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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00915109
Other study ID # CDHA-RS-2010-026
Secondary ID
Status Completed
Phase N/A
First received June 3, 2009
Last updated September 18, 2012
Start date June 2009
Est. completion date August 2012

Study information

Verified date September 2012
Source Nova Scotia Health Authority
Contact n/a
Is FDA regulated No
Health authority Canada: Health Canada
Study type Observational

Clinical Trial Summary

The purpose of this study is to evaluate whether there are quantifiable differences in walking stability, as measured by the acceleration of the trunk or the variation in step length, between people with unilateral below-knee amputations from vascular reasons or from trauma reasons.


Recruitment information / eligibility

Status Completed
Enrollment 50
Est. completion date August 2012
Est. primary completion date August 2012
Accepts healthy volunteers Accepts Healthy Volunteers
Gender Both
Age group 18 Years and older
Eligibility Inclusion Criteria:

- be over the age of 18;

- 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.

Study Design

Observational Model: Case Control, Time Perspective: Prospective


Related Conditions & MeSH terms


Locations

Country Name City State
Canada Nova Scotia Rehabilitation Centre Halifax Nova Scotia

Sponsors (1)

Lead Sponsor Collaborator
Kim Parker

Country where clinical trial is conducted

Canada, 

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