Acute Effects of Kinesiology Taping in Handball Players

January 11, 2023 updated by: Amasya University

Acute Effects of Kinesiology Taping On Functional Performance And Physical Parameters In Handball Players: Randomised Placebo-Controlled Trial

The aim of this randomised placebo-controlled study was to investigate the acute effect of kinesiology taping in the gastro-soleus muscle group of handball players.

Researchers compared the placebo and the kinesiology taping groups to see if there were any effects on foot plantar and dorsiflexion muscle strength, balance, proprioception, horizontal jumping and injury proneness.

Study Overview

Status

Completed

Conditions

Detailed Description

This randomised placebo-controlled and double blinded study aimed to investigate the acute effect of kinesiology taping in the gastro-soleus muscle group, which has the key role in jumping, of handball players on foot plantar and dorsiflexion muscle strength, balance, proprioception, horizontal jumping and injury proneness. There were two groups in the study: the experimental group was applied 'Y shaped' kinesiology taping on gastro-soleus muscle group, based on facilitation technique with 25-50% stretching. The control (placebo) group was applied kinesiology taping on gastro-soleus muscle group without any stretching. Participants' muscle strength, proprioception, balance, horizontal jumping and injury proneness was measured before and two hours after taping.

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

      • Amasya, Turkey
        • Amasya University

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

18 years to 35 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  • Licensed handball player
  • Volunteer to participate the study

Exclusion Criteria:

  • Any discomfort that is contraindicated for the measurements
  • Have suffered any injury in the last 6 months

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: Screening
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Double

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Kinesiology Taping Group
The experimental group was applied 'Y shaped' kinesiology taping on gastro-soleus muscle group, based on facilitation technique with 25-50% stretching.
Placebo Comparator: Placebo Control Group
Placebo Taping Group
The placebo group was applied kinesiology taping on gastro-soleus muscle group without any stretching.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Muscle strength
Time Frame: 2 hours
Foot dorsiflexion and plantar flexion muscle strength were measured using a manual dynamometer (MicroFET2 (Hogan Inc., West Jordan, USA). This device; shows the peak force in Newtons on its own screen. Measurements were made in three repetitions after a 30-second records. The highest value was recorded.
2 hours
Proprioception
Time Frame: 2 hours
Ankle proprioception was measured using Baseline Digital Inclinometer (New York, USA) device. This was measured on the dominant and non-dominant ankle with eyes open and eyes closed. Ankle dorsiflexion at 10 degrees, ankle plantar flexion at 11 degrees, and 25 degrees was measured in active reproduction test positions.
2 hours

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Horizontal jump performance
Time Frame: 2 hours
This was measured by standing long jump with the direction of movement develops from vertical to horizontal. The distance between the zero point and the last point of contact of the foot was measured in centimetres. Three repetitions were performed and the highest value was recorded.
2 hours
Balance
Time Frame: 2 hours
Dynamic balance was measured with Y-balance test. The participant reached anterior, posteromedial, and posterolateral directions with one foot, while other foot was on the centre. The test was repeated three times in each direction and the average was recorded in centimetres.
2 hours
Injury proneness
Time Frame: 2 hours
Injury proneness was measured using Functional Movement Screen test. This test consists of seven different positions to measure strength, flexibility, balance and such various motor skills. The movements are deep squats, high stepping, single-line stepping forward, shoulder mobility, active straight leg raise, trunk stability push-ups, rotation stability. Each movement is scored between 0 and 3 points, the score that the participant can get from the test is between 0 and 21. It was scored 3 points if the movement was performed completely well, 2 points if the movement was performed with an error, 1 point if the movement was not performed according to the specified instruction, and 0 points if pain was experienced during the movements.
2 hours

Collaborators and Investigators

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

August 1, 2022

Primary Completion (Actual)

October 1, 2022

Study Completion (Actual)

October 1, 2022

Study Registration Dates

First Submitted

January 11, 2023

First Submitted That Met QC Criteria

January 11, 2023

First Posted (Actual)

January 20, 2023

Study Record Updates

Last Update Posted (Actual)

January 20, 2023

Last Update Submitted That Met QC Criteria

January 11, 2023

Last Verified

January 1, 2023

More Information

Terms related to this study

Other Study ID Numbers

  • AmasyaU12

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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