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Article

Effects of Whole-Body Vibration Exercises on Parameters Related to the Sleep Quality in Metabolic Syndrome Individuals: A Clinical Trial Study

by
Claudia Figueiredo Azeredo
1,2,
Patrícia de Castro de Paiva
1,2,
Leandro Azeredo
3,
Aline Reis da Silva
1,2,
Arlete Francisca-Santos
2,4,
Laisa Liane Paineiras-Domingos
2,4,5,
Adriana Lírio Pereira da Silva
2,
Camila Leite Bernardes-Oliveira
1,5,
Juliana Pessanha-Freitas
2,
Márcia Cristina Moura-Fernandes
2,6,
Rubens Guimarães Mendonça
2,
José Alexandre Bachur
7,
Ygor Teixeira-Silva
2,5,
Eloá Moreira-Marconi
2,6,
Eliane de Oliveira Guedes-Aguiar
2,4,5,
Bruno Bessa Monteiro de Oliveira
2,4,
Mário Fritsch Neves
5,
Luiz Felipe Ferreira-Souza
2,
Vinicius Layter Xavier
8,
Daniel Lago Borges
9,
Ana Cristina Lacerda
10,
Vanessa Amaral Mendonça
10,
Anelise Sonza
11,
Redha Taiar
12,*,
Alessandro Sartorio
13,
Mario Bernardo-Filho
2 and
Danúbia da Cunha de Sá-Caputo
2,4,5
add Show full author list remove Hide full author list
1
Programa de Pós-graduação em Saúde, Medicina Laboratorial e Tecnologia Forense, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ 20950-003, Brazil
2
Laboratório de Vibrações Mecânicas e Práticas Integrativas, Departamento de Biofísica e Biometria, Instituto de Biologia Roberto Alcântara Gomes e Policlínica Piquet Carneiro, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ 20950-003, Brazil
3
Departamento de Fisioterapia, Hospital Central da Polícia Militar, Rio de Janeiro, RJ 20211-270, Brazil
4
Faculdade Bezerra de Araújo, Rio de Janeiro, RJ 23052-180, Brazil
5
Programa de Pós-Graduação em Ciências Médicas, Faculdade de Ciências Médicas, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ 20551-030, Brazil
6
Programa de Pós-Graduação em Fisiopatologia Clínica e Experimental, Instituto de Biologia Roberto Alcântara Gomes, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ 20550-900, Brazil
7
Cursos de Medicina e Fisioterapia da Universidade de Franca, Franca, SP 14401-426, Brazil
8
Departamento de Estatística, Instituto de Matemática e Estatística, Universidade do Estado do Rio de Janeiro, Rio de Janeiro, RJ 20550-900, Brazil
9
Hospital Universitário, Universidade Federal do Maranhão, São Luís do Maranhão, MA 65080-805, Brazil
10
Faculdade de Ciências Biológicas e da Saúde, Universidade Federal dos Vales do Jequitinhonha e Mucuri, Diamantina, MG 39100-000, Brazil
11
Programa de Pós-graduação em Fisioterapia, Universidade do Estado de Santa Catarina, Florianópolis, SC 88080-350, Brazil
12
GRESPI, Université de Reims, 51100 Reims, France
13
Istituto Auxologico Italiano, IRCCS, Experimental Laboratory for Auxo-Endocrinological Research, Division of Metabolic Diseases & Auxology, 28824 Milan and Verbania, Italy
*
Author to whom correspondence should be addressed.
Appl. Sci. 2019, 9(23), 5183; https://doi.org/10.3390/app9235183
Submission received: 24 October 2019 / Revised: 11 November 2019 / Accepted: 22 November 2019 / Published: 29 November 2019
(This article belongs to the Special Issue Biomechanical Spectrum of Human Sport Performance)

Abstract

:
Metabolic syndrome (MetS) is an undesirable clinical condition with physiological, biochemical, clinical, and metabolic factors that contribute to increased cardiovascular risks (CR). A poor sleep quality might be found in obese and MetS individuals. Whole-body vibration (WBV) exercise has been used on the management of MetS individuals. This clinical trial investigated the effect of WBV exercise on parameters related to the sleep quality in MetS individuals. After randomization, nine individuals (seven women and two men) were exposed to a fixed frequency (FF) and ten individuals (eight women and two men) were exposed to a variable frequency (VF). Both groups performed the protocol twice a week, for 6 weeks. All of the evaluations were performed before the first and after the last sessions. Anthropometric and cardiovascular parameters were measured before and after the 6-week intervention. Pittsburgh Sleep Quality Index (PSQI), Epworth Sleepiness Scale (ESS), and Berlin Questionnaire were also used to evaluate the quality of the sleep. A significant (p ≤ 0.05) reduction of the waist circumference in the VFG and an increase of the heart rate were found in the FFG and VFG group. The score of the PSQI of the both groups decreased significantly (p = 0.01). The score of the ESS decreased (p = 0.04) only in the VF group. The scores of the Berlin Questionnaire were not altered in both groups. In conclusion, WBV intervention was capable in interfering with physiological mechanisms with effects on the WC and HR, leading to the improvement of the quality of sleep in MetS individuals. WBV exercise might be an important clinical intervention to the management of some factors associated with poor quality of sleep (FFG and VFG) and in the daytime sleepiness in MetS individuals with variable frequencies (5–16 Hz) (VFG).

