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Traditional Chinese Cervical Manipulation for Cervicogenic Headache

StatusActive, Not Recruiting
PhaseNot applicable
Started
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Record status
This record was last updated May 11, 2026 (before its estimated August 30, 2026 completion). Its status may not reflect the trial's current state.

Record History

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  1. Notable Primary completion date: Dec 30, 2025 to Aug 30, 2026
    • Trial status: Not Yet Recruiting to Active, Not Recruiting
    • Study completion date: Mar 30, 2026 to Aug 30, 2026
    v4
  2. Notable Start date: Jul 1, 2024 to Nov 1, 2024v3
  3. Minor Study title shortened, about 9 wordsv2
  4. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
Background Cervical spondylosis is a prevalent condition. Studies has shown that it is a leading cause for headache, which is termed cervicogenic headache (CGH). The prevlance of CGH among severe headache is 17.5%. While conventional treatments, such as physical therapy and surgery, is effective in controlling symptoms, the effect was found to be short-lasting. There is existing clinical evidence supporting traditional Chinese cervical manipulation (CCM) as a viable treatment for CGH. Objective To preliminarily assess the feasibility, safety, and effectiveness of CCM on patients with CGH, and to optimize parameters for a future large-scale trial. Method This study is a pilot randomized, controlled, single-blind trial. 84 participants will be randomized evenly to receive either CCM or sham manipulation for 4 weeks. Outcome measurements will be conducted at baseline, week 2, week 4 and week 8 on cervical functional disability, cervical range of motion, and data on headache onset and painkiller assumption. Adverse events will be recorded using the Common Terminology Criteria for Adverse Events (CTCAE).
Trial Details
NCT Number NCT06434051
Lead Sponsor Hong Kong Baptist University
Conditions
(from sponsor)
Cervicogenic Headache
Related terms Post-Traumatic Headache
Enrollment 84 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov