- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06739785
Turkish Translation of SportsConcussion Assesment Tool 6 (SCAT 6-tr)
Turkish Translation And Cross-Cultural Adaptation of The Sport Concussion Assessment Tool 6th Edition (SCAT6)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Concussions constitute an important part of sports injuries. Concussion is a head trauma caused by blows to the head, face and neck. Head injuries are common in contact sports. They are usually minor injuries. However, injuries should be taken seriously. Because mismanagement can be fatal in cases of misdiagnosis. Therefore, it is among medical emergencies .
A sports concussions group has been established for the correct management of concussions seen in sports. In 2022, the group met in Amsterdam, renewed the existing consensus and published it in the British Journal of Sports Medicine in 2023 . The Sport Concussion Assessment Tool (SCAT), developed by the sports concussion group (CISG), is a valid and reliable approach to assessing sports-related head injuries ('Sport Concussion Assessment Tool 6 (SCAT6),' 2023). The main purpose of SCAT is to assess head injuries with a standardised method and to manage the return to sport process of athletes. SCAT is an assessment tool that evaluates adult athletes over the age of 13 in terms of physical, mental and cognitive aspects and includes different sections.
In the literature, there are adaptations of previous and current versions of SCAT in different languages (Korean, Chinese, Persian, Arabic). However, no Turkish translation and adaptation study of any version has been conducted before. Turkishisation of this assessment tool is an important step in terms of accurately evaluating concussion injuries in Turkish-speaking athletes and managing the return to sport process correctly. The aim of this study is to translate the SCAT 6 into Turkish and to provide intercultural adaptation of the SCAT 6 to the literature.
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Locations
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Ordu, Turkey
- Ordu University
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Child
- Adult
- Older Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
To be 13 years old
- Talking in Turkish
- Being a Professional Athlete
Exclusion Criteria:
- Athletes who experience any injury during the test, retest process will be excluded from the study.
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Lawshe Analysis
Time Frame: Before the create last verison of SCAT6-tr .It is planned to take 1 month.
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The appropriateness of the assessment tool will be determined by analysing the expert opinion forms reported by the experts.
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Before the create last verison of SCAT6-tr .It is planned to take 1 month.
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
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Inter-rater reliability
Time Frame: After the last version created. It is planned to take 2 months
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Scat 6-Tr will be applied randomly to 30 athletes by 2 different assessors.
Scat 6-Tr will be applied randomly to 30 athletes by 2 different assessors.
Inter-rater correlation will be analysed by Intra-class Correlation Coefficient (ICC).
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After the last version created. It is planned to take 2 months
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Test-retest reliability.
Time Frame: After the last version created. It is planned to take 2 months
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SCAT6-tr will be administered to 30 athletes 2 times by the same assessor at 1 week intervals.
The correlation between measurements will be evaluated with Intra-class Correlation Coefficient (ICC).
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After the last version created. It is planned to take 2 months
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Collaborators and Investigators
Sponsor
Collaborators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- E-1467249-000-1071258
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
product manufactured in and exported from the U.S.
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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