Evaluating a Behavioral Activities Treatment Program for Depressed Nursing Home Residents (BE-ACTIV)
|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.|
|ClinicalTrials.gov Identifier: NCT00536406|
Recruitment Status : Completed
First Posted : September 27, 2007
Last Update Posted : April 13, 2017
|Condition or disease||Intervention/treatment||Phase|
|Depression||Behavioral: BE-ACTIV Behavioral: Treatment as usual (TAU)||Not Applicable|
Depression is a common mental disorder that affects nearly half of all older people living in nursing homes. Depression can severely impact people's lives, causing them to often feel sad and hopeless, as well as affect people's sleep patterns, concentration, and energy levels. In addition, nursing homes are often understaffed and very busy, making it difficult for older people with depression to receive a proper diagnosis and adequate treatment. Recent studies have shown that an increase in pleasurable activities among residents in nursing homes can improve symptoms of depression. The purpose of this study is to determine whether symptoms of depression can be reduced by increasing opportunities for nursing home residents to engage in pleasant events and build better relationships with nursing home staff members.
Participating nursing homes will be randomly assigned to have their residents receive behavioral activity treatment (BE-ACTIV) or treatment as usual for 12 weeks. Potential participating nursing home residents will complete two brief tests regarding memory, attention, and symptoms of depression. An hour-long interview will then be conducted during which eligible participating residents will discuss their symptoms of depression, rate their health and level of functioning, and assess the quality of their relationship with a staff member. Residents receiving BE-ACTIV will meet with a therapist for weekly 30-minute sessions for 10 weeks. During these sessions, residents will discuss their activity participation and any pleasant events that they recently experienced. Therapists and nursing home activities staff will work together to incorporate more activities of interest into each resident's schedule. Residents of nursing homes assigned to receive treatment as usual will be asked to rate their mood once a week for 10 weeks. Researchers will observe each resident, regardless of treatment group, for 5-minute intervals at various times during the study to assess mood and activity levels. All participating residents will undergo a second interview after 10 weeks to discuss any changes or improvements in mood, symptoms of depression, activity level, or their relationship with staff members. All participating residents will be assessed after 3 months and again after 6 months post-treatment to determine whether the BE-ACTIV program was successful in improving symptoms of depression.
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||20 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Single (Outcomes Assessor)|
|Official Title:||BE-ACTIV: Treating Depression in Nursing Homes|
|Study Start Date :||August 2007|
|Actual Primary Completion Date :||July 2013|
|Actual Study Completion Date :||November 2013|
Participants will receive the BE-ACTIV treatment
BE-ACTIV is 10-week behavioral treatment involving increasing pleasant events.
Active Comparator: B
Participants will receive treatment as usual
Behavioral: Treatment as usual (TAU)
TAU includes usual treatment in nursing care facility.
- Depression diagnosis and depressive symptoms as assessed by the Geriatric Depression Scale [ Time Frame: Measured at Weeks 12, 24, and 48 ]
- Functioning as assessed by the Dartmouth COOP Scales for Social Functioning [ Time Frame: Measured at Weeks 12, 24, and 48 ]
- Staff attention [ Time Frame: Measured at Weeks 12, 24, and 48 ]
- Positive affect [ Time Frame: Measured at Weeks 12, 24, and 48 ]
- Activity participation [ Time Frame: Measured at Weeks 12, 24, and 48 ]
- Behavior problems [ Time Frame: Measured at Weeks 12, 24, and 48 ]
- Resident satisfaction [ Time Frame: Measured at Weeks 12, 24, and 48 ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT00536406
|United States, Kentucky|
|University of Louisville|
|Louisville, Kentucky, United States, 40292|
|Principal Investigator:||Suzanne Meeks, PhD||University of Louisville|