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Not yet recruiting NCT06640322

Craniocervical Dysfunction Index in Turkish Patients With Non-specific Neck Pain

— Observational Neck Pain Craniocervical Disfunction

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
The protocol lists: Reliability and validity.
Who it may be relevant to
Registry conditions: Neck Pain, Craniocervical Disfunction. Basic parameters: 20 years — 60 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 →

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Official title

Turkish Validity and Reliability of the Craniocervical Dysfunction Index in Patients With Non-specific Neck Pain

Overview

The aims of this study were to perform cultural adaptation of the Craniocervical Dysfunction Index in patients with non-specific neck pain, reliability and validity of the index Turkish speaking adults.

Interventions

  • Other Reliability and validity
    Reliability and validity of Craniocervical Dysfunction Index in Turkish Patients With Non-specific Neck Pain

Primary outcome measures

  • Craniocervical Dysfunction Index [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Between the ages of 20-60 years
  • Clinical diagnosis of non-specific neck pain
  • Being able to communicate in Turkish
  • Volunteering to participate in the study

Exclusion criteria

  • Over 60 years of age
  • Those with impairments in cervical mobility that affected the postural assessment

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

Healthy volunteers: No

Study design

Observational model
Other

Study locations

Turkey (Türkiye) · 1 center
  • Alanya Alaadin Keykubat University — Antalya

Identifiers

NCT: NCT06640322 · 11.10.2024/CDI-NNP

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