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Safety and Efficacy of NeuroTechR3 System for Upper Extremity Recovery After Stroke

Safety and Efficacy of NeuroTechR3 System for Upper Extremity Recovery After Stroke

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07769281
Acronym
R3
Enrollment
10
Registered
2026-08-17
Start date
2025-08-21
Completion date
2026-12-31
Last updated
2026-08-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Stroke

Keywords

stroke, upper extremity rehab

Brief summary

This research aims to understand the feasibility and effectiveness of using the NeuroTechR3 System to improve upper extremity function after stroke.

Interventions

DEVICENeuroTechR3 Computer Rehabilitation System

Participants will complete three sessions a week, each lasting for 30 minutes. The sessions consist of upper extremity rehabilitation games on the computer.

Sponsors

Brooks Rehabilitation
Lead SponsorOTHER
NeuroTechR3
CollaboratorINDUSTRY

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years at the time of enrollment * Diagnosed with stroke * No other peripheral or central neurological condition limiting target upper extremity function (previous stroke is ok) * Indicated for upper extremity training procedures by participant's treating physician, occupational therapist, or physical therapist * Capable of providing informed consent * Participant demonstrates active extension of wrist and activation of at least two other digits plus thumb activation

Exclusion criteria

* In the opinion of the investigators, the study is not safe or appropriate for the participant, and/or the participant is unlikely to return for the follow-up visits per the protocol to return the device at 4 weeks post discharge * Visual impairment that would severely limit ability to see a computer screen for participation in sessions, including severe spatial neglect making the person unable to interact with an entire computer screen * Inability to follow a 3-step motor command * Severe upper extremity tone that will limit participation in study * No internet access at home * Severe receptive aphasia * Severe arthritis that limits hand and arm movements * Not independent in functional activities/mobility prior to stroke

Design outcomes

Primary

MeasureTime frameDescription
Upper Extremity Strength and FunctionPre-intervention, mid-intervention within 3 days of discharging from the inpatient rehabilitation facility, and post-intervention at 6 weeks.The Fugle-Meyer test is a simple, standardized test used to assess a person's exercise capacity and functional mobility. An increase in score reflects an improvement in mobility and upper extremity function.
QuestionnairesMid-intervention within 3 days of discharging from the inpatient rehabilitation facility and post-intervention at 6 weeks.The System Usability Scale measures the perceived usability, ease of use, and learnability of the system. An increase in score indicates better usability.

Secondary

MeasureTime frameDescription
Care TransitionPre-intervention, mid-intervention within 3 days of discharging from the inpatient rehabilitation facility, and post-intervention at 6 weeks.The NeuroTechR3 System evaluates range of motion, speed, and accuracy for the hand and arm. An increase in kinematic data indicates improved functioning.

Countries

United States

Contacts

CONTACTHannah Grimes
hannah.grimes@brooksrehab.org904-528-3159

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 18, 2026