The Effects of Kinesio Taping in Archery

December 29, 2022 updated by: Eylül Pınar KISA, Biruni University

Does Kinesio Taping Affect Shooting Performance Acutely in Archery Athletes?

The aim of the study is to investigate the effects of KT on archery athletes' performance.

Study Overview

Status

Completed

Intervention / Treatment

Detailed Description

Archery is a sport that requires strength, endurance, stabilization, and coordination of the upper body and shoulder girdle muscles. Kinesio taping (KT), which increased in popularity with the use in the athletes in the 2008 summer Olympics, is commonly investigated in the literature. KT is claimed to reduce pain and edema, increase functional performance, joint position sense, and blood-lymph flow, provide stability, and improve range of motion, flexibility, and strength. The aim of the study is to investigate the effects of KT on archery athletes' performance.

Study Type

Observational

Enrollment (Actual)

43

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

      • Istanbul, Turkey
        • Biruni 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

11 years to 14 years (Child)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Sampling Method

Probability Sample

Study Population

Archery athletes

Description

Inclusion Criteria:

  • To be archery in the elite category for at least 1 year
  • Attending training sessions at least 2 days a week

Exclusion Criteria:

  • Having any neurological problems
  • Having a Turkish-speaking and reading disability

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

  • Observational Models: Other
  • Time Perspectives: Prospective

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of Archery Shooting Performance
Time Frame: 15 minutes
The archery shooting performance will be assessed with the target paper which includes 5 scoring colors. The subject will be placed within 18 meters distance of the target paper. The subjects will have 12 arrows to make the shoot. The best 6 shoots will be taken to calculate the total score.
15 minutes

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Assessment of Proprioception
Time Frame: 15 minutes
The proprioception will be assessed with the angle reproduction test.
15 minutes
Evaluation of Scapular Dyskinesis
Time Frame: 5 minutes
Dyskinesis will be assessed with scapular lateral slide test.
5 minutes

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Eylül Pınar Kısa, PhD, Biruni 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)

August 4, 2022

Primary Completion (Actual)

September 4, 2022

Study Completion (Actual)

September 18, 2022

Study Registration Dates

First Submitted

July 26, 2022

First Submitted That Met QC Criteria

July 27, 2022

First Posted (Actual)

July 29, 2022

Study Record Updates

Last Update Posted (Estimate)

January 2, 2023

Last Update Submitted That Met QC Criteria

December 29, 2022

Last Verified

September 1, 2022

More Information

Terms related to this study

Other Study ID Numbers

  • ARCHERY (Other Identifier: San Raffaele Hospital)

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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