New Rear Anti-tip Device for Manual Wheelchairs: Subjective Input (RAD-SI)
Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorNova Scotia Health Authority
About this trial
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.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
at least 18 years of age
willing to participate
alert
co-operative
Disqualifiers
None
Trial population
Local wheelchair service providers will be Occupational Therapists or Occupational Therapy Assistants. Global wheelchair service providers will be people who self-identify as wheelchair service providers. End-users will be wheelchair users and, for some, their caregivers.
Trial design
Design model
Cohort
Time perspective
Cross-sectional
Treatments tested in this trial
Local wheelchair service provider questionnaires
Other interventionThe 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 interventionThe 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 interventionThe 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.
Treatment groups
150 Participants
are divided into 3 treatment groupsGroup A: Local wheelchair service providers1 intervention
Group B: Global wheelchair service providers1 intervention
Group C: End-users1 intervention
Trial outcomes
Primary outcomes
1
Qualitative comments
For each of a set of problems that have been identified for conventional rear anti-tip devices and a set of potential uses for a new design, study participants will be asked for their subjective comments.
Time frame
By 12 monthsSecondary outcomes
1
Questions with categorical responses
For each of a set of problems that have been identified for conventional rear anti-tip devices , study participants will be asked questions for which there are Yes/No answers possible.
Time frame
By 12 months2
Questions with ordinal-scale answers
For each of a set of potential uses for a new design, study participants will be asked to provide a score from 1-5 on an ordinal scale of potential usefulness.
Time frame
By 12 monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
Source ClinicalTrials.gov
This trial is not recruiting at the moment. You can still explore other options: