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Article

Effects of Endurance Exercise Intensities on Autonomic and Metabolic Controls in Children with Obesity: A Feasibility Study Employing Online Exercise Training

by
Valeria Calcaterra
1,2,
Giuseppina Bernardelli
3,4,
Mara Malacarne
5,
Matteo Vandoni
6,
Savina Mannarino
7,
Vittoria Carnevale Pellino
6,8,
Cristiana Larizza
9,
Massimo Pagani
3,
Gianvincenzo Zuccotti
1,10 and
Daniela Lucini
3,5,*
1
Pediatric Unit, Pediatric Department, Buzzi Children’s Hospital, 20154 Milan, Italy
2
Department of Internal Medicine, University of Pavia, 27100 Pavia, Italy
3
Exercise Medicine Unit, Istituto Auxologico Italiano, IRCCS, 20135 Milan, Italy
4
DISCCO Department, University of Milan, 20122 Milan, Italy
5
BIOMETRA Department, University of Milan, 20129 Milan, Italy
6
Laboratory of Adapted Motor Activity (LAMA), Department of Public Health, Experimental Medicine and Forensic Science, University of Pavia, 27100 Pavia, Italy
7
Pediatric Cardiology Unit, Pediatric Department, Buzzi Children’s Hospital, 20154 Milan, Italy
8
Department of Industrial Engineering, University of Rome Tor Vergata, 00133 Rome, Italy
9
Department of Electrical, Computer and Biomedical Engineering, University of Pavia, 27100 Pavia, Italy
10
Department of Biomedical and Clinical Science, University of Milano, 20157 Milan, Italy
*
Author to whom correspondence should be addressed.
Nutrients 2023, 15(4), 1054; https://doi.org/10.3390/nu15041054
Submission received: 20 January 2023 / Revised: 9 February 2023 / Accepted: 16 February 2023 / Published: 20 February 2023

Abstract

:
Exercise is one of the major determinants of a healthy lifestyle, which is particularly important in childhood and serves as a powerful preventive tool. On the other hand, obesity and arterial hypertension rates are increasing in children, representing a huge risk for developing major cardiovascular and metabolic diseases in adult life. Of fundamental importance is the modality and volume of exercise required to obtain benefits. In this feasibility study, we considered a group of obese children, studied before and after a 12-week online exercise training program, and subdivided the participants into two groups considering the volume of exercise performed (above or below 1200 MET·min/week). This threshold level was applied in two different ways: subdivision A considered the total weekly physical activity volume (considering both time spent walking for at least 10 min consecutively and time spent performing structured exercise) and subdivision B considered only the weekly volume of structured exercise. We assessed autonomic and metabolic control and auxological and lifestyle parameters. We observed that the improved volume of structured exercise was associated with reduced arterial pressure percentile only in subdivision B and an improvement in markers of vagal and metabolic control was evident. Moreover, the 12-week online exercise training program, defined considering individual fitness level and progressively adapted as the goal was reached, proved to be sustainable from an economical and organizational point of view.

1. Introduction

Childhood and youth are ideally the best periods in life to instill healthy behaviors [1], thereby fostering wellbeing and preventing chronic non-communicable diseases (CNCD). On the other hand, overweight, obesity, and the prevalence of hypertension are increasing, particularly in the initial phases of life [2,3], thus determining a dramatic increase in the risk of diseases such as diabetes, coronary artery disease, and cancer [3,4]. Unhealthy lifestyles, such as poor nutrition and sedentariness, contribute to this phenomenon. Additionally, recent data show that obesity [5] and an unhealthy lifestyle, in particular sedentariness [6], are linked to poor prognosis in COVID-19 patients, thus expanding the role of lifestyle in determining health status further to CNCD.
Physical activity is one of the major determinants of a healthy lifestyle, in addition to healthy nutrition, not smoking, good sleep hygiene, and the capability to manage stress [7,8]. Regular physical activity is particularly important in childhood and youth as it grants immediate (improvement of wellbeing, scholastic performance, social relationships [9], etc.), and long-term benefits (prevention/treatment of many diseases), and it may be considered a sustainable tool [10] for the individual and environment. On the other hand, epidemiological data from the USA show that only 28.3% of youth aged 6 to 11 years are active for ≥60 min every day of the week, thus meeting more recent guideline recommendations [3,11,12,13], and this decreases to 16.5% of youth aged 12 to 17 years [4]. European Commission data show that 32.4% of Italian children aged 8–9 years are estimated to meet sufficient physical activity levels (considering WHO guidelines), and this percentage decreases to 11.9% of children aged 11 years old and further decreases to 6.8% of children aged 15 years old [14].
International guidelines [11,12,13] indicate that children and adolescents should perform moderate-to-vigorous intensity, mostly aerobic, physical activity at least an average of 60 min every day of the week and that vigorous-intensity aerobic activities, as well as activities that strengthen muscle and bone, should be incorporated at least 3 days a week. A recent paper [15] reported that a minimum of 20 min/day of vigorous endurance exercise may be best for maximizing cardiorespiratory fitness in adolescence, a parameter that a growing body of epidemiological and clinical evidence [16] considers to be a potentially strong predictor of mortality, showing that the intensity of endurance exercise may be a determinant of the beneficial effect of exercise programs.
Recent data on the association between walking pace and telomere length [17] (a parameter associated with chronic diseases and proposed as a marker of biological age) underlined the importance of exercise intensity, showing that only brisk walkers had significantly longer telomeres than slow walkers.
An exercise program, and a lifestyle program in general, may be considered efficacious only if it leads to an improvement of the underlying pathogenetic mechanisms that determine a disease or risk of developing a disease. The mechanisms that are potentially improved by exercise are multifarious and complex, ranging from improved immunological and metabolic profiles to an improvement in hemodynamics [1,4,7,8,11,16,18]. An amelioration in cardiac autonomic regulation (CAR, autonomic control of cardiovascular system) may also play an additional, but little recognized, beneficial role [19], generating a “risk factor gap” above and beyond usual treatments. Several chronic diseases, such as arterial hypertension and diabetes, are characterized in adulthood [20,21] and also in childhood and adolescence [22,23] by autonomic nervous system (ANS) impairment, which may be reversed by exercise training and/or healthy nutrition programs [10,22,24,25,26,27].
The literature is particularly rich with scientific data demonstrating that exercise may positively interfere with many mechanisms underlying chronic diseases, rendering it a well-recognized preventive and therapeutic tool [1,4,7,8,11,16,18,22,24,25,26,27,28]. However, the implementation of efficacious exercise programs is less defined [7,8,12,29]. Generally, programs that group children together, such as school-based programs or participation in team sports [12], are considered more effective than home-based exercise programs, since they also foster socialization and play an educational role. On the other hand, these approaches may present some economical and organizational barriers [30,31], such as the need for transportation to the gym or sports field, lack of parental support, cost, and family time management. These barriers may have a particular impact on families of low socio-economical level or in a country, such as Italy, where time spent at school is limited. Moreover, other important barriers, such as lack of skills, motivation, enjoinment, and peer support, as well as feeling shy about physical activity in public [31,32], need to be accounted for in the case of obese children and adolescents. Home-based exercise intervention programs may help in overcoming some of these barriers [33,34,35]. As previously reported [36], remote physical activity programs may provide a valuable strategy for fostering compliance with physical activity guidelines, representing an opportunity for pediatric subjects with obesity to stay healthy. On the other hand, their effectiveness may vary [12,33,37] according to the level of support granted by exercise professionals and the level of personalization of the proposed program.
The goal of this feasibility study was to verify the effectiveness on cardiac autonomic regulation and metabolic parameters of a supervised, home-based exercise program specifically designed to meet obese children’s needs and be enjoyable and sustainable from an economical and organizational point of view in order to facilitate acceptance and compliance. In particular, we assessed the autonomic and metabolic effects considering the volume of physical activity actually performed by children.

2. Materials and Methods

We consecutively enrolled 35 Caucasian children and adolescents (14 females/21 males) admitted to our pediatric outpatient clinic for obesity by their general practitioner or by their primary care pediatric consultant between March 2021 and December 2021. We studied them before (T0) and after (T1) a 12-week online exercise training protocol.
To be included in our study, the children must have been aged between 8 and 13 years, have a body mass index (BMI) z-score ≥ 2 (according to World Health Organization [38]), and have Italian language competency. The exclusion criteria were: known secondary obesity conditions, no comprehension of Italian language, cardiovascular and respiratory chronic diseases, orthopedic problems, and absolute contraindications to practicing physical activity.
This study was approved by the institutional ethics committee (Milano Area 1 protocol number 2020/ST/298, approval date 2 December 2020) and conducted in accordance with the Helsinki Declaration of 1975, as revised in 2008.Written consent was obtained by all participants or their responsible guardians once they were well informed about the study.

2.1. Clinical Evaluations

All children underwent the following assessments.

