NCT04536025

Shared Decision Making Aid for Prosthetic Design

University of Colorado, Denver·ClinicalTrials.gov·otherNot yet recruiting
View on ClinicalTrials.gov
Study focus
Drug/Device/Intervention
Qualitative focus group interviews
Study type
Observational
Intervention type
other
Sponsor & location
Primary sponsor
University of Colorado, Denver
Location
Aurora, United States of America
Timeline & enrollment
Phase
N/A
Start date
Jun 06, 2020
End date
Jun 01, 2022
Enrollment
62 participants
Primary outcome

Qualitatively identified decisional needs of patients and prosthetists for Prosthetic Design Decisions, to be used as content in the development of a decision aid for prosthetic design,Accuracy of the decision aid prototype, as measured in percentage.,Comprehensibility of the decision aid prototype, as measured by a Likert Scale,Usability of the decision decision aid prototype, as measured by a Likert scale

Summary

This study is designed to learn more about decision making for prosthetic design, with the
 goal of producing a decision making aid for prosthetic design decisions.

ICD-10 classifications
Amputation of limb(s)Traumatic amputation of upper and lower limbs, any combination [any level]Traumatic amputations involving other combinations of body regionsTraumatic amputation of one hand and other arm [any level, except hand]Traumatic amputation of lower limb, level unspecified
Data source
Registry
ClinicalTrials.gov
Trial ID
NCT04536025
Type
Non-Device Trial
About this record

Access comprehensive clinical trial information for NCT04536025 through Pure Global AI's free database. This phase not specified trial is sponsored by University of Colorado, Denver and is currently Not yet recruiting. The study focuses on Amputation,Prosthesis User. Target enrollment is 62 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.