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Evaluation of a Power Assistance Device for Wheelchair-DUO

Evaluation of a Power Assistance Device for Wheelchair-DUO

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03386799
Acronym
EVALDUO
Enrollment
27
Registered
2017-12-29
Start date
2018-03-20
Completion date
2021-04-21
Last updated
2022-07-12

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hemiplegia, Paraplegia

Keywords

Power assistance device, Wheelchair

Brief summary

Power assisted wheelchairs have specific advantages compared to manual propelled or powered Wheelchair. Autonomad Mobility has developed a new device (DUO), the assistance being triggered by the motion of the wheelchair and not an push on the hand rim, people who use their foot to move or people pushing the wheelchair can be helped by the device as people propelling the wheelchair with their arms. Furthermore DUO has an option with a longer assistance (AEP+) which can be preferred by some people. To be referenced and reimbursed by the French health insurance, DUO has to be compared with an other power assistance device for wheelchairs, already referenced. The study is a comparative study between DUO and the ALBER E Motion. Each patient is his own control and is assessed in 4 experimental conditions, with intervals of 3 or 4 days, manually propelled, with the E mtion device, with the DUO device and the single push configuration, with the DUO device and the AEP+ configuration. The main outcome measure will be the user's satisfaction (using 8 items of the ESAT questionnaire)

Interventions

DEVICEE-motion device

Powered assisted Wheelchair with the E-motion device. Outdoor and indoor runs

Sponsors

University Hospital, Lille
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* with a motor deficiency (of any origin) needing a manual wheelchair * propelling his wheelchair with both arms or with one foot and one arm. * covered by the French national health insurance. * living at less than 30km form the investigation center

Exclusion criteria

* subject of a guardianship or tutelage measure * owning already a power wheelchair or a powered assisted wheelchair * with cognitive impairments that affect the steering capacity or the understanding of the instructions. * Patient unable to use a manual wheelchair indoor without help, * Contraindication in keeping a seating position especially the occurrence of ulcers.

Design outcomes

Primary

MeasureTime frameDescription
ESAT questionnaireat 12 daysUser satisfaction, using 8 items of the ESAT (Echelle de Satisfaction envers une Aide Technique) questionnaire

Secondary

MeasureTime frameDescription
Success rate during the indoor test (wheelchair skill program)at 12 days
Time to perform the wheelchair skill programat 12 days
Time runat 12 daysDuring a 500 m outdoor run
Maximal heart rateat 12 daysDuring a 500 m outdoor run
Effort assessment by the Borg scaleat 12 daysDuring a 500 m outdoor run The 10-point Borg scale ranges from 0 nothing at all to 10 maximal/extremely strong and will be used to rate the intensity of dyspnea

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026