Improving Mood and Behavior in Assisted Living Residents Through Skills Training for Their Caregivers

Sponsor
University of Washington (Other)
Overall Status
Completed
CT.gov ID
NCT00255866
Collaborator
National Institute of Mental Health (NIMH) (NIH)
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Study Details

Study Description

Brief Summary

This study will develop a treatment program to reduce mood and behavior problems in assisted living residents who have dementia.

Condition or Disease Intervention/Treatment Phase
  • Behavioral: Skills training for the care of dementia patients
Phase 2/Phase 3

Detailed Description

Assisted living is rapidly becoming one of the most common methods of caring for older adults with dementia in long-term care. Over half of assisted living residents have dementia and many exhibit affective and behavioral problems related to the condition; residents' care and quality of life may suffer as a result of these problems. Despite the seriousness of this condition, interventions to teach direct care staff how to care for these residents are limited. This study will develop a program for teaching assisted living staff how to deal with the issues of patients with dementia and reduce mood and behavioral problems among this population.

Caregivers will be randomly assigned to attend skills training sessions as two 4-hour workshops, four 30 minute individual training sessions, or two 30 minute in-services. Training will focus on dementia, depression and anxiety, the incidence of behavior problems, and skills and techniques for alleviating care challenges associated with behavior problems. Caregivers will complete self-report scales and questionnaires at the beginning and at the end of the study; these measures will assess job satisfaction, reactions to resident behavioral problems, and job skills. Residents will also be recruited for this study; they will complete questionnaires about their depressive episodes, anxiety, behavioral problems, and quality of life at the beginning and at the end of the study.

Study Design

Study Type:
Interventional
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Official Title:
Improving Affect and Behavior in Assisted Living Residents
Study Start Date :
Jan 1, 2004
Actual Primary Completion Date :
Dec 1, 2006
Actual Study Completion Date :
Dec 1, 2006

Outcome Measures

Primary Outcome Measures

  1. Skills to effectively deal with resident behavioral problems []

Secondary Outcome Measures

  1. Resident depression, anxiety, behavioral problems, and quality of life []

Eligibility Criteria

Criteria

Ages Eligible for Study:
21 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes

Inclusion Criteria for Assisted Living Staff

  • Work in the assisted living residence for at least 6 months prior to study entry

  • Work in the assisted living residence at least 5 days a week, for at least 4 hours a day on day or afternoon-evening shifts

  • Provide direct care for at least 1 assisted living resident

  • Agree to attend all training sessions and complete assessment forms

  • Able to speak, read, and understand English at a 6th grade level

Inclusion Criteria for Assisted Living Residents:
  • Diagnosis of dementia

  • Identified by caregiving staff as having mood or behavioral problems

  • Have lived at the assisted living residence for at least 3 months prior to study entry

  • Have a family member with power of attorney

Exclusion Criteria for Assisted Living Residents:
  • Plan to receive medication for affective or behavioral problems during the study

  • History of alcohol or drug abuse

  • Have attempted suicide within 1 year prior to study entry

Contacts and Locations

Locations

Site City State Country Postal Code
1 University of Arkansas for Medical Sciences Little Rock Arkansas United States 72205
2 Rush University School of Nursing Chicago Illinois United States 60612

Sponsors and Collaborators

  • University of Washington
  • National Institute of Mental Health (NIMH)

Investigators

  • Principal Investigator: Linda Teri, PhD, University of Washington

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Linda Teri, Principal Investigator, University of Washington
ClinicalTrials.gov Identifier:
NCT00255866
Other Study ID Numbers:
  • 26082-ED
  • R21MH069651
  • DSIR 82-SEDR
First Posted:
Nov 21, 2005
Last Update Posted:
Dec 2, 2015
Last Verified:
Dec 1, 2013
Keywords provided by Linda Teri, Principal Investigator, University of Washington
Additional relevant MeSH terms:

Study Results

No Results Posted as of Dec 2, 2015