Plantar Fascia and Achilles Tendon Thickness and Flexibility in Pes Planus (NCT06987422) | Clinical Trial Compass
CompletedNot Applicable
Plantar Fascia and Achilles Tendon Thickness and Flexibility in Pes Planus
Turkey (Türkiye)93 participantsStarted 2025-05-25
Plain-language summary
The aim of this study is to examine the plantar fascia and Achilles tendon thickness and flexibility in individuals with pes planus. Individuals between the ages of 18-45 who have been diagnosed with pes planus by an orthopedist and healthy individuals with similar demographic characteristics will be included in the study as a control group. Demographic information of the individuals will be recorded and clinical evaluations will be made. The foot posture of the individuals participating in the study will be evaluated with the Foot Posture Index, and the degree of flat feet will be evaluated with the Navicular Drop Test. The Achilles tendon and plantar fascia thicknesses of the individuals participating in the study will be measured with ultrasound, and the plantar fascia and Achilles tendon flexibility will be measured with a myotonometer.
Who can participate
Age range
18 Years – 45 Years
Sex
ALL
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
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.
Questions worth asking your doctor
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
Questions for the trial coordinator
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.