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Article

Attendance-Based Adherence and Outcomes of Obesity Management Program in Arab Adolescents

1
Chair for Biomarkers of Chronic Diseases, Biochemistry Department, College of Science, King Saud University, Riyadh 11451, Saudi Arabia
2
Department of Community Health Sciences, College of Applied Medical Sciences, King Saud University, Riyadh 11451, Saudi Arabia
3
Department of Food Science and Nutrition, College of Food Science and Agriculture, King Saud University, Riyadh 11451, Saudi Arabia
*
Author to whom correspondence should be addressed.
Children 2023, 10(9), 1449; https://doi.org/10.3390/children10091449
Submission received: 25 July 2023 / Revised: 21 August 2023 / Accepted: 24 August 2023 / Published: 25 August 2023

Abstract

:
Pediatric obesity has become a global pandemic in the last century, contributing to short and long-term medical conditions that heighten the risk of morbidity and mortality in children. The 12-month school-based obesity management educational program aims to assess the effect of adherence to the lifestyle educational program and target outcomes, obesity, and hypertension. A total of 363 (nonadherent, N = 179; adherent, N = 184) Saudi school adolescents aged 12–18 were recruited from 60 schools in Riyadh City, Saudi Arabia. Anthropometrics, lipid profile, and blood glucose were measured at baseline and post-intervention. The level of adherence was based on the number of attended educational sessions, and participants were grouped accordingly into two groups: adherent group (attended ≥ 3 sessions) and nonadherent group (attended 1–2 sessions) out of a total of five sessions. Results demonstrated that significantly more participants in the adherent group achieved the primary program goal of reducing obesity indices [body weight, body mass index (BMI), and BMI z-score] than the nonadherent group. Additionally, among adherent obese participants, BMI z-score significantly decreased after the 12-month intervention (post-intervention: 1.5 ± 0.7 vs. baseline: 1.7 ± 0.6, p < 0.05), while the trend in BMI z-score modestly increased in the nonadherent obese participants post-intervention (post-intervention: 1.8 ± 0.7 vs. baseline: 1.7 ± 0.6, p > 0.05). Moreover, there was a substantial reduction in hypertension prevalence only in the adherent group (p = 0.003) and among adherent obese participants in particular (p = 0.03). Furthermore, adherence to session attendance was higher in girls than boys, which led to better outcomes among girls than boys. For the secondary outcomes, lipid profile indices increased in both groups, while no changes were observed in the glycemic profile. In conclusion, greater adherence to educational sessions achieved modest but favorable weight changes and improved blood pressure among obese adolescents. Future intervention studies should take into consideration the need to improve attendance to enhance adherence to the program among adolescents at risk.

1. Introduction

Obesity is a key risk factor for several chronic, non-communicable diseases, estimated as the principal cause of 74% of all-cause mortality globally as of 2022 [1]. It has been established as a significant risk factor for atherosclerotic disease [2,3] and type 2 diabetes mellitus [4], leading to amplified risk of morbidity and mortality [5]. Consequently, pediatric obesity is increasingly becoming a public health threat affecting most industrialized countries worldwide, influenced by health behaviors, psychosocial factors, biology, and genetics [6]. The key modifiable contributors to childhood obesity are physical inactivity and overnutrition, reflected as visceral adiposity, which, if untreated over time, increases the risk for more serious chronic diseases and mortality, subsequently aggravating the family and community’s economic health burden [7,8]. Compared to individuals who maintained a healthy weight during childhood, obese children and adolescents are five times likelier to remain obese in adulthood [9]. Childhood overweight and obesity prevalence have risen significantly from 4% in 1975 to 18% in 2016 among those aged 5 to 19 years [10]. Obese children and adolescents are more prone to dyslipidemia [2], cardiovascular diseases [11], non-alcoholic fatty liver disease [12], and asthma and lung functioning [13]. Pediatric hypertension is an important healthcare concern. Several epidemiological studies have found that pediatric hypertension prevalence ranges from 3% in the general population to 25% in obese children [14]. Previous research has indicated that pediatric hypertension is linked to obesity and unhealthy behaviors, e.g., increased caloric/salt intake and a sedentary lifestyle [14,15].
In Saudi Arabia, one out of every four girls and one of every three boys aged 12–18 years is overweight or obese [16]. Several lifestyle factors appear to be key drivers for being overweight or obese, including physical inactivity, skipping breakfast, dining outside, and eating too much-sweetened beverages [10]. Locally, there has been a shift from diets composed of whole foods and low in refined oils and sugars to an energy-dense and nutrient-poor diet composed of fat and sugar-rich diets and processed foods [17,18]. Previous intervention studies targeting children and adolescents demonstrated that school-based intervention has the potential to be effective in preventing obesity, as most children and adolescents consume a significant portion of their daily calories and spend half of their waking hours at school [18].
Lifestyle intervention is the primary treatment for childhood obesity as recommended by the National Institute for Health and Care Excellence (NICE) guidance [19]. This includes changes in dietary habits to reduce daily caloric intake [20]. Ojeda-Rodriguez et al. [12] demonstrated that lifestyle intervention (nutritional education, exercise, and reducing calorie intake) successfully reduced BMI standard deviation score in obese children [21]. Recent studies have documented a favorable association between adherence to lifestyle intervention programs, such as compliance with self-monitoring of physical activity and food intake, session attendance and outcomes of the intervention program. Higher levels of session attendance in children have been linked to more substantial weight loss [22,23].
Similarly, it has been shown that successful weight management in adolescents with obesity was related to accurate self-monitoring in lifestyle modification programs [24,25]. Furthermore, evidence pointed out that weight loss in adolescents was associated with parent self-monitoring [26]. Due to the necessity to improve the effectiveness of intervention programs to prevent pediatric obesity, there is a strong rationale to examine the role of adherence in lifestyle intervention programs more closely.
Despite the plethora of successful interventions to prevent and manage childhood obesity [27,28], most lifestyle modification programs done in Saudi Arabia focused on adult obesity and individuals at high risk for diabetes [29,30], while pediatric obesity studies are mostly observational [31,32]. The current study investigates the efficacy of attendance-based adherence to a lifestyle obesity management program and its association with changes in obesity indices and hypertension in a cohort of Arab children and adolescents. The current study hypothesizes that attendance-based adherence is positively associated with the intervention outcomes.

2. Materials and Methods

Our study’s primary outcomes are changes in anthropometric indices (body weight, waist, and BMI) and blood pressure. Secondary outcomes are improvements in serum lipids and glycated hemoglobin (HbA1c).

2.1. Participants

This 12-month (November 2019–November 2020) lifestyle intervention study was a collaborative project by the Chair for Biomarkers of Chronic Diseases (CBCD) at King Saud University (KSU) and the Saudi Charity Association of Diabetes (SCAD). Six hundred (600) healthy school-attending Saudi boys and girls aged 12–18 years from randomly selected 60 preparatory and high schools in Riyadh City, Saudi Arabia. Students with chronic diseases or those on medications that may affect parameters of interest were excluded. Parental informed consent was obtained from each participant before the study started. At baseline, all participants were asked to provide fasting blood samples. Baseline anthropometric and glycemic status were assessed. At the end of the study, due to the COVID-19 lockdown, only 363 participants out of 600 students were able to come for the extraction of fasting blood samples and endpoint measurements. A flow chart describing the study population is provided in Figure 1. Baseline characteristics of participants are provided in Supplementary Table S1. This study was approved by the Institutional Review Board (IRB) of the College of Medicine, King Saud University (KSU), Riyadh, Saudi Arabia (No. E-19-4239, 29 October 2019). An English-translated copy of the brochures provided to the parents is provided as Supplementary File S1.

2.2. Intervention

The full protocol, including the materials provided to the participants, was published previously [33,34]. In brief, education on diet and exercise was given to all participants by certified health professionals, with the primary aim of reducing body weight by 5% or more. The topics covered include mindful eating, such as decreasing portion sizes to reduce caloric intake, having low-fat lunches to school and discontinuing juice/soda intake, and increasing physical activity (outdoor if no restrictions) and 30-min aerobic exercise 5 times per week. The exercise type, duration, and frequency were personalized according to their lifestyle or health conditions.
Educational materials were supplied to all study staff to provide consistent educational programs across sites. Also, all participants were given booklets, pamphlets, gamification, and infographic videos about the recommended lifestyle changes. During the 12-month intervention, participants were educated every three months about the essential lifestyle modifications to prevent obesity, the first of five sessions that were given in classrooms. Unfortunately, due to COVID-19 lockdown regulations, the follow-up educational activities were done through a virtual meeting platform (Zoom) and social media platforms: Telegram, WhatsApp, Twitter, and Facebook. Participants’ online attendance (a measure of adherence) was taken using Google Forms during the educational sessions. Overweight and obese participants, in particular, were monitored by phone by a registered nutritionist.

