Ischemic Compression Technique Versus Jones Technique in Cervicogenic Headache Patients
Recruiting
N/A
Interventional Study
Cervicogenic Headache
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 25 – 35
- Sex
- Any
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 32 (estimated)
- Sponsor
- Riphah International University · Other
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About This Trial
The primary objective of the study is to determine the effects of Jones and Ischemic compression technique on pain, range of motion and disability in patients with cervicogenic headache. Cervicogenic headache is a distinctive type of secondary headache where the pain originates from structures in the neck or cervical spine and radiates to the head. Trigger point release has been associated with de…
Trial Locations
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Eligibility 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 f…
Contacts