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Recruiting Observational

Predictors of Functional Status in Chronic Neck Pain

NCT07544108 · tracked via the Priya Life Science Turkey tracker
Phase
Observational
Started
2025-10-20
Last updated
2026-04-27

Condition(s) studied

Neck Pain

Investigational drug(s) / intervention(s)

assesment

assesment: only single assessment

Study summary

Although it has been reported that these problems seen together with neck pain are related to functional limitations and disability, there is still insufficient evidence regarding the relationship between factors affecting functional status and chronic neck pain symptoms in individuals with chronic neck pain. Furthermore, a mixed methodology approach has not been used to comprehensively investigate this relationship. Identifying factors affecting functional status in CNP will help guide the prevention, treatment, and management of neck pain. Therefore, the aim of this study is to investigate the relationships between functional status and psychosocial and bodily functions in CNP.

Eligibility

Sex
ALL
Min age
18 Years
Max age
65 Years
Healthy volunteers
No
Inclusion Criteria: * patients aged 18-65 * patients have experienced non-specific neck pain for at least 3 months, patients who are literate, and no cognitive impairment. Exclusion Criteria: * patients with serious and secondary musculoskeletal diseases (inflammatory, neuropathic and malignancy) * patiens who have undergone spinal and abdominal surgery and trauma * patients who smoke * patients if any lung disease that will affect respiration, * patients with a body mass index greater than 40 * patients who cannot operate.

Primary outcome measure(s)

  • NDI — 1. day
    ın the questionnaire, whose Turkish validity and reliability were established by Aslan , subjective symptoms (pain, headache, concentration, sleep) and daily living activities (personal care, carrying, reading, work, driving and recreation activities) are evaluated with a 6-option answer. Each option is scored with a value between 0 (no limitation) and 5 (maximum limitation), and 0-4 points are recorded as no disability, 5-14 points as mild, 15-24 points as moderate, 25-34 points as severe and 35-50 points as complete functional disability

Trial sites (1)

FacilityCityRegionStatus
Kütahya Health Sciences University, Kütahya City Hospital Kütahya Kütahya Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07544108 on ClinicalTrials.gov ↗ ← All trials in Turkey