2.3. Anthropometrics and Biochemical Parameters

Blood samples and anthropometrics were collected at two time points: baseline and after a 12-month follow-up. Height (cm), weight (cm), body mass index BMI (kg/m2), waist (cm) and hip (cm) circumferences, Systolic and diastolic blood pressures (SBP and DBP, respectively, measured as the average of 2 readings with a 15-min interval, using pediatric cut-offs appropriate for children’s sizes).
All participants were instructed to come in a 10-h overnight fasting state to their respective schools. Fasting blood samples were collected by trained nurses at baseline and after intervention. Fasting blood glucose, high-density lipoprotein cholesterol (HDL-c), total cholesterol (TC), and triglycerides (TG) were measured using a standard routine laboratory analysis (Konelab, Finland). Low-density lipoprotein cholesterol (LDL-c) was calculated using the Friedwald equation. HbA1c was analyzed using the D-10 Hemoglobin Testing System (ion-exchange chromatography) (Bio-Rad, Hercules, CA, USA). Overweight and obese were classified according to sex, age and BMI percentile for children as done previously [35,36].

2.4. Obesity and Hypertension Cut-Offs

Overweight and obese children and adolescents were defined according to the criteria of the International Obesity Task Force (IOTF) cut-offs [37]. Definition of hypertension, systolic blood pressure (SBP) and/or diastolic blood pressure (DBP) ≥ 95th percentile for age, sex and height based on 2017 clinical practice guidelines [38].

2.5. Statistical Analysis

SPSS version 28.0 (SPSS, Inc., Chicago, IL, USA) was used to analyze the data. We used the Kolmogorov-Smirnov test to ensure that our data were normally distributed. Normally distributed data were presented as mean and standard deviation (SD). Non-normal data were presented as median (1st and 3rd quartiles). Non-Gaussian variables were log-transformed before parametric analysis. Categorical variables were shown as frequencies (percentages) and analyzed by the MC-Nemar test. Student independent t-test was performed for mean difference between Adherent vs. Non-Adherent at baseline Further Pair Student T-Test was performed to check overtime interval there was mean change in adherent and non-adherent group. General repeated measurement analysis was performed to check the overweight and obese participants’ time interval change effect, time effect by gender and gender, group effect and time effect interval. Statistical significance p < 0.05 is considered significant.
The sample size was calculated based on the results reported by Berkowitz et al. [39]. who noticed attendance was significantly associated with achieving a ≥5% reduction in BMI at month 12. Berkowitz et al. revealed that among the participants of a group lifestyle modification program (Group LMP), only 8% of low attendees lost ≥ 5% of initial BMI at month 12, compared with 27% of high attenders (p = 0.045). Based on these statistics, the total required sample size at 95% power and 5% level of significance is 182.

3. Results

After a 12-month follow-up interrupted by COVID-19 pandemic lockdown regulations, only a total of 363 out of 600 participants (60%) were able to provide follow-up anthropometrics and fasting blood samples. Participants’ online attendance was taken using Google Forms during the educational sessions. Based on the number of attended sessions for each participant, participants were grouped into two groups (nonadherent group, defined as participants who attended 1–2 sessions; and adherent group, defined as participants who attended ≥ 3 sessions). Baseline characteristics of all participants are provided in Supplementary Table S1, as well as differences in the effects of intervention in boys and girls (Supplementary Table S2).

3.1. Comparison of Clinical Characteristics in Adherent and Nonadherent Groups after 12-Month Follow-Up

Table 1 shows the pre-and post-intervention clinical characteristics of all participants in both groups. Participants’ weight significantly increased in both groups overtime (p < 0.001). BMI significantly decreased in both groups but more in the adherent group (p < 0.01). BMI z-score decreased modestly in the adherent group (p = 0.09), while it was significantly increased in the nonadherent group (0.093 ± 1.05 vs. −0.015 ± 0.98, p < 0.007). The waist was significantly increased only in the nonadherent group (85.6 ± 10.4 vs. 75.0 ± 17.3, p < 0.001). Hip circumference significantly increased in the nonadherent group (92.3 ± 11.6 vs. 81.6 ± 23.6, p < 0.001), while it significantly decreased in the adherent group (80.6 ± 15.0 vs. 88.8 ± 16.1, p < 0.001). WHR significantly increased in both groups (both p < 0.001). SBP significantly decreased in both groups over time (nonadherent, 116.6 ± 8.7 vs. 120.6 ± 13.5, p = 0.003; adherent, 106.1 ± 13.6 vs. 121.2 ± 16.4, p < 0.01). DBP significantly increased over time only in the nonadherent group (75.7 ± 7.1 vs. 68.7 ± 8.8, p < 0.001). Lastly, blood glucose, HbA1c, TC, HDL-c, LDL-c, and TG significantly increased in both groups.

3.2. Primary Outcomes

Only 23 (6%) participants were able to achieve the study’s main goal (body weight reduction by ≥5%). More participants in the adherent group achieved this goal than in the nonadherent group, but this was not significant (8% vs. 4%, p = 0.11) (not mentioned in the table). Furthermore, a significant reduction in the incidence of hypertension among adherent participants was seen overall (p = 0.003), and among adherent obese participants only (p = 0.03) (Table 2). These were not observed in the normal and overweight participants regardless of adherence status.

3.3. Pre- and Post-Intervention Comparison of Overweigh and Obese Participants in Both Groups

Table 3 shows pre- and post-intervention clinical characteristics of overweight and obese participants in both groups. Participants’ weight significantly increased only in the nonadherent group overtime (p < 0.01). BMI significantly decreased in both groups, more so in the adherent group (nonadherent, 28.2 ± 4.9 vs. 29.8 ± 4.4; adherent, 26.6 ± 4.7 vs. 29.3 ± 4.5, p < 0.01). BMI z-score significantly decreased only in the adherent group (0.87 ± 0.80 vs. 1.05 ± 0.75, p < 0.01). BMI z-score. Waist significantly increased in the nonadherent group (88.7 ± 9.5 vs. 81.3 ± 21.8, p < 0.05) while significantly decreased in the adherent group (75.7 ± 15.9 vs. 82.2 ± 16.7, p < 0.01). SBP significantly decreased post-intervention in both groups while DBP was significantly increased only in the nonadherent group (p < 0.01). Lipid profile indices significantly increased in both groups. No changes over time were observed in blood glucose or HbA1c levels in both groups.

3.4. Pre- and Post-Intervention Comparison of Overweigh Participants in Both Groups

Table 4 shows the pre- and post-intervention clinical characteristics of overweight participants in both groups. BMI significantly decreased in both groups (p < 0.01). WHR significantly increased in both groups (nonadherent: 0.92 ± 0.04 vs. 0.84 ± 0.07, p < 0.05; adherent, 0.91 ± 0.07 vs. 0.83 ± 0.12, p < 0.01). SBP significantly in both groups (p < 0.01). DBP significantly increased only in the nonadherent group (75.4 ± 8.1 vs. 69.3 ± 10.5, p < 0.05). Lipid and glycemic profile findings were similar to Table 3.

3.5. Pre- and Post-Intervention Comparison of Obese Participants in Both Groups

Table 5 shows the characteristics of obese participants over time. BMI significantly decreased in both groups (p < 0.01). BMI z-score significantly decreased only in the adherent group (p < 0.05). WHR significantly increased in both groups (p < 0.01). SBP significantly decreased post-intervention in both groups (p < 0.01). DBP significantly increased only in the nonadherent group (p < 0.01) while it significantly decreased in the adherent group (p < 0.05). The rest were similar to Table 3.

