Actively Recruiting

Phase Not Applicable
Age: 18Years - 65Years
All Genders
NCT07309874

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

Led by Texas Tech University Health Sciences Center · Updated on 2026-04-01

50

Participants Needed

1

Research Sites

13 weeks

Total Duration

On this page

Sponsors

T

Texas Tech University Health Sciences Center

Lead Sponsor

T

Texas Woman's University

Collaborating Sponsor

AI-Summary

What this Trial Is About

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.

CONDITIONS

Official Title

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

Who Can Participate

Age: 18Years - 65Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • 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 65 2/10
  • No history of cervical spine surgery or neurological disorders
Not Eligible

You will not qualify if you...

  • History of cervical spine trauma or surgery
  • Diagnosed bleeding disorder
  • Currently using anticoagulant medications
  • Currently using anti-platelet medications
  • Diagnosed systemic joint diseases such as rheumatoid arthritis
  • Active infection
  • Diabetes
  • Cancer
  • Fibromyalgia
  • Cervical radiculopathy
  • Inability to tolerate prone positioning for the duration of the procedure.

AI-Screening

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Trial Site Locations

Total: 1 location

1

Texas Tech University Health Sciences Center

Lubbock, Texas, United States, 79430-0001

Actively Recruiting

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Research Team

G

Gary A Kearns, PT, ScD

CONTACT

J

Jace A Brown, PT, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

TREATMENT

Number of Arms

1

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