Evaluation of Physiological and Biomechanical Efficiency of the PAPAW
NCT ID: NCT02506712
Last Updated: 2020-09-04
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
44 participants
INTERVENTIONAL
2015-07-15
2017-10-01
Brief Summary
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Comparison of energy expenditure with and without the use of a system SmartDrive 6 minute propulsion test.
Comparison the risk of musculoskeletal disorders of the wrist during a 6 minute propulsion test.
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Detailed Description
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22 SCI manual wheelchair users. 22 caregivers (healthy subjects)
Conditions
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Study Design
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RANDOMIZED
CROSSOVER
OTHER
NONE
Study Groups
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spinal cord injury
use a wheelchair with and without a assisting device to power manuel wheelchair
SmartDrive assisting device
oxygen consumption
Standard manuel wheelchair
oxygen consumption
volunteer
push a wheelchair with and without a assisting device to power manuel wheelchair
SmartDrive assisting device
oxygen consumption
Standard manuel wheelchair
oxygen consumption
Interventions
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SmartDrive assisting device
oxygen consumption
Standard manuel wheelchair
oxygen consumption
Eligibility Criteria
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Inclusion Criteria
* spinal cord injury
* having given free and informed consent
Exclusion Criteria
* Refusal to participate in the clinical trial
* Patient under guardianship
* Major cognitive disorder
* Bedsores
* Acute complication or systemic organ
18 Years
70 Years
ALL
Yes
Sponsors
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Fondation Garches
OTHER
Centre d'Investigation Clinique et Technologique 805
OTHER
Responsible Party
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Principal Investigators
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Caroline Hugeron, PH
Role: PRINCIPAL_INVESTIGATOR
Raymond Poincaré Hospital
Locations
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hopital R Poincare
Garches, , France
Countries
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Other Identifiers
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2015-A00758-41
Identifier Type: -
Identifier Source: org_study_id
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