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

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age20-60
SponsorAlanya Alaaddin Keykubat University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Over 60 years of age

Those with impairments in cervical mobility that affected the postural assessment

Trial population

aproximately 5o patients with non-specific neck pain between the ages of 20-60 years

Trial design

Design model

Other

Time perspective

Prospective

Treatments tested in this trial

  • Reliability and validity

    Other intervention

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

Treatment groups

No treatment groups listed

Trial outcomes

Primary outcomes

1

Craniocervical Dysfunction Index

The assessment of craniocervical dysfunction is performed objectively and comprehensively through the Craniocervical Dysfunction Index (CDI), which was developed based on the Helkimo Dysfunction Index. The CDI numerically grades the severity of the functional disorders of the cervical spine. Through this index it is possible to assess the craniocervical dysfunction, regardless of the opinion of the patients, of the severity of the symptoms, and of the need for treatment. The CDI objectively indicates the dysfunction of the cervical region by numerical average, assessing the degree of dysfunction and enabling the differential diagnosis, suggesting the priority and monitoring of the treatment these changes may be reassessed over time.

Time frame
Baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

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