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| Sponsor: | National Institute of Mental Health (NIMH) |
|---|---|
| Collaborator: |
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 |
| Study Type: | Interventional |
| Study Design: | Randomized, Open Label, Active Control, Parallel Assignment, Efficacy Study |
| Official Title: | Behavioral Intervention for Depression in Nursing Homes |
| Estimated Enrollment: | 40 |
| Study Start Date: | April 2002 |
| Study Completion Date: | August 2006 |
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 |
Inclusion Criteria:
Contacts and Locations| United States, Kentucky | |
| University of Louisville | |
| Louisville, Kentucky, United States, 40292 | |
| 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 |
| Study First Received: | March 14, 2003 |
| Last Updated: | January 16, 2008 |
| ClinicalTrials.gov Identifier: | NCT00056485 History of Changes |
| Health Authority: | United States: Federal Government |
|
Nursing homes Aging |
|
Depression Mental Disorders Mood Disorders Depressive Disorder Behavioral Symptoms |