4. Discussion

The current school-based study investigated the relationship between attendance-adherence to obesity management lifestyle intervention programs and program outcomes with an emphasis on blood pressure. The present investigation is one of the few to focus on pediatric hypertension and the first in Saudi Arabia.
Hypertension is a key risk factor for cardiovascular disease and has been increasing among pediatrics [40]. The prevalence of hypertension among children is about 3% in the general population and about 25% among obese children [14]. Martinovic et al. [41], in a school-based study on 3254 children aged 7–13 years, reported that childhood obesity raised the probability of child hypertension by 68% (p < 0.001). Our results showed positive changes in blood pressure, particularly in adherent participants. This is in line with a previous study on 85 children (aged 5–8 years) found decreased DBP in the intervention group compared to the control group post-intervention [42]. In Saudi Arabia, pediatric hypertension is a growing problem. A previous large national study screened 16,226 pediatrics; results have revealed that blood pressure was steadily increasing with age [43]. Authors found that SBP was annually increasing with an average of 1.44 mmHg among girls and 1.66 mmHg among boys, while DBP was increasing annually by 0.83 mmHg among boys and 0.77 mmHg among girls [43].
Our results showed that adherence was a contributing factor in achieving the primary intervention goal of reducing participants’ body weight by 5% or more. However, the difference between adherence and nonadherence was insignificant, which could be attributed to the small sample size. Kim J et al. [44], in a 16-week nutritional intervention study, included monthly 30-min nutritional sessions on children (mean age 12.4 ± 2.0 years), found significant differences in body weight reduction between adherent and nonadherent children, where adherent children achieved lower body weight post-intervention comparing to nonadherent children (−0.2 kg vs. 3.3 kg, p < 0.001). A novel finding, however, under-highlighted in other investigations was the significant improvement in the prevalence of hypertension in the adherent group compared with the nonadherent group. Moreover, results demonstrated that session attendance was associated with a reduction in BMI, where adherent participants achieved better reductions in BMI than non-adherent participants. In our cohort, adherence to session attendance was not associated with glycemic control and didn’t improve lipid profile. Several previous pediatric obesity trials have used sessions as a program adherence proxy [22,23].
In the present study, we targeted childhood obesity and hypertension. Both hypertension and obesity have been increasing among pediatrics. Both can track into adulthood, which increases heart disease prevalence and its related mortality [25]. Obese children are at a significantly increasing risk for CVD as they have higher SBP and DBP [26]. Previous research has demonstrated that BMI influences BP in pediatrics [25]. In our study, we have incorporated education about switching to a healthy lifestyle, which included dietary and physical activity changes, which were effective in BMI and BP reductions among our adherent group. Several intervention studies on obese and overweight pediatrics (aged 6–16 years) have demonstrated that weight loss was successful in decreasing BP in pediatrics [25]. These intervention studies (5- to 12-month) have incorporated education, physical activity, and diet and demonstrated that intervention was effective in decreasing SBP [27,28]. In a recent large retrospective study that recruited 101,606 of pediatrics (aged 3–17 years) who were followed for several years, authors found that obese and severely obese participants had increased BP at baseline and greater odds of developing hypertension in adulthood compared with pediatrics with normal BMI [37]. Changes in dietary habits are a significant part of lifestyle modifications in treating obesity-related hypertension [25]. The American Academy of Pediatrics published 2011 an updated dietary recommendation for hypertension treatment [37]. They stated that regardless of the hypertension stage or its etiology, hypertensive children should follow the dietary approaches and lifestyle for cardiovascular health to prevent hypertension [37].
The present results show that about 50% of participants attended at least one session of the intervention sessions, and 50% attended more than 60% of the planned sessions. Our attendance rates were lower than those obtained in studies from the West [22,23]. Kalarchian et al. [22], over a 6-month period, found that 63% of attendance rate and attendance rate was related to weight reduction. Another study by Berkowitz et al. [39] reported a median of 75% attendance rate at intervention sessions. Children with better attendance also had significantly higher BMI reductions than children with less attendance.
In line with previous programs for the management of childhood obesity [45,46], our participants’ BMI z-score significantly reduced post-intervention. We analyzed BMI and BMI z-score instead of the absolute change in weight as our participants were still growing in height. In the present analysis, although participants did not have significant weight loss, BMI and BMI z-score were significantly improved as they still grew in height during the intervention. In previous lifestyle modification intervention studies, authors reported a significant reduction in BMI and BMI z-scores among obese children and adolescents in the intervention group compared to the control group [47,48]. BMI z-score is a pediatric and adolescent obesity assessment tool that considers age and sex into account [48]. Previous research has validated BMI z-scores values for pediatric obesity and demonstrated that BMI z-score was a more accurate obesity indicator for children and adolescents [49,50]. The US Preventive Services Task Force proposed a reduction in BMI z-score with more than 0.20–0.25 could be clinically significant [37]. Moreover, a previous intervention study noted a decrease of ≥0.2 SD in BMI z-score, indicating a successful intervention outcome [48]. It can be speculated that without the current lifestyle intervention, our participants would have continued to gain weight and increased their BMI and BMI z-score.
The present study demonstrates sex differences in program determinants and outcomes, where adherence to session attendance was higher in girls than in boys, with better improvements in program outcomes among girls. Previously, a Canadian study reported that girls were identified to have higher odds of adhering to precautionary COVID-19 measures [51]. To maximize intervention outcomes, reasons for non-adherence among males should be examined in future studies. Gender-adapted strategies to improve compliance have to be developed, for instance, increasing targeted education towards males engaging their families [52]. Additionally, there is a need to reveal sex differences in determinants of low adherence and intervention effects to improve adherence. Sex differences in determinants of adherence have been previously identified [53].
An important aspect not investigated in the present study is parental influence. Parental adherence to healthier lifestyles may prove pivotal in controlling childhood weight gain since this approach has been tied to a significantly lower risk of pediatric obesity [54]. Furthermore, the switching from school-based to internet-based implementation of the program was relatively new. Several internet-based studies provided promising outcomes [55,56], but an approach that is personalized and family-based remains superior to other strategies, at least in children [57]. In general, there are still significant gaps in our understanding of how best to tailor interventions that increase children’s adherence, different types of nonadherence (e.g., intentional vs. unintentional), and different preferences for delivery (e.g., technology-mediated vs. face-to-face) [58,59,60].
The present study has some limitations. First, we had no control group. Second, the high dropout rate in our study after intervention limited the actual effect of the intervention in the study duration. The high dropout rate was definitely due to the COVID-19 lockdown and the mobility restrictions during the study period. However, this large dropout might also suggest that sustaining interest in lifestyle change is difficult to do, particularly among our cohort of youth, and they may revert to their previous habits in time. Also, this dropout might indicate difficulties in sustaining interest in lifestyle change, particularly among our study population of children and adolescents, and they may revert with time to their previous unhealthy habits. It is worth noting that a high dropout rate is common in Saudi Arabia for intervention studies. Previously, in a 6-month intervention study on 150 type 2 diabetes Saudi patients, only 61 completed the trial [61]. Another Saudi 18-month lifestyle intervention study started with 180 prediabetes participants, and at the end of the study, only 28 participants completed the study [62]. Behavioral techniques such as self-efficacy, goal-setting and provision of feedback should be applied more aggressively in future studies. Lastly, the study focused on weight loss and hypertension and not on biochemical parameters since glycemic and lipid parameters undergo fluctuations within the normal range during growth, as seen in the present results. Therefore, the increase in glucose and lipid profile observed over time may not necessarily reflect that the participants’ lifestyle got worse after intervention but more of a combination of physiological changes and external factors, some of which were not accounted for in the present study [63,64]. Despite these limitations, this study highlights the modest but positive effects of adherence in lifestyle intervention, particularly in the reduction of pediatric hypertension among obese youth. Apart from obesity management, lifestyle interventions with healthy dietary and exercise behaviors have been effective in achieving favorable metabolic effects [65]. Additionally, lifestyle modification approaches were demonstrated previously to have positive effects that can be long-lasting [66,67].

5. Conclusions

Our results indicate that greater participant adherence to the intervention improved target outcomes, particularly in reducing pediatric hypertension among Arab obese adolescents. Our results add to the current literature and have clinical value, given the ethnic and cultural variations in compliance with such an obesity management intervention program. Future intervention studies should be geared towards improving adherence by direct involvement of parents and a more personalized approach involving a multi-disciplinary team, especially among children at the highest risk of obesity-related complications. The use of a virtual platform in the implementation of lifestyle modifications among Saudi children still has a lot of room for improvement, including, but not limited to, the addition of educational content that is both encouraging and entertaining to children, which hopefully can translate to better adherence.

