Skip to main content
Evidence-based Complementary and Alternative Medicine : eCAM logoLink to Evidence-based Complementary and Alternative Medicine : eCAM
. 2021 Aug 25;2021:6702767. doi: 10.1155/2021/6702767

Effects of Continuous Yoga on Body Composition in Obese Adolescents

Marisa Poomiphak Na Nongkhai 1,, Rodsarin Yamprasert 2, Chuchard Punsawad 3
PMCID: PMC8410386  PMID: 34484400

Abstract

Overweight/obesity is a pressing international health concern, and conventional treatments demonstrate poor long-term efficacy. Several studies have shown that yoga can control risk factors for cardiovascular disease, obesity, and psychosocial stress. The present study aimed to assess the effect of continuous yoga (asanas, pranayama, and Surya Namaskar yoga) on body composition in overweight participants. Forty adolescents with obesity were enrolled in this study. The study was conceived as a prospective, single-center, single-blinded randomized controlled trial. The participants were divided into 2 groups: the intervention group (n = 20), which undertook a continuous yoga practice, and the control group (n = 20). Body composition, including body weight (BW), body mass index (BMI), body fat mass (BFM), and muscle mass, was evaluated using tetrapolar bioelectrical impedance (BIA). Our results showed that the mean BMI and BFM of the yoga intervention group were significantly decreased at week 8 and week 12. The muscle mass of the yoga group continued to improve at a rate of 0.515 per week, which was statistically significant. In conclusion, a continuous yoga practice had a tendency to decrease BMI and BFM and increase muscle mass. These findings demonstrate intervention effectiveness similar to that observed in other clinical research and indicate that continuous yoga practice may be used as an alternative therapy for obesity prevention and health promotion in adolescents with obesity.

1. Introduction

Obesity is a metabolic disorder with excessive fat accumulation in different parts of the body, and it is a risk factor for cardiovascular and metabolic disorders [1]. One-third of the world's population is now categorized as overweight, and all signs point to a further escalation of this situation in the years to come [1]. This health problem is increasing worldwide, especially in developing countries and newly industrializing countries [2]. Improvements in living standards and changes in lifestyle, physical inactivity, sedentary behavior, and excessive energy intake have resulted in a rapid increase in overweight and obesity rates among children and adolescents [24]. An estimated 38.2 million children under the age of 5 years were overweight or obese in 2019. Once considered a high-income country problem, overweight and obesity are now on the rise in low- and middle-income countries, particularly in urban settings. In Africa, the number of overweight children under 5 has increased by nearly 24% since 2000. Almost half of the children under 5 who were overweight or obese in 2019 lived in Asia. The prevalence of overweight and obesity among children and adolescents aged 5–19 has risen dramatically from 4% in 1975 to just over 18% in 2016. This increase occurred in boys and girls; in 2016, 18% of girls and 19% of boys were overweight [5]. The results of a 2014 nationwide health survey of Thai people found that Thai people over 15 years old were more likely to be overweight and obese (body mass index (BMI) of 25 kg/m2 or more) than people who participated in the survey in 2009; the rate among women increased from 40.7% to 41.8%, and the rate among men increased from 28.4% to 32.9% [6]. Moreover, the Department of Health, Ministry of Public Health, Thailand, reported that 13.1% of school-aged children were on the verge of becoming overweight or obese in 2016, and 1 in 4 children and 3 in 4 teenagers were obese and may grow to become obese adults. Obesity increases the risk of developing chronic noncommunicable diseases (NCDs) [7]. College and university students may be especially at risk for sedentary behavior because much of their campus day consists of classroom lectures and studying while sitting still. However, young adults are typically in good health, and educational institutions and student welfare associations facilitate student's engagement in various forms of physical activity. Studies suggested that university students are highly sedentary and highly active [1, 8].

