Ultrasound-Guided Dry Needling for Headaches
This study is looking at how a treatment called dry needling might help people with headaches, including tension-type, migraine, and cervicogenic (neck-related) headaches. Dry needling involves inserting very thin needles into tight muscles, specifically the rectus capitus posterior major muscles at the base of your skull, which can contribute to headaches. Researchers will use ultrasound to guide the needles and test two different insertion angles (30 degrees and 45 degrees). They want to see if this treatment reduces headache pain and disability. You might be able to join if you are between 18 and 65 years old, have had headaches in the last six months, and have tenderness in your neck muscles. The study will measure how much soreness you feel after needling, your pain levels, and how headaches affect your daily life. The current status of this study is unclear.
- Study design
- This is a single-arm study, meaning all participants will receive the dry needling intervention. It plans to enroll 50 participants.
- What's involved
- You will have one study visit lasting about 60 minutes. During this visit, you will be screened, complete pain and disability questionnaires, and receive the dry needling procedure.
- Compensation
- Not stated in the trial record.
- Follow-up
- Your post-needling soreness, pain levels, and headache disability will be measured again 24-48 hours after the data collection session.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Effect of Ultrasound-Guided Dry Needling Targeting Rectus Capitus Posterior Major on Individuals With Headaches
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Gary A Kearns, PT, ScD · PRINCIPAL_INVESTIGATOR · Texas Tech University Health Sciences Center
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Post-needling soreness24-48 hours post-data collection
Subjective outcome measures: • Post-data collection reports of post-needling soreness (Dichotomous report: Yes or No)
- Numeric Pain Rating ScaleBaseline immediately pre-data collection and then again 24-48 hours post-data collection
Numeric Pain Rating Scale (0 = no pain; 10 = worst pain): Pre-data collection will include Current rating, Best rating in past 6 months, and Worst rating in past 6 months. Post-data collection will include Current rating, Best rating in past 24-48 hours, and Worst rating in past 24-48 hours
- Headache Disability IndexBaseline immediately pre-data collection and then again 24-48 hours post-data collection
Headache Disability Index: Scores range from 0 to 100. A total score of 10-28 is considered mild disability. A total score of 30-48 is considered moderate disability. A total score of 50-68 is severe disability. A total score of 72-100 is considered complete disability. Participants will complete the Headache Disability Index immediately pre-data collection and then 24-48 hours post-data collection