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CompletedNCT05648045Updated Apr 29, 2026

Weight Status, Resilience, and Quality of Life in Indian Children

An observational study in Childhood Obesity, Overweight (BMI > 25) and Underweight, sponsored by Maastricht University Medical Center. Completed at 16 sites in India. Open to participants aged 14 Years to 16 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-04-29.

Sponsored by Maastricht University Medical Center · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
720
Ages
14 Years to 16 Years
Sex
All
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Study summary

A school-based cross-sectional study that aims to generate context-specific evidence on how weight status is related to resilience, health behaviour, and quality of life among Indian adolescents.

Primary Objective

To assess differences in overall resilience (total score of Adolescent Resilience score from ARQ49) between normal-weight and overweight/obese Indian adolescents aged 14-16 years.

Secondary Objectives

  1. To compare differences in Adolescent Resilience Questionnaire (ARQ49) subscale scores between normal-weight and overweight/obese adolescents. The internal resilience factors assessed by the ARQ49 include confidence, emotional insight, negative cognition, social skills, empathy, and tolerance, while the external resilience factors include family connectedness, family availability, peer connectedness, peer availability, supportive school environment, school connectedness, and community connectedness.
  2. To assess differences in internal resilience factors (diet self-efficacy, physical activity self-efficacy, self-esteem, and optimism) between normal-weight and overweight/obese adolescents and to examine parental nutrition knowledge as an external resilience resource and moderator in association analyses.
  3. To compare dietary behaviors, physical activity patterns, and Pediatric Quality of Life Inventory (PedsQL) scores between normal-weight and overweight/obese adolescents.
  4. To examine the associations among resilience, dietary and physical activity behaviors, and PedsQL within the overall sample and within different weight groups, and to evaluate parental nutrition knowledge as a moderator of the relationship between weight status and resilience or health outcomes.

    Exploratory Objective

  5. To explore differences in resilience, health behaviors, and PedsQL between normal-weight and underweight Indian adolescents.

Study hypotheses

The investigators hypothesized that adolescents with overweight/obesity, compared with their normal-weight peers, would demonstrate lower scores on total resilience (primary outcome), as well as on internal and external resilience indices; report lower diet self-efficacy, physical activity self-efficacy, self-esteem, and optimism; report less frequent health-promoting behaviors (including lower fruit and vegetable intake and fewer days achieving ≥ 60 min/day of moderate-to-vigorous physical activity); and report lower PedsQL scores.

Parental nutrition knowledge will not be treated as a between-group outcome; instead, it will be tested as a moderator in association analyses, examining whether parental nutrition knowledge influences the relationship between weight status and resilience or health outcomes.

Furthermore, the investigators hypothesized that higher resilience scores would be positively associated with healthier dietary behaviors, greater physical activity participation, and higher PedsQL scores across the overall sample, with these associations expected to hold true within both normal-weight and overweight/obese groups. In addition, analyses involving underweight adolescents will be exploratory and descriptive in nature. We will explore whether underweight adolescents show different levels of resilience, health behaviors, and HRQoL compared with adolescents with normal weight.

Read the detailed description

Childhood and adolescent obesity is associated with adverse physical, psychological, and social outcomes, including reduced health-related quality of life (HRQoL). In India, the coexistence of underweight and overweight highlights the need to examine behavioural and psychosocial factors alongside anthropometric measures.

Resilience, defined as the capacity to adapt to stress and challenges, is a multidimensional construct encompassing individual, family, peer, school, and community domains. Internal resilience-related traits such as diet and physical activity self-efficacy, self-esteem, and optimism may influence adolescents' health behaviours and well-being. However, evidence examining these factors together, particularly in relation to weight status among Indian adolescents, remains limited.

This study is a school-based cross-sectional investigation conducted among adolescents aged 14-16 years in Kolkata, India. The primary objective is to assess differences in overall resilience (ARQ49 total score) between normal-weight and overweight/obese adolescents. Secondary objectives include comparing internal resilience-related traits, dietary behaviours, physical activity patterns, and HRQoL (PedsQL), and examining associations among these variables within the overall sample. An exploratory objective assesses similar outcomes among underweight adolescents.

Participants are recruited from public and private secondary schools using non-probability and snowball sampling through existing professional networks. One parent or guardian per adolescent participates to provide data on parental nutrition knowledge and related contextual factors.

Data collection includes validated self-administered questionnaires and anthropometric measurements (height and weight) to calculate BMI-for-age z-scores using international standards. Statistical analyses include group comparisons across weight categories and multivariable models examining associations among resilience, health behaviours, parental factors, and HRQoL, accounting for clustering at the school level.

This study aims to generate context-specific evidence on how psychosocial resilience and behavioural factors relate to weight status and well-being among Indian adolescents.

02

Conditions studied

  • Childhood Obesity
  • Overweight (BMI > 25)
  • Underweight

Keywords

  • psychosocial resilience
  • self-efficacy
  • self-esteem
  • optimism
  • physical activity
  • dietary behavior
  • health related quality of life
03

In context

Pediatric Obesity

1,129 studies on the registry are indexed under Pediatric Obesity; 187 are open to participants now.

This study's enrollment of 720 is above the median of 180 across 235 observational studies indexed under Pediatric Obesity.

Browse Pediatric Obesity studies →

Lead sponsor

Maastricht University Medical Center is the lead sponsor of 853 studies on the registry; 114 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
14 Years to 16 Years
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

School-going Indian adolescents aged 14 to 16 years, studying in grades 8 to 10 in secondary schools in Kolkata, India. Participants were recruited from public and private schools. One parent or guardian of each participating adolescent was also invited to participate. Weight status categories (underweight, normal weight, and overweight/obese) were defined analytically using BMI-for-age z-scores based on IOTF cut-offs.

