- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05604027
Pain Types and Pain Severity in Chronic Low Back Pain
October 27, 2022 updated by: Konya Beyhekim Training and Research Hospital
The Effects of Pain Types on Pain Severity and Quality of Life in Chronic Low Back Pain
The aim of this study is to characterize the distribution of pain phenotypes in people with chronic low back pain and to determine the effects of pain phenotypes on pain severity, functional status and quality of life.
Participants will be examined to determine the type of pain and questions will be asked to identify the effects.
Study Overview
Status
Not yet recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
200
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
-
-
Selçuklu
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Konya, Selçuklu, Turkey, 42060
- Konya Beyhekim Research and training hospital
-
-
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 90 years (Adult, Older Adult)
Accepts Healthy Volunteers
N/A
Genders Eligible for Study
All
Sampling Method
Probability Sample
Study Population
Patients who come to the hospital for chronic low back pain
Description
Inclusion Criteria:
- having chronic low back pain
- be over 18 years old
Exclusion Criteria:
- Those under the age of 18
- Those with major psychiatric illness,
- Those with communication problems
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: Case-Control
- Time Perspectives: Cross-Sectional
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
identification of pain types(determination of nociceptive, neuropathic, nociplastic pain rates)
Time Frame: 01.03.2023
|
Neuropathic pain with PainDETECT scale, Clinical criteria and rating system for nociplastic pain affecting the musculoskeletal system nosplastic pain will be evaluated
|
01.03.2023
|
|
Pain levels of those with nociplastic, neuropathic and nociceptive pain
Time Frame: 01.03.2023
|
Pain severity with Visual Analogue Scale,(0-10)higher scores indicate more pain
|
01.03.2023
|
|
pain effect
Time Frame: 01.03.2023
|
quality of life with SF-36,
|
01.03.2023
|
|
disability,
Time Frame: 01.03.2023
|
disability with Roland Morris Disability Questionnaire,
|
01.03.2023
|
|
patient's feelings, thoughts, and feelings about pain and disaster.
Time Frame: 01.03.2023
|
The Pain Catastrophizing Scale is used to assess the patient's feelings, thoughts, and feelings about pain and disaster.
|
01.03.2023
|
Collaborators and Investigators
This is where you will find people and organizations involved with this 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 (Anticipated)
December 15, 2022
Primary Completion (Anticipated)
July 1, 2023
Study Completion (Anticipated)
September 1, 2023
Study Registration Dates
First Submitted
October 10, 2022
First Submitted That Met QC Criteria
October 27, 2022
First Posted (Actual)
November 3, 2022
Study Record Updates
Last Update Posted (Actual)
November 3, 2022
Last Update Submitted That Met QC Criteria
October 27, 2022
Last Verified
October 1, 2022
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 2022-15/20
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Undecided
IPD Plan Description
will be shared upon request.
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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