Effects of Windlass Versus Calcaneal Taping in Football Player With Plantar Fasciitis.

January 1, 2025 updated by: Riphah International University

Effects of Windlass Versus Calcaneal Taping on Pain, Flexibility and Lower Extremity Function in Football Player With Plantar Fasciitis.

Plantar fasciitis is a prevalent ailment that affects the plantar fascia, a dense tissue strip that spans the underside of the foot, from the heel bone to the toes. Football players are especially susceptible to this ailment because of the sport's high-impact nature, which includes repetitive sprinting, jumping, and quick changes in direction. Taping has been used for many years for various ailments. The purpose of this study is to determine the effects of two taping techniques i.e. windlass taping and calcaneal taping on pain, flexibility and lower extremity function in football players.

Study Overview

Status

Recruiting

Conditions

Detailed Description

The study will be a randomized clinical trial conducted at the Pakistan Sports Board and The Raider's football club over a duration of 10 months after synopsis approval. The required sample size for each group, after accounting for a 10% attrition rate, will be 17. Two study groups will be established: Group A, which will receive calcaneal taping among football players, and Group B, which will receive windlass taping among football players. Nonprobability purposive sampling will be employed. Data will be collected using the Numeric Pain Rating Scale (NPRS), Hubscher maneuver, goniometer, and lower extremity functional scale (LEFS) to assess pain severity, flat foot type flexibility, joint range of motion, and lower limb function, respectively. This comprehensive study aims to contribute valuable insights into the effects of calcaneal and windlass taping on football players.

Study Type

Interventional

Enrollment (Estimated)

34

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 Contact

Study Locations

    • Punjab
      • Lahore, Punjab, Pakistan, 54700
        • Not yet recruiting
        • Raiders football club
        • Contact:
        • Principal Investigator:
          • Maheen Shahid, MS-SPT
        • Sub-Investigator:
          • Muhammad Asrar Yousaf, Mphil
      • Lahore, Punjab, Pakistan, 619
        • Recruiting
        • Pakistan Sports Board
        • Contact:
        • Principal Investigator:
          • Maheen Shahid, MS-SPT
        • Sub-Investigator:
          • Muhammad Asrar Yousaf, Mphil

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • positive windlass test
  • Pain can appear after a period of intense training, normally declines with the warm up and reappears at the end of training.
  • Intense and acute heel pain localized primarily where plantar fascia attaches to the anterior calcaneus.
  • The pain presents on first walking in the morning or after a rest period.

Exclusion Criteria:

  • Congenital deformity of ankle and foot.
  • History of foot and ankle fracture.
  • History of ankle and foot surgery.
  • Previous surgery or treatment for plantar fasciitis in the previous 6 months.
  • Use of an assistive device for ambulation
  • Use of an assistive device for ambulation
  • Refuse to participate in the 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: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Calcaneal taping
Calcaneal taping is a method employed to offer assistance and relieve discomfort in the heel and ankle area. Start with a clean surface and apply first tape from lateral malleolus, pulling calcaneus in medial direction and attach to medial malleolus. Apply two more tapes in the same manner going distally. Apply an anchor tape at back of heel.
Calcaneal taping is a method employed to offer assistance and relieve discomfort in the heel and ankle area. Start with a clean surface and apply first tape from lateral malleolus, pulling calcaneus in medial direction and attach to medial malleolus. Apply two more tapes in the same manner going distally. Apply an anchor tape at back of heel.
Experimental: Windlass taping
Begin by anchoring the tape just above the ball of the foot (metatarsal heads). Tear or cut a strip of tape, approximately 2-3 inches long, and place it horizontally around the foot, securing the starting point. Pull the tape diagonally across the bottom of the foot, aiming to support the arch. The tape should be applied with moderate tension to provide support without causing discomfort. While keeping tension on the tape, extend the big toe (great toe) upward. As the toe extends, the tape should tighten, activating the windlass mechanism and providing additional arch support.
Begin by anchoring the tape just above the ball of the foot (metatarsal heads). Tear or cut a strip of tape, approximately 2-3 inches long, and place it horizontally around the foot, securing the starting point. Pull the tape diagonally across the bottom of the foot, aiming to support the arch. The tape should be applied with moderate tension to provide support without causing discomfort. While keeping tension on the tape, extend the big toe (great toe) upward. As the toe extends, the tape should tighten, activating the windlass mechanism and providing additional arch support.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
numeric pain rating scale
Time Frame: 1 week
This is a self-report assessment where participants evaluate their pain using a number scale. The scale normally spans from 0 to 10, where 0 signifies the absence of pain and 10 signifies the most severe agony imaginable.
1 week
hubscher maneuver
Time Frame: 1 week
It is a method of evaluating the flexibility of a pes planus or flat foot type. The test is performed with the patient weight bearing, with the foot flat on the ground, while the clinician dorsiflexors the hallux and watches for an increasing concavity of the Arches of the foot
1 week
calcaneal stance phase angle
Time Frame: 1 week
it is the sngle between calcaneal bisection and vertical line to floor when patient is standing erect on flat surface.
1 week
lower extremity functional scale
Time Frame: 1 week
The Lower Extremity Functional Scale (LEFS) is a patient-reported instrument used to assess the level of functioning in cases of lower extremity musculoskeletal (MSK) disorders. The LEFS has 20 questions with scores ranging from 0 (severe difficulty/inability to execute activity) to 4 (no difficulties). The overall score can be calculated by adding the points for each item.
1 week

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Muhammad Asrar Yousaf, Mphil, Riphah International University

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

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)

October 10, 2024

Primary Completion (Estimated)

January 1, 2025

Study Completion (Estimated)

January 1, 2025

Study Registration Dates

First Submitted

October 10, 2024

First Submitted That Met QC Criteria

October 10, 2024

First Posted (Actual)

October 15, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

January 1, 2025

Last Verified

January 1, 2025

More Information

Terms related to this study

Other Study ID Numbers

  • REC/RCR&AHS/24/0407

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.

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