ACTRN12618001463268
Withdrawn
未知
Effectiveness of home-based occupational therapy to optimise performance in daily occupations for adults with both Down syndrome and dementia, and reduce caregiving strain for their informal caregivers: a single-case experimental design study
niversity of South Australia0 sites6 target enrollmentAugust 30, 2018
Overview
- Phase
- 未知
- Intervention
- Not specified
- Conditions
- Not specified
- Sponsor
- niversity of South Australia
- Enrollment
- 6
- Status
- Withdrawn
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •1\) Inclusion criteria for participants with both Down syndrome and dementia:
- •\-Confirmed medical diagnosis of both Down syndrome and dementia.
- •\-Report of requiring assistance with daily activities, which includes self\-care, productivity and leisure (Creek \& Lawson\-Porter, 2010\).
- •\-Living within the metropolitan area of Adelaide.
- •\-Living in their own homes with their informal caregiver(s) or residing in close proximity to informal caregiver(s) who provide daily care and support.
- •\-English speaking or if informal caregiver could speak English.
- •\-Provides verbal consent to participate if capable.
- •2\) Inclusion criteria for informal caregiver participants:
- •\-Participants consider themselves as informal caregiver for the person with both Down syndrome and dementia.
- •\-Who provide continuing daily care and support to their family member with both Down syndrome and dementia.
Exclusion Criteria
- •Exclusion criteria for participants with both Down syndrome and dementia :
- •\-Pre\-existing diagnosis of mental health issues (e.g. Depression or anxiety), as it may mask the clinical problems related to dementia..
- •\-Having an active Occupational Therapy or Physiotherapy interventions for dementia prior to or during the study.
- •\-Not living within the metropolitan area of Adelaide.
- •\-Does not consent to the study.
- •2\) Exclusion criteria for informal caregiver participants:
- •\-Does not consent to the study.
Outcomes
Primary Outcomes
Not specified
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