- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03175510
Reliabılıty,Validity Of The Turkish Version Of The Back Pain Function Scale
September 22, 2017 updated by: GÖKHAN MARAŞ, Gazi University
This study, we performed the Turkish version validity and reliability of the Back Pain Function Scale.
Study Overview
Status
Completed
Conditions
Detailed Description
Low back pain is defined as the pain that can occur in the region between the lower border of the scapula and the hip, sometimes spreading to the lower extremities, which causes activity limitation and is one of the most common health problems in the society.
Appropriate use of assessment questionnaires is one of the most important steps in the evaluation of the functional level of the patient and in deciding on an effective treatment protocol.
The purpose of our study is to determine the Turkish version, validity and reliability of Back Pain Function Scale.
180 patients with chronic low back pain were included in the study.
Test-retest and internal consistency analysis were conducted to determine the reliability of the questionnaire.
Test-retest results were evaluated using the Intraclass Correlation Coefficient method.
Intraclass Correlation Coefficient results vary between 0.857 and 0.951, and the total Intraclass Correlation Coefficient value is found to be 0.961.
These results indicate that the test-retest responses have a high degree of correlation.
For internal consistency analysis, the Cronbach Alpha score was fou nd to be 0.910, indicating that the survey has high internal consistency.
The total score obtained from the Back Pain Function Scale was assessed using the Pearson correlation analysis with the total scores obtained from the Roland Morris Disability Scale , Oswestry Disability Scale.
Pearson's correlation coefficient was -0.840 with Oswestry Disability Scale of Back Pain Function Scale, Pearson's correlation coefficient was -0.803 with Roland Morris Disability Scale.
The results show that the Back Pain Function Scale correlates perfectly with the Oswestry Disability Scale and the Roland Morris Disability Scale.
In conclusion, Turkish version of Bac Pain Function Scale is valid and reliable.
Study Type
Observational
Enrollment (Actual)
180
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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Ankara, Turkey, 06500
- Gazi 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
18 years to 65 years (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
Yes
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients with chronic back pain between the ages of 18-65
Description
Inclusion Criteria:
Having a low back pain Literate
Exclusion Criteria:
pregnant canser trauma
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
Cohorts and Interventions
Group / Cohort |
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patients group
Patients with low back pain (18-65 years)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Roland Morris disability questionnaire
Time Frame: 10 minute
|
Roland Morris Disability Questionnaire, a widely used health status measure for low back pain.
The RMDQ can be used in research or clinical practice.
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10 minute
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Oswestry Low Back Pain Disability Questionnaire
Time Frame: 10 minute
|
The Oswestry Disability Index (ODI) has become one of the principal condition-specific outcome measures used in the management of spinal disorders
|
10 minute
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Study Chair: seyit citaker, Gazi 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)
May 15, 2016
Primary Completion (ACTUAL)
August 1, 2017
Study Completion (ACTUAL)
September 1, 2017
Study Registration Dates
First Submitted
June 1, 2017
First Submitted That Met QC Criteria
June 1, 2017
First Posted (ACTUAL)
June 5, 2017
Study Record Updates
Last Update Posted (ACTUAL)
September 25, 2017
Last Update Submitted That Met QC Criteria
September 22, 2017
Last Verified
June 1, 2017
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2017-72
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
YES
IPD Sharing Supporting Information Type
- CSR
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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