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Journal of Medicine and Life logoLink to Journal of Medicine and Life
. 2023 Apr;16(4):559–570. doi: 10.25122/jml-2022-0006

Impact of a lifestyle intervention program on cardio-metabolic parameters among obese adults: A comparative population-based study in West Bengal, India

Chaitali Bose 1, Amol Dilip Kinge 2, Julekha Sultana 2, Ajoy Kumar Biswas 3, Koushik Bhattacharya 4, Alak Kumar Syamal 1,*
PMCID: PMC10251381  PMID: 37305820

Abstract

The obesity epidemic is not only limited to high-income or urbanized societies, but has also become prevalent among rural communities, even in India. Approaches to modifiable behaviors, like unhealthy dietary habits or a sedentary lifestyle, could bring positive results among obese populations. This research aimed to assess the effectiveness of lifestyle intervention programs to prevent obesity and cardio-metabolic risks among Bengali obese adults (Body Mass Index of 25-30kg/m2). The population was selected from rural and urban communities of Hooghly district in west Bengal, India and included 121 participants (20-50 years), divided into four groups (rural male, rural female, urban male, and urban female) who underwent a 12-month intervention program. Anthropometric parameters, systolic and diastolic blood pressure, biochemical parameters (fasting blood glucose, fasting plasma insulin, Homeostatic Model Assessment for Insulin Resistance [HOMA-IR] and lipid profile), dietary habits, and physical activity profiles were assessed before the study (baseline), after 12 months of intervention (post-intervention), and after 24 months (follow-up), among all groups, to evaluate changes in data within and between the groups (rural vs. urban). The results showed a significant decline in anthropometric parameters and fasting blood glucose levels among all intervention groups, HOMA-IR in rural females, and serum triglyceride levels in urban groups. A significant improvement was noted regarding dietary habits and physical activity, even during follow-up. The impact of the intervention program did not show any rural-urban difference. The lifestyle intervention program was effective in reducing obesity and related health risks and promoting a healthy lifestyle among the target population.

Keywords: cardio-metabolic risks, dietary modification, lifestyle, non-communicable diseases, obesity, physical activity

ABBREVIATIONS: BMI – Body Mass Index, DBP – Diastolic Blood Pressure, FBG – Fasting Blood Glucose, HDL-C – High Density Lipo-protein Cholesterol, HOMA-IR – Homeostatic Model Assessment for Insulin Resistance, LDL-C – Low Density Lipo-protein Cholesterol, MET – Metabolic Equivalent, NCDs – Non-Communicable Diseases, N.S. – Non-Significant i.e. p>0.05, PA – Physical Activity, SBP – Systolic Blood Pressure, SD – Standard Deviation, TC – Total Cholesterol, TG – Triglyceride, WC – Waist Circumference, WHR – Waist to Hip Ratio, WHtR – Waist to Height Ratio

INTRODUCTION

Obesity can be defined as an accumulation of excess adipose tissue in the body resulting in health risks. The obesity surge has become prominent since 1975 across the world. According to the World Health Organization (WHO), in 2016 nearly 1.9 billion adults were overweight, and 650 million among them were obese. This global epidemic was not only confined to high-income countries, but also sprawling in low- or middle-income countries like India. Research revealed that among such countries, obesity prevalence is increasing at a similar or faster pace in rural areas compared to urban settings [1]. Obesity is a major risk for non-communicable diseases (NCDs) as it substantially raises the threat of metabolic, cardiovascular, respiratory, musculoskeletal, and mental health disorders, as well as for different forms of cancer [2]. Certain NCDs such as cardiovascular diseases, diabetes, and different cancers account for >70% of global deaths yearly and are the leading causes of premature mortality and disabilities [3]. In 2011, the United Nations general assembly recognized unhealthy diet and physical inactivity as key factors to be modified for the prevention and control of NCDs. Obesity, which is a salient risk for NCDs, results from the complex interplay among one’s genetic or epigenetic factors, environment (including intra-uterine environment), and behavior (faulty dietary habits and sedentary living) [4]. Even though the fundamental reason behind obesity is the long-term energy imbalance, a high intake of calories with low expenditure leads to a positive energy balance [5]. WHO also remarked that high-calorie dense food, rich in fat or sugar, a sedentary living promoted by urbanization, and developing social, economic, industrial, agricultural, health, or marketing sectors foster lifestyle transitions that may lead to lifestyle diseases or NCDs [6].

In response to the alarming rate and severity of NCDs globally, the WHO Global Strategy on Diet, Physical Activity and Health 2004 fostered the promotion of healthy living structured around healthy diet and physical activity and maintaining energy balance, as the key factor to prevent obesity. The management of obesity needs a ‘two-pronged’ initiative to (1) provide better surgical, pharmacological, and behavioral interventions, and (2) prevent obesity by tackling environmental factors [7].

Among the interventional measures, behavioral or lifestyle management programs have been gaining ground globally over the last few decades. Many research teams have undertaken such programs to address lifestyle diseases like obesity, diabetes, or other cardio-metabolic disorders [8-9]. These initiatives are mainly based on health or nutrition education and group or individual counseling to adopt modified dietary habits and increased physical activity (PA). The duration of programs varied from three months to two years or more and was supervised by medical practitioners with or without other paramedical staff (e.g., nutritionists, dieticians, nurses, or trained physiotherapists). The Diabetes Prevention Program (DPP) in the USA in 2002 successfully reverted pre-diabetic patients to patients with normal blood glucose levels [10]. In India, the Kerala-Diabetes Prevention Program (K-DPP), a clustered randomized controlled trial, was implemented and resulted in significant improvements regarding cardiovascular risks [11]. Other interventional studies based on lifestyle modification for several NCDs have been implemented in various age groups at different places (schools, outdoor hospitals, clinics, and workplaces), with positive results [12-13]. Studies from West Bengal on the Bengalee population have shown their increasing risks regarding the anthropometric, cardiovascular, and metabolic profile, also accompanied by excess intake of calories and their sedentary lifestyle, both in rural and urban areas, especially among upper-class women [14-15]. No such research was available in West Bengal, so it is the first-ever attempt to administer a lifestyle intervention program targeting an approach to obesity and other cardio-metabolic parameters through dietary modification and increased PA recommendation in both the rural and urban populations.

MATERIAL AND METHODS

Research design and framework

This study implemented a longitudinal research design. 121 subjects selected from rural and urban backgrounds of the Hooghly district (age group 20-50 years; both male and female; Body Mass Index of 25-30 kg/m2) underwent a lifestyle intervention program for 12 months. The study included measurements of anthropometric characteristics [body weight, height, BMI, Waist Circumference (WC), Waist to Hip Ratio (WHR), Waist to Height Ratio (WHtR)], blood pressure (systolic and diastolic), and biochemical parameters [fasting blood glucose (FBG), fasting insulin, Homeostatic Model Assessment for Insulin Resistance (HOMA-IR), lipid profile] at baseline (before the commencement of the lifestyle program), post-intervention (at 12 months), and at follow-up, which was after another 12 months (i.e., at 24 months). The study was conducted from September 2017 to September 2019. Participants received lifestyle modification and awareness training regarding obesity and related lifestyle diseases, their risks of having various NCDs, the need for weight reduction, and the importance of dietary changes and increased physical exercise. Self-reported dietary behavior and PA levels were checked at regular intervals. Subjects were encouraged by the research team to adopt modified health behaviour through small group sessions at definite intervals.

