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NCT07769281Recruiting

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

Source: ClinicalTrials.gov · Last updated 17 Aug 2026

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Study type
Interventional
Enrollment
10 (estimated)
First submitted
12 Aug 2026
Start date
21 Aug 2025
Primary completion date
31 Dec 2026
Lead sponsor
Brooks Rehabilitation
Diseases
Stroke
NCT number
NCT07769281

What you commit to

  • Study type: Interventional
  • Planned participants: 10
  • From 21 Aug 2025 to the primary completion date, 31 Dec 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Not independent in functional activities/mobility prior to stroke

Other illness

  • 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

Other

  • 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
  • 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

Who the study is looking for

  • 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

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Brooks Rehabilitation Hospital - Bartram Campus
Coordinator of this site? Confirm its status
JacksonvilleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.