Pain Types and Pain Severity in Chronic Low Back Pain

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

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
      • 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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