Study setting

At first, general data, anthropometric parameters, resting blood pressure (both systolic and diastolic), and dietary and physical activity profiles were collected from the urban and rural areas by a home visit. After screening, the eligible subjects were invited to attend mobile clinics, which were community buildings (school buildings or mobile health check-up camps) and were asked to fast for 8-12 hours before a blood test. Participants with a fasting blood glucose ≥126 mg/dl were rejected for the intervention program as per the study criteria and suggested to visit government health clinics. The intervention program, including data collection, counselling sessions, and meeting with participants, was conducted in community buildings on Saturdays or Sundays, at the convenience of the participants. The study settings had the necessary equipment and spaces ensured by the local volunteers (club members, non-teaching staff, students) along with the research team consisting of trained dieticians, nutritionists, health professionals, lab technicians, and physiologists.

Eligibility and Recruitment of subjects

Eligible participants were recruited from rural and urban areas of the Hooghly district. Urban areas were municipal areas, and rural areas were the villages under the gram panchayat of Community Development Blocks of Hooghly. The locations were purposively selected depending on accessibility, distance, or familiarity of the research team. After selecting municipal areas wards, the streets were chosen randomly. In rural areas, the process was similar. The households were selected by systematic random sampling, and the subjects were recruited based on study criteria.

Inclusion criteria

Subjects were Bengali-speaking Hindus, permanent residents of the selected areas, male or female, aged 20-50 years, had at least upper primary or high-school education (8th grade to 12th grade), a BMI of 25-30 kg/m2, were free from any clinically diagnosed diseases, were not consuming alcohol or any form of tobacco, had a diet with excess of calories, sugar, or refined carbohydrates, saturated and trans fats, and high in sodium, and were physically inactive (Metabolic Equivalent or MET score <600).

Exclusion criteria

The research excluded pregnant or lactating women or those planning for conception, people on medication (e.g., steroids, anti-depressant, anti-hypertensive drugs), participants on weight reduction therapy or who have undergone surgery, non-ambulatory participants, or those with physical or mental disabilities, people with eating disorders and those who were diagnosed with certain medical problems before or during the study period (e.g., hypertension, diabetes, stroke) and were not willing to participate [16].

Sample size

A total of 300 subjects with a BMI of 25-30 kg/m2 (150 from rural areas, 75 male and 75 female; 150 from the urban area, 75 male and 75 female) were screened before undergoing the intervention program. Obese subjects with a MET score >600 whose diets were not faulty or deficient with macronutrients and were excluded. Subjects matched based on study criteria and with similar socio-demographic backgrounds and occupations from both rural and urban areas were recruited. Out of 300 subjects, 190 (107 in urban areas [Male=48 & Female=59] and 83 in rural areas [Male=39 & Female=44]) were selected. Out of the 190 participants, 41 were excluded after the blood test; thus, the program was started with 149 people (81 from urban areas, 68 from rural areas). A total of 121 (61 from rural area, 60 from the urban area) completed the lifestyle modification program and participated in the follow-up at 12 months and at 24 months. Therefore, we considered 121 participants as the sample size for this study. The sample selection is represented in Figure 1.

Figure 1.

Figure 1

Selection of subjects for the intervention study

Intervention period

The intervention program was initiated in September 2017 and continued for 12 months. After the follow-up, at 24 months from the initiation (September 2019), the program ended.

Program activities and content

The activities were based on previous interventions for reducing obesity, diabetes, or cardiovascular risks through lifestyle modification in India or other countries for adults with metabolic risks [17-19].

The program included: the inaugural session, individual and group-based counseling sessions for dietary modification, PA recommendations, behavioral modification, and sessions on motivation, problem-solving, and encouragement to adaptation. The tracked variables included participants' self-recorded data, anthropometric parameters, blood pressure, and biochemical parameters, assessed at 12 months and 24 months [20].

Program goals

The goals of the program were the following:

  1. At least 7% of initial body weight loss at the end of the intervention program and maintenance of weight post-program;

  2. Increase in PA (at least 150 minutes of moderate-intensity activity per week);

  3. Promotion of healthy eating habits;

  4. Decrease in weekly sedentary time;

  5. Decrease of cardio-metabolic risks from baseline.

Counseling sessions

The program, both in rural and urban study centers, started with an inaugural session addressing the participants of that area on different days (the rural program was started on the 1st Sunday of September, and the urban program started the following Sunday). The participants interacted with the study team, their health risks and future complications were discussed, and the importance of the program was delivered. Program-related leaflets and folders written in Bengali and activity logbooks were also distributed. All the participants in an area were divided into small groups based on their gender (15-16 in each group). A total of 16 individual or group sessions were arranged in each study center (rural & urban) for the first 24 weeks, and then it was limited to at least one session per month for each group. Each session usually lasted for 60-90 minutes. The topics were interdisciplinary and delivered by personnel trained in the respective field [21].

Educational session

The educational session discussed obesity, its link with other NCDs, complications, prevalence and severity, economic burden, and possible treatment (lifestyle modification, medication, and surgery). The behavioral change includes prudential shopping of food, reading the food labels, or choosing the right foods [22].

Dietary counseling

The principle of the individualized diet plans was a low-calorie, low-fat, and high-fiber diet that included a reduction of 500-1000 kcal/day. The total calorie distribution is likely to be 50-60% from carbohydrates, 15% from protein, 20%-30% from unsaturated fat, and 8-10% from saturated fat. Dietary salt was limited to 6 gm/day. The program advised the consumption of low glycemic index foods, an increase in fruit and vegetable (except potato) intake of up to 5 servings per day, the consumption of whole fruits instead of fruit juices and the replacement of carbonated beverages with milk. After attaining a desirable body weight, a maintenance diet was recommended. Participants were asked to record their daily intake, including portion size, in activity logbooks and were given leaflets with a list of foods along with their nutritional composition from a standard portion size (100gm) [23].

Physical activity session

The participants were encouraged to increase moderate-intensity activity to at least 150 minutes a week, initially, and to increase the activity time gradually. They were advised to find their own way to accomplish the required activities. Two approaches were recommended, one was self-programmed exercise (e.g., brisk walking, bicycling), and the second was lifestyle exercise (e.g., using stairs instead of lifts, avoiding vehicles for short distances). In general, it was advised to walk for 30-45 minutes with more intensity 3-5 days/week and to reduce sedentary hours (e.g., screen time) to <2 hours/day. Participants were asked to record their activities, daily, in diaries, along with the time and intensity [24, 25]. The program also allotted a few sessions for encouragement, problem-solving, or motivational activities, so the participants could better adapt and adhere to the modified lifestyle.