2.1.1. Clinical, Auxological, and Hemodynamic Assessment

In all patients, weight, height, waist circumference (WC), pubertal stage according to Marshall and Tanner [39,40], BMI, waist-to-height ratio (WHtR) [41], triponderal mass index [42], and visceral adiposity index (VAI) [43] were considered as adiposity indexes related to cardiometabolic risk [44]. A basal musculoskeletal assessment was employed in order to exclude the presence of musculoskeletal limitations to the exercise program. Weight was measured with patients not wearing shoes and in light clothing, standing upright in the center of the scale platform (Seca, Hamburg, Germany), facing the recorder, hands at the sides, and looking straight ahead. Standing height was measured using a Harpenden stadiometer (Holtain Ltd., Cross-well, Crymych, UK) with a fixed vertical backboard and adjustable headpiece [44].
WC was performed in the horizontal plane midway between the lowest ribs and iliac crest, using a flexible inch tape [44].
BMI was calculated as body weight (kilograms) divided by height (meters squared) and was transformed into BMI z-scores using WHO reference values [38].
Other adiposity indexes were calculated as follows [42,43]:
WHtR = WC/Ht
TMI = weight (kg)/height (m)3
VAI
Male = [WC/(39.68  +  (1.88 × BMI))] × (TG/1.03) × (1.31/HDL-C);
Female = [WC/(36.58  +  (1.89 × BMI))] × (TG/0.81) × (1.52/HDL-C)
Pubertal stages according to Tanner were classified as follows: prepubertal stage 1 = Tanner 1; middle puberty stage 2 = Tanner 2–3; and late puberty stage 3 = Tanner 4–5 [39,40].
Systolic arterial pressure (SAP) and diastolic arterial pressure (DAP) were measured twice, in the supine position, using an electronic mercury sphygmomanometer (A & D Medical, Tokyo, Japan) with an appropriately sized cuff on the right arm after 5 min of rest [45]; the second measurement was used for analysis. We determined the blood pressure percentile for each child, following recent guidelines [46,47,48]. Moreover, every child underwent a basal electrocardiogram and echocardiogram in order to verify the absence of main cardiac diseases that might contraindicate or limit exercise training, particularly at high intensities.

2.1.2. Metabolic Assessment

A blood sample for the evaluation of fasting blood glucose (FBG), total cholesterol (TOT Cho), high-density lipoprotein (HDL C) cholesterol, triglycerides (TG), and insulin was obtained in fasting state between 8:30 and 9:00 a.m. and analyzed the same morning by standard methods (Advia XPT, Siemens Healthcare). As a surrogate of insulin resistance (IR), we considered the homeostasis model assessment (HOMA-IR) calculated as insulin resistance = (insulin × glucose)/22.5 [49] and the triglyceride and glucose (TyG) index was calculated as ln[fasting triglycerides (mg/dL) × fasting plasma glucose (mg/dL)/2 ]) [50].

2.1.3. Lifestyle Assessment

An ad hoc questionnaire was employed to quantify lifestyle [51,52,53,54,55]:
-
Nutrition was assessed using the American Heart Association Healthy Diet Score (AHA score) [8], taking into consideration fruit/vegetables, fish, sweetened beverages, whole grain, and sodium consumption (assessment of the latter was adapted to Italian eating habits) [55].
-
The lifestyle questionnaire inquired also about hours of sleep/day, hours of sedentariness/week, and perceptions of quality of sleep, health, and school performance (assessed using evaluation scales from 0 (‘worst quality’) to 10 (‘best quality’) for each measure).
-
Physical activity (total activity volume) was assessed by a modified version of the commonly employed short version of the International Physical Activity Questionnaire (IPAQ) [52,53], which focuses on intensity (nominally estimated in metabolic equivalents (METs) according to the type of activity) and duration (in min) of physical activity. We decided to employ this questionnaire, even if it was designed for adults, because it has the advantage of furnishing a numeric parameter of exercise volume (expressed in METs) capable of reflecting the total exercise volume.
We considered the following levels: brisk walking (≈3.3 METs), other activities of moderate intensity (≈4.0 METs), and activities of vigorous intensity (≈8.0 METs).
In accordance with current guidelines [11,12], these levels were used to assess the weekly exercise volume, using the following equations:
(METsTOT) Total weekly physical activity volume [MET·min/week] = (3.3 × minutes of brisk walking × days of brisk walking) + (4.0 × minutes of other moderate intensity activity × days of other moderate intensity activities) + (8.0 × minutes of vigorous intensity activity × days of vigorous intensity activity).
(METsMV) Weekly physical activity volume calculated only considering other activities of moderate intensity and activities of vigorous intensity [MET·min/week] = (4.0 × minutes of other moderate intensity activity × days of other moderate intensity activities) + (8.0 × minutes of vigorous intensity activity × days of vigorous intensity activity). METsMV may be considered as the total weekly volume of structured exercise.
The population of our study was subdivided into two groups: those reaching the physical activity goals suggested by the latest guidelines [11,12], corresponding to at least an average of 60 min/day of moderate-to-vigorous intensity, mostly aerobic, physical activity (above 1200 MET·min/week, and those who did not reach the physical activity goals (below 1200 MET·min/week. Accordingly, we considered the physical activity volume reached at the end of the training.
The threshold level of 1200 MET·min/week was obtained in two different ways:
-
Subdivision A considered the total weekly physical activity volume (METsTOT), i.e., considering both time spent walking (at least for 10 min consecutively) and time spent performing structured exercise (other moderate intensity activities and vigorous intensity activities)
-
Subdivision B considered only the weekly volume of structured exercise (METsMV) (only other moderate intensity activities and vigorous intensity activities).
The results considering these two different subdivisions are reported respectively in Table 1 and Table 2.
We considered these two different subdivisions in order to unveil the possible different effects associated with structured exercise (generally of higher intensity) or with physical activities of less intensity, such as walking.
All children were equipped with an activity tracker (Fitbit Charge 2 ©, Fitbit Inc, San Francisco, CA, USA) to monitor their heart rate during the day and during the supervised training sessions.

2.1.4. Physical Fitness (PF) Assessment

Prior to starting the training program, all the children were tested for cardiovascular fitness, as follows:
-
Six-minute walk test (6MWT). This field test is considered a valid and reliable tool for measuring PF in children and is widespread, has inexpensive equipment, and is easy to administer in a clinical setting [56]. The 6MWT was performed according to international administration guidelines [57]. The children were instructed by the trainers to walk the greatest distance possible while maintaining their own pace. Standardized encouragement and information about the remaining time were given to the children every minute; for example, “you are doing well” or “keep up the good work” [58]. Children were permitted to stop (if required) during the test but were instructed to resume walking once able and the covered distance was registered in meters. Test-retest reliability was undertaken, and the intraclass correlation coefficient (95% confidence interval) was calculated as 0.94 (0.89–0.96).
-
After an adequate recovery time, children were interviewed by the same investigator to assess perceived physical fitness and physical activity level, respectively, using the International Fitness Enjoyment Scale (IFIS) and Physical Activity Questionnaire for Older Children (PAQ-C) questionnaires.
-
The International Fitness Enjoyment Scale (IFIS) questionnaire is a self-reported, easy, and rapid fitness scale previously validated in several European countries and languages. It describes physical fitness as an indicator of physical competence [59]. The IFIS is composed of a 5-point Likert scale (from 1 ‘very poor’ to 5 ‘very good’), with questions focused on five areas of fitness: general fitness, cardiorespiratory, strength, speed-agility, and flexibility. The IFIS has high validity and moderate-to-good reliability (average weighted Kappa: 0.70 and 0.59) for school-aged children.
-
The Physical Activity Questionnaire for Older Children (PAQ-C) evaluates the weekly amount of physical activity reported by children. This questionnaire was verified to be adequate for school-aged children (approximate ages between 8 and 14). The PAQ-C is recognized as a valid and reliable measurement of general physical activity level from childhood to adolescence. The PAQ-C utilizes cues such as break time at school and evening physical activity to ameliorate the recall ability of children. The PAQ-C is cost- and time-efficient, simple to administer, and displays normal distribution properties. The PAQ-C is shown to have good reliability and an intraclass correlation (ICC) = 0.96 [60].

2.1.5. Cardiac Autonomic Regulation (CAR) Assessment

On the day of autonomic evaluation, all subjects arrived at the clinic avoiding caffeinated beverages since awakening as well as heavy physical exercise in the preceding 24 h. Recordings were performed between 04:00 am and 06:00 pm in an air conditioned, quiet room. After a preliminary 10-min rest period in the supine position, electrocardiogram (ECG) and respiratory activity (piezoelectric belt) were continuously recorded over a minimum 5-min period using a two-way radiotelemetry system (Marazza, Monza Italy). Subsequently, subjects were asked to stand up unaided and remain in the upright position for 5 min, during which recordings were maintained. Data were acquired with a PC at 250 samples/second using a custom built software tool (HeartScope) that automatically provided a series of indices describing heart rate variability (HRV) in the time domain: RR interval (in msec) and RR interval variability (RRTP) (assessed as total power, i.e., variance, in msec2), taken as simple classifiers typical of vagal control [21,61,62]. A series of indices were also provided in the frequency domain: autoregressive spectral components both in the low frequency (LF, center frequency ≈ 0.1 Hz) and high frequency (HF, centered with respiration, ≈0.25 Hz) (assessed in msec2 as well as in normalized units [nu]) and markers of prevalent sympathetic and vagal activities, indicating sinoatrial node function [21,62].
Based on all of these assessments before starting the training, a medical exercise prescription defining the modality, intensity, duration, frequency, and progression of exercise was created for each participant, who were individually followed by exercise physiologists using a Zoom online platform.

2.2. Exercise Training Protocol

Children performed a 12-week online training program supervised by two sport specialists using the Zoom online platform (California, USA). The training protocol consisted of three 60-min sessions per week, over 12 weeks, for a total of 36 sessions. Each session was streamed in real-time using the Zoom platform, which allowed live interaction among the instructors and children. Two sport specialists supervised every training session, which usually consisted of different typology and intensity of exercises, defined considering individual fitness levels and progressively adapted as each individual reached the goal. In detail, all sessions were divided into three sub-sessions: an initial warm-up of approximately 5 min to ensure the correct preparation of the children for the subsequent exercises, the main training that consisted of a combination of aerobic and muscular routines for approximately 50 min, and a final part of cool down of approximately 5 min to ensure the return of the body to the rest condition. The exercise physiologist recorded that the training session was actually performed by the child. All the proposed exercises were playful and recreative activities; for example, we proposed motor and active fabulation, dancing to music, imitation games, circuit training in a playful way, playing with small objects such as balls, books, pencils, and paper, and paths through the furniture. The activities started from low intensity and progressed through the training to moderate and high intensities with values of maximum heart rate ranging from 50% to 80%, as calculated using the Tanaka equation [63] after clinical verification that no cardiovascular contraindications were present for the execution of vigorous exercise. Shorter bouts of yoga and mindfulness were proposed as cool-down activities [64]. The main goal of the intervention was to administer a simple and enjoyable online training sessions with interaction and adaptable loads that were affordable and sustainable for families and had no cost or transportation difficulties. Starting 30 min from the beginning of the session, the trainers acquired the children’s heart rates in order to control the intensity of the training using the Fitbit Charge 2 © (Fitbit Inc, San Francisco, CA, USA).
To better comply with the guidelines [11,12] recommending 60 min of moderate-to-vigorous exercise per day for children and adolescents, we provided a dedicated YouTube channel “LAMA Junior” with adapted exercise routines for days without supervised training [34]. See Figure 1.
Throughout the exercise program, patients were asked to maintain a healthy diet but no standard modifications were made.

