Clinical Outcomes With Non-Powered vs. Powered Prosthetic Knees by K2-level Amputees (NCT06194838)
Clinical Outcomes Associated With At Home Use of Non-Powered vs. Powered Prosthetic Knees by K2-level Individuals With Transfemoral Amputations
🩺 Plain-English Summary (8th-Grade Level)
The goal of this proposed project is to gather community-based data from the K2-level Transfemoral Amputee (TFA) population to aid in evidence-based prescription of powered prosthetic knees (i.e., choosing the right device to maximize the benefit for each patient). The investigators intend to use this trial data along with a concurrent study being conducted within the K3-K4 level population to guide the implementation of effective prescriptions towards those that can benefit most from a given device and limit prescription to those who would not see benefit in order to ensure the most judicious use of Department of Defense (DoD) and Veteran's Affairs healthcare dollars. The findings will also be shared with the research community to help drive the design of future devices by identifying what features and functions are most beneficial to which patient populations when the devices are used outside of the laboratory. In summary, more community-based data on how powered prosthetic knees compare with the current standard in TFA populations is needed to allow for improved clinical decision making and clinical outcomes.
Who can join: Review the eligibility criteria below.
Location: Hanger Clinic — Austin, Texas
Age range: 18 Years
🧪 Interventions in This Study
📋 "Do I Qualify?" — 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria ↗
📍 All Participating Trial Locations (1 Sites)
- Hanger Clinic — Austin, Texas
📞 Contact the Study Coordinator
Phone: (402) 290-8051
Email: swurdeman@hanger.com
Coordinator details come directly from the registered NIH protocol. Confirm the study is still recruiting before traveling.
💰 Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA § 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Amputation
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- GaMA Metric to Quantify Functional Importance of Various Upper Limb Prosthetic Devices — Chicago, Illinois
- Transfemoral Osseointegrated Prosthesis Limb-Load Symmetry Training — Aurora, Colorado
- Magnetic Bead Tracking System and eOPRA Implant System With Bionic Prosthesis for Transtibial Amputees — Boston, Massachusetts
- Personalized Mobility Interventions Using Smart Sensor Resources for Lower-Limb Prosthesis Users — Chicago, Illinois
- Optimizing Prosthetic Prescription to Mitigate the Effects of Perspiration — Seattle, Washington
Explore by condition: All Amputation clinical trials
💡 How to Participate
- Check the checklist above to see if you may qualify.
- Contact the study coordinator using the phone/email above.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.