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Status unknownNCT05572489Updated Oct 26, 2022

Cervicogenic Headache, Cognitive Dysfunction

An observational study in Cervicogenic Headache, sponsored by Konya Beyhekim Training and Research Hospital. Status unknown at 1 site in Turkey. Open to participants aged 18 Years to 65 Years. Per ClinicalTrials.gov, last updated 2022-10-26.

Sponsored by Konya Beyhekim Training and Research Hospital · Observational

The sponsor has not verified this record recently (last verified Oct 2022), so the status shown — last known as Recruiting — may be out of date.
Study type
Observational
Model
Case-only
Time perspective
Cross-sectional
Enrollment
60
Ages
18 Years to 65 Years
Sex
All
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Study summary

The goal of this study was to determine the frequency of cognitive dysfunction in patients with cervicogenic headache.

participants will be asked questions to determine their cognitive status at once.

Read the detailed description

A set of survey-type questions will be asked to the participants. Pain and fatigue levels of the patients were measured by visual pain scale (VAS), mood states by Beck depression scale (BDI) and Pain catastrophizing scale (Pain catastrophizing scale), quality of life by Short Form-36 (SF-36), and cognitive status by Standard Mini. mental test (SMMT) and Montreal cognitive assessment scale (MOCA).

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Conditions studied

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In context

Post-Traumatic Headache

188 studies on the registry are indexed under Post-Traumatic Headache; 50 are open to participants now.

This study's planned enrollment of 60 is below the median of 90 across 19 observational studies indexed under Post-Traumatic Headache.

Browse Post-Traumatic Headache studies →

Lead sponsor

Konya Beyhekim Training and Research Hospital is the lead sponsor of 31 studies on the registry; 15 are open to participants now.

Counted across the registry records on this site, refreshed daily.

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Who can participate

Ages eligible
18 Years to 65 Years
Sexes eligible
All
Sampling method
Probability sample

Study population

30 patients with cervicogenic headache and 30 healthy volunteers

Inclusion criteria

Clinical Diagnosis of cervicogenic headache be over 18

Exclusion criteria

Exclusion Criteria:

those under the age of 18 Those with neurological deficits Those with rheumatic diseases such as fibromyalgia, polymyalgia rheumatica, ankylosing spondylitis, rheumatoid arthritis Surgery in the cervical region in the past 6 months Those with widespread pain, significant pain in another anatomical location (eg, gonarthrosis) Those who use drugs or substances (alcohol, drugs, etc.) that may cause cognitive impairment Those with known neurological diseases such as cerebrovascular disease, MS, Parkinson's, dementia Those with major psychiatric illness Those with communication problems Those who have started psychiatric medical treatment in the last three months Those with significant hearing or vision problems Those with a history of uncontrollable systemic disease (cardiovascular, pulmonary, hepatic, renal, hematological, endocrine..)

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Study design

Observational model
Case-only
Time perspective
Cross-sectional
Enrollment
60 participants (estimated)
Target follow-up
1 Day
Patient registry
Yes

Groups and cohorts

  • patients with cervicogenic headache

    visual pain scale Beck depression scale Pain catastrophizing scale Short Form-36 Standard Mini mental test Montreal cognitive assessment scale

    Diagnostic Test: visual pain scale Beck depression scale Pain catastrophizing scale Short Form-36 Standard Mini mental test Montreal cognitive assessment scale

  • healthy controls

    visual pain scale Beck depression scale Pain catastrophizing scale Short Form-36 Standard Mini mental test Montreal cognitive assessment scale

    Diagnostic Test: visual pain scale Beck depression scale Pain catastrophizing scale Short Form-36 Standard Mini mental test Montreal cognitive assessment scale

Interventions

  • Diagnostic testvisual pain scale Beck depression scale Pain catastrophizing scale Short Form-36 Standard Mini mental test Montreal cognitive assessment scale

    evaluation of pain, fatigue, mood, quality of life, cognitive status

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What researchers measure

Primary outcomes

  1. cognitive status

    Time frame: 01.12.2022

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Study locations

1 of 1 sites recruiting
  • Konya Beyhekim Research and Training Hospital
    Konya, Selçuklu 42060, Turkey
    • Savaş Karpuz · Contact · svskrpz@hotmail.com · 05552057860
    • Ramazan YIlmaz, MD · Sub investigator
    Recruiting
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References and documents

Publications

  • Bogduk N, Govind J. Cervicogenic headache: an assessment of the evidence on clinical diagnosis, invasive tests, and treatment. Lancet Neurol. 2009 Oct;8(10):959-68. doi: 10.1016/S1474-4422(09)70209-1. PubMed 19747657 ↗
  • Sjaastad O. Cervicogenic headache: comparison with migraine without aura; Vaga study. Cephalalgia. 2008 Jul;28 Suppl 1:18-20. doi: 10.1111/j.1468-2982.2008.01610.x. PubMed 18494988 ↗

Individual participant data

Plan to share: Undecided — Shared on request.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Oct 26, 2022, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
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Registry details

Key details

Study ID
NCT05572489
Lead sponsor
Konya Beyhekim Training and Research Hospital
Responsible party
Savaş Karpuz (Medical doctor, Konya Beyhekim Training and Research Hospital) — Principal investigator
First posted
Oct 7, 2022
Start date
Jan 1, 2022
Primary completion
Dec 1, 2022 (estimated)
Completion
Jan 1, 2023 (estimated)
Last update
Oct 26, 2022

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is status unknown, as verified in Oct 2022. You cannot join it, but the record below documents what was studied.

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