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Effect of Depressin Screening and Care Program at Community Health Center

This study has been completed.
Sponsor:
ClinicalTrials.gov Identifier:
NCT01626703
First Posted: June 25, 2012
Last Update Posted: March 10, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
Information provided by (Responsible Party):
Hyeon Woo Yim, National Clinical Research Coordination Center, Seoul, Korea
June 20, 2012
June 25, 2012
March 10, 2016
June 2012
December 2012   (Final data collection date for primary outcome measure)
Reuptake rate [ Time Frame: 12 weeks ]
Same as current
Complete list of historical versions of study NCT01626703 on ClinicalTrials.gov Archive Site
  • reduced depressive symptoms [ Time Frame: 12 weeks ]
    Geriatric Depression Scale Short Form (SGDS)
  • changed perceived heath status [ Time Frame: 12 weeks ]
    Visual Analogue Scale (VAS)
Same as current
Not Provided
Not Provided
 
Effect of Depressin Screening and Care Program at Community Health Center
Not Provided

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.

Not Provided
Interventional
Not Provided
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Double (Participant, Outcomes Assessor)
Primary Purpose: Screening
  • Depression
  • Screening
  • Elderly
Other: Reminding call
  • Experimental: intervention
    remiding call
    Intervention: Other: Reminding call
  • No Intervention: Control
    No intervention
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
86
March 2013
December 2012   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  • 60 or more
  • 10 or more in GDS scor

Exclusion Criteria:

  • severe cognitive problem
Sexes Eligible for Study: All
60 Years and older   (Adult, Senior)
No
Contact information is only displayed when the study is recruiting subjects
Korea, Republic of
 
 
NCT01626703
A102065_2012_2
Not Provided
Not Provided
Not Provided
Hyeon Woo Yim, National Clinical Research Coordination Center, Seoul, Korea
National Clinical Research Coordination Center, Seoul, Korea
Not Provided
Not Provided
National Clinical Research Coordination Center, Seoul, Korea
March 2016

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP