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Dry Needling Versus Intramuscular Stimulation in the Management of the Myofascial Trigger Points

U

University of Alcala

Status

Completed

Conditions

Trigger Point Pain, Myofascial
Myofascial Pain Syndrome
Muscle Pain

Treatments

Other: Dry needling and electric stimulation
Other: Dry needling

Study type

Interventional

Funder types

Other

Identifiers

NCT03025230
M2012119/20130409

Details and patient eligibility

About

Hypothesis The application of intramuscular electrostimulation will be more effectiveness than the dry needling in myofascial trigger points treatment.

Objetives:

To determine the effectiveness of intramuscular electrostimulation in the treatment of trigger points of the levator scapula muscle for the improvement of pain in mechanical cervicalgia.

Participants: Subjects with diagnosed of myofascial pain syndrome in cervical region and active trigger points in levator scapulae muscle, randomly assigned to experimental or control group.

Intervention: Control group: one session of dry needling in active trigger points; experimental group: one session of intramuscular stimulation in active trigger points.

Main Outcomes Measures: Pain, pressure pain threshold (PPT), active cervical range of motion and strength muscle . The measures will be taken before, after and one week after the interventions.

Full description

The muscle pain is one of the most common forms of musculoskeletal pain. Within muscular pain, the presence of myofascial trigger points (PG) in the musculature is a important and prevalent problem.

Currently one the techniques most used in the treatment of PG is dry needling. Dry needling has been shown effective in the treatment of neck pain associated with PGs.

To our knowledge, there are no studies that they have compared the effectiveness of dry needling and intramuscular stimulation by applying an electric current.

This study is a randomized clinical trial that aims to demonstrate that the application of an electric current associated with dry needling in the treatment of PG.

In this study we will treat subjects with cervical pain who they have active PGs in the levator scapulae muscle.

Enrollment

80 patients

Sex

All

Ages

18 to 65 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Cervical pain.
  • Active trigger points in levator scapulae muscle

Exclusion criteria

  • Pain Irradiation toward upper limb
  • Psychological disorders
  • Whiplash.
  • Neuropathic symptoms
  • Cervical and / or Shoulder Spine Surgery

Trial design

Primary purpose

Treatment

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

80 participants in 2 patient groups

Experimental group
Experimental group
Description:
Dry needling technique and the application of a rectangular, biphasic, asymmetric analgesic electric current by selecting a frequency of 2 Hz with a pulse width 40 μs, with an intensity located at the tolerance threshold and for a time of 20 minutes.
Treatment:
Other: Dry needling and electric stimulation
Control group
Active Comparator group
Description:
Dry technique in PG.The needle will be moved in-and-out into different directions to encounter sensitive spots in PG region.
Treatment:
Other: Dry needling

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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