School- and Family-Based Lifestyle Programme for Primary School Children in Punjab, Pakistan: A Feasibility Study
NCT07932028, Not applicable, Completed, Central South University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | School- and Family-Based Lifestyle Programme for Primary School Children in Punjab, Pakistan: A Feasibility Study | ClinicalTrials.gov |
| NCT number | NCT07932028 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 1,200 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Central South University | ClinicalTrials.gov |
| Conditions | Pediatric Obesity, Overweight , Obesity | ClinicalTrials.gov |
| Interventions | School- and family-based lifestyle programme | ClinicalTrials.gov |
| First posted | 2026-11-12 | ClinicalTrials.gov |
| Last updated | 2026-11-12 | ClinicalTrials.gov |
Registered outcomes 16
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | School recruitment rate | Baseline (before the programme started) | Proportion of eligible primary schools that agreed to participate. | ClinicalTrials.gov |
| Primary | Child recruitment rate | Baseline (before the programme started) | Proportion of eligible children in grades 3-5 whose parents gave written consent. | ClinicalTrials.gov |
| Primary | Retention rate | 18 weeks after baseline | Proportion of enrolled children followed up at 18 weeks. | ClinicalTrials.gov |
| Primary | Data completeness | Baseline and 18 weeks | Proportion of enrolled children (baseline) and followed-up children (18 weeks) with complete data for each measure: anthropometry, blood pressure, child questionnaire sections and parent questionnaire. | ClinicalTrials.gov |
| Primary | Time needed for data collection | Baseline and 18 weeks | Mean minutes per class required to complete the child questionnaire and to measure anthropometry and blood pressure. | ClinicalTrials.gov |
| Primary | Programme delivery and attendance | During the 17-week programme | Proportion of planned child and parent sessions delivered; mean attendance (%) of children at classroom sessions and of parents at group sessions; frequency (days per week) and duration (minutes per day) of school physical activity. | ClinicalTrials.gov |
| Primary | Standard deviation of change and intracluster correlation coefficient of BMI-for-age z-score | Baseline to 18 weeks | Parameters for the sample size calculation of the definitive trial. BMI-for-age z-score was calculated from measured height and weight using the WHO 2007 growth reference. | ClinicalTrials.gov |
| Secondary | Change in BMI-for-age z-score | Baseline to 18 weeks | Calculated from measured height and weight using the WHO 2007 growth reference. | ClinicalTrials.gov |
| Secondary | Change in prevalence of overweight and obesity | Baseline to 18 weeks | Proportion of children with overweight (BMI-for-age z-score \> +1 to +2) or obesity (z-score \> +2) according to WHO 2007 cut-offs. | ClinicalTrials.gov |
| Secondary | Change in waist circumference | Baseline to 18 weeks | Measured in centimetres midway between the lowest rib and the iliac crest. | ClinicalTrials.gov |
| Secondary | Change in systolic and diastolic blood pressure | Baseline to 18 weeks | Measured in mmHg with a validated oscillometric device; classified using the American Academy of Pediatrics 2017 tables. | ClinicalTrials.gov |
| Secondary | Change in physical activity score | Baseline to 18 weeks | Child-reported summary score (range 0-19) based on days with at least 60 minutes of activity, days walking or cycling to school, and days with physical education in the past 7 days; higher scores indicate more activity. | ClinicalTrials.gov |
| Secondary | Change in diet score | Baseline to 18 weeks | Child-reported dietary questionnaire on intake of fruit and vegetables, sugar-sweetened beverages and fast food in the past 7 days. | ClinicalTrials.gov |
| Secondary | Change in screen and sedentary time score | Child-reported score (range 0-8) from four items on screen and sedentary time, each scored 0-2 (<1 h, 1-2 h, >2 h per day); higher scores indicate more screen time. | Child-reported score (range 0-8) from four items on screen and sedentary time, each scored 0-2 (\<1 h, 1-2 h, \>2 h per day); higher scores indicate more screen time. | ClinicalTrials.gov |
| Secondary | Change in sleep duration | Baseline to 18 weeks | Child-reported usual nightly sleep duration in hours. | ClinicalTrials.gov |
| Secondary | Change in parental knowledge, attitudes and practices | Baseline to 18 weeks | Parent questionnaire scores for knowledge, attitudes and practices regarding childhood healthy weight, diet and physical activity. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)