2.3. Statistical Analysis

Data are presented as the median (25–75 percentile). The significance of differences was assessed with repeated measures GLM (General Linear Model), considering group and intervention as factors. Differences in pubertal stage between T0 and T1 were assessed using the Chi-squared test. Bivariate Pearson’s correlation analysis was employed with two-tailed significance.
Computations were performed using IBM SPSS Statistics for Windows, version 27 (IBM Corp., Armonk, NY, USA) with a PC (DELL). A value of p < 0.05 was taken as the threshold for statistical significance.

3. Results

Throughout the program period, no significant changes in pubertal stage were noted. (Stage 1 = 19 vs. 17, Stage 2 = 6 vs. 8, Stage 3 = 10 vs. 10, p = 0.82).
As specified in the methods, we subdivided the population into two groups: those reaching the physical activity goals suggested by the latest guidelines (corresponding to at least an average of 60 min/day of moderate-to-vigorous intensity, mostly aerobic, physical activity, i.e., above 1200 MET·min/week) and those who did not reach the physical activity goals (i.e., below 1200 MET·min/week).
Table 1 reports the results of subdivision A considering the total weekly physical activity volume (METsTOT) (i.e., both time spent walking and time spent performing structured exercise), while Table 2 reports the results of subdivision B considering only the weekly volume of structured exercise (METsMV). The tables report data before (T0) and after (T1) exercise intervention.

3.1. Clinical, Auxological, Hemodynamical and Metabolic Data

Subdivision A showed that significant differences were present between conditions in clinical auxological parameters (BMI z-score p = 0.004 and TMI p < 0.001) and between groups in metabolic parameters (total cholesterol p = 0.048). No significant differences were noted regarding systolic arterial pressure, diastolic arterial pressure percentile, and heart rate. Similarly, there was no difference in autonomic parameters for RRV.
Subdivision B showed significant differences between conditions in clinical auxological parameters (BMI z-score p = 0.033, TMI p = 0.003, and VAI p = 0.012) and metabolic parameters (total cholesterol p = 0.048), with an interaction for HOMA-IR (p = 0.05) and VAI (p = 0.048). No significant differences were noted regarding systolic arterial pressure, diastolic arterial pressure percentile, and heart rate. Borderline significance was noted in RR interval (p = 0.062).

3.2. Lifestyle Data

No significant differences were noted in subdivisions A and B regarding hours sleep/day and school performance. Quality of sleep and health perceptions were slightly different between groups in subdivision A. Hours of sedentariness/week was slightly different between groups in subdivisions A and B. The AHA score (quality of nutrition index) was slightly different between groups only in subdivision B, and it improved after training. As expected, the volume of performed physical activity was significantly increased after intervention in both subdivisions A and B (p = 0.008 and p < 0.001, respectively). Interestingly, in both subdivisions, the subjects who performed higher volumes of physical activity after intervention were also characterized by higher volumes of physical activity before intervention (p < 0.001 and p = 0.012, respectively), with significant interaction (p = 0.030 and p = 0.012, respectively), suggesting that the increase was significantly higher in group 2 for both subdivisions.

3.3. Physical Fitness Assessment Data

The covered distance of 6MWT and PAQ-C score were significantly increased after intervention in groups 1 and 2, for both subdivisions A and B. No significant differences between groups or conditions were observed in the IFIS score for both subdivisions A and B.

3.4. Cardiac Autonomic Regulation Data

No significant differences between groups or condition were observed in any of the autonomic variables in subdivision A.
Subdivision B unveiled an interaction effect in RRHFnu (marker of prevalent vagal modulation of the sinoatrial node) and LF/HF ratio, being slightly increased only in those subjects who performed higher volumes of structured exercise.
Table 3 reports the Pearson’s correlations among changes (Δ) between T0 and T1 for the major variables. Notably, ΔMETsTOT was correlated, as expected, with ΔRRTP (change in total variance of heart rate variability), while ΔMETsMV was significantly correlated not only with ΔRRTP but also with ΔRR (change in RR interval) and ΔHFnu. Moreover, ΔMETsMV was significantly correlated (r = −0.400, p = 0.017) with Δ SAPpc (change in percentile of systolic arterial pressure), suggesting that only structured exercise was associated with a reduction of the percentile of SAP. Additionally, ΔRRTP and ΔRR were significantly correlated with ΔSAPpc.

4. Discussion

In this feasibility study, we observed that only the improvement in the volume of structured exercise was associated with the reduction in arterial pressure percentile and improvement of markers of vagal control in obese children. Moreover, structured exercise improved the auxological and metabolic parameters. The increase in volume of structured exercise was obtained through a 12-week exercise training protocol delivered online by exercise physiologists [34,54], using an individualized exercise prescription that was progressively adapted as each individual reached their goal and was specifically designed to meet the needs of obese children and their families, while being economically and organizationally sustainable.
The beneficial effects of exercise are well reported in the literature and exercise is now considered a mandatory preventive and therapeutic strategy in all CNCD, particularly in youth [11,12,13], as underlined in the introduction. Of fundamental importance is the dose/volume of physical activity required to obtain such benefits. While international guidelines [11,12,13] clearly indicate the volume of required physical activity and the need to perform moderate and vigorous exercise at a young age, their practical translation into everyday life is sometimes less specific. Simply walking or practicing sports, without paying attention to the volume and particularly the intensity of exercise, is considered efficacious. This phenomenon is well emblemized by the importance given to the number of steps walked every day [65] independent of the speed of walking. On the contrary, the literature shows that the benefits of endurance exercise are also linked to the level of cardiorespiratory fitness [15,16] in children and that only brisk walkers had significantly longer telomeres than slow walkers among adults [17], thereby showing a direct correlation between exercise intensity and longevity. In this paper, we observed that only the volume of exercise due to structured moderate-to-vigorous intensity exercise was associated with improved cardiac autonomic control, reduced systolic arterial pressure, and improved auxologic and metabolic parameters. Of particular interest is the reduction in the HOMA-IR index, which suggested reduced insulin resistance after training, confirming the relevant influence of different types of exercise on insulin resistance [66]. In contrast, we observed only a slight change in the auxologic parameters, such as BMI z-score and TMI, considering that the MET count also included METs linked to simple walking for more than 10 min.
The data in our study, albeit preliminary, suggest that only structured exercise was capable of inducing an improvement in autonomic and metabolic control. Of particular interest is the observation that the change in the SAP percentile with training was associated with the change in structured exercise volume and changes in ANS variable markers of vagal control. Arterial hypertension is a condition that characterizes childhood obesity [2,3,6] and increases the risk of major cardiovascular disease over the lifespan. Many studies have demonstrated that exercise is a powerful tool to prevent/treat arterial hypertension and obesity [11,12,13]. The data in the current study corroborate previous observations in which improved autonomic cardiac regulation was among the benefits of exercise in the management of hypertension and obesity [10,22,24,25,26,27].
Another interesting point to discuss is the methodology employed to help children with obesity become physically active. Participation in team sports or programs that generally group children together are considered more effective, but they may present some practical barriers (economical, organizational, and psychological), as reported in the introduction. In this paper, we observed that a home-based, online exercise training program could overcome, albeit in part, these barriers, and could be enjoyable and sustainable from an economical and organizational point of view, thus facilitating acceptance and compliance of children and their families. This observation was corroborated by 86% of children in our study remaining in the program after completing the final evaluations.
In addition, the possibility of starting exercise at home, thus avoiding interaction with peers while improving their physical performance, may result in an improvement of self-efficacy [67] and, consequently, motivate obese children to exercise in a different environment close to their peers. A fundamental characteristic of the employed protocol [34] was the balance between the possibility of being delivered online and tailoring the proposed modality/intensity of exercises to the child’s needs, preferences, and reached goals [54]. An individualized clinical assessment and exercise prescription was essential to the achievement of this goal, which required exercise physiologists to interact online with children, design enjoyable exercises, and adjust the program during the training period. In contrast [12,37,68], home-base exercise programs that were not tailored to individual needs showed poor or no efficacy in previous studies.
In this observational study, we also observed that children with obesity who significantly increased their exercise volume through the intervention program were already characterized by higher exercise volumes and less sedentary hours (considering both subdivisions) before starting the intervention program. This finding suggests that other factors, in addition to the methodology employed in the exercise program, need to be considered, such as psychological and social conditions [9,67]. Although we do not have data to support this hypothesis, we observed that the group of children who actually increased their exercise volume in subdivision A were characterized before the intervention by slightly higher health and quality of sleep perceptions.
Throughout the exercise program, children with obesity were asked to maintain a healthy diet but no standard modifications were made. Nevertheless, the group of subjects who significantly increased the volume of structured exercise was also characterized by a higher AHA score, suggesting an improvement in the quality of nutrition. Further supporting the hypothesis expressed in the previous paragraph, we also observed that this group was characterized by better AHA scores before the intervention.
Some limitations of this study must be acknowledged. First, this study was an observational feasibility study and the group size was small, thus limiting the interpretative value of the results. Additionally, we did not consider a control group (subjects studied before and after sham intervention). Nevertheless, we observed in other studies that sham interventions did not induce modifications of the autonomic nervous system per se [69,70], corroborating the idea that the observed changes were attributable to functional remodeling. Second, only 19 children (54.29%) wore the activity tracker both during the day and during the training sessions and were considered for the specific analysis. Interestingly, we observed a significant correlation (r = 0.445, p = 0.049) between the total steps recorded by the tracker and the total volume of structured exercise (METsMV), while no significant correlation (r = 0.235, p = 0.3.19) was observed with the total volume of physical activity (METsTOT). Third, the children’s diets were not standardized, allowing for a potential bias. Moreover, we did not have data regarding immunological control (another main control system that plays an important role in cardiometabolic conditions) and psychological and social aspects. These are important factors to consider when studying the effects of intervention programs in subjects with obesity. In addition, the intervention lasted only 12 weeks and we do not have data regarding the long-lasting effects of our model. Therefore, in view of the small number of subjects and overall feasibility of the design, generalizing the results is not possible.

