Next Article in Journal
Multicast Routing Based on Data Envelopment Analysis and Markovian Decision Processes for Multimodal Transportation
Previous Article in Journal
Artificial Intelligence and Forensic Genetics: Current Applications and Future Perspectives
Previous Article in Special Issue
The Mulberry Juice Fermented by Lactiplantibacillus plantarum O21: The Functional Ingredient in the Formulations of Fruity Jellies Based on Different Gelling Agents
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Effectiveness of a Nutrition Education Program for Patients with Type 2 Diabetes Mellitus

1
Department of Agriculture Crop Production and Rural Environment, School of Agriculture Sciences, University of Thessaly, 38446 Volos, Greece
2
Laboratory of Clinical Nutrition and Dietetics, Department of Nutrition and Dietetics, University of Thessaly, 42132 Trikala, Greece
3
Department of Endocrinology and Metabolic Diseases, Faculty of Medicine, School of Health Sciences, University Hospital of Larissa, University of Thessaly, 41334 Larissa, Greece
*
Authors to whom correspondence should be addressed.
Appl. Sci. 2024, 14(5), 2114; https://doi.org/10.3390/app14052114
Submission received: 14 January 2024 / Revised: 22 February 2024 / Accepted: 23 February 2024 / Published: 4 March 2024

Abstract

:
Diabetes is a metabolic disease that is a major health problem globally. Dietary interventions contribute to the management of the disease and the improvement in patients’ quality of life. The aim of the present study was to assess the effects of a nutrition and lifestyle education intervention on a sample of patients with diabetes. The duration of the intervention was 3 months, and it focused on the promotion of the Mediterranean diet through information pamphlets, diet plans and healthy lifestyle guidelines, which were provided in addition to patients’ standard medical treatment. Patients were enrolled in the outpatient clinic of the University Hospital of Larissa (Greece). Anthropometric and biochemical parameters were recorded at baseline and follow-up using standardized equipment and methods. The intervention improved patients’ body mass index, body composition, fasting glucose, postprandial glucose, triglycerides, HDL/LDL cholesterol and cholesterol. For smoking status, alcohol consumption and physical activity categorization, physical activity improved but not the other two indices. The results of this study show that patient education should be provided according to the nutritional recommendations for T2DM plus a more individually structured intervention. It is therefore necessary to direct the attention of doctors to the need for continuous and detailed discussions with patients in relation to both the standards of a healthy diet and the benefits it brings. Patients, for their part, need to commit to following an appropriate, healthy diet.

1. Introduction

The prevalence of type 2 diabetes mellitus (T2DM) worldwide is increasing at epidemic proportions [1]. Chronic hyperglycemia is considered a major risk factor for cardiovascular and kidney disease, retinopathy and neuropathy [2]. The Center for Disease Control (CDC) estimates that almost 33% of adults in the U.S. have prediabetes; therefore, preventing or delaying T2DM is a public health imperative to help extend and improve the lives of millions of people [3].
The increase in the prevalence of T2DM is paralleled with the increase in overweight/obesity, and it has become particularly evident in the last decade [4]. Undoubtedly, as a person’s body mass index (BMI) increases, the risk of developing T2DM increases in a “dose-dependent” manner. The prevalence of T2DM is 3–7 times higher in obese than in normal-weight adults [4], and people with a BMI > 35 kg/m2 are 20 times more likely to develop T2DM than those with a BMI between 18.5 and 24.9 kg/m2 [5]. Obesity also complicates the management of T2DM by increasing insulin resistance and blood glucose concentrations [6]. Obesity is also an independent risk factor for dyslipidemia, hypertension and cardiovascular complications and cardiovascular mortality in patients with T2DM [2].
Attaining and maintaining a healthy body weight is a major therapeutic target in the management of T2DM. Governments are looking to identify the most effective services to support overweight/obese patients with T2DM to lose weight and improve their health status and quality of life [7]. Data from the Diabetes Prevention Program (DPP) showed that weight loss (7% of weight lost in the first year), increased physical activity (150 min of walking per week) and improvements in other lifestyle behaviors (e.g., dietary behavior) decreased the 4-year incidence of T2DM by 58% in men and women with glucose tolerance disorders [8].
Some strategies associated with successful long-term weight loss include lifestyle modification, specifically the adoption of low-caloric diets, frequent body weight monitoring, and participation in regular physical activity. Successful weight loss is accompanied by a reduction in the portion size of meals, foods and snacks, daily breakfast consumption, and 3 or less hours of screen-watching (television, computer, tablets/smartphone) per week on average [9,10]. The link between overweight and obesity and many non-communicable diseases is well known [11]. Weight loss has a major impact on improving glycemic control and reducing the risk of cardiovascular disease [12].
Dietary recommendations need to be based on personal choices, access to food and the patient’s culture and ability to make behavioral changes [13]. Interventions in the patient’s lifestyle to increase physical activity and reduce caloric intake aim to reduce body weight by 5%, as this can improve HbA1c and cholesterol and reduce cardiovascular risk [14]. The American Diabetes Association emphasizes the importance of educating the patient to make conscious food choices that take into account personal preferences, culture and religion and individualized metabolic goals. The diet patterns with the most beneficial effect on the metabolic profile have been mentioned as the Mediterranean diet and the vegetarian diet [15,16].
Long-term improvements to lifestyle, especially nutrition and physical activity, are challenging for most patients. The role of healthcare professionals working with diabetic patients is to encourage, monitor and support them in this effort [17]. Several techniques can be used to promote behavioral change. First, behaviors need to be screened, and personalized goals need to be set by the healthcare professional in agreement with the patient. Setting realistic and achievable goals allows patients to achieve success, which can be a starting point for further lifestyle change [18,19]. Strategies such as self-monitoring, avoidance of situations that trigger food intake and problem-solving (to the extent possible) may support self-regulation over time. Frequent communication and educational meetings (e.g., every fortnight) are associated with better long-term maintenance of weight loss [20].
The purpose of this study was to investigate the effectiveness of a nutrition and lifestyle education intervention in patients with T2DM for a patient-approach medicine. At the same time, the level of nutritional knowledge of the patients was assessed and their problems in adopting appropriate nutritional approaches were recorded with the ultimate aim of improving them. Some small studies promote nutritional supplementation [21] or a diet that may affect postprandial glucose or other metabolic biomarkers [22,23,24] or alter the metabolic profile through intermittent fasting [25], but only a few have examined the impact of behavioral [26] and patient-centric therapeutic approaches [27] for diabetes, so original research could close the gap. This study aims to present multifaceted strategies compared with the clinical studies conducted in the last years, with diet playing a pivotal role in T2DM management, with a special focus not only on the Mediterranean diet but also on personalized dietary recommendations for patients and shedding light on the efficacy of a multidisciplinary team of health professionals.

2. Participants and Methods

2.1. Study Designed

The study was approved by the competent Bioethics Committee of the University of Thessaly (approval numbers 49162/13-10-2017 and 49161/13-10-2017), and it was in line with the Declaration of Helsinki. All volunteers signed a written informed consent prior to their participation in the study. The study period was from October 2017 to January 2018.

2.2. Participant Recruitment

Eighty-eight T2DM patients (forty males and forty-eight females, average age 51.4 years) were admitted to the Larissa General University Hospital, Greece, for 90.0 ± 3.3 days. Criteria for participation in the study were a diagnosis of diabetes established by hemoglobin A1C (HbA1c) or plasma glucose concentration. In addition, individuals with a recent diagnosis of T2DM (<3 months) and who were treatment-naive, 30–70 years of age, clinically and biochemically stable and without any acute metabolic complications of diabetes were also considered for the study. Individuals with history of recent alcohol use (<6 months), pregnant women and those in a severe comorbid state were excluded. The clinical samples for analysis were collected at the baseline (t = 0 months) and at the end (t = 3 months) of the study.

