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Laser and Therapeutic Ultrasound in the Management of the Chronic Non-specific Low Back Pain

Not Applicable
Conditions
Chronic Low Back Pain
Interventions
Other: continuous ultrasound group
Other: low level laser therapy group
Other: pulsed ultrasound group
Registration Number
NCT02150096
Lead Sponsor
University of Sao Paulo General Hospital
Brief Summary

The objective of this study is evaluate the laser and ultrasound effect on pain and disability in women with non-specific chronic low back pain.

Detailed Description

Not available

Recruitment & Eligibility

Status
UNKNOWN
Sex
Female
Target Recruitment
150
Inclusion Criteria
  • non-specific chronic low back pain
  • moderate pain
  • eutrophics women
Exclusion Criteria
  • disk herniation
  • cardiac diseases
  • psychiatrics diseases
  • endocrinous diseases
  • fractures of the spine
  • fractures of lower members
  • diabetics
  • dental emergency
  • local infections
  • local non sensibility
  • analgesics and anti-inflammatories in use
  • neurologic diseases
  • pregnancy

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Pulsed ultrasound grouplow level laser therapy groupthe group will be treated with 1,5 W/cm² 6 minutes in each side of the lumbar spine in 6 points around the lumbar spine
low level laser therapy groupcontinuous ultrasound groupthe group will be treated with 3J during 6 minutes in each side of the lumbar spine in 6 points around the lumbar spine
low level laser therapy grouppulsed ultrasound groupthe group will be treated with 3J during 6 minutes in each side of the lumbar spine in 6 points around the lumbar spine
Continuous ultrasound grouppulsed ultrasound groupthe group will be treated with 1,5 W/cm² 6 minutes in each side of the lumbar spine in 6 points around the lumbar spine
Continuous ultrasound grouplow level laser therapy groupthe group will be treated with 1,5 W/cm² 6 minutes in each side of the lumbar spine in 6 points around the lumbar spine
Pulsed ultrasound groupcontinuous ultrasound groupthe group will be treated with 1,5 W/cm² 6 minutes in each side of the lumbar spine in 6 points around the lumbar spine
Primary Outcome Measures
NameTimeMethod
Pain evaluationThe pain will be evaluate before and after 25 days of the treatment

The visual analogic scale will be used for evaluate the pain.

Secondary Outcome Measures
NameTimeMethod
Disability evaluationThe disability will be evaluate before and after 25 days of the treatment

The Roland Morris questionaire will be used to evaluate the disability.

Trial Locations

Locations (1)

Sâo Lucas College

🇧🇷

Porto Velho, Rondônia, Brazil

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