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NCT07254949Not yet recruiting

Vision and Proprioception Evaluation With Robotics After Stroke

Source: ClinicalTrials.gov · Last updated 28 Nov 2025

Brief summary (registry, in English)

Stroke is highly prevalent in Canada and can lead to profound upper limb impairments in motor and sensory function, as well and vision. Clinical assessments for these functions often lack sensitivity making detecting impairments and tracking their recovery after stroke difficult. It is known that sensory function and vision interact to inform motor behaviours, yet how each of these modalities might contribute to motor impairments and subsequent recovery after stroke is undetermined. Using robotics to assess neurologic function after a stroke can be very beneficial, as they can measure on the scale of millimetres and milliseconds which can more easily detect subtle deficits in a persons function. Compared to current clinical tools, robotics offer greater objectivity and reliability, as they do not rely on the examiners clinical experience and/or impression. The use of robotics not only offers a more precise measurement, but robotics assessments can be completed in a relatively short amount of time, in comparison to some of the current clinical assessment tools, which can take along time to complete. In addition to robotics, collecting neuroimaging (MRI/CT) will allow us to relate our robotic and eye-tracking measures to neuroanatomical information about the person's stroke. With this data, we will assess how the brain changes post-stroke in relation to the recovery of motor, sensory and visual functions. This research will: 1) examine the relationship between visual and proprioceptive impairment on motor and eye movement behaviour over time after stroke, and 2) identify neuroanatomical correlates of visual, proprioceptive and sensory integrative dysfunction that impact motor recovery after stroke and examine the ability of regional damage and network disruption to predict recovery. Objectives: 1. Determine the impact of visual field loss and visual neglect in stroke survivors with impaired movement over the first 6 months post-stroke. 2. Identify the impact of Proprioceptive Impairment and Sensory Integration Impairment on recovery post-stroke using robotics and eye tracking. 3. Understand the impact of damage to neuroanatomic structures involved in vision, proprioception and sensory integration on motor recovery using MRI after stroke. The VIPERS study is recruiting both stroke and control participants. Stroke participants are recruited within the first 28 days post-stroke and are assessed longitudinally across the first 6-months post-stroke (four study timepoints). Control participants just complete a single session.

Status (registry)
Not yet recruiting
Study type
Observational
Enrollment
425 (estimated)
First submitted
19 Nov 2025
Start date
Jan 2026
Primary completion date
Jan 2031
Lead sponsor
Dr. Sean Dukelow
Diseases
Stroke
NCT number
NCT07254949

What you commit to

  • Study type: Observational
  • Planned participants: 425
  • From Jan 2026 to the primary completion date, Jan 2031
  • 2 sites 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

  • Prior history of stroke/significant neurologic problem (e.g. Parkinson's)

Other illness

  • Symptomatic medical conditions that would interfere with participation (e.g. uncontrolled angina)
  • Pre-stroke history of visual field/oculomotor abnormalities.

Other

  • Contraindications to Magnetic Resonance Imaging (MRI)

Who the study is looking for

  • 18 years of age or older
  • First clinical diagnosis of stroke
  • No recent muscle skeletal injuries to the arms, neck, or back
  • No history of other neurological disease/injury (Ie. MS, Parkinson's, Brain Tumour, etc.)
  • Corrected vision 20/50 or better
  • Able to follow multi-step commands.
  • Living independently prior to stroke
  • Can consent to participate in research
  • 18 years of age or older
  • No history stroke, or Trans Ischemic Attack (TIA)
  • No recent muscle skeletal injures to the arms, neck, or back
  • No history of other neurological disease/ injury (Ie. MS, Parkinson's, Brain Tumour, etc)
  • No pre-stroke history of eye movement disorders
  • Corrected vision 20/50 or better
  • Able to follow multi-step commands
  • Can consent to participate in research

Age in the registry: 18 years to - · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
Foothills Medical Centre
Coordinator of this site? Confirm its status
CalgaryCanadaUnknown status
Carewest Dr Vernon Fanning Centre
Coordinator of this site? Confirm its status
CalgaryCanadaUnknown status

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