- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04063202
Development of a Predictive Index for Probable Depression Among Secondary School Students
A Longitudinal Study for Identifying Predictors of Incidence/Remission of Probable Depression and Developing a Predictive Index for Probable Depression Among Secondary School Students
Study Overview
Detailed Description
A 12-month longitudinal study will be conducted in secondary school settings.
The investigators will investigate incidence of probable depression (i.e., from non-depression, CESD<16, at baseline to probable depression, CESD≥16, at month 12) and remission of probable depression.
The investigators will investigate factors that can prospectively predict new cases/remission of probable depression, including both well-documented risk/protective factors and some under-examined but potentially important local factors (e.g. school/academic stress, psychological resilience). The relative importance of the risk/protective factors at different socio-ecological levels will be compared and their combined effect will be identified.
Based on the selected factors, the investigators will derive a new prediction index called the Adolescent Depression Prediction Index (ADPI) in a model building sample and test its performance in predicting incidence of depression in a validation sample among secondary school students in Hong Kong.
Study Type
Enrollment (Anticipated)
Contacts and Locations
Study Locations
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Hong Kong, Hong Kong
- Recruiting
- China Holiness Church Living Spirit College
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Contact:
- Phone Number: 2958 9694
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Hong Kong, Hong Kong
- Recruiting
- Christian Alliance SW Chan Memorial College (Christian Alliance SW Chan Memorial Secondary School)
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Contact:
- Phone Number: 2670 9229
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Hong Kong, Hong Kong
- Recruiting
- Ho Ngai College ( Sponsored By Sik Sik Yuen)
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Contact:
- Phone Number: 2441 7100
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Hong Kong, Hong Kong
- Recruiting
- Kit Sam Lam Bing Yim Secondary Schoo
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Contact:
- Phone Number: 2337 9594
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- Secondary 1 (seventh year of formal education) to Secondary 4 Chinese students, who are studying local mainstream schools in Hong Kong.
- Able to read Chinese and speak either Cantonese or Mandarin.
Exclusion Criteria:
- Eligible students whose parents refuse to give consent to take part in the study.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
Non-cases
Secondary school students (seventh to tenth years of education) without probable depression at baseline interview.
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The anonymous structured questionnaire will be self-administered by the participating students in the absence of their teachers in class-room settings.
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Incidence of probable depression
Time Frame: 12 months
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To examine the incidence of probable depression from non-depression (CESD<16) at baseline to probable depression (CESD>=16) at month 12.
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12 months
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Adolescent Depression Prediction Index (ADPI)
Time Frame: 12 months
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To develop a new prediction index ADPI and test test its performance in predicting incidence of depression.
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12 months
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Collaborators and Investigators
Sponsor
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- HMRF16171001
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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