5. Conclusions

In conclusion, this study showed the feasibility of an online exercise program as a practical tool to improve cardiac autonomic control and hemodynamic, metabolic, and auxological parameters in a group of children with obesity, rendering it a valuable strategy for fostering compliance with physical activity guidelines and providing an opportunity for pediatric subjects with obesity to stay healthy, thus managing the increased risk of CNCD. Moreover, by guaranteeing that an adequate level of exercise intensity was reached, this study underlines the importance of structured exercise in obtaining significant health benefits. The benefits of exercise overcome those of “simple” weight reduction (which in this study was present when considering subdivision A), which are also linked to improvements in important endocrine and autonomic control mechanisms (which in this study was evident when considering subdivision B). In addition, the ability of exercise to affect control mechanisms, particularly cardiac autonomic control, seems only to be evident if exercise reaches an adequate intensity, i.e., even at the same exercise volume (1200 METs), the effect may differ depending on the intensity of the exercise performed. With this in mind, we have to consider that this was a feasibility study. Therefore, the capability of the exercise program to affect CAR and its economical/organizational sustainability must be verified. On the basis of the present observations, larger and longer lasting studies aimed at confirming these preliminary satisfactory data seem justified.

Author Contributions

Conceptualization, D.L., V.C. and M.V.; methodology, D.L., M.P., M.V., V.C.P., V.C. and G.Z.; software, D.L., M.P., M.V. and C.L.; formal analysis, D.L., G.B. and M.M.; investigation, D.L., G.B., M.M., V.C.P., V.C. and S.M.; resources, D.L., G.Z., M.V., D.L., M.M. and G.B.; writing—original draft preparation, D.L. and M.P.; writing—review and editing, D.L., G.B., M.M., M.V., V.C.P., V.C., S.M., C.L., G.Z. and M.P.; supervision, D.L., V.C., G.Z. and M.V.; project administration, M.V. and D.L.; funding acquisition, D.L. and G.Z. All authors have read and agreed to the published version of the manuscript.

Funding

This research was partially funded by the Italian Ministry of Health.

Institutional Review Board Statement

This study were approved by the institutional ethics committee (Milano Area 2 proto-col number 2020/ST/298, approval date 2 December 2020).

Informed Consent Statement

Written consent was obtained by all participants or their responsible guardians once they were well informed about the study.

Data Availability Statement

Data will be available on justified request. We have not yet uploaded the data because they are part of an ongoing study on the effects of exercise in children and other papers may be prepared using them.

Acknowledgments

We thank Fitbit Inc., San Francisco, CA, USA to have furnished activity trackers (Fitbit Charge 2 ©).

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Turco, J.V.; Inal-Veith, A.; Fuster, V. Cardiovascular health promotion: An issue that can no longer wait. J. Am. Coll. Cardiol. 2018, 72, 908–913. [Google Scholar] [CrossRef] [PubMed]
  2. Song, P.; Zhang, Y.; Yu, J.; Zha, M.; Zhu, Y.; Rahimi, K.; Rudan, I. Global Prevalence of Hypertension in Children: A Systematic Review and Meta-analysis. JAMA Pediatr. 2019, 173, 1154–1163. [Google Scholar] [CrossRef]
  3. Hampl, S.E.; Hassink, S.G.; Skinner, A.C.; Armstrong, S.C.; Barlow, S.E.; Bolling, C.F.; Avila Edwards, K.C.; Eneli, I.; Hamre, R.; Joseph, M.M.; et al. Clinical Practice Guideline for the Evaluation and Treatment of Children and Adolescents With Obesity. Pediatrics 2023, 151, e2022060640. [Google Scholar] [CrossRef] [PubMed]
  4. Tsao, C.W.; Aday, A.W.; Almarzooq, Z.I.; Alonso, A.; Beaton, A.Z.; Bittencourt, M.S.; Boehme, A.K.; Buxton, A.E.; Carson, A.P.; Commodore-Mensah, Y.; et al. Heart Disease and Stroke Statistics—2022 Update: A Report From the American Heart Association. Circulation 2022, 145, e153–e639. [Google Scholar] [CrossRef] [PubMed]
  5. Gao, M.; Wang, Q.; Piernas, C.; Astbury, N.M.; Jebb, S.A.; Holmes, M.V.; Aveyard, P. Associations between body composition, fat distribution and metabolic consequences of excess adiposity with severe COVID-19 outcomes: Observational study and Mendelian randomisation analysis. Int. J. Obes. 2022, 46, 943–950. [Google Scholar] [CrossRef] [PubMed]
  6. Sallis, R.; Young, D.R.; Tartof, S.Y.; Sallis, J.F.; Sall, J.; Li, Q.; Smith, G.N.; Cohen, D.A. Physical inactivity is associated with a higher risk for severe COVID-19 outcomes: A study in 48 440 adult patients. Br. J. Sports Med. 2021, 55, 1099–1105. [Google Scholar] [CrossRef] [PubMed]
  7. Artinian, N.T.; Fletcher, G.F.; Mozaffarian, D.; Kris-Etherton, P.; Van Horn, L.; Lichtenstein, A.H.; Kumanyika, S.; Kraus, W.E.; Fleg, J.L.; Redeker, N.S.; et al. Interventions to Promote Physical Activity and Dietary Lifestyle Changes for Cardiovascular Risk Factor Reduction in Adults: A scientific statement from the American Heart Association. Circulation 2010, 122, 406–441. [Google Scholar] [CrossRef] [Green Version]
  8. Lloyd-Jones, D.M.; Hong, Y.; Labarthe, D.; Mozaffarian, D.; Appel, L.J.; Van Horn, L.; Greenlund, K.; Daniels, S.; Nichol, G.; Tomaselli, G.F.; et al. Defining and setting national goals for cardiovascular health promotion and disease reduction: The American heart association’s strategic impact goal through 2020 and beyond. Circulation 2010, 121, 586–613. [Google Scholar] [CrossRef] [Green Version]
  9. Centers for Disease Control and Prevention. The Association Between School-Based Physical Activity, Including Physical Education, and Academic Performance; US Department of Health and Human Services: Atlanta, GA, USA, 2010.
  10. Jackson, T.; Dixon, J. The New Zealand Resource Management Act: An exercise in delivering sustainable development through an ecological modernisation agenda. Environ. Plan. B Plan. Des. 2007, 34, 107–120. [Google Scholar] [CrossRef]
  11. Chaput, J.-P.; Willumsen, J.; Bull, F.; Chou, R.; Ekelund, U.; Firth, J.; Jago, R.; Ortega, F.B.; Katzmarzyk, P.T. 2020 WHO guidelines on physical activity and sedentary behaviour for children and adolescents aged 5–17 years: Summary of the evidence. Int. J. Behav. Nutr. Phys. Act. 2020, 17, 141. [Google Scholar] [CrossRef]
  12. Wyszyńska, J.; Ring-Dimitriou, S.; Thivel, D.; Weghuber, D.; Hadjipanayis, A.; Grossman, Z.; Ross-Russell, R.; Dereń, K.; Mazur, A. Physical Activity in the Prevention of Childhood Obesity: The Position of the European Childhood Obesity Group and the European Academy of Pediatrics. Front. Pediatr. 2020, 8, 662. [Google Scholar] [CrossRef] [PubMed]
  13. Steinberger, J.; Daniels, S.R.; Hagberg, N.; Isasi, C.R.; Kelly, A.S.; Lloyd-Jones, D.; Pate, R.R.; Pratt, C.; Shay, C.M.; Towbin, J.A.; et al. Cardiovascular Health Promotion in Children: Challenges and Opportunities for 2020 and Beyond: A Scientific Statement From the American Heart Association. Circulation 2016, 134, e236–e255. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  14. Available online: https://www.euro.who.int/__data/assets/pdf_file/0009/513756/Physical-activity-2021-Italy-eng.pdf (accessed on 12 January 2023).
  15. Burden, S.J.; Weedon, B.D.; Turner, A.; Whaymand, L.; Meaney, A.; Dawes, H.; Jones, A. Intensity and Duration of Physical Activity and Cardiorespiratory Fitness. Pediatrics 2022, 150, e2021056003. [Google Scholar] [CrossRef]
  16. Ross, R.; Blair, S.N.; Arena, R.; Church, T.S.; Despres, J.P.; Franklin, B.A.; Haskell, W.L.; Kaminsky, L.A.; Levine, B.D.; Lavie, C.J.; et al. Importance of Assessing Cardiorespiratory Fitness in Clinical Practice: A Case for Fitness as a Clinical Vital Sign: A Scientific Statement from the American Heart Association. Circulation 2016, 134, e653–e699. [Google Scholar] [CrossRef]
  17. Dempsey, P.C.; Musicha, C.; Rowlands, A.V.; Davies, M.; Khunti, K.; Razieh, C.; Timmins, I.; Zaccardi, F.; Codd, V.; Nelson, C.P.; et al. Investigation of a UK biobank cohort reveals causal associations of self-reported walking pace with telomere length. Commun. Biol. 2022, 5, 381. [Google Scholar] [CrossRef] [PubMed]
  18. Fiuza-Luces, C.; Santos-Lozano, A.; Joyner, M.; Carrera-Bastos, P.; Picazo, O.; Zugaza, J.L.; Izquierdo, M.; Ruilope, L.M.; Lucia, A. Exercise benefits in cardiovascular disease: Beyond attenuation of traditional risk factors. Nat. Rev. Cardiol. 2018, 15, 731–743. [Google Scholar] [CrossRef]
  19. Joyner, M.J.; Green, D.J. Exercise protects the cardiovascular system: Effects beyond traditional risk factors. J. Physiol. 2009, 587, 5551–5558. [Google Scholar] [CrossRef] [PubMed]
  20. Esler, M.; Rumantir, M.; Wiesner, G.; Kaye, D.; Hastings, J.; Lambert, G. Sympathetic nervous system and insulin resistance: From obesity to diabetes. Am. J. Hypertens. 2001, 14, S304–S309. [Google Scholar] [CrossRef] [Green Version]
  21. Lucini, D.; Mela, G.S.; Malliani, A.; Pagani, M. Impairment in cardiac autonomic regulation preceding arterial hypertension in humans: Insights from spectral analysis of beat-by-beat cardiovascular variability. Circulation 2002, 106, 2673–2679. [Google Scholar] [CrossRef] [Green Version]
  22. Lucini, D.; Zuccotti, G.; Malacarne, M.; Scaramuzza, A.; Riboni, S.; Palombo, C.; Pagani, M. Early Progression of the Autonomic Dysfunction Observed in Pediatric Type 1 Diabetes Mellitus. Hypertension 2009, 54, 987–994. [Google Scholar] [CrossRef] [Green Version]
  23. Calcaterra, V.; Palombo, C.; Malacarne, M.; Pagani, M.; Federico, G.; Kozakova, M.; Zuccotti, G.; Lucini, D. Interaction between Autonomic Regulation, Adiposity Indexes and Metabolic Profile in Children and Adolescents with Overweight and Obesity. Children 2021, 8, 686. [Google Scholar] [CrossRef] [PubMed]
  24. Grassi, G.; Seravalle, G.; Colombo, M.; Bolla, G.; Cattaneo, B.M.; Cavagnini, F.; Mancia, G. Body Weight Reduction, Sympathetic Nerve Traffic, and Arterial Baroreflex in Obese Normotensive Humans. Circulation 1998, 97, 2037–2042. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Soares-Miranda, L.; Sattelmair, J.; Chaves, P.; Duncan, G.E.; Siscovick, D.S.; Stein, P.K.; Mozaffarian, D. Physical Activity and Heart Rate Variability in Older Adults: The Cardiovascular Health Study. Circulation 2014, 129, 2100–2110. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  26. Lucini, D.; Milani, R.V.; Costantino, G.; Lavie, C.J.; Porta, A.; Pagani, M. Effects of cardiac rehabilitation and exercise training on autonomic regulation in patients with coronary artery disease. Am. Heart J. 2002, 143, 977–983. [Google Scholar] [CrossRef] [Green Version]
  27. Lucini, D.; Zuccotti, G.V.; Scaramuzza, A.; Malacarne, M.; Gervasi, F.; Pagani, M. Exercise might improve cardiovascular autonomic regulation in adolescents with type 1 diabetes. Acta Diabetol. 2012, 50, 341–349. [Google Scholar] [CrossRef]
  28. Calcaterra, V.; Vandoni, M.; Rossi, V.; Berardo, C.; Grazi, R.; Cordaro, E.; Tranfaglia, V.; Pellino, V.C.; Cereda, C.; Zuccotti, G. Use of Physical Activity and Exercise to Reduce Inflammation in Children and Adolescents with Obesity. Int. J. Environ. Res. Public Health 2022, 19, 6908. [Google Scholar] [CrossRef]
  29. Lucini, D.; Pagani, M. Exercise Prescription to Foster Health and Well-Being: A Behavioral Approach to Transform Barriers into Opportunities. Int. J. Environ. Res. Public Health 2021, 18, 968. [Google Scholar] [CrossRef]
  30. Abu-Omar, K.; Messing, S.; Sarkadi-Nagy, E.; Kovács, V.A.; Kaposvari, C.; Brukało, K.; Hassapidou, M.; Janssen, D.; Sandu, P.; Tecklenburg, E.; et al. Barriers, facilitators and capacities for childhood obesity prevention in 12 European Union Member States: Results of a policy-maker survey. Public Health Panor. 2018, 4, 360–367. [Google Scholar]
  31. Shahsanai, A.; Bahreynian, M.; Fallah, Z.; Hovsepian, S.; Kelishadi, R. Perceived barriers to healthy lifestyle from the parental perspective of overweight and obese students. J. Educ. Health Promot. 2019, 8, 79. [Google Scholar] [CrossRef]
  32. Zabinski, M.F.; Saelens, B.E.; Stein, R.; Hayden-Wade, H.A.; Wilfley, D.E. Overweight Children’s Barriers to and Support for Physical Activity. Obes. Res. 2003, 11, 238–246. [Google Scholar] [CrossRef]
  33. Kirwan, M.; Chiu, C.L.; Laing, T.; Chowdhury, N.; Gwynne, K. A Web-Delivered, Clinician-Led Group Exercise Intervention for Older Adults with Type 2 Diabetes: Single-Arm Pre-Post Intervention. J. Med. Internet Res. 2022, 24, e39800. [Google Scholar] [CrossRef] [PubMed]
  34. Calcaterra, V.; Iafusco, D.; Pellino, V.C.; Mameli, C.; Tornese, G.; Chianese, A.; Cascella, C.; Macedoni, M.; Redaelli, F.; Zuccotti, G.; et al. “CoVidentary”: An online exercise training program to reduce sedentary behaviours in children with type 1 diabetes during the COVID-19 pandemic. J. Clin. Transl. Endocrinol. 2021, 25, 100261. [Google Scholar] [CrossRef] [PubMed]
  35. Calcaterra, V.; Verduci, E.; Vandoni, M.; Rossi, V.; Di Profio, E.; Pellino, V.C.; Tranfaglia, V.; Pascuzzi, M.C.; Borsani, B.; Bosetti, A.; et al. Telehealth: A Useful Tool for the Management of Nutrition and Exercise Programs in Pediatric Obesity in the COVID-19 Era. Nutrients 2021, 13, 3689. [Google Scholar] [CrossRef] [PubMed]
  36. Vandoni, M.; Pellino, V.C.; Gatti, A.; Lucini, D.; Mannarino, S.; Larizza, C.; Rossi, V.; Tranfaglia, V.; Pirazzi, A.; Biino, V.; et al. Effects of an Online Supervised Exercise Training in Children with Obesity during the COVID-19 Pandemic. Int. J. Environ. Res. Public Health 2022, 19, 9421. [Google Scholar] [CrossRef] [PubMed]
  37. Showell, N.N.; Fawole, O.; Segal, J.; Wilson, R.F.; Cheskin, L.J.; Bleich, S.N.; Wu, Y.; Lau, B.; Wang, Y. A Systematic Review of Home-Based Childhood Obesity Prevention Studies. Pediatrics 2013, 132, e193–e200. [Google Scholar] [CrossRef] [Green Version]
  38. Available online: https://www.who.int/tools/child-growth-standards (accessed on 12 January 2023).
