New Rear Anti-tip Device for Manual Wheelchairs: Subjective Input (RAD-SI)

Sponsor
Nova Scotia Health Authority
Study ID
NCT06831240
Status
Not Yet Recruiting

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Conditions

  • Amputation
  • Caregivers
  • Spinal Cord Injury
  • Stroke
  • Wheelchair Service Providers
  • Wheelchair Users

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Accepted

Interventions

  • Local wheelchair service provider questionnaires — OTHER
    The local wheelchair service providers will complete a questionnaire that includes demographic data, to allow us to describe the sample, and a questionnaire about rear anti-tip devices for manual wheelchairs.
  • Global wheelchair service provider questionnaires — OTHER
    The global wheelchair service providers will complete a questionnaire that includes demographic data, to allow us to describe the sample, and a questionnaire about rear anti-tip devices for manual wheelchairs.
  • End-users questionnaires — OTHER
    The end-users will complete a questionnaire that includes demographic and clnical data, to allow us to describe the sample, and a questionnaire about rear anti-tip devices for manual wheelchairs.

Study Details

The objective of this study is to obtain subjective input from wheelchair service providers and end-users about their experiences with conventional rear anti-tip devices (C-RADs) of manual wheelchairs and the potential usefulness of a new design.

Key Dates

First listed
Feb 18, 2025
Start date
Apr 15, 2025
Status verified
Feb 2025
Primary completion
Apr 14, 2026
Completion
Apr 14, 2026

Study Design

Enrollment
150 participants (estimated)

Arms

  • Arm: Local wheelchair service providers
    Wheelchair service providers will be Occupational Therapists or Occupational Therapy Assistants for the focus groups.
  • Arm: Global wheelchair service providers
    For the online survey, participants will be people who self-identify as wheelchair service providers.
  • Arm: End-users
    For end-users, we will study wheelchair users, in some cases with their caregivers.

Primary Outcome Measure

Qualitative comments [ Time Frame: By 12 months ]

Central Contacts

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