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NCT Number: NCT07254949

Vision and Proprioception Evaluation With Robotics After Stroke

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.

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Carewest Dr. Vernon Fanning Centre, Calgary, Alberta, Canada

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Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

for stroke participants:

  • 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

Inclusion criteria

for control participants:

  • 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

Exclusion criteria

  • Prior history of stroke/significant neurologic problem (e.g. Parkinson's)
  • Symptomatic medical conditions that would interfere with participation (e.g. uncontrolled angina)
  • Contraindications to Magnetic Resonance Imaging (MRI)
  • Pre-stroke history of visual field/oculomotor abnormalities.

Treatment and study plan

Primary outcomes

  1. Visually Guided Reaching Score

    Time frame: Enrolment to six-months post stroke

Other outcomes

  1. Visually Guided Reaching Score (no vision)

    Time frame: Enrolment to six-months post stroke

  2. Proprioceptive Saccade task scores

    Time frame: Enrolment to six-months post stroke

  3. Arm Movement Matching (vision)

    Time frame: Enrolment to six-months post stroke

  4. Arm Movement Matching

    Time frame: Enrolment to six-months post stroke

  5. Arm position matching (vision)

    Time frame: Enrolment to six-months post stroke

  6. Arm Position Matching Score

    Time frame: Enrolment to six-months post stroke

  7. Visually Guided Reaching Score

    Time frame: From enrolment to six-months post stroke

  8. Anti-saccade task score

    Time frame: Enrolment to six-months post stroke

  9. Pro-saccade task score

    Time frame: Enrolment to six-months post-stroke

  10. Behavioural Inattention Test (BIT)

    Time frame: Enrolment to six-months post-stroke

  11. Visual Impairment Screening Assessment (VISA)

    Time frame: Enrolment to six-months post-stroke

  12. Humphrey's Visual Field Analyzer (VFA)

    Time frame: Enrolment to six-months post stroke

  13. Thumb Localization Test (TLT)

    Time frame: Enrolment to six-months post stroke

  14. Medical Research Council Strength Scale

    Time frame: Enrolment to six-months post stroke

  15. Modified Ashworth Scale (MAS)

    Time frame: Enrolment to six-months post stroke

  16. Fugl-Meyer Assessment-Upper Extremity (FMA-UE)

    Time frame: Enrolment to six-months post stroke

  17. Functional Independence Measure (FIM)

    Time frame: Enrolment to six-months post stroke

Sponsors and collaborators

Lead sponsor

Dr. Sean Dukelow

Other

Registry information

Acronym: VIPERS

Important dates

Study start
2026
Primary completion
2031
Study completion
2031
First posted
Nov 28, 2025
Registry last updated
Nov 28, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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