Recruiting

NeuroTechR3 System

Sponsor:

Brooks Rehabilitation

Code:

NCT07769281

Conditions

Stroke

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

NeuroTechR3 Computer Rehabilitation System

Study Details

Brief summary:

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

Conditions

Stroke

Study ID

NCT07769281

Start date

Aug 21, 2025

Status verified date

Aug, 2026

Completion date

Dec 31, 2026

Anticipated

Primary completion date

Dec 31, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

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

Study Design

Enrollment

10 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: NeuroTechR3 System

Participants will be engaging in six weeks of intervention sessions using the NeuroTechR3 System while in the Brooks Rehabilitation Hospital under the direct supervision of a study staff member. Participants will then take the NeuroTechR3 System and a laptop home to complete intervention sessions in their home after discharge without the supervision of study staff. Each session is 30 minutes and 3 times a week.

Interventions

NeuroTechR3 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.

Primary outcome measure

  • Upper Extremity Strength and Function [ Time Frame: Pre-intervention, mid-intervention within 3 days of discharging from the inpatient rehabilitation facility, and post-intervention at 6 weeks. ]
  • Questionnaires [ Time Frame: Mid-intervention within 3 days of discharging from the inpatient rehabilitation facility and post-intervention at 6 weeks. ]

Central Contacts and Locations

Central contacts

Hannah Grimes

904-528-3159hannah.grimes@brooksrehab.org

Locations

Brooks Rehabilitation Hospital - Bartram Campus

Recruiting

Jacksonville, Florida, United States, 32258

Contacts

Hannah Grimes

904-528-3159hannah.grimes@brooksrehab.org

More Information

Sponsor

Brooks Rehabilitation

Last update posted

Aug 17, 2026

Last verified

Aug, 2026

Keywords

  • stroke
  • upper extremity rehab

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by Brooks Rehabilitation on 2026-08-17.