Clinical trial No longer in our active list Interventional Ages 18 and up

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 typeInterventional
Ages18 Years and up
SexAll
Enrollment100 (estimated)
SponsorCampus Bio-Medico University
Academic / other
Locations1 site (Roma, RM)
Trial IDNCT05990153 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

Similar studies

Other studies for the same condition or treatment. Recruiting studies are listed first.

How to take part

  1. Review the eligibility criteria above with your treating physician.
  2. Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
  3. Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.
Last reviewed 2026-11-14 by the Find a Trial editorial team. Information on this page is for educational purposes and is not medical advice. Always consult qualified healthcare professionals about clinical trial participation.