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Clinical Trial Details — Status: Enrolling by invitation

Administrative data

NCT number NCT06146959
Other study ID # P.T.REC/012/004632
Secondary ID
Status Enrolling by invitation
Phase N/A
First received
Last updated
Start date July 1, 2023
Est. completion date February 28, 2024

Study information

Verified date February 2024
Source Beni-Suef University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The aim of this study is to find the effect of a program of corrective kinesiotaping on pain intensity, foot function, and the sonographic picture of plantar fascia in adolescents with pronated feet.This study hypothesizes that there will be a statistically significant effect of a program of application of the corrective technique of kinesiotaping on plantar heel pain, foot function, and the sonographic picture of plantar fascia in a sample of Egyptian adolescents suffering from pronated feet.


Description:

This study will be conducted to find the effect of a program of corrective kinesiotaping on pain intensity, foot function, and the sonographic picture of the plantar fascia in adolescents with pronated feet. Thirty adolescents suffering from plantar heel pain associated with pronated feet will be included in this study. They will be distributed randomly into 2 groups: Group A will receive corrective kinesiotaping (50-75% stretch) for 4 weeks, 2 times per week with 1 day of rest; Group B will receive a placebo non-corrective kinesiotaping (without tension) with no mechanical correction of the calcaneus; and Group C will receive a home program of intrinsic foot strengthening and stretching exercises. Data will be collected pre- and post-intervention for all groups by using the visual analog scale (VAS), the first two subscales of foot function index (FFI), and a sonographic picture of the foot for each adolescent. Participants will be recruited from outpatient clinics and schools.


Recruitment information / eligibility

Status Enrolling by invitation
Enrollment 30
Est. completion date February 28, 2024
Est. primary completion date January 30, 2024
Accepts healthy volunteers No
Gender All
Age group 12 Years to 18 Years
Eligibility Inclusion Criteria: - Children with unilateral or bilateral plantar fasciitis. - pronated foot or foot on weightbearing in the navicular drops test. - Pain and tenderness to palpation at the medial tubercle of the calcaneus for a minimum of 6 weeks and maximum of 6 months Exclusion Criteria: - Corticosteroid injection of the heel within the past 3 months. - Posterior heel pain. - Systemic inflammatory conditions. - Diabetes. - Surgery of the foot. - Neuromuscular conditions e.g. CP. - Individuals with BMI > 25. - Individuals engaged in regular athletic activities

Study Design


Related Conditions & MeSH terms


Intervention

Device:
Corrective Kinesiology taping
corrective kinesiology tape is a form of biomechanical tape that is used with specific tension to get a corrective effect
Non corrective kinesiology tape
Non-corrective kinesiology tape is a form of biomechanical tape that is used without any tension
Other:
Home exercise program
Intrinsic foot strengthening and stretching exercises

Locations

Country Name City State
Egypt Tayseer Younes Cairo Al Qahirah

Sponsors (2)

Lead Sponsor Collaborator
Beni-Suef University Azhar University

Country where clinical trial is conducted

Egypt, 

Outcome

Type Measure Description Time frame Safety issue
Other Diagnostic ultrasound A sonographic picture of plantar fascia 4 weeks
Primary Pain Visual Analogue Scale minimum score is 0, and the maximum score is 10 ; higher scores means worse outcome 4 weeks
Secondary Foot function Index This questionnaire has been designed to give therapists information on how foot pain has affected your ability to to manage in everyday life. each question on a scale from 0 (no pain) to 10 (worst pain imaginable) 4 weeks
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