Graphical Abstract

1. Introduction

Metabolic syndrome (MetS) is an undesirable clinical condition with physiological, biochemical, clinical, and metabolic factors, including alterations on the level of the lipids on the plasma, arterial hypertension, central adiposity, insulin resistance (IR), and hyperglycemia. These conditions strongly contribute to increased cardiovascular risks (CR) [1], and they are interconnected by pathophysiological basis in low-grade chronic inflammation, increase of the risk of type 2 diabetes mellitus (T2DM), and all-cause mortality [2]. MetS is also related to the increased deposit of central adiposity and ectopic fat infiltration (muscle and liver) associated with overeating and/or sedentary lifestyles. These conditions are related to various deleterious consequences in late life [3,4].
Lian et al. [5], in a systematic review and meta-analysis, reported that the overall sleep quality as well as sleep complaints have significant positive associations with MetS. Massar et al. [6] and Tsai et al. [7] pointed out that this condition of the sleep is linked with cardiovascular disease. Massar et al. [6] reported in individuals with poor habitual sleep efficiency during the week before stress induction (Trier Social Stress Test) responded with higher stress-related elevations of blood pressure and cortisol levels as compared to subjects with high sleep efficiency. This relationship between poor sleep efficiency and elevated blood pressure persisted during the post-stress recovery period. In addition, poor sleep health is also associated with MetS and mental illness [8,9]. Iftikhar et al. [10], in a meta-analysis reported that some investigations demonstrated the association between sleep quality and MetS. It was verified that the poor sleep quality characterized by sleep fragmentation was related to impaired glucose metabolism, independent of sleep duration [11], however, the studies of the meta-analysis analyzed had not reached a consensus. Mesas et al. [12] reported that the difficulty falling asleep is associated with MetS and, in particular, with high blood pressure, and this association would be independent of sleep duration and would be not due to lifestyles related to poor sleep.
Ying et al. [5] reported in a systematic review and meta-analysis that the overall sleep quality, as well as sleep complaints have significant positive associations with MetS. Moreover, it is estimated [13,14] that 50% to 60% of obese and MetS individuals can present obstructive sleep apnea (OSA).
Some tools have been used to verify parameters (such as sleep duration, sleep inertia, sleep latency, snoring, disorientation or confusion during sleep, and daytime sleepiness) related to the quality of the sleep, such as the Pittsburgh Sleep Quality Index (PSQI) [15], Epworth Sleepiness Scale (ESS) [16] and the Berlin Questionnaire [17]. Moreover, the neck circumference (NC) [16] and waist circumference (WC) [18,19] have also been used.
There is moderate evidence supporting the use of physical exercise (PE) programs to counter MetS, although the optimal dose and type of PE is not well established. It is the main challenge for health care professionals to persuade individuals to have adherence to perform PE to the prevention and management of MetS [20]. In this case, it is relevant to consider the whole-body vibration (WBV) exercise, a modality of PE, an option. WBV exercise has been used as a clinical intervention in individuals with different clinical disorders, including MetS [21,22,23,24,25,26] and it can be considered a feasible, safe, and low-cost technique [27].
WBV exercise is generated in an individual who is on the base of a vibrating platform. It produces a mechanical vibration (MV) that is transmitted to the body inducing muscle contractions, with physiological responses like those produced by other types of PE, such as aerobic conditioning and strength training [28,29,30]. Biomechanical parameters, such as the frequency (f) and the peak-to-peak displacement (PPD) of the MV must be considered in the WBV exercise protocols [26,31,32].
As it is suggested that the sleep quality plays an important role in development of MetS [5] and putting together all of the previous considerations, to our knowledge, this is a first work aiming to study the effect of WBV exercise on the sleep quality of MetS individuals using the PSQI, ESS, and Berlin Questionnaire. It is hypothesized that the WBV exercise would be able in improving the sleep quality of MetS individuals.

2. Materials and Methods

2.1. Individuals

In this cross-sectional and randomized study, 31 subjects were recruited and 19 performed the protocol (58.79 ± 12.55 years old, 1.62 ± 0.09 m height, 86.27 ± 15.03 kg body mass). The recruitment of the participants occurred from January 2018 to January 2019, in the Hospital Universitário Pedro Ernesto (HUPE), in the Universidade do Estado do Rio de Janeiro (UERJ). The WBV protocol was performed in the Laboratório de Vibrações Mecânicas e Práticas Integrativas (LAVIMPI).
This project was approved by the Research Ethics Committee of HUPE-UERJ with the number CAAE 54981315.6.0000.5259, the registry in the Brazilian Registry of Clinical Trials (ReBEC) with the number RBR 2bghmh and UTN: U1111-1181-1177. The participants of both groups signed a consent form.
Consolidated Standards of Reporting Trials (CONSORT) was used to report all of the different steps of the interventions utilized in this work [33].
In the randomization, a blinded envelope was used for the cards with the name of the groups: fixed frequency group (FFG) (control group) or variable frequency group (VFG) (WBVE group).
The inclusion criteria were individuals of both sexes, over 18 years of age, with MetS according to the International Diabetes Federation.
The exclusion criteria were: (i) individuals with high blood pressure (BP) levels (systolic blood pressure (SBP) ≥ 180 mmHg and diastolic blood pressure (DBP) ≥ 110 mmHg); (ii) cardiovascular disease (CVD) clinically evident in the last 6 months, manifested by a myocardial infarction or a stroke; (iii) a neurological, muscular, or rheumatologic disease that difficulte the position of the individual on the vibrating platform; (iv) disabling clinical disease according to the evaluation; (v) speech therapy or respiratory physiotherapy in the last 3 months; (vi) body mass index (BMI) > 40 kg/m²; (vii) orthodontic therapy with intraoral device; (viii) individuals who refuse to sign the consent form.
The participants declared that they were sedentary. They were instructed to continue their daily activities, dietary habits, and medications during the period of the investigation. The drugs used by the participants of both groups were diuretics, beta blockers, calcium channel blockers, angiotensin converting enzyme inhibitors, and angiotensin receptor antagonists.

2.2. Interventions

2.2.1. Fixed Frequency Group (Control Group)

After the randomization, nine individuals (seven women and two men) allocated in the FFG performed a protocol twice a week, for 6 weeks. In this protocol, the individuals were positioned in a squat position, barefoot and with 130° knee flexion (Figure 1A). The biomechanical parameters were 2.5, 5 and 7.5 mm (Figure 1B–D) of PPD and 5 Hz for 10 s of vibration and 110 s of non-vibration in each bout. From 1 to 4 weeks, were performed 3 bouts in each session, totaling 18 min of total time. From 5 to 8 weeks, were performed 4 bouts in each session, totaling 24 min of total time. From 9 to 12 weeks, were performed 5 bouts in each session, totaling 30 min of total time. The participants performed dynamic and static squats in the sessions.

2.2.2. Variable Frequency Group (WBVE Group)

After the randomization, ten individuals (eight women and two men) allocated in the VFG performed the protocol twice a week, for 6 weeks. In this protocol, the individuals were positioned in a squat position, barefoot and with 130° knee flexion (Figure 1) The biomechanical parameters of the MV were 2.5, 5 and 7.5 mm (Figure 1B–D) of the PPD; the frequency was 5 Hz in the first session and it increased by one Hz in each session, and it was 16 Hz in the last session. During the intervention, were performed 60 s of MV and 60 s of non-vibration in each bout. From 1 to 4 weeks were performed 3 bouts in each session, for a total time of 18 min. From 5 to 8 weeks, were performed 4 bouts in each session, for a total time of 24 min. From 9 to 12 weeks were performed 5 bouts in each session, for a total time of 30 min. Dynamic and static squats were performed in interspersed sessions.

