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

F

Florida Gulf Coast University

Status

Terminated

Conditions

Cervicogenic Headache

Treatments

Procedure: Dry needling

Study type

Interventional

Funder types

Other

Identifiers

NCT03730896
FGCU IRB 2018-49

Details and patient eligibility

About

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

Full 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)

Enrollment

17 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

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

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

17 participants in 2 patient groups

standard care group
No Intervention group
Description:
Normal manual therapy interventions Clinician will decide normal course of treatment
Dry needling
Experimental group
Description:
Dryneedling group Clinician will decide normal course of treatment and dry needling of the Sternocleidomastoid muscle (SCM) muscle will be added to that treatment
Treatment:
Procedure: Dry needling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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