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NCT06967415

Comparison of Pain, Sensitisation, Function and Quality of Life According to Stenosis Degree in Chronic Neck Pain

Not yet recruiting NA Last updated 5 January 2026
What this trial tests

NA trial testing Pain, central sensitization,functional status and quality of life. in Central Sensitisation in 88 participants. Not yet recruiting.

Timeline
15 December 2025
Primary endpoint
15 February 2026
15 August 2026

Quick facts

Lead sponsorIzmir Democracy University
PhaseNA
StatusNot yet recruiting
Study typeINTERVENTIONAL
Allocationrandomized
Designparallel
Maskingnone
Primary purposeother
Enrollment88
Start date15 December 2025
Primary completion15 February 2026
Estimated completion15 August 2026
Sites1 location across Turkey (Türkiye)

Drugs / interventions tested

Conditions studied

Sponsor

Izmir Democracy University

Who can join

Adults 18 to 65, any sex, with Central Sensitisation or Cervical Spine Stenosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The cervical spine is a structure that bears the weight of the head and has important functions, but is susceptible to mechanical stress and degenerative processes. Cervical stenosis can lead to compression of the nerve roots as a result of narrowing of the spinal canal and symptoms such as pain, numbness and weakness. Central sensitisation (CS) causes even innocuous stimuli to cause pain due to hypersensitivity of the central nervous system and negatively affects the quality of life by increasing pain intensity in individuals with chronic neck pain. Progression of cervical stenosis can lead to symptoms such as walking difficulties, loss of balance and loss of proprioception. Furthermore, CS causes patients to avoid physical activity, increasing muscle weakness and pain, which further reduces quality of life. For this reason, our study will be carried out to determine the effect of cervical stenosis on patients with neck pain whom applied to Izmir Democracy University Physical Medicine and Rehabilitation outpatient clinic and had cervical MRI. Participants' pain status, central sensitisation, sensory loss, range of motion and proprioception will be recorded. Pressure pain threshold will be measured with algometer, sensory loss will be examined with Semmes-Weinstein Monofilament (SWM) Test, joint movements and proprioception will be evaluated with Pa CROM Basic device. In addition, the effects of cervical stenosis on functional status and quality of life will be measured by questionnaires. The data obtained will be compared and analysed with appropriate statistical methods. This study is aimed to contribute to the development of treatment methods and improvement of patient care, and will provide important information in terms of pain management and improvement of quality of life.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Central Sensitisation

Currently open trials in the same condition.

Other Izmir Democracy University trials

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Data sources for this page

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