2.3. Data Collection and Measures

At baseline, patients filled out the questionnaire (demographic characteristics, personal information, complications of the disease), and data were recorded for biochemical indicators, including fasting glucose, blood glucose, HbA1c, total cholesterol, HDL cholesterol, LDL cholesterol and triglycerides, and also medications. Anthropometric data were also collected. Participants’ weight was measured in light clothing and without shoes using a portable calibrated electronic weighing scale precision scale (TAN- ITA MC-780U Multi Frequency Segmental Body Composition Analyzer, Amsterdam, the Netherlands). Height was measured with portable measuring inflexible bars (Seca model 220, Seca, Hamburg, Germany). Waist (at umbilicus) and hip (at widest point) circumferences (WC and HC) were measured according to standard conditions using a measuring tape, and waist/hip circumference ratio (WHR) was calculated. Blood pressure was measured with a clever blood monitor (FYGB-869). All measurements were taken twice, and the average of the two values was reported, as suggested [28]. The follow-up was planned after 3 months and aimed to evaluate potential changes in the collected variables. Subjects recorded their physical activity using the International Physical Activity Questionnaire [29] and a validated diet recall Food Frequency Intake form [30].
Low-density lipoprotein cholesterol (LDL) was calculated according to the Friedewald formula [31]. Fasting glucose was calculated [32], and glycated hemoglobin (HbA1c) was measured by high-performance liquid chromatography (HPLC). All participants were evaluated for their changes in the collected variables.

2.4. Lifestyle and Nutritional Intervention

Each patient was allocated to one dietitian, a nutritionist, who was responsible for educating, measuring and adhering to the intervention. The intervention included one face-to-face meeting about nutrition under the direction of a dietician and the patient. During this visit, the patients were informed about the purpose of the study, answered the 24 h diet recall questionnaire [33] and were given an individualized nutritional plan (the energy requirements were calculated and personalized according to the preferences/needs of each patient) and detailed nutritional instructions, recommendations and advice, both for their diet and eating behavior. Patients were also educated regarding the choices of foods containing carbohydrates, with the aim of regulating sugar levels within normal limits as well as easily forming their daily diet. There were written specific nutritional recommendations: to have 5–6 meals per day, dividing the foods containing carbohydrates, to prefer foods rich in soluble fiber (legumes, fruits, vegetables, whole grains), to avoid the consumption of pure sugar and products containing it (sweets, cookies with sugar, cakes, jelly, ice creams with sugar, candies, sugared drinks, etc.), to reduce salt consumption and to avoid the consumption of saturated fat contained mainly in red meat, cold meats, egg yolks (up to 3 times/week) and butter. Emphasis was given to the consumption of vegetable fats, mainly olive oil, and to replace red meat with fish as much as possible. All participants’ diets were evaluated to assess their compliance with the Mediterranean diet and standards recommended by the American Diabetes Association [34] and the Hellenic Diabetes Association [35]. Some dietary recommendations were given by the dietician, such as reducing the intake of calories, total fat to <30% of daily energy intake and saturated fat (including trans fatty acids) to <10% of daily energy intake and increasing fiber intake (15g to 30g/day) [36]. The patients were given a form with the food categories mentioned above and an individualized nutritional plan (55% carbohydrate, 15% protein, and 30% fat) that they could follow for weight loss, as this was a key target of the intervention for those who were overweight or obese. They also received instructions for exercise. More precisely, participants were instructed to follow a Mediterranean-type diet and to perform at least 150 min of moderate-intensity exercise a week. Adherence to recommendations from dietitians was reported after the three-month intervention. Finally, the patients could communicate, either through calling, messaging or visiting the dietician during the three-month intervention, for questions or for support for their efforts.

2.5. Statistical Analyses

Statistical analysis was performed with the Statistical Package for the Social Sciences (SPSS 21). A frequency analysis was performed for each of the variables in the questionnaires. The Kolmogorov–Smirnov test was used to test the variables for a normal distribution. Data are presented as mean ± standard deviation (SD) or as median value (interquartile range). A paired t-test was used to compare parametric variables before and after three months of the nutrition education intervention; the Wilcoxon test was used for non-parametric data; and the chi-square test was used for categorical variables. p-values < 0.05 (two-tailed) were considered statistically significant.

3. Results

3.1. Study Population

Individuals with a history of recent alcohol use (<3 months) or in a severe comorbid state were excluded. The study population consisted of 48 females (mean age 50.1 ± 9.1 years) and 40 males (mean age 51.4 ± 6.8 years). The average interval between baseline and the end of the follow-up was 90.0 ± 3.3 days, and all participants completed the study. The study was explained to all the individuals initially considered. Only 88 of the initial 100 patients gave informed written consent and so participated in the intervention at the Hospital of Thessaly.

3.2. Socio-Economic Data, Nutritional Knowledge and Perception of T2DM Treatment

Although, risk factors for people with T2DM [3] are well known. it is therefore necessary to select socio-economic data and clinical characteristics of the T2DM patients.
More than half of the patients were treating diabetes with antidiabetic medication only (56.8%), with 3.4% injecting insulin and only 9.1% taking diabetic medications and eating a balanced diet (Table 1).
The amount patients spent on food each month was also checked for correlation with dietary guidelines. Most (52% of the sample) spent EUR 200–300, 32% spent EUR 300–400, 11% spent less than EUR 200 and just under 5% spent more than EUR 400.
As part of the interview, patients were questioned about their educational level. The results showed that almost half of the patients had a high school degree (42.5%), while only 4.6% had an elementary school degree. The rest of the patients had a university degree (Table 1).
No comorbidities were recorded in 25 patients; 57.5% had a family history of diabetes. The frequency of comorbidities for the remaining 63 patients is recorded in Figure 1.
When asked about the frequency of blood glucose monitoring by the patients, 50% answered 1 time/day. After analyzing the patients’ responses to the questionnaire, it was found that 90% of patients reported the frequency of their visits to the doctor for diabetes was every 3 months and 10% every year. A total of 89.8% of patients responded that they were not informed about the severity of the disease, while 10.2% of patients were informed. When asked if dietary instructions were given after the onset of the disease, the physician responded that it was the patient’s responsibility. Almost half of the patients exercised every day. Finally, patients were asked if they smoked, and 25% of patients answered yes (Table 2).
Figure 2 shows the percentage of participants who adhered to the dietary guidelines prior to the intervention. Before the intervention, half the patients had not received clear dietary guidelines related to treating their diabetes. The others had been given some kind of dietary plan by the research dietician. For the majority of patients (56%), reducing carbohydrate intake was the most important dietary goal; 20% of patients tried to increase their intake of fruit and vegetables; 42% chose to include low-fat foods in their diet; 27% of patients did not follow any dietary guidelines. In terms of sodium consumption, only 5% restricted the consumption of processed foods, and 35% refrained from eating particularly salty foods.
When asked about their knowledge of the proper diet for someone with diabetes, the largest percentage (57.5%) rated this as moderate, while 37.9% felt they were adequately informed. A small percentage of 3.4% felt that they had very good knowledge and 1.1% felt that they had no knowledge in this area.

