- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT00817570
Evaluation of Balance Reactions of Transfemoral Amputees Using the Virtual Analysis System
October 21, 2009 updated by: Sheba Medical Center
Evaluation of Balance Reactions of Transfemoral Amputees Using the Virtual
The purpose of this study is to test and compare the balance reactions of Tranfemoral Amputees and able bodied subjects in response to perturbations given by a highly advanced Virtual Reality system.
Study Overview
Status
Suspended
Conditions
Study Type
Observational
Enrollment (Anticipated)
60
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
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Ramat- Gan, Israel
- Sheba Medical Center
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years to 60 years (Adult)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
Male
Sampling Method
Non-Probability Sample
Study Population
Transfemoral Amputees and Able bodied.
Description
Inclusion Criteria:
- Transfemoral Amputees, walking without any assistive device, at least one year.
Exclusion Criteria:
- Amputees who suffer from a Neurological Injury/ disease that has implication on balance control.
- Amputees who suffer from Orthopedic Injury that has implication on balance control.
- Amputees who suffer from Cardiology disease that has implication on balance reactions.
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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1
Transfemoral Amputees using the C- Leg knee.
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2
Transfemoral Amputees using a Multiaxial Knee.
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3
Able bodied.
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
April 1, 2009
Study Registration Dates
First Submitted
January 4, 2009
First Submitted That Met QC Criteria
January 5, 2009
First Posted (Estimate)
January 6, 2009
Study Record Updates
Last Update Posted (Estimate)
October 22, 2009
Last Update Submitted That Met QC Criteria
October 21, 2009
Last Verified
October 1, 2009
More Information
Terms related to this study
Other Study ID Numbers
- SHEBA-5610-08-IS-CTIL
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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