  39. Marshall, W.A.; Tanner, J.M. Variations in the Pattern of Pubertal Changes in Boys. Arch. Dis. Child. 1970, 45, 13–23. [Google Scholar] [CrossRef] [Green Version]
  40. Marshall, W.A.; Tanner, J.M. Variations in pattern of pubertal changes in girls. Arch. Dis. Child. 1969, 44, 291–303. [Google Scholar] [CrossRef] [Green Version]
  41. Maffeis, C.; Banzato, C.; Talamini, G.; Obesity Study Group of the Italian Society of Pediatric Endocrinology and Diabetology. Waist–to–Height Ratio, a Useful Index to Identify High Metabolic Risk in Overweight Children. J. Pediatr. 2008, 152, 207–213. [Google Scholar] [CrossRef]
  42. Ramírez-Vélez, R.; Correa-Bautista, J.E.; Carrillo, H.A.; González-Jiménez, E.; Schmidt-RioValle, J.; Correa-Rodríguez, M.; García-Hermoso, A.; González-Ruíz, K. Tri-Ponderal Mass Index vs. Fat Mass/Height3 as a Screening Tool for Metabolic Syndrome Prediction in Colombian Children and Young People. Nutrients 2018, 10, 412. [Google Scholar] [CrossRef] [Green Version]
  43. Mameli, C.; Krakauer, N.Y.; Krakauer, J.C.; Bosetti, A.; Ferrari, C.M.; Moiana, N.; Schneider, L.; Borsani, B.; Genoni, T.; Zuccotti, G. The association between a body shape index and cardiovascular risk in overweight and obese children and adolescents. PLoS ONE 2018, 13, e0190426. [Google Scholar] [CrossRef] [Green Version]
  44. Calcaterra, V.; Verduci, E.; Schneider, L.; Cena, H.; De Silvestri, A.; Vizzuso, S.; Vinci, F.; Mameli, C.; Zuccotti, G. Sex-Specific Differences in the Relationship between Insulin Resistance and Adiposity Indexes in Children and Adolescents with Obesity. Children 2021, 8, 449. [Google Scholar] [CrossRef] [PubMed]
  45. National High Blood Pressure Education Program Working Group on High Blood Pressure in Children and Adolescents. The fourth report on the diagnosis, evaluation, and treatment of high blood pressure in children and adolescents. Pediatrics 2004, 114, 555–576. [Google Scholar] [CrossRef]
  46. Rosner, B.; Cook, N.; Portman, R.; Daniels, S.; Falkner, B. Determination of Blood Pressure Percentiles in Normal-Weight Children: Some Methodological Issues. Am. J. Epidemiol. 2008, 167, 653–666. [Google Scholar] [CrossRef] [PubMed]
  47. Flynn, J.T.; Kaelber, D.C.; Baker-Smith, C.M.; Blowey, D.; Carroll, A.E.; Daniels, S.R.; De Ferranti, S.D.; Dionne, J.M.; Falkner, B.; Flinn, S.K.; et al. Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents. Pediatrics 2017, 140, e20171904. [Google Scholar] [CrossRef] [Green Version]
  48. Available online: https://www.bcm.edu/bodycomplab/BPappZjs/BPvAgeAPPz.html (accessed on 12 January 2023).
  49. Matthews, D.R.; Hosker, J.P.; Rudenski, A.S.; Naylor, B.A.; Treacher, D.F.; Turner, R.C. Homeostasis model assessment: Insulin resistance and β-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia 1985, 28, 412–419. [Google Scholar] [CrossRef] [Green Version]
  50. Vieira-Ribeiro, S.A.; Fonseca, P.C.; Andreoli, C.S.; Ribeiro, A.Q.; Hermsdorff, H.H.; Pereira, P.F.; Priore, S.E.; Franceschini, S.C. The TyG index cutoff point and its association with body adiposity and lifestyle in children. J. Pediatr. 2019, 95, 217–223. [Google Scholar] [CrossRef]
  51. Lucini, D.; Solaro, N.; Lesma, A.; Gillet, V.B.; Pagani, M.; Dickerson, J.; Ivannikov, M. Health Promotion in the Workplace: Assessing Stress and Lifestyle with an Intranet Tool. J. Med. Internet Res. 2011, 13, e88. [Google Scholar] [CrossRef]
  52. Craig, C.L.; Marshall, A.L.; Sjöström, M.; Bauman, A.E.; Booth, M.L.; Ainsworth, B.E.; Pratt, M.; Ekelund, U.L.; Yngve, A.; Sallis, J.F.; et al. International Physical Activity Questionnaire: 12-Country Reliability and Validity. Med. Sci. Sports Exerc. 2003, 35, 1381–1395. [Google Scholar] [CrossRef] [Green Version]
  53. Minetto, M.A.; Motta, G.; Gorji, N.E.; Lucini, D.; Biolo, G.; Pigozzi, F.; Portincasa, P.; Maffiuletti, N.A. Reproducibility and validity of the Italian version of the International Physical Activity Questionnaire in obese and diabetic patients. J. Endocrinol. Investig. 2017, 41, 343–349. [Google Scholar] [CrossRef]
  54. Lucini, D.; Pagani, E.; Capria, F.; Galliano, M.; Marchese, M.; Cribellati, S. Evidence of Better Psychological Profile in Working Population Meeting Current Physical Activity Recommendations. Int. J. Environ. Res. Public Health 2021, 18, 8991. [Google Scholar] [CrossRef]
  55. Lucini, D.; Zanuso, S.; Blair, S.; Pagani, M. A simple healthy lifestyle index as a proxy of wellness: A proof of concept. Acta Diabetol. 2014, 52, 81–89. [Google Scholar] [CrossRef] [PubMed]
  56. Ruiz, J.R.; Castro-Pinero, J.; Espana-Romero, V.; Artero, E.G.; Ortega, F.B.; Cuenca, M.M.; Jimenez-Pavon, D.; Chillon, P.; Girela-Rejon, M.J.; Mora, J.; et al. Field-based fitness assessment in young people: The ALPHA health-related fitness test battery for children and adolescents. Br. J. Sports Med. 2011, 45, 518–524. [Google Scholar] [CrossRef]
  57. Holland, A.E.; Spruit, M.A.; Troosters, T.; Puhan, M.A.; Pepin, V.; Saey, D.; McCormack, M.C.; Carlin, B.W.; Sciurba, F.C.; Pitta, F.; et al. An official European Respiratory Society/American Thoracic Society technical standard: Field walking tests in chronic respiratory disease. Eur. Respir. J. 2014, 44, 1428–1446. [Google Scholar] [CrossRef] [PubMed]
  58. Vandoni, M.; Correale, L.; Puci, M.V.; Galvani, C.; Codella, R.; Togni, F.; La Torre, A.; Casolo, F.; Passi, A.; Orizio, C.; et al. Six minute walk distance and reference values in healthy Italian children: A cross-sectional study. PLoS ONE 2018, 13, e0205792. [Google Scholar] [CrossRef]
  59. Ortega, F.B.; Ruiz, J.R.; España-Romero, V.; Vicente-Rodriguez, G.; Martínez-Gómez, D.; Manios, Y.; Béghin, L.; Molnar, D.; Widhalm, K.; Moreno, L.A.; et al. The International Fitness Scale (IFIS): Usefulness of self-reported fitness in youth. Int. J. Epidemiol. 2011, 40, 701–711. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  60. Benítez-Porres, J.; López-Fernández, I.; Raya, J.F.; Carnero, S.; Alvero-Cruz, J.R.; Carnero, E. Reliability and Validity of the PAQ-C Questionnaire to Assess Physical Activity in Children. J. Sch. Heal. 2016, 86, 677–685. [Google Scholar] [CrossRef]
  61. La Rovere, M.T.; Bigger, J.T., Jr.; Marcus, F.I.; Mortara, A.; Schwartz, P.J. Baroreflex sensitivity and heart-rate variability in prediction of total cardiac mortality after myocardial infarction. Lancet 1998, 351, 478–484. [Google Scholar] [CrossRef]
  62. Solaro, N.; Pagani, M.; Lucini, D. Altered Cardiac Autonomic Regulation in Overweight and Obese Subjects: The Role of Age-and-Gender-Adjusted Statistical Indicators of Heart Rate Variability and Cardiac Baroreflex. Front. Physiol. 2021, 11, 567312. [Google Scholar] [CrossRef]
  63. Cicone, Z.S.; Holmes, C.J.; Fedewa, M.V.; MacDonald, H.V.; Esco, M.R. Age-Based Prediction of Maximal Heart Rate in Children and Adolescents: A Systematic Review and Meta-Analysis. Res. Q. Exerc. Sport 2019, 90, 417–428. [Google Scholar] [CrossRef]
  64. Calcaterra, V.; Vandoni, M.; Pellino, V.C.; Cena, H. Special Attention to Diet and Physical Activity in Children and Adolescents With Obesity During the Coronavirus Disease-2019 Pandemic. Front. Pediatr. 2020, 8, 407. [Google Scholar] [CrossRef]
  65. Paluch, A.E.; Bajpai, S.; Bassett, D.R.; Carnethon, M.R.; Ekelund, U.; Evenson, K.R.; Galuska, D.A.; Jefferis, B.J.; Kraus, W.E.; Lee, I.M.; et al. Daily steps and all-cause mortality: A meta-analysis of 15 international cohorts. Lancet Public Health 2022, 7, e219–e228. [Google Scholar] [CrossRef] [PubMed]
  66. Calcaterra, V.; Verduci, E.; Vandoni, M.; Rossi, V.; Fiore, G.; Massini, G.; Berardo, C.; Gatti, A.; Baldassarre, P.; Bianchi, A.; et al. The Effect of Healthy Lifestyle Strategies on the Management of Insulin Resistance in Children and Adolescents with Obesity: A Narrative Review. Nutrients 2022, 14, 4692. [Google Scholar] [CrossRef] [PubMed]
  67. Han, S.-S.; Li, B.; Wang, G.-X.; Ke, Y.-Z.; Meng, S.-Q.; Li, Y.-X.; Cui, Z.-L.; Tong, W.-X. Physical Fitness, Exercise Behaviors, and Sense of Self-Efficacy Among College Students: A Descriptive Correlational Study. Front. Psychol. 2022, 13, 932014. [Google Scholar] [CrossRef] [PubMed]
  68. Pamungkas, R.A.; Chamroonsawasdi, K. Home-Based Interventions to Treat and Prevent Childhood Obesity: A Systematic Review and Meta-Analysis. Behav. Sci. 2019, 9, 38. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  69. Lucini, D.; Malacarne, M.; Solaro, N.; Busin, S.; Pagani, M. Complementary medicine for the management of chronic stress: Superiority of active versus passive techniques. J. Hypertens. 2009, 27, 2421–2428. [Google Scholar] [CrossRef]
  70. Lucini, D.; Riva, S.; Pizzinelli, P.; Pagani, M. Stress management at the worksite: Reversal of symptoms profile and cardiovascular dysregulation. Hypertension 2007, 49, 291–297. [Google Scholar] [CrossRef] [Green Version]
Figure 1. Exercise program.
Figure 1. Exercise program.
Nutrients 15 01054 g001
Table 1. Summary of descriptive data of the study population subdivided into two groups considering total volume of physical activity (METsTOT) (Subdivision A).
Table 1. Summary of descriptive data of the study population subdivided into two groups considering total volume of physical activity (METsTOT) (Subdivision A).
IndicesGroupsSignificance
Group 1 n = 12Group 2 n = 23
Below 1200 METsAbove 1200 METsBetween GroupsBetween T0–T1Interaction
Median (Percentile 25°; 75°)Median (Percentile 25°; 75°)
HR T0 [b/min]90.76 (83.38; 97.48)82.15 (75.67; 85.90)0.2830.8430.163
HR T190.80 (78.83; 95.34)83.52 (77.86; 95.90)
RR T0 [msec]661.20 (615.73; 719.99)730.38 (698.48; 792.92)0.1860.8980.289
RR T1660.93 (629.34; 761.20)718.41 (625.64; 770.63)
RRTP T0 [msec2]2015.38 (700.66; 4175.22)2070.68 (1174.64; 4358.51)0.7260.6940.604
RRTP T11941.73 (1036.30; 2996.04)1974.04 (880.01; 3978.67)
RRLFa T0 [msec2]278.57 (152.21; 1536.34)569.95 (324.55; 1064.11)0.6130.9110.795
RRLFa T1414.05 (246.20; 1126.03)679.74 (218.92; 1833.57)
RRHFa T0 [msec2]565.22 (124.40; 1610.27)600.91 (198.91; 1718.47)0.9170.4230.331
RRHFa T1461.04 (252.52; 1177.21)630.36 (235.87; 1128.62)
RRLFnu T0 [nu]30.66 (25.04; 48.65)46.38 (31.23; 55.80)0.2670.2640.727
RRLFnu T141.86 (34.10; 44.14)41.52 (33.52; 65.68)
RRHFnu T0 [nu]52.41 (37.54; 61.06)46.00 (28.39; 59.02)0.8080.3100.367
RRHFnu T147.47 (32.09; 56.59)43.79 (28.31; 57.69)
RRLF/HF T0 [.]0.58 (0.41; 1.30)1.01 (0.46; 2.27)0.2990.6600.691
RRLF/HF T10.91 (0.55; 1.46)0.95 (0.59; 2.32)
SAPpc T0 [%]78.00 (35.50; 87.00)80.00 (63.00; 92.00)0.0580.4640.895
SAPpc T158.50 (49.50; 65.00)80.00 (51.00; 93.00)
DAPpc T0 [%]75.00 (56.00; 92.00)71.00 (59.00; 95.00)0.3480.3760.068
DAPpc T161.50 (42.50; 84.50)78.00 (59.00; 91.00)
AHA score T0 [.]1.50 (1.00; 2.50)2.00 (1.00; 3.00)0.1570.1800.180
AHA score T12.00 (1.00; 2.50)3.00 (2.00; 3.00)
Hours of sleep T0 [h/day]8.00 (8.00; 9.00)8.50 (8.00; 9.00)0.1560.2080.402
Hours of sleep T19.00 (7.00; 9.00)9.00 (8.00; 9.00)