Outcome measures and timing of measurements

Primary outcomes

Data regarding anthropometric and clinical variables were measured at three levels (1) baseline (before intervention), (2) post-intervention (at 12 months), and (3) at follow-up (at 24 months). Anthropometric measurements, including body weight, height, BMI (kg/m2), WC (cm), WHR, WHtR were assessed at the respective study centers by using standard protocols and instruments [26, 27]. SBP (mmHg) and DBP (mmHg) were measured in a seated position, after at least 10 minutes of rest, by standard sphygmomanometer with adult cuffs. These measurements were taken twice at an interval of 3 minutes, and the mean was calculated and recorded [28]. Venous blood samples (5 ml) were drawn by expert lab technicians after 8-12 hours of overnight fasting for biochemical tests (e.g., FBG, fasting plasma insulin level, and lipid profile which includes TC, HDL-C and LDL-C, and TG). The blood collection, storage, and tests were done following standard protocols [29]. HOMA was used to evaluate insulin resistance (IR) by using the formula [HOMA-IR = fasting insulin (µIU/mL) X fasting glucose (mmol/L)/22.5] [30].

Secondary outcomes

The assessment of the self-reported PA level and dietary habits was done through a standardized questionnaire and multiple non-consecutive 24-hours recall methods, to evaluate the impact of the intervention program [31-33].

Statistical analysis

Data were analyzed using descriptive statistics like mean and standard deviation (SD); the difference between two and more groups was assessed by independent t-test and one-way ANOVA, respectively. The chi-square test was used for categorical data. The results were considered significant at p-value ≤0.05. All data were analyzed using SPSS version 2017 (IBM, USA).

RESULTS

After screening 300 obese people, 121 subjects were selected from similar socio-demographic backgrounds. Their socio-demographic profile is shown in Table 1.

Table 1.

Sociodemographic characteristics of participants (n=121).

Characteristics Rural n=61 (%) Urban n=60 (%) P-value
Gender
Male 30 (49.2) 30 (50) N.S.**
Female 31 (50.8) 30 (50)
Age (mean±SD) 34.3±10.5 34.5±7.8 N.S.*
Marital status
Not married 13 (19.7) 15 (25) N.S.**
Married 48 (80.3) 45 (75)
Occupation
Professional/skilled worker 8 (13.1) 16 (26.7) N.S.**
Self-employed 6 (9.8) 9 (15)
Semi professional 16 (26.3) 9 (15)
Housewives 21 (34.4) 17 (28.3)
Students/unemployed 10 (16.4) 9 (15)
Education
8–12 grades 23 (37.7) 16 (26.7) N.S.**
University or more 38 (62.3) 44 (73.3)
Monthly income (Rs)
>25000 48 (78.7) 54 (90) N.S.**
<25000 13 (21.3) 6 (10)
*

– independent t-test; ** – chi-square test; N.S. – non-significant differences.

No significant differences were found between rural and urban groups regarding the socio-demographic profile. The mean age was 34.3 years for the rural and 34.5 years for the urban group. Professionally, all were sedentary workers.

No significant differences between the groups (rural and urban) were found regarding dietary and PA profiles (Table 2).

Table 2.

Baseline dietary and physical activity profiles of participants (n=121).

Baseline profiles Rural male (n=30) Rural female (n=31) Rural total (n=61) Urban male (n=30) Urban female (n=30) Urban total (n=60) Statistical significance
Calorie (kcal) 2402.09±170.05 1921.1±125 2130±376.6 2462.4±179.2 2019.2±173 2211.1±384 N.S.
Sitting Time/Screen Time (minutes) 335.4±66.9 357.09±55.5 346.2±61.3 355.7±79.8 368.9±52.3 368.1±64.9 N.S.
MET Score/Week 542.13±82.4 522.8±89.2 532.5±87.3 535.06±87.3 489.7±123.2 512.4±108.3 N.S.

Independent t-test; N.S. – non-significant differences.

Result of Primary outcomes included:

  1. Changes in the anthropometric profile of subjects at baseline (prior-intervention), at 12 months (post-intervention), and 24 months (follow-up), represented in Table 3.

  2. Changes in cardio-metabolic risks (blood pressure, FBG, plasma insulin, HOMA-IR, lipid profile) from baseline to follow-up, presented in Table 4 A, B.

Table 3.

Changes in anthropometric parameters between rural and urban participants from baseline to follow-up (n=121).

Outcomes Male (n=60) Female (n=61)
Anthropometric Rural (30) mean±SD Urban (30) mean±SD P-value Rural (31) mean±SD Urban (30) mean±SD P-value
Bodyweight (kg)
Baseline
79.57±5.77 83.63±4.68 0.004 71.16±4.42 72.39±4.88 N.S.
Post-intervention 74.42±6.18 78.46±4.67 0.006 65.64±4.25 67±4.66 N.S.
Follow-up 75.6±6.6 79.9±5.12 0.007 66.6±4.5 67.98±4.84 N.S.
F value 2.92 4.95 7.006 5.612
P-value** 0.015 0.001 0.001 0.001
BMI (kg/m2)
Baseline
27.2±1.11 27.9±1.23 0.02 27.95±1.28 28.11±1.19 N.S.
Post-intervention 25.43±1.3 26.2±1.27 0.02 25.8±1.3 26.02±1.18 N.S.
Follow-up 25.84±1.47 26.68±1.52 0.03 26.15±1.48 26.4±1.37 N.S.
F-value 8.33 7.37 11.34 13.84
P-value** 0.001 0.001 0.001 0.001
WC (cm)
Baseline
99.33±3.12 101.07±2.66 0.024 93.81±2.42 94±2.88 N.S.
Post-intervention 97.3±3.01 99.3±2.9 0.01 90.7±3.08 91.7±2.64 N.S.
Follow-up 98.5±3.02 100.5±2.91 0.01 92.85±2.38 93.37±2.62 N.S.
F-value 3.31 3.04 11.5 5.5
P-value** 0.04 0.05 <0.0001 0.006
WHR
Baseline
0.988±0.026 0.998±0.017 N.S. 0.89±0.017 0.9±0.015 N.S.
Post-intervention 0.967±0.024 0.977±0.02 N.S. 0.87±0.015 0.88±0.013 0.002
Follow-up 0.98±0.024 0.992± 0.02 N.S. 0.88±0.017 0.89±0.012 N.S.
F-value 5.47 9.43 15.04 14.74
P-value** 0.005 0.0002 <0.0001 <0.0001
WHtR
Baseline
0.578±0.015 0.581±0.015 N.S. 0.583±0.01 0.582±0.015 N.S.
Post-intervention 0.564±0.01 0.568±0.014 N.S. 0.57±0.012 0.571±0.016 N.S.
Follow-up 0.574±0.016 0.578±0.018 N.S. 0.580±0.011 0.580±0.013 N.S.
F-value 6.59 4.87 9.05 4.57
P-value** 0.002 0.009 0.0003 0.012
**

– ANOVA and * – t-test. F-value: the degree of variation between the means of two or more groups. N.S. – non-significant (p>0.05).

Table 4.

Change in primary outcomes among rural and urban subjects from baseline to follow-up (n=121).

