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Manipulation and Dry Needling in Patients With Cervicogenic Headache and WAD II

A

Alabama Physical Therapy & Acupuncture

Status

Enrolling

Conditions

Cervicogenic Headache
Whiplash Injuries

Treatments

Other: Dry Needling,Thrust Manipulation
Other: Exercise,Non-thrust Mobilization

Study type

Interventional

Funder types

Other

Identifiers

NCT06502951
AAMT0018

Details and patient eligibility

About

The purpose of this research is to compare two different approaches for treating patients with cervicogenic headaches associated with type II whiplash associated disorder: non-thrust mobilization and exercise versus thrust manipulation and dry needling. Physical therapists commonly use all of these techniques to treat cervicogenic headaches. This study is attempting to find out if one treatment strategy is more effective than the other.

Full description

Patients with cervicogenic headaches and type II whiplash associated disorder will be randomized to receive 1-2 treatment sessions per week for 4 weeks (up to 8 sessions total) of either: (1) dry needling and upper cervical high-velocity low-amplitude thrust manipulation, or (2) exercise and non-thrust mobilization.

Enrollment

120 estimated patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Subacute (> 4 weeks) or chronic type II whiplash associated disorder. Neck pain and headache following motor vehicle accident with reduced range of motion & point tenderness.
  2. Diagnosis of cervicogenic headache as defined by Cervicogenic Headache International Study Group criteria.
  3. Headache frequency of at least one per week since the whiplash injury.
  4. Headache intensity of greater than 2/10 on the NPRS.
  5. Neck pain intensity of greater than 2/10 on the NPRS.
  6. Neck Disability Index score of greater than 10/50 on the NDI.

Exclusion criteria

  1. WAD I (neck pain, but no physical signs), WAD III (neck pain and neurological signs), WAD IV (neck pain + fracture/dislocation).

  2. Positive screen for cervical radiography (Canadian C-Spine Rules).

  3. Bilateral headaches (typical of tension type headaches).

  4. Diagnosis / signs & symptoms of concussion (confusion, disorientation, or impaired consciousness; loss of memory for events immediately before or after the MVA; and one or more of the following: nausea, vomiting, visual disturbances, vertigo, gait and/or postural imbalance, and impaired memory and/or concentration).

  5. Diagnosis of fibromyalgia.

  6. Presence of any of the following atherosclerotic risk factors: hypertension, diabetes, heart disease, stroke, transient ischemic attack, peripheral vascular disease, smoking, hypercholesterolemia, or hyperlipidemia.

  7. Red flags noted in the patient's Neck Medical Screening Questionnaire (i.e., tumor, fracture, metabolic diseases, RA, osteoporosis, prolonged history of steroid use, etc.).

  8. Diagnosis of cervical spinal stenosis.

  9. Bilateral upper extremity symptoms.

  10. 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).

  11. 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 deep tendon reflex of the biceps, brachioradialis, triceps or superficial flexors
    3. Diminished or absent sensation to pinprick in any UE dermatome.
  12. Prior surgery to the head, neck, or thoracic spine.

  13. Physical therapy or chiropractic treatment for neck pain and/or headache in the past 3 months.

  14. Any condition that might contraindicate spinal manipulative therapy or dry needling.

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

120 participants in 2 patient groups

Dry Needling,Thrust Manipulation
Experimental group
Description:
Dry needling to the craniofacial, upper cervical, and cervicothoracic regions. High-velocity thrust manipulation to the upper cervical spine, mid/lower cervical spine, and cervicothoracic spinal regions.
Treatment:
Other: Dry Needling,Thrust Manipulation
Exercise,Non-thrust Mobilization
Active Comparator group
Description:
Nonthrust joint mobilization to the upper cervical spine, mid/lower cervical spine, and cervicothoracic spinal regions. Cranio-cervical flexion exercises, peri-scapular progressive resistance exercises, and electrothermal modalities
Treatment:
Other: Exercise,Non-thrust Mobilization

Trial contacts and locations

1

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Central trial contact

James Dunning, PhD, DPT; Ian Young, DSc, PT

Data sourced from clinicaltrials.gov

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