- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06700707
Turkish Adaptation, Validity and Reliability Study of the Athlete Disability Index Questionnaire (ADI_Turkish)
Turkish Adaptation, Validity and Reliability Study
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
In the study, firstly, the translation of the Athlete Disability Index Questionnaire (ADI) into the target language, comparison of the two translated versions of the scale, back translation of the preliminary version, synthesis, pilot test of the pre-final version and psychometric test studies will be carried out by 3 independent translators and 2 linguists in 6 stages.
Then, 120 athletes with low back pain will be asked to fill out the ADI, Roland Morris Disability Questionnaire (RMDQ) and Oswestry Low Back Pain Disability Index (ODI). 7 days later, the ADI will be filled out again by 60 athletes.
After the surveys are completed, the structural validity of the scale will be tested, and reliability will be measured by performing test-retest reliability and internal consistency analyses.
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
-
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Beykoz
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Istanbul, Beykoz, Turkey (Türkiye), 34810
- Gülay Aras Bayram
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- Low back pain that has persisted for at least 6 weeks
- Pain that worsens with changes in posture, movement, or physical activity
- Elite athletes with a regular training/match schedule of more than 10 hours per week
Exclusion Criteria:
- Not knowing Turkish
- Acute inflammatory conditions
- Acute musculoskeletal trauma
- Long-term corticosteroid use
Study Plan
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Athlete Disability Index Questionnaire (ADI)
Time Frame: 7 days
|
The Athlete Disability Index Questionnaire (ADI) is a self-administered questionnaire to assess disability related to low back pain in athletes.
The ADI measures athletes' functional disability in activities of daily living as well as their disability in sports and exercise activities.
The ADI consists of 12 questions that include pain intensity, stretching exercises, strengthening/weight training exercises, sport-specific skills (technical skills), rotational waist movements/changing direction, fear of pain or re-injury, sitting, walking, recreational activities, sexual activity, sleep, and personal care (ability to put on socks and shoes, ability to go to the bathroom).
Each question is scored from 0 to 3, with higher scores indicating a more severe condition.
|
7 days
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Oswestry Low Back Pain Disability Index (ODI)
Time Frame: 1 day
|
Oswestry Low Back Pain Disability Index (ODI) is a Likert-type scale that questions pain intensity, personal care, lifting, walking, sitting, standing, sleeping, sexual life, social life and traveling in 10 items. Each item is scored between 0-5 (0: normal, 5: maximum difficulty) and the total score is 50. In it's calculation; (Final score = [total score] / [(number of marked questions) x5] x 100) formula is used to convert it to a percentage system. A high percentage indicates that the level of disability perceived by the patient is also high. Turkish validity and reliability study has been conducted. |
1 day
|
|
Roland Morris Disability Questionnaire (RMDQ)
Time Frame: 1 day
|
Roland Morris Disability Questionnaire (RMDQ): This scale, which was developed by selecting 24 of the 136 items of the Disease Impact Profile, evaluates activity level, daily living activities, eating and sleeping.
Yes is scored as 1, no is scored as 0, and a higher total score indicates worse functionality.
A Turkish validity and reliability study was conducted by Küçükdeveci et al.
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1 day
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Gülay Aras Bayram, PhD, Medipol University
Publications and helpful links
Helpful Links
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
- 20112024
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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