Effect of Depressin Screening and Care Program at Community Health Center

This study has been completed.

Sponsor:

Information provided by (Responsible Party):

Hyeon Woo Yim, National Clinical Research Coordination Center, Seoul, Korea

ClinicalTrials.gov Identifier:

NCT01626703

First received: June 20, 2012

Last updated: March 9, 2016

Last verified: March 2016

History of Changes

Purpose

Depression affect between 5% and 10% of older adults seen in the primary care setting.Late-life depression is often chronic or recurrent and is associated with substantial suffering, functional impairment, and diminished health-related quality of life.Depressed, older primary care patients are frequent users of general medical services and may have poor adherence to medical treatments.They are also at increased risk of death from suicide and medical illnesses. The aim of this study is to examine whether depression screening and health care practitioner feedback are increased depression treatment rate.

Depression screening is provided 60 or more who visited community health care center with a 15-item Geriatric Depression Scale.GDS scores of 10 or more were classified depression positive. Intervention group participants received twice remind calls from primary care nurse.

Condition	Intervention
Depression Screening Elderly	Other: Reminding call


Study Type:	Interventional
Study Design:	Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Parallel Assignment Masking: Double Blind (Subject, Outcomes Assessor) Primary Purpose: Screening

Further study details as provided by National Clinical Research Coordination Center, Seoul, Korea:

Primary Outcome Measures:

Reuptake rate [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]

Secondary Outcome Measures:

reduced depressive symptoms [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
Geriatric Depression Scale Short Form (SGDS)
changed perceived heath status [ Time Frame: 12 weeks ] [ Designated as safety issue: No ]
Visual Analogue Scale (VAS)


Enrollment:	86
Study Start Date:	June 2012
Study Completion Date:	March 2013
Primary Completion Date:	December 2012 (Final data collection date for primary outcome measure)

Arms	Assigned Interventions
Experimental: intervention remiding call	Other: Reminding call
No Intervention: Control No intervention

Eligibility


Ages Eligible for Study:	60 Years and older (Adult, Senior)
Genders Eligible for Study:	Both
Accepts Healthy Volunteers:	No

Criteria

Inclusion Criteria:

60 or more
10 or more in GDS scor

Exclusion Criteria:

severe cognitive problem

Contacts and Locations

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Please refer to this study by its ClinicalTrials.gov identifier: NCT01626703

Locations


Korea, Republic of
Chungju community health care center
Chungju, Choongbuk, Korea, Republic of, 123456

Sponsors and Collaborators

National Clinical Research Coordination Center, Seoul, Korea

More Information


Responsible Party:	Hyeon Woo Yim, professor, National Clinical Research Coordination Center, Seoul, Korea
ClinicalTrials.gov Identifier:	NCT01626703 History of Changes
Other Study ID Numbers:	A102065_2012_2
Study First Received:	June 20, 2012
Last Updated:	March 9, 2016
Health Authority:	Korea: Ministry of Health and Welfare

ClinicalTrials.gov processed this record on September 27, 2016

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