Research on Suicidal Ideation of University Students in Harbin City and Cognitive Behavior Therapy
Primary Purpose
Suicide
Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
cognitive behavior therapy
Sponsored by
About this trial
This is an interventional prevention trial for Suicide focused on measuring Suicidal ideation, cognitive behavior therapy
Eligibility Criteria
Inclusion Criteria:
- Suicidal ideation or the scores of Beck Depression Inventory ≧14
Exclusion Criteria:
- have no Suicidal ideation and the scores of Beck Depression Inventory <14
Sites / Locations
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
A,2
Arm Description
Outcomes
Primary Outcome Measures
suicidal ideation; depression
Secondary Outcome Measures
Full Information
NCT ID
NCT00575575
First Posted
December 15, 2007
Last Updated
February 25, 2009
Sponsor
Harbin Medical University
1. Study Identification
Unique Protocol Identification Number
NCT00575575
Brief Title
Research on Suicidal Ideation of University Students in Harbin City and Cognitive Behavior Therapy
Official Title
the Research on Suicidal Ideation of University Students in Harbin City and Intervention on Them
Study Type
Interventional
2. Study Status
Record Verification Date
February 2009
Overall Recruitment Status
Completed
Study Start Date
June 2007 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
February 2009 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
Harbin Medical University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purposes of this research are:
to understand the status of suicidal ideation, suicidal behavior, and depression in Harbin University students; and
to analyse the infect factors of suicidal ideation and suicidal behavior.
With cognitive behavior interventions on students with suicidal ideation, suicidal behavior, and middle or high degree of depression, the researchers can provide a scientific and effective intervention to the students.
Cognitive therapy for the prevention of suicide attempts: a randomized controlled trial.
Brown GK, Ten Have T, Henriques GR, Xie SX, Hollander JE, Beck AT. Department of Psychiatry, University of Pennsylvania, Philadelphia 19104, USA. gregbrow@mail.med.upenn.edu JAMA. 2005 Aug 3;294(5):563-70.
Detailed Description
By using suicidal ideation scale, to assess the status of suicidal ideation and suicidal attempt in 6000 university students in Harbin city. About 300 students with suicidal ideation and depression disorder randomized into two groups (control and intervention groups) accept the cognitive behavior intervention. We will assess the depression after intervention.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Suicide
Keywords
Suicidal ideation, cognitive behavior therapy
7. Study Design
Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
355 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A,2
Arm Type
Experimental
Intervention Type
Behavioral
Intervention Name(s)
cognitive behavior therapy
Intervention Description
cognitive behavior therapy once a week
Primary Outcome Measure Information:
Title
suicidal ideation; depression
Time Frame
half a year
10. Eligibility
Sex
All
Minimum Age & Unit of Time
17 Years
Maximum Age & Unit of Time
35 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria:
Suicidal ideation or the scores of Beck Depression Inventory ≧14
Exclusion Criteria:
have no Suicidal ideation and the scores of Beck Depression Inventory <14
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Yanjie Yang, doctor
Organizational Affiliation
Harbin Medical University
Official's Role
Study Director
12. IPD Sharing Statement
Learn more about this trial
Research on Suicidal Ideation of University Students in Harbin City and Cognitive Behavior Therapy
We'll reach out to this number within 24 hrs