Supplementary Materials

The following supporting information can be downloaded at https://www.mdpi.com/article/10.3390/children10091449/s1, File S1: Study brochure distributed to parents and participants; Table S1: Baseline clinical characteristic of all participants; Table S2: Pre- and post-intervention comparison of boys and girls in both groups.

Author Contributions

N.M.A.-D. and O.E.A. designed the study. O.E.A. did the biochemical analyses. M.N.K.K. and S.D.H. did the statistical analysis. G.A., H.A.A. and M.A.E. helped in the investigations and data curation. O.E.A. wrote the manuscript. S.S. revised the manuscript. N.M.A.-D. did the study supervision. All authors have read and agreed to the published version of the manuscript.

Funding

The authors extend their appreciation to the Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia, for funding this research (grant number IFKSURC-1-1601).

Institutional Review Board Statement

IRB approved by the College of Medicine, King Saud University, Riyadh, Saudi Arabia (No. E-19-4239, 29 October 2019).

Informed Consent Statement

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

Data Availability Statement

The data presented in this study are available on request from the corresponding author. The data are not publicly available due to privacy protection.

Acknowledgments

The authors extend their appreciation to the Deputyship for Research & Innovation, Ministry of Education in Saudi Arabia, for their continuous support.

Conflicts of Interest

The authors declare that they have no competing interests.

