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Clinical Trials/NCT03345238
NCT03345238
Completed
Not Applicable

Neurophysiological Effects of Dry Needling in Patients With Neck Pain

Universidad Rey Juan Carlos1 site in 1 country65 target enrollmentStarted: March 13, 2017Last updated:

Overview

Phase
Not Applicable
Status
Completed
Enrollment
65
Locations
1
Primary Endpoint
Efficacy of Deep Dry Needling applied on Active Myofascial Trigger Points (MTP) vs. latent MTP versus outside MTP, on pain reduction in patients with chronic neck pain.

Overview

Brief Summary

The present study aims to evaluate the differences that may be experienced in pain and cervical disability, before, during and just after the intervention of the Deep Dry Needling in the upper trapezius muscle in active, passive myofascial trigger points (MTP) or non-MTP in Patients with neck pain, assessing, in turn, the neurophysiological effects on the Autonomic Nervous System.

Hypothesis: Deep Dry Needling of active myofascial trigger points produces a greater decrease of pain and cervical disability index and increase of pressure pain threshold; Than the Deep Dry Needling of Myofascial Trigger Points latent or out of Myofascial Trigger Points in patients with chronic neck pain.

Objective: To determine the efficacy of Deep Dry Needling applied on Active Myofascial Triggers (MTP) vs. latent MTP versus MTP, on pain reduction and cervical disability, in patients with chronic neck pain attributable to Myofascial Pain Syndrome.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Factorial
Primary Purpose
Treatment
Masking
Double (Participant, Outcomes Assessor)

Eligibility Criteria

Ages
18 Years to 65 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Non-specific neck pain, unilateral or bilateral.
  • Neck pain ≥ 3 months of duration.
  • Presence of active and latent MTP in the upper, left, right or bilateral trapezius muscle, in relation to the patient's neck pain.
  • Clinical criteria recommended to identify active and latent MTP:
  • Tensile band palpable.
  • Exquisite local pain at the pressure of a taut band node.
  • Recognition by the patient of their usual pain when pressing on the sensitive nodule (to identify an active MTP).
  • Painful limitation of range of mobility to complete stretching. It is considered positive when 3 of the 4 clinical criteria are found.

Exclusion Criteria

  • Unsurpassed fear of needles.
  • Coagulation disorders.
  • Specific alterations of the cervical region in the clinical history.
  • Infiltration of corticosteroids or local anesthetics during a year before the study.
  • Surgical intervention of the cervical region or previous shoulder.
  • Skin lesions in the area, as well as infection or inflammation.
  • Taking analgesic, anti-inflammatory or anticoagulant medication the week before the study.
  • Treatment of MTP or Deep Dry Needling in the neck region in the 6 months prior to the intervention.
  • Cognitive deficit in the medical history.

Outcomes

Primary Outcomes

Efficacy of Deep Dry Needling applied on Active Myofascial Trigger Points (MTP) vs. latent MTP versus outside MTP, on pain reduction in patients with chronic neck pain.

Time Frame: Baseline, during intervention, immediately after intervention, 1, 6, 12, 24, 48 and 72 hours after intervention, a week after intervention and one month after the intervention

Checkin the Intensity of pain with the Visual Analogic Scale. It is a 100 mm line that measures the intensity of pain.The left end of the line represents the absence of pain, while the far right represents the worst pain imaginable. The numerical scale of intensity of pain adds a numerical ranking where 1 is no pain and 10 the worst pain imaginable.

Secondary Outcomes

  • Threshold of pain to pressure(Baseline and immediately after intervention)
  • Changes related to the Autonomic Nervous System(Baseline, during intervention and after intervention (1 and 10 minutes after intervention))
  • Cervical pain and dysfunction(Baseline, a week after intervention and one month after the intervention)

Investigators

Sponsor Class
Other
Responsible Party
Principal Investigator
Principal Investigator

Josue Fernandez Carnero

Tesis Director

Universidad Rey Juan Carlos

Study Sites (1)

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