Corrective Calcaneal Kinesiology Tape in Adolescents With Pronated Foot

Sponsor
Beni-Suef University (Other)
Overall Status
Enrolling by invitation
CT.gov ID
NCT06146959
Collaborator
Azhar University (Other)
30
1
3
8
3.8

Study Details

Study Description

Brief 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.

Condition or Disease Intervention/Treatment Phase
  • Device: Corrective Kinesiology taping
  • Device: Non corrective kinesiology tape
  • Other: Home exercise program
N/A

Detailed 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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
30 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Investigator, Outcomes Assessor)
Primary Purpose:
Treatment
Official Title:
Effect of Corrective Calcaneal Kinesiology Tape on Pain, Function and Sonographic Picture of Plantar Fascia in Adolescents With Pronated Foot
Actual Study Start Date :
Jul 1, 2023
Anticipated Primary Completion Date :
Dec 30, 2023
Anticipated Study Completion Date :
Feb 28, 2024

Arms and Interventions

Arm Intervention/Treatment
Experimental: Group A

Group A: will receive corrective kinesiotaping (50-75% stretch) for 4 weeks, 2 times per week, with 1 day rest

Device: Corrective Kinesiology taping
corrective kinesiology tape is a form of biomechanical tape that is used with specific tension to get a corrective effect
Other Names:
  • Kinesiotape
  • Active Comparator: Group B

    Group B: will receive a placebo non-corrective kinesio taping (without tension) with no mechanical correction of calcaneus

    Device: Non corrective kinesiology tape
    Non-corrective kinesiology tape is a form of biomechanical tape that is used without any tension

    Placebo Comparator: Group C

    Group C: will receive a home program of intrinsic foot strengthening and stretching exercises.

    Other: Home exercise program
    Intrinsic foot strengthening and stretching exercises

    Outcome Measures

    Primary Outcome Measures

    1. Pain Intenisty [4 weeks]

      Visual Analogue Scale

    Secondary Outcome Measures

    1. Foot function [4 weeks]

      first two subscales of Foot Function Index

    Other Outcome Measures

    1. Sonographic picture of plantar fascia [4 weeks]

      Diagnostic ultrasound

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    12 Years to 18 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Children with unilateral or bilateral Plantar Fasciitis.

    • Pronated foot/feet 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:
    • 1- Corticosteroid injection of the heel within the past 3 months. 2- Posterior heel pain. 3- Systemic inflammatory conditions. 4- Diabetes. 5- Surgery of the foot. 6- Neuromuscular conditions e.g. CP. 7- Individuals with BMI > 25. 8- Individuals engaged in regular athletic activities

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Tayseer Younes Cairo Al Qahirah Egypt 11411

    Sponsors and Collaborators

    • Beni-Suef University
    • Azhar University

    Investigators

    • Principal Investigator: Tayseer S Abdeldayem, PhD, Beni-Suef University

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Sherin Hassan Mohammed Mehani, Professor, Beni-Suef University
    ClinicalTrials.gov Identifier:
    NCT06146959
    Other Study ID Numbers:
    • P.T.REC/012/004632
    First Posted:
    Nov 27, 2023
    Last Update Posted:
    Nov 27, 2023
    Last Verified:
    Nov 1, 2023
    Studies a U.S. FDA-regulated Drug Product:
    No
    Studies a U.S. FDA-regulated Device Product:
    No
    Keywords provided by Sherin Hassan Mohammed Mehani, Professor, Beni-Suef University

    Study Results

    No Results Posted as of Nov 27, 2023