Comparison of User Experience With Wheelsoft Wheels Intalled on a Wheelchair Compared With Normal Wheels.
NCT ID: NCT02925910
Last Updated: 2018-02-28
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
24 participants
INTERVENTIONAL
2017-02-01
2018-02-10
Brief Summary
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
SINGLE
Study Groups
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softwheels at second round
Begining with regular wheelchair for 2 days and then changing for shock absorbing wheelchair for 2 days
Shock absorbing wheelchair
2 randomised groups will try the softwheel wheelchair compare to regular one, but in different order.
softwheels at first round
starting with Shock absorbing wheelchair for 2 days and then changing for regular wheelchair for 2 days
Shock absorbing wheelchair
2 randomised groups will try the softwheel wheelchair compare to regular one, but in different order.
Interventions
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Shock absorbing wheelchair
2 randomised groups will try the softwheel wheelchair compare to regular one, but in different order.
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
Exclusion Criteria
* over 95 kg of weight (wheel limit)
18 Years
ALL
No
Sponsors
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HaEmek Medical Center, Israel
OTHER
Responsible Party
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Principal Investigators
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uriel giwnewer, MD
Role: PRINCIPAL_INVESTIGATOR
haemek medical center
Locations
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haemek MC
Afula, , Israel
Countries
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Other Identifiers
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115-16emc
Identifier Type: -
Identifier Source: org_study_id
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