Implementation Research on the Intervention Mode of " Comorbidity-Co-causes-Joint-prevention" Comprehensive Demonstration District of Depression and Obesity Among Children and Adolescents in Beijing

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

NOT_YET_RECRUITING

Clinical Phase

NA

Total Enrollment

440 participants

Study Classification

INTERVENTIONAL

Study Start Date

2024-08-01

Study Completion Date

2026-12-31

Brief Summary

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Depression and obesity have become the most prominent health problems among adolescents and have caused a heavy burden on the health and social economy of the whole population. There are high incidence, comorbidity and co-pathogenic factors of depression and obesity in adolescents, but there is still a lack of research on joint prevention strategies and multi-sectoral collaborative prevention and control network. This project plans to screen and integrate effective intervention measures based on multi-stage optimization strategy, developing an intervention mode of \[Comorbidity-Co-causes-Joint-prevention\] for adolescents with depression or/and obesity, and then carry out with children or adolescents in Beijing based on digital platform. The investigators will be considering the accessibility, sustainability and replicability of the implement based on the RE-AIM framework including the coverage of population and organizations as well as the effect, implement and sustainability of the interventions. The research will be promoted with the help of the National Clinical Research Center for Mental Disorders and Monitoring of Student Common Diseases and Health Influencing Factors. The results of the research will establish an intervention mode of \[Comorbidity-Co-causes-Joint-prevention\] and a promotion model for adolescents' depression and obesity in Beijing, providing support for the realization of Healthy China 2030 and Healthy Beijing 2030 Plans.

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Detailed Description

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Conditions

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Depression Obesity High Risk of Depression Overweight

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

NONE

Study Groups

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intervention group

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

Group Type ACTIVE_COMPARATOR

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

Intervention Type COMBINATION_PRODUCT

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

control group

receiving routine health education and mental health knowledge

Group Type PLACEBO_COMPARATOR

routine health education and mental health knowledge

Intervention Type COMBINATION_PRODUCT

routine health education and mental health knowledge

Interventions

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

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

Intervention Type COMBINATION_PRODUCT

routine health education and mental health knowledge

Intervention Type COMBINATION_PRODUCT

Eligibility Criteria

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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.

Eligible Sex

ALL

Accepts Healthy Volunteers

No