- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05356065
The Turkish Version of the OSTRC Questionnaires
The Turkish Version of the Oslo Sports Trauma Research Center (OSTRC) Questionnaire on Overuse Injuries and Health Problems; Validity and Reliability Study
Exposure to repetitive activities and heavy workloads makes athletes vulnerable to overuse injuries over time. Well-timed detection of these injuries is crucial to maintaining their sports career healthily. The Oslo Sports Trauma Research Centre questionnaires for Overuse Injury (OSTRC-O) and Health Problems (OSTRC-H) are universally used as valid and reliable tools in athlete health screening. This study aims to make them available for Turkish athletes.
The internal consistency, reproducibility, and validity of the questionnaires were analyzed. Data were obtained from 72 athletes from different sports types. 33 participants were screened weekly for six weeks to detect score changes and calculate effect sizes. Participants filled out the OSTRC-O, the OSTRC-H, the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ), and the Nottingham Health Profile (NHP) for validity analyses. The internal consistency and test-retest reliability values were very high for both questionnaires. There was a moderate correlation between OSTRC-O and OSTRC-H scores with CMDQ and NHP. The area under the curve (AUC) values were adequate for all scales. The effect size values were moderate for all scales. Turkish versions of the OSTRC-O and OSTRC-H questionnaires are valid and reliable tools for Turkish-speaking athletes in different sports branches.
Study Overview
Detailed Description
Introduction and Aims All athletes are vulnerable to acute traumas or cumulative injuries throughout their sports life. Thus, screening the health levels of athletes and investigating whether they have overuse injuries is essential both to prevent acute traumas and improve health and performance. There is no valid and reliable subjective measurement tool to perform this screening in athletes in Turkish currently. However, the valid and reliable "Oslo Sports Trauma Research Centre Overuse Injury Questionnaire - (OSTRC)" questionnaires are available in English. So the investigators aimed to adapt the OSTRC- Overuse (OSTRC-O) and the OSTRC-Health Questionnaire (OSTRC-H) into Turkish.
Methods Permission was obtained from the developer authors. Then, ethical approval was acquired from the clinical researches ethics committee. Questionnaires were adapted into Turkish systematically. A pilot study was conducted to ensure the accuracy of meaning and comprehensibility of translated questionnaires. Next, the validity and reliability of the new tools were estimated. 72 athletes aged between 18 and 35, who can understand and speak Turkish fluently from various sports branches, were included. Informed consent was obtained from all athletes. The demographics of the participants were recorded. All participants were administered the Cornell Musculoskeletal Discomfort Questionnaire (CMDQ), Nottingham Health Profile (NHP), OSTRC-O, and OSTRC-H questionnaires. The OSTRC-O OSTRC-H and CMDQ questionnaires were repeated weekly for six weeks on 33 athletes.
Reliability was analyzed by internal consistency and test-retest methods. The validity of the scale was evaluated in terms of content validity and concurrent validity. Content validity was verified with reports of participants at the end of the sixth week. To evaluate the concurrent validity, total OSTRC scores were compared with the total scores of CMDQ and NHP. Correlations of the OSTRC-O and OSTRC-H change scores with CMDQ change scores separately were assessed throughout the six weeks in point of the Effect Size (ES) for responsiveness. Receiver Operating Characteristic (ROC) Curve test based on the area under the curve (AUC) depicted to define the performance of these assessment tools. Statistical analyses were performed with the Statistical Package for Social Sciences Program.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
-
-
Ankara, Turkey, 006450
- Gazi University
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
- accepting to participate in the study
- Participating in sports
Exclusion Criteria:
- Being illiterate
- Being younger than 18 years or older than 35 years
Study Plan
How is the study designed?
Design Details
- Observational Models: Cohort
- Time Perspectives: Prospective
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Oslo Sports Trauma Research Centre Questionnaires for Overuse Injury (OSTRC-O)
Time Frame: Baseline
|
The "Oslo Sports Trauma Research Centre Questionnaires for Overuse Injury" is a self-reported outcome measure.
