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Clinical Trials/NCT04759014
NCT04759014
Completed
N/A

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

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital1 site in 1 country42 target enrollmentFebruary 18, 2021
ConditionsAmputation

Overview

Phase
N/A
Intervention
Not specified
Conditions
Amputation
Sponsor
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Enrollment
42
Locations
1
Primary Endpoint
The six-minute walking test (6MWT)
Status
Completed
Last Updated
4 years ago

Overview

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.

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).

Registry
clinicaltrials.gov
Start Date
February 18, 2021
End Date
July 1, 2021
Last Updated
4 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
Gaziler Physical Medicine and Rehabilitation Education and Research Hospital
Responsible Party
Principal Investigator
Principal Investigator

Yasin Demir

Physical Medicine and Rehabilitation Associate Professor

Gaziler Physical Medicine and Rehabilitation Education and Research Hospital

Eligibility Criteria

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.

Outcomes

Primary Outcomes

The six-minute walking test (6MWT)

Time Frame: 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.

Visual Analogue Scale

Time Frame: 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)).

Short Form 36 (SF-36)

Time Frame: 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.

Secondary Outcomes

  • Likert scale(through study completion, an average of one and a half months)

Study Sites (1)

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