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Investigation of the Cultural Adaptation, Validity, and Reliability of the Turkish Version of the CAP Questionnaire

H

Hacettepe University

Status

Enrolling

Conditions

Fibromyalgia
Back Pain
Osteoarthritis

Treatments

Other: Questionnaire study

Study type

Observational

Funder types

Other

Identifiers

NCT06825650
SBA 24/997

Details and patient eligibility

About

The "CAP questionnaire," developed by modifying the CAP-Knee questionnaire to assess potential nociplastic pain features in painful musculoskeletal disorders, has been described. The "CAP questionnaire" is used in people with musculoskeletal pain and diagnostic subgroups of osteoarthritis, back pain, and fibromyalgia. There is no Turkish version of the CAP questionnaire. This study aims to investigate the cultural adaptation, validity, and reliability of the Turkish version of the "CAP questionnaire."

Full description

Chronic pain is a symptom shared by many musculoskeletal conditions, even when disease management is optimized. Musculoskeletal pathologies are reported to be an essential therapeutic target in pain management. However, these pathologies often do not adequately explain the pain or the reason for its persistence.

Central sensitization is the increased sensitivity of Central Nervous System (CNS) neurons to a standard nociceptive input. Pain that increases in intensity and distribution beyond that explained by musculoskeletal pathology has been termed "nociplastic pain." Measuring these CNS aspects of pain is a prerequisite for understanding their mechanistic basis and predicting future pain and responses to treatment. Chronic pain is associated with CNS dysfunction in several areas, including depression, anxiety, pain catastrophizing, cognitive dysfunction, sleep disturbance, and fatigue. Considering the increasing importance of assessing mood-related pain (nociplastic pain) The "CAP questionnaire," developed by modifying the CAP-Knee questionnaire to assess potential nociplastic pain features in painful musculoskeletal disorders, has been described.

Enrollment

300 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • People with musculoskeletal pain and in diagnoses with OA, back pain, or FM
  • Above 18 years of age
  • Informed consent of the participant

Exclusion criteria

  • Diagnosis of uncontrolled/other clinically significant diseases (chronic obstructive pulmonary disease, congestive heart failure, endocrine system diseases, neurological, psychological diseases, etc.)
  • Pregnant women

Trial design

300 participants in 3 patient groups

Individuals with osteoarthritis
Treatment:
Other: Questionnaire study
Individuals with back pain
Treatment:
Other: Questionnaire study
Individuals with fibromyalgia
Treatment:
Other: Questionnaire study

Trial contacts and locations

1

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Central trial contact

Orkun Tüfekçi, PT, PhD (c)

Data sourced from clinicaltrials.gov

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