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Corrective Calcaneal Kinesiology Tape in Adolescents With Pronated Foot

B

Beni-Suef University

Status

Invitation-only

Conditions

Physical Disability
Physical Therapy Modalities

Treatments

Other: Home exercise program
Device: Corrective Kinesiology taping

Study type

Interventional

Funder types

Other

Identifiers

NCT06146959
P.T.REC/012/004632

Details and patient eligibility

About

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.

Full 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.

Enrollment

30 estimated patients

Sex

All

Ages

12 to 18 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

30 participants in 2 patient groups

Group A
Experimental group
Description:
Group A: will receive corrective kinesiotaping (50-75% stretch) for 4 weeks, 2 times per week, with 1 day rest
Treatment:
Device: Corrective Kinesiology taping
Group B
Active Comparator group
Description:
Group B will receive a home program of intrinsic foot strengthening and stretching exercises.
Treatment:
Other: Home exercise program

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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