Department of Mechanical Engineering, Stanford University, Stanford, CA.
Department of Bioengineering, Stanford University, Stanford, CA.
Arch Phys Med Rehabil. 2023 Oct;104(10):1565-1572. doi: 10.1016/j.apmr.2023.03.031. Epub 2023 May 4.
To test the feasibility and efficacy of the VibroTactile Stimulation (VTS) Glove, a wearable device that provides VTS to the impaired limb to reduce spastic hypertonia.
Prospective 2-arm intervention study-including 1 group of patients who use Botulinum toxin (BTX-A) for spasticity and 1 group of patients who do not use BTX-A.
Participants were recruited through rehabilitation and neurology clinics.
Patients with chronic stroke (N=20; mean age=54 years, mean time since stroke=6.9 years). Patients who were previously receiving the standard of care (BTX-A injection) were eligible to participate and started the intervention 12 weeks after their last injection.
Participants were instructed to use the VTS Glove for 3 hours daily, at home or during everyday activities, for 8 weeks.
Spasticity was assessed with the Modified Ashworth Scale and the Modified Tardieu Scale at baseline and then at 2-week intervals for 12 weeks. Primary outcomes were the difference from baseline and at week 8 (end of VTS Glove use) and week 12 (4 weeks after stopping VTS Glove use). Patients who were receiving BTX-A were also assessed during the 12 weeks preceding the start of VTS Glove use to monitor the effect of BTX-A on spastic hypertonia. Range of motion and participant feedback were also studied.
A clinically meaningful difference in spastic hypertonia was found during and after daily VTS Glove use. Modified Ashworth and Modified Tardieu scores were reduced by an average of 0.9 (P=.0014) and 0.7 (P=.0003), respectively, at week 8 of daily VTS Glove use, and by 1.1 (P=.00025) and 0.9 (P=.0001), respectively, 1 month after stopping VTS Glove use. For participants who used BTX-A, 6 out of 11 showed greater change in Modified Ashworth ratings during VTS Glove use (mean=-1.8 vs mean=-1.6 with BTX-A) and 8 out of 11 showed their lowest level of symptoms during VTS Glove use (vs BTX-A).
Daily stimulation from the VTS Glove provides relief of spasticity and hypertonia. For more than half of the participants who had regularly used BTX-A, the VTS Glove provided equal or greater symptom relief.
测试 VibroTactile 刺激(VTS)手套的可行性和疗效,这是一种可穿戴设备,可向受损肢体提供 VTS,以减轻痉挛性肌强直。
前瞻性 2 臂干预研究-包括使用肉毒杆菌毒素(BTX-A)治疗痉挛的患者组和未使用 BTX-A 的患者组。
参与者通过康复和神经病学诊所招募。
20 名慢性中风患者(平均年龄 54 岁,中风后平均时间为 6.9 年)。以前接受标准治疗(BTX-A 注射)的患者有资格参加,并在最后一次注射后 12 周开始干预。
参与者被指示每天在家中或日常活动期间使用 VTS 手套 3 小时,持续 8 周。
基线时以及之后每 2 周评估 12 周,采用改良 Ashworth 量表和改良 Tardieu 量表评估痉挛程度。主要结果是与基线和第 8 周(VTS 手套使用结束时)和第 12 周(停用 VTS 手套 4 周后)的差异。在开始使用 VTS 手套之前的 12 周内,还对接受 BTX-A 的患者进行了评估,以监测 BTX-A 对痉挛性肌强直的影响。还研究了运动范围和参与者的反馈。
在使用 VTS 手套期间和之后,发现痉挛性肌强直有明显的临床改善。在每天使用 VTS 手套 8 周时,改良 Ashworth 和改良 Tardieu 评分分别平均降低 0.9(P=.0014)和 0.7(P=.0003),停用 VTS 手套 1 个月后分别降低 1.1(P=.00025)和 0.9(P=.0001)。对于使用 BTX-A 的患者,在使用 VTS 手套期间,有 6 名患者的改良 Ashworth 评分变化更大(均值为-1.8,而使用 BTX-A 时为均值-1.6),8 名患者的症状最低水平出现在使用 VTS 手套期间(而不是 BTX-A)。
VTS 手套的日常刺激可缓解痉挛和肌强直。对于超过一半经常使用 BTX-A 的参与者来说,VTS 手套提供了同等或更大的症状缓解。