A. Bio-chemical changes
Outcomes Males (n=60) Females (n=61)
Biochemical Rural (30) mean±SD Urban (30) mean±SD P-level Rural (31) mean±SD Urban (30) mean±SD P-level
FBG (mg/dl)
Baseline
110.03±8.88 110±9.86 N.S. 106.84±8.77 107.03±8.77 N.S.
Post-intervention 98.93±7.6 97.9±6.82 N.S. 98.22±7.7 95.6±6.21 N.S.
Follow-up 98.8±6.81 97.36±8.06 N.S. 97.06±6.5 97.63±6.89 N.S.
F-value 20.38 21.98 14.8 20.53
P-value** 0.001 0.001 0.001 0.001
Plasma Insulin (microU/L)
Baseline
11.21±3.48 13.25±4.4 N.S. 9.93±1.34 13.14±3.71 0.001
Post-intervention 10.71±3.43 12.77±4.17 0.04 9.52±1.16 12.75±3.61 0.001
Follow-up 10.79±3.47 12.83±3.98 0.04 9.7±1.21 12.9±3.5 0.001
F-value 0.17 0.116 0.845 0.88
P-value** N.S. N.S. N.S. N.S.
HOMA-IR
Baseline
3.07±1.16 3.65±1.44 N.S. 2.64±0.48 3.49±1.19 0.001
Post-intervention 2.65±1.06 3.1±1.1 N.S. 2.3±0.37 3.02±0.97 0.001
Follow-up 2.66±1.09 3.11±1.14 N.S. 2.32±0.37 3.11±0.91 0.001
F-value 1.41 1.9 6.52 1.752
P-value** N.S. N.S. 0.002 N.S.
TC (mg/dl)
Baseline
228±36.34 249.82±34.71 0.02 227.32±32.25 238.5±38.21 N.S.
Post-intervention 210.1±35.31 232.12±29.11 0.01 211.29±32.22 220.7±38.54 N.S.
Follow-up 211.7±34.7 235.22±29.68 0.006 213.39±32.95 228.13±31.27 N.S.
F-value 2.34 2.73 2.32 1.83
P-value** N.S. N.S. N.S. N.S.
HDL-C (mg/dl)
Baseline
40.2±3.18 39.86±2.56 N.S. 40.51±1.89 41.16±2.29 N.S.
Post-intervention 40.3±3.04 40.3±2.15 N.S. 40.74±2.29 41.6±2.23 N.S.
Follow-up 40.3±3.24 40.06±2.18 N.S. 40.26±2.25 41.03±2.37 N.S.
F-value 0.014 0.26 0.39 0.49
P-value** N.S. N.S. N.S. N.S.
TG (mg/dl)
Baseline
150.93±26.62 169.07±23.3 0.007 142.04±25.96 158.77±25.09 0.01
Post-intervention 145.19±39.81 155.77±20.3 N.S. 131.9±24.1 144.43±22.32 0.04
Follow-up 140.1±23.85 157.9±22.7 0.004 134.8±19.03 150.63±19 0.04
F-value 0.92 3.1 1.8 3.12
P-value** N.S. 0.05 N.S. 0.04
LDL-C
Baseline
132.3±9.86 140.96±11.27 0.002 131.06±8.15 134.9±10.07 N.S.
Post-intervention 131.3±9.93 140.13±11.66 0.003 131.19±8.13 133.3±9.64 N.S.
Follow-up 132±9.81 141.23±11.32 0.001 132.42±7.77 135.4±9.71 N.S.
F-value 0.75 0.075 0.269 0.375
P-value** N.S. N.S. N.S. N.S.
B. Changes in blood pressure
Outcomes Males (n=60) Females (n=61)
Blood Pressure (B.P) Rural (30) mean±SD Urban (30) mean±SD p≤0.05 (between both groups) * Rural (31) mean±SD Urban (30) mean±SD p≤0.05 (between both groups) *
SBP (mmHg)
Baseline
132.23±4.81 133.5±4.55 N.S. 132.32±5.5 132.57±4.56 N.S.
Post-intervention 131.46±4.93 132.16±4.44 N.S. 131.71±6.5 131.46±4.59 N.S.
Follow-up 132.86±3.72 133.93±4.96 N.S. 134.39±6.4 133.8±4.81 N.S.
F-value 0.72 1.16 1.052 1.08
P-value** N.S. N.S. N.S. N.S.
DBP (mmHg)
Baseline
80.96±2.78 82.7±2.47 0.01 81.06±3.28 80.4±2.94 N.S.
Post-intervention 80.93±3.11 81.86±3.35 N.S. 81.09±3.6 80.4±2.47 N.S.
Follow-up 81.73±3.53 82.9±2,55 N.S. 82.9±4.06 81.5±3.27 N.S.
F-value 0.61 1.13 1.404 0.8
P-value** N.S. N.S. N.S. N.S.
**

– ANOVA and * – t-test. F-value: the degree of variation between the means of two or more groups. N.S. – non-significant (p>0.05).

Among rural subjects, 60.7% attained 7% weight loss from the initial values, whereas in the urban setting, the percentage of subjects was 61.7%. However, this difference was statistically insignificant (p=0.9**, chi-square test). All anthropometric parameters changed significantly across all groups from baseline.

Among all clinical parameters, FBG significantly decreased among all groups over time. HOMA-IR declined in the rural female group, and the TG level changed significantly among urban participants. No other significant changes were observed.

Secondary outcomes included a change in food behaviour and physical activity levels after intervention and adherence to this modified behaviour during the follow-up period, i.e., after 24 months (Table 5 A, B).

Table 5.

Change in secondary outcomes among rural and urban subjects from baseline to follow-up (n=121).

A. Dietary pattern
Outcomes Males (n=60) Females (n=61)
Dietary profile Rural (30) mean±SD Urban (30) mean±SD Rural (31) mean±SD Urban (30) mean±SD
Calorie (kcal)
Baseline
2402.09±170.05 2462.4±179.2 1921.1±125 2019.2±173
Post-intervention 2006.17±99.82 2010.7±118.85 1806.9±103.8 1824.3±113.21
Follow-up 2064.17±134.98 2083.7±130.37 1888.84±119.33 1900.33±98.78
F-value 72.06 83.64 7.64 16.5
P-value** <0.0005 <0.0005 0.0008 <0.0005
Cereals (whole & refined) g
Baseline
309.63±38.1 301.6±22.7 294.04±26.3 301.8±14.6
Post-intervention 270.4±37.31 260.2±59.12 237.13±52.2 243.03±42.7
Follow-up 277.5±29.8 269.9±57.16 239.6±52.05 246.5±49.8
F-value 10.52 5.79 15.24 21.6
P-value** <0.0005 0.004 <0.0005 <0.0005
Milk & products (ml)
Baseline
91.9±18.9 88.06±12.7 65.8±24.5 84.1±23.8
Post-intervention 111.4±30.4 98.6±19.3 110.9±46.41 107.9±30.27
Follow-up 105.73±23.96 102.7±21.74 103.32±36.95 98.33±29.27
F-value 4.87 5.11 13.13 4.38
P-value** 0.009 0.007 <0.0005 0.015
Vegetables (except potato) g
Baseline
92.3±19.4 91.4±21.7 82.6±17.1 73.8±19.9
Post-intervention 114.6±31.7 107.6±24.7 111.42±19.6 102.9±17.35
Follow-up 107.5±21.5 107.7±8 112.3±19.1 101.9±11.5
F-value 6.33 6.92 25.6 29.7
P-value** 0.002 0.0016 <0.0005 <0.0005
Fruits (g)
Baseline
40.6±10.5 45.5±9.6 40.61±10.6 47.3±27.6
Post-intervention 95.4±24.2 98.9±25.13 92.2±29.7 102.4±30.7
Follow-up 90.6±30.5 88.9±23 86.3±26.5 91.4±26.5
F-value 51.14 57.9 43.58 34.9
P-value** <0.0005 <0.0005 <0.0005 <0.0005
Visible fat/oils (g)
Baseline
39.4±8.5 43.4±9 40.6±10.6 41.8±8.1
Post-intervention 38.9±9.15 41.6±6.7 38.3±8.7 39.3±5.3
Follow-up 40.53±11.4 42.9±6.8 39.2±7.7 41.4±5.8
F-value 0.22 0.43 0.53 1.31
P-value** N.S. N.S. N.S. N.S.
Added sugar (g)
Baseline
31.8±5.9 34.8±9 34.83±8.8 34.5±6
Post-intervention 31.3±4.5 33.8±4.8 33.8±4.8 33.23±6.34
Follow-up 31.57±4.42 34.53±5.4 34.53±5.4 34.2±6.04
F-value 0.087 0.19 0.015 0.35
P-value** N.S. N.S. N.S. N.S.
B. PA pattern
Outcomes Males (60) Females (61)
PA profile Rural (30) mean±SD Urban (30) mean±SD Rural (31) mean±SD Urban (30) mean±SD
Sitting time/ day (minutes)
Baseline
335.4±67 357.09±55.5 355.7±79.8 368.9±52.3
Post-intervention 235.43±60.8 237.9±79.6 262.8±68.9 301.2±40
Follow-up 262.5±64.03 263.8±77.2 284.2±60 317.8±48
F-value 19.6 23.8 14.5 16.9
P-value** <0.0005 <0.0005 <0.0005 <0.0005
MET score/week
Baseline
542.13±82.4 522.9±89.17 535.06±87.29 489.7±123
Post-intervention 684.53±134.3 681.9±140.9 702.06±148.4 690.9±155
Follow-up 652.2±154 646.7±110.3 671.26±139.05 633.3±174
F-value 10.3 16.2 14.5 13.9
P-value** <0.0005 <0.0005 <0.0005 <0.0005
**

