光生物调制疗法与运动控制训练相结合治疗慢性非特异性腰背痛的效果:随机安慰剂对照试验方案。

IF 3.9 Q1 SPORT SCIENCES BMJ Open Sport & Exercise Medicine Pub Date : 2024-09-26 eCollection Date: 2024-01-01 DOI:10.1136/bmjsem-2024-002199
Marcelo Ferreira Duarte de Oliveira, Jan Magnus Bjordal, Jociane Schardong, Rodrigo Della Méa Plentz, Heliodora Leão Casalechi, Ernesto Cesar Pinto Leal-Junior, Shaiane Silva Tomazoni
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引用次数: 0

摘要

光生物调节疗法(PBMT)作为运动的辅助疗法,可以减轻肌肉骨骼疾病的疼痛。此外,光生物调制疗法与运动相结合还能通过不同的训练方案减轻疲劳、加速肌肉恢复并提高运动表现和收益。虽然尚未进行过研究,但将 PBMT 与运动疗法结合起来可能是一种替代方法,可提高运动对非特异性腰背痛(LBP)患者的积极作用。因此,我们旨在评估在慢性非特异性腰背痛患者中,PBMT 与运动控制训练(MCE)相结合与安慰剂与运动控制训练相结合的效果。这是一项前瞻性注册、双臂、随机、安慰剂对照、三重盲法试验。共有 148 名慢性非特异性腰痛患者将被随机分配到与 MCE 相关的主动 PBMT 或与 MCE 相关的安慰剂 PBMT 中。治疗疗程为每周两次,为期 6 周。主要结果是在治疗结束时测量疼痛强度和全身残疾程度。次要结果是治疗结束后 1 个月、随机分配后 3、6 和 12 个月测量的疼痛强度和全身残疾程度,以及治疗结束时测量的前列腺素 E2 水平。将在所有时间点测量药物摄入量、共同干预和不良事件。这项研究已获得阿雷格里港圣卡萨圣母医院研究伦理委员会的批准。研究结果将通过科学出版物和科学会议上的演讲进行传播。试验注册号:NCT05487118:NCT05487118。
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Effects of photobiomodulation therapy associated with motor control exercise for chronic non-specific low back pain: protocol for a randomised placebo-controlled trial.

Photobiomodulation therapy (PBMT), as an adjunct therapy to exercise, can reduce pain in musculoskeletal disorders. In addition, PBMT associated with exercise decreases fatigue, accelerates muscle recovery and enhances performance and gain through different training protocols. Although it has not been investigated, the association of PBMT and exercise therapy could be an alternative to improve the positive effects of exercise in patients with non-specific low back pain (LBP). Therefore, we aim to evaluate the effects of PBMT associated with motor control exercise (MCE) versus placebo associated with MCE in patients with chronic non-specific LBP. This is a prospectively registered, two-arm, randomised, placebo-controlled, triple-blind trial. A total of 148 patients with chronic non-specific LBP will be randomised to either active PBMT associated with MCE or placebo PBMT associated with MCE. Treatment sessions will be provided twice a week for 6 weeks. The primary outcomes will be pain intensity and general disability measured at the end of the treatment. The secondary outcomes will be pain intensity and general disability measured 1 month after the end of the treatment, 3, 6 and 12 months after randomisation, in addition to levels of prostaglandin E2 measured at the end of the treatment. Medication intake, cointerventions and adverse events will be measured at all time points. This study was approved by the Research Ethics Committee of Irmandade de Santa Casa de Misericórdia de Porto Alegre. The results will be disseminated through scientific publications and presentations at scientific meetings. Trial registration number: NCT05487118.

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CiteScore
7.10
自引率
4.20%
发文量
106
审稿时长
20 weeks
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