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Study Evaluating the Benefit of Dry Needling for Patients With Neck Pain

The Effectiveness of Dry Needling for Patients With Neck Pain: A Randomized Clinical Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01301170
Enrollment
66
Registered
2011-02-23
Start date
2011-02-28
Completion date
2012-03-31
Last updated
2011-02-23

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

Conditions

Neck Pain

Keywords

Neck pain, Dry Needling, Manual Therapy, Manipulation

Brief summary

The purpose of this study is to determine whether individuals with neck pain will respond favorably to a program of manual therapy, directed at the cervical and thoracic spine (including thrust manipulation), and exercise, in combination with dry needling, as compared to manual therapy, directed to the cervical and thoracic spine (including thrust manipulation), and an exercise program alone.

Interventions

PROCEDUREdry needling

The needling will take place bilaterally at both the suboccipital region and the paravertebral muscles between C4 and T4. The needling will take place with the patient in the prone position. Following all needle placement, they will rotated clockwise till the point that tension on the needle is felt by the therapist. This will create more tension between the needle and tissue fibers, after which the needles were removed.

Sponsors

Integrated Therapy Practice PC
Lead SponsorOTHER

Study design

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

Eligibility

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

Inclusion criteria

1. Age between 18-60 years old 2. Primary complaint of neck pain 3. Restricted cervical extension/and or cervical rotation ROM 4. Neck Disability Index \> 20 points

Exclusion criteria

1. Red flags noted in the patient's Neck Medical Screening Questionnaire (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: * Muscle weakness involving a major muscle group of the upper extremity * Diminished upper extremity muscle stretch reflex (biceps brachii, brachioradialis, or triceps) * 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 12-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 frame
neck disability index (NDI)4,12, 24 weeks

Secondary

MeasureTime frame
Patient Global Rating of Change (GROC)4, 12, 24 weeks

Countries

United States

Outcome results

None listed

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