3.3. Efficacy of the Nutrition Education Intervention

At the end of the dietary intervention period, changes were seen in all anthropometric and biochemical variables measured. Body weight and body mass index (BMI) decreased significantly, as did systolic blood pressure, fasting and mean glucose, total and LDL cholesterol and triglycerides (TGs) (Table 3). The most important outcome was the change in body composition (average body fat and vascular fat percentage averages) and waist circumference (Table 3).
The atherosclerotic index and uric acid also decreased significantly at the end of the study period, while no significant changes occurred in HbA1c, HDL cholesterol, diastolic blood pressure and muscle mass (Table 3).
Based on the 24 h reminders at the beginning and end of the study, 73.4% of patients reduced their daily calorie intake and 5.9% increased their consumption of high-fiber foods by the third month, a large percentage (from 67.8% at the first visit to 59.8% in the third month) reduced their alcohol consumption, 5.9% opted for plant-based foods in place of meat, chicken and fish, while 5.2% made no changes to their dietary habits (Figure 3). Regarding patients’ participation in physical activities, the percentage increased slightly by the third month, such as brisk walking, cycling or playing a friendly game of basketball or soccer (moderate to vigorous physical activity) (Figure 1). A significant percentage of patients skipped meals both at the beginning and at the end of the study (especially dinner (55.2%)) (Figure 4), although skipping breakfast and afternoon snacks was less frequent in the third month of the intervention and the differences were statistically significant (p < 0.05) (Figure 4). Lunch was the only meal that was not skipped by anyone.
Since dietitians should focus on individualized nutritional care to gain a holistic understanding of their patients, we recorded the frequency of patient communication with the dietitian during the three-month intervention and the results are shown in Figure 5.

4. Discussion

In this study, the nutritional and lifestyle recommendations given to diabetic patients appeared to cause significant changes in anthropometric characteristics and biochemical markers 3 months after a face-to-face meeting with a specialized dietitian. This is due to dietary instructions and changes in their physical activity (Table 1 and Table 2). Main role in achieving and maintaining an appropriate body weight, preventing complications of the disease (Figure 1) and improving the overall clinical picture play also the appropriate dietary changes (Figure 2).
Other studies have also examined a similar research topic [37,38,39]. In most of them, a significant trend of a decrease in the recorded anthropometric characteristics and biochemical indices was observed [40]. In our study, body weight decreased from 81.8 to 77.8 kg after 3 months, and BMI also decreased from 28.8 to 27.1 kg/m2. There was also a significant reduction in the average fasting blood glucose from 110.7 to 99.5 mg/dL and in the mean value of lipids (total cholesterol, LDL cholesterol, HDL cholesterol and triglycerides). The greatest change was observed in the mean total cholesterol and the mean triglyceride values. According to a recent study with a 3-month intervention to improve glucose control in individuals with type 2 diabetes through education, the HbA1c value was reduced by 1.1% [41]. In the ANODE study (2017), other secondary endpoints in the intention-to-treat analysis with web-based nutritional coaching were fasting blood glucose 1.46 mmol/L, total cholesterol 0.21 mg/dL, LDL-c 0.2 mg/dL, HDL-c 0.05 mg/dL, triglycerides 1.05 mg/dL and uric acid 45.45 µmol/L [42]. In our study, the changes in the other biomarkers were higher, with the exception of fasting blood glucose and uric acid, which were the same: fasting blood glucose 1.12 mmol/L, total cholesterol 17.2 mg/dL, LDL-c 6.8 mg/dL, HDL-c 1.1 mg/dL, triglycerides 35 mg/dL and uric acid 30 µmol/L. Other studies had positive results [41,42], as our study has. A possible explanation is the multi-layered strategies such as a personalized diet plan, written instructions with healthy food choices and personal contact with the dietician.
Some studies found varying effects of nutritional education [43,44,45]. For example, one study of 100 patients with type 2 diabetes found no significant effects on BMI or daily intake of fruit and vegetables, but there were positive changes in fasting blood glucose and HbA1c as well as weekly consumption of fruit and vegetables. Weekly moderate physical activity also improved [46]. Awareness about diabetes complications and consequent improvements in dietary knowledge, attitude and practices lead to better control of the disease [47]. Different medications may also have different effects [48] and it is important to provide appropriate motivation for physical activity [49]. Our study did not find any significant change in HbA1c values, although significant changes occurred in fasting blood glucose levels. The biggest change was found in those who followed the dietitian’s nutritional advice.
Our results agree with other studies that both dietary guidelines and nutritional interventions contribute to the reduction in anthropometric characteristics and biochemical indicators of people with type 2 diabetes. Following specific dietary interventions also gives better results for weight loss than are found in people who follow more general dietary recommendations [50].
Our sample consisted of patients admitted to the hospital due to uncontrollable diabetes. It is possible that being admitted to the hospital and being given information about the possible complications that can occur if T2DM is not controlled contributed to their more positive attitude toward making changes in their behavior, both in terms of diet and physical activity (Figure 3). The intervention in the 88 adults with T2DM played an important role in their overall health.
Multiple supportive connections in community settings can also help people lose weight.
A study by Pellegrini and colleagues [47] aimed to evaluate the effectiveness of a technology-based system (TECH) on weight loss when used alone or in combination with a 6-month, in-person, behavioral weight loss intervention [47]. In another study of 212 patients [48], biomarkers such as fasting glucose, postprandial plasma glucose, triglyceride and HbA1c were lower at each follow-up meeting with the dietitian, which highlighted the improved patients’ knowledge and behavior using the mobile interactive system as a helpful tool [49].
Nutrition is unquestionably important in the progression of T2DM, but most people rely more heavily on medication to manage their disease. In our study, the majority of the patients managed their diabetes by taking medicinal tablets (26.4%) or by combining antidiabetic drugs with appropriate nutrition/diet (27.6%). One review of 22 studies of overweight adults with type 2 diabetes [51] found that the most successful weight loss occurred with multicomponent interventions, including more intense physical activity and very low-calorie diets or low-calorie diets [51].
Programs delivered in primary care can produce meaningful weight loss. In our study, the average weight loss was 4 Kg. It is reported that a 5% to 10% weight loss is associated with health benefits, including lower systolic blood pressure along with reduced triglyceride and glucose levels, which may impact cardiac health [52]. In addition to weight control, the first goal is macronutrient and micronutrient intakes at the right amounts according to national dietary recommendations, i.e., a high-quality diet [34]. The proper dietary plan could be helpful for patients to follow the advice, as many do not realize that following the proper dietary rules prevents the occurrence of complications of the disease and improves the overall clinical picture of the patient [43]. In addition, more than half of the participants did not correctly identify alcohol as a factor that plays a role in the progression of the disease. Although abstaining from alcohol does not “reverse” diabetes per se, it significantly improves glycemic control and reduces the likelihood of complications [53]. Our study also showed that the consumption of breakfast is a factor in better metabolic biomarkers (Figure 4). This concurs with findings from a study of adults in families at high risk of T2DM in six European countries [54]. Another important finding of our study, as shown in the initial interviews of the patients with the dietitian, is that patients ignore the basic parameters of the disease. Although they know the importance of regulating blood glucose concentrations, they consider that reducing the calories they consume is enough to protect them from adverse situations. Observance of the frequency of meals by diabetic patients is of particular importance, but there was also a number of patients who skipped meals. Finally, the Mediterranean diet is considered a well-formed diet plan. However, with all dietary changes, we know that institutions and organizations need behavioral scientists to assist consumers in becoming more aware of healthy eating habits, nutritional labeling and checking overall health [27].
According to the Academy of Nutrition and Dietetics and the Endocrine Society, another factor that affects the success of a nutrition education program and may minimize the frequency of visits to a dietitian is the cost [55]. A potential solution could be for primary care to support the recommendations from the organizations through consultations with health professionals [56].
Other factors, such as emotional support as well as fast and effective access to care, have been found to be important [57]. A greater number of contacts between patients and providers led to greater weight loss (Figure 5). The dietitian in all the studies followed some strategies for weight loss (>1 kg/month) such as dietary plans with detailed diet information or advice on cooking and minimizing the frequency of eating out and some other support tools like a food exchange list. Some specifically list replacement foods organized by food groups and guidelines on healthy food choices or even healthy recipes [58].
After the nutritional intervention, a change was observed in all biochemical indices and anthropometric characteristics studied. Therefore, the adoption of a careful dietary pattern based on the Mediterranean diet can lead to significant and long-term changes in metabolic profile due to minimizing ultra-processed foods, which are high in saturated fats and added sugars. Such changes protect against cardiovascular complications [59,60].
Diet advice via individual sessions as treatment has occurred in many studies [61]. A single dietary counseling session [62], as in our study and others, did not have the same results as can occur in more intensified interventions such as weekly [63], fortnightly [64] or monthly sessions [20].
Dietary patterns such as the Mediterranean diet as well as physical activity are crucial for improving the metabolic disturbances seen in patients with diabetes [65]. The primary goal is to reduce saturated and trans fatty acids. Dietary plans documented to reduce body weight at least by 5% in overweight and obese people should also reduce total fat to <30% of daily energy intake, reduce saturated fat (including trans fatty acids) to <10% of daily energy intake, increase fiber intake (14g/1000 Kcal) [66], minimize refined and processed foods [67] and increase omega-3 fatty acid intake [68]. Increasing the daily consumption of natural foods rich in dietary antioxidants (tocopherols, carotenoids, vitamin C, flavonoids, polyphenols), trace elements and vitamins by increasing vegetable and fruit intake to 400 g/day should be encouraged [69]. Educational meetings with the dietitian in primary care will possibly help patients better understand type 2 diabetes and show how they can control it with easy-to-apply lifestyle changes. The interaction and exchanges between different specialists, a friendly atmosphere of meetings, weight loss tips, including the latest research-backed strategies, healthy eating plans, smart nutritional secrets, meal-planning help and lifestyle strategies to help manage diabetes could help patients control diabetes. Moreover, effective social support with assistance and encouragement from family members, adequate self-management skills and self-efficacy (confidence) may reduce the risk of developing diabetes complications [70].
In our study, despite recommendations from health professionals to adopt a healthier lifestyle, many patients avoided exercising, while a high percentage of patients smoked. These practices are anything but helpful in controlling the disease. This finding should concern and activate health professionals to mobilize change in the behavior and habits of patients. Exercise seems to have a positive association not only with the regulation of systolic and diastolic blood pressure [71] but also with glycemic control [72] and variability, insulin sensitivity, lipid profile, oxidative stress/antioxidative capacity and/or chronic inflammation [73]. Although there is limited evidence, stopping smoking has been shown to have benefits in reducing or slowing the risk of cardiovascular morbidity and mortality in people with diabetes [74].
The nutritional intervention adopted by our patients was based on the principles of the Mediterranean diet [69]. The Mediterranean diet is considered to be a model of healthy eating. Its beneficial actions are generally accepted both in the general population and in patients with T2DM [66]. It is a food pattern that satisfies all the conditions of a suitable diet for the regulation of the disease. It is therefore necessary to inform patients about the beneficial effects of this nutritional model in order to adopt it in their daily lives. Many people with diabetes initiate a conversation about diet with a health professional themselves [75]. The primary reason clinicians initiate a conversation about weight management is to avoid follow-on complications from T2DM [76]. A key strategic theme is to strengthen research-based understanding of T2DM and public health to improve the lives of young people and adults living with or at high risk of developing T2DM.
Therapeutic patient education for obesity or diabetes is a cost-effective intervention that improves patient outcomes [51]. The first step is to learn about the patient’s circumstances and perspective, the second step is to help the patient identify their goals, the third step is to help the patient develop a plan (especially a dietary plan and oral health routine), the fourth step is to help the patient implement their plan and the fifth step is to review progress and adjust to changing circumstances. According to the most recently published WHO guidelines (2023), this review identified the factors that could be helpful for doctors, dietitians, nutritionists and other health professionals to promote health and prevent T2DM complications through education [27].
The main objective is to give health professionals better access to effective nutrition education for all people by identifying risk factors such as obesity, malnutrition, excessive sugar intake, weight, age, smoking, alcohol consumption and physical inactivity. A fundamentally different approach is then needed, one that emphasizes disease prevention and health management through a multidisciplinary, integrated and patient-centered approach to overall health [76].
The limitations of this study include the small sample size. The primary care physician was recommended and notified. Future research needs to be conducted using artificial intelligence and its applications to diabetes in order to detect and manage the disease and capture more data to be recorded for personalized healthcare with lower costs. A fully automated web-based program improves lifestyle habits and HbA1c in patients with type 2 diabetes and could be the next step for the researchers.