It queries sports participation, training volume, sports performance, and pain for a selected body location-e.g.
knee taking into account the last seven days.
A severity score is between 0-100 points.
Higher points show worse health conditions.
|
Baseline
|
Oslo Sports Trauma Research Centre questionnaires on Health Problems (OSTRC-H)
Time Frame: Baseline
|
"Oslo Sports Trauma Research Centre questionnaires on Health Problems" is a self-reported outcome measure.
It is applied to determine the effects of general health problems on sports participation, training volume, sports performance, and pain for the last seven days.
A severity score is between 0 and 100 points.
Higher points show worse health conditions.
|
Baseline
|
Cornell Musculoskeletal Discomfort Questionnaire (CMDQ)
Time Frame: Baseline
|
Cornell Musculoskeletal Discomfort Questionnaire is used to ascertain the musculoskeletal problems experienced in the last week during work life.
Participants marked the frequency, discomfort, and interference categories for 20 different regions on the body map diagram.
The total score of the questionnaire is between 0 (best condition) and 90 (worst health status).
|
Baseline
|
Nottingham Health Profile (NHP)
Time Frame: Baseline
|
Nottingham Health Profile is a self-reported outcome measure.
It is a general health questionnaire consisting of 6 sub-parameters (pain, physical mobility, emotional reactions, sleep, energy level, social isolation) and 38 items.
Participants marked yes or no for each item.
The total score ranges from 0 to 600, and the total score is inversely proportional to the quality of life.
|
Baseline
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Oslo Sports Trauma Research Centre Questionnaires for Overuse Injury (OSTRC-O)
Time Frame: Change from baseline score at 6 weeks
|
The "Oslo Sports Trauma Research Centre Questionnaires for Overuse Injury" is a self-reported outcome measure.
It queries sports participation, training volume, sports performance, and pain for a selected body location-e.g.
knee taking into account the last seven days.
A severity score is between 0-100 points.
Higher points show worse health conditions
|
Change from baseline score at 6 weeks
|
Oslo Sports Trauma Research Centre questionnaires on Health Problems (OSTRC-H)
Time Frame: Change from baseline score at 6 weeks
|
"Oslo Sports Trauma Research Centre questionnaires on Health Problems" is a self-reported outcome measure.
It is applied to determine the effects of general health problems on sports participation, training volume, sports performance, and pain for the last seven days.
A severity score is between 0 and 100 points.
Higher points show worse health conditions.
|
Change from baseline score at 6 weeks
|
Cornell Musculoskeletal Discomfort Questionnaire (CMDQ)
Time Frame: Change from baseline score at 6 weeks
|
Cornell Musculoskeletal Discomfort Questionnaire is used to ascertain the musculoskeletal problems experienced in the last week during work life.
Participants marked the frequency, discomfort, and interference categories for 20 different regions on the body map diagram.
The total score of the questionnaire is between 0 (best condition) and 90 (worst health status).
|
Change from baseline score at 6 weeks
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Şeyda ÖZAL, Ph.D. (c), Gazi University Faculty of Health Sciences
- Study Director: Nihan KAFA, Asoc. Prof., Gazi University Faculty of Health Sciences
- Principal Investigator: Fuat YUKSEL, Ph.D. (c), Gazi University Faculty of Health Sciences
- Study Chair: Nevin A GÜZEL, Prof. Dr., Gazi University Faculty of Health Sciences
Publications and helpful links
General Publications
- Beaton DE, Bombardier C, Guillemin F, Ferraz MB. Guidelines for the process of cross-cultural adaptation of self-report measures. Spine (Phila Pa 1976). 2000 Dec 15;25(24):3186-91. doi: 10.1097/00007632-200012150-00014. No abstract available.
- Clarsen B, Myklebust G, Bahr R. Development and validation of a new method for the registration of overuse injuries in sports injury epidemiology: the Oslo Sports Trauma Research Centre (OSTRC) overuse injury questionnaire. Br J Sports Med. 2013 May;47(8):495-502. doi: 10.1136/bjsports-2012-091524. Epub 2012 Oct 4.
