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临床试验/NCT07602933
NCT07602933招募中不适用

Effects of Photobiomodulation on Fatigue and Muscle Damage Induced by Neuromuscular Electrical Stimulation in Healthy Individuals: a Randomized Clinical Trial

Federal University of Rio Grande do Sul1 个研究点 分布在 1 个国家目标入组 36 人开始时间: 2026年6月1日最近更新:
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
36
试验地点
1

研究概览

简要总结

Neuromuscular electrical stimulation (NMES) is widely used to improve muscle strength and mitigate atrophy. However, its clinical efficacy is often limited by early neuromuscular fatigue, muscle damage, and discomfort, which reduce patient tolerance and contraction time. Photobiomodulation (PBM) has emerged as a potential therapy to enhance muscle performance and accelerate recovery by minimizing fatigue and damage. Despite its potential, few studies have investigated the effects of PBM applied specifically before an NMES-evoked fatigue protocol. This randomized, double-blind, placebo-controlled trial aims to evaluate the acute effects of PBM on neuromuscular fatigue, muscle damage, and functional outcomes in healthy young subjects. Participants will receive either active PBM (cluster probe: 5 lasers 810nm/200mW; 4 LEDs 660nm/10mW; Total Energy: 249.6 J per limb) or sham treatment 5 minutes before a fatiguing NMES protocol (80 contractions at 20% MVIC, 80 Hz, 1ms pulse width) applied to the quadriceps muscle. Assessments will be performed at baseline, immediately post-intervention, and at 24h, 48h, and 72h post-intervention. Primary outcomes include maximum and evoked isometric strength, mechanical work, and electrical muscle activity. Secondary outcomes include muscle damage (ultrasound echo-intensity), delayed onset muscle soreness (DOMS), functional performance (unilateral vertical jump), and clinical discomfort. The study seeks to determine if PBM can effectively modulate NMES-induced fatigue and muscle damage, potentially optimizing its clinical application.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Triple (Participant, Investigator, Outcomes Assessor)

盲法说明

Participants and outcome assessors will be blinded to the intervention groups. The investigator responsible for data analysis will also be blinded. Due to the nature of the equipment operation, the individual administering the treatment (care provider) will not be blinded.

入排标准

年龄范围
18 Years 至 45 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Healthy male and female volunteers.
  • Age between 18 and 45 years.
  • Practice physical activity regularly
  • No history of musculoskeletal injuries in the lower limbs in the last 6 months
  • Ability to tolerate NMES

排除标准

  • Have sensory intolerable changes due to NMES
  • Consumed coffee or another stimulant in the last 12 hours
  • Have a body mass index (BMI) greater than 30 kg/m2 (grade I obesity)
  • Present any contraindication for the performance of maximum effort
  • Abnormal increase in blood pressure after maximal exertion

研究组 & 干预措施

Photobiomodulation (PBM)

Experimental

Participants in this arm will receive active photobiomodulation therapy.

干预措施: NMES-evoked fatigue protocol (Other)

Sham PBM

Sham Comparator

Participants in this arm will receive an inactive (placebo) photobiomodulation treatment.

干预措施: Placebo Photobiomodulation (Device)

Sham PBM

Sham Comparator

Participants in this arm will receive an inactive (placebo) photobiomodulation treatment.

干预措施: NMES-evoked fatigue protocol (Other)

Photobiomodulation (PBM)

Experimental

Participants in this arm will receive active photobiomodulation therapy.

干预措施: Active Photobiomodulation (Device)

研究者

发起方
Federal University of Rio Grande do Sul
申办方类型
Other
责任方
Principal Investigator
主要研究者

Marco Aurélio Vaz, PhD

Full Professor

Federal University of Rio Grande do Sul

研究点 (1)

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