2.3. Anthropometric Measurements and Physiological Parameters

All of the measurements were performed in the same location, at room temperature. Height and body mass were measured on a digital balance (MIC 200 PPA, Micheletti, São Paulo, Brazil). The BMI was calculated by dividing body mass (in kg) by square of height (in m) [34]. WC was obtained with a flexible measuring tape connecting the midpoints between the last costal arch and iliac crest, at the end of the soft exhalation and in the orthostatic position [34]. NC was obtained using a flexible metric tape just below the prominence of the larynx [35].
An automated device (OMRON, model HEM-7113, Dalian, China) was utilized to record the SBP and DBP (mm Hg), and the HR (beats/min) was measured on the left arm of seated patient after a 10-min rest. Three measurements were performed with 1 min of rest after each measurement. The mean of these 3 records of SBP and DBP and HR was used in the analyses of the WBV exercise group and the control group [36]. These evaluations were performed before and after the 6-week intervention in both groups.
The data of these parameters were expressed in mean and standard derivation and the Wilcoxon rank test was performed.

2.4. Questionnaires

The PSQI [15] was used to assess sleep quality and disturbances over a 1-month period. This questionnaire is composed of 19 self-rated questions and 5 questions that should be answered by bedmates or roommates. The 19 questions are separated into 7 categories and there is a score from 0 to 3. The components of this questionnaire are subjective sleep quality, sleep latency, sleep duration, habitual sleep efficiency, sleep disturbances, use of medication, and daytime dysfunction. The maximum PSQI score is 21 points. Higher scores indicate poor quality of sleep [37].
The ESS [16] is composed of 8 self-reported questions and it is used to assess the self-reported level of daytime sleepiness [38]. These items have a four-point scale (0 indicating “would never nod off” and 3 indicating a “strong chance of nodding off”). The questionnaire questions are related to daily activities. The questionnaire score ranges between 0 and 24. Higher total scores are related to more sleepiness [39].
The Berlin Questionnaire [17] has been proposed as a tool in screening OSA and validated in primary care. The subjects were classified into high risk (if there were 2 or more categories where the score was positive), and low risk (if there was only 1 or no categories where the score was positive). The percentage os individuals with high risk to OSA was calculated in both groups [40,41].
The PSQI, ESS, and Berlin Questionnaire were only measured before and after the 6-week intervention in both groups.

2.5. Statistical Analyses

For the sample size calculation, we used a standard deviation of 3.1, a margin of error of 2, the significance level of 5%, and a sample size of 9 individuals in each group, considering the PSQI [42].
The Wilcoxon signed-rank test with continuity correction was used in the analyses of the DBP, SBP, HR, WC, NC, the PSQI, and ESS. Descriptive statistics, median, and interquartile range (IQR) are also reported. Wilcoxon signed-rank test is a nonparametric test that was used to determine if paired samples, before and after intervention, have the same distribution. Fisher’s exact test was applied to the qualitative variable, Berlin, to asses if the proportion of people in each class (high risk and low risk) have been affected by the experiment. In the analyses of the PSQI and ESS, the values are expressed in scores. The statistical analyses of the Berlin Questionnaire considered only the percentage of individuals with a high risk to OSA.
All statistical analysis was performed using R software, version 3.5.0 [43] and the R Librarie Table 1 [44]. Results are considered statistically significant if the p-value is under 0.05 (p ≤ 0.05).

3. Results

The flow diagram with the enrolment of the study is shown in Figure 2. Thirty-one individuals were recruited, two individuals were excluded because they did not have risk of sleep apnea, three declined to participate, and seven individuals declined due to other reasons (economical problem related to the transportation).
Table 1 shows some anthropometric parameters of the individuals that were exposed to WBV exercise (FV group) and to only 5 Hz (FF group). An analysis is shown of both groups before and just after the treatments. It was verified that the BMI, NC, SBP, and DBP (p > 0.05) were not significantly altered in both groups. However, a significant increase in the HR (p < 0.05) was found in both groups exposed to mechanical vibration, only 5 Hz (FFG) and variable frequency 5–16Hz (VFG). Furthermore, a reduction was found in the group that was submitted to the variable frequency 5–16 Hz (VFG) in the WC.
Figure 3 shows the values of the scores of the PSQI of the individuals of the group exposed only to mechanical vibration of 5 Hz (FFG-control). A significant decrease was found (p = 0.01) of the score (after and before) of the individuals of the FF group (exposure to 5 Hz).
Figure 4 shows the values of the scores of the PSQI of the individuals of the groups exposed to the treatment with WBV exercises (VFG). It is observed that an important and significant (p = 0.008) decrease of score in the group after the exposure to various frequencies (intervention) was seen. This finding indicates an improvement of quality of the sleep.
Figure 5 shows the values of the scores of the ESS of the individuals of the group exposed only to mechanical vibration of 5 Hz (FFG). It is observed that there was no significant decrease (p = 1.0) of the score (after and before) of the individuals. This finding indicates no reduction of daytime sleepiness.
Figure 6 shows the values (before and after the interventions) of the scores of the ESS scale of the individuals of the groups exposed to the treatment with WBV exercises (VFG). It is observed that there was a significant (p = 0.04) decrease of the score in the group after the exposure to various frequencies (intervention). This finding indicates a reduction of daytime sleepiness.
Considering the Berlin Questionnaire, no alteration in ter percentage of individuals with risk to OSA were significantly found in both groups, the FF p = 0.29 and FVG p = 1.00.

