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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT00808873
Other study ID # 2008-7
Secondary ID
Status Recruiting
Phase N/A
First received December 15, 2008
Last updated December 15, 2008
Start date November 2008
Est. completion date March 2011

Study information

Verified date November 2008
Source Beijing HuiLongGuan Hospital
Contact Xianyun Li, Bachelor, Master of Medicine
Phone 86-10-82951464
Email xianyunl@public3.bta.net.cn
Is FDA regulated No
Health authority China: Ethics Committee
Study type Interventional

Clinical Trial Summary

Compared to a treatment-as-usual group, providing brief mental health education to suicide attempters from rural parts of China at the time of their treatment in the emergency departments of general hospitals or local clinics and 6 home-visits (FOR those subjects WITH PHONES refuse home visits, THE INTERVIEWS WILL BE CONDUCTED OVER THE PHONE) over the twelve months after the attempt demonstrate continuing concern about the attempters ('befriending'), strengthen their social support networks and improve their problem-solving skills will significantly reduce their hopelessness, the severity of depressive symptoms, and level of suicidal ideation.


Recruitment information / eligibility

Status Recruiting
Enrollment 450
Est. completion date March 2011
Est. primary completion date February 2011
Accepts healthy volunteers No
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- suicide attempters

- must be 18 years or older

- no-zero intent to die

Exclusion Criteria:

- with communication difficulties

- living outside of the research sites

Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind (Investigator)


Related Conditions & MeSH terms


Intervention

Other:
socio-educational intervention
brief mental health education and 6 follow-up visits

Locations

Country Name City State
China People's Hospital of Yuncheng County Yuncheng County Shandong

Sponsors (6)

Lead Sponsor Collaborator
Beijing HuiLongGuan Hospital Bureau of Health of Ji County, Harvard University, People's Hospital of Yuncheng County, Suicide Prevention International, University of Rochester

Country where clinical trial is conducted

China, 

Outcome

Type Measure Description Time frame Safety issue
Primary the severity of depressive symptoms one year No
Secondary frequency and intensity of suicidal ideation one year No
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