RECRUITING

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

Conditions

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Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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

Official Title

A Comparison of the Effectiveness of OrthoFeet HandsFree Therapeutic Shoes in Reducing Foot Pain and Peak Plantar Pressure

Quick Facts

Study Start:2024-06-05

Study Completion:2025-12-31

Study Type:Not specified

Phase:Not Applicable

Enrollment:Not specified

Status:RECRUITING

Study ID

NCT06516900

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:50 Years to 70 Years

Sexes Eligible for Study:ALL

Accepts Healthy Volunteers:Yes

Standard Ages:ADULT, OLDER_ADULT

Inclusion Criteria	Exclusion Criteria
* be able to give written, informed consent * self-reported foot pain including heel pain, arch or ball of the foot pain, and hallux limitus/rigidus joint pain * not engaged in any physician prescribed treatment plan * in-tact protective sensation as determined using Semmes Weinstein monofilament	* patients with plantar ulcer * patients with major foot deformities such as charcot foot, pes cavus * patients with lower extremity amputation including minor amputation * foot pain because of nail disorder of keratotic lesions * patients with unstable conditions such as recent stroke, anticipated changes in medication regime * acute fractures of the foot * patients with major cognitive impairment or major depression * patients with lower extremity decreased protective sensation * engaged in any treatment of foot pain including icing, oral anti-inflammatories, creams, injections, physical therapy * swelling

Inclusion Criteria

Exclusion Criteria

* be able to give written, informed consent
* self-reported foot pain including heel pain, arch or ball of the foot pain, and hallux limitus/rigidus joint pain
* not engaged in any physician prescribed treatment plan
* in-tact protective sensation as determined using Semmes Weinstein monofilament

* patients with plantar ulcer
* patients with major foot deformities such as charcot foot, pes cavus
* patients with lower extremity amputation including minor amputation
* foot pain because of nail disorder of keratotic lesions
* patients with unstable conditions such as recent stroke, anticipated changes in medication regime
* acute fractures of the foot
* patients with major cognitive impairment or major depression
* patients with lower extremity decreased protective sensation
* engaged in any treatment of foot pain including icing, oral anti-inflammatories, creams, injections, physical therapy
* swelling

Contacts and Locations

Study Contact

Hafizur Rahman, PhD

CONTACT

9562962035

hafizur.rahman@utrgv.edu

Study Locations (Sites)

Hafizur Rahman

Harlingen, Texas, 78550

United States

Collaborators and Investigators

Sponsor: University of Texas Rio Grande Valley

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2024-06-05

Study Completion Date2025-12-31

Study Record Updates

Study Start Date2024-06-05

Study Completion Date2025-12-31

Terms related to this study

Additional Relevant MeSH Terms

Foot Pain