Recruiting

Observational Study

Sponsor:

Louis Stokes VA Medical Center

Code:

NCT04855214

Conditions

Prosthesis User

Amputation

Upper Limb Amputation at the Wrist

Upper Limb Amputation Above Elbow (Injury)

Upper Limb Amputation Below Elbow (Injury)

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Qualitative Analysis

Study Details

Brief summary:

The goal is to understand the critical factors associated with outcome acceptance following upper limb loss. The investigators aim to develop a unified theoretical model that describes the psychosocial experience of upper limb prosthesis use and predicts outcome acceptance following upper limb loss. The investigators will also examine experiences with prosthesis education, selection, and training as well as how psychological and social issues impact prosthesis use. In addition, the investigators will use the findings to develop a prototype decision tool to assist with matching persons to prostheses. Study findings will help providers, technology developers, and researchers better understand the complex experience of upper limb prosthesis use.

This conceptual framework will enable clinicians and researchers to evaluate and predict patient outcomes following limb loss, and to design interventions that improve outcomes. The proposed study is a mixed methods (qualitative and quantitative) study using an observational design. The qualitative component of the study will involve data collection through telephone interviews with 42 participants and analyses using a grounded theory approach with constant comparison methods. The quantitative component involves administration of standardized measures quantifying constructs of the theoretical model in 120 participants and analyses to produce a structural equation model of outcome acceptance. Participants will include persons with unilateral acquired upper limb loss at the trans radial or trans humeral level who use currently available prosthetic devices. Up to 16 individuals will participate in a series of focus groups that will be conducted to provide feedback on the model generated from previous data.

Conditions

Prosthesis User

Amputation

Upper Limb Amputation at the Wrist

Upper Limb Amputation Above Elbow (Injury)

Upper Limb Amputation Below Elbow (Injury)

Study ID

NCT04855214

Start date

Dec 16, 2020

Status verified date

Aug, 2026

Completion date

Sep 30, 2026

Anticipated

Primary completion date

Sep 30, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • 18 years or older
  • Ability to give verbal informed consent
  • Ability to speak and understand English
  • Unilateral acquired trans-radial or trans-humeral amputee
  • At least six months from time of limb loss
  • Current user of an upper limb prosthesis
  • Use of the device they will be describing for at least six months (with the exception of sensory augmentation)

Exclusion Criteria:

  • Significant hearing impairment which would prevent telephone communication.
  • Unwillingness or inability to discuss experiences with prostheses
  • Emotional disturbance related to discussion the prosthesis or limb loss

Study Design

Enrollment

178 participants

Anticipated

Interventions and Outcome Measures

Arms

Body-powered Prosthesis User

Individuals who use a prosthesis that relies on a system of cables or harnesses which are operated using other parts of the body like the shoulders, chest, or elbows.

Single degree-of-freedom (DOF) myoelectric prosthesis users

Individuals who use a myoelectric prosthesis that can perform only one movement.

Multi-DOF myoelectric prosthesis users

Individuals who use a myoelectric prosthesis that can perform more than one movement.

Sensory Augmentation

Individuals who experience augmented prosthesis sensory feedback through vibrating devices or pressure bladders, using electrical stimulation applied to the residual limb, or using neural implants.

Interventions

Qualitative Analysis

Mixed methods analysis of the user's experience with upper limb prosthetics.

Primary outcome measure

  • Patient Experience Measure (PEM) [ Time Frame: Two years ]

Central Contacts and Locations

Central contacts

Locations

Louis Stokes VA Medical Center

Recruiting

Cleveland, Ohio, United States, 44106

Contacts

More Information

Sponsor

Louis Stokes VA Medical Center

Last update posted

Aug 26, 2026

Last verified

Aug, 2026

Keywords

  • Upper Limb Prosthesis User
  • Survey
  • Interview
  • User Experience
  • Body-powered
  • Myoelectric
  • Multiple degree of freedom
  • Sensory Feedback
  • Prosthetic device features
  • Upper Limb Loss
  • Amputee
  • Outcome Acceptance
  • Qualitative Research

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Louis Stokes VA Medical Center on 2026-08-26.