Headache
Conditions
Brief summary
Currently, it is unknown if dry needling when performed to the trigeminal innervation field improves neck pain and or headache for patients with cervicogenic headaches. The aim of this study is to determine if dry needling of the trigeminal innervation field improves pain, pain-pressure thresholds, and neck mobility in patients with cervicogenic headaches, with or without migraine.
Detailed description
Dry needling is a widely used intervention performed by physical therapists for a wide range of musculoskeletal and neurological conditions. Dry needling has been shown to be beneficial for cervicogenic headaches but treatment is typically applied to the neck. It is well-established that cervical pain can upregulate the trigeminal nerve and vice versa in various forms of headaches. Thus, it is plausable that reducing inflammation and irritation of the trigeminal nerve may in fact reduce neck pain and impairments. This study aims to look investigate whether dry needling the trigeminal innervation field will reduce pain and impairments known to exist in patients with cervicogenic headaches compared to a sham comparator. The study is a pilot trial for a larger RCT and will look at immediate effects only.
Interventions
OTHERDry Needling
1/2 needles will placed into defined innervation fields of the trigeminal nerve and rotated. Total time will be 5-7 minutes.
OTHERSham Dry Needling
Needle handles inside of guide tubes will be tapped in a way similar to an actual needle being set but the sham needles will be blunted.
Sponsors
Youngstown State University
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Outcomes Assessor)
Masking description
Patients will be asked to keep their eyes closed during the treatment. Clinicians will be blinded to group and outcomes
Intervention model description
Double blinded, sham controlled, randomized trial.
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Aged 18 or older * Symptoms: (1)Unilateral pain starting in the neck and radiating to the frontotemporal region or posterior fossa, (2) pain aggravated by neck movement, (3) restricted cervical range of motion, (4) non-throbbing and non-lancinatingnpain, 5) dysfunction/headache pain in at least one of the joints of the upper cervical spine(C0-C4), and (6) headache frequency of at least 1 per week over a period greater than 3 months.
Exclusion criteria
* Pain \<2/10 * Contraindications to the interventions * Whiplash associated disorder within 6 weeks * Pending litigation for neck pain and/or headache.
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Headache or neck pain intensity on a Numeric pain rating scale (0-10) | <1 hour | 0-10 scale pain intensity |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Active Range of Motion of the Cervical Spine in degrees of measurement | <1 hour | Active range of motion will be measured in the most painful and or limited plane of movement. |
| Flexion-rotation test in degrees of measurement | <1 hour | Flexion-rotation test for CGH will be measured to determine any change in measure for c1-c2 mobility. |
| Pain-pressure threshold in lbs of pressure | <1 hour | Pain-pressure threshold will be measured using an algometer at the innervation zones of the trigeminal nerve and the upper cervical spine. |
Countries
United States
Contacts
Primary ContactDavid W Griswold, PhD
Outcome results
None listed