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Augmented Reality-based Telerehabilitation Platform for Patients With Stroke

Stanford University logo

Stanford University

Status

Not yet enrolling

Conditions

Stroke

Treatments

Device: AR rehabilitation app

Study type

Interventional

Funder types

Other

Identifiers

Details and patient eligibility

About

The study is to 1) determine the feasibility of the use of our augmented reality (AR) rehabilitation program, including its preliminary efficacy, 2) determine the feasibility of obtaining an augmented reality assessment based on the Fugl-Meyer Assessment - Upper Extremity (FMA-UE).

Enrollment

30 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. 18 years or older
  2. ≥3 months post ischemic or hemorrhagic stroke
  3. Upper extremity deficit with an FMA-UE score between 20-50
  4. Able to operate the AR device independently or with the help of a caregiver
  5. Sufficiently proficient in the English language to follow instructions from Reia

Exclusion criteria

  1. History of developmental, neurological or psychological impairment leading to functional disability
  2. Vision or visual field impairment that interferes with the use of the AR headset
  3. Severe photosensitivity that makes use of the AR headset uncomfortable
  4. History of visually provoked seizures
  5. Hearing aids
  6. Cardiac pacemaker
  7. Implantable cardioverter-defibrillator (ICD)

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

30 participants in 1 patient group

Telerehabilitation Group
Experimental group
Description:
Participants will use a mobile medical device in a augmented reality (AR) headset for 30 minutes daily to support their rehabilitation process after stroke by completing assessments and training programs.
Treatment:
Device: AR rehabilitation app

Trial contacts and locations

1

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Central trial contact

Study Team

Data sourced from clinicaltrials.gov

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