– ANOVA. F-value: the degree of variation between the means of two or more groups. N.S. – non-significant (p>0.05).

Except for the consumption of fats, oils, and added sugar, all other dietary and PA variables changed significantly among all groups.

DISCUSSION

This lifestyle intervention study for the management of obesity and reduction of cardio-metabolic complications of rural and urban obese subjects of both sexes is the first ever attempt in West Bengal, as per our knowledge. In this research, we aimed to explore the effect of lifestyle intervention programs through a change in dietary patterns and PA profiles of participants with similar socio-demographic backgrounds in the Hooghly district of West Bengal. Lifestyle modification brought significant changes among all anthropometric parameters and FBG (mg/dl) levels across all four groups (rural male, urban male, rural female, and urban female) from baseline to follow-up. A significant reduction has been noticed in serum TG (mg/dl) levels among urban obese participants (both male and female groups), and insulin sensitivity improved among rural women only. A between-group comparison (rural male vs. urban male; rural female vs. urban female), indicated significant differences regarding serum TG (mg/dl) and DBP (mmHg) at baseline between the two groups, which became insignificant after intervention. However, during follow-up, TG (mg/dl) differences between groups became significant, though DBP (mmHg) remained unchanged.

The secondary outcome, the adaptation and adherence to a modified lifestyle, showed a remarkably significant decrease with respect to calorie and cereal consumption; notably, consumption of milk beverages and products, fruits, and vegetables (except potato) showed excellent improvements. No significant change was found regarding oil or fat and added sugar intake among all four groups over time. Sitting time (minutes) declined significantly from baseline to post-intervention; though the mean value increased during the follow-up period. Mean values of MET-score among all groups indicated that subjects kept active even during the follow-up period, as per the recommendation of WHO to prevent NCDs.

This interventional study presented a significant effect in reducing the cardio-metabolic complications of obese participants of both sexes from rural and urban areas. Obesity is the most common outcome of a modern, fast-paced lifestyle which dysregulates inflammatory markers, resulting in several metabolic or cardiovascular disorders. Insulin resistance, diabetes, hypertension, dyslipidemia, metabolic syndrome, are among the long-term consequences of obesity. Studies proved that prevention or treatment of obesity could effectively lessen the cardio-metabolic risks [34, 35]. Dietary management or improvement of PA level alone could not produce a better result than their combined effect in preventing obesity. Therefore, lifestyle intervention through a combination of dietary modification and improved PA among target populations showed a positive impact on tackling various health issues related to obesity (e.g., diabetes, insulin resistance, cardio-metabolic or liver abnormalities, and osteoarthritis) [36].

Many interventional studies on obesity or related complications used lifestyle modification as a potential tool to shed extra weight, produce a better insulin response, revert pre-hyperglycaemic to normoglycemic, and proved to improve lipid or other cardio-metabolic profiles [37]. Several randomized controlled trials (RCT) or longitudinal studies were carried in South Asia to prevent obesity among children and adults over decades. The meta-analysis by Brown et al. 2015 outlined that the outcomes of such intervention studies varied [38]. One RCT program designed for 3 years, based on a calorie deficit diet and brisk walking for 30 minutes daily, produced a significant reduction in body weight, BMI, or WC in the intervention group, whereas other research did not showcase such prominent effects. This could be partly explained by the variation in study design [38-40]. Chapman et al. 2013 reviewed that diet and PA have significantly improved anthropometric parameters, but no effect was found regarding insulin sensitivity, though few studies noted the change in DBP or lipid profile after the intervention. In this study, male participants showed better weight loss than female participants. However, the subjects were from different religions, which affected the results due to the fact that the physical activity sessions included both genders. As a result, many women might have been unwilling to attend, influencing the result [41]. In our study, we targeted the same religious and cultural group, and counseling or activity sessions were scheduled separately for both sex groups, revealing that female obese participants presented better results than their male counterparts, as they attended more counseling sessions and showcased better adherence to modified lifestyles. This observation was similar to the rural-urban study done in Tamilnadu, India, in 2011, which noted that women were more cooperative than men, leading to better outcomes [42]. Sex difference became insignificant where attendance and completion of counseling sessions was the independent factor in the weight loss program [43].

In our study, we used a calorie, carbohydrate, and saturated fat-restricted diet with plenty of fibers, along with moderate PA, to reduce body fat and to improve other cardio-metabolic profiles. 60.7% of rural and 61.7% of urban obese participants achieved 7% of the initial body weight loss goal at 12 months. The mean change in body weight ranged from -5.1 kg to -5.6 kg; BMI -1.7 to -2.08 kg/m2; WC -1.8 to -3.1 cm across all four groups after intervention. This finding goes in line with observations noted in other research on various populations [36, 42, 44-46]. Research in Kerala showed that at 24 months subjects who received intervention did not produce better results, with little loss in body weight, WC, non-significant change in fruit intake, and sedentary behavior. This may be due to a difference in study criteria and subject selection, which was based on IDRS (Indian Diabetes Risk Score) but not obesity, so subjects with lower body weight or WC with high IDRS were included [13].

