Completed

School-Based Intervention for Healthy Lifestyle Promotion Among Qatari Youth

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Study Aim

This study aims to promote a healthy lifestyle among Qatari youth by implementing a school-based intervention, with the primary goal of achieving weight loss, measured through changes in Body Mass Index (BMI) over a period of 26 weeks.

What is being tested

Weight loss program for school children

Behavioral
Who is being recruted

Body Weight+6

+ Nutrition Disorders

+ Nutritional and Metabolic Diseases

From 9 to 12 Years
+2 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Prevention Study

Interventional
Study Start: August 2013
See protocol details

Summary

Principal SponsorQatar University
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: August 1, 2013

Actual date on which the first participant was enrolled.

This study aims to tackle overweight and obesity among Qatari youth, specifically children aged 9-12. The project plans to adapt a school-based intervention that combines behavioral and cognitive approaches to promote a healthy lifestyle. It also aims to integrate behavioral economics and cognitive behavioral therapy in a multi-cohort prevention/intervention study. The study will select and use technological tools for enhanced outcomes and adoption of the intervention nationally. The ultimate goal is to package the study findings into a lifestyle change intervention for national implementation, in collaboration with Hamad Medical Corporation and the Supreme Education Council. This project could provide the basis for a national program to reduce obesity in Qatar through lifestyle changes and decrease related health conditions. During the study, participants will have their weight loss progress assessed by measuring their Body Mass Index (BMI) at various stages: the start of the study, post-camp, post-clubs, and post-maintenance/end of intervention. The change in BMI Standard Deviation Scores (SDS) between the start and week 26 will be used to evaluate the effectiveness of the intervention, compared to the BMI-SDS for the control group. A one-year follow-up of the change in BMI-SDS for both intervention and control groups will gauge the long-term benefits of the intervention. A multilevel mixed effects model will be used to assess both individual- and school-level effects, including covariates such as demographic factors of the children and time (cohort). Subgroup analyses will be conducted by gender and age.

Official TitleAdapted Cognitive Behavioural Approach to Addressing Overweight and Obesity Among Qatari Youth
NCT02972164
Principal SponsorQatar University
Last updated: January 27, 2026
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

799 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Prevention Study

Prevention studies aim to stop a disease from developing. They often involve people at risk and test things like vaccines, lifestyle changes, or preventive medications.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

From 9 to 12 Years

Range of ages for which participants are eligible to join.

Healthy volunteers allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Body WeightNutrition DisordersNutritional and Metabolic DiseasesObesitySigns and SymptomsPathological Conditions, Signs and SymptomsOvernutritionOverweightPediatric Obesity

Criteria

1 inclusion criteria required to participate
School children within age range of 9-12 yrs, at or above 95th percentile of BMI by age using International Obesity TaskForce (IOTF) cut off, and parental consent.

1 exclusion criteria prevent from participating
Psychiatric or neurological disorders, learning disability, dyslexia, current or past drug abuse, head injury and psychotropic medication.

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

One single intervention group is designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Experimental
Each year, 100 school children age 9-12 who meet inclusion criteria are selected from 5 randomly chosen schools to participate in the intervention group. The intervention children take part in the integrated approach for weight management consisting of (1) intensive weight loss camp (2) twelve weeks of after school clubs for consolidation purposes, and (3) social media and wearable sensors for support and monitoring.

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Suspended

Qatar University

Doha, QatarOpen Qatar University in Google Maps
CompletedOne Study Center
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