Visual exploration training: Visual exploration of natural scenes guided by closed-loop auditory biofeedback through eye-tracking
Standard neuropsychological rehabilitation: Standard rehabilitation delivered at the IRCCS San Camillo hospital
Study summary
The current study evaluates first the assumption that eye-movements during free viewing behavior are potential biomarkers of visuospatial deficits in stroke population. Second, it assesses the feasibility of a novel visual exploration training to ameliorate visuospatial deficits, by exploiting an auditory biofeedback system coupled with online parsed fixations.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
Accepted
Inclusion Criteria:
* Vigilant
* First unifocal ischemic or hemorragic stroke
* Presence of maximum two lacunae, clinically silent, smaller than 15 mm. in the structural MRI
* Evident symptoms in the visual, attentive, memory, motor or language domain supported by the radiological exam
Exclusion Criteria:
* Previous stroke history, visible at the radiological exam
* Multifocal deficit
* Incapacity to remain vigilant during the required assessments
* Claustrophobia and/or metallic objects which could prevent MRI acquisition
* Presence of other neurological, psychiatric or medical conditions which may undermine interpretation of behavioral and neuroimaging results
Primary outcome measure(s)
Change pre-post rehabilitation in eye movements patterns during free viewing — At day 0 and day 30 (i.e., end of the rehabilitation) Eye movements patterns described by fixations, saccades and blinks related features summarized by principal component analysis (PCA)
Change pre-post rehabilitation in Behavioral Inattention Test score — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing visuospatial deficits
Change pre-post rehabilitation in Trail Making Test score — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing visuospatial abilities, scored as the time to complete the task
Change pre-post rehabilitation in Posner Test reaction times — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing visuospatial abilities, scored with the measured reaction times
Change pre-post rehabilitation in Attention Matrices Test — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing visuospatial deficits
Change pre-post rehabilitation in Brief Visuospatial Memory Test Revised — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing visuospatial memory
Change pre-post rehabilitation in Bells Test — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing visuospatial deficits
Change pre-post rehabilitation in Apple Test score — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing visuospatial deficits
Change pre-post rehabilitation in Comb and Razor Test — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing functional activities to investigate spatial attention deficits
Change pre-post rehabilitation in Mental Number Interval Bisection — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test investigating spatial biases in the mental number line
Change pre-post rehabilitation in Anosognosia — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test investigating deficits awareness
Change pre-post rehabilitation in Load Test — At day 0 and day 30 (i.e., end of the rehabilitation) Neuropsychological test assessing spatial attentional deficits with cognitive load as a moderator
Change pre-post rehabilitation in the Catherine-Bergego Scale score — At day 0 and day 30 (i.e., end of the rehabilitation) Test assessing activities of daily living involving spatial attention
Trial sites (2)
Facility
City
Region
Status
Azienda Ospedaliera di Padova
Padova
PD
Recruiting
IRCCS San Camillo
Venice-Lido
VE
Recruiting
More IRCCS San Camillo, Venezia, Italy trials in Italy
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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