Calcaneal Low Dye Taping Plantar Fascial Stretching and Sham Taping in Football Players

February 20, 2023 updated by: Riphah International University

Comparative Effects of Calcaneal Low Dye Taping Plantar Fascial Stretching and Sham Taping on Acute Plantar Heal Pain and Functional Activity Level in Football Players

Showing the effect of calcaneal Low-dye Taping on acute planter heel pain and functional activity level in football players.

Study Overview

Detailed Description

Planter fascia is a fibrous connective tissue originate from the medial calcaneal tubercle and help support the arch of the foot repetitive tensile overload from standing for long periods of time or running causes changes in the aponeurosis. Patient mostly present with pain on first step in the morning or after long non-weight bearing , Tenderness to anterior medial head. Its can first be treated conservatively where 90 % cases treated greater then 6 months of duration. Baseline treatment is given as Rest , Ice , compression and Elevation , with this NSAID ,shoe inset ,Taping, orthotics, deep friction massage and precautions are advised to the patients. Arch taping is most probably used and orthotics in acute treatment is commonly preferred due to its cost.Taping effects most probably overlooked in general gait parameters, patient feedback on pain relief and function recovery.

Study Type

Interventional

Enrollment (Actual)

21

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

    • Punjab
      • Lahore, Punjab, Pakistan, 54000
        • Surya Azeem Hospital

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

20 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Both male and female football players
  • Age (20-45 yrs)
  • Pain with the first step upon walking
  • Pain located at the heel or Planter surface of Mid-foot consistent with Planter fasciitis
  • Presence of an everted calcaneus greater than or equal to 2°

Exclusion Criteria:

  • Patient with surgery and treatment with previous 6 month
  • History of Ankle or foot fracture
  • Congenital deformity of the foot and ankle
  • Sever Spasticity
  • Use of an Assistive device
  • Bilateral Planter heel pain
  • Refusal to participate in study

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: Crossover Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Low-Dye taping
out of 21 participants 7 will be included in the study design as an experimental group using low-dye taping in acute stage
Low-dye taing using 4 tapes around calcaneam
Active Comparator: Plantar fascia stretching
out of 21 participants 7 will be included in the study design as an active participants group using plantar fscia stretching in acute stage
out of 21 participants 7 will be included in the study design as an active participants group using plantar fscia stretching in acute stage
Placebo Comparator: Sham taping
out of 21 participants 7 will be included in the study design as an active participants group using plantar fscia stretching in acute stage
out of 21 participants 7 will be included in the study design as an plecebo group using sham taping in acute stage

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
numeric pain rating scale
Time Frame: 3 week
The Numeric Pain Rating Scale (NPRS) is a famous strategy to evaluate Pain. The NPRS has a dependable, substantial and delicate instrument to survey torment. Torment score as per the NPRS (0-10), made during the principal strides toward the beginning of the day, was the essential result (0 as "no aggravation" and 10 as "exceptionally serious agony").
3 week
foot and ankle disability index
Time Frame: 3 week
It is utilized to evaluate the utilitarian restrictions connected with foot and lower leg, action of day to day living and most troublesome errand that are vital for sports e.g., Walk, word related execution, Agony, Rest and Strength. The foot and ankle disability index (FADI) is scored out of 104, with a score of 0 indicating maximum disability and a score of 104 indicating no disability. The total FADI score corresponds to the sum of Activity and Pain subscale scores (maximum score of 88 for Activity and 16 for Pain).
3 week

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Investigators

  • Principal Investigator: Fatima Dr Tariq, Phd, Riphah International 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 19, 2022

Primary Completion (Anticipated)

February 1, 2023

Study Completion (Anticipated)

February 1, 2023

Study Registration Dates

First Submitted

January 4, 2023

First Submitted That Met QC Criteria

February 20, 2023

First Posted (Estimate)

February 21, 2023

Study Record Updates

Last Update Posted (Estimate)

February 21, 2023

Last Update Submitted That Met QC Criteria

February 20, 2023

Last Verified

February 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • 30162

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

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.

Clinical Trials on Sports Physical Therapy

Clinical Trials on Low-dye taping

Subscribe