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Enrolling by invitation NCT06777862

Chronic Non-Specific Neck Pain and Quality of Life

Observational Neck Pain Quality of Life

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
This is an observational study: the protocol does not assign a study treatment.
Who it may be relevant to
Registry conditions: Neck Pain, Quality of Life. Basic parameters: 18 years — 65 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
Turkey (Türkiye)
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Investigation of Factors Affecting Quality of Life in Chronic Non-Specific Neck Pain

Overview

The factors affecting the quality of life in individuals with chronic non-specific neck pain are not fully known in the studies conducted to date. The aim of this study was to examine the factors affecting the quality of life of individuals with chronic non-specific neck pain.

Primary outcome measures

  • Pain Level [Time frame: 6 weeks]
Secondary outcome measures (7)
  • RANGE OF MOTION [Time frame: 6 weeks]
  • MUSCLE STRENGTH [Time frame: 6 weeks]
  • Cervical Region Proprioception Sense [Time frame: 6 weeks]
  • Depression symptoms [Time frame: 6 weeks]
  • Quality of Life Level [Time frame: 6 weeks]
  • Sleep Quality [Time frame: 6 weeks]
  • Neck Disability Level [Time frame: 6 weeks]

Eligibility criteria

Inclusion criteria

No history of radicular pain, trauma or surgery in the cervical region,

  • Between the ages of 18-65,
  • Having neck pain for at least 6 months,
  • Not having received any treatment for neck pain in the last year
  • Volunteers with chronic non-specific neck pain

Exclusion criteria

  • Those with any systemic disease
  • Those with cervical pathology
  • Previous surgery in the neck region
  • Those with neuromuscular disease
  • Those with rheumatology disease
  • Infection

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: Yes

Study design

Observational model
Cohort

Study locations

Turkey (Türkiye) · 1 center
  • Kirsehir Ahi Evran University — Kırşehir

Identifiers

NCT: NCT06777862 · KAEU-M.ASLAN-001

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