NCT07317739Not yet recruiting
Screening and Rehabilitation of Visual Field Defects in Post-Stroke Patients
SCRiCaViPS Screening and Rehabilitation of Visual Field Defects in Post-Stroke Patients
Source: ClinicalTrials.gov · Last updated 5 Jan 2026
Brief summary (registry, in English)
In this study, the investigators will use a wearable device capable of performing this bedside assessment to evaluate the incidence of visual field loss in post-stroke patients. Furthermore, for those with visual field loss, the investigators will investigate whether integrating multisensory audio-visual rehabilitation into the standard physical rehabilitation protocol can help improve visual field loss compared to standard rehabilitation alone.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 300 (estimated)
- First submitted
- 4 Dec 2025
- Start date
- 1 Jan 2026
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- Fondazione David Chiossone - Impresa Sociale
- Diseases
- Stroke
- NCT number
- NCT07317739
What you commit to
- Study type: Interventional
- Planned participants: 300
- From 1 Jan 2026 to the primary completion date, 31 Dec 2026
- No sites listed in no 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.
Other illness
- Presence of cognitive impairment (with an MMSE score less than 24), which limits the understanding of the informed consent or the ability to perform the test.
- Presence of ocular comorbidity that could affect visual field assessment before stroke.
Other
- Difficulty moving both upper limbs.
- Presence of fluent aphasia, neglect, or head and gaze deviation.
- Presence of disturbances in the state of consciousness
- Presence of delirium
Who the study is looking for
- Patients aged 18 to 99 years with stroke (excluding isolated cerebellar, brainstem, or spinal cord strokes), admitted to Neurology in IRCCS San Martino Polyclinic Hospital with the ability to understand and sign the informed consent for study participation.
- Mobility of at least one upper limb.
Age in the registry: 18 years to 99 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.