Implementation of IVS3 for Upper Limb Motor Recovery

Recruiting now · Not applicable

Conditions studied: Neglect, Hemispatial, Stroke, Cardiovascular, Mirror Movement, Motor Activity

In brief

This study measures participant satisfaction and upper extremity function in outpatients with chronic stroke when exposed to the IVS3 device. Investigators hypothesize that treatment with the IVS3 device will be feasible and tolerable for use in the outpatient setting.

Key facts

Study ID

NCT06483230

Run by

Weill Medical College of Cornell University

People needed

25

Starts

2024-10-02

Expected to finish

2027-06-01

Last updated by the study team

2025-10-29

Who can join

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

You may qualify if…

• Age ≥ 18 years old
• English speaking
• History of ischemic or hemorrhagic stroke ≥ 6 months prior to study enrolment
• FMA-UE: 20 < x < 50 (moderate impairments)
• With or without hemi spatial neglect

You may not qualify if…

• Spasticity or increased tone with MAS ≥3 in the upper extremity
• Unable to communicate effectively or provide informed consent
• Significant visual impairments
• Concurrent occupational therapy being received outside of the study
• Pregnant or incarcerated individuals

Where it is running

• Weill Cornell Medicine, 525 E. 68th St, Baker Pavilion, F-2106 — New York, New York, United States (enrolling)

Full record on ClinicalTrials.gov

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