Research on Suicidal Ideation of University Students in Harbin City and Cognitive Behavior Therapy

Suicide Clinical Trial

Official title:

the Research on Suicidal Ideation of University Students in Harbin City and Intervention on Them

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00575575
• Other study ID #: 196781
• Secondary ID: 19678181
• Status: Completed
• Phase: N/A
• First received: December 15, 2007
• Last updated: February 25, 2009
• Start date: June 2007
• Est. completion date: February 2009

Study information

• Verified date: February 2009
• Source: Harbin Medical University
• Contact: n/a
• Is FDA regulated: No
• Health authority: China: Ministry of Health
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 355
• Est. completion date: February 2009
• Est. primary completion date: December 2008
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Both
• Age group: 17 Years to 35 Years

Eligibility

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

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Prevention

Related Conditions & MeSH terms

• Suicidal Ideation
• Suicide

Intervention

Behavioral:
• cognitive behavior therapy
cognitive behavior therapy once a week

Locations

Country	Name	City	State
n/a

Sponsors (1)

Lead Sponsor	Collaborator
Harbin Medical University

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	suicidal ideation; depression		half a year	No