References

  1. World Health Organization. Noncommunicable Diseases. Available online: https://www.who.int/news-room/fact-sheets/detail/noncommunicable-diseases (accessed on 15 June 2023).
  2. Turer, C.B.; Brady, T.M.; de Ferranti, S.D. Obesity, Hypertension, and Dyslipidemia in Childhood Are Key Modifiable Antecedents of Adult Cardiovascular Disease: A Call to Action. Circulation 2018, 3, 1256–1259. [Google Scholar] [CrossRef] [PubMed]
  3. Charakida, M.; Deanfield, J.E. BMI Trajectories from Childhood: The Slippery Slope to Adult Obesity and Cardiovascular Disease. Eur. Heart J. 2018, 39, 2271–2273. [Google Scholar] [CrossRef] [PubMed]
  4. Bjerregaard, L.G.; Baker, J.L. Change in Overweight from Childhood to Early Adulthood and Risk of Type 2 Diabetes. New Engl. J. Med. 2018, 378, 2537–2538. [Google Scholar] [CrossRef] [PubMed]
  5. Reilly, J.J.; Kelly, J. Long-Term Impact of Overweight and Obesity in Childhood and Adolescence on Morbidity and Premature Mortality in Adulthood: Systematic Review. Int. J. Obes. 2011, 35, 891–898. [Google Scholar] [CrossRef]
  6. Smith, J.D.; Fu, E.; Kobayashi, M.A. Prevention and Management of Childhood Obesity and Its Psychological and Health Comorbidities. Annu. Rev. Clin. Psychol. 2020, 16, 351–378. [Google Scholar] [CrossRef]
  7. Al-Daghri, N.M.; Al-Attas, O.S.; Alokail, M.; Alkharfy, K.; Wani, K.; Amer, O.E.; Ul Haq, S.; Rahman, S.; Alnaami, A.M.; Livadas, S.; et al. Does visceral adiposity index signify early metabolic risk in children and adolescents? Association with insulin resistance, adipokines, and subclinical inflammation. Pediatr. Res. 2014, 75, 459–463. [Google Scholar] [CrossRef]
  8. Hamilton, D.; Dee, A.; Perry, I.J. The Lifetime Costs of Overweight and Obesity in Childhood and Adolescence: A Systematic Review. Obes. Rev. Off. J. Int. Assoc. Study Obes. 2018, 19, 452–463. [Google Scholar] [CrossRef]
  9. Simmonds, M.; Llewellyn, A.; Owen, C.G.; Woolacott, N. Predicting Adult Obesity from Childhood Obesity: A Systematic Review and Meta-Analysis. Obes. Rev. Off. J. Int. Assoc. Study Obes. 2016, 17, 95–107. [Google Scholar] [CrossRef]
  10. Mistry, S.K.; Puthussery, S. Risk factors of overweight and obesity in childhood and adolescence in South Asian countries: A systematic review of the evidence. Public Health 2015, 129, 200–209. [Google Scholar] [CrossRef]
  11. Luca, A.-C.; Curpan, A.-S.; Braha, E.E.; Ţarcă, E.; Iordache, A.-C.; Luca, F.-A.; Adumitrachioaiei, H. Increasing Trends in Obesity-Related Cardiovascular Risk Factors in Romanian Children and Adolescents—Retrospective Study. Healthcare 2022, 10, 2452. [Google Scholar] [CrossRef]
  12. Di Sessa, A.; Umano, G.R.; Miraglia Del Giudice, E.; Santoro, N. From the Liver to the Heart: Cardiac Dysfunction in Obese Children with Non-Alcoholic Fatty Liver Disease. World J. Hepatol. 2017, 9, 69–73. [Google Scholar] [CrossRef] [PubMed]
  13. Liang, Y.; Qi, Y. Developmental trajectories of adolescent overweight/obesity in China: Socio-economic status correlates and health consequences. Public Health 2020, 185, 246–253. [Google Scholar] [CrossRef]
  14. Shatat, I.F.; Brady, T.M. Editorial: Pediatric Hypertension: Update. Front. Pediatr. 2018, 6, 209. [Google Scholar] [CrossRef] [PubMed]
  15. Valerio, G.; Maffeis, C.; Saggese, G.; Ambruzzi, M.A.; Balsamo, A.; Bellone, S.; Bergamini, M.; Bernasconi, S.; Bona, G.; Calcaterra, V.; et al. Diagnosis, Treatment and Prevention of Pediatric Obesity: Consensus Position Statement of the Italian Society for Pediatric Endocrinology and Diabetology and the Italian Society of Pediatrics. Ital. J. Pediatr. 2018, 44, 88. [Google Scholar] [CrossRef]
  16. World Health Organization. Noncommunicable Diseases Country Profiles. 2014. Available online: https://apps.who.int/iris/handle/10665/128038 (accessed on 12 November 2022).
  17. Almughamisi, M. The Co-Development of a School-Based Nutrition Intervention to Prevent Childhood Obesity in Jeddah, Saudi Arabia. Ph.D. Thesis, King’s College, London, UK, 2021. [Google Scholar]
  18. Aboul-Enein, B.H.; Bernstein, J.; Neary, A.C. Dietary Transition and Obesity in Selected Arabicspeaking Countries: A Review of the Current Evidence. East. Mediterr. Health J. 2017, 22, 763–770. [Google Scholar] [CrossRef]
  19. NICE. Obesity: Identification, Assessment and Management. Clinical Guideline [CG189]. 2014. Available online: https://www.nice.org.uk/guidance/cg189 (accessed on 21 July 2023).
  20. Gungor, N.K. Overweight and obesity in children and adolescents. J. Clin. Res. Pediatr. Endocrinol. 2014, 6, 129–143. [Google Scholar] [CrossRef] [PubMed]
  21. Almughamisi, M.; O’Keeffe, M.; Harding, S. Adolescent Obesity Prevention in Saudi Arabia: Co-Identifying Actionable Priorities for Interventions. Front. Public Health 2022, 10, 863765. [Google Scholar] [CrossRef]
  22. Kalarchian, M.A.; Levine, M.D.; Arslanian, S.A.; Ewing, L.J.; Houck, P.R.; Cheng, Y.; Ringham, R.M.; Sheets, C.A.; Marcus, M.D. Family-Based Treatment of Severe Pediatric Obesity: Randomized, Controlled Trial. Pediatrics 2009, 124, 1060–1068. [Google Scholar] [CrossRef]
  23. Theim, K.R.; Sinton, M.M.; Goldschmidt, A.B.; Van Buren, D.J.; Doyle, A.C.; Saelens, B.E.; Stein, R.I.; Epstein, L.H.; Wilfley, D.E. Adherence to Behavioral Targets and Treatment Attendance during a Pediatric Weight Control Trial. Obesity 2013, 21, 394–397. [Google Scholar] [CrossRef]
  24. Brady, T.M. Obesity-Related Hypertension in Children. Front. Pediatr. 2017, 5, 197. [Google Scholar] [CrossRef]
  25. Friedemann, C.; Heneghan, C.; Mahtani, K.; Thompson, M.; Perera, R.; Ward, A.M. Cardiovascular disease risk in healthy children and its association with body mass index: Systematic review and meta-analysis. BMJ 2012, 345, e4759. [Google Scholar] [CrossRef] [PubMed]
  26. Reinehr, T.; Schaefer, A.; Winkel, K.; Finne, E.; Toschke, A.M.; Kolip, P. An effective lifestyle intervention in overweight children: Findings from a randomized controlled trial on “Obeldicks light”. Clin. Nutr. 2010, 29, 331–336. [Google Scholar] [CrossRef]
  27. Herouvi, D.; Paltoglou, G.; Soldatou, A.; Kalpia, C.; Karanasios, S.; Karavanaki, K. Lifestyle and Pharmacological Interventions and Treatment Indications for the Management of Obesity in Children and Adolescents. Children 2023, 10, 1230. [Google Scholar] [CrossRef] [PubMed]
  28. Scotto di Luzio, S.; Martinent, G.; Popa-Roch, M.; Ballereau, M.; Chahdi, S.; Escudero, L.; Guillet-Descas, E. Obesity in Childhood and Adolescence: The Role of Motivation for Physical Activity, Self-Esteem, Implicit and Explicit Attitudes toward Obesity and Physical Activity. Children 2023, 10, 1177. [Google Scholar] [CrossRef] [PubMed]
  29. Al-Hamdan, R.; Avery, A.; Al-Disi, D.; Sabico, S.; Al-Daghri, N.M.; McCullough, F. Efficacy of lifestyle intervention program for Arab women with prediabetes using social media as an alternative platform of delivery. J. Diabetes Investig. 2021, 12, 1872–1880. [Google Scholar] [CrossRef]
