An observational study in Stroke and Control Condition, sponsored by Dr. Sean Dukelow. Not yet recruiting at 2 sites in Canada. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-11-28.
Sponsored by Dr. Sean Dukelow · Observational
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:
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.
7,286 studies on the registry are indexed under Stroke; 2,007 are open to participants now.
This study's planned enrollment of 425 is above the median of 160 across 1,692 observational studies indexed under Stroke.
Browse Stroke studies →This is the only study on the registry with Dr. Sean Dukelow as lead sponsor.
Counted across the registry records on this site, refreshed daily.
425 participants will be recruited for this study (225 stroke participants and 200 matched control participants who have not experienced a stroke). All participant will be aged 18 or older.
Inclusion criteria for stroke participants:
Inclusion criteria for control participants:
Exclusion Criteria:
Stroke Participants - Individuals with first time stroke
Control Participants - Individuals not suffering stroke or other neurological disorders
Visually Guided Reaching Score
Time frame: Enrolment to six-months post stroke
Visually Guided Reaching Score (no vision)
Time frame: Enrolment to six-months post stroke
Proprioceptive Saccade task scores
Time frame: Enrolment to six-months post stroke
Arm Movement Matching (vision)
Time frame: Enrolment to six-months post stroke
Arm Movement Matching
Time frame: Enrolment to six-months post stroke
Arm position matching (vision)
Time frame: Enrolment to six-months post stroke
Arm Position Matching Score
Time frame: Enrolment to six-months post stroke
Visually Guided Reaching Score
Time frame: From enrolment to six-months post stroke
Anti-saccade task score
Time frame: Enrolment to six-months post stroke
Pro-saccade task score
Time frame: Enrolment to six-months post-stroke
Behavioural Inattention Test (BIT)
Time frame: Enrolment to six-months post-stroke
Visual Impairment Screening Assessment (VISA)
Time frame: Enrolment to six-months post-stroke
Humphrey's Visual Field Analyzer (VFA)
Time frame: Enrolment to six-months post stroke
Thumb Localization Test (TLT)
Time frame: Enrolment to six-months post stroke
Medical Research Council Strength Scale
Time frame: Enrolment to six-months post stroke
Modified Ashworth Scale (MAS)
Time frame: Enrolment to six-months post stroke
Fugl-Meyer Assessment-Upper Extremity (FMA-UE)
Time frame: Enrolment to six-months post stroke
Functional Independence Measure (FIM)
Time frame: Enrolment to six-months post stroke
Plan to share: No — Formal data transfer agreements/legal contracts are required to share IPD with other researchers outside of the main study site.
No publications or documents are linked to this record.
This study is not yet recruiting, as verified in Nov 2025. You cannot join it, but the record below documents what was studied.
Get an email when the registry record changes — status, dates, results — or when someone posts here.
Sign in to followQuestions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.
Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.
Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.