Therapeutic intervention programs for obese individuals aim at long-term weight maintenance and normalization of body weight and body fat. These programs modify the eating and exercise behaviors of obese children and establish new, healthier behaviors and lifestyles. Treatment programs must include behavioral components to permanently change the nutrition and physical exercise habits of obese children and adolescents [9]. All of this information shows that adolescent obesity remains a major public health problem that must be addressed. Control of eating habits and physical activity is recommended in medical guidelines as the most important therapeutic option in nonmorbid obesity [10]. However, a substantial proportion of obese persons not adhering to such recommendations supports the study of alternative forms of physical activity to reduce weight [11]. Yoga is a holistic mind-body intervention aimed at physical, mental, emotional, and spiritual wellbeing. Several studies showed that yoga and/or meditation controlled risk factors for cardiovascular diseases, such as hypertension, type II diabetes, insulin resistance, obesity, lipid profile abnormalities, psychosocial stress, and smoking. Some randomized studies suggest that yoga/meditation retards or even regresses early and advanced coronary atherosclerosis [12]. A recent study suggests that transcendental meditation may be extremely useful in the secondary prevention of coronary heart disease [13] and may decrease body weight [11].

Yoga is one such intervention, with studies reporting long-term adherence and benefits in various health conditions, including obesity. The various postures of yoga, especially forward bending, twisting and backward bending, help reduce fat near the abdomen, hips, and other areas [14]. Therefore, yoga is a solution for a healthy lifestyle because the practice of yoga is a complete package with wonderful cardiovascular, dynamic workouts that do not require any machines or much space [15].

Therefore, yoga may be a way to prevent obesity in adolescents. It is necessary to study forms of exercise that are appropriate and beneficial for weight. The present study examined the effects of a continuous yoga program on weight loss and body composition. This study provides new exercise knowledge on classic yoga plus aerobic exercise for decreasing body weight and increasing fat-burning in female adolescents.

2. Materials and Methods

2.1. Study Design and Participants

The study was conceived as a single-center, single-blinded randomized controlled trial (RCT) before patients were recruited. All procedures performed in studies involving human participants were in accordance with the ethical standards of the Mae Fah Luang University Ethics Committee on Human Research (MFU EC) at Mae Fah Luang University, Chiang Rai, Thailand (approved no. REH-61202). The total duration of the study was from June 2018 to July 2019.

Forty participants were selected at the beginning of the study and invited to participate in this research. The type of sampling was purposive sampling, which was set up for the main purpose of this study. The selection criteria included (1) female students who studied exercise and weight control as first priority and other subjects who were interested in participating in the research project, (2) age between 19 and 22 years, (3) BMI of 23–29.5 kg/m2 and not greater than 30 kg/m2, (4) BFM between 26 and 36%, and (5) absence of a disease that could have contributed to obesity (e.g., hypothyroidism and polycystic ovarian syndrome). Participants who had other diseases that were disabling or were not controlled with medication or were participating in another research project were also excluded. Written informed consent was obtained from all participants prior to enrollment in this study.

The sample size determination was calculated from the formula N (each group) = (r + 1) (/2 + Z1 − β)2 σ2/rd2 [1416], where is the normal deviate at a level of significance ( is 1.96 for 5%) and Z1 − β is the normal deviate at 1 − β% power with β% of type II error (0.84 at 80% power). R = n1/n2 is the ratio of the sample size required for 2 groups, which generally creates equal sample sizes for 2 groups. σ and d are the pooled standard deviation and difference of means of 2 groups, respectively. We performed a pilot study, and the minimal detectable difference of means (d) of two groups was 2.8 scores of body fat mass (BFM), with a standard deviation (σ) of 3.00. Therefore, the minimum sample size for each group to detect the mean difference between the two means was 18 persons/group. Considering a 10% of drop-out, twenty patients per treatment group were required for the study.

