Autonomy Among Physically Frail Older People in Nursing Homes

Sponsor
University of Southern Denmark (Other)
Overall Status
Completed
CT.gov ID
NCT00783055
Collaborator
(none)
66
1
1
29
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Study Details

Study Description

Brief Summary

The purpose of this study is to assess the status of perceived autonomy and to evaluate the effectiveness of individually tailored programmes on perceived autonomy in physically frail older people living in nursing homes.

Condition or Disease Intervention/Treatment Phase
  • Other: Individually tailored programmes
N/A

Detailed Description

Experiencing autonomy is recognised to promote health and well-being for all age groups. Perceived lack of control has been found to be detrimental to physical and mental health. There is a lack of evidence-based knowledge elucidating how frail older people in nursing home settings perceive autonomy. Further, there are no studies on the extent to which this perception can be influenced positively by participating in an individually tailored programme based on individual wishes for daily activities.

The purpose of this study was to evaluate the effectiveness of individually tailored programmes on perceived autonomy in physically frail older people in nursing homes.

Study Design

Study Type:
Interventional
Actual Enrollment :
66 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Single (Investigator)
Primary Purpose:
Supportive Care
Official Title:
Autonomy Among Physically Frail Older People in Nursing Homes: a Study Protocol for an Intervention Study
Study Start Date :
Mar 1, 2005
Actual Primary Completion Date :
Aug 1, 2007
Actual Study Completion Date :
Aug 1, 2007

Arms and Interventions

Arm Intervention/Treatment
Experimental: Treatment

12 weeks of individually tailored intervention programmes based on participants individual wishes for daily activities e.g.ADL, mobility, social, mental or creative that they want to improve, conserve - and/or to revive.

Other: Individually tailored programmes
Individualised intervention programmes based on individual wishes for daily activities
Other Names:
  • activity
  • autonomy
  • Outcome Measures

    Primary Outcome Measures

    1. The Autonomy Sub-dimension [baseline, after 12 weeks, anfter 24 weeks]

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years and Older
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Aged 65 years or older

    • All kinds of diseases leading to physical frailty

    • Dependent on assistance in minimum one P-ADL activity

    • Able to understand verbal instructions

    • Willing to participate

    • Expected to live in the nursing home during the 24 weeks

    • Both men and women

    Exclusion Criteria:
    • Terminal stages of disease

    • MMSE-score below 16

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Centre of Applied and Clinical Excercise Sciences, Institute of Sports Science and Clinical Biomechanics, University of Southern Denmark Odense Denmark 5000

    Sponsors and Collaborators

    • University of Southern Denmark

    Investigators

    • Study Director: Lis Puggaard, PhD, University of Southern Denmark

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    , ,
    ClinicalTrials.gov Identifier:
    NCT00783055
    Other Study ID Numbers:
    • 2004-1-52G
    First Posted:
    Oct 31, 2008
    Last Update Posted:
    Oct 31, 2008
    Last Verified:
    Aug 1, 2008
    Keywords provided by , ,
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Oct 31, 2008