5. Conclusions

In conclusion, this study adds to the existing scientific evidence of the benefits of a nutrition education program for patients with type 2 diabetes mellitus by demonstrating relevant outcomes in both glycemic responses and dietary behaviors in a real-world setting. Overall, these data suggest that more frequent face-to-face contact with the dietitian may also be more helpful, and meal frequency and a daily breakfast followed by an afternoon snack of healthier foods may help to break down barriers and facilitate dietary self-management of diabetes. To achieve this, people with diabetes need education about their condition. They need to understand how to self-regulate their blood sugar not only in normal situations but also in stressful situations, such as intense physical activity, and when to seek early medical help. The earlier treatment begins, the better the prognosis.

Author Contributions

Conceptualization, O.G., A.B. and O.A.; methodology, O.G., A.B. and O.A.; software, M.D., A.V. and H.G.; validation, A.B., O.G., O.A. and M.D.; formal analysis, M.D.; investigation, M.D., A.V. and H.G.; resources, M.D.; data curation, O.G., A.B., O.A. and M.D.; writing—original draft preparation, M.D.; writing—review and editing, A.B., O.A., M.D. and O.G.; visualization, O.A. and A.B.; supervision, O.G.; project administration, O.G. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Institutional Review Board Statement

The study was approved by the competent Bioethics Committee of the University of Thessaly (approval numbers 49162/13-10-2017 and 49161/13-10-2017), and it was in line with the Declaration of Helsinki.

Informed Consent Statement

Informed consent was obtained from all subjects involved in the study.

Data Availability Statement

The data presented in this study are available on request from the corresponding author. Data are unavailable due to privacy restrictions.

Acknowledgments

This work was supported by the Department of Endocrinology and Metabolic Diseases, Medical School, University of Thessaly, Larissa, Greece, and specifically by Bargiota Alexandra, Endocrinologist and Director of the Endocrinology Clinic of the University Hospital of Larissa, who granted us permission to enter the clinic and allowed us to talk with the patients. Additionally, Tsolaki Catherine, Clinical Dietitian and Head of the Dietetics Department of the University Hospital of Larisa, and Sotiriou Evangelia, Dietitian, for their cooperation in collecting data and conducting interviews with the patients.

Conflicts of Interest

The authors declare no conflicts of interest.