2.2. Continuous Yoga Intervention

Participants were given all of the equipment needed for the yoga classes to use free of charge during the intervention. Equipment included a mat, 2-3 m straps, 3 blankets, and 2 wooden blocks. The intervention was implemented three times per week for twelve weeks, and each class lasted 50 min. The yoga curriculum is shown in Table 1. This curriculum was designed to focus primarily on the physicality of yoga practice. Continuous yoga is a cyclic yoga practice with minimal rest periods. The purpose of this study was to adjust the form of yoga to obtain an aerobic workout and increase the processes used for energy metabolism. Asanas were specifically chosen to strengthen and align the trunk and lower extremities [1517]. Pranayama, also called breathing exercises, involves manipulation of the breath, which is a dynamic bridge between the body and mind [1618]. Classes included instructions/demonstrations of each asana, followed by participant practice. Participants reported current pain intensity at the beginning of each class. The instructor actively modified asanas where necessary for pain and/or other limitations (e.g., body habitus) and gave instructions on breathing techniques throughout. The exercise sessions consisted of three phases for a total of 50 mins: 10 min of warming up/stretching in standing poses and a sitting pose, 30 min of continuous yoga involving 12 poses that were performed continuously with no rest or break, and 10 min of relaxation (cooldown) in sitting poses and a corpse pose. Exercise was performed at 65–75% of the maximum heart rate (HRmax). The frequency of exercise was Monday, Wednesday, and Friday from 5 : 00 to 5 : 50 p.m. for 12 weeks. The continuous yoga program, including the asanas technique, was validated by five yoga experts and sports science teachers, and the accepted exercise program was tried out on 20 female students. The continuous yoga practices, which included stretching techniques, sun salutations, and meditation and breathing exercises, were introduced in the yoga curriculum in Table 1.

Table 1.

Yoga curriculum.

FITT principle Items Details
F 3 times/week Mon., Wed., Fri.
I 65–75% of maximum heart rate 135–145 times/min
T 50 min Warm-up/stretching, 10 min
yoga exercise, 12 poses, 30 min
cooldown/relaxation, 10 min
T Continuous yoga Continuous yoga, 12 poses

FITT: frequency, intensity, time, and type.

2.3. Assessments of Body Composition

Height was assessed using an FBT height scale. Body composition, including body weight (BW), BMI, BFM, and muscle mass, was measured three times before the intervention (week 0) and at week 8 and week 12 from 4 : 00 to 5 : 00 p.m. Body composition measurement methods are continuously being perfected, with the most commonly used method being bioelectrical impedance analysis (BIA) (INBODY 720 BIOSPACE, USA). Before BIA, participants were instructed to remove their shoes and socks, and the bottoms of the feet and palms of the hands were wiped using tissue. Participants were asked to step onto the BIA device, place the soles of their feet on the foot electrodes, and grip the hand electrodes with their hands. Participants were asked to stand with their arms straight and away from their trunks so they were not touching their bodies to achieve a proper testing posture, as described in the manufacturer's guidelines. The target heart rate (HR) was checked after 30 min of yoga asanas. Participants checked their own HR for 1 min.

2.4. Statistical Analysis

All statistical analyses were performed using IBM SPSS® Statistics version 26. The Mann–Whitney U test was used to compare the mean values between groups. Friedman's test was used to analyze changes in the mean values from baseline to the 8th and 12th week for each group. Univariable analysis was used to examine the crude odds ratio (COR) of the binary outcome variable for each independent variable. All variables in the univariable analysis were subjected to multivariable analysis to adjust for possible confounders. The final analysis was interpreted as adjusted odds ratios (AORs) with 95% CIs. A P value less than 0.05 indicated statistical significance.

3. Results

3.1. Demographic Characteristics of the Study Participants

Forty participants were initially screened between October 2018 and January 2019. They were studying at Mae Fah Luang University, Chiang Rai Province, Thailand, and were randomized into 2 groups (20 participants in each group). The first group was the yoga or intervention group, and the second group served as the control group. The results demonstrated that the mean weight (kg), BMI (kg/m2), BFM, and muscle mass were not different between the control group and the yoga group. The mean height (cm) of the control group was significantly greater than the yoga group (Table 2). There was no significant difference between the two groups in weight, BMI, or BFM. At baseline, the participants in the control group had a lower percentage of body fat and less muscle mass than the participants in the yoga group (Table 2).

Table 2.

Demographic characteristics of the study participants.

Characteristics Groups P value
Yoga (n = 20) Control (n = 20)
Weight (kg) 65.60 ± 10.15 67.53 ± 4.72 0.587
Height (cm) 164.25 ± 7.82 172.20 ± 6.61 >0.001
BMI (kg/m2) 22.70 ± 3.51 23.37 ± 1.63 0.433
BFM 29.25 ± 3.49 29.22 ± 3.86 0.968
Muscle mass 25.31 ± 1.60 24.25 ± 1.76 0.059

Data are presented as the means ± SD. P < 0.05, significantly different compared to the control group.

