Comparing two techniques for treating cervicogenic headaches
Comparative Effects of Jones and Ischemic Compression Technique on Pain, Range of Motion and Disability in Patients With Cervicogenic Headache
NA · Riphah International University · NCT06875869
This study is testing two different physiotherapy treatments for cervicogenic headaches to see which one helps reduce pain and improve movement better.
Quick facts
| Phase | NA |
|---|---|
| Study type | Interventional |
| Enrollment | 32 (estimated) |
| Ages | 25 Years to 35 Years |
| Sex | All |
| Sponsor | Riphah International University (other) |
| Locations | 1 site (Bahawalpur, Punjab Province) |
| Trial ID | NCT06875869 on ClinicalTrials.gov |
What this trial studies
This study aims to evaluate the effectiveness of two physiotherapy interventions, the Jones technique and Ischemic compression therapy, in treating cervicogenic headaches. It will involve a randomized clinical trial with 32 participants who will be divided into two groups, each receiving one of the treatment techniques. The primary outcomes measured will include pain levels, range of motion, and disability associated with cervicogenic headaches. The study will take place at Bahawal Victoria Hospital in Bahawalpur, Punjab.
Who should consider this trial
Good fit: Ideal candidates for this study are males and females aged 25-35 who meet the criteria for cervicogenic headaches and have positive Simon's criteria for trigger points.
Not a fit: Patients with primary headaches, bilateral headaches, or any significant cervical spine issues may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could provide a more effective treatment option for patients suffering from cervicogenic headaches.
How similar studies have performed: While there is ongoing research into treatment techniques for cervicogenic headaches, this specific comparison of the Jones technique and Ischemic compression therapy is relatively novel.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Both males and females * 25-35 years of age * Individuals satisfying the Cervicogenic Headache criteria * Positive Simon's criteria for trigger points Exclusion Criteria: * primary headaches (i.e., migraine, tension type headache) * bilateral headache * Presence of any red flags * cervical spinal stenosis * evidence of central nervous system involvement * prior surgery to the head or neck
Where this trial is running
Bahawalpur, Punjab Province
- Bahaval Victoria Hospital — Bahawalpur, Punjab Province, Pakistan (RECRUITING)
Study contacts
- Principal investigator: Ghulam Fatima, PHD* — Riphah International University
- Study coordinator: Imran Amjad, PHD*
- Email: imran.amjad@riphah.edu.pk
- Phone: 03324390125
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.
Conditions: Cervicogenic Headache, Cervicogenic headache, Disability evaluation, Ischemic compression therapy, Pain assessment, Range of motion, Trigger point