Improving Mobility and Function Following Transfemoral Amputation: A Novel Approach to Reverse Volumetric Muscle Loss

Description

The purpose of this study is to investigate the relationship between thigh strength and walking ability and assess if using a blood pressure cuff on the leg improves strength and walking performance.

Conditions

Traumatic Amputation of Lower Extremity

Study Overview

Study Details

Study overview

The purpose of this study is to investigate the relationship between thigh strength and walking ability and assess if using a blood pressure cuff on the leg improves strength and walking performance.

Improving Mobility and Function Following Transfemoral Amputation: A Novel Approach to Reverse Volumetric Muscle Loss

Improving Mobility and Function Following Transfemoral Amputation: A Novel Approach to Reverse Volumetric Muscle Loss

Condition
Traumatic Amputation of Lower Extremity
Intervention / Treatment

-

Contacts and Locations

Chicago

UIC Physical Therapy Faculty Practice, Chicago, Illinois, United States, 60608

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.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • * At least 18 years old
  • * History of lower limb unilateral transfemoral amputation.
  • * At least two years post lower limb amputation
  • * Able to ambulate independently without the use of aids (i.e., walking cane).
  • * Able to walk at least 10 minutes continuously without stopping.
  • * Has a safe residuum with no open wounds on either the residual or intact limb.
  • * Has a prosthetic limb with materials that are sound and safe to withstand the mobility requirements of the study.
  • * Younger than 18 years old.
  • * Inability to give informed consent.
  • * Neurological disorder that affects gait.
  • * Participants with significant metal (greater than one orthopaedic screw) in either the residual limb or the sound/intact limb
  • * Participants who begin taking medications or change dosage of medications that could affect gait, balance, and cardiovascular function during the course of the study.
  • * Currently pregnant (or intend to become pregnant while participating in study).
  • * History of any condition where fatiguing contractions or resisted leg contractions are contraindicated.
  • * Blood clots in the leg, or any condition in which compression of the thigh or transient ischemia is contraindicated (e.g. open wounds in the leg).
  • * History of uncontrolled hypertension.
  • * History of heart failure.
  • * Head injury within the previous 6 months.
  • * Seizure disorder.
  • * History of vascular disease.
  • * History of thrombosis.
  • * History of sickle cell trait.
  • * History of genetic disease

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

University of Illinois at Chicago,

Lindsay Slater, PRINCIPAL_INVESTIGATOR, University of Illinois at Chicago

Study Record Dates

2027-12-31