3.2. Body Mass Index

BMI is a measure of body fat based on height and weight that applies to individuals aged approximately 19–20 years. BMI was calculated based on self-reported body weight (kg) divided by height squared (m2) [1719]. Participants were categorized based on BMI according to World Health Organization Western Pacific Region (WPRO) criteria, as recommended for Asians. BMI was categorized as follows: 23.0–24.9 kg/m2 was overweight, 25.0–29.9 kg/m2 was obesity level 1, and over 30.0 kg/m2 was obesity level 2 [20]. Our study showed that the mean BMI of the yoga group decreased significantly at week 8 and week 12 (Table 3 and Figure 1). However, the mean BMI of the control group did not change compared to the yoga group. When considering differences between the groups, the mean BMI of the yoga group decreased consistently by week 12 (Table 3).

Table 3.

Body mass index (BMI) of the yoga and control groups.

Follow-up Groups P value
Yoga (n = 20) Control (n = 20)
Week 0 22.70 (3.51) 23.37 (1.63) 0.433
Week 8 22.26 (3.37) ††† 23.32 (1.61) 0.087
Week 12 22.02 (3.33) ††† 23.42 (1.65) 0.018
Mean difference 0.681 0.058 NT
95% CI for difference 0.204–0.630 0.278–0.395
P value∗∗ ≤0.001 0.664

Data are represented as the means (SD). NT: not detected. Statistical analysis.Mann–Whitney U test.∗∗Friedman's test. †Significant difference from day 0 within group (P ≤ 0.05).††Significant difference from day 0 within group (P ≤ 0.01). †††Significant difference from day 0 within group (P ≤ 0.001).

Figure 1.

Figure 1

Trends in body mass index (BMI) at baseline, week 8, and week 12 in the yoga and control groups. Data are presented in means (SD).

3.3. Body Fat Mass

The BFM of the yoga group decreased consistently at week 8 and week 12, whereas the BFM of the control group did not change from baseline (Table 4 and Figure 2). At week 12, the mean BFM of the yoga group had consistently decreased compared with that of the control group (Table 4 and Figure 2).

Table 4.

Body fat mass of the yoga and control groups.

Follow-up Groups P value
Yoga (n = 20) Control (n = 20)
Week 0 29.25 (3.49) 29.22 (3.86) 0.968
Week 8 27.49 (3.55) ††† 28.68 (3.50) † 0.406
Week 12 26.37 (3.47) ††† 29.02 (3.54) 0.013
Mean difference 2.879 0.200 NT
95% CI for difference 2.119–3.639 0.444–0.844
P value∗∗ ≤0.001 0.030

Data are presented as the means (SD). NT: not detected. Statistical analysis.Mann–Whitney U test. ∗∗Friedman's test. †Significant difference from day 0 within group (P ≤ 0.05). ††Significant difference from day 0 within group (P ≤ 0.01). †††Significant difference from day 0 within group (P ≤ 0.001).

Figure 2.

Figure 2

Trends in body fat mass (BFM) at baseline, week 8, and week 12 in the yoga and control groups. Data are presented in means (SD).

3.4. Muscle Mass

The muscle mass of the yoga group was significantly improved at week 8 and week 12, with an improvement rate of 0.515 per week (Table 5 and Figure 3). In contrast, the muscle mass of the control group was significantly decreased compared with the baseline (Table 5 and Figure 3).

Table 5.

Muscle mass of the yoga and control groups.

Follow-up Groups P value
Yoga (n = 20) Control (n = 20)
Week 0 25.31 (1.60) 24.25 (1.76) 0.059
Week 8 25.39 (1.59) 23.62 (1.86) †† 0.005
Week 12 25.83 (1.45) †† 23.81 (1.83) † 0.002
Mean difference 0.515 −0.440 NT
95% CI for difference 0.130–0.900 (−0.888)–0.008
P value∗∗ 0.002 0.002

Data are presented as the means (SD). NT: not detected. Statistical analysis. Mann–Whitney U test. ∗∗ Friedman's test. †Significant difference from day 0 within group (P ≤ 0.05). ††Significant difference from day 0 within group (P ≤ 0.01). †††Significant difference from day 0 within group (P ≤ 0.001).

