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Clinical Trials/NCT01626716
NCT01626716
Completed
Not Applicable

Collaborative Care for Depressed Elderly in Korea

National Clinical Research Coordination Center, Seoul, Korea1 site in 1 country80 target enrollmentJune 2012

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Depression
Sponsor
National Clinical Research Coordination Center, Seoul, Korea
Enrollment
80
Locations
1
Primary Endpoint
Reduced depression symptoms
Status
Completed
Last Updated
10 years ago

Overview

Brief Summary

Late-life depression is associated with physical limitations, greater functional impairment, increased utilization and cost of health care, and suicide. Collaborative care, linking primary and mental health specialty care, has been shown to be effective for the treatment of late-life depression in primary care settings in Western countries. The primary aim of this project is to implement a depression care management intervention, and examine its effectiveness on the depressive symptoms of older patients in Korean primary care settings. Based on chronic disease management theory and previous Collaborative care management studies in western countries, we propose to test a Depression Care Management intervention,which includes care manager to support a primary care physician of depression in their old patients. Care manager'd role are monitoring the progress of treatment, supporting patient's adherence, educating patients/ family and facilitate communication between providers. Also psychiatrists provide consultation and supervision of care managers. Using a randomized controlled design, we will examine whether the Depression care management is an effective treatment for patients with late life depression in rural Korea. The primary outcome would be the improvement of depressive symptoms of patients in primary care setting.

Registry
clinicaltrials.gov
Start Date
June 2012
End Date
December 2013
Last Updated
10 years ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
National Clinical Research Coordination Center, Seoul, Korea
Responsible Party
Principal Investigator
Principal Investigator

Hyeon Woo Yim

Professor

National Clinical Research Coordination Center, Seoul, Korea

Eligibility Criteria

Inclusion Criteria

  • 60 year or older
  • diagnosed depression based on DSM-IV criteria

Exclusion Criteria

  • impairment of hearing
  • other psychiatric disorders

Outcomes

Primary Outcomes

Reduced depression symptoms

Time Frame: 3 months

HAMD (Hamilton Depression Ratind Scale) Difference HAMD score between the intervention and control group from baseline to 3 month follow-up

Secondary Outcomes

  • Depression response and remissionhealth related quality of life(3months and 6months)
  • Reduced suicide ideation(3 months and 6 months)
  • Improvement of Quality of life(3 months and 6 months)

Study Sites (1)

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