Skip to content

Photobiomodulation Therapy Combined With Static Magnetic Field on the Subsequent Performance

Immediate Effects of Photobiomodulation Therapy Combined With Static Magnetic Field on the Subsequent Performance: a Randomized Crossover Triple-blinded Placebo-controlled Trial

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04934709
Enrollment
12
Registered
2021-06-22
Start date
2015-05-31
Completion date
2015-09-30
Last updated
2021-06-22

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Skeletal Muscle Performance

Keywords

Photobiomodulation Therapy, Static Magnetic Field, Subsequent performance

Brief summary

There is evidence about the effects of photobiomodulation therapy (PBMT) alone and combined with static magnetic field (PBMT-sMF) on skeletal muscle fatigue, physical performance and post-exercise recovery in different types of exercise protocols and sports activity. However, it is unknown the effects of PBMT-sMF to improve the subsequent performance after a first set of exercise. Therefore, the aim of this study was to investigate the effects of PBMT-sMF, applied between two sets of exercises, on the subsequent physical performance.

Detailed description

A randomized, crossover, triple-blinded (assessors, therapist and volunteers), placebo-controlled trial was carried out. Healthy non-athletes' male volunteers were randomized and treated with a single application of PBMT-sMF and placebo between two sets of an exercise protocol performed on isokinetic dynamometer. The order of interventions was randomized. The primary outcome was fatigue index, measured by isokinetic dynamometer during the exercise protocol. The secondary outcomes were total work and peak torque measured by isokinetic dynamometer during the exercise protocol; and blood lactate, measured by blood samples collected before, 3 minutes after the first set of the exercise protocol, 3 minutes after the application of the intervention and 3 minutes after the second set of the exercise protocol. Statistical analysis: The findings were tested for normality using the Kolmogorov-Smirnov test and were determined to have a normal distribution. Data were expressed as the mean and standard deviation, and a two-way repeated measures ANOVA was performed to test between-group differences at each timepoint (treatment effects), mean difference (MD) and 95% confidence intervals (CI), followed by the Bonferroni post hoc test. The significance level was set at p \< 0.05.

Interventions

PBMT-sMF was applied employing the Multi Radiance Medical Super Pulsed Laser MR4 console (Solon, Ohio, USA) with a LaserShower cluster probe as emitter. Six different sites of the knee extensor muscles (two medial, two lateral and two central points) were irradiated at the same time.

Placebo PBMT-sMF was applied employing the Multi Radiance Medical Super Pulsed Laser MR4 console (Solon, Ohio, USA) with a LaserShower cluster probe as emitter, but without any emission of therapeutic dose. Placebo PBMT-sMF was applied at six different sites of the knee extensor muscles (two medial, two lateral and two central points).

Sponsors

University of Nove de Julho
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
PREVENTION
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Masking description

A researcher programmed the device (placebo or PMBT-sMF) and was instructed not to inform the volunteers or other researchers as to the type of treatment (placebo or PBMT-sMF). Therefore, the researcher responsible for the treatment was blinded to the type of treatment administered to the volunteers. The sounds and signals emitted from the device as well as the information displayed on the screen was identical, regardless of the type of treatment (placebo or PBMT).

Eligibility

Sex/Gender
MALE
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

* Male healthy volunteers; * Non-athletes or those who practiced physical activity up to once a week; * Aged 18-35 years.

Exclusion criteria

* History of musculoskeletal injuries in the hip and knee regions in the two months prior to the study; * Use of pharmacological agents and nutritional supplements; * Chronic joint disease in the non-dominant lower limb.

Design outcomes

Primary

MeasureTime frameDescription
Fatigue index1 minute after the end of exercise protocol.Variable provided directly by the isokinetic dynamometer during the exercise protocol.

Secondary

MeasureTime frameDescription
Total work1 minute after the end of exercise protocol.Variable provided directly by the isokinetic dynamometer during the exercise protocol.
Peak torque1 minute after the end of exercise protocol.Variable provided directly by the isokinetic dynamometer during the exercise protocol.
Blood lactate3 minutes after the first set of the exercise protocol, 3 minutes after the application of the intervention and 3 minutes after the second set of the exercise protocol.Measured by blood samples.

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026