Figure 3.

Figure 3

Trends in muscle mass (BFM) at baseline, week 8, and week 12 in the yoga and control groups. Data are presented in means (SD).

3.5. Logistic Regression Analysis

The results of the univariable and multivariable analyses of the risk factors associated with overweight are shown in Table 6. Univariable analysis revealed that BFM and muscle mass were significantly associated with overweight (odds ratios (OR) = 1.75; 95% confidence intervals (CI) 1.27–2.71, OR = 4.53; 95% CI 1.75–11.69). No significant associations were found between overweight and age or yoga (P < 0.05) (Table 6). Multivariable analysis also showed that muscle mass was significantly associated with overweight. When muscle mass increased by 1 unit, the odds of becoming overweight increased 3.88 times after adjusting for age, BFM, and yoga (adjusted odds ratios (AOR) = 3.88; 95% CI 1.08–13.93) (Table 6).

Table 6.

Univariate and multivariate logistic regression analyses.

Characteristics n OR (95% CI) P value AOR (95% CI) P value
Age 20.00 ± 0.75 1.20 (0.51–2.81) 0.670 0.71 (0.21–2.46) 0.590
BFM 29.23 ± 3.63 1.85 (1.27–2.71) 0.001∗∗ 1.23 (0.78–1.95) 0.360
Muscle mass 24.77 ± 1.74 4.53 (1.75–11.69) 0.002∗∗ 3.88 (1.08–13.93) 0.030∗∗
Yoga
No 20 (50.00) Ref. Ref.
Yes 20 (50.00) 0.81 (0.23–2.83) 0.750 0.39 (0.04–3.50) 0.400

Data are presented as the means ± SD. ∗∗Statistically significant at P < 0.05.

4. Discussion

The prevalence of obesity is increasing worldwide, and obesity is an important risk factor for cardiovascular and metabolic disorders. Particularly worrisome is that children and teenagers with obesity may become obese adults. Obesity is associated with an increased risk of developing chronic NCD. Therefore, alternative therapies for obesity prevention and promotion of health in overweight adolescents are important. The effectiveness of yoga for weight control and improved body composition is evident from surveys [21] and clinical studies [22], and yoga has the potential to increase fat loss, develop muscle tone, and build flexibility, leading to better shape and good proportions. Many types of yoga also help build muscle strength and endurance [23].

The present study assessed the effect of a continuous yoga intervention on body composition in overweight participants. BMI is a parameter of body composition that may be used in the diagnosis of obesity [24]. It is a measure of body fat based on height and weight. Therefore, BMI does not measure body fat directly, but it is moderately correlated with more direct measures of body fat. BMI appears to be strongly correlated with various metabolic and disease outcomes, but there are more direct measures of body fatness [24].

Our results showed that significantly reduced BMI and BFM were found in the yoga group. The Mama study (2019) reported that 12 weeks of yoga led to a significant decrease in body fat. The decrease in body fat may be because the volunteers experienced an abnormal state of yoga exercise over some stretch of time, which produced a decrease in the body fat rate. Yoga includes profound nostril breathing, adaptability of limbs, and extension of various body parts, which may be the reason for the decrease in body fat of the volunteers performing yoga. The decrease in body fat may impact body mass, and the present examination found a significant decrease in body mass in the volunteers performing yoga. Comparable perceptions were noted in numerous studies, where a decrease in body fat was noted after yoga training [23]. A previous study found that an increase in frequency, a longer duration, and the use of complex yoga interventions with multiple components affected anthropometric measures. The combination of yoga with dietary/nutritional recommendations, especially a vegetarian diet with or without calorie reduction, also affected anthropometric measures [25].

The mean BW and muscle mass in the present study were significantly decreased in the yoga group after continuous yoga practice. A controlled trial in India supported that yogic practices contributed to a reduction in excess body fat in school students and obese patients [26]. This finding suggests that yoga plays a role as a safety measure. Participants in the continuous yoga group also had significantly increased muscle mass, which may be due to yoga poses that included strengthening exercises.

