MedPath

Dry Needling Dosage in the Treatment of Myofascial Neck Pain

Not Applicable
Completed
Conditions
Neck Pain
Interventions
Procedure: Dry needling
Procedure: Control
Registration Number
NCT02190890
Lead Sponsor
Universidad Rey Juan Carlos
Brief Summary

The purpose of this study are (1) to determine the effectiveness of different dry needling dosages in the treatment of myofascial trigger points in the upper trapezius muscle in patients with myofascial neck pain, (2) to assess postneedling soreness and tenderness and (3) evaluate the influence of psychological factors on the perception of postneedling soreness.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
94
Inclusion Criteria
  • Diagnosis of an active myofascial trigger point. Neck pain: Superior to 3 cm in VAS
Exclusion Criteria
  • Neck area: Fracture, radiculopathy, previous surgery, previous needling treatment in the last 6 months, previous analgesic medication (24 hours), psychiatric disease

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Dry needling: Until no more local twitch responses elicitedDry needlingDeep dry needling in the active myofascial trigger point in the upper trapezius muscle. The muscle fibers were repeatedly perforated by rapidly inserting and partially withdrawing the needle from the MTrP until no more local twitch responses were elicited.
Dry needling: 4 local twitch responsesDry needlingDeep dry needling in the active myofascial trigger point in the upper trapezius muscle. The muscle fibers were repeatedly perforated by rapidly inserting and partially withdrawing the needle from the MTrP until 4 local twitch responses were elicited.
Dry needling: 6 local twitch responsesDry needlingDeep dry needling in the active myofascial trigger point in the upper trapezius muscle. The muscle fibers were repeatedly perforated by rapidly inserting and partially withdrawing the needle from the MTrP until 6 local twitch responses were elicited.
ControlControlThe needle was inserted 1.5 cm away from the trigger point in the trapezius muscle and withdrawn without any consecutive insertion.
Primary Outcome Measures
NameTimeMethod
Postneedling soreness1 week

Visual analog scale. A 100mm VAS, ranging from 0mm (no pain) to 100mm (worst imaginable pain).

Pain1 week

Visual analog scale. A 100mm VAS, ranging from 0mm (no pain) to 100mm (worst imaginable pain).

Secondary Outcome Measures
NameTimeMethod
Psychological factorsPre-intervention

Pain Catastrophizing Scale

Pressure pain threshold1 week

Three consecutive trials of pressure pain threshold on the active trigger point at a rate of 1 kg/sec at intervals of 30 seconds were conducted.

Pain in cervical range of motion1 week

Pain in a numerical pain rating scale during all cervical movements was recorded.

Neck disability1 week

Neck Disability Index questionnarie was completed.

Cervical range of motion1 week

The subjects sat in a chair and a CROM goniometer was placed over the head. They were asked to perform active neck movements to the fullest extent of their mobility. Each movement was recorded three times and the average value was calculated.

© Copyright 2025. All Rights Reserved by MedPath