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Clinical Trials/NCT01598519
NCT01598519
Unknown
Not Applicable

School-based Comprehensive Suicide Intervention in Shanghai, China

Shanghai Mental Health Center1 site in 1 country3,000 target enrollmentFebruary 2011
ConditionsSuicide

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Suicide
Sponsor
Shanghai Mental Health Center
Enrollment
3000
Locations
1
Primary Endpoint
students' score of mediating factors and suicide behaviors
Last Updated
13 years ago

Overview

Brief Summary

The primary aim of this study is to examine whether a school-based suicide intervention is effective in reducing suicide related risk factors in a population of middle and high students. It hypothesized that receiving the intervention will reduce the severity of suicide related risk factors such as depression, hopelessness, suicidal behaviors and increasing protective factors such as social support, self esteem, suicide knowledge and attitude and so on, as compared to the control group.

Detailed Description

A total of 3000 students from two junior schools (grade 7 and 8) and two senior schools (grade 10 and 11) in Shanghai Pu Dong district were recruited in our study. All students were randomly assigned into universal study group or universal control group by class level. In those two groups, high risk of suicidal students were identified by screening. A universal suicide intervention was conducted in the universal study group; an indicated suicide intervention was conducted in the indicated study group. All students in universal study group and universal control group completed the self-administered questionnaire before and 6 months after the end of universal intervention. High risk of suicidal students in the indicated study group and indicated control group completed another self-administered questionnaire before, 6 months and 18 months after the end of the indicated intervention.

Registry
clinicaltrials.gov
Start Date
February 2011
End Date
December 2012
Last Updated
13 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • students of grade 6,7,9,10 from four schools (2 middle schools, 2 high schools)

Exclusion Criteria

  • students who are not attending school because of long term sickness or moving to other school,or going aboard, etc.
  • students whose parents don't agree to participate the study

Outcomes

Primary Outcomes

students' score of mediating factors and suicide behaviors

Time Frame: "Change from baseline in suicide behavior at 6 months after the end of the intervention" and "Change from baseline in suicide behavior at 18 months after the end of intervention"

Secondary Outcomes

  • students' score of suicide knowledge and attitude("Change from baseline in suicide knowledge at 6 months after the end of the intervention" and "Change from baseline in suicide knowledge at 18 months after the end of intervention")

Study Sites (1)

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