References

  1. Saeedi, P.; Petersohn, I.; Salpea, P.; Malanda, B.; Karuranga, S.; Unwin, N.; Colagiuri, S.; Guariguata, L.; Motala, A.A.; Ogurtsova, K. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas. Diabetes Res. Clin. Pract. 2019, 157, 107843. [Google Scholar] [CrossRef]
  2. Iacobini, C.; Vitale, M.; Pesce, C.; Pugliese, G.; Menini, S. Diabetic complications and oxidative stress: A 20-year voyage back in time and back to the future. Antioxidants 2021, 10, 727. [Google Scholar] [CrossRef] [PubMed]
  3. Echouffo-Tcheugui, J.B.; Perreault, L.; Ji, L.; Dagogo-Jack, S. Diagnosis and Management of Prediabetes: A Review. JAMA 2023, 329, 1206–1216. [Google Scholar] [CrossRef] [PubMed]
  4. Abdullah, A.; Peeters, A.; de Courten, M.; Stoelwinder, J. The magnitude of association between overweight and obesity and the risk of diabetes: A meta-analysis of prospective cohort studies. Diabetes Res. Clin. Pract. 2010, 89, 309–319. [Google Scholar] [CrossRef] [PubMed]
  5. Field, A.E.; Coakley, E.H.; Must, A.; Spadano, J.L.; Laird, N.; Dietz, W.; Rimm, E.; Colditz, G.A. Impact of overweight on the risk of developing common chronic diseases during a 10-year period. Arch. Intern. Med. 2001, 161, 1581–1586. [Google Scholar] [CrossRef] [PubMed]
  6. Taylor, R. Insulin resistance and type 2 diabetes. Diabetes 2010, 61, 778–779. [Google Scholar] [CrossRef]
  7. Forouhi, N.G.; Misra, A.; Mohan, V.; Taylor, R.; Yancyet, W. Dietary and nutritional approaches for prevention and management of type 2 diabetes. BMJ 2018, 361, k2234. [Google Scholar] [CrossRef]
  8. Wing, R.R. Looking back and forward from the Diabetes Prevention Program (DPP): A commentary on the importance of research aimed at intervention optimization. Health Psychol. 2021, 40, 1009–1016. [Google Scholar] [CrossRef]
  9. Powers, M.A.; Bardsley, J.K.; Cypress, M.; Funnell, M.M.; Harms, D.; Hess-Fischl, A.; Hooks, B.; Isaacs, D.; Mandel, E.D.; Maryniuk, M.D.; et al. Diabetes self-management education and support in adults with type 2 diabetes: A consensus report of the American Diabetes Association, the Association of Diabetes Care & Education Specialists, the Academy of Nutrition and Dietetics, the American Academy of Family Physicians, the American Academy of PAs, the American Association of Nurse Practitioners, and the American Pharmacists Association. Diabetes Care 2020, 43, 1636–1649. [Google Scholar]
  10. Haynes, A.; Kersbergen, I.; Sutin, A.; Daly, M.; Robinson, E. A systematic review of the relationship between weight status perceptions and weight loss attempts, strategies, behaviours and outcomes. Obes. Rev. 2018, 19, 347–363. [Google Scholar] [CrossRef]
  11. Rawshani, A.; Rawshani, A.; Franzén, S.; Sattar, N.; Eliasson, B.; Svensson, A.M.; Zethelius, B.; Miftaraj, M.; McGuire, D.K.; Rosengren, A.; et al. Risk factors, Mortality, and Cardiovascular Outcomes in patients with type 2 diabetes. N. Engl. J. Med. 2018, 379, 633–644. [Google Scholar] [CrossRef]
  12. Magkos, F.; Hjorth, M.F.; Astrup, A. Diet and exercise in the prevention and treatment of type 2 diabetes mellitus. Nat. Rev. Endocrinol. 2020, 16, 545–555. [Google Scholar] [CrossRef]
  13. Han, H.H.; Cao, Y.; Feng, C.; Zheng, Y.; Dhana, K.; Zhu, S.; Shang, C.; Yuan, C.; Zong, G. Association of a Healthy Lifestyle with All-Cause and Cause-Specific Mortality Among Individuals with Type 2 Diabetes: A Prospective Study in UK Biobank. Diabetes Care 2022, 45, 319–329. [Google Scholar] [CrossRef] [PubMed]
  14. Swift, D.L.; McGee, J.E.; Earnest, C.P.; Carlisle, Ε.; Nygard, Μ.; Johannsen, Ν.Μ. The Effects of Exercise and Physical Activity on Weight Loss and Maintenance. Progress. Cardiovasc. Dis. 2018, 61, 206–213. [Google Scholar] [CrossRef] [PubMed]
  15. Meng, Y.; Bai, H.; Wang, S.; Li, Ζ.; Wang, Q.; Chen, L. Efficacy of low carbohydrate diet for type 2 diabetes mellitus management: A systematic review and meta-analysis of randomized controlled trials. Diabetes Res. Clin. Pract. 2017, 131, 124–131. [Google Scholar] [CrossRef] [PubMed]
  16. McMacken, M.; Shah, S. A plant-based diet for the prevention and treatment of type 2 diabetes. J. Geriatr. Cardiol. 2017, 14, 342–354. [Google Scholar] [CrossRef]
  17. Hall, K.D.; Kahan, S. Maintenance of lost weight and long-term management of obesity. Med. Clin. 2018, 102, 183–197. [Google Scholar] [CrossRef] [PubMed]
  18. Bailey, R.R. Goal setting and action planning for health behavior change. Am. J. Lifestyle Med. 2019, 13, 615–618. [Google Scholar] [CrossRef] [PubMed]
  19. Sheeran, P.; Klein, W.M.; Rothman, A.J. Health behavior change: Moving from observation to intervention. Annu. Rev. Psychol. 2017, 68, 573–600. [Google Scholar] [CrossRef]
  20. Newson, L.; Parody, F.H. Investigating the experiences of low-carbohydrate diets for people living with Type 2 Diabetes: A thematic analysis. PLoS ONE 2022, 17, e0273422. [Google Scholar] [CrossRef]
  21. Behrouz, V.; Dastkhosh, A.; Sohrab, G. Overview of dietary supplements on patients with type 2 diabetes. Diabetes Metab. Syndr. Clin. Res. Rev. 2020, 14, 325–334. [Google Scholar] [CrossRef] [PubMed]
  22. Papakonstantinou, E.; Oikonomou, C.; Nychas, G.; Dimitriadis, G.D. Effects of Diet, Lifestyle, Chrononutrition and Alternative Dietary Interventions on Postprandial Glycemia and Insulin Resistance. Nutrients 2022, 14, 823. [Google Scholar] [CrossRef]
  23. Vlachos, D.; Malisova, S.; Lindberg, F.A.; Karaniki, G. Glycemic Index (GI) or Glycemic Load (GL) and Dietary Interventions for Optimizing Postprandial Hyperglycemia in Patients with T2 Diabetes: A Review. Nutrients 2020, 12, 1561. [Google Scholar] [CrossRef]
  24. Esposito, K.; Maiorino, M.I.; Di Palo, C.; Giugliano, D. Adherence to a Mediterranean diet and glycaemic control in Type 2 diabetes mellitus. Diabet. Med. 2009, 26, 900–907. [Google Scholar] [CrossRef]
  25. Rajpal, A.; Ismail-Beigi, F. Intermittent fasting and ‘metabolic switch’: Effects on metabolic syndrome, prediabetes and type 2 diabetes. Diabetes Obes. Metab. 2020, 22, 1496–1510. [Google Scholar] [CrossRef]
  26. Salvia, M.G.; Quatromoni, P.A. Behavioral Approaches to Nutrition and Eating Patterns for Managing Type 2 Diabetes: A Review. Am. J. Med. Open 2023, 9, 100034. [Google Scholar] [CrossRef]
