Trial record 58 of 3551 for:    Louisville | ( Map: United States )

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. Identifier: NCT00536406
Recruitment Status : Completed
First Posted : September 27, 2007
Last Update Posted : April 13, 2017
National Institute of Mental Health (NIMH)
Information provided by (Responsible Party):
Suzanne Meeks, University of Louisville

Brief Summary:
This study will evaluate whether a behavioral activities treatment program improves symptoms of depression in nursing home residents.

Condition or disease Intervention/treatment Phase
Depression Behavioral: BE-ACTIV Behavioral: Treatment as usual (TAU) Not Applicable

Detailed Description:

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
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Treatment
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

Resource links provided by the National Library of Medicine

MedlinePlus related topics: Nursing Homes

Arm Intervention/treatment
Experimental: A
Participants will receive the BE-ACTIV treatment
Behavioral: BE-ACTIV
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.

Primary Outcome Measures :
  1. Depression diagnosis and depressive symptoms as assessed by the Geriatric Depression Scale [ Time Frame: Measured at Weeks 12, 24, and 48 ]
  2. Functioning as assessed by the Dartmouth COOP Scales for Social Functioning [ Time Frame: Measured at Weeks 12, 24, and 48 ]

Secondary Outcome Measures :
  1. Staff attention [ Time Frame: Measured at Weeks 12, 24, and 48 ]
  2. Positive affect [ Time Frame: Measured at Weeks 12, 24, and 48 ]
  3. Activity participation [ Time Frame: Measured at Weeks 12, 24, and 48 ]
  4. Behavior problems [ Time Frame: Measured at Weeks 12, 24, and 48 ]
  5. Resident satisfaction [ Time Frame: Measured at Weeks 12, 24, and 48 ]

Information from the National Library of Medicine

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Ages Eligible for Study:   Child, Adult, Older Adult
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No

Inclusion Criteria:

  • Nursing home residents in long-term care beds with an expected stay of 3 months or more
  • Geriatric Depression Scale score of at least 11
  • Meets DSM-IV criteria for major depressive disorder or research diagnostic criteria for minor depressive disorder

Exclusion Criteria:

  • Mini Mental State Exam score below 14
  • Referred to hospice care for a terminal condition
  • Current unstable or terminal medical condition
  • Suicidal
  • Meets DSM-IV criteria for bipolar disorder

Information from the National Library of Medicine

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 identifier (NCT number): NCT00536406

United States, Kentucky
University of Louisville
Louisville, Kentucky, United States, 40292
Sponsors and Collaborators
University of Louisville
National Institute of Mental Health (NIMH)
Principal Investigator: Suzanne Meeks, PhD University of Louisville

Responsible Party: Suzanne Meeks, Principal Investigator, University of Louisville Identifier: NCT00536406     History of Changes
Other Study ID Numbers: R01MH074865 ( U.S. NIH Grant/Contract )
R01MH074865 ( U.S. NIH Grant/Contract )
First Posted: September 27, 2007    Key Record Dates
Last Update Posted: April 13, 2017
Last Verified: April 2017

Keywords provided by Suzanne Meeks, University of Louisville:
Nursing Homes

Additional relevant MeSH terms:
Depressive Disorder
Behavioral Symptoms
Mood Disorders
Mental Disorders