The cardio-vascular and biochemical results were comparable with other studies like Backes et al. 2008, where carbohydrate and calorie-restricted diet reduced body weight, FBG, TG, and DBP but showcased no significant difference in TC, HDL-C, and LDL-C [47]. IDPP-1 (Indian diabetic prevention Program) showed insignificant change in the lifestyle modified intervention group regarding body weight or WC, but improved insulin sensitivity, which may be due to the lower BMI of subjects at baseline, and adapting dietary modification and increased PA might have reduced metabolic risk among those subjects [48]. Nanditah et al. (2014) showed men on lifestyle modification for 24 months improved insulin response and the observed obesity was associated with dysglycemia, which again related to cardio-metabolic risks [49]. A 12-month lifestyle intervention program in Germany in 2018 also showed a beneficial result for obese subjects, as losing weight led to a better cardio-metabolic profile [9]. Weight loss through lifestyle modification has also been proven to improve liver function [50]. Yadav et al. (2018) showed that yoga-based lifestyle modification has a better result than dietary intervention alone on inflammatory markers of metabolic syndrome [51]. In our study, participants lost a significant portion of body weight or abdominal fat but failed to influence biochemical parameters except for blood glucose and TG level, which indicate the underlying metabolic complications, genetic influence, body composition, or requirement of more fat to lose [52].

Secondary outcomes showed subjects adopted healthier food habits, but it was not as per recommendations by ICMR-NIN (Indian Council of Medical Research–National Institute of Nutrition). The consumption of calories and cereals have declined, and fruit, vegetables (except potato), and milk intake have raised significantly, yet no significant difference was found regarding consumption of visible fat or added sugar among all groups. PA level has raised, and all groups became active (MET-score >600 MET) even during the follow-up. Sedentary time has fallen among all groups significantly as well. Though the mean values of MET score and sedentary time have declined from post-intervention values, they did not cross the baseline in any group. Other interventional studies have also identified improved dietary habits and PA profiles adopted by a good proportion of the target group and succeeded in attaining their study goal. K-DPP also showed improvement in dietary habits and PA behavior among 99% and 96% of participants, respectively [53]. Mathews et al. (2021) in their study on the effectiveness of PA among sedentary women in Thiruvanthapuram, India, noted that women preferred moderate-intensity activity like walking or household work, and MET minute increased significantly from baseline with a simultaneous reduction in WC, similarly to our results [54].

The Diabetes Community Lifestyle Improvement Program (D-CLIP) trial in Chennai, India, also showed improvement in Moderate to Vigorous Physical Activity (MPVA) among intervention groups in diabetes prevention programs in India [55]. Another study noted lifestyle management is more effective than drug treatment to prevent diabetes, and 450±26 kcal energy intake was reduced by the intervention group; fat intake was decreased, and 74% adhered with the recommendation of >150 minutes MVPA and resulting in average weight loss of 5.6 kg (mean value) and succeeded to improve diabetes. Vadheim et al. 2010 in a lifestyle intervention program to lower cardio-metabolic risks in the rural community, reported that 52% of participants who received the intervention achieved a 7% weight loss goal after 16 weekly sessions, and 65% of them met the PA goal [56]. Other interventional research also showed an increase in MET score, fruit and vegetable consumption, and successive weight loss. The mean values of primary or secondary outcomes started to increase during follow-up, as supported by other studies [24, 34, 57].

Limitations

This study has certain limitations, like a high attrition rate (28 out of 149 subjects, i.e., 18.8%), gradually lower attendance in counseling sessions, and declined responses after the first 6 months, which may indicate that the program was not attractive or motivating. Self-reported dietary and activity log books for dietary and PA assessment could be biased, and the findings cannot be generalized due to a small sample size.

CONCLUSION

The lifestyle intervention program is of utmost importance in the present society to prevent obesity and its deleterious consequences among all age groups worldwide. Such intervention programs can enhance mass awareness regarding healthy living as the cheapest way to prevent NCDs. Lifestyle intervention programs can be applied in educational settings or workplaces. Government initiatives and other stakeholders should come forward to support resources like trained health personnel, funds, or accommodation of community buildings to conduct such programs more, which not only lessen the economic burden for diseases of the countries but also get healthy active posterity.

ACKNOWLEDGMENTS

Conflict of interest

The authors declare no conflict of interest.

Ethical approval

The study was approved by the Human Ethical Committee of Serampore College, Serampore, West Bengal, India, under the University of Calcutta in Hooghly District (Approval Number SC/HEC/2021/1).

Consent to participate

Written informed consent was obtained from the participants before the commencement of the study.

Special thanks

The authors convey their heartfelt thanks to Mr. HemantaRouth, senior dietitian of the Department of Nutrition and Dietetics in IQ City Medical College, Burdwan, West Bengal, for his relentless support and cooperation in this program.

Authorship

AKS and AKB contributed for conceptualization and methodology; CB and JS contributed to data collection and writing the original draft; AKS, ADK and KB contributed to editing the manuscript; ADK and CB contributed to data curation and data analysis.

