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Treatment of Depression in Nursing Homes

This study has been completed.

Sponsors and Collaborators: National Institute of Mental Health (NIMH)
University of Louisville
Information provided by: National Institute of Mental Health (NIMH)
ClinicalTrials.gov Identifier: NCT00056485
  Purpose

This study will implement a treatment for depression in a nursing home setting.


Condition Intervention Phase
Depression
Behavioral: Pleasant Events-Based Behavioral Intervention
Phase I

MedlinePlus related topics:   Depression    Nursing Homes   

U.S. FDA Resources

Study Type:   Interventional
Study Design:   Other, Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study
Official Title:   Behavioral Intervention for Depression in Nursing Homes

Further study details as provided by National Institute of Mental Health (NIMH):

Estimated Enrollment:   40
Study Start Date:   April 2002
Study Completion Date:   August 2006

Detailed Description:

Depression in long-term care facilities is a significant public health issue. Up to 50% of nursing home residents are affected by significant depressive symptoms. The decreased health and limited cognitive ability of many nursing home residents makes treatment and research extremely challenging. This study will attempt to identify and implement treatments for depressed nursing home residents.

Participants are randomly assigned to receive either an active intervention or treatment as usual for 6 weeks. The active intervention is followed by 4 weeks of maintenance. The intervention is implemented primarily by existing nursing facility staff and focuses on increasing opportunities for residents to experience pleasant events through increased levels of activity and positive affect. The maintenance treatment involves incorporation of protocol-based activities into patient care plans. Patients have a follow-up visit 12 weeks after the study. Psychiatric evaluations, depression and mood rating scales, observed affect and activity participation, behavior problems, and staff burden are assessed.

  Eligibility
Ages Eligible for Study:   60 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No

Criteria

Inclusion Criteria:

  • Nursing home residents
  • DSM-IV criteria for major depressive disorder or dysthymia or Research Diagnostic Criteria for minor depressive disorder with current Geriatric Depression Scale scores > 11 and Mini Mental State scores >= 14
  Contacts and Locations

Please refer to this study by its ClinicalTrials.gov identifier: NCT00056485

Locations
United States, Kentucky
University of Louisville    
      Louisville, Kentucky, United States, 40292

Sponsors and Collaborators

Investigators
Principal Investigator:     Suzanne Meeks, PhD     University of Louisville    
  More Information

Responsible Party:   University of Louisville ( Suzanne Meeks, Ph.D., Professor )
Study ID Numbers:   R21 MH63073, DSIR GT-GS
First Received:   March 14, 2003
Last Updated:   January 16, 2008
ClinicalTrials.gov Identifier:   NCT00056485
Health Authority:   United States: Federal Government

Keywords provided by National Institute of Mental Health (NIMH):
Nursing homes  
Aging  

Study placed in the following topic categories:
Depression
Mental Disorders
Mood Disorders
Depressive Disorder
Behavioral Symptoms

ClinicalTrials.gov processed this record on September 05, 2008




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