- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05691946
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
Intervention / Treatment
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
-
-
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Amasya, Turkey
- Amasya University
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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.
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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.
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2 hours
|
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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.
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2 hours
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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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