Actively Recruiting
Investigation of the Cultural Adaptation, Validity, and Reliability of the Turkish Version of the Central Aspects of Pain (CAP) Questionnaire
Led by Hacettepe University · Updated on 2025-02-13
300
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying the Turkish version of the Central Aspects of Pain (CAP) questionnaire, which is designed to assess features of nociplastic pain in people with musculoskeletal disorders such as osteoarthritis, back pain, and fibromyalgia. This study aims to culturally adapt, validate, and test the reliability of this questionnaire for Turkish-speaking patients. Chronic pain in these conditions is often linked to nervous system changes that are not fully explained by physical problems alone. The study involves administering the Turkish CAP questionnaire along with other related questionnaires that assess biopsychosocial factors, anxiety, depression, pain catastrophizing, central sensitization, and pain quality. Participants include adults with osteoarthritis, back pain, or fibromyalgia who will complete these assessments over a three-month period. There is no drug or device intervention, as this is an observational study focused on questionnaire validation. Participants will be involved for at least three months during which they will complete the CAP questionnaire and other related scales. Researchers will evaluate the questionnaires' validity and reliability based on responses. The primary outcome measured is the CAP questionnaire score at three months, with secondary outcomes including several other pain and psychological assessment tools. This study helps improve tools for understanding and managing chronic pain in Turkish-speaking patients.
CONDITIONS
Brief Title
Investigation of the Cultural Adaptation, Validity, and Reliability of the Turkish Version of the CAP Questionnaire
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- People with musculoskeletal pain diagnosed with osteoarthritis, back pain, or fibromyalgia
- Participants who provide informed consent
You will not qualify if you...
- Diagnosis of uncontrolled or clinically significant diseases such as chronic obstructive pulmonary disease, congestive heart failure, endocrine, neurological, or psychological diseases
- Pregnant women
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 3 months
Participants complete questionnaires to assess central aspects of pain and related biopsychosocial factors.
1 baseline visit and 1 follow-up visit
Trial Site Locations
Total: 1 location
1
Hacettepe University
Ankara, Altındağ, Turkey (Türkiye), 06100
Actively Recruiting
Research Team
O
Orkun Tüfekçi, PT, PhD (c)
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
3
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