NCT00732329
Completed
Not Applicable
Effectiveness of an Optimized Home Based Occupational Therapy for Patients With Dementia.
ConditionsDementia
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Dementia
- Sponsor
- Technische Universität Dresden
- Enrollment
- 160
- Locations
- 3
- Primary Endpoint
- Alzheimer's Disease Cooperative Study/Activities of Daily Living
- Status
- Completed
- Last Updated
- 11 years ago
Overview
Brief Summary
The purpose of this study is to determine if a home based occupational therapy is effective in the treatment of dementia.
Investigators
Dr. Matthias Schützwohl
PD Dr.
Technische Universität Dresden
Eligibility Criteria
Inclusion Criteria
- •Dementia (according to DSM-IV TR)
- •A score 26 to 12 on the MMSE
- •Must be 55 or older
- •Patient is living at home or therapeutical flat sharing
- •Primary care giver at least 2 days / week available at home
- •Written informed consent from patient and care giver
- •German as dominant language
Exclusion Criteria
- •Other dementia (p.e. frontotemporal dementia, dementia with Lewy Bodies, Creutzfeldt-Jakob disease, Parkinson's disease or atypical Parkinson's syndromes
- •Dementia with relevant displaying behavioural problems (neuropsychiatric Inventory; NPI, Subscore ≥ 8)
- •Depressive episodes (Geriatric Depression Scale, GDS (short version) ≥ 6)
- •Mental disability
- •Home Based Occupational Therapy for Dementia within the last 6 months
- •Impairment of visual and/or acoustic cognition which does not allow Occupational Therapy
- •Apoplexy with movement disorders which does not allow Occupational Therapy
- •Severe physical/systemic illnesses (cardio-pulmonal, Hematological or metabolic) which do not allow participating
- •Recent history of addictive disorder
- •Intermittent intake of depressant medication, that likely causes an impairment of cognitive performance during the trial
Outcomes
Primary Outcomes
Alzheimer's Disease Cooperative Study/Activities of Daily Living
Time Frame: 2 weeks, 3 and 6 months after invention or 9, 19 and 31 weeks after randomization (treatment-as-usual-group)
Secondary Outcomes
- - for patients: cognitive performance, displaying behavioural problems, satisfaction with occupational therapy, costs of occupational therapy - for family care givers: burden, medical condition, life-satisfaction(2 weeks, 3 and 6 months after invention or 9, 19 and 31 weeks after randomization (treatment-as-usual-group))
Study Sites (3)
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