Exercise program for treating cervicogenic headache
The Effects of a Specific Exercise Program on Subjects With Cervicogenic Headache
This study tests whether a special exercise program can help people with cervicogenic headaches by improving the strength and function of certain neck muscles.
Quick facts
| Phase | Not applicable |
|---|---|
| Study type | Interventional |
| Enrollment | 40 (estimated) |
| Ages | 18 Years to 65 Years |
| Sex | All |
| Sponsor | Florida Gulf Coast University Academic / other |
| Locations | 1 site (Fort Myers, Florida) |
| Trial ID | NCT05500378 on ClinicalTrials.gov |
What this trial studies
This study investigates the effects of a specific exercise program on individuals suffering from cervicogenic headaches. Using musculoskeletal (MSK) ultrasound imaging, the research aims to determine if subjects can selectively contract the obliquus capitis minor and rectus capitis major muscles through head extension and rotation while maintaining neck position. The study will measure changes in muscle length and width to assess the effectiveness of the exercise intervention.
Who should consider this trial
Good fit: Ideal candidates are individuals aged 18-65 with no history of neck pain or surgery who can actively move their neck.
Not a fit: Patients with current neck pain or a history of neck surgery will not benefit from this study.
Why it matters
Potential benefit: If successful, this program could provide a non-invasive treatment option for patients suffering from cervicogenic headaches.
How similar studies have performed: While there is limited data on this specific approach, similar studies exploring targeted exercise interventions for musculoskeletal conditions have shown promising results.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * No history of surgery, No current neck pain, Being able to move the neck actively, being able to read English, between ages 18-65 Exclusion Criteria: * Neck pain, History of surgery, unable to move the head into extension, outside age requirements, unable to read English
Where this trial is running
Fort Myers, Florida
- Florida Gulf Coast University — Fort Myers, Florida, United States (Recruiting)
Study contacts
- Principal investigator: Rob Sillevis, phD — Florida Gulf Coast University
- Study coordinator: Rob Sillevis, PhD
- Email: rsillevis@fgcu.edu
- Phone: 2397454312
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.