Muscle mass includes skeletal muscles, smooth muscles, such as cardiac and digestive muscles, and the water contained in these muscles. Muscles act as an engine in consuming energy. As muscle mass increases, the rate at which energy (calories) is burned increases, which accelerates the basal metabolic rate (BMR) and helps reduce excess body fat and weight in a healthy manner. When exercising hard, muscle mass increases and metabolism is efficient. It is important to monitor body measurements regularly to observe the impact of a training program on muscle mass [27].

A study in Tampere, Finland, also supports the present study and indicated that the practice of yoga was associated with significant decreases in total cholesterol and triglycerides in subjects with cardiovascular disease [28]. A study in Connecticut, USA, used a six-week program of yoga and meditation to observe brachial artery reactivity, and significant reductions in blood pressure, heart rate, and BMI were observed in the cohort that practiced yoga [29]. BW decreased significantly after Hatha yogic practices in a previous study. A controlled trial in India showed that yogic practices contributed to a reduction in excess body fat in school students and obese patients [30]. Ha et al. [31] reported that regular and continuous modified Hatha yoga exercise effectively improved body composition, decreased plasma malondialdehyde (MDA) concentration, and increased plasma superoxide dismutase (SOD) activity in female patients with shoulder pain. Therefore, Hatha yoga exercise should be effective at preventing shoulder pain of various causes in female patients with skeletal muscle pain syndrome [31]. The current study found that continuous yoga reduced BW, decreased BFM, and increased muscle mass. However, yoga must be practiced on a regular basis until it is a daily habit. Effective strategies for weight loss require management strategies with a combination of dietary therapy and physical activity using behavioral interventions [32]. Yoga practices lead to an increase in energy expenditure, which results in statistically significant changes in body composition [33, 34]. The practice of only Hatha yoga for 30 min daily increased the metabolic equivalent of task (MET) to 2.5 in females [35].

The limitations of this study were the small sample size and the inclusion of only women, which limits the generalizability to men. Further research should be performed on male subjects or different age groups to determine the effect of this intervention. Our study reported only BMI, BFM, and muscle mass but not fat-free mass. We suggest that future work evaluate more accurate parameters, such as fat-free mass.

5. Conclusions

The current study demonstrated that the mean BMI and BFM of a yoga intervention group decreased significantly at week 8 and week 12. The muscle mass of the yoga group continued to improve at a rate of 0.515 per week. Multivariate logistic regression analysis confirmed that continuous yoga practice affected muscle mass. These findings demonstrated intervention effectiveness that was similar to other clinical research and indicated that continuous yoga practice may be used as an alternative therapy for obesity prevention and health promotion in adolescents with obesity.

Acknowledgments

The authors acknowledge Mae Fah Luang University, Thailand, for financial support and the sports science equipment used in this study. The authors thank Dr. Udomsak Narkkul, Department of Medical Science, Walailak University, for analyzing and interpreting the logistic regression analysis.

Data Availability

The data used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that there are no conflicts of interest regarding the publication of this paper.

Authors' Contributions

MP conceived the design, performed the experiments, and collected the data. RY analyzed the data and designed the figures and tables. MP, RY, and CP wrote the paper, provided critical feedback, helped shape the research and analysis, and approved the final submission.

