A Comparison of External Mechanical Work Between Different Prosthetic Feet (SEW)

This study has been completed.
Sponsor:
Information provided by:
Miami VA Healthcare System
ClinicalTrials.gov Identifier:
NCT01340807
First received: April 19, 2011
Last updated: April 22, 2011
Last verified: February 2011

April 19, 2011
April 22, 2011
March 2008
January 2010   (final data collection date for primary outcome measure)
Symmetry in External Work [ Time Frame: up to 12 weeks ] [ Designated as safety issue: No ]
Work done by the intact and prosthetic limb
Same as current
Complete list of historical versions of study NCT01340807 on ClinicalTrials.gov Archive Site
Self Report and Performance Based Assessment Instruments [ Time Frame: up to 12 weeks ] [ Designated as safety issue: No ]
PEQ-13, LCI-5, AMPPRO, 6MWT, and SAM.
Same as current
Not Provided
Not Provided
 
A Comparison of External Mechanical Work Between Different Prosthetic Feet
A Comparison of External Mechanical Work Between Bionic and Conventional Prosthetic Feet in Transtibial Amputees During Functional Activities

Recent dysvascular and diabetic amputees as well as older, long-term traumatic amputees are at risk of functional decline, joint degeneration, skin breakdown and further limb loss due to the forces placed on the contralateral limb through prosthetic ambulation. If specialized prosthetic gait training and proper use of the appropriate prosthetic foot can decrease forces on the intact limb, the long term health and quality of life of veterans with amputations could be substantially improved. We will address two key questions:

Key Question 1: After receiving specialized gait training and a new prosthetic socket, will subjects demonstrate differences in gait symmetry and external mechanical work between the bionic and conventional prosthetic feet, while performing various functional activities.

Key Question 2: Can external mechanical work be used as a clinically friendly measure to differentiate between prosthetic feet?

The study examined the application of outcome measures to determine changes in function of unilateral transtibial amputees (TTAs) caused by specialized functional prosthetic training (training) and the use of four different prosthetic feet. Two self-report measures i.e. the Prosthetic Evaluation Questionnaire (PEQ-13) and Locomotor Capability Index (LCI-5), and three performance-based measures i.e. the Amputee Mobility Predictor (AMPPRO), Six-minute Walk Test (6MWT), and Step Activity Monitor (SAM) were utilized. Healthy unilateral Transtibial Amputees between the age of 40-65 will participate in the study. Subjects were tested at baseline, after receiving training with their existing prosthesis, and with the study socket and four prosthetic feet i.e. SACH, SAFE, Talux and PROPRIO FOOT over an 8-10 week period. Training was administered between testing sessions.

Interventional
Not Provided
Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: Open Label
Primary Purpose: Treatment
Traumatic Amputation of Lower Extremity
Other: Specialized Functional Prosthetic Training
Each subject receives specialized functional prosthetic training
Other Name: Proshetic Feet
Experimental: Prosthetic Feet
Randomized to 4 different prosthetic feet (SACH, SAFE, TALUX, and Proprio Foot)
Intervention: Other: Specialized Functional Prosthetic Training
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
15
January 2011
January 2010   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Males and/or Females between the ages of 40 and 65. b. People with unilateral transtibial amputations for vascular reasons or from traumatic events.

    c. At the lowest level of function candidates will have the ability to use a prosthesis for ambulation on level surfaces at a fixed cadence.

    d. People with a diagnosis of diabetes mellitus and/or peripheral vascular disease leading to amputation or people who have been amputated as a result of trauma.

    e. People comfortably fitted with a prosthesis for a period of at least 6 months.

    f. Candidates who score within the range of 29 to 47 on the Amputee Mobility Predictor which would indicate that subjects achieved the minimum required score to be fitted with a prosthesis.

    g. Able to tolerate the testing protocol and would not fatigue at any time during testing.

    h. Men's shoe size should be between 7.5 (25 cm) and 12.5 (29 cm). i. Women's shoe size should be between 8.5 (25 cm) and 13.5 (29 cm).

Exclusion Criteria:

  • People who weigh more than 255 pounds at baseline visit. People receiving renal dialysis b. People with severe cardiac or pulmonary disease limiting ability to exercise including angina or poorly controlled hypertension.

    c. People with neurological disorder such as or stroke that affecting ability to ambulate d. People with severe lower limb arthritis e. People with wound on non-amputated side f. People experiencing problems with prosthetic fit g. People with poor control of diabetes

Both
40 Years to 65 Years
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
NCT01340807
8497.01, 01
Yes
Ronald Tolchin, DO, Miami VAHS
Miami VA Healthcare System
Not Provided
Principal Investigator: Ronald Tolchin, DO Miami VAHS
Miami VA Healthcare System
February 2011

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP