Effects of low-power laser auriculotherapy on chronic spinal pain: Randomized clinical trial

被引:3
作者
Menezes, Flavia da Silva [1 ,2 ]
Lopes Chaves, Erika de Cassia [3 ,4 ]
Aparecida Mantuani, Ana Paula [1 ,2 ]
Marino, Ligia de Sousa [1 ,2 ]
Roquim Alcantara, Marcela Albertini [1 ]
Nassif, Melissa Santos [3 ,4 ]
Moura, Caroline de Castro [5 ]
Carvalho, Leonardo Cesar [1 ,2 ]
Iunes, Denise Hollanda [1 ,2 ]
机构
[1] Univ Fed Alfenas, Motor Sci Inst, 2600 Jovino Fernandes Sales Ave, BR-37133840 Alfenas, MG, Brazil
[2] Univ Fed Alfenas, Postgrad Program Rehabil Sci, 2600 Jovino Fernandes Sales Ave, BR-37133840 Alfenas, MG, Brazil
[3] Univ Fed Alfenas, Nursing Sch, 700 Gabriel Monteiro da Silva St, BR-37130001 Alfenas, MG, Brazil
[4] Univ Fed Alfenas, Postgrad Program Nursing, 700 Gabriel Monteiro da Silva St, BR-37130001 Alfenas, MG, Brazil
[5] Univ Fed Minas Gerais, Sch Nursing, 190 Prof Alfredo Balena St, BR-30130100 Belo Horizonte, MG, Brazil
关键词
Auricular acupuncture; Musculoskeletal pain; Complementary therapies; Gallium arsenide laser; Rehabilitation; RBR-7cs387; Clinical trial registration: Brazilian registry of clinical trials; LOW-BACK-PAIN; ACUPUNCTURE; METAANALYSIS; INTENSITY; LEVEL;
D O I
10.1016/j.ctcp.2022.101578
中图分类号
R [医药、卫生];
学科分类号
10 ;
摘要
Aims and objectives: To evaluate the effect of laser auriculotherapy on chronic spinal pain. It is a randomized controlled clinical trial. Methods: Volunteers with chronic spinal pain underwent three evaluations: an initial evaluation, a final evaluation immediately after the last intervention session, and a 15-day follow-up. Pain intensity, nociceptive threshold in relation to mechanical stimulus, and degree of pain (the greatest and least pain) in the last seven days were the assessed variables. The experimental group (EG, n = 24) underwent 10 sessions of laser auriculotherapy twice a week, while the control group (CG, n = 23) did not receive any intervention. Results: The EG showed great clinical improvement in relation to the variable pain intensity between pre-and post-interventions (65.2%) and pre-intervention and follow-up (58.62%) compared to the CG. There was a significant increase in the nociceptive threshold for the EG. In contrast, the CG showed a significant reduction in the nociceptive threshold. The intergroup analysis indicated an improvement in pain intensity for the EG (0.006). This result remained at the follow-up (0.012). The nociceptive threshold increased over time for the EG (0.016). In contrast, the CG showed a reduction in this variable with a significant difference over time (< 0.001). Conclusion: The results of this clinical trial suggest that the proposed intervention may be effective in reducing pain intensity and increasing the nociceptive threshold. The effect of the intervention remained 15 days after the end of the treatment, when the volunteers were re-evaluated.
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页数:7
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