A Study on Improving Detection and Management of Suicide Risk Among Depressed Patients in Primary Care
Primary Purpose
Depression, Suicide
Status
Unknown status
Phase
Phase 1
Locations
China
Study Type
Interventional
Intervention
training on identification of suicide risk and depression
Sponsored by
About this trial
This is an interventional prevention trial for Depression focused on measuring suicide, depressed patients, primary care
Eligibility Criteria
Inclusion Criteria:
- consecutive outpatient
Exclusion Criteria:
- severe physical conditions
Sites / Locations
- Nanjing Brain Hospital
Outcomes
Primary Outcome Measures
Kappa of diagnostic consistency
Secondary Outcome Measures
ratio of optimal managment
Full Information
NCT ID
NCT00386711
First Posted
October 10, 2006
Last Updated
October 10, 2006
Sponsor
Nanjing Medical University
1. Study Identification
Unique Protocol Identification Number
NCT00386711
Brief Title
A Study on Improving Detection and Management of Suicide Risk Among Depressed Patients in Primary Care
Official Title
A Study on Improving Detection and Management of Suicide Risk Among Depressed Patients in Primary Care
Study Type
Interventional
2. Study Status
Record Verification Date
October 2006
Overall Recruitment Status
Unknown status
Study Start Date
October 2006 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
January 2007 (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Nanjing Medical University
4. Oversight
5. Study Description
Brief Summary
improve detection and management of suicide risk among depressed patients in primary care
Detailed Description
After intervention of training on the identification and management of depression and suicide risk in primary health care professionals, the ability of detection and management of suicide risk among depressed patients in primary care is expected to be improved compared to baseline evaluation.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Depression, Suicide
Keywords
suicide, depressed patients, primary care
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
Single
Allocation
Non-Randomized
Enrollment
2160 (false)
8. Arms, Groups, and Interventions
Intervention Type
Behavioral
Intervention Name(s)
training on identification of suicide risk and depression
Primary Outcome Measure Information:
Title
Kappa of diagnostic consistency
Secondary Outcome Measure Information:
Title
ratio of optimal managment
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
consecutive outpatient
Exclusion Criteria:
severe physical conditions
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yong Tang, Doctor
Phone
13851603705
Email
tangyong1967@gmail.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
SHUTAO ZHAI, DOCTOR
Organizational Affiliation
Nanjing Brain Hospital
Official's Role
Study Director
Facility Information:
Facility Name
Nanjing Brain Hospital
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
210029
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yong Tang, doctor
Phone
13851603705
Email
tangyong1967@gmail.com
12. IPD Sharing Statement
Learn more about this trial
A Study on Improving Detection and Management of Suicide Risk Among Depressed Patients in Primary Care
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