4. Discussion

The underlying etiology of MetS is multifactorial, however, they are not well known, but sedentary lifestyles and unhealthy dietary habits favor the appearance of MetS [45]. Considering the high prevalence and strong and undesirable complications, early identifying and controlling the modified risk factors are key prevention methods to counter the development of MetS and its progression to CVD.
It is relevant to point out that, to our knowledge, this is the first work that was performed to evaluate the effect of WBV exercise in sleep quality of MetS individuals. As it was hypothesized that the WBV exercise would be able to improve the sleep quality of MetS individuals, the quality of sleep was improved (PSQI) and a reduction of daytime sleepiness (ESS) in the MetS was found due to a protocol with variable frequencies (5–16 Hz) of WBV. A protocol with fixed frequency (5 Hz) also improved the quality of sleep (PSQI).
It was shown (Table 1) that the 6-week intervention with WBV exercise with variable frequencies (from 5 up to 16 Hz) (VF group) did not alter significantly the BMI, NC, SBP, and DBP. The same finding was verified in the individuals with fixed frequency (5 Hz). These findings agree with other studies. Feairheller et al. [46], in a study of six months, have shown that aerobic exercise training is enough to elicit improvements in vascular structure and function in African Americans, even without alterations on BP measurements (SBP and DBP) in African Americans. Moreover, Sá-Caputo et al. [31] have reported that, in individuals with MetS exposed to acute WBV exercise, the SBP and DBP were not altered. Figueroa et al. [21] have reported that the BMI of overweight/obese women was not modified after 6 weeks of WBV exercises.
Considering the HR (Table 1), an increase was verified in FFG (only 5 Hz) and VFG (variable 5–16 Hz), and this is in agreement with Sunita et al. [47] that have also observed an increase of the HR in response to exercise. Moreover, Kang et al. [48] have described an association between resting HR and cardiorespiratory fitness with an elevated resting HR.
The findings presented in Table 1 indicated no alterations on SBP and DBP due to WBVE (a possible stressor), however, Massar et al. [6] reported that individuals with poor habitual sleep efficiency during the week before stress induction (Trier Social Stress Test) responded with higher stress-related elevations of blood pressure and cortisol levels as compared to subjects with high sleep efficiency.
In the current study, no alterations on the NC were found. However, a decrease on the WC was found (Table 1). Sîrbu et al. [49] have compared some anthropometric parameters in trained and sedentary healthy young students. It was found that in moderately aerobic trained students, the BMI and BP were not significantly different between the two groups. However, a significantly lower NC was found in the trained students. Considering the WC, in agreement with our results, King et al. [50] have verified that a 12-week supervised aerobic exercise intervention has reduced significantly the WC of overweight/obese men and women. But, Sîrbu et al. [49], have not found alteration in the WC due to exercise.
WBV exercise is an intervention with several improvements in populations with various diseases [23,24,25,31]. In this current study, it was verified that WBV exercise has improved the quality of the sleep in MetS when we used the PSQI (Figure 3 and Figure 4) and ESS (Figure 6). This finding is partially in agreement with Souza et al. [51] who have evaluated, in a population of 16 individuals with OSA, the effectiveness of inspiratory muscle training (IMT) on sleep and functional capacity to exercise. It was a significant improvement in sleep quality was seen with PSQI values, but no significant changes were seen in daytime sleepiness (ESS) after the intervention. Furthermore, Reid et al. [52] have verified that moderate aerobic PE improved the sleep quality of sedentary adults considering the PSQI and the ESS. Brandão et al. [53] have reported that home exercise improves the quality of sleep and daytime sleepiness of elderlies considering, respectively, the PSQI and the ESS.
The findings of the current work have verified that the sleep quality was not altered when the Berlin Questionnaire was used. This result agrees with Brandão et al. [53] who have reported that home exercise does not alter the risk to OSA when the same questionnaire was used.
Kline et al. [54], evaluated the utility of PE for improving daytime functioning in adults with OSA. Sleepiness and functional impairment due to sleepiness also were improved following exercise versus control, though these changes were not statistically significant. It is suggested that PE may be helpful for improving aspects of daytime functioning of adults with OSA. Moreover, Yilmaz Gokmen et al. [55] have investigated the effects of Tai Chi and Qigong training on severity of OSA for 12-weeks. In the intervention group, there was a statistically significant decrease in the ESS. However, Itoh et al. [56], in a cross-sectional study among non-obese male workers in Japan, found no significant association between physical activity and the risk of sleep-disordered breathing.
Considering the MetS, not all forms of exercise are equally effective and safe; although aerobic exercise [57] or resistance training have been associated with decreased cardiovascular disease risk factors, obesity, or MetS severity [58,59]. Due to the pain or even the low physical fitness, most individuals are unable or unwilling to perform these exercises [60]. Given the limitations for some types of exercises that many individuals report, different forms of exercise are being suggested for MetS individuals [61]. WBV exercise has improved several parameters in MetS individuals [26,31,32] and in the current study a decrease of the WC was found (Table 1).
This study has some limitations, no control of daily activity, daily working, lifestyle habits, smoking, PE, and daily energy intake. The follow-up data were not available after the intervention. The external validity of this intervention considering its generalizability to other settings (like the everyday-living condition) was not explored and only a small sample was used. The big ratio of female to male would be also considered as a limitation of the study. Moreover, a sham group and a group of individuals without MetS were not used. Furthermore, the analysis of the questionnaires was not done in the weeks in which there were changes of the frequency and duration of the intervention in the VFG. Some points of the questionnaires are influenced by factors that are not taken into account in the current study, as categories of individuals (good-sleepers and bad-sleepers), sleep duration, sleep inertia, and sleep latency. In consequence, further investigations are required. However, putting together all the considerations, the strength was to verify that a WBV exercise might be suggested as an option to the management of MetS individuals with some important outcomes, and it would be expected that a WBV exercise might lead to responses that can reflect in improvements of the sleep quality.

5. Conclusions

In conclusion, WBV intervention was capable of interfering with physiological mechanisms with effects on the WC and HR, leading to the improvement of the quality of sleep in MetS individuals. Although the calculated sample size determined a study with a small number of individuals, WBV exercise might be an important clinical intervention to the management of some factors associated with poor quality of sleep (FFG and VFG) and in the daytime sleepiness in MetS individuals with variable frequencies (5–16Hz) (VFG). However, further investigations are necessary to try to understand the mechanisms that underlines this positive effect of the WBV exercise in the studied population, as well as with individuals with sleep disturbances without MetS.

Author Contributions

Conceptualization, R.T., A.S. (Alessandro Sartorio), M.B.-F., and D.d.C.d.C.D.S.-C.; data curation, C.F.A., J.A.B., V.L.X., and D.L.B.; formal analysis, J.A.B., V.L.X., D.L.B., A.C.L., V.A.M., A.S. (Anelise Sonza), and R.T.; funding acquisition, M.B.-F.; Investigation, C.F.A., P.d.C.d.P., L.A., A.R.d.S., A.F.-S., L.L.P.-D., A.L.P.d.S., C.L.B.-O., J.P.-F., M.C.M.-F., R.G.M., Y.T.-S., E.M.-M., E.d.O.G.-A., B.B.M.d.O., M.F.N., and L.F.F.-S.; methodology, C.F.A., P.d.C.d.P., L.A., A.R.D.S., A.F.-S., L.L.P.-D., A.L.P.d.S., C.L.B.-O., J.P.-F., M.C.M.-F., R.G.M., J.A.B., Y.T.-S., E.M.-M., E.d.O.G.-A., B.B.M.d.O., M.F.N., L.F.F.-S., and A.S.(Alessandro Sartorio); project administration, M.B.-F. and D.d.C.d.C.D.S.-C.; resources, C.F.A., P.d.C.d.P., L.A., A.R.d.S., R.G.M., and B.B.M.d.O.; software, V.L.X.; supervision, M.B.-F. and D.d.C.d.C.D.S.-C.; validation, V.L.X., M.B.-F., and D.d.C.d.C.D.S.-C.; visualization, A.S.(Anelise Sonza) and R.T.; writing—original draft, C.F.A.; Writing—review and editing, A.C.L., V.A.M., A.S. (Anelise Sonza), A.S. (Alessandro Sartorio), M.B.-F., and D.d.C.d.C.D.S.-C.

Funding

This study was supported in part by the Coordenação de Aperfeiçoamento de Pessoal de Nível Superior - Brazil (CAPES) - Finance Code 001, the Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) and the Fundação de Amparo à Pesquisa do Estado do Rio de Janeiro (FAPERJ).

