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NCT06937242 · ClinicalTrials.gov registry record · NA

Effects of Microprocessor-controlled Prosthetic Knees on Fall-related Health Outcomes in Limited Community Ambulators

A NA study of Amputation and Prosthesis User, sponsored by Hanger Institute for Clinical Research and Education.

Recruiting
Registry status
NA
Development phase
100
Enrollment target
1
Study location

NCT06937242: Recruiting NA study of Amputation and Prosthesis User, sponsored by Hanger Institute for Clinical Research and Education.

NCT06937242 is a NA study of Amputation and Prosthesis User that is actively recruiting participants, run by Hanger Institute for Clinical Research and Education. The registered enrollment target is 100 participants, below the 131-participant average among 65 other Amputation trials with a reported enrollment target (24% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06937242, a NA study of Amputation and Prosthesis User, is actively recruiting participants, sponsored by Hanger Institute for Clinical Research and Education.

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

Study Summary

The goal of this study is to find out if using microprocessor-controlled prosthetic knees (MPKs), prosthetic knees with a built-in computer, improves health outcomes related to falls in adults who use above-knee prostheses. The main questions are: * Do individuals with MPKs have fewer fall-related health issues compared to those with non-microprocessor-controlled prosthetic knees (nMPKs)? * Do individuals with MPKs have increased mobility, faster walking speed, and improved quality of life compared to those with nMPKs? Participants who have recently received an nMPK as part of their regular care can join the study. Those randomized to the control group will keep using their nMPK, while those randomized to the intervention group will receive a stance-and-swing MPK or a stance-only MPK.

Primary Outcome

The PLUS-F-SEF is a 15-item self-report instrument we developed in the present study to measure perceived ability to avoid a loss of balance while performing an activity. Respondents rate their degree of confidence on a 5-point scale from "not at all confident" (1) to "very much confident" (5). A standardized T-score is generated for the PLUS-F-SEF using a lookup table that converts the raw score to a T-score.

Interventions

  • DEVICE Ottobock C-Leg 4 Microprocessor Knee
  • DEVICE Ottobock Kenevo

Study Locations (1)

Texas

  • Hanger Inc. - Austin

Trial Details

FieldValue
Enrollment Target 100 participants
Start Date 2025-07-11
Est. Completion 2027-02
Phase NA

What NCT06937242 shows while recruiting

NCT06937242 is an interventional study that assigns participants to a tested intervention. The registered 100 participants enrollment target is mid-sized for trials with a published cap, below the 131-participant average among 65 other Amputation trials with a reported enrollment target (24% lower).

The record links to 6 conditions, with Amputation appearing as the primary indexed condition, and to 2 interventions - of which Ottobock C-Leg 4 Microprocessor Knee is the first listed.

NCT06937242 reports a single indexed study location in Texas.

Frequently Asked Questions

What is clinical trial NCT06937242 about?

NCT06937242 is a clinical study titled "Effects of Microprocessor-controlled Prosthetic Knees on Fall-related Health Outcomes in Limited Community Ambulators". The goal of this study is to find out if using microprocessor-controlled prosthetic knees (MPKs), prosthetic knees with a built-in computer, improves health outcomes related to falls in adults who use above-knee prostheses. The main questions are: * Do individuals with MPKs have fewer fall-related ...

What is the current status of trial NCT06937242?

This trial is currently recruiting. It is a NA study. The enrollment target is 100 participants. The study started on 2025-07-11. Estimated completion is 2027-02.

What conditions does trial NCT06937242 study?

This clinical trial studies the following conditions: Amputation, Prosthesis User, Lower Limb Amputation Above Knee (Injury), Limb; Absence, Congenital, Lower, Amputation; Traumatic, Leg: Thigh, Between Hip and Knee.

What interventions are being tested in trial NCT06937242?

The interventions under investigation include: Ottobock C-Leg 4 Microprocessor Knee (DEVICE), Ottobock Kenevo (DEVICE).

Who is sponsoring clinical trial NCT06937242?

This trial is sponsored by Hanger Institute for Clinical Research and Education, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06937242 being conducted?

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

Similar trials for Amputation

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06937242's enrollment target sits among peer trials

100 9th of 65 higher than 55 of 65 other Amputation trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Amputation trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06937242, the US trial registry maintained by the National Library of Medicine. NCT06937242 (mid enrollment · single site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.