About this trial
Our primary aim is to compare diaphragm function (resting thickness, activity/resting thickness ratio indicating contractility), postural control, and plantar pressure between individuals with pes planus and healthy controls without pes planus.
Eligibility criteria
Qualifiers
Willing to participate in the study voluntarily
Having a Navicular drop test value of 10mm or above
Being between the ages of 18-30
Having the physical capacity to perform assessments and tests
Disqualifiers
Termination of voluntariness
Those with rigid flatfoot, pes cavus, hallux valgus, hallux rigidus, or calcaneal spur deformity
Those with chronic systematic and metabolic diseases (e.g., diabetes mellitus, rheumatoid arthritis, etc.) and musculoskeletal problems (e.g., pes planus) that may affect foot functions and gait
Those with any surgical history likely to affect balance, lower extremity strength, and postural control
Trial design
Treatments tested in this trial
- Determination of Foot Deformity Level
- Foot Function Index
- UFAA-International Physical Activity Questionnaire
- Diaphragm ultrasound measurements
- NeuruCom Balance Master Balnce and Performans Test
- Plantar Pressure Assessment