Conflicts of Interest

There is no conflict of interest.

References

  1. Kaur, J. Retracted: A Comprehensive Review on Metabolic Syndrome. Cardiol. Res. Pract. 2019, 2019, 4301528. [Google Scholar]
  2. Seaman, D.R.; Palombo, A.D. An Overview of the Identification and Management of the Metabolic Syndrome in Chiropractic Practice. J. Chiropr. Med. 2014, 13, 210–219. [Google Scholar] [CrossRef]
  3. Dominguez, L.J.; Barbagallo, M. The Biology of the Metabolic Syndrome and Aging:2006. Curr. Opin. Clin. Nutr. & Metab. Care 2016, 9, 5–11. [Google Scholar]
  4. Alberti, K.G.M.M.; Zimmet, P.; Shaw, J. Metabolic syndrome-a new world-wide definition. A Consensus Statement from the International Diabetes Federation. Diabet. Med. 2006, 23, 469–480. [Google Scholar] [CrossRef]
  5. Lian, Y.; Yuan, Q.; Wang, G.; Tang, F. Association between sleep quality and metabolic syndrome: A systematic review and meta-analysis. Psychiatry Res. 2019, 274, 66–74. [Google Scholar] [CrossRef]
  6. Massar, S.A.A.; Liu, J.C.J.; Mohammad, N.B.; Chee, M.W.L. Poor habitual sleep efficiency is associated with increased cardiovascular and cortisol stress reactivity in men. Psychoneuroendocrinology 2017, 81, 151–156. [Google Scholar] [CrossRef]
  7. Tsai, H.-J.; Kuo, T.B.J.; Lin, Y.-C.; Yang, C.C.H. The association between prolonged sleep onset latency and heart rate dynamics among young sleep-onset insomniacs and good sleepers. Psychiatry Res. 2015, 230, 892–898. [Google Scholar] [CrossRef]
  8. Salo, P.; Sivertsen, B.; Oksanen, T.; Sjösten, N.; Pentti, J.; Virtanen, M.; Kivimäki, M.; Vahtera, J. Insomnia symptoms as a predictor of incident treatment for depression: Prospective cohort study of 40,791 men and women. Sleep Med. 2012, 13, 278–284. [Google Scholar] [CrossRef]
  9. Wang, S.; Wu, Y.; Ungvari, G.S.; Ng, C.H.; Forester, B.P.; Gatchel, J.R.; Chiu, H.F.K.; Kou, C.; Fu, Y.; Qi, Y.; et al. Sleep duration and its association with demographics, lifestyle factors, poor mental health and chronic diseases in older Chinese adults. Psychiatry Res. 2017, 257, 212–218. [Google Scholar] [CrossRef]
  10. Iftikhar, I.H.; Donley, M.A.; Mindel, J.; Pleister, A.; Soriano, S.; Magalang, U.J. Sleep Duration and Metabolic Syndrome. An Updated Dose–Risk Metaanalysis. Ann. Am. Thorac. Soc. 2015, 12, 1364–1372. [Google Scholar] [CrossRef]
  11. Stamatakis, K.A.; Punjabi, N.M. Effects of Sleep Fragmentation on Glucose Metabolism in Normal Subjects. Chest 2010, 137, 95–101. [Google Scholar] [CrossRef]
  12. Mesas, A.E.; Guallar-Castillón, P.; López-García, E.; León-Muñoz, L.M.; Graciani, A.; Banegas, J.R.; Rodríguez-Artalejo, F. Sleep quality and the metabolic syndrome: The role of sleep duration and lifestyle. Diabetes. Metab. Res. Rev. 2014, 30, 222–231. [Google Scholar] [CrossRef]
  13. Resta, O.; Foschino-Barbaro, M.P.; Legari, G.; Talamo, S.; Bonfitto, P.; Palumbo, A.; Minenna, A.; Giorgino, R.; De Pergola, G. Sleep-related breathing disorders, loud snoring and excessive daytime sleepiness in obese subjects. Int. J. Obes. 2001, 25, 669–675. [Google Scholar] [CrossRef]
  14. Drager, L.F.; Lopes, H.F.; Maki-Nunes, C.; Trombetta, I.C.; Toschi-Dias, E.; Alves, M.J.N.N.; Fraga, R.F.; Jun, J.C.; Negrão, C.E.; Krieger, E.M.; et al. The Impact of Obstructive Sleep Apnea on Metabolic and Inflammatory Markers in Consecutive Patients with Metabolic Syndrome. PLoS ONE 2010, 5, e12065. [Google Scholar] [CrossRef]
  15. Kline, C.E.; Crowley, E.P.; Ewing, G.B.; Burch, J.B.; Blair, S.N.; Durstine, J.L.; Davis, J.M.; Youngstedt, S.D. The Effect of Exercise Training on Obstructive Sleep Apnea and Sleep Quality: A Randomized Controlled Trial. Sleep 2011, 34, 1631–1640. [Google Scholar] [CrossRef]
  16. Soler, X.; Liao, S.-Y.; Marin, J.M.; Lorenzi-Filho, G.; Jen, R.; DeYoung, P.; Owens, R.L.; Ries, A.L.; Malhotra, A. Age, gender, neck circumference, and Epworth sleepiness scale do not predict obstructive sleep apnea (OSA) in moderate to severe chronic obstructive pulmonary disease (COPD): The challenge to predict OSA in advanced COPD. PLoS ONE 2017, 12, e0177289. [Google Scholar] [CrossRef]
  17. Qu, X.-X.; Esangbedo, I.C.; Zhang, X.-J.; Liu, S.-J.; Li, L.-X.; Gao, S.; Li, M. Obstructive Sleep Apnea Syndrome is Associated with Metabolic Syndrome among Adolescents and Youth in Beijing. Chin. Med. J. 2015, 128, 2278–2283. [Google Scholar] [CrossRef]
  18. Hoffstein, V.; Mateika, S. Differences in abdominal and neck circumferences in patients with and without obstructive sleep apnoea. Eur. Respir. J. 1992, 5, 377–381. [Google Scholar]
  19. Horner, R.L.; Shea, S.A.; McIvor, J.; Guz, A. Pharyngeal size and shape during wakefulness and sleep in patients with obstructive sleep apnoea. QJM 1989, 72, 719–735. [Google Scholar]
  20. Paley, C.A.; Johnson, M.I. Abdominal obesity and metabolic syndrome: Exercise as medicine? BMC Sports Sci. Med. Rehabil. 2018, 10, 7. [Google Scholar] [CrossRef]
  21. Figueroa, A.; Kalfon, R.; Madzima, T.A.; Wong, A. Whole-body vibration exercise training reduces arterial stiffness in postmenopausal women with prehypertension and hypertension. Menopause 2014, 21, 131–136. [Google Scholar] [CrossRef]
  22. Wong, A.; Alvarez-Alvarado, S.; Kinsey, A.W.; Figueroa, A. Whole-Body Vibration Exercise Therapy Improves Cardiac Autonomic Function and Blood Pressure in Obese Pre- and Stage 1 Hypertensive Postmenopausal Women. J. Altern. Complement. Med. 2016, 22, 970–976. [Google Scholar] [CrossRef]
  23. Anwer, S.; Alghadir, A.; Zafar, H.; Al-Eisa, E. Effect of whole body vibration training on quadriceps muscle strength in individuals with knee osteoarthritis: A systematic review and meta-analysis. Physiotherapy 2016, 102, 145–151. [Google Scholar] [CrossRef]
  24. Alev, A.; Mihriban, A.; Bilge, E.; Ayça, E.; Merve, K.; Şeyma, C.; Uğur, E.; Adnan, B.; Zeynel, K.; Mahmut, G.S. Effects of whole body vibration therapy in pain, function and depression of the patients with fibromyalgia. Complement. Ther. Clin. Pract. 2017, 28, 200–203. [Google Scholar] [CrossRef]
  25. Zhou, J.; Pang, L.; Chen, N.; Wang, Z.; Wang, C.; Hai, Y.; Lyu, M.; Lai, H.; Lin, F. Whole-body vibration training-better care for COPD patients: A systematic review and meta-analysis. Int. J. COPD 2018, 13, 3243–3254. [Google Scholar] [CrossRef]
  26. Sá-Caputo, D.; Paineiras-Domingos, L.L.; Francisca-Santos, A.; dos Anjos, E.M.; Reis, A.S.; Neves, M.F.T.; Oigman, W.; Oliveira, R.; Brandão, A.; Machado, C.B.; et al. Whole-body vibration improves the functional parameters of individuals with metabolic syndrome: An exploratory study. BMC Endocr. Disord. 2019, 19, 6. [Google Scholar] [CrossRef]
