Experimental Control Investigation of the Impact of Assistive Technology on the User-caregiver Dyad: a Multi-site Trial
- Conditions
- Mobility Limitations
- Interventions
- Device: Assistive technology updating and tune up intervention
- Registration Number
- NCT00927706
- Lead Sponsor
- Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal
- Brief Summary
The purpose of this study is to determine the effectiveness of an assistive technology updating and tune up intervention on users and their caregivers. This intervention includes 4 components:
* an in-residence assessment of the mobility preferences of the older person and his/her caregiver
* a detailed review of forms of assistance, technological and human, that are currently being used
* recommendations by an occupational therapist for possible changes in the older person's mobility assistive technology or assistance strategy
* therapist negotiation of an mobility assistive technology updating and tune-up intervention plan with the individual and his or her caregiver. The intervention is provided to the immediate treatment following the administration of baseline measures and the delayed intervention group six weeks later, after an additional baseline measurement. The treatment is six weeks long and the follow-up is 26 weeks.
Hypothesis 1: For community-dwelling older people, an intervention that increases the appropriateness of existing or new assistive technology(AT) for mobility or self-care will alter established patterns of human assistance, such that caregiver burden is reduced or eliminated.
Hypothesis 2: At the same time, AT users will report less difficulty in mobility or self-care, as well as enhanced subjective well-being, and satisfaction with their modified personal assistance strategy.
Hypothesis 3: Following the AT intervention, caregivers will report reduced physical and/or psychological demands and increased satisfaction with their caregiving-related activities compared with
* the pre-intervention period
* caregivers in a delayed intervention control group. Hypothesis 4: Decreased physical and/or psychological demands on helpers will be associated with increases in device users' satisfaction with their personal assistance strategies.
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 88
- Users: Aged 65 years and over
- Have moderate to severe disability that limits their ability to move from place to place independently and/or to perform self-care activities.
- Living at home
- Receiving 2 or more hour per week of assistance with mobility and/or self-care activities from a non-professional, caregiver who is also willing to take part in the study.
- Those caregivers will be adults aged 18 years and over.
- Assistive technology users will be excluded if they have severe aphasia, are currently on a community occupational therapist caseload, or are unable to communicate in English or French.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Immediate intervention Assistive technology updating and tune up intervention Subjects and their caregivers randomized to this arm receive the intervention immediately after baseline data is collected. Delayed Intervention Assistive technology updating and tune up intervention Subjects and their caregivers who are randomized to this group will receive the intervention after baseline measurements are administered twice (6 weeks apart).
- Primary Outcome Measures
Name Time Method Assessment of Life Habits baseline (1or 2 times), 6 weeks (immediately after intervention), 16 weeks later Caregivers: Caregiver Assistive Technology Outcome Measure base line (1 or 2), 6 weeks (immediately after intervention), 16 weeks later
- Secondary Outcome Measures
Name Time Method Functional Autonomy Measurement System Baseline (1 or 2 times), Immediately after intervention, 16 weeks later Psychological Impact of Assistive Devices Scale Imediately after intervention. 16 weeks later Individually Prioritized Problem Assessment Baseline (1 or 2 times), Immediately after intervention, 16 weeks later Satisfaction with Personal Assistance Strategy Baseline (1 or 2 times), Immediately after intervention, 16 weeks later
Trial Locations
- Locations (4)
the Centre de santé et des services sociaux de Laval
🇨🇦Montreal, Quebec, Canada
Simon Fraser University
🇨🇦Vancovuer, British Columbia, Canada
the Centre de santé et des services sociaux Cavendish
🇨🇦Montreal, Quebec, Canada
Centre de santé et des services sociaux de Bordeaux-Cartierville--St-Laurent
🇨🇦Montreal, Quebec, Canada