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CompletedNCT01626716Updated Mar 11, 2016

Collaborative Care for Depressed Elderly in Korea

An interventional study of care management in Depression, Elderly and Korean, sponsored by National Clinical Research Coordination Center, Seoul, Korea. Completed at 1 site in Korea, Republic of. Open to participants aged 60 Years and older. Per ClinicalTrials.gov, last updated 2016-03-11.

Sponsored by National Clinical Research Coordination Center, Seoul, Korea · Not applicable, Interventional, and Treatment

Phase
Not applicable
Study type
Interventional
Enrollment
80
Allocation
Randomized
Ages
60 Years and older
Sex
All
01

Study 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.

02

Conditions studied

  • Depression
  • Elderly
  • Korean
  • Collaborative Care

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03

In context

Depression

8,057 studies on the registry are indexed under Depression; 1,643 are open to participants now.

This study's enrollment of 80 is close to the median of 84 across 6,718 interventional studies indexed under Depression.

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Lead sponsor

National Clinical Research Coordination Center, Seoul, Korea is the lead sponsor of 5 studies on the registry; none are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
60 Years and older
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

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

Exclusion criteria

Exclusion Criteria:

  • impairment of hearing
  • dementia
  • other psychiatric disorders
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
80 participants (actual)

Study arms

  • Experimental
    case management

    patients who assigned to the intervention group will take 7 times phone calls from case manager

    Other: care management

  • No intervention
    control

    usual care

Interventions

  • Othercare management

    patients who assigned to the intervention group will take 7 times phone calls from case manager

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What researchers measure

Primary outcomes

  1. Reduced depression symptoms

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

    Time frame: 3 months

Secondary outcomes

  1. Depression response and remissionhealth related quality of life

    HAMD (Hamilton Depression Ratind Scale) Depression response is defined by improvement 50% or more HAMD scores from baseline to each follow-up periods. Depression remission is defined by 7 or less of HAMD score at each follow-up periods

    Time frame: 3months and 6months

  2. Reduced suicide ideation

    SSI (Beck's suicide ieation scale) Difference total SSI scores Between the two groups from baseline to each follow-up periods

    Time frame: 3 months and 6 months

  3. Improvement of Quality of life

    EQ5D Difference EQ5D scores Between the two groups from baseline to each follow-up periods

    Time frame: 3 months and 6 months

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Study locations

1 site
  • Chungju community health care center
    Chungju, ChoongBuk 123456, Korea, Republic of
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 11, 2016, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT01626716
Lead sponsor
National Clinical Research Coordination Center, Seoul, Korea
Responsible party
Hyeon Woo Yim (Professor, National Clinical Research Coordination Center, Seoul, Korea) — Principal investigator
First posted
Jun 25, 2012
Start date
Jun 2012
Primary completion
Dec 2013
Completion
Dec 2013
Last update
Mar 11, 2016
View the source record on ClinicalTrials.gov ↗

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This study is completed, as verified in Mar 2016. You cannot join it, but the record below documents what was studied.

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