Association of High PainDETECT Scores With Pain Region and Diagnosis in Patients Attending a Musculoskeletal and Sports Medicine Clinic (PD-MSK)

February 19, 2026 updated by: Prof. Dr. Deniz Demirci, Uskudar University

Evaluation of the Association Between PainDETECT Scores, Pain Localization, and Diagnosis in a Musculoskeletal and Sports Medicine Outpatient Population

This observational study aims to evaluate the relationship between PainDETECT questionnaire scores, pain regions, and clinical diagnoses in patients presenting to a musculoskeletal and sports medicine clinic. Patients attending the clinic will complete the PainDETECT questionnaire, and their pain localization and clinical diagnoses will be recorded. The findings are expected to contribute to a better understanding of neuropathic pain components in musculoskeletal conditions.

Study Overview

Status

Recruiting

Intervention / Treatment

Detailed Description

This is an observational, non-interventional study conducted in a musculoskeletal and sports medicine outpatient clinic. Adult patients presenting with pain will be included. The PainDETECT questionnaire will be used to assess neuropathic pain components. Pain regions and clinical diagnoses determined during routine clinical evaluation will be recorded.

No interventions, experimental treatments, or changes to standard clinical care will be applied. The study will analyze the association between PainDETECT scores, pain localization, and clinical diagnoses. Data will be collected prospectively and analyzed using appropriate statistical methods to explore potential relationships between variables.

Study Type

Observational

Enrollment (Estimated)

150

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

      • Istanbul, Turkey (Türkiye)
        • Recruiting
        • Dr. Cavit Meclisi - Istanbul Orthopaedics Group, Musculoskeletal and Sports Medicine Clinic
        • Contact:

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

  • Adult
  • Older Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Adult patients aged 18 years and older who presented to a musculoskeletal and sports medicine clinic with pain complaints and had available PainDETECT questionnaire data.

Description

Inclusion Criteria:

  • Patients aged 18 years and older
  • Patients who presented to the musculoskeletal and sports medicine clinic with pain complaints
  • Availability of complete medical records including PainDETECT questionnaire data

Exclusion Criteria:

  • Patients younger than 18 years
  • Incomplete clinical or questionnaire data

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
Intervention / Treatment
Patients with musculoskeletal pain
Adult patients with musculoskeletal pain whose retrospective clinical data and PainDETECT scores are analyzed.
This is an observational retrospective study. No interventions are assigned to participants.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
PainDETECT Score
Time Frame: At baseline, based on retrospective review of existing medical records.
The PainDETECT score is a validated patient-reported outcome measure used to assess the likelihood of neuropathic pain components. The score is calculated based on responses recorded in existing medical records. No additional assessments or interventions are performed as part of this study.
At baseline, based on retrospective review of existing medical records.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

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)

February 19, 2026

Primary Completion (Estimated)

March 15, 2026

Study Completion (Estimated)

March 20, 2026

Study Registration Dates

First Submitted

January 11, 2026

First Submitted That Met QC Criteria

January 19, 2026

First Posted (Actual)

January 21, 2026

Study Record Updates

Last Update Posted (Actual)

February 23, 2026

Last Update Submitted That Met QC Criteria

February 19, 2026

Last Verified

February 1, 2026

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

IPD Plan Description

Individual participant data will not be shared due to the retrospective nature of the study and the absence of a predefined data sharing plan.

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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