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School-based Comprehensive Suicide Intervention in Shanghai, China

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01598519
Enrollment
3000
Registered
2012-05-15
Start date
2011-02-28
Completion date
2012-12-31
Last updated
2012-05-15

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Suicide

Keywords

school-based, adolescent suicide, intervention, screening

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.

Interventions

BEHAVIORALsuicide intervention

universal intervention:(1)students: 4 sections about cherishing life, coping strategies, suicide and depression disorder during 2 semesters, each session lasting 45 minutes.(2)gatekeeper: 4 sessions about teenagers psychological crisis intervention strategies during 2 semesters, 30minutes per session. indicated intervention: (1)student: 2 semesters, 20 sessions' group life skill and cognitive-behavioral psychological training lesson, including Youth rational emotive group tutoring(eight classroom sessions), Coping skill group tutoring(six classroom sessions)and Behavior group tutoring(six classroom sessions), once a week, each session lasting 1.5hours.(2)gatekeeper: a social support net.

Sponsors

Shanghai Pu Dong Institute of Education Development
CollaboratorUNKNOWN
Shanghai Sanling North Junior Middle School
CollaboratorUNKNOWN
Shanghai Shangnan East Junior Middle School
CollaboratorUNKNOWN
Shanghai Sanling Senior Middle School
CollaboratorUNKNOWN
Shanghai Yangsi Senior Middle School
CollaboratorUNKNOWN
Shanghai Mental Health Center
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
12 Years to 19 Years
Healthy volunteers
Yes

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

Design outcomes

Primary

MeasureTime frame
students' score of mediating factors and suicide behaviorsChange 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

MeasureTime frame
students' score of suicide knowledge and attitudeChange 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

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026