  27. Braz, D.S.; de Andrade, A.D.; Teixeira, A.S.; Cavalcanti, C.A.; Morais, A.B.; Marinho, P.E.M. Whole-body vibration improves functional capacity and quality of life in patients with severe chronic obstructive pulmonary disease (COPD): A pilot study. Int. J. COPD 2015, 10, 125–132. [Google Scholar]
  28. Rønnestad, B.R. Comparing the Performance-Enhancing Effects of Squats on a Vibration Platform With Conventional Squats in Recreationally Resistance-Trained Men. J. Strength Cond. Res. 2004, 18, 839–845. [Google Scholar]
  29. Merkert, J.; Butz, S.; Nieczaj, R.; Steinhagen-Thiessen, E.; Eckardt, R. Combined whole body vibration and balance training using Vibrosphere®. Z. für Gerontol. und Geriatr. 2011, 44, 256–261. [Google Scholar] [CrossRef]
  30. Cardim, A.B.; Marinho, P.E.; Nascimento, J.F.; Fuzari, H.K.; de Andrade, A.D. Does Whole-Body Vibration Improve the Functional Exercise Capacity of Subjects With COPD? A Meta-Analysis. Respir. Care 2016, 61, 1552–1559. [Google Scholar] [CrossRef]
  31. Sá-Caputo, D.C.; Paineiras-Domingos, L.L.; Oliveira, R.; Neves, M.F.T.; Brandão, A.; Marin, P.J.; Sañudo, B.; Furness, T.; Taiar, R.; Bernardo-Filho, M. Acute Effects of Whole-Body Vibration on the Pain Level, Flexibility, and Cardiovascular Responses in Individuals With Metabolic Syndrome. Dose-Response 2018, 16, 155932581880213. [Google Scholar] [CrossRef]
  32. Paineiras-Domingos, L.L.; da Cunha Sá-Caputo, D.; Reis, A.S.; Francisca Santos, A.; Sousa-Gonçalves, C.R.; dos Anjos, E.M.; dos Santos Pereira, M.J.; Sartorio, A.; Bernardo-Filho, M. Assessment Through the Short Physical Performance Battery of the Functionality in Individuals With Metabolic Syndrome Exposed to Whole-Body Vibration Exercises. Dose-Response 2018, 16, 155932581879453. [Google Scholar] [CrossRef]
  33. Moher, D.; Hopewell, S.; Schulz, K.F.; Montori, V.; Gøtzsche, P.C.; Devereaux, P.J.; Elbourne, D.; Egger, M.; Altman, D.G. CONSORT 2010 explanation and elaboration: Updated guidelines for reporting parallel group randomised trials. Int. J. Surg. 2012, 10, 28–55. [Google Scholar] [CrossRef]
  34. Casadei, K.; Kiel., J. Anthropometric Measurement; StatPearls Publishing LLC: Treasure Island, FL, USA, 2019. Available online: https://www.ncbi.nlm.nih.gov/books/NBK537315/ (accessed on 24 October 2019).
  35. Gasa, M.; López-Padrós, C.; Monasterio, C.; Salord, N.; Mayos, M.; Vilarrasa, N.; Fernandez-Aranda, F.; Montserrat, J.M.; Dorca, J.; López-Padrós, C.; et al. Anthropometrical phenotypes are important when explaining obstructive sleep apnea in female bariatric cohorts. J. Sleep Res. 2019, 28, e12830. [Google Scholar] [CrossRef]
  36. De Cardiologia, S.B. III Diretrizes Brasileiras Sobre Dislipidemias e Diretriz de Prevenção da Aterosclerose do Departamento de Aterosclerose da Sociedade Brasileira de Cardiologia. Arq. Bras. Cardiol. 2001, 77, 48. [Google Scholar]
  37. Kim, T.Y.; You, S.E.; Ko, Y.S. Association between Sasang constitutional types with obesity factors and sleep quality. Integr. Med. Res. 2018, 7, 341–350. [Google Scholar] [CrossRef]
  38. Schwab, R.J.; Pasirstein, M.; Pierson, R.; Mackley, A.; Hachadoorian, R.; Arens, R.; Maislin, G.; Pack, A.I. Identification of Upper Airway Anatomic Risk Factors for Obstructive Sleep Apnea with Volumetric Magnetic Resonance Imaging. Am. J. Respir. Crit. Care Med. 2003, 168, 522–530. [Google Scholar] [CrossRef]
  39. Duarte, R.L.; Mello, F.C.; Magalhães-da-Silveira, F.J.; Oliveira-e-Sá, T.S.; Rabahi, M.F.; Gozal, D. Comparative performance of screening instruments for obstructive sleep apnea in morbidly obese patients referred to a sleep laboratory: A prospective cross-sectional study. Sleep Breath. 2019, 23, 1123–1132. [Google Scholar] [CrossRef]
  40. Netzer, N.C.; Stoohs, R.A.; Netzer, C.M.; Clark, K.; Strohl, K.P. Using the Berlin Questionnaire to Identify Patients at Risk for the Sleep Apnea Syndrome. Ann. Intern. Med. 1999, 131, 485. [Google Scholar] [CrossRef]
  41. Ng, S.S.; Tam, W.; Chan, T.O.; To, K.W.; Ngai, J.; Chan, K.K.P.; Yip, W.H.; Lo, R.L.; Yiu, K.; Ko, F.W.; et al. Use of Berlin questionnaire in comparison to polysomnography and home sleep study in patients with obstructive sleep apnea. Respir. Res. 2019, 20, 40. [Google Scholar] [CrossRef] [Green Version]
  42. Cizza, G.; de Jonge, L.; Piaggi, P.; Mattingly, M.; Zhao, X.; Lucassen, E.; Rother, K.I.; Sumner, A.E.; Csako, G. Neck Circumference Is a Predictor of Metabolic Syndrome and Obstructive Sleep Apnea in Short-Sleeping Obese Men and Women. Metab. Syndr. Relat. Disord. 2014, 12, 231–241. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  43. Team, R. R Development Core Team. R A Lang. Environ. Stat. Comput. 2013, 3, 201. [Google Scholar]
  44. Yoshida, K.; Bohn, J.; Yoshida, M.K. Package ‘Tableone’; R Foundation for Statistical Computing: Vienna, Austria, 2016. [Google Scholar]
  45. Rao, D.P.; Orpana, H.; Krewski, D. Physical activity and non-movement behaviours: Their independent and combined associations with metabolic syndrome. Int. J. Behav. Nutr. Phys. Act. 2016, 13, 26. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  46. Feairheller, D.L.; Diaz, K.M.; Kashem, M.A.; Thakkar, S.R.; Veerabhadrappa, P.; Sturgeon, K.M.; Ling, C.; Williamson, S.T.; Kretzschmar, J.; Lee, H.; et al. Effects of Moderate Aerobic Exercise Training on Vascular Health and Blood Pressure in African Americans. J. Clin. Hypertens. 2014, 16, 504–510. [Google Scholar] [CrossRef] [Green Version]
  47. Mahajan, A.; Mishra, T.; Singh, N.; Jain, A. Heart rate and blood pressure response to exercise and recovery in subclinical hypothyroid patients. Int. J. Appl. Basic Med. Res. 2013, 3, 106. [Google Scholar] [CrossRef] [Green Version]
  48. Kang, S.J.; Ha, G.C.; Ko, K.J. Association between resting heart rate, metabolic syndrome and cardiorespiratory fitness in Korean male adults. J. Exerc. Sci. Fit. 2017, 15, 27–31. [Google Scholar] [CrossRef]
  49. Sîrbu, E.; Buzaș, R.; Mihăescu, R.; Suceava, I.; Lighezan, D. Influence of exercise training and eating behavior on arterial stiffness in young healthy students. Wien. Klin. Wochenschr. 2015, 127, 555–560. [Google Scholar] [CrossRef]
  50. King, N.A.; Hopkins, M.; Caudwell, P.; Stubbs, R.J.; Blundell, J.E. Beneficial effects of exercise: Shifting the focus from body weight to other markers of health. Br. J. Sports Med. 2009, 43, 924–927. [Google Scholar] [CrossRef] [Green Version]
  51. Souza, A.K.F.; de Andrade, A.D.; de Medeiros, A.I.C.; de Aguiar, M.I.R.; de Souza Rocha, T.D.; Pedrosa, R.P.; de Lima, A.M.J. Effectiveness of inspiratory muscle training on sleep and functional capacity to exercise in obstructive sleep apnea: A randomized controlled trial. Sleep Breath. 2018, 22, 631–639. [Google Scholar] [CrossRef]
