School-Based Intervention for Healthy Lifestyle Promotion Among Qatari Youth
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.
Weight loss program for school children
Body Weight+6
+ Nutrition Disorders
+ Nutritional and Metabolic Diseases
Prevention Study
Summary
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.
Protocol
This section provides details of the study plan, including how the study is designed and what the study is measuring.799 patients to be enrolled
Total number of participants that the clinical trial aims to recruit.Prevention Study
Eligibility
Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.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
Criteria
Study Plan
Find out more about all the medication administered in this study, their detailed description and what they involve.One single intervention group is designated in this study
This study does not include a placebo group
Treatment Groups
Group I
ExperimentalStudy 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