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Dry Needling vs. Manual Therapy for Headaches

N/A
Recruiting
Led By David Griswold, PhD
Research Sponsored by Youngstown State University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Headache frequency of at least 1 per week over a period greater than 3 months
18 years or older
Must not have
Non-English speaking patients
Tension-type headache
Timeline
Screening 3 weeks
Treatment Varies
Follow Up baseline 1 week, 1 month, 3 months, 12 months
Awards & highlights
No Placebo-Only Group

Summary

This trial compares dry needling and orthopedic manual therapy for patients with headaches caused by neck problems. Dry needling uses thin needles to relieve muscle tension, while manual therapy involves hands-on adjustments to the neck. Both treatments aim to reduce headache pain by addressing issues in the neck. Dry needling is a treatment technique used by clinicians to relieve symptoms in patients with tension-type headache (TTH), cervicogenic headache (CGH), or migraine.

Who is the study for?
This trial is for adults over 18 with cervicogenic headaches (CGH) occurring at least once a week for more than three months. Participants must meet specific criteria and have neck dysfunction. It's not for those with mild headache pain, non-English speakers, certain medical conditions or surgeries, metal allergies, migraine or tension-type headaches, needle phobia, or cervical arterial issues.
What is being tested?
The study compares the effectiveness of cervical-cranial dry needling versus orthopedic manual therapy in managing CGH symptoms. Both treatments are accompanied by patient education, thoracic manipulation, and exercise. The outcomes will be measured at various intervals up to one year.
What are the potential side effects?
Potential side effects may include discomfort at the needle site from dry needling and soreness from manual therapy. There could also be temporary increased headache or neck pain following treatment.

Eligibility Criteria

Inclusion Criteria

You may be eligible if you check “Yes” for the criteria below
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I have had headaches at least once a week for more than 3 months.
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I am 18 years old or older.
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I have had headaches at least once a week for more than 3 months.
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I have trouble moving parts of my body even when helped.

Exclusion Criteria

You may be eligible for the trial if you check “No” for criteria below:
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I do not speak English.
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I experience tension-type headaches.
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I do not have conditions like cancer, spinal cord issues, fractures, metabolic diseases, rheumatoid arthritis, or long-term steroid use that would prevent me from receiving certain treatments.
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My headache does not worsen with certain neck movements.
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I am extremely afraid of needles.
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I have had surgery on my neck or upper back.
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I experience headaches that suggest a neck artery issue.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~baseline 1 week, 1 month, 3 months, 12 months
This trial's timeline: 3 weeks for screening, Varies for treatment, and baseline 1 week, 1 month, 3 months, 12 months for reporting.

Treatment Details

Study Objectives

Study objectives can provide a clearer picture of what you can expect from a treatment.
Primary study objectives
Change in NPRS headache intensity
Secondary study objectives
Change in Medication intake
Change in current NPRS neck or headache intensity
Change in disability using Headache Disability Index (HDI)
+5 more

Awards & Highlights

No Placebo-Only Group
All patients enrolled in this study will receive some form of active treatment.

Trial Design

2Treatment groups
Experimental Treatment
Active Control
Group I: Cervical-cranial dry needlingExperimental Treatment4 Interventions
Patients randomized to this arm will receive cervical-cranial dry needling, thoracic manipulation, and exercise.
Group II: Orthopedic Manual TherapyActive Control4 Interventions
Patients randomized to this arm will receive orthopedic manual therapy to cervical spine, thoracic manipulation, and exercise.

Research Highlights

Information in this section is not a recommendation. We encourage patients to speak with their healthcare team when evaluating any treatment decision.
Mechanism Of Action
Side Effect Profile
Prior Approvals
Other Research
Cervical-Cranial Dry Needling (Trigger Point Release) involves inserting thin needles into specific muscle trigger points to relieve tension and pain by disrupting the pain cycle and promoting muscle relaxation. Orthopedic Manual Therapy (Spinal Mobilization) includes techniques such as thrust and non-thrust mobilizations to the cervical spine, which aim to improve joint mobility, reduce muscle tension, and alleviate pain by restoring normal movement patterns. These treatments are significant for Cervicogenic Headache patients as they directly target the musculoskeletal sources of their headaches, potentially providing relief from pain and improving overall function.

Find a Location

Who is running the clinical trial?

Youngstown State UniversityLead Sponsor
26 Previous Clinical Trials
1,884 Total Patients Enrolled
Franklin Pierce UniversityOTHER
15 Previous Clinical Trials
986 Total Patients Enrolled
David Griswold, PhDPrincipal InvestigatorAssociate Professor at Youngstown State University
~13 spots leftby Oct 2025