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OpenTrials
Completed

NCT Number: NCT01347138

Health Care Management for the Elderly in Community Through Screening

Depression in late life has been associated with losses in functioning and quality of life, mortality, and increased health care costs. Although late life depression can be successfully treated with antidepressant medication or psychotherapy, few older adults receive adequate trials of such treatment in community in Korea. Barriers, such as loss of loved ones, medical illnesses, and social stigma associated with depression, lack of social and financial support, to effective treatment of depression can be especially problematic for older adult. Screening has been valuable in overcoming barriers to diagnosis. Over 60 year old community dwelling people will be screened for symptoms of four geriatric conditions (depression, dementia, urinary incontinence, and sleep disorder). Those who will be screened positive for each condition will be refer to clinic for diagnosis. Among them only those cases confirmed as depression by psychiatrists will be enrolled in this study. Enrolled patients will be randomly assigned to either case management or usual care conditions.

The objective of the study is to test whether a system of screening, assessment, and follow-up provided by case manager improves in recognizing the target geriatric conditions (depression, dementia, urinary incontinence, and sleep disorder) and healthcare outcomes.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

City of Choongju public health center

Choongju, Choongchungbuk-Do, South Korea

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • over 60 year old
  • having medicare insurance

Exclusion criteria

  • dementia and other psychiatric disorders

Treatment and study plan

Case management

Other

confirmation of hospital visit date, checking the adverse effect and treatment compliance

Primary outcomes

  1. Geriatric Depression Score

    Time frame: 6 months after baseline

Secondary outcomes

  1. quality of life

    Time frame: 6 months after baseline

  2. treatment compliance

    Time frame: 6 months after baseline

  3. suicide ideation

    Time frame: 6 months after baseline

Sponsors and collaborators

Lead sponsor

National Clinical Research Coordination Center, Seoul, Korea

Other Gov

Registry information

Important dates

Study start
2011
Primary completion
2012
Study completion
2012
First posted
May 4, 2011
Registry last updated
Mar 11, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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