References

  • 1.Cramer H., Thoms M. S., Anheyer D., Lauche R., Dobos G. Yoga in women with abdominal obesityߞa randomized controlled trial. Deutsches Ärzteblatt international. 2016;113(39):645–652. doi: 10.3238/arztebl.2016.0645. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.NCD Risk Factor Collaboration (NCD-RisC) Trends in adult body-mass index in 200 countries from 1975 to 2014: a pooled analysis of 1698 population-based measurement studies with 19·2 million participants. Lancet. 2016;387(10026):1377–1396. doi: 10.1016/S0140-6736(16)30054-X. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3.Finkelstein E. A., Trogdon J. G., Cohen J. W., Dietz W. Annual medical spending attributable to obesity: payer-and service-specific estimates. Health Aff (Millwood) 2009;28(5):822–831. doi: 10.1377/hlthaff.28.5.w822. [DOI] [PubMed] [Google Scholar]
  • 4.Hales C. M., Carroll M. D., Fryar C. D., Ogden C. L. Prevalence of Obesity Among Adults and Youth: United States, 2015-2016. NCHS Data Brief. 2017;288:1–8. [PubMed] [Google Scholar]
  • 5.World Health Organization. Obesity and overweight. 2020. https://www.who.int/news-room/fact-sheets/detail/obesity-and-overweight.
  • 6.Aekplakorn W. Thai national health examination survey, NHES V. 2014. http://www.thaiheart.org/images/column_1387023976/NHES5_EGATMeeting13Dec13.pdf. [DOI] [PMC free article] [PubMed]
  • 7.Chaiyapak S. Department of health annual report 2017. 2017. https://planning.anamai.moph.go.th/download/D_report_year/Report_DoH61.pdf.
  • 8.Telles S., Naveen V. K., Balkrishna A., Kumar S. Short term health impact of a yoga and diet change program on obesity. Medical Science Monitor. 2010;16(1):35–40. [PubMed] [Google Scholar]
  • 9.Zwiauer K. F. Prevention and treatment of overweight and obesity in children and adolescents. Eur J Pediatr. 2000;159(1):56–68. doi: 10.1007/pl00014367. [DOI] [PubMed] [Google Scholar]
  • 10.American College of Cardiology/American Heart Association Task Force on Practice Guidelines. Expert Panel Report: Guidelines (2013) for the management of overweight and obesity in adults. Obesity (Silver Spring) 2014;22(2):41–410. doi: 10.1002/oby.20821. [DOI] [PubMed] [Google Scholar]
  • 11.Manchanda S. C., Madan K. Yoga and meditation in cardiovascular disease, Clinical Research in Cardiology. 2014;103(9):675–80. doi: 10.1007/s00392-014-0663-9. [DOI] [PubMed] [Google Scholar]
  • 12.Swift D. L., Johannsen N. M., Lavie C. J., Earnest C. P., Church T. S. The role of exercise and physical activity in weight loss and maintenance. Progress in Cardiovascular Diseases. 2014;56(4):441–447. doi: 10.1016/j.pcad.2013.09.012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Tian D., Meng J. Exercise for Prevention and Relief of Cardiovascular Disease: Prognoses, Mechanisms, and Approaches. Oxidative Medicine and Cellular Longevity. 2019;2019:11. doi: 10.1155/2019/37567502019.3756750 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Telles S., Sharma S. K., Kala N., Pal S., Gupta R. K., Balkrishna A. Twelve weeks of yoga or nutritional advice for centrally obese adult females. Frontiers in Endocrinology. 2018;9:p. 466. doi: 10.3389/fendo.2018.00466. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Angus P. Y., Ugwu F. N., Tam B. T., et al. One year of yoga training alters ghrelin axis in centrally obese adults with metabolic syndrome. Frontiers in Physiology. 2018;9 doi: 10.3389/fphys.2018.01321.1321 [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Suresh K., Chandrashekara S. Sample size estimation and power analysis for clinical research studies. Journal of Human Reproductive Sciences. 2012;5(1):7–13. doi: 10.4103/0974-1208.97779. [DOI] [PMC free article] [PubMed] [Google Scholar] [Retracted]
  • 17.Hainsworth K. R., Liu X. C., Simpson P. M., et al. A pilot study of iyengar yoga for pediatric obesity: effects on gait and emotional functioning. Children (Basel) 2018;5(7):p. 92. doi: 10.3390/children5070092. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Mamatha Shree C., Prashanth K. S., Girija B. Effect of short-term pranayama on perceived stress, sleep quality, heart rate, and blood pressure. International Journal of Physiology. 2019;7(2):111–115. doi: 10.5958/2320-608x.2019.00054.4. [DOI] [Google Scholar]