  30. Wani, K.; Alfawaz, H.; Alnaami, A.M.; Sabico, S.; Khattak, M.N.K.; Al-Attas, O.; Alokail, M.S.; Alharbi, M.; Chrousos, G.; Kumar, S.; et al. Effects of a 12-Month Intensive Lifestyle Monitoring Program in Predominantly Overweight/Obese Arab Adults with Prediabetes. Nutrients 2020, 12, 464. [Google Scholar] [CrossRef]
  31. Al Enazi, S.; Al Ajlan, R.; Al Khalaf, H.; Abolfotouh, M.; Alharbi, O.; Alfawaz, R.; Aldebasi, B.; Alghnam, S. Prevalence of Obesity among Children and Adolescents in Saudi Arabia: A Multicenter Population-Based Study. Saudi J. Med. Med. Sci. 2023, 11, 19–25. [Google Scholar] [PubMed]
  32. El-Setouhy, M.; Safhi, A.M.; Dallak, M.Y.; Ayoub, A.Y.; Suwaid, O.A.H.; Moafa, A.K.; Al-Ahmed, A.M.; Zaino, M.; Al Sayed, A. Prevalence and associated factors of pediatric hypertension in Jazan region, south of the Kingdom of Saudi Arabia. A pilot cross-sectional study. PLoS ONE 2023, 18, e0287698. [Google Scholar] [CrossRef]
  33. Al-Daghri, N.M.; Amer, O.E.; Hameidi, A.; Alfawaz, H.; Alharbi, M.; Khattak, M.N.K.; Alnaami, A.M.; Aljohani, N.J.; Alkhaldi, G.; Wani, K.; et al. Effects of a 12-Month Hybrid (In-Person + Virtual) Education Program in the Glycemic Status of Arab Youth. Nutrients 2022, 14, 1759. [Google Scholar] [CrossRef]
  34. Al-Daghri, N.M.; Wani, K.; Khattak, M.N.K.; Alnaami, A.M.; Amer, O.E.; Aljohani, N.J.; Hameidi, A.; Alfawaz, H.; Alharbi, M.; Sabico, S. Cardiometabolic Effects of a 12-Month, COVID-19 Lockdown-Interrupted Lifestyle Education Program for Arab Adolescents. Front Pediatr. 2022, 10, 887138. [Google Scholar] [CrossRef]
  35. Amer, O.E.; Sabico, S.; Khattak, M.N.K.; Alnaami, A.M.; Aljohani, N.J.; Alfawaz, H.; AlHameidi, A.; Al-Daghri, N.M. Increasing Prevalence of Pediatric Metabolic Syndrome and Its Components among Arab Youth: A Time-Series Study from 2010–2019. Children 2021, 8, 1129. [Google Scholar] [CrossRef] [PubMed]
  36. Al-Daghri, N.M.; Al-Othman, A.; Albanyan, A.; Al-Attas, O.S.; Alokail, M.S.; Sabico, S.; Chrousos, G.P. Perceived stress scores among Saudi students entering universities: A prospective study during the first year of university life. Int. J. Environ. Res. Public Health 2014, 11, 3972–3981. [Google Scholar] [CrossRef]
  37. US Preventive Services Task Force; Grossman, D.C.; Bibbins-Domingo, K.; Curry, S.J.; Barry, M.J.; Davidson, K.W.; Doubeni, C.A.; Epling, J.W., Jr.; Kemper, A.R.; Krist, A.H.; et al. Screening for Obesity in Children and Adolescents: US Preventive Services Task Force Recommendation Statement. JAMA 2017, 317, 2417–2426. [Google Scholar] [CrossRef] [PubMed]
  38. Flynn, J.T.; Kaelber, D.C.; Baker-Smith, C.M.; Blowey, D.; Carroll, A.E.; Daniels, S.R.; de Ferranti, S.D.; Dionne, J.M.; Falkner, B.; Flinn, S.K.; et al. Clinical Practice Guideline for Screening and Management of High Blood Pressure in Children and Adolescents. Pediatrics 2017, 140, e20171904. [Google Scholar] [CrossRef]
  39. Berkowitz, R.I.; Rukstalis, M.R.; Bishop-Gilyard, C.T.; Moore, R.H.; Gehrman, C.A.; Xanthopoulos, M.S.; Cochran, W.J.; Louden, D.; Wadden, T.A. Treatment of Adolescent Obesity Comparing Self-Guided and Group Lifestyle Modification Programs: A Potential Model for Primary Care. J. Pediatr. Psychol. 2013, 38, 978–986. [Google Scholar] [CrossRef] [PubMed]
  40. Reinehr, T.; de Sousa, G.; Toschke, A.M.; Andler, W. Long-term follow-up of cardiovascular disease risk factors in children after an obesity intervention. Am. J. Clin. Nutr. 2006, 84, 490–496. [Google Scholar] [CrossRef] [PubMed]
  41. Martinovic, M.; Belojevic, G.; Evans, G.W.; Kavaric, N.; Asanin, B.; Pantovic, S.; Jaksic, M.; Boljevic, J. Hypertension and correlates among Montenegrin schoolchildren—A cross-sectional study. Public Health 2017, 147, 15–19. [Google Scholar] [CrossRef] [PubMed]
  42. Novotny, R.; Nigg, C.R.; Li, F.; Wilkens, L.R. Pacific Kids DASH for Health (PacDASH) Randomized, Controlled Trial with DASH Eating Plan plus Physical Activity Improves Fruit and Vegetable Intake and Diastolic Blood Pressure in Children. Child. Obes. 2015, 11, 177–186. [Google Scholar] [CrossRef]
  43. Al Salloum, A.A.; El Mouzan, M.I.; Al Herbish, A.S.; Al Omar, A.A.; Qurashi, M.M. Blood Pressure Standards for Saudi Children and Adolescents. Ann. Saudi Med. 2009, 29, 173–178. [Google Scholar] [CrossRef]
  44. Kim, J.; Kim, Y.; Seo, Y.-G.; Park, K.-H.; Jang, H.B.; Lee, H.-J.; Park, S.I.; Lim, H. Evidence-Based Customized Nutritional Intervention Improves Body Composition and Nutritional Factors for Highly-Adherent Children and Adolescents with Moderate to Severe Obesity. Nutr. Res. Pract. 2020, 14, 262–275. [Google Scholar] [CrossRef]
  45. Parker, E.D.; Sinaiko, A.R.; Kharbanda, E.O.; Margolis, K.L.; Daley, M.F.; Trower, N.K.; Sherwood, N.E.; Greenspan, L.C.; Lo, J.C.; Magid, D.J.; et al. Change in weight status and development of hypertension. Pediatrics 2016, 137, e20151662. [Google Scholar] [CrossRef] [PubMed]
  46. Monzavi, R.; Dreimane, D.; Geffner, M.E.; Braun, S.; Conrad, B.; Klier, M.; Kaufman, F.R. Improvement in Risk Factors for Metabolic Syndrome and Insulin Resistance in Overweight Youth Who Are Treated with Lifestyle Intervention. Pediatrics 2006, 117, e1111–e1118. [Google Scholar] [CrossRef] [PubMed]
  47. Chung, S.J. Effect of Physical Activity on Adolescent Obesity Status over Time: A Latent Growth Modeling Approach. Healthcare 2021, 9, 1018. [Google Scholar] [CrossRef]
  48. Markert, J.; Herget, S.; Petroff, D.; Gausche, R.; Grimm, A.; Kiess, W.; Blüher, S. Telephone-based adiposity prevention for families with overweight children (T.A.F.F.-Study): One year outcome of a randomized, controlled trial. Int. J. Environ. Res. Public Health 2014, 11, 10327–10344. [Google Scholar] [CrossRef] [PubMed]
  49. Lobstein, T.; Baur, L.; Uauy, R. IASO International Obesity TaskForce. Obesity in children and young people: A crisis in public health. Obes. Rev. 2004, 5 (Suppl. S1), 4–104. [Google Scholar] [CrossRef] [PubMed]
  50. Cole, T.J.; Faith, M.S.; Pietrobelli, A.; Heo, M. What is the best measure of adiposity change in growing children: BMI, BMI %, BMI z-score or BMI centile? Eur. J. Clin. Nutr. 2005, 59, 419–425, Erratum in Eur. J. Clin. Nutr. 2005, 59, 807. [Google Scholar] [CrossRef]
  51. Yang, X.Y.; Gong, R.N.; Sassine, S.; Morsa, M.; Tchogna, A.S.; Drouin, O.; Chadi, N.; Jantchou, P. Risk Perception of COVID-19 Infection and Adherence to Preventive Measures among Adolescents and Young Adults. Children 2020, 7, 311. [Google Scholar] [CrossRef]
  52. Griffith, D.M.; Sharma, G.; Holliday, C.S.; Enyia, O.K.; Valliere, M.; Semlow, A.R.; Stewart, E.C.; Blumenthal, R.S. Men and COVID-19: A Biopsychosocial Approach to Understanding Sex Differences in Mortality and Recommendations for Practice and Policy Interventions. Prev. Chronic Dis. 2020, 17, E63. [Google Scholar] [CrossRef]
  53. Holt, E.; Joyce, C.; Dornelles, A.; Morisky, D.; Webber, L.S.; Muntner, P.; Krousel-Wood, M. Sex Differences in Barriers to Antihypertensive Medication Adherence: Findings from the Cohort Study of Medication Adherence among Older Adults. J. Am. Geriatr. Soc. 2013, 61, 558–564. [Google Scholar] [CrossRef]
