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
50 participants
OBSERVATIONAL
2009-06-30
2012-08-31
Brief Summary
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Detailed Description
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Conditions
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Keywords
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Study Design
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CASE_CONTROL
PROSPECTIVE
Study Groups
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vascular
People with a unilateral below-knee amputations due to a vascular reason
No interventions assigned to this group
nonvascular
People with a below-knee amputation due to nonvascular reasons
No interventions assigned to this group
Control
People with no gait impairments.
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* be able to walk comfortably for a minimum of two (2) minutes;
* be willing to take part in the study, including signing the consent after carefully reading it;
* be able to read and understand English and follow verbal and visual instructions;
* are competent to give informed consent or have a proxy with power of attorney.
* have an unilateral, transtibial amputation;
* been fitted with a prosthesis for over six weeks.
18 Years
ALL
Yes
Sponsors
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Kim Parker
OTHER
Responsible Party
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Kim Parker
Rehabilitation Engineer
Locations
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Nova Scotia Rehabilitation Centre
Halifax, Nova Scotia, Canada
Countries
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Other Identifiers
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CDHA-RS-2010-026
Identifier Type: -
Identifier Source: org_study_id