A Study on Improving Detection and Management of Suicide Risk Among Depressed Patients in Primary Care

NCT ID: NCT00386711

Last Updated: 2006-10-12

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

UNKNOWN

Clinical Phase

PHASE1

Total Enrollment

2160 participants

Study Classification

INTERVENTIONAL

Study Start Date

2006-10-31

Study Completion Date

2007-01-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

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

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

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.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Depression Suicide

Keywords

Explore important study keywords that can help with search, categorization, and topic discovery.

suicide depressed patients primary care

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Allocation Method

NON_RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

PREVENTION

Blinding Strategy

SINGLE

Interventions

Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.

training on identification of suicide risk and depression

Intervention Type BEHAVIORAL

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* consecutive outpatient

Exclusion Criteria

* severe physical conditions
Minimum Eligible Age

18 Years

Maximum Eligible Age

80 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Nanjing Medical University

OTHER

Sponsor Role lead

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

SHUTAO ZHAI, DOCTOR

Role: STUDY_DIRECTOR

Nanjing Brain Hospital

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

Nanjing Brain Hospital

Nanjing, Jiangsu, China

Site Status

Countries

Review the countries where the study has at least one active or historical site.

China

Central Contacts

Reach out to these primary contacts for questions about participation or study logistics.

Yong Tang, Doctor

Role: CONTACT

Phone: 13851603705

Email: [email protected]

Facility Contacts

Find local site contact details for specific facilities participating in the trial.

Yong Tang, doctor

Role: primary

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

NBH038

Identifier Type: -

Identifier Source: org_study_id