Purdue University, Lafayette, IN.
J Athl Train. 1999 Oct;34(4):334-7.
To examine the efficacy of microcurrent electrical neuromuscular stimulation (MENS) treatment on pain and loss of range of motion (ROM) associated with delayed-onset muscle soreness (DOMS).
We assigned subjects to 1 of 2 groups. Group 1 received treatment with microcurrent stimulation (200 muA, 30 Hz, for 10 minutes, then 100 muA, 0.3 Hz, for 10 minutes) 24, 48, and 72 hours after DOMS induction. Group 2 served as a sham group and was treated using a machine altered by the manufacturer so that no current could flow through the electrodes.
DOMS was induced in the biceps brachii of the nondominant arm of 18 subjects (3 males, 15 females: age = 20.33 +/- 2.3 years, ht = 170.81 +/- 7.3 cm, wt = 69.61 +/- 13.1 kg). Dominance was defined as the arm used by the subject to throw a ball.
Subjective pain and active elbow extension ROM were evaluated before and after treatment each day. Two methods were used to assess pain: constant pressure using a weighted Orthoplast sphere and full elbow extension to the limit of pain tolerance. Subjective pain was measured with a graphic rating scale and active elbow extension ROM using a standard, plastic, double-armed goniometer. Three repeated-measures ANOVAs (between-subjects variable was group, within- subjects variables were day and test) were used to assess ROM and pain scores for the 2 groups.
We found no significant difference in the measurement of subjective pain scores or elbow extension ROM when the MENS group was compared with the sham group.
Our results indicate that the MENS treatment, within the parameters used for this experiment, was not effective in reducing the pain or loss of ROM associated with delayed-onset muscle soreness.
研究微电流电神经肌肉刺激(MENS)治疗对延迟性肌肉酸痛(DOMS)相关疼痛和运动范围(ROM)丧失的疗效。
我们将受试者分为两组。第 1 组在 DOMS 诱导后 24、48 和 72 小时接受微电流刺激(200 μA,30 Hz,持续 10 分钟,然后 100 μA,0.3 Hz,持续 10 分钟)治疗。第 2 组为假治疗组,使用制造商修改的机器进行治疗,使电流无法通过电极。
18 名受试者(3 名男性,15 名女性;年龄=20.33±2.3 岁,身高=170.81±7.3cm,体重=69.61±13.1kg)非优势手臂肱二头肌诱导 DOMS。优势定义为受试者投掷球所使用的手臂。
每天治疗前后评估主观疼痛和主动肘部伸展 ROM。使用两种方法评估疼痛:使用带重的 Orthoplast 球的恒定压力和充分伸展肘部至疼痛耐受极限。使用图形评分量表测量主观疼痛,使用标准塑料双臂量角器测量主动肘部伸展 ROM。使用 3 个重复测量的 ANOVA(组间变量为组,组内变量为天和测试)评估两组的 ROM 和疼痛评分。
与假治疗组相比,我们发现 MENS 组在主观疼痛评分或肘部伸展 ROM 的测量上没有显著差异。
我们的结果表明,在所进行的实验参数范围内,MENS 治疗对减轻与延迟性肌肉酸痛相关的疼痛或 ROM 丧失无效。