Clinical trial Recruiting at 1 site Interventional Ages 18 to 70

Barefoot Walking vs Standardised Conservative Care for Plantar Fasciopathy

Official title: Clinical and Economic Effectiveness of Barefoot Walking Compared to Standardised Conservative Care for the Treatment of Plantar Fasciopathy: a Pragmatic Randomised Controlled Trial

Run by South East Technological University · NCT07600229 · Data updated 2026-11-12

This trial tests whether a barefoot walking program can reduce heel pain and improve foot function in adults with plantar fasciopathy compared with a standard stretching and strengthening program.

More Plantar Fasciitis trials

Quick facts

Study typeInterventional
Ages18 Years to 70 Years
SexAll
Enrollment74 (estimated)
SponsorSouth East Technological University
Academic / other
Locations1 site (Carlow, Carlow County)
StatusRecruiting
StartedMay 7, 2026
Main results expectedOctober 31, 2027
Study endsOctober 31, 2027
Registry record updatedMay 22, 2026
Trial IDNCT07600229 on ClinicalTrials.gov

Is this trial a fit for you?

Likely a good fit

Adults aged 18-70 with clinically diagnosed plantar fasciopathy, experiencing first-step pain and a symptom duration longer than four weeks, able to walk unaided and provide informed consent.

Probably not a fit

People with severe comorbidities affecting the lower limb, prior foot surgery, BMI over 40, or inability to walk without aid may not benefit from this intervention.

A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.

What this trial studies

Adults with plantar fasciopathy are randomly assigned to either a barefoot walking program or a standardized stretching and strengthening routine for 12 weeks, with weekly short surveys and follow-up surveys over six months. The study uses a home-based exercise approach and provides load-management education for plantar fasciopathy. Outcomes focus on changes in heel pain, foot function, and quality of life. Results will indicate whether barefoot walking is a viable conservative option for managing heel pain due to plantar fasciopathy.

Why it matters

Potential benefit: If successful, this approach could offer a simple, at-home option to reduce heel pain and improve daily functioning for people with plantar fasciopathy.

How similar studies have gone: Previous research has explored conservative care for plantar fasciopathy, with mixed results; this study tests a novel barefoot approach against standard therapy.

Who can join: the full rules

Show full inclusion / exclusion criteria
Inclusion Criteria:

* Aged 18-70 years;
* Clinical diagnosis of Plantar Fasciopahty, defined by: a) Pain localised to the medial calcaneal tubercle of sharp or stabbing quality; b) Pain worst with the first few steps in the morning or after a period of rest (first-step pain); c) Pain reproduced with palpation of the medial calcaneal tubercle OR positive Windlass Test;
* Symptom duration greater than 4 weeks;
* Able to walk independently without a mobility aid
* Able to provide informed consent and comply with study protocol

Exclusion Criteria:

* Prior surgery on the affected foot
* Diabetes with peripheral neuropathy or other neurological condition affecting lower limb sensation or motor control
* Active inflammatory arthropathy, uncontrolled vascular disease, or inability to walk unaided
* Current or recent (less than 6 months) bony stress fracture or other acute foot or ankle injury on the affected side
* Pregnancy during the intervention period
* BMI greater than 40 kg/m²
* Corticosteroid injection to the affected foot within the previous 3 months
* Night splints initiated less than 4 weeks prior to enrolment
* Any condition that would make participation unsafe, including open foot wounds

Where it's running

  • South East Technological University
    Carlow, Carlow County, Ireland
    Recruiting

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How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.