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Short-Term Response of Thoracic Spine Manipulation With or Without Trigger Point Dry Needling for Mechanical Neck Pain

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Brooke Army Medical Center

Status

Completed

Conditions

Neck Pain

Treatments

Device: Seirin J-type stainless steel needles, 0-2-0.3 x 40-50 mm
Procedure: Thoracic spinal manipulation
Procedure: Trigger point dry needling sham
Behavioral: Cervical range of motion exercises
Behavioral: Posterior neck muscle activation exercise
Procedure: Trigger point dry needling

Study type

Interventional

Funder types

Other U.S. Federal agency

Identifiers

NCT02415660
404153-1

Details and patient eligibility

About

This study will assess the short term response of thoracic spinal manipulation with or without trigger point dry needling in 58 subjects with a primary complaint of mechanical neck pain.

Full description

Neck pain is common, and return to duty rates after medical evacuation from theater for spinal pain is low. Muscles comprise the majority of the stability for the cervical spine, yet neck muscle function can be altered in the presence of pain. Research has consistently shown the benefit of including thoracic spine manipulation (SMT) in the treatment of patients with mechanical neck pain. Emerging evidence is now also showing promising benefit of including trigger point dry needling (TDN) for the treatment of mechanical neck pain. Treatment regimens commonly address anterior cervical stabilizing musculature, but little is known regarding the response to treatment of the deep posterior stabilizing musculature.

This study will assess the short term response of thoracic SMT with or without TDN in 58 subjects with a primary complaint of mechanical neck pain. Subjects will be randomized to receive 2 treatment visits approximately 2-3 days apart of either SMT+sham TDN or SMT+TDN. TDN will be directed to the upper trapezius and deep cervical extensor muscles of the neck. Outcomes of interest will be changes in function and pain. Assessments will be made at baseline, immediately after the first treatment, at the 2nd treatment, and approximately 5-7 days after the 2nd treatment visit. A subgroup of 20 subjects (10 per group) will also have the upper trapezius and deep cervical extensor muscle activation assessed via shear wave elastography, and deep cervical flexor activation assessed via the craniocervical flexion test.

Enrollment

42 patients

Sex

All

Ages

18 to 64 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Age 18-64 years and eligible for military health care
  2. Primary complaint of mechanical neck pain provoked by posture, movement or palpation of neck musculature, with or without unilateral upper extremity symptoms.
  3. Presence of active trigger points in either the upper trapezius or deep cervical extensor muscles.
  4. Able to make one initial appointment at the Army Medical Department Center and School at Fort Sam Houston, one treatment visit approximately 2-3 days after the initial visit, and then a final outcome visit approximately 5-7 days after 2nd visit.
  5. No less than 10 points (0-50 range) on the Neck Disability Index.

Exclusion criteria

  1. Prior history of whiplash injury resulting in neck pain which required medical treatment.

  2. Any prior physical therapy, chiropractic, acupuncture treatment or injections for neck pain within the past 3 months.

  3. History of cervical spine surgery.

  4. History of any systemic disorder in which thoracic spine manipulation and TDN would be contraindicated (i.e. osteoporosis, bleeding disorders or anticoagulant medication use)

  5. Signs and symptoms consistent with nerve root compression (i.e. diminished upper extremity strength, sensation or reflexes), cervical artery insufficiency (i.e. nystagmus, gait disturbances, Horner Syndrome) or upper cervical ligament instability (i.e. Sharp-Purser, alar ligament, transverse ligament tests).

  6. Current primary complaint of headaches

  7. Pending legal action regarding their neck pain

  8. Inability to read and understand English

  9. Females known or thought to be pregnant

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Double Blind

42 participants in 2 patient groups

SMT and TDN
Experimental group
Description:
Thoracic spinal manipulation and trigger point dry needling using Seirin J-type stainless steel needles, 0-2-0.3 x 40-50 mm. Exercise program consists of cervical range of motion exercises and posterior neck muscle activation exercise.
Treatment:
Device: Seirin J-type stainless steel needles, 0-2-0.3 x 40-50 mm
Behavioral: Cervical range of motion exercises
Behavioral: Posterior neck muscle activation exercise
Procedure: Trigger point dry needling
Procedure: Thoracic spinal manipulation
SMT and Sham TDN
Sham Comparator group
Description:
Thoracic spinal manipulation and trigger point dry needling sham. Exercise program consists of cervical range of motion exercises and posterior neck muscle activation exercise.
Treatment:
Procedure: Trigger point dry needling sham
Behavioral: Cervical range of motion exercises
Behavioral: Posterior neck muscle activation exercise
Procedure: Thoracic spinal manipulation

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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