Effect of Rigid Tapping on Chronic Functional Ankle Instability in Basketball Players

January 15, 2024 updated by: Islam Gomaa Mohamed Eid, Cairo University
This study aims rigid tapping on chronic functional ankle instability in professional basketball players.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Lateral ankle sprains (LASs) are common injuries in sports and physical activities, with up to 40% of individuals experiencing a first-time LAS developing chronic ankle instability (CAI). LASs predominantly affect the anterior talofibular ligament, and residual symptoms can persist in a significant percentage of patients. However, many individuals with ankle sprains do not seek professional treatment, leading to potential underestimation of the injury severity. CAI is characterized by recurrent episodes of ankle giving way, ongoing symptoms, reduced ankle range of motion, diminished self-reported function, and persistent ankle sprains beyond one year. It is attributed to both mechanical and functional instability, with factors such as proprioceptive deficits and mechanical insufficiencies contributing to the condition. Taping, particularly rigid taping, is commonly used by athletes to enhance joint stability and improve dynamic balance and functional performance. Rigid taping limits joint movement, improves joint position, and provides external support without compromising functional performance. Taping is especially prevalent in multidirectional sports like basketball, where ankle sprains are frequent. The use of tapes aims to restrict ankle movement, increase joint stability, and enhance proprioception without hindering athletic performance.

Study Type

Interventional

Enrollment (Actual)

28

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

      • Giza, Egypt, 12613
        • Faculty of physical therapy

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

Accepts Healthy Volunteers

No

Description

Inclusion Criteria:

  • Basketball players with age range from 18-40 years old.
  • Body mass index (BMI) range from 18-25 H/m2.
  • Participants had episodes of subjective sensation of instability in the last six months.
  • Participants have at least moderate ankle instability, defined as a score of <25 on the Cumberland Ankle Instability Tool (CAIT).

Exclusion Criteria:

  • Participants had a history of surgery or fractures in the ankle joints.
  • Participants had a neurological or vestibular disorder.
  • Participants were unable to understand the nature of the protocol and test instructions.

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: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: study group
this study group assessed by 3 functional tests (Figure of 8 hopping , single leg stance test and y balance test) pre and post receiving rigid ankle tapping

The patient was rested in supine or long sitting position on a table Pre-wrap was applied to cover all the area before tapping Two strips used separately as anchors at the two ends of the pre-wrap. Two Longitudinal stirrup of tape were used from medial side of the superior anchor to lateral side of the same anchor.

Two horizontal stirrup of tape were used from medial side of the distal anchor to lateral side of the same anchor to support the medial side of the foot.

Figure-of-eight straps were utilized for the taping. Lateral heel lock was applied.The tape then proceeded from the lateral side of the foot, looping around the heel, and returning to the same starting point by crossing over the Achilles tendon from behind.

Medial heel lock was applied, the tape application was similar to the lateral heel lock but was at the opposite direction.

Superior and inferior anchors were applied to support all the previous strips

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Ankle Stability
Time Frame: 3 days
measured by y balance test and single leg stance test
3 days
functional performance
Time Frame: 3 days
measured by Figure of 8 hopping test
3 days

Collaborators and Investigators

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

Investigators

  • Study Chair: Salwa Fa Abdel-Majeed, phd, Cairo 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)

October 12, 2022

Primary Completion (Actual)

April 10, 2023

Study Completion (Actual)

August 1, 2023

Study Registration Dates

First Submitted

August 29, 2023

First Submitted That Met QC Criteria

August 29, 2023

First Posted (Actual)

September 5, 2023

Study Record Updates

Last Update Posted (Actual)

January 17, 2024

Last Update Submitted That Met QC Criteria

January 15, 2024

Last Verified

January 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • 012/003958

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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