Evaluation of Vibration-based Wearable Upper Limb Rehabilitation Device

Stopped early · Not applicable

Conditions studied: Stroke

In brief

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.

Key facts

Study ID

NCT04698369

Run by

University of Oklahoma

People needed

4

Starts

2021-08-30

Expected to finish

2021-12-31

Last updated by the study team

2026-04-06

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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)

You may not qualify if…

• 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

Where it is running

• University of Oklahoma Health Sciences Center — Oklahoma City, Oklahoma, United States

Full record on ClinicalTrials.gov

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