Evaluating manual therapy and exercise for headache pain relief
Official title: Evaluation of the Efficacy of Manual Therapy, Therapeutic Exercise and the Two Modalities Combined in Pain Reduction in Patients Suffering From Cervicogenic Headache, or Primary Headache (Tension-type Headache, Migraine, Trigeminal Autonomic Headache)
Run by Campus Bio-Medico University · NCT05990153 · Data updated 2026-05-14
This study is no longer in our active list. It may have stopped recruiting or finished. The details below are as of 2026-05-14 and are kept for reference. Check ClinicalTrials.gov for its current status, or see similar studies below.
This study is testing three different non-drug treatments for people with various types of headaches to see which one helps reduce headache pain and frequency the most.
Quick facts
| Study type | Interventional |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 100 (estimated) |
| Sponsor | Campus Bio-Medico University Academic / other |
| Locations | 1 site (Roma, RM) |
| Trial ID | NCT05990153 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include adults over 18 years old who experience primary headaches or cervicogenic headaches.
✕Probably not a fit
Patients with upper cervical spine instability, cervical arterial insufficiency, cervical spine fractures, pregnancies, rheumatoid arthritis, or severe cognitive impairment may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This study evaluates the effectiveness of three non-pharmacological treatment methods for patients suffering from various types of primary headaches, including tension-type headaches, trigeminal autonomic headaches, and migraines. Participants will be assigned to one of three intervention groups: therapeutic exercise, myofascial release combined with therapeutic exercise, or Mulligan's manual therapy combined with therapeutic exercise. The study will assess the reduction in headache episodes, pain intensity, and duration over a series of evaluations conducted before treatment, immediately after treatment, and at three and six months post-treatment. The control group will receive standard pharmacological treatment and may later switch to one of the intervention groups if desired.
Why it matters
Potential benefit: If successful, this study could provide effective non-drug treatment options for patients suffering from chronic headaches.
How similar studies have gone: Other studies have shown promising results with non-pharmacological approaches for headache management, indicating potential success for this study's methodology.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients suffering from primary headache or cervicogenic headache; * Age \> 18 years; * signature of the informed consent. Exclusion Criteria: * upper cervical spine instability; * cervical arterial insufficiency * cervical spine fractures * pregnancies * rheumatoid arthritis * severe cognitive impairment
Where it's running
-
Rehabilitation Department Fondazione Policlinico Universitario Campus Bio-Medico
Roma, Rm, Italy Recruiting
Study contacts
- Principal investigator: Silvia Sterzi, MD — Fondazione Policlinico Universitario Campus Bio-Medico
- Study coordinator: Silvia Sterzi, MD
- Email: s.sterzi@policlinicocampus.it
- Phone: +390622541624
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.