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
18 participants
INTERVENTIONAL
2016-09-30
2017-05-31
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NON_RANDOMIZED
PARALLEL
DIAGNOSTIC
NONE
Study Groups
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paraplegic
Well-trained participants with a spinal cord injury (\<Th1) were included in this group.
upper-body double-poling
An incremental peak test to exhaustion and four 5-min submaximal stages were performed in the upper-body double-poling mode.
arm crank ergometry
An incremental peak test to exhaustion and four 5-min submaximal stages were performed in the arm crank ergometry mode.
able bodied
Upper-body trained, able-bodied participants were included in this group.
upper-body double-poling
An incremental peak test to exhaustion and four 5-min submaximal stages were performed in the upper-body double-poling mode.
arm crank ergometry
An incremental peak test to exhaustion and four 5-min submaximal stages were performed in the arm crank ergometry mode.
Interventions
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upper-body double-poling
An incremental peak test to exhaustion and four 5-min submaximal stages were performed in the upper-body double-poling mode.
arm crank ergometry
An incremental peak test to exhaustion and four 5-min submaximal stages were performed in the arm crank ergometry mode.
Eligibility Criteria
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Inclusion Criteria
* well upper-body-trained participants with or without paraplegia
Exclusion Criteria
18 Years
50 Years
ALL
No
Sponsors
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St. Olavs Hospital
OTHER
Norwegian University of Science and Technology
OTHER
Responsible Party
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Principal Investigators
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Jorunn Helbostad, phd prof
Role: STUDY_DIRECTOR
Dept of Neuromedicine and Movement Science, Norwegian University of Science and Technology
Locations
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Centre for Elite Sports Research
Trondheim, , Norway
Countries
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Other Identifiers
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2015/2008
Identifier Type: -
Identifier Source: org_study_id