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Eligibility Criteria

Inclusion criteria

Inclusion Criteria:

  • Adolescents aged 14 to 16 years
  • Studying in grades 8, 9, or 10
  • Enrolled in participating secondary schools in Kolkata, India
  • Able to provide assent, with written consent from a parent or legal guardian
  • One parent or guardian willing to participate in the parent survey

Exclusion criteria

Exclusion Criteria:

  • Age below 14 years or above 16 years
  • Not enrolled in grades 8, 9, or 10
  • No parental/legal guardian consent or no adolescent assent
  • Incomplete eligibility for participation in the survey procedures
05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
720 participants (actual)
Target follow-up
1 Year
Patient registry
Yes

Groups and cohorts

  • Groups classified based on BMI

    Adolescent participants (14-16 years): Participants will be categorized into weight status groups (underweight, normal-weight, overweight/obese) based on BMI-for-age z-scores for analysis. Group 1: Overweight BMI Cut-Off Points (kg/m²) by International Obesity Task Force; IOTF Overweight (including obesity) ≥25.00 Group 2: Obese BMI Cut-Off Points (kg/m²) by International Obesity Task Force; IOTF Obese ≥30.00 Group 3: Normal-weight BMI Cut-Off Points (kg/m²) by International Obesity Task Force; IOTF Normal Weight - 18.5-24.99

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What researchers measure

Primary outcomes

  1. Overall resilience (ARQ49 total score)

    Overall resilience will be assessed using the Adolescent Resilience Questionnaire (ARQ49). The total score will be calculated by summing responses across all items, with higher scores indicating higher levels of psychosocial resilience.

    Time frame: At baseline (single time-point assessment)

Secondary outcomes

  1. Health-related quality of life (HRQoL)

    HRQoL will be assessed using the Pediatric Quality of Life Inventory (PedsQL). Scores will be transformed to a 0-100 scale, with higher scores indicating better quality of life.

    Time frame: At baseline (single time-point assessment)

  2. Diet and Physical activity self-efficacy

    Self-efficacy will be assessed using a validated Diet and Physical Activity Self-Efficacy Scale. The scale includes multiple domains related to confidence in engaging in physical activity and making healthy dietary choices. Subscale scores will be calculated for each domain, with higher scores indicating greater self-efficacy.

    Time frame: At baseline (single time-point assessment)

  3. Optimism

    Optimism will be assessed using the Youth Life Orientation Test (Y-LOT). A total score will be calculated, with higher scores indicating a more optimistic outlook.

    Time frame: At baseline (single time-point assessment)

  4. Dietary and PA behaviour

    Dietary and physical activity behaviour will be assessed using selected items from the Global School-based Student Health Survey (GSHS), including frequency of consumption of key food groups and hours/days of physical activity (weekly/monthy). Responses will be analysed as categorical or frequency-based variables.

    Time frame: At baseline (single time-point assessment)

  5. Self-esteem

    Self-esteem will be measured using the Rosenberg Self-Esteem Scale (RSES). Total scores will be calculated, with higher scores indicating higher self-esteem.

    Time frame: At baseline (single time-point assessment)

07

Study locations

16 sites
  • Mitra Institution (Main)
    Kolkata, West Bengal 700009, India
  • Victoria Institution High School
    Kolkata, West Bengal 700009, India
  • Ballygunge Government High School
    Kolkata, West Bengal 700020, India
  • Andhra Association High School (AAHS)
    Kolkata, West Bengal 700026, India
  • Lycee School
    Kolkata, West Bengal 700029, India
  • National High School For Boys
    Kolkata, West Bengal 700029, India
  • National High School For Girls
    Kolkata, West Bengal 700029, India
  • Tollygunge Adarsh Hindi High School (Girls and Boys)
    Kolkata, West Bengal 700033, India
  • New Alipore Multipurpose School
    Kolkata, West Bengal 700053, India
  • New Vista Academy
    Kolkata, West Bengal 700063, India
  • Sakhawat Memorial Govt. Girls' High School
    Kolkata, West Bengal 700071, India
  • Calcutta Public School, Bidhan Park
    Kolkata, West Bengal 700090, India
  • Indus Valley World School
    Kolkata, West Bengal 700094, India
  • Calcutta Public School, Kalikapur
    Kolkata, West Bengal 700099, India
  • Holy Mission school
    Kolkata, West Bengal, India
  • St. Joseph and Mary's school
    Kolkata, West Bengal, India
08

References and documents

Individual participant data

Plan to share: No — Individual participant data will not be shared publicly because the study involves adolescent participants and linked parent data, and open sharing would raise ethical and privacy concerns. De-identified data may be considered upon reasonable request, subject to review by the research team, applicable ethical approvals, and a data-sharing agreement, in accordance with Maastricht University data governance requirements.

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Feb 2023 to primary completion in Feb 2024, 12 months.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 22, 2022
First posted
Dec 13, 2022
StartActual
Feb 20, 2023
Primary completionActual
Feb 28, 2024
CompletionActual
Apr 30, 2024
Last update
Apr 29, 2026
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Apr 29, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05648045
Collaborators
Maastricht University
Responsible party
Sponsor
First posted
Dec 13, 2022
Start date
Feb 20, 2023
Primary completion
Feb 28, 2024
Completion
Apr 30, 2024
Last update
Apr 29, 2026

Study contacts

Poulami Dasgupta
principal investigator · Maastricht University/MaastrichtUMC

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Apr 2026. You cannot join it, but the record below documents what was studied.

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