- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05201716
Turkish Validity and Reliability of the UW Concerns About Pain Scale
July 7, 2022 updated by: Ismail Saracoglu, Kutahya Health Sciences University
Brief Summary:
The aim of this study was to determine the Turkish validity and reliability of ''UW Concerns About Pain Scale'' developed by Dr. Amtmann.
Study Overview
Status
Completed
Conditions
Detailed Description
Chronic pain is a common condition, affecting an estimated 20% of people worldwide.
The biopsychosocial model of chronic pain is the most current accepted approach to understanding the complexity of pain and disability.
One of the most important psychosocial factors in this approach is pain-related self-efficacy, which is defined as the individual's confidence in their ability to tolerate pain and participate in daily activities despite pain.
The aim of this study is to determine the Turkish version, validity, and reliability of ''UW Concerns About Pain Scale''.
60 people with chronic low back pain will include in the study.
In order to determine the reliability of the scale, the intraclass correlation coefficient (ICC) will be used to determine the level of the relationship between the results of the first and second measurements.
Cronbach's alpha coefficient will be used for the homogeneity of the questions in the scale.
For construct validity, the correlation coefficient will be used to determine the agreement between the Turkish version of Pain catastrophizing scale and, Turkish version of "Fear Avoidance Beliefs Questionnaire" and The ''UW Concerns About Pain Scale''.
Study Type
Observational
Enrollment (Actual)
100
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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Kütahya, Turkey, 43100
- Kutahya Health Sciences 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
16 years to 63 years (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
People with Chronic low back pain
Description
Inclusion Criteria:
- To be between 18-65 years old
- Having a complaint of low back pain for at least 6 months
- Low back pain severity to be 3 points or above according to the Numerical Graded Pain Scale.
Exclusion Criteria:
- Using antidepressant-derived drugs
- Having a history of spinal surgery
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 |
---|---|---|
UW Concerns About Pain
Time Frame: 8 minutes
|
The UW Concerns About Pain is intended measure an individual's level of pain catastrophizing.
We will use to 8 item form, in study.
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8 minutes
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Turkish version of Pain Catastrophizing Scale (PCS)
Time Frame: 10 minutes
|
PCS was developed by Sullivan et al. in order to identify the catastrophic thoughts or feelings of the patients about the pain and ineffective coping strategies.The scale is a Likert-type self-assessment scale consisting of 13 items.Each item is scored between 0-4 points.The total score ranges from 0 to 52.High scores indicate a high level of catastrophizing.
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10 minutes
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Turkish version of "Fear Avoidance Beliefs Questionnaire"
Time Frame: 10 minutes
|
FABQ was developed Waddell et al. in 1993.
FABQ consists of 16 questions and 2 parts.
While the first part of the scale evaluates attitudes about physical activities, the second part evaluates attitudes about occupational work.
Scoring of the questionnaire is done with a 7-point Likert type scale.
The Physical Activity section is scored between 0-24 and the labor section is scored between 0-36.
A high score in KKTS indicates an increased level of fear-avoidance attitudes related to low back pain.
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10 minutes
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Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Director: İsmail SARACOGLU, PhD, Kutahya Health Sciences University
- Principal Investigator: Cihan Caner AKSOY, PhD, Kutahya Health Sciences University
- Principal Investigator: Hasan Hüseyin GÖKPINAR, MD, Kutahya Health Sciences 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)
February 1, 2022
Primary Completion (Actual)
May 1, 2022
Study Completion (Actual)
June 1, 2022
Study Registration Dates
First Submitted
January 9, 2022
First Submitted That Met QC Criteria
January 9, 2022
First Posted (Actual)
January 21, 2022
Study Record Updates
Last Update Posted (Actual)
July 8, 2022
Last Update Submitted That Met QC Criteria
July 7, 2022
Last Verified
July 1, 2022
More Information
Terms related to this study
Keywords
Additional Relevant MeSH Terms
Other Study ID Numbers
- KutahyaHSU2
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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