  • 19.Grasdalsmoen M., Eriksen H. R., Lønning K. J., Sivertsen B. Physical exercise and body-mass index in young adults: a national survey of Norwegian university students. BMC Public Health. 2019;19(1):p. 1354. doi: 10.1186/s12889-019-7650-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.World Health Organization. Regional Office for the Western Pacific. (2000). The Asia-Pacific perspective: redefining obesity and its treatment. Sydney, Australia: Health Communications Australia; 2000. https://apps.who.int/iris/handle/10665/206936. [Google Scholar]
  • 21.Kristal A. R., Littman A. J., Benitez D., White E. Yoga practice is associated with attenuated weight gain in healthy, middle-aged men and women. Alternative Therapies in Health and Medicine. 2005;11(4):28–33. [PubMed] [Google Scholar]
  • 22.Lauche R., Langhorst J., Lee M. S., et al. A systematic review and meta-analysis on the effects of yoga on weight-related outcomes. Preview Medicine. 2016;87:213–232. doi: 10.1016/j.ypmed.2016.03.013. [DOI] [PubMed] [Google Scholar]
  • 23.Manna I. Effects of Yoga training on Body composition, cardiovascular and biochemical parameters in healthy adult Male Volunteers. Al Ameen Journal of Medical Sciences. 2018;10(3):156–2017. [Google Scholar]
  • 24.Rothman K. J. BMI-related errors in the measurement of obesity. International Journal of Obesity. 2008;32(3):56–59. doi: 10.1038/ijo.2008.87. [DOI] [PubMed] [Google Scholar]
  • 25.Rioux J. G, Ritenbaugh C. Narrative review of yoga intervention clinical trials including weight-related outcomes. Alternative Therapies in Health and Medicine. 2013;19(3):32–46. [PubMed] [Google Scholar]
  • 26.Kumar K. Effect of yogic intervention on general body weight of the subjects: A study report. International Journal of Yoga & Allied Sciences. 2015;4(1):2278–5159. [Google Scholar]
  • 27.Schoenfeld B. J., Ogborn D., Krieger J. W. Dose-response relationship between weekly resistance training volume and increases in muscle mass: a systematic review and meta-analysis. Journal of Sports Science. 2017;35(11):1073–1082. doi: 10.1080/02640414.2016.1210197. [DOI] [PubMed] [Google Scholar]
  • 28.Asikainen T. M., Miilunpalo S., Kukkonen-Harjula K., et al. Walking trials in post-menopausal women: effect of low doses of exercise and exercise fractionization on coronary risk factors. Scandinavian Journal of Medicine & Science. 2003;13(5):284–92. doi: 10.1034/j.1600-0838.2003.00331.x. [DOI] [PubMed] [Google Scholar]
  • 29.Sivasankaran S., Sachdeva S., Sachdeva R., et al. The effect of a six-week program of yoga and meditation on brachial artery reactivity: do psychosocial interventions affect vascular tone? Clinical Cardiology. 2006;29(9):393–8. doi: 10.1002/clc.4960290905. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Bera T. K., Gore M. M., Kulkarni D. D., Bhogal R. S., Oak J. P. Residential and non-residential yoga training on health related physical fitness of obese patients. Yoga-Mimamsa. 2003;34:166–87. [Google Scholar]
  • 31.Ha M. S., Kim D. Y., Baek Y. H. Effects of Hatha yoga exercise on plasma malondialdehyde concentration and superoxide dismutase activity in female patients with shoulder pain,”. Journal of Physical Therapy Science. 2015;27(7):2109–2112. doi: 10.1589/jpts.27.2109. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Lang A., Froelicher E. S. Management of overweight and obesity in adults: behavioral intervention for long-term weight loss and maintenance. European Journal of Cardiovascular Nursing. 2006;5(2):102–14. doi: 10.1016/j.ejcnurse.2005.11.002. [DOI] [PubMed] [Google Scholar]
  • 33.Sahay B. K. Role of yoga in diabetes. JAPI: Journal of the Association of Physicians of India. 2007;55:121–26. [PubMed] [Google Scholar]
  • 34.Bera T. K., Rajapurkar M. V. Body composition, cardiovascular endurance and anaerobic power of yogic practitioner. Indian Journal of Physiology and Pharmacology. 1993;37:225–228. [PubMed] [Google Scholar]
  • 35.Clay C. C., Lloyd L. K., Walker J. L., Sharp K. R., Pankey R. B. The metabolic cost of hatha yoga. Journal of Strength and Conditioning Research. 2005;19:604–610. doi: 10.1519/15144.1. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

The data used to support the findings of this study are available from the corresponding author upon request.


Articles from Evidence-based Complementary and Alternative Medicine : eCAM are provided here courtesy of Wiley

RESOURCES