- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06146959
Corrective Calcaneal Kinesiology Tape in Adolescents With Pronated Foot
April 12, 2025 updated by: Tayseer Saber Abdeldayem, Beni-Suef University
Effect of Corrective Calcaneal Kinesiology Tape on Pain, Function and Sonographic Picture of Plantar Fasciitis 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.
Study Overview
Status
Enrolling by invitation
Conditions
Intervention / Treatment
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 Type
Interventional
Enrollment (Estimated)
30
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Al Qahirah
-
Cairo, Al Qahirah, Egypt, 11411
- Tayseer Younes
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
Accepts Healthy Volunteers
No
Description
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 Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / 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
|
corrective kinesiology tape is a form of biomechanical tape that is used with specific tension to get a corrective effect
Other Names:
|
|
Active Comparator: Group B
Group B will receive a home program of intrinsic foot strengthening and stretching exercises.
|
Intrinsic foot strengthening and stretching exercises
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Pain Visual Analogue Scale
Time Frame: 4 weeks
|
minimum score is 0, and the maximum score is 10 ; higher scores means worse outcome
|
4 weeks
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
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)
|
4 weeks
|
Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Diagnostic ultrasound
Time Frame: 4 weeks
|
A sonographic picture of plantar fascia
|
4 weeks
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Collaborators
Investigators
- Principal Investigator: Tayseer S Abdeldayem, PhD, Beni-Suef University
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 1, 2023
Primary Completion (Actual)
July 28, 2024
Study Completion (Estimated)
December 30, 2025
Study Registration Dates
First Submitted
November 18, 2023
First Submitted That Met QC Criteria
November 18, 2023
First Posted (Actual)
November 27, 2023
Study Record Updates
Last Update Posted (Actual)
April 17, 2025
Last Update Submitted That Met QC Criteria
April 12, 2025
Last Verified
April 1, 2025
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- P.T.REC/012/004632
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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