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Completed

NCT Number: NCT00927706

Experimental Control Investigation of the Impact of Assistive Technology on the User-caregiver Dyad: a Multi-site Trial

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.

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Key information

Age range

65 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Simon Fraser University, Vancovuer, British Columbia, Canada

Loading trial locations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • 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.

Exclusion criteria

  • 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.

Treatment and study plan

Assistive technology updating and tune up intervention

Device

This intervention includes 4 components: 1) an in-residence assessment of the mobility preferences of the older person and his/her caregiver; 2) a detailed review of forms of assistance, technological and human, that are currently being used; 3) recommendations by an occupational therapist for possible changes in the older person's mobility assistive technology or assistance strategy; and 4) therapist negotiation of an mobility assistive technology updating and tune-up intervention plan with the individual and his or her caregiver.

Primary outcomes

  1. Assessment of Life Habits

    Time frame: baseline (1or 2 times), 6 weeks (immediately after intervention), 16 weeks later

  2. Caregivers: Caregiver Assistive Technology Outcome Measure

    Time frame: base line (1 or 2), 6 weeks (immediately after intervention), 16 weeks later

Secondary outcomes

  1. Individually Prioritized Problem Assessment

    Time frame: Baseline (1 or 2 times), Immediately after intervention, 16 weeks later

  2. Functional Autonomy Measurement System

    Time frame: Baseline (1 or 2 times), Immediately after intervention, 16 weeks later

  3. Psychological Impact of Assistive Devices Scale

    Time frame: Imediately after intervention. 16 weeks later

  4. Satisfaction with Personal Assistance Strategy

    Time frame: Baseline (1 or 2 times), Immediately after intervention, 16 weeks later

Sponsors and collaborators

Lead sponsor

Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal

Other

Registry information

Official study title

Experimental Control Investigation of the Impact of an Assistive Technology Updating and Tune up Intervention on the User-caregiver Dyad: a Multi-site Trial

Acronym: ATUTI

Important dates

Study start
2009
Primary completion
2011
Study completion
2011
First posted
Jun 25, 2009
Registry last updated
Feb 19, 2014

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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