Performance Developement of Patients With Paraplegia During First Rehabilitation
NCT ID: NCT03405558
Last Updated: 2023-03-13
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
14 participants
OBSERVATIONAL
2018-01-01
2023-01-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Interventions
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No intervention
As this is an observational study, we will only supervise testing and training sessions which were performed anyway during first rehabilitation as daily therapeutic routine
Eligibility Criteria
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Inclusion Criteria
* male or female, paraplegia (AIS A-C, lesion Level Th1-Th12)
* Age 18-65 years
* Manual wheelchair user
* Patient during first rehabilitation
Exclusion Criteria
* unable to use an arm-crank Ergometer due to e.g. spasticity
* physical impairment, which makes it impossible to perform an arm-crank ergometry
* Progressive disease (g.g. tumor, MS)
* Ventilator dependent
* existing cardiopulmonary disease
* Unstable medical situation
18 Years
65 Years
ALL
Yes
Sponsors
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Swiss Paraplegic Research, Nottwil
NETWORK
Responsible Party
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Principal Investigators
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Claudio Perret
Role: PRINCIPAL_INVESTIGATOR
Swiss Paraplegic Research, Nottwil
Locations
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Swiss Paraplegic Centre
Nottwil, Canton of Lucerne, Switzerland
Countries
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Other Identifiers
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2017-01
Identifier Type: -
Identifier Source: org_study_id
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