  52. Reid, K.J.; Baron, K.G.; Lu, B.; Naylor, E.; Wolfe, L.; Zee, P.C. Aerobic exercise improves self-reported sleep and quality of life in older adults with insomnia. Sleep Med. 2010, 11, 934–940. [Google Scholar] [CrossRef] [Green Version]
  53. Brandão, G.S.; Gomes, G.S.B.F.; Brandão, G.S.; Callou Sampaio, A.A.; Donner, C.F.; Oliveira, L.V.F.; Camelier, A.A. Home exercise improves the quality of sleep and daytime sleepiness of elderlies: A randomized controlled trial. Multidiscip. Respir. Med. 2018, 13, 2. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  54. Kline, C.E.; Ewing, G.B.; Burch, J.B.; Blair, S.N.; Durstine, J.L.; Davis, J.M.; Youngstedt, S.D. Exercise Training Improves Selected Aspects of Daytime Functioning in Adults with Obstructive Sleep Apnea. J. Clin. Sleep Med. 2012, 8, 357–365. [Google Scholar] [CrossRef] [PubMed]
  55. Yilmaz Gokmen, G.; Akkoyunlu, M.E.; Kilic, L.; Algun, C. The Effect of T’ai Chi and Qigong Training on Patients with Obstructive Sleep Apnea: A Randomized Controlled Study. J. Altern. Complement. Med. 2019, 25, 317–325. [Google Scholar] [CrossRef] [PubMed]
  56. Itoh, H.; Yokoyama, K.; Matsukawa, T.; Kitamura, F. Association between physical activity and sleep-disordered breathing in male Japanese workers: A cross-sectional study. BMC Res. Notes 2017, 10, 37. [Google Scholar] [CrossRef] [Green Version]
  57. Dixit, S.; Maiya, A.; Shastry, B. Effect of aerobic exercise on quality of life in population with diabetic peripheral neuropathy in type 2 diabetes: A single blind, randomized controlled trial. Qual. Life Res. 2014, 23, 1629–1640. [Google Scholar] [CrossRef]
  58. Farias, D.L.; Tibana, R.A.; Teixeira, T.G.; Vieira, D.C.L.; Tarja, V.; Nascimento, D.D.C.; Silva, A.D.O.; Funghetto, S.S.; Coura, M.A.D.S.; Valduga, R.; et al. Elderly women with metabolic syndrome present higher cardiovascular risk and lower relative muscle strength. Einstein 2013, 11, 174–179. [Google Scholar] [CrossRef] [Green Version]
  59. World Health Organization. GLOBAL STATUS REPORT on Noncommunicable Diseases 2014—“Attaining the Nine Global Noncommunicable Diseases Targets; A Shared Responsibility”; WHO Libr. Cat. Data: Geneva, Switzerland, 2014; p. 298. [Google Scholar]
  60. Callaghan, B.C.; Xia, R.; Reynolds, E.; Banerjee, M.; Rothberg, A.E.; Burant, C.F.; Villegas-Umana, E.; Pop-Busui, R.; Feldman, E.L. Association Between Metabolic Syndrome Components and Polyneuropathy in an Obese Population. JAMA Neurol. 2016, 73, 1468. [Google Scholar] [CrossRef] [Green Version]
  61. Sossa, C.; Delisle, H.; Agueh, V.; Sodjinou, R.; Ntandou, G.; Makoutodé, M. Lifestyle and dietary factors associated with the evolution of cardiometabolic risk over four years in West-African adults: The Benin study. J. Obes. 2013, 2013, 298024. [Google Scholar] [CrossRef]
Figure 1. Biomechanical parameters during the intervention (fixed frequency (FF) and variable frequency (VF) groups) using the side alternating vibratory platform; (A) individual in a stand position, barefoot and with 130° knee flexion; (B) individual in 2.5 mm of peak-to-peak displacement (PPD) on the base of the vibrating platform with medial malleoli together; (C) individual in 5 mm of PPD on the base of the vibrating platform 21 cm apart between the medial malleoli; (D) individual in 7.5 mm of PPD on the base of the vibrating platform 38 cm apart between the medial malleoli.
Figure 1. Biomechanical parameters during the intervention (fixed frequency (FF) and variable frequency (VF) groups) using the side alternating vibratory platform; (A) individual in a stand position, barefoot and with 130° knee flexion; (B) individual in 2.5 mm of peak-to-peak displacement (PPD) on the base of the vibrating platform with medial malleoli together; (C) individual in 5 mm of PPD on the base of the vibrating platform 21 cm apart between the medial malleoli; (D) individual in 7.5 mm of PPD on the base of the vibrating platform 38 cm apart between the medial malleoli.
Applsci 09 05183 g001
Figure 2. Flow diagram of the intervention.
Figure 2. Flow diagram of the intervention.
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Figure 3. Scores of the Pittsburgh Sleep Quality Index (PSQI) of the individuals of the group exposed only to a mechanical vibration of 5 Hz (FFG) (before and after).
Figure 3. Scores of the Pittsburgh Sleep Quality Index (PSQI) of the individuals of the group exposed only to a mechanical vibration of 5 Hz (FFG) (before and after).
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Figure 4. Scores of the PSQI of the individuals exposed to the whole-body vibration (WBV) intervention with variable frequency (VFG).
Figure 4. Scores of the PSQI of the individuals exposed to the whole-body vibration (WBV) intervention with variable frequency (VFG).
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Figure 5. Scores of the Epworth Sleepiness Scale (ESS) of the individuals of the SG individuals of the FFG (before and after).
Figure 5. Scores of the Epworth Sleepiness Scale (ESS) of the individuals of the SG individuals of the FFG (before and after).
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Figure 6. Scores of the ESS of the individuals of the group exposed to the intervention with WBV exercises (VFG).
Figure 6. Scores of the ESS of the individuals of the group exposed to the intervention with WBV exercises (VFG).
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Table 1. Anthropometrical parameters of the individuals exposed to variable frequency group (intervention 5–16 Hz) and to only 5 Hz (fixed frequency group).
Table 1. Anthropometrical parameters of the individuals exposed to variable frequency group (intervention 5–16 Hz) and to only 5 Hz (fixed frequency group).
FFG before
(Median [IQR])
FFG after
(Median [IQR])
pVFG before
(Median [IQR])
VFG after
(Median [IQR])
p
BMI (kg/m2)29.50
[29.0, 34.20]
29.60
[28.90, 34.10]
0.5435.40
[32.40, 36.60]
34.70
[32.88, 36.08]
0.23
WC (cm)105.00
[101.20, 106.30]
101.00
[100.00, 105.00]
0.23108.90
[103.75, 116.10]
107.00
[102.17, 112.85]
0.02
NC (cm)38.00
[36.40, 38.50]
36.60
[35.60, 39.50]
0.2938.00
[37.58, 38.88]
38.30
[37.17, 39.00]
0.25
SBP
(mm Hg)
129.00
[128.00, 130.00]
127.00
[121.00, 128.00]
0.12130.00
[122.50, 132.50]
130.00
[120.00, 132.00]
0.76
DBP
(mm Hg)
78.00
[75.00, 83.00]
75.00
[68.00, 87.00]
1.0074.00
[72.25, 75.75]
70.00
[60.75, 74.75]
0.18
HR
(bpm)
57.00
[56.00, 62.00]
62.00
[60.00, 66.00]
0.0563.50
[59.75, 66.00]
72.00
[61.25, 83.00]
0.05
BMI—body mass index, WC—waist circumference, NC—neck circumference, SBP—systolic blood pressure, DBP—diastolic blood pressure, HR—heart rate, FF—fixed frequency group, VF—variable frequency group.

