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NCT05601869 · ClinicalTrials.gov registry record · NA

Impact of Improving Footwear Options

A NA study of Amputation, sponsored by VA Office of Research and Development.

Recruiting
Registry status
NA
Development phase
18
Enrollment target
1
Study location

NCT05601869 is a NA study of Amputation that is actively recruiting participants, run by VA Office of Research and Development. The registered enrollment target is 18 participants, below the 133-participant average among 65 other Amputation trials with a reported enrollment target (86% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05601869, a NA study of Amputation, is actively recruiting participants, sponsored by VA Office of Research and Development.

RECRUITING
Registry status
NA
Development phase
18 participants
Enrollment target
1
Study location

Study Summary

Veterans with leg amputations have limited footwear options because their artificial feet do not change shapes for different shoes. Studies have shown that women with amputations receive more frequent prosthetics care than men, but are less satisfied with the fit, comfort, and appearance of their prostheses. The investigators' previous research indicates that women Veterans would like to be able to wear a broader variety of footwear, and those who perceive more footwear limitations tend to have poorer body image and community participation. A new prosthesis designed by the investigators' group allows Veterans with amputations to use their footwear of choice using 3D-printed artificial feet with a single ankle. The novel prosthesis will be tested in this project with women Veterans with amputations to determine the impact of improving footwear options on body image and community participation.

Conditions Studied

Interventions

  • DEVICE RECOVER Prosthetic Ankle-Feet System

Study Locations (1)

Minnesota

  • Minneapolis VA Health Care System, Minneapolis, MN - Minneapolis

Trial Details

FieldValue
Enrollment Target 18 participants
Start Date 2023-09-01
Est. Completion 2026-03-31
Phase NA

Sponsor

VA Office of Research and Development

1,668 total trials

What the Registry Record Tells You About NCT05601869

The ClinicalTrials.gov registry entry for NCT05601869 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 18 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 133-participant average among 65 other Amputation trials with a reported enrollment target (86% lower). The listed sponsor is VA Office of Research and Development, which has 1,668 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Amputation appearing as the primary indexed condition, and to 1 intervention - of which RECOVER Prosthetic Ankle-Feet System is the first listed.

NCT05601869 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT05601869 about?

NCT05601869 is a clinical study titled "Impact of Improving Footwear Options". Veterans with leg amputations have limited footwear options because their artificial feet do not change shapes for different shoes. Studies have shown that women with amputations receive more frequent prosthetics care than men, but are less satisfied with the fit, comfort, and appearance of their pr...

What is the current status of trial NCT05601869?

This trial is currently recruiting. It is a NA study. The enrollment target is 18 participants. The study started on 2023-09-01. Estimated completion is 2026-03-31.

What conditions does trial NCT05601869 study?

This clinical trial studies the following conditions: Amputation.

What interventions are being tested in trial NCT05601869?

The interventions under investigation include: RECOVER Prosthetic Ankle-Feet System (DEVICE).

Who is sponsoring clinical trial NCT05601869?

This trial is sponsored by VA Office of Research and Development, which has 1,668 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05601869 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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