Effects of Community Occupational Therapy in Older Patients With Dementia and Their Caregivers.
|ClinicalTrials.gov Identifier: NCT00295152|
Recruitment Status : Unknown
Verified February 2006 by Radboud University.
Recruitment status was: Active, not recruiting
First Posted : February 22, 2006
Last Update Posted : November 17, 2011
|Condition or disease||Intervention/treatment|
|Community Occupational Therapy Dementia Patients Primary Caregivers of Dementia Patients||Behavioral: community occupational therapy in dementia|
- Objective To determine the effects of community occupational therapy on the daily performance of older patients with mild to moderate dementia and the sense of competence of their primary caregivers.
- design: a randomized controlled single-blind design is used with 3 measurement moments. We measure at baseline (before start of OT intervention), after 6 weeks (the effect measurement)and after 3 months after baseline (follow-up measurement).
- patients: 135 patients and their primary caregivers are needed to determine effects on the primary outcome measures of this intervention, with a power of 80% and alpha = 0.05/3. This power calculation is based on the outcomes of a pilot study (Graff, et al., 2003).
- intervention: 5 weeks client-centered community occupational therapy directed at both patients and primary caregivers using an OT guideline.The control group receives no OT intervention, but usual care.
- main outcome measures are: Assessment of Motor and Process Skills, Interview in Deterioration of Daily Activities in Dementia (IDDD)and Sense of Competence Questionnaire (SCQ)
- Analysis: analyses of covariance on intention-to-treat basis (Last Observation Carried Forward (LCOF))will be used to determine the effects of community OT on the daily performance of older patients with dementia and the sense of competence of their primary caregivers. Also secondary patients'and caregivers' health outcomes will be analyzed by analyses of covariance on intention-to-treat basis.
Cost-effectiveness: the costs of this OT intervention will also be determined and a cost-effectiveness analysis will be carried out.
3)Results: Results at baseline, at 6 weeks and at 3 months follow-up on primary outcome measures and on patients' and caregivers' secondary health outcomes and also the cost effectiveness of this intervention, will be analyzed and described in international publications.
|Study Type :||Interventional (Clinical Trial)|
|Estimated Enrollment :||135 participants|
|Intervention Model:||Factorial Assignment|
|Official Title:||Effects of Community Occupational Therapy on the Daily Performance of Older Patients With Mild to Moderate Dementia and on the Sense of Competence of Their Primary Caregivers.|
|Study Start Date :||April 2001|
|Estimated Study Completion Date :||February 2005|
- 1.process skills scores of the patients on the Assessment of Motor and Process Skills (AMPS);
- 2. performance scores in daily activities of the patients on the Interview of Deterioration in Daily Activities in Dementia (IDDD);
- 3. Sense of competence scores of the primary caregivers on the Sense of Competence Questionnaire (SCQ).
- 1. motor skills scores on the AMPS
- 2. initiative in performing daily activities on the IDDD
- 3. general health scores on the General Health Questionnaire (GHQ-12)
- 4.Quality of life scored on the Dementia Quality of Life Instrument (DQOL)
- 5. Self-perception scores in occupational performance and satisfaction scores with this performance, scored on the Canadian Occupational Performance Measurement (COPM)
- 6. Mood/depression scored on the Cornell Depression Scale (CDS)
- 1. mastery skills scored on the Mastery Scale
- 2. general health scores on the GHQ-12
- 3. quality of life scores on the DQOL
- 4. self-perception scores in occupational performance and satisfaction scores on the COPM
- 5. mood/depression scores on the Center for Epidemiologic Studies Depression Scales (Ces-D)
- 6. Copings skills scores on the JCS
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): NCT00295152
|Memory Clinic and Geriatic Department Radboud University Nijmegen Medical Centre|
|Nijmegen, Netherlands, PO Box 9101, 6500 HB|
|Principal Investigator:||Marcel GM Olde-Rikkert, PhD, MD||Department of Geriatrics Radboud University Nijmegen Medical Centre|