Examining foot structure and flexibility in flat feet
Investigation of Plantar Fascia and Achilles Tendon Thickness and Flexibility in Individuals With Pes Planus
This study is testing the thickness and flexibility of certain foot structures in people with flat feet and comparing them to those with normal feet to see how they differ.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 100 (estimated) |
| Ages | 18 Years to 45 Years |
| Sex | All |
| Sponsor | Hacettepe University Academic / other |
| Locations | 1 site (Ankara) |
| Trial ID | NCT06987422 on ClinicalTrials.gov |
What this trial studies
This study investigates the thickness and flexibility of the plantar fascia and Achilles tendon in individuals diagnosed with pes planus, also known as flat feet. Participants aged 18 to 45 will be recruited, including those with pes planus and a control group of healthy individuals. Clinical evaluations will be conducted, including demographic data collection, foot posture assessment using the Foot Posture Index, and the Navicular Drop Test to evaluate the degree of flat feet. Ultrasound will be utilized to measure tendon thickness, while flexibility will be assessed with a myotonometer.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18 to 45 diagnosed with pes planus by a physician.
Not a fit: Patients with severe visual impairment, neurological disorders, or those who have undergone lower extremity surgery may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of foot mechanics in pes planus, potentially leading to improved treatment strategies.
How similar studies have performed: While similar studies have explored foot mechanics, this specific investigation into the relationship between tendon thickness and flexibility in pes planus is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Age 18 to 45 * Mini Mental State Examination (MMSE) score of 24 to 30 * Diagnosed with Pes Planus by a physician Exclusion Criteria: * Inability to communicate verbally * Use of walking aids * Any history of surgery involving the lower extremities * People with severe visual impairment, neurological disorders and/or congestive heart failure.
Where this trial is running
Ankara
- Atılım University — Ankara, Turkey (Recruiting)
Study contacts
- Study coordinator: Büşra Seçkinoğulları Korkusuz, PhD
- Email: bskorkusuz@ankara.edu.tr
- Phone: +905442436914
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.