Quality of Sleep T0 [.]8.50 (6.00; 10.00)10.00 (8.00; 10.00)0.0200.3510.829
Quality of SleepT18.50 (4.50; 9.50)9.00 (9.00; 10.00)
Health T0 [.]7.00 (6.00; 9.00)8.00 (6.00; 10.00)0.0510.2150.215
Health T16.50 (5.00; 9.00)8.00 (6.00; 9.00)
School Performance T0 [.]8.00 (7.00; 10.00)9.00 (7.00; 10.00)0.4500.2150.907
School Performance T18.50 (7.00; 9.00)8.00 (7.00; 9.00)
Sedentariness T0 [h/week]68.00 (61.00; 82;00)56.00 (49.00; 68.00)0.0380.2290.775
Sedentariness T166.50 (52.00; 84.50)61.00 (28; 68.00)
METsMV T0 [MET·min/week]240.00 (0.00; 880.00)480.00 (0.00; 720.00)0.0560.1190.117
METsMV T1480.00 (330.00; 670.00)960.00 (720.00; 1800.00)
METsTOT T0 [MET·min/week]361.50 (153.00; 966.25)918.00 (495.00; 1635.00)0.0000.0080.030
METsTOT T1752.25 (538.50; 960.50)1860.00 (1395.00; 2580.00)
BMI z-score T0 [.]2.13 (1.65; 2.52)2.04 (1.84; 2.41)0.6780.0040.200
BMI z-score T12.00 (1.35; 2.54)1.97 (1.82; 2.49)
WHtR T0 [.]0.59 (0.57; 0.62)0.59 (0.57; 0.64)0.7020.2230.142
WHtR T10.58 (0.54; 0.60)0.58 (0.55; 0.60)
FBG T0 [mg/dL]89.50 (87.00; 91.50)87.00 (85.00; 95.00)0.6380.6830.406
FBG T193.00 (86.50; 99.00)89.00 (85.00; 95.00)
Insulin T0 [mg/dL]17.55 (11.25; 25.85)17.40 (13.14; 30.70)0.3430.5150.375
Insulin T115.40 (8.80; 30.75)18.00 (12.00; 30.10)
HOMA-IR T0 [.]3.97 (2.50; 5.59)3.87 (2.76; 6.64)0.3540.5960.363
HOMA-IR T13.78 (1.86; 7.02)3.78 (2.77; 5.72)
TG T0 [mg/dL]93.00 (64.50; 117.50)113.00 (73.00; 150.00)0.2810.8860.331
TG T191.00 (60.00; 119.00)110.00 (65.00; 148.00)
TOT Chol T0 [mg/dL]149.00 (123.00; 156.00)170.00 (150.00; 190.00)0.0480.3140.068
TOT Chol T1143.00 (129.00; 183.00)167.00 (144.00; 172.00)
HDL C T0 [mg/dL]47.00 (37.00; 53.50)45.00 (41.00; 50.00)0.9900.4270.567
HDL C T149.00 (43.00; 52.00)47.00 (40.00; 50.00)
TMI T0 [.]19.13 (18.17; 21.30)18.64 (17.24; 20.53)0.6370.0000.160
TMI T118.62 (17.47; 20.91)18.32 (16.72; 19.68)
VAI T0 [.]3.33 (1.60; 4.90)3.30 (1.58; 4.96)0.3300.1370.392
VAI T13.01 (2.01; 4.53)4.46 (2.48; 5.58)
TyG T0 [.]8.26 (8.01; 8.54)8.56 (7.90; 8.82)0.5230.7220.306
TyG T18.35 (7.94; 8.47)8.47 (7.93; 8.80)
6MWT T0 [m]464.00 (427.00; 540.00)472.00 (438.00; 504.00)0.5960.0000.122
6MWT T1516.00 (482.00. 560.00)540.00 (500.00; 574.00)
PAQ-C score T0 [.]1.92 (1.74; 2.17)1.97 (1.57; 2.30)0.8400.0430.858
PAQ-C score T12.39 (1.90; 2.53)2.25 (1.77; 2.69)
IFIS score T0 [.]3.40 (3.20; 4.20)3.00 (2.80; 3.80)0.1590.5430.653
IFIS score T13.80 (3.20; 4.00)3.40 (2.80; 4.00)
Abbreviations: T0 = before intervention; T1 = after intervention; HR = heart rate; RR= RR interval; RRTP = RR total power (RR interval variance); LF = low frequency component of RR variability; HF = high frequency component of RR variability; nu = normalized unit; LF/HF = RRLF on RRHF ratio; SAPpc = percentile of systolic arterial pressure; DAPpc = percentile of diastolic arterial pressure; AHA score = American Heart Association Nutrition Score; METsTOT = total weekly physical activity volume; METsMV = weekly physical activity volume calculated only considering other activities of moderate intensity and activities of vigorous intensity volume (i.e., volume of structured exercise); BMI= body mass index; WHtR = waist-to-height ratio; FBG = fasting blood glucose; HOMA-IR = homeostasis model assessment—insulin resistance; TG = triglycerides; TOT Chol = total cholesterol; HDL C = HDL cholesterol; TMI = triponderal mass index; VAI = visceral adiposity index; TyG = triglyceride and glucose index; 6MWT = 6-min walk test; PAQ-C = physical activity questionnaire—children; IFIS = international fitness scale; [.] = arbitrary units. Significant values are evidenced in bold.
Table 2. Summary of descriptive data of the study population subdivided into two groups considering weekly volume of structured exercise (METsMV) (Subdivision B).
Table 2. Summary of descriptive data of the study population subdivided into two groups considering weekly volume of structured exercise (METsMV) (Subdivision B).
Indices GroupsSignificance
Below 1200 METs Above 1200 METs Between GroupsBetween
T0–T1
Interaction
Median (Percentile 25°; 75°)Median (Percentile 25°; 75°)
HR T0 [b/min]86.61 (81.86; 95.46)77.07 (73.44; 83.37)0.1390.5550.344
HR T189.55 (80.08; 95.83)80.87 (68.25; 94.11)
RR T0 [msec]692.84 (628.57; 732.96)778.47 (719.76; 816.99)0.0620.7210.675
RR T1670.07 (626.13; 749.24)741.94 (637.58; 879.14)
RRTP T0 [msec2]1602.01 (775.36; 3131.09)3215.74 (2070.68; 4532.33)0.6860.9960.552
RRTP T11711.46 (1036.30; 2996.04)2342.19 (815.39; 4338.19)
RRLFa.T0 [msec2]392.29 (165.69; 1052.10)952.41 (465.37; 1154.68)0.9950.7400.702
RRLFa T1498.63 (246.86; 1390.14)679.74 (138.87; 1833.57)
RRHFa. T0 [msec2]551.61 (158.16; 1360.03)773.98 (269.76; 2289.90)0.7540.9420.266
RRHFa T1474.34 (252.52; 1092.48)777.43 (235.87; 1485.89)
RRLFnu T0 [nu]44.24 (27.10; 51.30)48.20 (26.04; 69.70)0.9470.7350.063
RRLFnu.T142.13 (34.23; 57.47)34.69 (22.89; 67.94)
RRHFnu T0 [nu]49.16 (40.03; 59.66)49.43 (20.20; 67.22)0.6510.9520.032
RRHFnu. T142.55 (32.09; 55.36)55.05 (27.20; 70.76)
RRLF/HF T0 [.]0.87 (0.48; 1.29)0.98 (0.44; 3.53)0.4500.5460.015
RRLF/HF T11.09 (0.59; 1.68)0.60 (0.32; 2.58)
SAPpc T0 [%]77.00 (46.00; 87)86.00 (65.00; 94.00)0.3150.2430.197
SAPpc T164.5 (56.00; 91.00)83.00 (50.00; 92.00)
DAPpc T0 [%]75.00 (60.00; 92.00)65.00 (58.00; 95.00)0.9870.8640.768
DAPpc T179.5 (49.5; 90.5)76.00 (55.00; 89.00)
AHA score T0 [.]1.00 (1.00; 2.00)2.00 (2.00; 3.00)0.0190.0450.359
AHA score T12.00 (1.00; 3.00)3.00 (2.00; 4.00)
Hours of sleep T0 [h]8.5 (8.00; 9.00)8.00 (8.00; 9.00)0.5070.5750.141
Hours of sleep.T18.00 (7.50; 9.00)9.00 (8.00; 9.00)
Quality of Sleep T0 [.]9.00 (8.00; 10.00)10.00 (8.00;1 0.00)0.2330.4140.935
Quality of Sleep T19.00 (7.00; 10.00)9.00 (9.00; 10.00)
Health T0 [.]8.00 (6.00; 10.00)7.00 (6.00; 9.00)0.7440.7030.229
Health T18.00 (5.50; 9.00)7.00 (6.00; 9.00)
School Performance T0 [.]9.00 (7.00; 10.00)8.00 (7.00; 10.00)0.9210.1600.560
School Performance T18.00 (7.00; 9.00)8.00 (6.00; 9.00)
Sedentariness T0 [h/week]66.00 (56.00; 78.50)53.00 (48.00; 56.00)0.0100.1620.708
Sedentariness T163.00 (52.00; 79.50)54.00 (26.00; 67.00)
METsMV T0 [MET·min/week]240.00 (0.00; 480.00)720.00 (0.00;1 680.00)0.0000.0020.007
METsMV T1600.00 (480.00; 720.00)1800 (1200.00; 2080.00)
METsTOT T0 [MET·min/week]648.75 (268.50; 1333.00)819.00 (0.00; 1920.00)0.0120.0000.012
METsTOT T11207.50 (752.25; 1644.00)2493.00 (1860.00; 2773.00)
BMI z-score T0 [.]2.11 (1.91; 2.38)1.99 (1.69; 2.55)0.8850.0330.282
BMI z-score T11.99 (1.63; 2.35)1.90 (1.58; 2.52)
WHtR T0 [.]0.59 (0.57; 0.63)0.59 (0.56; 0.64)0.6470.8480.142
WHtR T10.57 (0.56; 0.60)0.59 (0.55; 0.63)
FBG T0 [mg/dL]89.00 (86.00; 92.50)87.00 (86.00; 96.00)0.7080.9390.594
FBG T190.00 (85.50; 96.00)88.00 (87.00; 96.00)
Insulin T0 [mg/dL]16.80 (11.75; 23.80)18.00 (13.14; 35.00)0.4200.0880.061
Insulin T116.00 (10.24; 30.15)18.20 (14.80; 30.10)
HOMA-IR T0 [.]3.80 (2.51; 5.36)3.87 (2.76; 7.78)0.3720.1030.053
HOMA-IR T13.75 (2.22; 6.46)4.27 (3.22; 5.72)
TG T0 [mg/dL]96.00 (69.50; 122.50)121.00 (62.00; 169.00)0.3620.8760.991
TG T191.00 (63.00; 120.00)112.00 (75.00; 156.00)
TOT Chol T0 [mg/dL]156.00 (139.00; 187.00)165.00 (150.00; 190.00)0.7820.0480.199
TOT Chol T1155.50 (133.00; 176.00)151.00 (144.00; 168.00)
HDL C T0 [mg/dL]47.50 (40.50; 55.50)43.00 (39.00; 48.00)0.3900.4450.675
HDL C T148.00 (43.00; 52.00)46.00 (39.00; 48.00)
TMI T0 [.]19.08 (18.30; 21.03)17.58 (17.15; 19.93)0.2850.0030.760
TMI T119.07 (17.69; 20.91)17.48 (16.38; 19.68)
VAI T0 [.]3.26 (1.79; 4.85)3.42 (1.51; 5.53)0.6110.0120.048
VAI T13.61 (2.07; 4.73)5.34 (2.65; 5.85)
TyG T0 [.]8.35 (7.99; 8.66)8.58 (7.88; 8.97)0.4540.9980.938
TyG T18.35 (7.92; 8.62)8.61 (8.09; 8.84)
6MWT T0 [m]464.00 (432.00; 509.00)490.00 (440.00; 509.00)0.5320.0000.263
6MWT T1520.00 (492.00; 560.00)564.00 (520.00; 580.00)
PAQ-C score T0 [.]1.97 (1.73; 2.17)1.84 (1.57; 2.39)0.8950.0460.731
PAQ-C score T12.30 (1.77; 2.53)2.25 (1.81; 2.69)
IFIS score T0 [.]3.00 (2.80; 3.60)3.20 (3.00; 4.20)0.6930.5780.214
IFIS score T13.60 (3.20; 4.00)3.40 (2.80; 4.00)
Abbreviations: T0 = before intervention; T1 = after intervention; HR = heart rate; RR = RR interval; RRTP = RR total power (RR interval variance); LF = low frequency component of RR variability; HF = high frequency component of RR variability; nu = normalized unit; LF/HF = RRLF on RRHF ratio; SAPpc = percentile of systolic arterial pressure; DAPpc = percentile of diastolic arterial pressure; AHA score = American Heart Association Nutrition Score; METsTOT = total weekly physical activity volume; METsMV = weekly physical activity volume calculated only considering other activities of moderate intensity and activities of vigorous intensity volume (i.e., volume of structured exercise); BMI= body mass index; WHtR = waist-to-height ratio; FBG = fasting blood glucose; HOMA-IR = homeostasis model assessment—insulin resistance; TG = triglycerides; TOT Chol = total cholesterol; HDL C = HDL cholesterol; TMI = triponderal mass index; VAI = visceral adiposity index; TyG = triglyceride and glucose index; 6MWT = 6-min walk test; PAQ-C = physical activity questionnaire—children; IFIS = international fitness scale; [.] = arbitrary units. Significant values are evidenced in bold.
Table 3. Pearson’s correlations among changes between T0 and T1 of main variables.
Table 3. Pearson’s correlations among changes between T0 and T1 of main variables.
Δ METsMV0.844 **
0.000
Δ RR0.2270.423 *
0.1890.011
Δ RRTP0.405 *0.509 **0.686 **
0.0160.0020.000
Δ RRLFnu−0.117−0.204−0.086−0.012
0.5040.2390.6220.946
Δ RRHFnu0.2160.335 *0.0610.088−0.872 **
0.2130.0490.7290.6170.000
Δ LF/HF−0.137−0.238−0.0040.0690.721 **0.716 **
0.4330.1680.9830.6920.0000.000
Δ SAPpc−0.136−0.400 *−0.512 **−0.368 *0.214−0.1870.061
0.4360.0170.0020.0300.2170.2810.729
Δ BMI z-score−0.088−0.008−0.189−0.2430.099−0.103−0.0790.094
0.6170.9630.2780.1600.5720.5550.6540.590
Δ METsTOTΔ METsMVΔ RRΔ RRTPΔ RRLFnuΔ RRHFnuΔ LF/HFΔ SAPpc
Abbreviations: Δ = change between T0 and T1; METsTOT = total weekly physical activity volume; METsMV = weekly physical activity volume calculated only considering other activities of moderate intensity and activities of vigorous intensity volume (i.e., volume of structured exercise); RR = RR interval; RRTP = RR total power (RR interval variance); LF = low frequency component of RR variability; HF = high frequency component of RR variability; nu= normalized unit; LF/HF= RRLF on RRHF ratio; SAPpc= percentile of systolic arterial pressure. BMI= body mass index. Significant values are evidenced in bold. **: correlation is significant at the 0.01 level (2-tailed). *: correlation is significant at the 0.05 level (2-tailed).
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Calcaterra, V.; Bernardelli, G.; Malacarne, M.; Vandoni, M.; Mannarino, S.; Pellino, V.C.; Larizza, C.; Pagani, M.; Zuccotti, G.; Lucini, D. Effects of Endurance Exercise Intensities on Autonomic and Metabolic Controls in Children with Obesity: A Feasibility Study Employing Online Exercise Training. Nutrients 2023, 15, 1054. https://doi.org/10.3390/nu15041054

