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School-based Comprehensive Suicide Intervention in Shanghai, China

Primary Purpose

Suicide

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
suicide intervention
Sponsored by
Shanghai Mental Health Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Suicide focused on measuring school-based, adolescent suicide, intervention, screening

Eligibility Criteria

12 Years - 19 Years (Child, Adult)All SexesAccepts Healthy Volunteers

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

Sites / Locations

  • Shanghai Mental Health CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

study group

control group

Arm Description

1500 students are randomized to receive a universal suicide intervention apart from usual school psychology classes. Furthermore, high risk of suicidal students screened in study group will receive an indicated suicide intervention in addition to usual school psychology classes.

1500 students are randomized to receive usual school psychology classes. High risk of suicidal students screened in control group will receive usual psychology classes.

Outcomes

Primary Outcome Measures

students' score of mediating factors and suicide behaviors

Secondary Outcome Measures

students' score of suicide knowledge and attitude

Full Information

First Posted
February 6, 2012
Last Updated
May 10, 2012
Sponsor
Shanghai Mental Health Center
Collaborators
Shanghai Pu Dong Institute of Education Development, Shanghai Sanling North Junior Middle School, Shanghai Shangnan East Junior Middle School, Shanghai Sanling Senior Middle School, Shanghai Yangsi Senior Middle School
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1. Study Identification

Unique Protocol Identification Number
NCT01598519
Brief Title
School-based Comprehensive Suicide Intervention in Shanghai, China
Study Type
Interventional

2. Study Status

Record Verification Date
May 2012
Overall Recruitment Status
Unknown status
Study Start Date
February 2011 (undefined)
Primary Completion Date
June 2012 (Anticipated)
Study Completion Date
December 2012 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Shanghai Mental Health Center
Collaborators
Shanghai Pu Dong Institute of Education Development, Shanghai Sanling North Junior Middle School, Shanghai Shangnan East Junior Middle School, Shanghai Sanling Senior Middle School, Shanghai Yangsi Senior Middle School

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicide
Keywords
school-based, adolescent suicide, intervention, screening

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
3000 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
study group
Arm Type
Experimental
Arm Description
1500 students are randomized to receive a universal suicide intervention apart from usual school psychology classes. Furthermore, high risk of suicidal students screened in study group will receive an indicated suicide intervention in addition to usual school psychology classes.
Arm Title
control group
Arm Type
No Intervention
Arm Description
1500 students are randomized to receive usual school psychology classes. High risk of suicidal students screened in control group will receive usual psychology classes.
Intervention Type
Behavioral
Intervention Name(s)
suicide intervention
Intervention Description
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.
Primary Outcome Measure Information:
Title
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 Outcome Measure Information:
Title
students' score of suicide knowledge and attitude
Time Frame
"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"

10. Eligibility

Sex
All
Minimum Age & Unit of Time
12 Years
Maximum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
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
Facility Information:
Facility Name
Shanghai Mental Health Center
City
Shanghai
State/Province
Shanghai
ZIP/Postal Code
200030
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Qian Bian, MD
Phone
+86-021-34289888
Ext
3284
Email
bianqian0602@qq.com

12. IPD Sharing Statement

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School-based Comprehensive Suicide Intervention in Shanghai, China

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