We updated the design of this site on September 25th. Learn more.
Show more
ClinicalTrials.gov
ClinicalTrials.gov Menu

Characterizing Ankle Function During Sloped Locomotion for Prosthesis Development

This study is currently recruiting participants.
Verified November 2016 by VA Eastern Colorado Health Care System
Sponsor:
ClinicalTrials.gov Identifier:
NCT01784003
First Posted: February 5, 2013
Last Update Posted: November 9, 2016
The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Know the risks and potential benefits of clinical studies and talk to your health care provider before participating. Read our disclaimer for details.
Information provided by (Responsible Party):
VA Eastern Colorado Health Care System
  Purpose
The proposed study aims to characterize biological ankle joint function during walking and running on slopes in order to further develop advanced powered ankle-foot prostheses. Ankle joint torque and angle data will be collected from non-amputees while walking and running at multiple speeds and slopes. This data will be used to develop control parameters for a powered ankle-foot prosthesis. Then, these parameters will be implemented and tested in a powered prosthesis worn by people with below the knee amputations.

Condition Intervention
Traumatic Amputation of Lower Extremity Device: Powered ankle-foot prosthesis

Study Type: Observational
Study Design: Time Perspective: Cross-Sectional
Official Title: Characterizing Ankle Function During Sloped Locomotion for Prosthesis Development

Resource links provided by NLM:


Further study details as provided by VA Eastern Colorado Health Care System:

Primary Outcome Measures:
  • Force-measuring treadmill and motion capture [ Time Frame: approximately 2 months ]
  • Metabolic analysis system [ Time Frame: approximately 2 months ]

Estimated Enrollment: 60
Study Start Date: June 2012
Estimated Study Completion Date: May 2018
Estimated Primary Completion Date: May 2017 (Final data collection date for primary outcome measure)
Groups/Cohorts Assigned Interventions
Non-amputee
People without an amputation will be recruited to participate in the study.
Below the knee amputee
People with a unilateral transtibial amputation will be recruited to participate in the study.
Device: Powered ankle-foot prosthesis

  Eligibility

Information from the National Library of Medicine

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.


Ages Eligible for Study:   18 Years to 45 Years   (Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   Yes
Sampling Method:   Probability Sample
Study Population
Study 1: Non-amputee Study 2: Unilateral transtibial amputee Study 3: Unilateral transtibial amputee Study 4: Non-amputee Study 5: Unilateral transtibial amputee
Criteria

Inclusion Criteria:

Study 1:

- Between 18-60 years old.

Study 2 and 3:

  • Between 18-60 years old.
  • At least 1 year post-amputation
  • no current problems with prosthesis or residual limb
  • At least a K3 level of ambulation

Study 4:

- Between 18-45 years old

Study 5:

  • Between 18-45 years old
  • At least 1 year post-amputation
  • no current problems with prosthesis or residual limb
  • Experience running with a passive prosthesis
  • At least a K4 level of ambulation

Exclusion Criteria:

Studies 1-5

  • Cardiovascular, pulmonary, or neurological disease or disorder
  • Musculoskeletal injury
  Contacts and Locations
Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01784003


Contacts
Contact: Alena Grabowski, PhD 303-492-5208 alena.grabowski@colorado.edu

Locations
United States, Colorado
University of Colorado Boulder Recruiting
Boulder, Colorado, United States, 80309
Contact: Alena Grabowski, PhD    303-492-5208    alena.grabowski@colorado.edu   
Principal Investigator: Alena Grabowski, PhD         
Sponsors and Collaborators
VA Eastern Colorado Health Care System
  More Information

Publications:
Responsible Party: VA Eastern Colorado Health Care System
ClinicalTrials.gov Identifier: NCT01784003     History of Changes
Other Study ID Numbers: A7972W
First Submitted: January 25, 2013
First Posted: February 5, 2013
Last Update Posted: November 9, 2016
Last Verified: November 2016

Additional relevant MeSH terms:
Amputation, Traumatic
Leg Injuries
Wounds and Injuries