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Turkish Version of the Pain Metacognitions Questionnaire

NCT07351617 · Status: NOT_YET_RECRUITING · Type: OBSERVATIONAL · Enrollment: 210

Last updated 2026-01-20

No results posted yet for this study

Summary

Pain-related thoughts and beliefs play an important role in how individuals experience and cope with chronic pain. Metacognitions about pain, such as beliefs about the uncontrollability or harmfulness of pain-related thoughts, may influence emotional distress and pain-related outcomes. The Pain Metacognitions Questionnaire was developed to assess these beliefs; however, a validated Turkish version is not currently available. The aim of this study is to translate the Pain Metacognitions Questionnaire into Turkish and to evaluate its validity and reliability in adults with chronic non-cancer pain. This observational study will include adult individuals experiencing chronic pain for at least three months. Data will be collected using self-report questionnaires administered in a single assessment session. The findings of this study are expected to provide a reliable and valid measurement tool for assessing pain-related metacognitions in Turkish-speaking populations and to support future clinical and research applications in chronic pain management.

Conditions

Interventions

OTHER

No Intervention (Observational Study)

This is an observational study. No intervention is administered. Data are collected using self-report questionnaires only.

Sponsors & Collaborators

  • Çankırı Karatekin University

    collaborator OTHER

  • Tokat Gaziosmanpasa University

    lead OTHER

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2026-02-01
Primary Completion
2026-05-19
Completion
2026-06-10

Countries

  • Turkey (Türkiye)

Study Locations

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Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07351617 on ClinicalTrials.gov