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NCT07765082 · Jennifer Xu

Textured Insoles to Restore Sensorimotor Function in Patients With Plantar Fasciopathy

(TIRE)

What this study is about

This study will evaluate the immediate effects of wearing textured insoles on gait, postural control, and sensorimotor function in adults with plantar fasciopathy. Researchers will compare functional performance while participants wear textured insoles to determine whether this intervention may improve stability, movement and future studies of longer-term treatment.

View original scientific description

This study will evaluate the immediate effects of wearing textured insoles on gait, postural control, and sensorimotor function in adults with plantar fasciopathy. Researchers will compare functional performance while participants wear textured insoles to determine whether this intervention may improve stability, movement and future studies of longer-term treatment.

Interventions

OTHER

Textured Insole

A textured shoe insole designed to provide plantar sensory stimulation by increasing cutaneous input to the foot during standing and walking.

OTHER

Smooth Insole

A smooth shoe insole without surface texture used as a control device for comparison with the textured insole.

Primary outcome measures

Change in Postural Control

Time frame: Baseline and immediately following completion of each intervention condition during the study visit

Postural control will be assessed while participants complete standardized balance testing under each study condition. Performance will be compared between the textured insole and smooth insole conditions to evaluate the acute effects of textured insoles on postural control.

Who can participate

This study lists these criteria on ClinicalTrials.gov. A study coordinator reviews eligibility during screening — this page does not determine whether you qualify.

Inclusion criteria

  • Diagnosis of plantar fasciopathy for at least 3 months
  • Able to walk continuously at a self-selected pace for at least 20 minutes
  • Able and willing to provide informed consent

Exclusion criteria

  • Concomitant lower extremity injury (example fracture)
  • History of lower extremity injury within the previous 6 months
  • History of hip, knee, or ankle surgery involving bones, joints, ligaments, tendons, or cartilage.
  • Any condition other than plantar fasciopathy that affects balance or plantar cutaneous sensation.
  • Neurological deficits, vestibular disorders, visual disturbances, or other conditions that impair movement or sensory function.
  • Unable to speak or understand English.

Where

  • Lexington, Kentucky

Collaborators

National Athletic Trainers' Association

Related conditions & keywords

Plantar Fasciopathy

Frequently asked questions

What is a clinical trial?

A clinical trial is a research study that tests new medical treatments, drugs, devices, or procedures to determine their safety and effectiveness. Trials are carefully designed and monitored to protect participants while advancing medical knowledge.

Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. Trials must be reviewed and approved, and participants are closely monitored by medical professionals throughout the study. You can withdraw at any time if you choose.

Will I be compensated?

Many clinical trials offer compensation for your time, travel expenses, and inconvenience. The specific compensation varies by study and will be discussed during the screening process. All study-related medical care is typically provided at no cost to participants.

Will I receive a placebo instead of treatment?

When effective treatment exists, participants typically receive either the standard treatment plus the study intervention, or the standard treatment plus placebo. You would not be denied effective care. Placebos are primarily used when no proven treatment is available, or in addition to standard care. Your trial consent form will clearly explain what treatments you may receive.

Can I leave a trial if I change my mind?

Absolutely. Participation in clinical trials is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty or loss of benefits to which you are otherwise entitled.

How long does a clinical trial last?

Trial duration varies widely depending on the study design and purpose. Some trials last just a few weeks, while others may continue for months or years. The study coordinator will provide specific timeline information during your screening call.

Data: ClinicalTrials.gov · synced Sep 24, 2026 · Source of record for eligibility and locations

📊
1 of 26 participants interested
4% interest

See if this study fits

A short prescreen based on this study's listed criteria. A coordinator confirms eligibility — this is not a medical assessment.

Preparing your pre-screening questions…

Study locations

Choose your preferred location, or select flexible during enrollment.

RECRUITING

Lexington

Kentucky

Location available

Express your interest

Share your contact details and a study coordinator can follow up about screening.

Secure & Confidential

Your information is protected and will only be shared with the research team.

What participation can include

  • Study-related care provided by the research team
  • Close monitoring by medical professionals
  • Possible compensation for time and travel*
  • The option to withdraw at any time
  • Contributing to medical research that may help future patients

*Compensation varies by study. Confirm details with coordinator.

Typical next steps

  1. 1.Submit this form
  2. 2.Phone screening
  3. 3.In-person assessment if eligible
  4. 4.Begin participation

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Looking for Plantar Fasciopathy Treatment in Lexington?

Join others in Kentucky exploring innovative treatment options through clinical research

Plantar Fasciopathy Treatment Options in Lexington, Kentucky

If you're searching for Plantar Fasciopathy treatment in Lexington, participating in a clinical research study may provide access to innovative approaches under expert medical supervision. This study is actively recruiting participants in Lexington and surrounding areas.

Clinical trials offer participants the opportunity to receive cutting-edge treatments while contributing to medical research that may help future patients with Plantar Fasciopathy. All study-related care is provided at no cost to participants.

Local Sites
1 locations in Kentucky
Now Enrolling
Up to 26 participants
Quick Start
Screening available now

Why Consider a Clinical Trial for Plantar Fasciopathy?

Potential Benefits

  • ✓Access to new treatment approaches before public availability
  • ✓Close monitoring by experienced medical professionals
  • ✓Study-related care provided at no cost
  • ✓Contribute to medical research for Plantar Fasciopathy

What to Expect

  • →Initial screening to determine eligibility
  • →Regular check-ups and monitoring visits
  • →Possible compensation for time and travel
  • →You can withdraw at any time

Frequently Asked Questions About This Plantar Fasciopathy Study

Important Clinical Trial Information

This information is provided for educational purposes and does not constitute medical advice. Clinical trial participation involves potential risks and benefits. Eligibility requirements apply and will be assessed during the screening process.

Study identifier: NCT07765082. For complete study details, visit ClinicalTrials.gov. Always consult with your healthcare provider before making decisions about your medical care or participating in clinical research.