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Effectiveness of Dry Needling of the Sternocleidomastoid in Patients With Cervicogenic Headaches

Effectiveness of Dry Needling of the Sternocleidomastoid in Patients With Cervicogenic Headaches - A Randomized Clinical Trial

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03730896
Enrollment
17
Registered
2018-11-05
Start date
2018-10-01
Completion date
2020-03-01
Last updated
2020-07-23

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervicogenic Headache

Keywords

Dry needling, Cervicogenic headache, Manual therapy

Brief summary

Evaluating the benefit of dry needling of the sternocleidomastoid muscle in subjects with cervicogenic headaches.

Detailed description

The purpose of this study is to determine whether individuals with cervicogenic headache respond favorably to a program of manual therapy in combination with dry needling of the major muscle between chest bone and the head (sternocleidomastoid muscle) compared to manual therapy directed to the upper body quadrant alone. The researchers will conduct a randomized clinical trial to assess the effectiveness of a manual therapy and dry needling approach (group 1) vs. manual therapy only. (group 2)

Interventions

PROCEDUREDry needling

Dryneedling of the sternocleidomastoid muscles within a standard treatment approach of physical therapy

Sponsors

Florida Gulf Coast University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Subject)

Masking description

Random assignment to dry needle group or control group with standard manual therapy interventions

Eligibility

Sex/Gender
ALL
Age
18 Years to 65 Years
Healthy volunteers
No

Inclusion criteria

1. Age between 18-65 years old 2. Primary complaint of cervicogenic headache 3. Restricted cervical Range of motion 4. Neck Disability Index \> 20 points

Exclusion criteria

1. Red flags identified during the patients physical therapy initial evaluation (i.e. tumor, fracture, metabolic diseases, RA, osteoporosis, prolonged history of steroid use, symptoms of vertebrobasilary insufficiency, pregnancy, cervical spinal stenosis, bilateral upper extremity symptoms etc. 2. Use of blood thinners 3. History of whiplash injury within the past six weeks 4. Evidence of central nervous system involvement, to include hyperreflexia, sensory disturbances in the hand, intrinsic muscle wasting of the hands, unsteadiness during walking, nystagmus, loss of visual acuity, impaired sensation of the face, altered taste, the presence of pathological reflexes (i.e. positive Hoffman's and/or Babinski reflexes), etc. 5. Two or more positive neurologic signs consistent with nerve root compression, including any two of the following: 1. Muscle weakness involving a major muscle group of the upper extremity 2. Diminished upper extremity muscle stretch reflex (biceps brachii, brachioradialis, or triceps) 3. Diminished or absent sensation to pinprick in any upper extremity dermatome 6. Prior surgery to the neck or thoracic spine 7. Chiropractic, Physical Therapy, or Acupuncture treatment for their neck pain in the last 6-months 8. Workers compensation or pending legal action regarding their headaches 9. Insufficient English language skills to complete all questionnaires 10. Inability to comply with treatment and follow-up schedule

Design outcomes

Primary

MeasureTime frameDescription
Change in Headache Disability Index (HDI) scoreAt initial evaluation (day 1), week three (day 21) and week 6 (day 42)Questionnaire for self report, this will be on a 0-100 score

Secondary

MeasureTime frameDescription
Change in cervical range of motion using an inclinometer/ change in high cervical range of motion using the Flexion-Rotation Test (FRT)At initial evaluation (day 1), week three (day 21) and week 6 (day 42)range of motion assessment, this will be measured in degrees with standardized goniometer measure
Change in the neck disability Index scoreAt initial evaluation (day 1), week three (day 21) and week 6 (day 42)Self report neck pain questionnaire, This is a 0-100 score
Change in visual analogue scale scoreAt initial evaluation (day 1), week three (day 21) and week 6 (day 42)Pain intensity scale,on a 10 cm line patient is asked to mark pain with one vertical mark

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026