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Effect of Ultrasound-Guided Dry Needling Targeting Rectus Capitus Posterior Major on Individuals With Headaches

Status: Recruiting
Location: See location...
Intervention Type: Other
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Headaches such as tension-type, migraine, and cervicogenic (neck-related) headaches are among the most common and disabling conditions worldwide. and are often associated with tight or sensitive muscles at the base of the skull, which can contribute to headaches. Dry needling involves inserting a very thin, sterile needle into tight muscle areas known as trigger points to relieve pain and muscle tension. When applied to the deep neck muscles, including those beneath the skull, dry needling may reduce headache symptoms. The suboccipital region contains important structures such as the vertebral artery, greater occipital nerve, and spinal cord, which requires precise needle placement to maintain safety. Many needling techniques used in this region have not been validated for accuracy or safety in living subjects. This study will use real-time ultrasound imaging to guide dry needling of the rectus capitis posterior major muscle and directly visualize nearby structures to minimize risk. The main goals of this research are to examine the effects of a single session of ultrasound-guided dry needling on headache symptoms and to confirm the safety, accuracy, and consistency of the proposed needling technique using ultrasound imaging.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 65
Healthy Volunteers: f
View:

• Reports of a headache within the last 6 months (no minimum or maximum frequency or duration)

• Current reports of headache

• Tenderness to palpation of suboccipital muscles with Numeric Pain Rating Scale score ≥ 2/10

• No history of cervical spine surgery or neurological disorders

Locations
United States
Texas
Texas Tech University Health Sciences Center
RECRUITING
Lubbock
Contact Information
Primary
Gary A Kearns, PT, ScD
gary.kearns@ttuhsc.edu
12142448398
Backup
Jace A Brown, PT, PhD
jbrown34@twu.edu
9406897716
Time Frame
Start Date: 2026-03-01
Estimated Completion Date: 2026-06-01
Participants
Target number of participants: 50
Treatments
Experimental: Dry needling
Related Therapeutic Areas
Sponsors
Collaborators: Texas Woman's University
Leads: Texas Tech University Health Sciences Center

This content was sourced from clinicaltrials.gov