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NCT Number: NCT06146959

Corrective Calcaneal Kinesiology Tape in Adolescents With Pronated Foot

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.

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Key information

Age range

12 year–18 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Tayseer Younes

Cairo, Cairo Governorate, 11411, Egypt

About this study

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 6 weeks, 2 times per week with 1 day of rest; Group B 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 the foot function index (FFI), and a sonographic picture of the foot for each adolescent. Participants will be recruited from outpatient clinics and schools.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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

Treatment and study plan

Corrective Kinesiology taping

Device

corrective kinesiology tape is a form of biomechanical tape that is used with specific tension to get a corrective effect

Other names: Kinesiotape

Home exercise program

Other

Intrinsic foot strengthening and stretching exercises

Primary outcomes

  1. Pain Visual Analogue Scale

    Time frame: 4 weeks

    minimum score is 0, and the maximum score is 10 ; higher scores means worse outcome

Secondary outcomes

  1. Foot function Index

    Time frame: 4 weeks

    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)

Other outcomes

  1. Diagnostic ultrasound

    Time frame: 4 weeks

    A sonographic picture of plantar fascia

Sponsors and collaborators

Lead sponsor

Beni-Suef University

Other

Collaborators

  • Al-Azhar University

Registry information

Official study title

Effect of Corrective Calcaneal Kinesiology Tape on Pain, Function and Sonographic Picture of Plantar Fasciitis in Adolescents With Pronated Foot

Important dates

Study start
2023
Primary completion
2024
Study completion
2025
First posted
Nov 27, 2023
Registry last updated
Apr 17, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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