  54. Qi, Y.; Lv, R.; Zhao, M.; Huang, Y.; Zhang, Y.; Zhang, H.; Song, P.; Li, Z.; Jia, P.; Zhang, H.; et al. Associations between parental adherence to healthy lifestyles and risk of obesity in offspring: A prospective cohort study in China. Lancet Glob. Health 2023, 11 (Suppl. S1), S6. [Google Scholar] [CrossRef]
  55. Ghofranipour, F.; Hamzavi Zarghani, N.; Mohammadi, E.; Mehrizi, A.A.H.; Tavousi, M.; De Craemer, M.; Cardon, G. An internet-based educational intervention for mothers targeting preschoolers’ weight management promotion (PWMP): A pilot study. BMC Public Health 2022, 22, 2220. [Google Scholar] [CrossRef] [PubMed]
  56. Chai, L.K.; Farletti, R.; Fathi, L.; Littlewood, R. A Rapid Review of the Impact of Family-Based Digital Interventions for Obesity Prevention and Treatment on Obesity-Related Outcomes in Primary School-Aged Children. Nutrients 2022, 14, 4837. [Google Scholar] [CrossRef] [PubMed]
  57. Varagiannis, P.; Magriplis, E.; Risvas, G.; Vamvouka, K.; Nisianaki, A.; Papageorgiou, A.; Pervanidou, P.; Chrousos, G.P.; Zampelas, A. Effects of Three Different Family-Based Interventions in Overweight and Obese Children: The “4 Your Family” Randomized Controlled Trial. Nutrients 2021, 13, 341. [Google Scholar] [CrossRef] [PubMed]
  58. Conn, V.S.; Ruppar, T.M.; Chase, J.-A.D.; Enriquez, M.; Cooper, P.S. Interventions to Improve Medication Adherence in Hypertensive Patients: Systematic Review and Meta-Analysis. Curr. Hypertens. Rep. 2015, 17, 94. [Google Scholar] [CrossRef]
  59. Conn, V.S.; Ruppar, T.M.; Enriquez, M.; Cooper, P. Medication Adherence Interventions that Target Subjects with Adherence Problems: Systematic Review and Meta-Analysis. Res. Social Adm. Pharm. 2016, 12, 218–246. [Google Scholar] [CrossRef]
  60. Hugtenburg, J.G.; Timmers, L.; Elders, P.J.; Vervloet, M.; van Dijk, L. Definitions, Variants, and Causes of Nonadherence with Medication: A Challenge for Tailored Interventions. Patient Prefer. Adherence 2013, 7, 675–682. [Google Scholar] [CrossRef]
  61. Sabico, S.; Al-Mashharawi, A.; Al-Daghri, N.M.; Wani, K.; Amer, O.E.; Hussain, D.S.; Ahmed Ansari, M.G.; Masoud, M.S.; Alokail, M.S.; McTernan, P.G. Effects of a 6-month multi-strain probiotics supplementation in endotoxemic, inflammatory and cardiometabolic status of T2DM patients: A randomized, double-blind, placebo-controlled trial. Clin. Nutr. 2019, 38, 1561–1569. [Google Scholar] [CrossRef]
  62. Amer, O.E.; Sabico, S.; Alfawaz, H.A.; Aljohani, N.; Hussain, S.D.; Alnaami, A.M.; Wani, K.; Al-Daghri, N.M. Reversal of Prediabetes in Saudi Adults: Results from an 18 Month Lifestyle Intervention. Nutrients 2020, 12, 804. [Google Scholar] [CrossRef]
  63. Schienkiewitz, A.; Truthmann, J.; Ernert, A.; Wiegand, S.; Schwab, K.O.; Scheidt-Nave, C. Age, maturation and serum lipid parameters: Findings from the German Health Survey for Children and Adolescents. BMC Public Health 2019, 19, 1627. [Google Scholar] [CrossRef]
  64. Maidowski, L.; Kiess, W.; Baber, R.; Dathan-Stumpf, A.; Ceglarek, U.; Vogel, M. Tracking of serum lipids in healthy children on a year-to-year basis. BMC Cardiovasc. Disord. 2023, 23, 386. [Google Scholar] [CrossRef]
  65. Mann, J.I. Evidence-Based Nutrition Recommendations for the Treatment and Prevention of Type 2 Diabetes and the Metabolic Syndrome. Food Nutr. Bull. 2006, 27, 161–166. [Google Scholar] [CrossRef] [PubMed]
  66. Conn, V.S.; Hafdahl, A.R.; Mehr, D.R.; LeMaster, J.W.; Brown, S.A.; Nielsen, P.J. Metabolic Effects of Interventions to Increase Exercise in Adults with Type 2 Diabetes. Diabetologia 2007, 50, 913–921. [Google Scholar] [CrossRef] [PubMed]
  67. Rodríguez-Muñoz, S.; Corella, C.; Abarca-Sos, A.; Zaragoza, J. Validation of three short physical activity questionnaires with accelerometers among university students in Spain. J. Sports Med. Phys. Fit. 2017, 57, 1660–1668. [Google Scholar] [CrossRef] [PubMed]
Figure 1. Flow chart of the study participants describing their participation and allocation.
Figure 1. Flow chart of the study participants describing their participation and allocation.
Children 10 01449 g001
Table 1. Comparison of clinical characteristics in both groups after 12-month follow-up.
Table 1. Comparison of clinical characteristics in both groups after 12-month follow-up.
ParametersOverall
Nonadherentp-ValueAdherent p-Value
BaselineFollow-UpBaselineFollow-Up
N179 184
Age14.97 ± 1.614.89 ± 1.7
Weight (Kg)58.2 ± 18.360.6 ± 17.2<0.00158.3 ± 17.560.2 ± 15.5<0.001
BMI (kg/m2)22.9 ± 5.922.1 ± 5.9<0.00123.82 ± 6.122.10 ± 5.6<0.001
BMI Z-score−0.015 ± 0.980.093 ± 1.050.0070.117 ± 1.00.069 ± 0.960.09
Waist (cm)75.0 ± 17.385.6 ± 10.4<0.00174.2 ± 14.673.4 ± 15.60.29
Hip (cm)81.6 ± 23.6 92.3 ± 11.6<0.00188.8 ± 16.180.6 ± 15.0<0.001
WHR0.86 ± 0.100.92 ± 0.10<0.0010.84 ± 0.120.91 ± 0.07<0.001
SBP (mmHg)120.6 ± 13.5116.6 ± 8.70.003121.2 ± 16.4106.1 ± 13.6<0.001
DBP (mmHg)68.7 ± 8.875.7 ± 7.1<0.00172.9 ± 11.671.7 ± 6.50.12
Glucose (mmol/L)5.3 ± 1.05.6 ± 2.20.035.2 ± 0.65.5 ± 2.30.06
HbA1c (%)5.2 ± 0.65.3 ± 1.10.045.1 ± 0.65.3 ± 1.30.007
TC (mmol/L)4.4 ± 0.86.0 ± 1.2<0.0014.4 ± 0.75.8 ± 1.4<0.001
HDL-c (mmol/L)1.0 ± 0.21.5 ± 0.50.0010.95 ± 0.31.5 ± 0.6<0.001
LDL-c (mmol/L)2.9 ± 0.73.7 ± 1.1<0.0013.0 ± 0.63.7 ± 1.2<0.001
TG (mmol/L)1.1 ± 0.51.8 ± 0.8<0.0011.1 ± 0.61.7 ± 0.8<0.001
Note: Data Presented mean ± SD. p-value significant at 0.05 and 0.01 level for baseline and after follow-up. BMI, Body Mass Index; WHR, waist-hip ratio; SBP, Systolic Blood Pressure; DBP, Diastolic Blood Pressure; HbA1c, glycated hemoglobin; TC, Total Cholesterol; HDL-c, High-Density Lipoprotein Cholesterol; LDL-c, Low-Density Lipoprotein Cholesterol; TG, Triglycerides.
Table 2. Prevalence of hypertension pre- and post-intervention among study groups.
Table 2. Prevalence of hypertension pre- and post-intervention among study groups.
Group (Total N)BaselineFollow-Upp-Value
Overall (N = 363)69 (19)51 (14)0.16
Nonadherent (N = 179) 21 (12)31 (17)0.23
Adherent (N = 184) 48 (26)20 (11)0.003
Normal body weight (N = 223)
Nonadherent (N = 122)9 (7)17 (14)0.15
Adherent (N = 101)23 (23)14 (14)0.18
Overweight (N = 72)
Nonadherent (N = 28)6 (21)7 (25)0.73
Adherent (N = 44)10 (23)4 (9)0.18
Obese (N = 68)
Nonadherent (N = 29)6 (25)4 (14)0.73
Adherent (N = 39)15 (38)5 (13)0.03
Note: Data presented N (%). p-value significant at <0.05 using Mc-Nemar test.
Table 3. Comparison of clinical characteristic in overweight and obese participants of both groups after 12-month follow-up.
Table 3. Comparison of clinical characteristic in overweight and obese participants of both groups after 12-month follow-up.
ParametersOverall Overweight & ObeseNonadherent Adherentp *p **p ***
BaselineFollow-UpBaselineFollow-UpBaselineFollow-Up
N (M/F)140 (89/51)57 (51/6)83 (38/45)
Age (years)15.0 ± 1.715.2 ± 1.714.9 ± 1.60.35
Weight (kg)74.5 ± 15.174.9 ± 13.877.1 ± 15.978.4 ± 15.0 **73.2 ± 14.573.1 ± 12.80.080.280.17
