- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05479084
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
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
-
-
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Istanbul, Turkey
- Biruni 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
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.
Sponsor
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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