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临床试验/NCT04698369
NCT04698369终止不适用

Development and Evaluation of Vibration-based Wearable Upper Limb Rehabilitation Device

University of Oklahoma1 个研究点 分布在 1 个国家目标入组 4 人开始时间: 2021年8月30日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
终止
入组人数
4
试验地点
1
主要终点
Usability of the WearUL as assessed by the System Usability Scale (SUS)

研究概览

简要总结

The investigators will perform a pilot 4-week at home study with 48 individuals with stroke and 10 therapists working with stroke patients to examine the feasibility and effect of a wearable focal muscle vibration device on upper limb strength and function.

详细描述

Stroke often leads to significant impairment of upper limb function and is associated with decreased quality of life. Patients have difficulty moving out of the upper extremity flexion synergies that often dominate attempts to function after stroke. Change in muscle activation is the key underlying factor. Despite study results from several interventions for muscle activation and motor coordination, wide-scale adoption remains largely elusive due to the lack of sustainability of those interventions. The main reasons for the unsustainability are under-doses of the interventions and low patient compliance and participation. Recent studies among individuals without disabilities as well as those with strokes have shown that with focal vibration, there is greater potential to increase and coordinate muscle recruitment and build muscle strength and endurance. This form of treatment could widely benefit stroke patients and therapists who are in need of sustainable intervention that is effective and efficient to building muscle work capacity for function. Thus, the aims of this study are to evaluate the usability and feasibility of a novel vibration-based wearable device for upper limb rehabilitation in stroke patients. Forty-eight stroke patients and 10 therapists working with those stroke patients will be recruited to evaluate the usability of the device. All stroke patients will participate in a 4-week in-home vibration treatment to evaluate the feasibility of the device. Patients will be randomized into four groups receiving vibrations with different frequency (60 Hz or 120 Hz) and amplitude (0.2mm or 2mm). All groups will follow a prescribed dose of vibration based on the therapists' recommendations. Strength and functional outcomes will be measured before and after the 4-week in-home intervention. The investigators hypothesize that all groups will show an increase in grip strength and upper limb function at the end of study compared to baseline and that the increases in outcomes will be different in different groups. The investigators also expect all participants will tolerate the wearable device without adverse side effects and report high levels of satisfaction with the device. This pilot study may help to develop a novel sustainable wearable system providing vibration-based muscle activation for upper limb function rehabilitation. It may provide patients opportunity to apply the prescribed vibratory stimuli in-home and/or at community settings. It may also allow therapists to monitor treatment usage and patient performance and to adjust the treatment doses based on progression.

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, Care Provider, Outcomes Assessor)

盲法说明

Participants will not know the vibration intensity they receive. The care provider will be blinded on the vibration intensity as well. The outcome assessor will be blinded on which group the participants are.

入排标准

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

入选标准

  • Ischemic or hemorrhagic stroke with Chedoke McMaster's Stroke Assessment (CMSA) level four or above;
  • over 18 years of age;
  • have been using a smartphone more than one year;
  • live within 40 miles from the University of Oklahoma Health Sciences Center (OUHSC)

排除标准

  • a history of fractures or dislocations in the shoulder, elbow, or wrist from which the participant has not fully recovered,
  • severe impairment of verbal communication ability (for example, severe aphasia),
  • inability to consent (for example, dementia),
  • simultaneous participation in another treatment study targeting stroke recovery

研究组 & 干预措施

low frequency low amplitude

Experimental

The vibration frequency is 60 Hz and amplitude is 0.2 mm

干预措施: Vibration Massage Therapy (Device)

low frequency high amplitude

Experimental

The vibration frequency is 60 Hz and amplitude is 2 mm

干预措施: Vibration Massage Therapy (Device)

high frequency low amplitude

Experimental

The vibration frequency is 120 Hz and amplitude is 0.2 mm

干预措施: Vibration Massage Therapy (Device)

high frequency high amplitude

Experimental

The vibration frequency is 120 Hz and amplitude is 2 mm

干预措施: Vibration Massage Therapy (Device)

结局指标

主要结局

Usability of the WearUL as assessed by the System Usability Scale (SUS)

时间窗: 4 weeks

SUS is a reliable tool for measuring the usability of a device or system

Changes in sensorimotor impairment as assessed by FMA-UE

时间窗: Change from Baseline FMA-UE at 4 weeks

Fugl-Meyer Assessment of the Upper Extremity

Changes in self-reported functional upper extremity performance as assessed by MAL

时间窗: Change from Baseline MAL at 4 weeks

Motor Activity Log

Changes in arm and hand function as assessed by CAHAI-7

时间窗: Change from Baseline CAHAI-7 at 4 weeks

Chedoke Arm and Hand Activity Inventory - 7

Usability of the WearUL app as assessed by the mHealth App Usability Questionnaire (MAUQ)

时间窗: 4 weeks

MAUQ is a reliable and valid questionnaire to assess mHealth app usability

Changes in grip strength

时间窗: Change from Baseline Grip Strength at 4 weeks

the affected side grip strength measured by a dynamometer

Changes in upper extremity performance as assessed by ARAT

时间窗: Change from Baseline ARAT at 4 weeks

Action Research Arm Test

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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