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.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years to 70 Years |
| Sex | All |
| Enrollment | 74 (estimated) |
| Sponsor | South East Technological University Academic / other |
| Locations | 1 site (Carlow, Carlow County) |
| Status | Recruiting |
| Started | May 7, 2026 |
| Main results expected | October 31, 2027 |
| Study ends | October 31, 2027 |
| Registry record updated | May 22, 2026 |
| Trial ID | NCT07600229 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
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South East Technological University
Carlow, Carlow County, Ireland Recruiting
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.