References

  • 1.Malik VS, Willet WC, Hu FB. Nearly a decade on-trends, risk factors and policy implications in global obesity. Nature Reviews Endocrinology. 2020;16:615–6. doi: 10.1038/s41574-020-00411-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 2.Bhattacharya K, Sengupta P, Dutta S, Bhattacharya S. Pathophysiology of Obesity: Endocrine, Inflammatory and Neural regulators. Research Journal of Pharmacy and Technology. 2020;13:4469–4478. doi: 10.5958/0974-360X.2020.00789.1. [DOI] [Google Scholar]
  • 3.Blüher M. Obesity: global epidemiology and pathogenesis. Nature Reviews Endocrinology. 2019;15:288–98. doi: 10.1038/s41574-019-0176-8. [DOI] [PubMed] [Google Scholar]
  • 4.Hruby A, Hu FB. The epidemiology of obesity: a big picture. Pharmacoeconomics. 2015;33:673–89. doi: 10.1007/s40273-014-0243-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5.Schwartz MW, Seeley RJ, Zeltser LM, Drewnowski A, et al. Obesity pathogenesis: an endocrine society scientific statement. Endocrine reviews. 2017;38:267–96. doi: 10.1210/er.2017-00111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 6.World Health Organization, Noncommunicable Disease; 13 April 2021. https://www.who.int/news-room/fact-sheets/detail/noncommunicable-diseases .
  • 7.Wadden TA, Brownell KD, Foster GD. Obesity: responding to the global epidemic. Journal of consulting and clinical psychology. 2002;70:510. doi: 10.1037//0022-006x.70.3.510. [DOI] [PubMed] [Google Scholar]
  • 8.Bondyra-Wiśniewska B, Myszkowska-Ryciak J, Harton A. Impact of lifestyle intervention programs for children and adolescents with overweight or obesity on body weight and selected cardiometabolic factors—A systematic review. International Journal of Environmental Research and Public Health. 2021;18:2061. doi: 10.3390/ijerph18042061. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9.König D, Hörmann J, Predel HG, Berg A. A 12-month lifestyle intervention program improves body composition and reduces the prevalence of prediabetes in obese patients. Obesity facts. 2018;11:393–9. doi: 10.1159/000492604. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Diabetes Prevention Program (DPP) Research Group The Diabetes Prevention Program (DPP): description of lifestyle intervention. Diabetes care. 2002;25:2165–71. doi: 10.2337/diacare.25.12.2165. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 11.Thankappan KR, Sathish T, Tapp RJ, Shaw JE, et al. A peer-support lifestyle intervention for preventing type 2 diabetes in India: A cluster-randomized controlled trial of the Kerala Diabetes Prevention Program. PLoS medicine. 2018;15:e1002575. doi: 10.1371/journal.pmed.1002575. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12.Nayak BS, Bhat VH. School based multicomponent intervention for obese children in Udupi district, South India–A randomized controlled trial. Journal of clinical and diagnostic research: JCDR. 2016;10:SC24. doi: 10.7860/JCDR/2016/23766.9116. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Mohan S, Jarhyan P, Ghosh S, Venkateshmurthy NS, Gupta R, Rana R, et al. UDAY: A comprehensive diabetes and hypertension prevention and management program in India. BMJ open. 2018;8:e015919. doi: 10.1136/bmjopen-2017-015919. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14.Sarkar D, Mondal N, Sen J. Obesity and blood pressure variations among the Bengali Kayastha population of North Bengal, India. Journal of Life Sciences. 2009;1(1):35–43. doi: 10.1080/09751270.2009.11885132. [DOI] [Google Scholar]
  • 15.Chakraborty SN, Roy SK, Rahaman MA. Epidemiological predictors of metabolic syndrome in urban West Bengal, India. J Family Med Prim Care. 2015;4(4):535–8. doi: 10.4103/2249-4863.174279. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Bose C, Syamal Ak, Bhattacharya K. Pattern of Dietary Intake and Physical activity among obese adults in rural vs urban areas in WestBengal: A cross-sectional study. Res J Pharm Technol. 2022;15(9):3924–3930. doi: 10.52711/0974-360X.2022.00657. [DOI] [Google Scholar]
  • 17.Wilfley DE, Hayes JF, Balantekin KN, Van Buren DJ, Epstein LH. Behavioral interventions for obesity in children and adults: Evidence base, novel approaches, and translation into practice. American Psychologist. 2018;73:981. doi: 10.1037/amp0000293. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18.Kandula NR, Patel Y, Dave S, Seguil P, et al. The South Asian Heart Lifestyle Intervention (SAHELI) study to improve cardiovascular risk factors in a community setting: Design and methods. Contemporary clinical trials. 2013;36:479–87. doi: 10.1016/j.cct.2013.09.007. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Azizi F, Ghanbarian A, Momenan AA, Hadaegh F, et al. Prevention of non-communicable disease in a population in nutrition transition: Tehran Lipid and Glucose Study phase II. Trials. 2009;10:1–5. doi: 10.1186/1745-6215-10-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Sathish T, Williams ED, Pasricha N, Absetz P, et al. Cluster randomised controlled trial of a peer-led lifestyle intervention program: study protocol for the Kerala diabetes prevention program. BMC public health. 2013;13:1035. doi: 10.1186/1471-2458-13-1035. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Spahn JM, Reeves RS, Keim KS, Laquatra I, et al. State of the evidence regarding behavior change theories and strategies in nutrition counseling to facilitate health and food behavior change. Journal of the American Dietetic Association. 2010;110:879–91. doi: 10.1016/j.jada.2010.03.021. [DOI] [PubMed] [Google Scholar]
  • 22.Behl S, Misra A. Management of obesity in adult Asian Indians. Indian heart journal. 2017;69:539–44. doi: 10.1016/j.ihj.2017.04.015. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23.Forouhi NG, Misra A, Mohan V, Taylor R, Yancy W. Dietary and nutritional approaches for prevention and management of type 2 diabetes. Bmj. 2018;361 doi: 10.1136/bmj.k2234. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 24.Lang A, Froelicher ES. Management of overweight and obesity in adults: behavioral intervention for long-term weight loss and maintenance. European Journal of Cardiovascular Nursing. 2006;5:102–14. doi: 10.1016/j.ejcnurse.2005.11.002. [DOI] [PubMed] [Google Scholar]
  • 25.Yuenyongchaiwat K. Effects of 10,000 steps a day on physical and mental health in overweight participants in a community setting: a preliminary study. Brazilian journal of physical therapy. 2016;20:367–73. doi: 10.1590/bjpt-rbf.2014.0160. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26.Sengupta P, Chaudhuri P, Bhattacharya K. Screening obesity by direct and derived anthropometric indices with evaluation of physical efficiency among female college students of Kolkata. Annals of medical and health sciences research. 2013;3(4):517–22. doi: 10.4103/2141-9248.122066. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 27.Bhattacharya K, Sengupta P, Dutta S, Chaudhuri P, et al. Waist-to-height ratio and BMI as predictive markers for insulin resistance in women with PCOS in Kolkata, India. Endocrine. 2021;72:86–95. doi: 10.1007/s12020-020-02555-3. [DOI] [PubMed] [Google Scholar]
  • 28.Bhattacharya K, Bhaduri D. Assessment of physical and physiological parameters among the male and female bakery workers from Palpa district of democratic Nepal. International Journal of Research in Pharmaceutical Sciences. 2018;9:226–235. doi: 10.26452/ijrps.v9i1.1251. [DOI] [Google Scholar]
  • 29.Shokeen D, Aeri BT. Prevalence of cardio-metabolic risk factors: a cross-sectional study among employed adults in urban Delhi, India. Journal of clinical and diagnostic research: JCDR. 2017;11:LC01. doi: 10.7860/JCDR/2017/29087.10336. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 30.Matthews DR, Hosker JP, Rudenski AS, Naylor BA, et al. Homeostasis model assessment: insulin resistance and β-cell function from fasting plasma glucose and insulin concentrations in man. Diabetologia. 1985;28:412–9. doi: 10.1007/BF00280883. [DOI] [PubMed] [Google Scholar]
  • 31.Chandrashekarappa SM, Puttannaiah SM, Mohandas A. Comparison of 24 h recall and 3-day dietary cycle with 7-day dietary cycle as a tool for dietary assessment at community level in a rural South Indian community: A cross-sectional study. International Journal of Medical Science and Public Health. 2020;9:174–178. doi: 10.5455/ijmsph.2020.1131522122019. [DOI] [Google Scholar]