AMA Style

Calcaterra V, Bernardelli G, Malacarne M, Vandoni M, Mannarino S, Pellino VC, Larizza C, Pagani M, Zuccotti G, Lucini D. Effects of Endurance Exercise Intensities on Autonomic and Metabolic Controls in Children with Obesity: A Feasibility Study Employing Online Exercise Training. Nutrients. 2023; 15(4):1054. https://doi.org/10.3390/nu15041054

Chicago/Turabian Style

Calcaterra, Valeria, Giuseppina Bernardelli, Mara Malacarne, Matteo Vandoni, Savina Mannarino, Vittoria Carnevale Pellino, Cristiana Larizza, Massimo Pagani, Gianvincenzo Zuccotti, and Daniela Lucini. 2023. "Effects of Endurance Exercise Intensities on Autonomic and Metabolic Controls in Children with Obesity: A Feasibility Study Employing Online Exercise Training" Nutrients 15, no. 4: 1054. https://doi.org/10.3390/nu15041054

APA Style

Calcaterra, V., Bernardelli, G., Malacarne, M., Vandoni, M., Mannarino, S., Pellino, V. C., Larizza, C., Pagani, M., Zuccotti, G., & Lucini, D. (2023). Effects of Endurance Exercise Intensities on Autonomic and Metabolic Controls in Children with Obesity: A Feasibility Study Employing Online Exercise Training. Nutrients, 15(4), 1054. https://doi.org/10.3390/nu15041054

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