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Clinical Trials/NCT06146959
NCT06146959
Enrolling By Invitation
Not Applicable

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

Beni-Suef University1 site in 1 country30 target enrollmentStarted: December 1, 2023Last updated:

Overview

Phase
Not Applicable
Status
Enrolling By Invitation
Enrollment
30
Locations
1
Primary Endpoint
Pain Visual Analogue Scale

Overview

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.

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 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.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Treatment
Masking
Double (Investigator, Outcomes Assessor)

Eligibility Criteria

Ages
12 Years to 18 Years (Child, Adult)
Sex
All
Accepts Healthy Volunteers
No

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 \>
  • Individuals engaged in regular athletic activities

Outcomes

Primary Outcomes

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

  • Foot function Index(4 weeks)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Tayseer Saber Abdeldayem

Lecturer

Beni-Suef University

Study Sites (1)

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