  27. WHO. Technical Advisory Group on Diabetes: Hybrid Meeting, 30 November–1 December 2022; World Health Organization: Geneva, Switzerland, 2023.
  28. WHO Multicentre Growth Reference Study Group; de Onis, M. Reliability of anthropometric measurements in the WHO Multicentre Growth Reference Study. Acta Paediatr. 2006, 95, 38–46. [Google Scholar]
  29. Craig, C.L.; Marshall, A.L.; Sjöström, M.; Bauman, A.E.; Booth, M.L.; Ainsworth, B.E.; Pratt, M.; Ekelund, U.; Yngve, A.; Sallis, J.F. International physical activity questionnaire: 12-country reliability and validity. Med. Sci. Sports Exerc. 2003, 35, 1381–1395. [Google Scholar] [CrossRef]
  30. Katsouyanni, K.; Rimm, Ε.Β.; Gnardellis, C.; Trichopoulos, D.; Polychronopoulos, E.; Trichopoulou, A. Reproducibility and relative validity of an extensive semi-quantitative food frequency questionnaire using dietary records and biochemical markers among Greek schoolteachers. Int. J. Epidemiol. 1997, 26, 118–127. [Google Scholar] [CrossRef]
  31. Friedewald, W.T.; Levy, R.I.; Fredrickson, D.S. Estimation of the concentration of low-density lipoprotein cholesterol in plasma, without use of the preparative ultracentrifuge. Clin. Chem. 1972, 18, 499–502. [Google Scholar] [CrossRef] [PubMed]
  32. Matthews, D.R.; Hosker, J.P.; Rudenski, A.S.; Naylor, B.; 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] [PubMed]
  33. Blanton, C.A.; Moshfegh, A.J.; Baer, D.J.; Kretsch, M.J. The USDA Automated Multiple-Pass Method accurately estimates group total energy and nutrient intake. J. Nutr. 2006, 136, 2594–2599. [Google Scholar] [CrossRef]
  34. ElSayed, N.A.; Aleppo, G.; Aroda, V.R.; Bannuru, R.R.; Brown, F.M.; Bruemmer, D.; Collins, B.S.; Hilliard, M.E.; Isaacs, D.; Johnson, E.L. 5. Facilitating Positive Health Behaviors and Well-being to Improve Health Outcomes: Standards of Care in Diabetes—2023. Diabetes Care 2023, 46 (Suppl. S1), S68–S96. [Google Scholar] [CrossRef] [PubMed]
  35. Bimpas, N.G.; Auyeung, V.; Tentolouris, A.; Tzeravini, H.; Eleutheriadou, I.; Tentolouris, N. Adoption of and adherence to the Hellenic Diabetes Association guidelines for the management of subjects with type 2 diabetes mellitus by Greek physicians. Hormones 2021, 20, 347–358. [Google Scholar] [CrossRef]
  36. Reynolds, A.N.; Akerman, A.P.; Mann, J. Dietary fibre and whole grains in diabetes management: Systematic review and meta-analyses. PLoS Med. 2020, 17, e1003053. [Google Scholar] [CrossRef]
  37. Group, L.A.R. The Look AHEAD study: A description of the lifestyle intervention and the evidence supporting it. Obesity 2006, 14, 737–752. [Google Scholar]
  38. Sharma, R.; Prajapati, P. Diet and lifestyle guidelines for diabetes: Evidence based ayurvedic perspective. Rom. J. Diabetes Nutr. Metab. Dis. 2014, 21, 335–346. [Google Scholar] [CrossRef]
  39. Ajala, O.; English, P.; Pinkney, J. Systematic review and meta-analysis of different dietary approaches to the management of type 2 diabetes. Am. J. Clin. Nutr. 2013, 97, 505–516. [Google Scholar] [CrossRef]
  40. ElSayed, N.A.; Aleppo, G.; Aroda, V.R.; Bannuru, R.R.; Brown, F.M.; Bruemmer, D.; Collins, B.S.; Hilliard, M.E.; Isaacs, D.; Johnson, E.L. 3. Prevention or Delay of Type 2 Diabetes and Associated Comorbidities: Standards of Care in Diabetes—2023. Diabetes Care 2023, 46 (Suppl. S1), S41–S48. [Google Scholar] [CrossRef]
  41. Chaib, A.; Zarrouq, Β.; El Amine Ragala, Μ.; Lyoussi, B.; Giesy, J.P.; Aboul-Soud, Μ.A.Μ.; Halim, Κ. Effects of nutrition education on Metabolic profiles of patients with type 2 diabetes mellitus to improve glycated hemoglobin and body mass index. J. King Saud. Univ. —Sci. 2023, 35, 1018–3647. [Google Scholar] [CrossRef]
  42. Hansel, B.; Giral, P.; Gambotti, L.; Lafourcade, A.; Peres, G.; Filipecki, C.; Kadouch, D.; Hartemann, A.; Oppert, J.; Bruckert, E.; et al. A fully automated web-based program improves lifestyle habits and HbA1c in patients with type 2 diabetes and abdominal obesity: Randomized trial of patient e-coaching nutritional support (the ANODE study). J. Med. Internet Res. 2017, 19, e360. [Google Scholar] [CrossRef]
  43. Maheri, A.; Asnaashari, Μ.; Joveini, H.; Tol, A.; Firouzian, A.A.; Rohban, A. The impact of educational intervention on physical activity, nutrition and laboratory parameters in type II diabetic patients. Electron. Physician 2017, 9, 4207. [Google Scholar] [CrossRef]
  44. Sami, W.; Ansari, T.; Butt, N.S.; Hamid, M.R.A. Effect of diet on type 2 diabetes mellitus: A review. Int. J. Health Sci. (Qassim) 2017, 11, 65–71. [Google Scholar] [PubMed]
  45. Vaccaro, O.; Masulli, Μ.; Bonora, Ε.; Del Prato, S.; Giorda, C.B.; Maggioni, A.P.; Mocarelli, P.; Nicolucci, A.; Rivellese, A.A.; Squatrito, S.; et al. Addition of either pioglitazone or a sulfonylurea in type 2 diabetic patients inadequately controlled with metformin alone: Impact on cardiovascular events. A randomized controlled trial. Nutr. Metab. Cardiovasc. Dis. 2012, 22, 997–1006. [Google Scholar] [CrossRef] [PubMed]
  46. Duclos, M.; Oppert, J.-M.; Verges, B.; Coliche, V.; Gautier, J.-F.; Guezennec, Y.; Reach, G.; Strauch, G. Physical activity and type 2 diabetes. Recommandations of the SFD (Francophone Diabetes Society) diabetes and physical activity working group. Diabetes Metab. 2013, 39, 205–216. [Google Scholar] [CrossRef] [PubMed]
  47. Pellegrini, C.A.; Verba, S.D.; Otto, A.D.; Helsel, D.L.; Davis, K.K.; Jakicic, J.M. The Comparison of a Technology-Based System and an In-Person Behavioral Weight Loss Intervention. Obesity 2012, 20, 356–363. [Google Scholar] [CrossRef]
  48. Hu, Y.; Wen, X.; Wang, F.; Yang, D.; Liu, S.; Li, P.; Xu, J. Effect of telemedicine intervention on hypoglycaemia in diabetes patients: A systematic review and meta-analysis of randomised controlled trials. J. Telemed. Telecare 2019, 25, 402–413. [Google Scholar] [CrossRef] [PubMed]
  49. Guo, S.H.-M. Assessing quality of glycemic control: Hypo- and hyperglycemia, and glycemic variability using mobile self-monitoring of blood glucose system. Health Inform. J. 2019, 26, 287–297. [Google Scholar] [CrossRef] [PubMed]
  50. ElSayed, N.A.; Aleppo, G.; VR Aroda, V.R.; RR Bannuruet, R.R. 8. Obesity and Weight Management for the Prevention and Treatment of Type 2 Diabetes: Standards of Care in Diabetes—2023. Diabetes Care 2023, 46 (Suppl. S1), S128–S139. [Google Scholar] [CrossRef]
