- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04099160
Turkish Version of Revised Neurophysiology of Pain Questionnaire
January 18, 2024 updated by: Hatice Gül, Akdeniz University
Cross-cultural Adaptation of Revised Neurophysiology of Pain Questionnaire Into Turkish Language
The Neurophysiology of Pain Questionnaire was first developed in English to test whether healthcare staff and patients could exactly understand pain neurophysiology.
This questionnaire which contains 19 items was developed from the exam questions of students interested in post-graduate pain medicine.
Catley et al. (2013) investigated the psychometric properties of the modified Neurophysiology of Pain Questionnaire with a few word differences from the original version by conducting a rash analysis on 300 patients with chronic spinal pain.
Acceptable internal consistency and test-retest reliability of the questionnaire were recorded.
However, it was stated that 7 items negatively affect psychometric properties of the questionnaire.
As a result, the author concluded that the questionnaire had sufficient psychometric properties for use in chronic spinal pain subjects, but further studies were needed.
The Neurophysiology of Pain Questionnaire was used to measure a knowledge about pain in different studies.
The validity and reliability studies of the Dutch, French and Brazlian Portuguese versions of the Neurophysiology of Pain Questionnaire were conducted in the literature.
The aim of our study was to translate the Revised Neurophysiology of Pain Questionnaire into Turkish language and to investigate its psychometric properties.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Actual)
182
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Hatice Gül, Ph.D
- Phone Number: +90-242-2274537
- Email: fzt-hatice@hotmail.com
Study Locations
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-
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Antalya, Turkey
- Akdeniz University Department of phyiotherapy
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Antalya, Turkey
- Akdeniz University Medical Ethics Committe
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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
No
Sampling Method
Probability Sample
Study Population
Patients with chronic spinal pain
Description
Inclusion Criteria:
- Patients with spinal pain lasting more than three months
- Patients who older than 18 years of age
- Patients who can understand and read Turkish.
Exclusion Criteria:
- Patients with specific spinal pain such as trauma, fracture, infection, inflammatory disease and tumor
- Patients who have undergone spinal surgery in the last 3 months
- Patients who have received pain neurophysiology education in the last year.
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
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
The Revised Neurophysiology of Pain Questionnaire
Time Frame: Two minute
|
The Revised Neurophysiology of Pain Questionnaire consists of 12 items and measuring the level of knowledge about pain neurophysiology.
High score indicates a high level of knowledge about pain neurophysiology.
|
Two minute
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Visual Analogue Scale
Time Frame: 1 minute
|
Visual Analogue Scale assessed pain severity.
Visual Analog Scale is a straight horizontal line of fixed length, usually 100 mm.
The ends are defined as the extreme limits of pain.
hence the left end is usually labeled 'no pain', and the right end usually labeled 'extreme pain'.
The score is determined by measuring the distance (mm) on the 10-cm line between the "no pain" anchor and the patient's mark by using a ruler.
The scale is provided a range of scores from 0-100.
High score indicates a high level of pain..
|
1 minute
|
Short Form-36
Time Frame: Ten minute
|
Short Form-36 (SF-36) questionnaire has 8 subscales such as physical function, role limitations due to physical problems, pain, general perception of health, energy, social function, role limitations due to emotional problems, mental health.
This questioonaire evaluate quality of life.
Scales have a fairly small range of response options, and scores are multiplied up to 0-100.
|
Ten minute
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Investigators
- Principal Investigator: Hatice Gül, Ph.D, Akdeniz University
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
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)
November 20, 2019
Primary Completion (Actual)
October 20, 2020
Study Completion (Actual)
January 20, 2021
Study Registration Dates
First Submitted
September 19, 2019
First Submitted That Met QC Criteria
September 20, 2019
First Posted (Actual)
September 23, 2019
Study Record Updates
Last Update Posted (Estimated)
January 19, 2024
Last Update Submitted That Met QC Criteria
January 18, 2024
Last Verified
January 1, 2024
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 34878437-199-E.115170
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
IPD Plan Description
The data obtained from patients at the beginning and a week later will be analyzed with SPSS program.
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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