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Figueiredo Azeredo, C.; de Castro de Paiva, P.; Azeredo, L.; Reis da Silva, A.; Francisca-Santos, A.; Liane Paineiras-Domingos, L.; Lírio Pereira da Silva, A.; Leite Bernardes-Oliveira, C.; Pessanha-Freitas, J.; Moura-Fernandes, M.C.; et al. Effects of Whole-Body Vibration Exercises on Parameters Related to the Sleep Quality in Metabolic Syndrome Individuals: A Clinical Trial Study. Appl. Sci. 2019, 9, 5183. https://doi.org/10.3390/app9235183

AMA Style

Figueiredo Azeredo C, de Castro de Paiva P, Azeredo L, Reis da Silva A, Francisca-Santos A, Liane Paineiras-Domingos L, Lírio Pereira da Silva A, Leite Bernardes-Oliveira C, Pessanha-Freitas J, Moura-Fernandes MC, et al. Effects of Whole-Body Vibration Exercises on Parameters Related to the Sleep Quality in Metabolic Syndrome Individuals: A Clinical Trial Study. Applied Sciences. 2019; 9(23):5183. https://doi.org/10.3390/app9235183

Chicago/Turabian Style

Figueiredo Azeredo, Claudia, Patrícia de Castro de Paiva, Leandro Azeredo, Aline Reis da Silva, Arlete Francisca-Santos, Laisa Liane Paineiras-Domingos, Adriana Lírio Pereira da Silva, Camila Leite Bernardes-Oliveira, Juliana Pessanha-Freitas, Márcia Cristina Moura-Fernandes, and et al. 2019. "Effects of Whole-Body Vibration Exercises on Parameters Related to the Sleep Quality in Metabolic Syndrome Individuals: A Clinical Trial Study" Applied Sciences 9, no. 23: 5183. https://doi.org/10.3390/app9235183

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