  51. Norris, S.L.; Zhang, X.; Avenell, A.; Gregg, E.; Bowman, B.; Serdula, M.; Brown, T.J.; Schmid, C.H.; Lau, J. Long-term effectiveness of lifestyle and behavioral weight loss interventions in adults with type 2 diabetes: A meta-analysis. Am. J. Med. 2004, 117, 762–774. [Google Scholar] [CrossRef]
  52. Ryan, D.H.; Yockey, S.R. Weight Loss and Improvement in Comorbidity: Differences at 5%, 10%, 15%, and Over. Curr. Obes. Rep. 2017, 6, 187–194. [Google Scholar] [CrossRef]
  53. Marathe, P.H.; Gao, H.X.; Close, K.L. American Diabetes Association Standards of Medical Care in Diabetes 2017. J. Diabetes 2017, 9, 320–324. [Google Scholar] [CrossRef]
  54. Apergi, K.; Karatzi, K.; Reppas, K.; Karaglani, E.; Usheva, N.; Giménez-Legarre, N.; Moreno, L.A.; Dimova, R.; Antal, E.; Jemina, K. Association of breakfast consumption frequency with fasting glucose and insulin sensitivity/b cells function (HOMA-IR) in adults from high-risk families for type 2 diabetes in Europe: The Feel4Diabetes Study. Eur. J. Clin. Nutr. 2022, 76, 1600–1610. [Google Scholar] [CrossRef]
  55. Sun, Y.; You, W.; Almeida, F.; Estabrooks, P.; Davy, B. The Effectiveness and Cost of Lifestyle Interventions Including Nutrition Education for Diabetes Prevention: A Systematic Review and Meta-Analysis. J. Acad. Nutr. Diet. 2017, 117, 404–421.e36. [Google Scholar] [CrossRef]
  56. Rosenfeld, R.M.; Kelly, J.H.; Agarwal, M.; Aspry, K.; Barnett, T.; Davis, B.C.; Fields, D.; Gaillard, T.; Gulati, M.; Guthrie, G.E. Dietary interventions to treat type 2 diabetes in adults with a goal of remission: An expert consensus statement from the American College of Lifestyle Medicine. Am. J. Lifestyle Med. 2022, 16, 342–362. [Google Scholar] [CrossRef]
  57. Flint, S.W.; Leaver, M.; Griffiths, A.; Kaykanloo, M. Disparate healthcare experiences of people living with overweight or obesity in England. eClinicalMedicine 2021, 41, 101140. [Google Scholar] [CrossRef]
  58. Early, K.B.; Stanley, K. Position of the Academy of Nutrition and Dietetics: The Role of Medical Nutrition Therapy and Registered Dietitian Nutritionists in the Prevention and Treatment of Prediabetes and Type 2 Diabetes. J. Acad. Nutr. Diet. 2018, 118, 343–353. [Google Scholar] [CrossRef]
  59. Acosta-Navarro, J.; Antoniazzi, L.; Oki, A.M.; Bonfim, M.C.; Hong, V.; Acosta-Cardenas, P.; Strunz, C.; Brunoro, E.; Miname, M.H.; Salgado Filho, W. Reduced subclinical carotid vascular disease and arterial stiffness in vegetarian men: The CARVOS Study. Int. J. Cardiol. 2017, 230, 562–566. [Google Scholar] [CrossRef]
  60. Afshin, A.; Sur, P.J.; Fay, K.A.; Cornaby, L.; Ferrara, G.; Salama, J.S.; Mullany, E.C.; Abate, K.H.; Abbafati, C.; Abebe, Z. Health effects of dietary risks in 195 countries, 1990–2017: A systematic analysis for the Global Burden of Disease Study 2017. Lancet 2019, 393, 1958–1972. [Google Scholar] [CrossRef]
  61. Cradock, K.A.; ÓLaighin, G.; Finucane, F.M.; Gainforth, H.L.; Quinlan, L.R.; Ginis, K.M. Behaviour change techniques targeting both diet and physical activity in type 2 diabetes: A systematic review and meta-analysis. Int. J. Behav. Nutr. Phys. Act. 2017, 14, 18. [Google Scholar] [CrossRef]
  62. BANERJEE, M.; MACDOUGALL, M.; LAKHDAR, A.F. Impact of a single one-to-one education session on glycemic control in patients with diabetes. J. Diabetes 2012, 4, 186–190. [Google Scholar] [CrossRef] [PubMed]
  63. Napoleone, J.M.; Miller, R.G.; Devaraj, S.M.; Rockette-Wagner, B.; Arena, V.C.; Venditti, E.M.; Kramer, K.; Strotmeyer, E.S.; Kriska, A.M. Impact of Maintenance Session Attendance and Early Weight Loss Goal Achievement on Weight Loss Success in a Community-Based Diabetes Prevention Program Intervention. Sci. Diabetes Self-Manag. Care 2021, 47, 279–289. [Google Scholar] [CrossRef]
  64. West, D.S.; DiLillo, V.; Bursac, Z.; Gore, S.A.; Greene, P.G. Motivational Interviewing Improves Weight Loss in Women with Type 2 Diabetes. Diabetes Care 2007, 30, 1081–1087. [Google Scholar] [CrossRef]
  65. Castro-Barquero, S.S.; Ruiz-León, A.M.; Sierra-Pérez, M.; Estruch, R.; Casas, R. Dietary strategies for metabolic syndrome: A comprehensive review. Nutrients 2020, 12, 2983. [Google Scholar] [CrossRef]
  66. American Diabetes Association Professional Practice Committee. 5. Facilitating behavior change and well-being to improve health outcomes: Standards of Medical Care in Diabetes—2022. Diabetes Care 2022, 45 (Suppl. S1), S60–S82. [Google Scholar] [CrossRef]
  67. American Diabetes Association Professional Practice Committee. 3. Prevention or delay of type 2 diabetes and associated comorbidities: Standards of Medical Care in Diabetes—2022. Diabetes Care 2022, 45 (Suppl. S1), S39–S45. [Google Scholar] [CrossRef]
  68. Chew, E.Y. Dietary Intake of Omega-3 Fatty Acids from Fish and Risk of Diabetic Retinopathy. JAMA 2017, 317, 2226–2227. [Google Scholar] [CrossRef]
  69. Tosti, V.; Bertozzi, B.; Fontana, L. Health benefits of the Mediterranean diet: Metabolic and molecular mechanisms. J. Gerontol. Ser. A 2018, 73, 318–326. [Google Scholar] [CrossRef]
  70. Adu, M.D.; Malabu, U.H.; Malau-Aduli, A.E.; Malau-Aduli, B.S. Enablers and barriers to effective diabetes self-management: A multi-national investigation. PLoS ONE 2019, 14, e0217771. [Google Scholar] [CrossRef]
  71. Heberle, I.; de Barcelos, G.T.; Silveira, L.M.P.; Costa, R.R.; Gerage, A.M.; Delevatti, R.S. Effects of aerobic training with and without progression on blood pressure in patients with type 2 diabetes: A systematic review with meta-analyses and meta-regressions. Diabetes Res. Clin. Pract. 2021, 171, 108581. [Google Scholar] [CrossRef]
  72. Savikj, M.; Zierath, J.R. Train like an athlete: Applying exercise interventions to manage type 2 diabetes. Diabetologia 2020, 63, 1491–1499. [Google Scholar] [CrossRef] [PubMed]
  73. Meuffels, F.M.; Isenmann, E.; Strube, M.; Lesch, A.; Oberste, M.; Brinkmann, C. Exercise Interventions Combined with Dietary Supplements in Type 2 Diabetes Mellitus Patients—A Systematic Review of Relevant Health Outcomes. Front. Nutr. 2022, 9, 817724. [Google Scholar] [CrossRef]
  74. Campagna, D.; Alamo, A.; Di Pino, A.; Russo, C.; Calogero, A.; Purrello, F.; Polosa, R. Smoking and diabetes: Dangerous liaisons and confusing relationships. Diabetol. Metab. Syndr. 2019, 11, 85. [Google Scholar] [CrossRef]
