The Effect of Using Two Different Prosthetic Feet in Patients With Unilateral Transtibial Amputation

Sponsor
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital (Other)
Overall Status
Completed
CT.gov ID
NCT04759014
Collaborator
(none)
42
1
4.4
9.6

Study Details

Study Description

Brief Summary

Background: Prescribing optimal prosthetic feet to ensure successful rehabilitation is difficult since there are no generally established clinical guidelines based on objective data.

Aim: To investigate the effect of using non-articulated dynamic foot (non-articulating ankle, NAA) and dynamic foot with hydraulic ankle (articulating hydraulic ankle, AHA) on functional capacity, pain severity, satisfaction level and quality of life (QoL) in high activity patients with unilateral transtibial amputation.

Condition or Disease Intervention/Treatment Phase
  • Other: The effect of using two different prosthetic feet on functional capacity, pain severity, satisfaction level and quality of life

Detailed Description

Background: Prescribing optimal prosthetic feet to ensure successful rehabilitation is difficult since there are no generally established clinical guidelines based on objective data.

Aim: To investigate the effect of using non-articulated dynamic foot (non-articulating ankle, NAA) and dynamic foot with hydraulic ankle (articulating hydraulic ankle, AHA) on functional capacity, pain severity, satisfaction level and quality of life (QoL) in high activity patients with unilateral transtibial amputation.

Methods: Forty-two patients with unilateral transtibial traumatic amputation will be participated in this cross-sectional study. Functional capacity will be evaluated using the six-minute walking test (6MWT). The severity of residual limb pain, sound limb pain and low back pain will be evaluated with a 10-point Visual Analogue Scale (VAS). The socket system, prosthetic foot and overall prosthesis satisfaction will be evaluated with a 10-point VAS. The QoL of each patient will be assessed using the Short Form 36 (SF-36).

Study Design

Study Type:
Observational
Actual Enrollment :
42 participants
Observational Model:
Cohort
Time Perspective:
Cross-Sectional
Official Title:
The Effect of Using Two Different Prosthetic Feet on Functional Capacity, Pain Severity, Satisfaction Level and Quality of Life in High Activity Patients With Unilateral Transtibial Amputation
Actual Study Start Date :
Feb 18, 2021
Actual Primary Completion Date :
Jul 1, 2021
Actual Study Completion Date :
Jul 1, 2021

Arms and Interventions

Arm Intervention/Treatment
Group 1

21 patients using non-articulated dynamic foot (non-articulating ankle, NAA)

Other: The effect of using two different prosthetic feet on functional capacity, pain severity, satisfaction level and quality of life
The effect of using two different prosthetic feet on functional capacity, pain severity, satisfaction level and quality of life

Group 2

21 patients using dynamic foot with hydraulic ankle (articulating hydraulic ankle, AHA)

Other: The effect of using two different prosthetic feet on functional capacity, pain severity, satisfaction level and quality of life
The effect of using two different prosthetic feet on functional capacity, pain severity, satisfaction level and quality of life

Outcome Measures

Primary Outcome Measures

  1. Visual Analogue Scale [through study completion, an average of one and a half months]

    All patients will mark the severity of residual limb pain, sound limb pain and low back pain on a Visual Analogue Scale (VAS; from 0 (no pain) to 10 (worst pain)). The socket system, prosthetic foot and overall prosthesis satisfaction will be evaluated with a 10-point VAS (from 0 (absolutely dissatisfied) to 10 (absolutely satisfied)).

  2. Short Form 36 (SF-36) [through study completion, an average of one and a half months]

    The QoL of each patient will be assessed using the Short Form 36 (SF-36). The validity and reliability of the Turkish version of SF-36 has been demonstrated. SF-36 consists of 36 questions on eight different subscales that include physical functioning, role limitations due to physical health problems, bodily pain, general health perceptions, energy and fatigue, vitality, social functioning, role limitations due to emotional problems and general mental health. Each subscale of SF-36 is scored between 0 and 100, and higher scores illustrate better QoL.

  3. The six-minute walking test (6MWT) [through study completion, an average of one and a half months]

    Functional capacity will be evaluated using the six-minute walking test (6MWT). The 6MWT evaluates walking function and endurance. Patients will be instructed to walk quickly, safely, and as much distance as possible along a rectangular path. The 6MWT is both valid and reliable among individuals with lower-limb loss.

Secondary Outcome Measures

  1. Likert scale [through study completion, an average of one and a half months]

    Level of difficulty experienced during walking on straight road, walking uneven road, ascending stairs, descending stairs, ascending ramps and descending ramps will be recorded on a 5-point Likert scale ((1) very easy, (2) easy , (3) neutral, (4) difficult, (5) very difficult).

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 65 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • aged 18-65 years

  • Medicare functional classification level K4 (very active)

  • using the prosthesis for at least 6 months and at least 6 hrs a day

  • using active vacuum-assisted suspension system

Exclusion Criteria:
  • bilateral amputation,

  • the presence of neurological, cardiovascular and pulmonary disease that could affect walking performance.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Gaziler Physical Medicine and Rehabilitation, Education and Research Hospital Ankara Turkey

Sponsors and Collaborators

  • Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Investigators

  • Principal Investigator: Merve Orucu Atar, MD, Gaziler Physical Medicine and Rehabilitation, Training and Research Hospital, Department of PMR

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Yasin Demir, Physical Medicine and Rehabilitation Associate Professor, Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
ClinicalTrials.gov Identifier:
NCT04759014
Other Study ID Numbers:
  • 11
First Posted:
Feb 17, 2021
Last Update Posted:
Nov 23, 2021
Last Verified:
Nov 1, 2021
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Yasin Demir, Physical Medicine and Rehabilitation Associate Professor, Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Study Results

No Results Posted as of Nov 23, 2021