Immediate Effect of Irradiation With Low-level Laser Therapy on the Electromyographic Activity of the Upper Trapezius Muscles and the Level of Pain Among Patients With Non-specific Neck Pain

NCT02498249 · Status: COMPLETED · Phase: PHASE1/PHASE2 · Type: INTERVENTIONAL · Enrollment: 20

Last updated 2015-07-15

No results posted yet for this study

Summary

The aim of the present study is to assess the immediate effect of irradiation with low level laser therapy (LLLT) on the electromyographic activity of upper trapezius muscles and the amount of pain felt by patients with non-specific neck pain (NS-NP).A total of 20 patients with non-specific neck pain will be enrolled in a randomized, single-blind, crossover study. Each subject will receive two forms of treatment in random order: a single session of LLLT and placebo LLLT. In order to eliminate carry-over treatment effects, a one-week wash-out period will be respected between sessions. Surface electromyography will be used to determine nerve conduction velocity and activity in the upper trapezius muscles before and after treatment. The outcome measures will be determined by a numerical pain rating scale. Comparisons before and after irradiation with LLLT will determine the activity of the upper trapezius muscles and the level of pain. The data will be submitted to statistical tests considering a p-value of p \< 0.05.

Conditions

  • Neck Pain Treatment

Interventions

DEVICE

low level laser therapy

Will be performed irradiation with low-intensity laser in upper trapezius muscle

DEVICE

Placebo low level laser therapy

Will be not performed irradiation with low-intensity laser in upper trapezius muscle

Sponsors & Collaborators

  • Simone Aparecida Penimpedo Calamita

    collaborator UNKNOWN
  • Fabiana Sarilho de Mendonça

    collaborator UNKNOWN
  • Daniela Aparecida Biasotto-Gonzalez

    collaborator UNKNOWN
  • Marco Antônio Fumagalli

    collaborator UNKNOWN
  • Paulo de Tarso Camilo de Camargo

    collaborator UNKNOWN
  • University of Nove de Julho

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2015-05-31
Primary Completion
2015-06-30
Completion
2015-07-31

Countries

  • Brazil

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02498249 on ClinicalTrials.gov