  75. ElSayed, N.A.; Aleppo, G.; Aroda, V.R.; Bannuru, R.R.; Brown, F.M.; Bruemmer, D.; Collins, B.S.; Hilliard, M.E.; Isaacs, D.; Johnson, E.L. 1. Improving Care and Promoting Health in Populations: Standards of Care in Diabetes—2023. Diabetes Care 2023, 46 (Suppl. S1), S10–S18.76. [Google Scholar] [CrossRef] [PubMed]
  76. American Diabetes Association. Standards of Care in Diabetes—2023 Abridged for Primary Care Providers. Clin. Diabetes 2023, 41, 4–31. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Comorbidity of the participants (%).
Figure 1. Comorbidity of the participants (%).
Applsci 14 02114 g001
Figure 2. The participants who followed the nutritional guidelines before the intervention (%).
Figure 2. The participants who followed the nutritional guidelines before the intervention (%).
Applsci 14 02114 g002
Figure 3. Percentage (%) of patients following the recommendations according to the ADA [22].
Figure 3. Percentage (%) of patients following the recommendations according to the ADA [22].
Applsci 14 02114 g003
Figure 4. Percentage (%) of meal-skipping in participants.
Figure 4. Percentage (%) of meal-skipping in participants.
Applsci 14 02114 g004
Figure 5. How often the patients communicated (either through calling, messaging or visiting) with the dietician during the three-month intervention.
Figure 5. How often the patients communicated (either through calling, messaging or visiting) with the dietician during the three-month intervention.
Applsci 14 02114 g005
Table 1. Socio-economic data and clinical characteristics of the T2DM patients (N = 88).
Table 1. Socio-economic data and clinical characteristics of the T2DM patients (N = 88).
%
SexMen45.5
Women54.5
EducationPrimary Education4.6
Secondary Education42.5
Higher Education52.9
Financial budget per month for foodEUR < 20111.4
EUR 201–30052.3
EUR 301–40031.8
EUR > 4004.5
Treatment of T2DMExercise and insulin1.1
Exercise. and medication1.1
Exercise and diet1.1
Diet, exercise and medication6.8
Diet and medication9.1
Insulin3.4
Medication56.8
Medication and insulin20.5
Table 2. Therapeutic approaches and treatment of T2DM (%).
Table 2. Therapeutic approaches and treatment of T2DM (%).
N %
Frequency of blood glucose measurementOccasionally3.4
Weekly8.0
1 time/day50.0
2–3 times/day34.1
>3 times/day4.5
Frequency of doctor visits for type 2 diabetes mellitusOnce a year13.6
Once per 6 months28.4
Once per 3 months35.2
1 time/month17.0
2 times/month5.7
Update on disease severity/consequences of non-regulationNo89.8
Yes10.2
With the onset of the disease, were dietary instructions given (immediately)? If so, by whom?No11.4
From the doctor52.3
By the dietitian with guidance from the attending physician36.4
From the dietitian during a visit on individual initiative0.0
Reason for not visiting a dietitianNo answer20.5
Negligence31.8
The doctor is enough36.4
Cost8.0
No time available3.4
Participation in physical activityNo27.3
Housework6.8
Outside work2.3
Walking53.4
Jogging2.3
Sport8.0
Frequency of exerciseNo answer27.3
1 time/week2.3
2 times/week4.5
3 times/week10.2
4 times/week3.4
5 times/week5.7
Every day46.6
SmokingNo75.0
Yes25.0
Table 3. Somatometric characteristics, biochemical variables and 24 h dietary recall results of the participants (N = 88) at baseline and after three months of the nutrition education intervention.
Table 3. Somatometric characteristics, biochemical variables and 24 h dietary recall results of the participants (N = 88) at baseline and after three months of the nutrition education intervention.
Characteristics *At Baseline
(t = 0 Months)
After Intervention
(t = 3 Months)
p-Value
Body weight (Kg)81.8 ± 17.277.8 ± 16.3<0.001 *
BMI (kg/m2)28.8 ± 5.027.1 ± 5.4<0.001 *
Waist circumference (cm)107.4 ± 26.0103.4 ± 25.5<0.001 *
Hip circumference (cm)96.8 ± 24.094.5 ± 23.6<0.001 *
Waist–hip ratio1.2 ± 0.11.1 ± 0.1<0.001 *
HbA1c (%)7.2 (6.4–8)7.6 (6.7–7.7)0.672 *
Postprandial blood glucose (mg/dL)161.6 ± 36.0131.9 ± 26.7<0.001 *
Fasting glucose (mg/dL)110.7 ± 19.599.5 ± 13.9<0.001 *
Total cholesterol (mg/dL)183.0 ± 41.1165.8 ± 26.8<0.001*
LDL-c (mg/dL)96.2 ± 35.489.4 ± 20.00.002 *
HDL-c (mg/dL)48.2 ± 15.547.1 ± 6.50.443 *
TG (mg/dL)154.7 (150.7–154.7)119.7 (69.7–120.7)<0.001 **
SBP (mmHg)14.2 ± 11.411.8 ± 0.90.056 *
DBP (mmHg)8.8 ± 7.98.0 ± 0.40.342 *
Atherogenic index4.1 ± 1.33.5 ± 0.5<0.001 *
Uric acid (mg/dL)6.5 ± 1.76.2 ± 1.40.0001 *
Body fat (%)32.9 ± 7.829.2 ± 7.6<0.001 *
Visceral fat (%)11.8 ± 0.110.2 ± 0.1<0.001 *
Muscle mass (%)88.7 ± 4.383.1 ± 5.80.331 *
Daily calorie intake (kcal)1659.7 ± 285.91631.4 ± 267.30.002 *
BW: body weight, BMI: body mass index, WC: waist circumference, HC: hip circumference, WHR: waist-to-hip ratio, HbA1c: glycated hemoglobin, ΒGP: blood glucose postprandial, FBG: fasting blood glucose, TC: total cholesterol, HDL: high-density lipoprotein cholesterol, LDL: low-density lipoprotein cholesterol, TG: triglycerides, SBP: systolic blood pressure, DBP: diastolic blood pressure, AΙ: atherogenic index, UA: uric acid, BF: body fat, VF: visceral fat, MM: muscle mass, DCI: daily calorie intake. Data are mean ± standard deviation (SD) or median value (interquartile range). * p values for the comparison with baseline by paired t-test. ** p values for the comparison with baseline by Wilcoxon test.
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Gortzi, O.; Dimopoulou, M.; Androutsos, O.; Vraka, A.; Gousia, H.; Bargiota, A. Effectiveness of a Nutrition Education Program for Patients with Type 2 Diabetes Mellitus. Appl. Sci. 2024, 14, 2114. https://doi.org/10.3390/app14052114

AMA Style

Gortzi O, Dimopoulou M, Androutsos O, Vraka A, Gousia H, Bargiota A. Effectiveness of a Nutrition Education Program for Patients with Type 2 Diabetes Mellitus. Applied Sciences. 2024; 14(5):2114. https://doi.org/10.3390/app14052114

Chicago/Turabian Style

Gortzi, Olga, Maria Dimopoulou, Odysseas Androutsos, Anna Vraka, Helen Gousia, and Alexandra Bargiota. 2024. "Effectiveness of a Nutrition Education Program for Patients with Type 2 Diabetes Mellitus" Applied Sciences 14, no. 5: 2114. https://doi.org/10.3390/app14052114

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop