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Photobiomodulation Therapy on Low Back Pain

Primary Purpose

Low Back Pain

Status
Completed
Phase
Not Applicable
Locations
Brazil
Study Type
Interventional
Intervention
Placebo PBMT
PBMT active
Sponsored by
Universidade Cidade de Sao Paulo
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Low Back Pain focused on measuring low back pain, photobiomodulation therapy, LLLT

Eligibility Criteria

18 Years - 65 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • patients seeking care for chronic non-specific low back pain (defined as pain or discomfort between the costal margins and the inferior gluteal folds, with or without referred symptoms in the lower limbs, for at least 3 month);
  • with a pain intensity of at least 3 points measured by a 0-10 points pain numerical rating scale;
  • aged between 18 and 65 years;
  • able to read Portuguese.

Exclusion Criteria:

  • evidence of nerve root compromise (i.e. one or more of motor, reflex or sensation deficit);
  • serious spinal pathology (such as fracture, tumor, inflammatory and infectious diseases);
  • serious cardiovascular and metabolic diseases;
  • previous back surgery;
  • pregnancy.

Sites / Locations

  • Centre for Excellence in Clinical Research in Physiotherapy of Universidade Cidade de São Paulo

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Active Comparator

Arm Label

Placebo PBMT

PBMT active

Arm Description

Application of PBMT (Photobiomodulation Therapy) without any dose (0 Joule) and The Back Book (educational information booklet).

Application of PBMT (Photobiomodulation Therapy) active and The Back Book (educational information booklet).

Outcomes

Primary Outcome Measures

Pain Intensity
Pain intensity will be measured by an 11-point (0-10) Numerical Rating Scale (Pain NRS)
Disability
Disability will be measured by the 24-item Roland Morris Disability Questionnaire

Secondary Outcome Measures

Pain intensity
Pain intensity will be measured by an 11-poin (0-10) Numerical Rating Scale (Pain NRS)
Disability
Disability will be measured by the 24-item Roland Morris Disability Questionnaire
Function
Function will be measured by an 11-point (0-10) Patient-Specific Functional Scale
Global perceived effect
Global perceived effect will be measured by an 11-point (-5 to +5) Global Perceived Effect Scale

Full Information

First Posted
March 20, 2017
Last Updated
September 15, 2020
Sponsor
Universidade Cidade de Sao Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo
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1. Study Identification

Unique Protocol Identification Number
NCT03089424
Brief Title
Photobiomodulation Therapy on Low Back Pain
Official Title
Effects of Photobiomodulation Therapy in Patients With Chronic Non-specific Low Back Pain: a Randomized Placebo-controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
September 2020
Overall Recruitment Status
Completed
Study Start Date
April 6, 2017 (Actual)
Primary Completion Date
June 4, 2019 (Actual)
Study Completion Date
June 20, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Universidade Cidade de Sao Paulo
Collaborators
Fundação de Amparo à Pesquisa do Estado de São Paulo

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Photobiomodulation therapy (PBMT) is a non-pharmacological method commonly used in treatment of musculoskeletal disorders. However, there are few high-quality scientific evidence to support the effectiveness of this therapy in the treatment of patients with chronic low back pain, at short, medium and long term. The present research project aims to evaluate the effects of PBMT in patients with chronic non-specific low back pain.
Detailed Description
This is a randomized, triple-blinded, placebo-controlled trial, with voluntary patients with chronic non-specific low back pain.One hundred and forty-eight patients will be randomly allocated to two treatment groups: Placebo or PBMT for 4 weeks (3 times per week, total of 12 sessions of 27 minutes each). The clinical outcomes will be obtained at the completion of treatment (4 weeks) and at 3, 6 and 12 months after randomization. The data will be collected by a blinded assessor. The statistical analysis will follow the intention-to-treat principles and the between-group differences will be calculated by using mixed linear models. The outcomes of interest are pain intensity, disability, function and global perceived effect.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Low Back Pain
Keywords
low back pain, photobiomodulation therapy, LLLT

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Masking Description
The mode of intervention (active or placebo photobiomodulation) will be coded by an independent researcher. The randomization schedule will contain only codes (not the actual intervention). The output from the laser device is exactly the same from either the active or the placebo interventions. These features will guarantee that participants, therapists and outcomes assessor will be blinded to the treatment arms.
Allocation
Randomized
Enrollment
148 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Placebo PBMT
Arm Type
Placebo Comparator
Arm Description
Application of PBMT (Photobiomodulation Therapy) without any dose (0 Joule) and The Back Book (educational information booklet).
Arm Title
PBMT active
Arm Type
Active Comparator
Arm Description
Application of PBMT (Photobiomodulation Therapy) active and The Back Book (educational information booklet).
Intervention Type
Device
Intervention Name(s)
Placebo PBMT
Intervention Description
The PBMT treatments will be performed using the Multi Radiance Medical™ Super Pulsed Laser MR4™ console (Solon, OH, USA), with the LS50 (emitter with an area of 20 cm2) and SE25 (emitter with an area of 4 cm2) cluster probes as emitters. Nine sites will be irradiated at patient's lumbar region: 3 central sites, using the SE25 (without any dose, 0 J); and 6 sites in the same direction, but laterally (both sides, 3 at a side), using the LS50 (without any dose, 0 J). Patients will be treated during 12 sessions over a period of four weeks (three sessions/week). At each treatment session, patients will receive a total dose of 0 J. At the end of the 12 treatment sessions, patients will receive a total dose of 0 J.
Intervention Type
Device
Intervention Name(s)
PBMT active
Intervention Description
The PBMT treatments will be performed using the Multi Radiance Medical™ Super Pulsed Laser MR4™ console (Solon, OH, USA), with the LS50 (emitter with an area of 20 cm2) and SE25 (emitter with an area of 4 cm2) cluster probes as emitters. Nine sites will be irradiated at patient's lumbar region: 3 central sites, using the SE25 (3000 Hz of frequency, 3 minutes of irradiation per site, 24.75 J per site, a totalizing 74.25 J irradiated from SE25); and 6 sites in the same direction, but laterally (both sides, 3 at a side), using the LS50 (1000 Hz of frequency, 3 minutes of irradiation per site, 24.30 J per site, a total of 145.80 J irradiated from LS50). Patients will be treated during 12 sessions over a period of four weeks (three sessions/week). At each treatment session, patients will receive a total dose of 220.05 J. At the end of the 12 treatment sessions, patients will receive a total dose of 2640.60 J.
Primary Outcome Measure Information:
Title
Pain Intensity
Description
Pain intensity will be measured by an 11-point (0-10) Numerical Rating Scale (Pain NRS)
Time Frame
4 weeks after randomization
Title
Disability
Description
Disability will be measured by the 24-item Roland Morris Disability Questionnaire
Time Frame
4 weeks after randomization
Secondary Outcome Measure Information:
Title
Pain intensity
Description
Pain intensity will be measured by an 11-poin (0-10) Numerical Rating Scale (Pain NRS)
Time Frame
3, 6 and 12 months after randomization
Title
Disability
Description
Disability will be measured by the 24-item Roland Morris Disability Questionnaire
Time Frame
3, 6 and 12 months after randomization
Title
Function
Description
Function will be measured by an 11-point (0-10) Patient-Specific Functional Scale
Time Frame
4 weeks, 3, 6 and 12 months after randomization
Title
Global perceived effect
Description
Global perceived effect will be measured by an 11-point (-5 to +5) Global Perceived Effect Scale
Time Frame
4 weeks, 3, 6 and 12 months after randomization

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
65 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: patients seeking care for chronic non-specific low back pain (defined as pain or discomfort between the costal margins and the inferior gluteal folds, with or without referred symptoms in the lower limbs, for at least 3 month); with a pain intensity of at least 3 points measured by a 0-10 points pain numerical rating scale; aged between 18 and 65 years; able to read Portuguese. Exclusion Criteria: evidence of nerve root compromise (i.e. one or more of motor, reflex or sensation deficit); serious spinal pathology (such as fracture, tumor, inflammatory and infectious diseases); serious cardiovascular and metabolic diseases; previous back surgery; pregnancy.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Leonardo Oliveira Pena Costa, PhD
Organizational Affiliation
Universidade Cidade de Sao Paulo
Official's Role
Study Director
Facility Information:
Facility Name
Centre for Excellence in Clinical Research in Physiotherapy of Universidade Cidade de São Paulo
City
São Paulo
State/Province
Sao Paulo
ZIP/Postal Code
03071000
Country
Brazil

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
33449509
Citation
Guimaraes LS, Costa LDCM, Araujo AC, Nascimento DP, Medeiros FC, Avanzi MA, Leal-Junior ECP, Costa LOP, Tomazoni SS. Photobiomodulation therapy is not better than placebo in patients with chronic nonspecific low back pain: a randomised placebo-controlled trial. Pain. 2021 Jun 1;162(6):1612-1620. doi: 10.1097/j.pain.0000000000002189.
Results Reference
derived
PubMed Identifier
29070637
Citation
Tomazoni SS, Costa LDCM, Guimaraes LS, Araujo AC, Nascimento DP, Medeiros FC, Avanzi MA, Costa LOP. Effects of photobiomodulation therapy in patients with chronic non-specific low back pain: protocol for a randomised placebo-controlled trial. BMJ Open. 2017 Oct 24;7(10):e017202. doi: 10.1136/bmjopen-2017-017202.
Results Reference
derived

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Photobiomodulation Therapy on Low Back Pain

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