NCT00386711

Brief Summary

improve detection and management of suicide risk among depressed patients in primary care

Trial Health

43
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
2,160

participants targeted

Target at P75+ for phase_1 depression

Timeline
Completed

Started Oct 2006

Shorter than P25 for phase_1 depression

Geographic Reach
1 country

1 active site

Status
unknown

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 1, 2006

Completed
9 days until next milestone

First Submitted

Initial submission to the registry

October 10, 2006

Completed
2 days until next milestone

First Posted

Study publicly available on registry

October 12, 2006

Completed
3 months until next milestone

Study Completion

Last participant's last visit for all outcomes

January 1, 2007

Completed
Last Updated

October 12, 2006

Status Verified

October 1, 2006

First QC Date

October 10, 2006

Last Update Submit

October 10, 2006

Conditions

DepressionSuicide

Keywords

suicidedepressed patientsprimary care

Outcome Measures

Primary Outcomes (1)

  • Kappa of diagnostic consistency

Secondary Outcomes (1)

  • ratio of optimal managment

Interventions

training on identification of suicide risk and depressionBEHAVIORAL

Eligibility Criteria

Age18 Years - 80 Years
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)

You may qualify if:

  • consecutive outpatient

You may not qualify if:

  • severe physical conditions

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Nanjing Brain Hospital

Nanjing, Jiangsu, 210029, China

Location

MeSH Terms

Conditions

DepressionSuicide

Condition Hierarchy (Ancestors)

Behavioral SymptomsBehaviorSelf-Injurious Behavior

Study Officials

  • SHUTAO ZHAI, DOCTOR

    Nanjing Brain Hospital

    STUDY DIRECTOR

Central Study Contacts

Yong Tang, Doctor

CONTACT

13851603705tangyong1967@gmail.com

Study Design

Study Type
interventional
Phase
phase 1
Allocation
NON RANDOMIZED
Masking
SINGLE
Purpose
PREVENTION
Intervention Model
PARALLEL
Sponsor Type
OTHER

Study Record Dates

First Submitted

October 10, 2006

First Posted

October 12, 2006

Study Start

October 1, 2006

Study Completion

January 1, 2007

Last Updated

October 12, 2006

Record last verified: 2006-10

Locations

CN(1)