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Clinical Trials in Turkey / NCT06034600
Active, not recruiting Not applicable

Effect of Augmented Low-dye* Taping and Exercise on Plantar Pressure, Navicular Drop and Foot Posture in Pes Planus

NCT06034600 · tracked via the Priya Life Science Turkey tracker
Phase
Not applicable
Started
2023-10-06
Last updated
2024-10-09

Condition(s) studied

Pes Planus

Investigational drug(s) / intervention(s)

tapingexercise

taping: Taping will be applied to the exercise and taping group after the exercises with theraband. Other exercises that are not performed will be performed with the tape on the skin.The application will be repeated three days a week for eight weeks.

exercise: Stretching and strengthening exercises will be applied to both groups three days a week for 8 weeks.The exercises performed with theraband will be performed in the same way in both groups. While the other exercises will be done after taping in the "taping and exercise group", the "exercise group" will be done without taping.

Study summary

Introduction: Pes planus is a deformity that affects the foot-ankle muscle complex as well as passive components of the foot such as bones and ligaments. Various approaches such as taping methods and exercise training are being investigated in the treatment of pes planus. The effect of the applied methods and their superiority over each other are still unclear. The effect of banding methods varies according to the band type and technique. Exercise methods currently focus on the intrinsic and extrinsic muscles of the foot. Pedobarographic evaluations are also performed in addition to clinical evaluations to evaluate the effectiveness of treatments.

Objective: It is planned to compare the effects of reinforced low-dye taping method, which is one of the rigid taping techniques used in the treatment of pes planus, and exercise training on foot plantar pressure, navicular drop and foot posture.

Material and method: 34 individuals with pes planus between the ages of 18-25 will be included in the study, which was designed as a single-blind randomized study. The universe of our study will be Lokman Hekim University Faculty of Health Sciences and Institute of Health Sciences. The whole universe will be tried to be reached and individuals who meet the inclusion criteria will be selected from the relevant universe. Consent form will be obtained from individuals who are deemed eligible to participate in the study. Pes planus evaluation; It will be done using the navicular drop test and the foot posture index. In order for the physical activity levels of the groups to be homogeneous, after stratified sampling, individuals will be randomly assigned to the exercise groups by taping and exercise with the closed envelope method. Evaluations will be made to each group at the beginning, at the eighth and twelfth week. Static evaluation of the foot will be made using navicular drop and foot posture index, and pedobarographic analysis will be done using a foot analyzer.

Conclusion: The effects of taping and exercise training on foot static and plantar pressure measurements will be interpreted.

Eligibility

Sex
ALL
Min age
18 Years
Max age
25 Years
Healthy volunteers
Accepted
Inclusion Criteria: * Be between the ages of 18-25 * Navicular drop (ND) test \>10 mm * Foot posture index ≥6 * Individuals in the 1st and 2nd category according to the international physical activity survey * Individuals who volunteered to participate in the study Exclusion Criteria: * Presence of systemic, neurological, rheumatological or orthopedic problems that may affect the lower extremity * Individuals who are allergic to the tape to be used * Individuals who cannot adapt to exercise or taping practices * Individuals who have received treatment for pes planus in the last 6 months * Individuals with a BMI ≥ 30 * Presence of pregnancy * Cases not wanting to take part in the study

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Inonu Univercity Malatya Turkey (Türkiye)

More Inonu University trials in Turkey

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06034600 on ClinicalTrials.gov ↗ ← All trials in Turkey