← Eichor
Study identifier: NCT06127264 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Reliability of Force Measurement Within the Carbon Fiber Orthosis Proximal Cuff

Condition: Healthy · Ankle Foot Orthosis (AFO) · Peripheral Neuropathy  ·  Sponsor: University of Iowa

PhaseNA
Planned participants60
Who can joinAll sexes, 18 Years to 90 Years
Healthy volunteersYes

About this study

The primary purpose of this research study is to determine if forces within carbon fiber custom dynamic orthoses (CDOs) can be reliability assessed using Loadpad and Loadsol force measuring sensors (Novel GMBH, St. Paul, MN). An improved understanding of the forces acting within orthoses may help to guide future orthosis related research studies, provision methods, and patient education. Study participants will consist of three groups; 1) healthy, able-bodied adult participants using generic sized CDOs, which consist of a proximal cuff that wraps around the leg just below the knee, a posterior carbon fiber strut that runs the length of the leg and bends to store and return energy, and a semi-rigid footplate that acts as a lever arm to bend the posterior strut, 2) individuals without peripheral neuropathy who use AFO(s) regularly, and 3) individuals with peripheral neuropathy who use AFO(s) regularly. . Group 1 participants will be asked to fasten the proximal cuff to a self-selected cuff tightness 'SSCT', as well as three different predefined force levels; 'Loose' where the proximal cuff is loosely fastened around the participants leg, 'Moderate' where the proximal cuff is fastened with moderate tightness, and 'Tight' where the proximal cuff is tightly fastened around the participants leg. Testing in the predetermined force levels (Loose, Moderate, Tight) will occur in a randomized order. Group 2 and Group 3 participants will be asked to fasten their AFO(s) to a self-select…

This description comes directly from the study's public registry record.

Talk to the study team

Jason M Wilken, PT, PhD  ·  3193356857  ·  jason-wilken@uiowa.edu

Kirsten M Anderson, PhD  ·  3193530431  ·  kirsten-m-anderson@uiowa.edu

Always discuss trial participation with your own doctor first.

Locations (1)

University of IowaIowa City, Iowa, United StatesRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT06127264