- Bahr R, Bahr IA. Incidence of acute volleyball injuries: a prospective cohort study of injury mechanisms and risk factors. Scand J Med Sci Sports. 1997 Jun;7(3):166-71. doi: 10.1111/j.1600-0838.1997.tb00134.x.
- Clarsen B, Ronsen O, Myklebust G, Florenes TW, Bahr R. The Oslo Sports Trauma Research Center questionnaire on health problems: a new approach to prospective monitoring of illness and injury in elite athletes. Br J Sports Med. 2014 May;48(9):754-60. doi: 10.1136/bjsports-2012-092087. Epub 2013 Feb 21.
- Hunt SM, McKenna SP, McEwen J, Williams J, Papp E. The Nottingham Health Profile: subjective health status and medical consultations. Soc Sci Med A. 1981 May;15(3 Pt 1):221-9. doi: 10.1016/0271-7123(81)90005-5. No abstract available.
- Erdinc O, Hot K, Ozkaya M. Turkish version of the Cornell Musculoskeletal Discomfort Questionnaire: cross-cultural adaptation and validation. Work. 2011;39(3):251-60. doi: 10.3233/WOR-2011-1173.
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
- GAZIUN
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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.
Clinical Trials on Sports Injury
-
Riphah International UniversityCompletedSports Physical Therapy | Sports InjuryPakistan
-
University of Alabama at BirminghamCompleted
-
University Rovira i VirgiliCompletedSports Physical Therapy | Injury;Sports | Musculoskeletal Injury | Biomechanical LesionsSpain
-
Linkoeping UniversitySwedish Athletics AssociationCompleted
-
Federation Internationale de Football AssociationActive, not recruiting
-
Istanbul Medipol University HospitalNot yet recruitingSports Physical Therapy | Stretch | Stretch InjuryTurkey
-
Peking University Third HospitalRecruiting
-
Universidad Católica San Antonio de MurciaCompleted
Clinical Trials on survey administration
-
Rutgers, The State University of New JerseyNational Cancer Institute (NCI)TerminatedHealth Status UnknownUnited States
-
Centre Oscar LambretCentre Hospitalier Universitaire de BesanconTerminated
-
Boston UniversityNational Heart, Lung, and Blood Institute (NHLBI)Completed
-
Roswell Park Cancer InstituteNational Cancer Institute (NCI)RecruitingAcute Lymphoblastic LeukemiaUnited States
-
M.D. Anderson Cancer CenterRecruitingHematopoietic and Lymphoid Cell Neoplasm | Malignant Solid NeoplasmUnited States
-
University of Southern CaliforniaNational Cancer Institute (NCI)RecruitingAnatomic Stage I Breast Cancer AJCC v8 | Anatomic Stage IA Breast Cancer AJCC v8 | Anatomic Stage IB Breast Cancer AJCC v8 | Anatomic Stage II Breast Cancer AJCC v8 | Anatomic Stage IIA Breast Cancer AJCC v8 | Anatomic Stage IIB Breast Cancer AJCC v8 | Anatomic Stage III Breast Cancer AJCC v8 | Anatomic... and other conditionsUnited States
-
M.D. Anderson Cancer CenterActive, not recruitingHematopoietic and Lymphoid Cell Neoplasm | Advanced Malignant Solid Neoplasm | Locally Advanced Malignant Solid Neoplasm | Recurrent Malignant Solid Neoplasm | Metastatic Malignant Solid Neoplasm | COVID-19 Infection | Recurrent Hematologic MalignancyUnited States
-
Thomas Jefferson UniversityNational Cancer Institute (NCI)CompletedHematopoietic and Lymphoid Cell Neoplasm | Malignant Solid NeoplasmUnited States
-
M.D. Anderson Cancer CenterNational Cancer Institute (NCI)CompletedPancreatic Adenocarcinoma | Gastric Adenocarcinoma | Pancreatic Neuroendocrine CarcinomaUnited States
-
M.D. Anderson Cancer CenterNational Cancer Institute (NCI)CompletedMalignant NeoplasmUnited States