Actively Recruiting

Phase Not Applicable
Age: 50Years - 70Years
All Genders
Healthy Volunteers
NCT06516900

Reducing Foot Pain and Peak Plantar Pressure in Patients With Foot Pain

Led by University of Texas Rio Grande Valley · Updated on 2026-02-20

50

Participants Needed

1

Research Sites

99 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The research project aims to evaluate the effectiveness of OrthoFeet Hands-Free therapeutic shoes and prefabricated inserts in patients with foot pain.

CONDITIONS

Official Title

Reducing Foot Pain and Peak Plantar Pressure in Patients With Foot Pain

Who Can Participate

Age: 50Years - 70Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Be able to give written, informed consent
  • Have self-reported foot pain including heel pain, arch or ball of the foot pain, or big toe joint pain
  • Not be currently engaged in any physician prescribed treatment plan for foot pain
  • Have intact protective sensation as determined using Semmes Weinstein monofilament test
Not Eligible

You will not qualify if you...

  • Have plantar ulcers
  • Have major foot deformities such as Charcot foot or high arches (pes cavus)
  • Have any lower extremity amputation including minor amputation
  • Have foot pain caused by nail disorders or keratotic lesions
  • Have unstable medical conditions such as recent stroke or expected medication changes
  • Have acute foot fractures
  • Have major cognitive impairment or major depression
  • Have decreased protective sensation in lower extremities
  • Currently be undergoing any treatment for foot pain including icing, anti-inflammatory drugs, creams, injections, or physical therapy
  • Have swelling

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Hafizur Rahman

Harlingen, Texas, United States, 78550

Actively Recruiting

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Research Team

H

Hafizur Rahman, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

RANDOMIZED

Model

CROSSOVER

Primary Purpose

TREATMENT

Number of Arms

2

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