Autonomy Among Physically Frail Older People in Nursing Homes
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ClinicalTrials.gov Identifier: NCT00783055 |
Recruitment Status :
Completed
First Posted : October 31, 2008
Last Update Posted : October 31, 2008
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Condition or disease | Intervention/treatment | Phase |
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Frailty | Other: Individually tailored programmes | Not Applicable |
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 Type : | Interventional (Clinical Trial) |
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 : | March 2005 |
Actual Primary Completion Date : | August 2007 |
Actual Study Completion Date : | August 2007 |

Arm | Intervention/treatment |
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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.
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Other: Individually tailored programmes
Individualised intervention programmes based on individual wishes for daily activities
Other Names:
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- The Autonomy Sub-dimension [ Time Frame: baseline, after 12 weeks, anfter 24 weeks ]

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Ages Eligible for Study: | 65 Years and older (Older Adult) |
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

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): NCT00783055
Denmark | |
Centre of Applied and Clinical Excercise Sciences, Institute of Sports Science and Clinical Biomechanics, University of Southern Denmark | |
Odense, Denmark, 5000 |
Study Director: | Lis Puggaard, PhD | University of Southern Denmark |
Responsible Party: | Mette Andresen/Senior Lecturer & PhD student, The University of Southern Denmark |
ClinicalTrials.gov Identifier: | NCT00783055 |
Other Study ID Numbers: |
2004-1-52G |
First Posted: | October 31, 2008 Key Record Dates |
Last Update Posted: | October 31, 2008 |
Last Verified: | August 2008 |
Autonomy Older people Physically frail Nursing home Intervention study |
Frailty Pathologic Processes |