CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 5 enrolled
Drug / intervention
multisensory rehabilitation paradigmdevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04963075
NCT04963075N/ACompleted
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Non-Invasive Multisensory Rehabilitation of Hemianopia

Wake Forest University Health Sciences·interventional·Posted Jul 15, 2021·Updated Apr 30, 2026

In Brief

A clinical study evaluating multisensory rehabilitation paradigm for Hemianopia. Completed, enrolled 5 participants across 1 site.

Detailed Summary

The current proposal is to generate "proof of concept" evidence that hemianopia can be successfully rehabilitated in humans when this multisensory rehabilitation paradigm is used.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsHemianopia
CountriesUnited States
CollaboratorsNeuroscience Clinical Trial and Innovation Center (NCTIC)

Timeline

N/ACompletedFinished
20222023202420252026
First PostedJul 15, 2021
Enrollment StartSep 22, 2021
Primary CompletionMar 18, 2025
Study CompletionSep 30, 2025
TodayJul 2, 2026
Enrollment to primary: 3.5 yearsPosted 5.0 years ago

Interventions

multisensory rehabilitation paradigmdevice

In initial ("training") sessions, subjects will be exposed (and respond) to spatiotemporally congruent pairs of visual-auditory stimuli presented within their blinded field, with occasional probes of unisensory visual stimuli on both sides of space. Once recovery of visual responsiveness in the contralesional field is observed, sessions will alternate between "training/testing" and "testing only" sessions in which performance on the visual battery will be re-assessed.