BMI (kg/m2)29.5 ± 4.527.2 ± 4.8 **29.8 ± 4.428.2 ± 4.9 **29.3 ± 4.526.6 ± 4.7 **0.350.150.18
BMI Z-score1.1 ± 0.70.99 ± 0.8 *1.2 ± 0.71.2 ± 0.91.05 ± 0.750.87 ± 0.80 **0.220.130.18
Waist (cm)81.9 ± 18.680.3 ± 15.281.3 ± 21.888.7 ± 9.5 *82.2 ± 16.775.7 ± 15.9 **<0.001<0.0010.02
Hip (cm)95.1 ± 21.386.9 ± 14.5 **90.6 ± 25.694.6 ± 10.497.4 ± 18.482.7 ± 14.9 **0.002<0.0010.03
WHR0.85 ± 0.100.92 ± 0.05 **0.88 ± 0.100.93 ± 0.04 **0.84 ± 0.100.92 ± 0.06 **0.460.150.95
SBP (mmHg)125.7 ± 15.4110.9 ± 12.6 **125.5 ± 13.0117.0 ± 8.3 **125.9 ± 16.6107.6 ± 13.4 **0.02<0.0010.26
DBP (mmHg)72.5 ± 11.174.2 ± 7.269.6 ± 9.976.9 ± 7.4 **74.1 ± 11.572.8 ± 6.8<0.001<0.0010.095
Glucose (mmol/L)5.4 ± 1.15.8 ± 2.75.6 ± 1.75.8 ± 2.15.3 ± 0.65.9 ± 3.00.890.710.95
HbA1c (%)5.2 ± 0.75.5 ± 1.65.3 ± 0.75.2 ± 0.95.2 ± 0.75.6 ± 1.80.060.030.50
TC (mmol/L)4.6 ± 0.76.0 ± 1.4 **4.6 ± 0.86.1 ± 1.2 **4.6 ± 0.75.9 ± 1.5 **<0.0010.0470.46
HDL-c (mmol/L)0.9 ± 0.31.4 ± 0.6 **1.0 ± 0.21.5 ± 0.4 **0.9 ± 0.31.4 ± 0.6 **0.002<0.0010.04
LDL-c (mmol/L)3.1 ± 0.73.8 ± 1.2 **3.1 ± 0.83.8 ± 1.0 **3.1 ± 0.63.8 ± 1.3 **<0.001<0.0010.06
TG (mmol/L)1.2 ± 0.61.7 ± 0.8 **1.3 ± 0.81.9 ± 0.7 **1.2 ± 0.61.7 ± 0.9 **0.0020.120.84
Note: Data Presented as mean ± SD; * and ** denotes p-value significant at 0.05 and 0.01 level pre- and post-intervention; p * denotes time effect; p ** denotes time effect * Sex; p *** denotes Sex * group * Time effect. BMI, Body Mass Index; WHR, Waist-Hip Ratio; SBP, Systolic Blood Pressure; DBP, Diastolic Blood Pressure; HbA1c, glycated hemoglobin; TC, Total Cholesterol; HDL-c, High-Density Lipoprotein Cholesterol; LDL-c, Low-Density Lipoprotein Cholesterol; TG, Triglycerides.
Table 4. Comparison of clinical characteristic in overweight participants of both groups after 12-month follow-up.
Table 4. Comparison of clinical characteristic in overweight participants of both groups after 12-month follow-up.
ParametersOverall OverweightNonadherent Adherentp *p **p ***
BaselineFollow-UpBaselineFollow-UpBaselineFollow-Up
N (M/F)72 (38/34)28 (22/6)44 (16/28)
Age (years)15.2 ± 1.715.3 ± 1.815.1 ± 1.60.66
Weight (kg)64.4 ± 10.365.9 ± 9.5 **66.3 ± 10.368.2 ± 9.5 **63.5 ± 10.364.7 ± 9.3 *0.0010.040.94
BMI (kg/m2)26.0 ± 1.724.0 ± 3.2 **26.4 ± 1.624.8 ± 3.3 **25.8 ± 1.823.6 ± 3.1 **0.350.510.49
BMI Z-score0.54 ± 0.300.47 ± 0.580.63 ± 0.270.67 ± 0.6050.50 ± 0.310.40 ± 0.550.500.430.41
Waist (cm)74.6 ± 17.178.1 ± 15.469.8 ± 21.388.6 ± 9.477.2 ± 13.972.3 ± 15.0<0.0010.020.28
Hip (cm)89.8 ± 20.485.1 ± 14.982.3 ± 25.695.9 ± 11.2 **93.7 ± 16.179.4 ± 13.6 **<0.001<0.0010.007
WHR0.8 ± 0.110.9 ± 0.06 **0.8 ± 0.070.9 ± 0.04 *0.83 ± 0.120.91 ± 0.07 **0.290.470.54
SBP (mmHg)124.0 ± 15.4109.1 ± 12.5 **124.4 ± 11.8116.9 ± 9.2 *123.8 ± 16.9105.1 ± 12.1 **0.180.0030.15
DBP (mmHg)70.9 ± 10.973.8 ± 7.869.3 ± 10.575.4 ± 8.1 *71.8 ± 11.272.9 ± 7.60.0030.020.77
Glucose (mmol/L)5.4 ± 1.55.7 ± 2.45.8 ± 2.35.7 ± 2.45.2 ± 0.75.63 ± 2.40.520.390.88
HbA1c (%)5.2 ± 0.85.3 ± 1.35.3 ± 0.95.2 ± 0.85.2 ± 0.75.37 ± 1.50.0010.0010.83
TC (mmol/L)4.5 ± 0.85.8 ± 1.2 **4.4 ± 0.85.7 ± 1.1 **4.6 ± 0.85.86 ± 1.3 **0.0010.130.32
HDL-c (mmol/L)0.9 ± 0.31.6 ± 0.5 **1.0 ± 0.21.6 ± 0.3 **0.9 ± 0.31.56 ± 0.6 **0.600.0030.55
LDL-c (mmol/L)3.1 ± 0.73.5 ± 1.1 **2.9 ± 0.73.3 ± 1.043.2 ± 0.73.62 ± 1.1 *<0.0010.0010.09
TG (mmol/L)1.2 ± 0.71.6 ± 0.7 **1.2 ± 0.51.7 ± 0.7 **1.2 ± 0.71.6 ± 0.7 *0.220.820.79
Note: Data Presented as mean ± SD; * and ** denotes p-value significant at 0.05 and 0.01 level pre- and post-intervention; p * denotes time effect; p ** denotes time effect * Sex; p *** denotes group * time effect. BMI, Body Mass Index; WHR, Waist-Hip Ratio; SBP, Systolic Blood Pressure; DBP, Diastolic Blood Pressure; HbA1c, glycated hemoglobin; TC, Total Cholesterol; HDL-c, High Density Lipoprotein Cholesterol; LDL-c, Low Density Lipoprotein Cholesterol; TG, Triglycerides.
Table 5. Comparison of clinical characteristic in obese participants of both groups after 12-month follow-up.
Table 5. Comparison of clinical characteristic in obese participants of both groups after 12-month follow-up.
ParametersOverall OverweightNonadherent Adherentp *p **p ***
BaselineFollow-UpBaselineFollow-UpBaselineFollow-Up
N (M/F)68 (51/17)29 (29/0)39 (22/17)
Age (years)14.9 ± 1.715.1 ± 1.614.7 ± 1.70.34
Weight (kg)85.1 ± 11.684.5 ± 10.987.5 ± 13.488.2 ± 12.683.7 ± 10.482.3 ± 9.3 *0.530.450.16
BMI (kg/m2)33.1 ± 3.430.5 ± 3.9 **33.0 ± 3.731.5 ± 3.9 **33.2 ± 3.330.0 ± 3.8 **0.740.060.51
BMI Z-score1.7 ± 0.581.6 ± 0.701.7 ± 0.631.8 ± 0.731.7 ± 0.61.5 ± 0.7 *0.130.080.55
Waist (cm)89.2 ± 17.282.6 ± 14.9 *92.9 ± 15.688.8 ± 9.787.2 ± 17.979.1 ± 16.2 *<0.0010.0010.62
Hip (cm)100.6 ± 21.088.8 ± 14.1 **99.0 ± 23.293.3 ± 9.7101.4 ± 19.986.2 ± 15.60.060.0080.87
WHR0.9 ± 0.090.9 ± 0.04 **0.9 ± 0.111.0 ± 0.020.8 ± 0.080.9 ± 0.050.730.470.30
SBP (mmHg)127.6 ± 15.3112.9 ± 12.6 **126.6 ± 14.2117.1 ± 7.5 **128.2 ± 15.9110.5 ± 14.3 **0.002<0.0010.43
DBP (mmHg)74.1 ± 11.274.8 ± 6.669.9 ± 9.578.3 ± 6.4 **76.6 ± 11.572.7 ± 5.9 *<0.0010.0020.06
Glucose (mmol/L)5.4 ± 0.56.0 ± 3.15.3 ± 0.55.8 ± 1.85.4 ± 0.56.1 ± 3.60.720.950.90
HbA1c (%)5.2 ± 0.66.6 ± 1.85.3 ± 0.65.19 ± 0.95.22 ± 0.65.89 ± 2.10.790.960.23
TC (mmol/L)4.7 ± 0.76.1 ± 1.6 **4.9 ± 0.86.6 ± 1.1 **4.6 ± 0.65.9 ± 1.7 **0.0060.370.94
HDL-c (mmol/L)1.0 ± 0.21.3 ± 0.6 **1.0 ± 0.111.4 ± 0.5 **0.9 ± 0.31.2 ± 0.6 *<0.001<0.0010.002
LDL-c (mmol/L)3.2 ± 0.74.1 ± 1.3 **3.2 ± 0.84.3 ± 0.7 **3.1 ± 0.64.0 ± 1.5<0.0010.020.51
TG (mmol/L)1.3 ± 0.61.9 ± 0.9 **1.4 ± 0.72.0 ± 0.6 *1.2 ± 0.61.8 ± 1.10 **0.0020.040.37
Note: Data Presented as mean ± SD; * and ** denotes p-value significant at 0.05 and 0.01 level pre- and post-intervention; p * denotes time effect; p ** denotes time effect * Sex; p *** denotes group * time effect. BMI, Body Mass Index; WHR, Waist Hip Ratio; SBP, Systolic Blood Pressure; DBP, Diastolic Blood Pressure; HbA1c, glycated hemoglobin; TC, Total Cholesterol; HDL-c, High Density Lipoprotein Cholesterol; LDL-c, Low Density Lipoprotein Cholesterol; TG, Triglycerides.
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MDPI and ACS Style

Al-Daghri, N.M.; Amer, O.E.; Khattak, M.N.K.; Hussain, S.D.; Alkhaldi, G.; Alfawaz, H.A.; Elsaid, M.A.; Sabico, S. Attendance-Based Adherence and Outcomes of Obesity Management Program in Arab Adolescents. Children 2023, 10, 1449. https://doi.org/10.3390/children10091449

AMA Style

Al-Daghri NM, Amer OE, Khattak MNK, Hussain SD, Alkhaldi G, Alfawaz HA, Elsaid MA, Sabico S. Attendance-Based Adherence and Outcomes of Obesity Management Program in Arab Adolescents. Children. 2023; 10(9):1449. https://doi.org/10.3390/children10091449

Chicago/Turabian Style

Al-Daghri, Nasser M., Osama E. Amer, Malak N. K. Khattak, Syed D. Hussain, Ghadah Alkhaldi, Hanan A. Alfawaz, Mohamed A. Elsaid, and Shaun Sabico. 2023. "Attendance-Based Adherence and Outcomes of Obesity Management Program in Arab Adolescents" Children 10, no. 9: 1449. https://doi.org/10.3390/children10091449

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