  • 32.Cleland CL, Hunter RF, Kee F, Cupples ME, et al. Validity of the global physical activity questionnaire (GPAQ) in assessing levels and change in moderate-vigorous physical activity and sedentary behaviour. BMC public health. 2014;14:1255. doi: 10.1186/1471-2458-14-1255. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Prince SA, Cardilli L, Reed JL, Saunders TJ, et al. A comparison of self-reported and device measured sedentary behaviour in adults: a systematic review and meta-analysis. International Journal of Behavioral Nutrition and Physical Activity. 2020;17:1–7. doi: 10.1186/s12966-020-00938-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34.Wijesuriya M, Fountoulakis N, Guess N, Banneheka S, et al. A pragmatic lifestyle modification programme reduces the incidence of predictors of cardio-metabolic disease and dysglycaemia in a young healthy urban South Asian population: a randomised controlled trial. BMC medicine. 2017;15:146. doi: 10.1186/s12916-017-0905-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 35.Rolleston A, Doughty RN, Poppe K. The effect of a 12-week exercise and lifestyle management programme on cardiac risk reduction: A pilot using a kaupapa Māori philosophy. International Journal of Indigenous Health. 2017;12:116–30. doi: 10.18357/ijih121201716905. [DOI] [Google Scholar]
  • 36.Patel RM, Misra R, Raj S, Balasubramanyam A. Effectiveness of a group-based culturally tailored lifestyle intervention program on changes in risk factors for type 2 diabetes among Asian Indians in the United States. Journal of diabetes research. 2016;2017 doi: 10.1155/2017/2751980. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 37.Mathews G, Alexander J, Rahemtulla T, Bhopal R. Impact of a cardiovascular risk control project for South Asians (KhushDil) on motivation, behaviour, obesity, blood pressure and lipids. Journal of Public Health. 2007;29:388–97. doi: 10.1093/pubmed/fdm044. [DOI] [PubMed] [Google Scholar]
  • 38.Brown T, Smith S, Bhopal R, Kasim A, Summerbell C. Diet and physical activity interventions to prevent or treat obesity in South Asian children and adults: a systematic review and meta-analysis. International journal of environmental research and public health. 2015;12:566–94. doi: 10.3390/ijerph120100566. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39.Ramachandran A, Snehalatha C, Ram J, Selvam S, et al. Effectiveness of mobile phone messaging in prevention of type 2 diabetes by lifestyle modification in men in India: a prospective, parallel-group, randomised controlled trial. The lancet Diabetes & endocrinology. 2013;1(3):191–8. doi: 10.1016/S2213-8587(13)70067-6. [DOI] [PubMed] [Google Scholar]
  • 40.Telle-Hjellset V, Kjøllesdal MK, Bjørge B, Holmboe-Ottesen G, et al. The InnvaDiab-DE-PLAN study: a randomised controlled trial with a culturally adapted education programme improved the risk profile for type 2 diabetes in Pakistani immigrant women. British Journal of Nutrition. 2013;109(3):529–38. doi: 10.1017/S000711451200133X. [DOI] [PubMed] [Google Scholar]
  • 41.Chapman J, Qureshi N, Kai J. Effectiveness of physical activity and dietary interventions in South Asian populations: a systematic review. British Journal of General Practice. 2013;63:e104–14. doi: 10.3399/bjgp13X663064. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 42.Shailaja K, Moideen M, Kumar A, Ramasamy C. Effectiveness of patient counseling on weight reduction in rural and urban overweight and obese patients. International Journal of Pharma and Bio Sciences. 2011;2:173–185. [Google Scholar]
  • 43.Diabetes Prevention Program Research Group Reduction in the incidence of type 2 diabetes with lifestyle intervention or metformin. New England journal of medicine. 2002;346:393–403. doi: 10.1056/NEJMoa012512. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Weber MB, Ranjani H, Staimez LR, Anjana RM, et al. The stepwise approach to diabetes prevention: results from the D-CLIP randomized controlled trial. Diabetes care. 2016;39:1760–7. doi: 10.2337/dc16-1241. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Taurio J, Järvinen J, Hautaniemi EJ, Eräranta A, et al. Team-based “Get-a-Grip” lifestyle management programme in the treatment of obesity. Preventive medicine reports. 2020;19:101119. doi: 10.1016/j.pmedr.2020.101119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 46.Wong VW, Chan RS, Wong GL, Cheung BH, et al. Community-based lifestyle modification programme for non-alcoholic fatty liver disease: a randomized controlled trial. Journal of hepatology. 2013;59:536–42. doi: 10.1016/j.jhep.2013.04.013. [DOI] [PubMed] [Google Scholar]
  • 47.Backes AC, Abbasi F, Lamendola C, McLaughlin TL, et al. Clinical experience with a relatively low carbohydrate, calorie-restricted diet improves insulin sensitivity and associated metabolic abnormalities in overweight, insulin resistant South Asian Indian women. Asia Pacific journal of clinical nutrition. 2008;17:669–71. [PubMed] [Google Scholar]
  • 48.Ramachandran A, Snehalatha C, Mary S, Mukesh B, et al. The Indian Diabetes Prevention Programme shows that lifestyle modification and metformin prevent type 2 diabetes in Asian Indian subjects with impaired glucose tolerance (IDPP-1) Diabetologia. 2006;49:289–97. doi: 10.1007/s00125-005-0097-z. [DOI] [PubMed] [Google Scholar]
  • 49.Nanditha A, Ram J, Snehalatha C, Selvam S, et al. Early improvement predicts reduced risk of incident diabetes and improved cardiovascular risk in prediabetic Asian Indian men participating in a 2-year lifestyle intervention program. Diabetes care. 2014;37:3009–15. doi: 10.2337/dc14-0407. [DOI] [PubMed] [Google Scholar]
  • 50.Berzigotti A, Albillos A, Villanueva C, Genescá J, et al. Effects of an intensive lifestyle intervention program on portal hypertension in patients with cirrhosis and obesity: the SportDiet study. Hepatology. 2017;65:1293–305. doi: 10.1002/hep.28992. [DOI] [PubMed] [Google Scholar]
  • 51.Yadav R, Yadav RK, Khadgawat R, Pandey RM. Comparative efficacy of a 12 week yoga-based lifestyle intervention and dietary intervention on adipokines, inflammation, and oxidative stress in adults with metabolic syndrome: a randomized controlled trial. Translational behavioral medicine. 2019;9:594–604. doi: 10.1093/tbm/iby060. [DOI] [PubMed] [Google Scholar]
  • 52.Vlaar EM, Nierkens V, Nicolaou M, Middelkoop BJ, et al. Effectiveness of a targeted lifestyle intervention in primary care on diet and physical activity among South Asians at risk for diabetes: 2-year results of a randomised controlled trial in the Netherlands. BMJ open. 2017;7:e012221. doi: 10.1136/bmjopen-2016-012221. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 53.Aziz Z, Mathews E, Absetz P, Sathish T, et al. A group-based lifestyle intervention for diabetes prevention in low-and middle-income country: implementation evaluation of the Kerala Diabetes Prevention Program. Implementation Science. 2018;13:1–4. doi: 10.1186/s13012-018-0791-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 54.Mathews E, Sauzet O, Thankappan KR. Effectiveness of a physical activity intervention program using peer support among sedentary women in Thiruvananthapuram City, India: results of a non-randomized quasi experimental study. Wellcomeopen research. 2021;6:87. doi: 10.12688/wellcomeopenres.16618.1. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 55.Ford CN, Do WL, Weber MB, Narayan KV, et al. Moderate-to-vigorous physical activity changes in a diabetes prevention intervention randomized trial among South Asians with prediabetes–The D-CLIP trial. Diabetes Research and Clinical Practice. 2021;174:108727. doi: 10.1016/j.diabres.2021.108727. [DOI] [PubMed] [Google Scholar]
  • 56.Vadheim LM, Brewer KA, Kassner DR, Vanderwood KK, et al. Effectiveness of a lifestyle intervention program among persons at high risk for cardiovascular disease and diabetes in a rural community. The Journal of Rural Health 2010 ; 26:266–72. doi: 10.1111/j.1748-0361.2010.00288.x. [DOI] [PubMed] [Google Scholar]
  • 57.Skender ML, Goodrick GK, Del Junco DJ, Reeves RS, et al. Comparison of 2-year weight loss trends in behavioral treatments of obesity: diet, exercise, and combination interventions. Journal of the American dietetic association. 1996;96:342–6. doi: 10.1016/S0002-8223(96)00096-X. [DOI] [PubMed] [Google Scholar]

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