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Intervention Strategy for Depression and Obesity in Beijing Adolescents

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Study Aim

This study aims to prevent depression and obesity in teenagers living in Beijing by using a specific intervention strategy and measuring its impact with a health questionnaire.

What is being tested

combination intervention strategy of [Comorbidity-Co-causes-Joint-prevention]

+ routine health education and mental health knowledge

Combination Product
Who is being recruted

Behavior+8

+ Behavioral Symptoms

+ Body Weight

See all eligibility criteria
How is the trial designed

Prevention Study

Placebo-Controlled
Interventional
Study Start: August 2024
See protocol details

Summary

Principal SponsorCapital Medical University
Study ContactLinghui Meng, PHDMore contacts
Last updated: January 28, 2026
Sourced from a government-validated database.Claim as a partner

Study start date: August 1, 2024

Actual date on which the first participant was enrolled.

This study is focused on finding better ways to prevent and manage depression and obesity among children and adolescents in Beijing. Both depression and obesity are common in young people, often occurring together and sharing similar causes, which can have significant impacts on their health and well-being. The study aims to develop a new prevention method called "Comorbidity-Co-causes-Joint-prevention", which combines different strategies to address these issues jointly. This approach is important because it seeks to create a sustainable and effective way to tackle these health problems, potentially reducing their burden on individuals and society. Participants in the study will be part of a program that uses a digital platform to deliver the intervention, aiming to ensure it is accessible and easy to use. The study will assess how well this intervention works across different groups and organizations, looking at factors like the reach and sustainability of the program. The effectiveness of the intervention will be measured using the RE-AIM framework, which evaluates its reach, effectiveness, adoption, implementation, and maintenance. The findings will help establish a model for preventing depression and obesity in young people, aligning with broader health goals for Beijing and China.

Official TitleImplementation Research on the Intervention Mode of " Comorbidity-Co-causes-Joint-prevention" Comprehensive Demonstration District of Depression and Obesity Among Children and Adolescents in Beijing
NCT06489990
Principal SponsorCapital Medical University
Study ContactLinghui Meng, PHDMore contacts
Last updated: January 28, 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

440 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.

Healthy volunteers not allowed

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

Conditions

Pathology

BehaviorBehavioral SymptomsBody WeightDepressionNutrition DisordersNutritional and Metabolic DiseasesObesitySigns and SymptomsPathological Conditions, Signs and SymptomsOvernutritionOverweight

Criteria

Inclusion Criteria: * Stage I (screening stage): 1. Middle school students in Beijing Economic-Technological Development Area and other districts of Beijing, both male and female; 2. Students themselves and their guardians are willing to participate in this study and sign written informed consent file. Stage Ⅱ: Middle school students who were identified as high risk of depression and/or obesity in Stage I in Beijing Economic-Technological Development Area and other districts of Beijing, the screening criteria are as follows: ① CES-DC score ≥16 points; ② BMI ≥WS/T586-2018: Screened as overweight and obesity among school-age children and adolescents, according to the recommendation by the National Health Commission; ③ Students themselves and their guardians are willing to participate in this study and provide written informed consent. Exclusion Criteria: * Stage I: 1. Having serious physical or genetic disease that is not suitable for participation in the study; 2. Have been evaluated that not suitable for this study by investigators. Stage Ⅱ: 1. Having serious physical or genetic disease that is not suitable for participation in the study; 2. Have been evaluated that not suitable for this study by investigators.

Study Plan

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

2 intervention groups are designated in this study

50% chance of being blinded to the placebo group

Treatment Groups

Group I

Active Comparator
the intervention is combination intervention strategy of " Comorbidity-Co-causes-Joint-prevention"

Group II

Placebo
receiving routine health education and mental health knowledge

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

Beijing Anding Hospital, Capital Medical University

Beijing, ChinaOpen Beijing Anding Hospital, Capital Medical University in Google Maps
Recruiting soonOne Study Center