N/A
N=5
Multisensory Rehabilitation of Hemianopia
Hemianopia
Bottom Line
View on ClinicalTrials.gov: NCT04963075 ↗Enrolled (actual)
5
Serious AEs
0.0%
Results posted
Apr 2026
Primary outcome: Primary: Number of Points Detected at Multiple Locations — 14.0; 94.9; 63.6; 95.4 Number of points
Study Design & Population
- Study type
- Interventional
- Phase
- N/A
- Interventions
- multisensory rehabilitation paradigm (Device)
- Age
- Adult, Older Adult · 18+ yrs
- Sex
- All
- Sponsor
- Wake Forest University Health Sciences
- Primary completion
- Mar 2025
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Number of Points Detected at Multiple Locations |
14.0; 94.9; 63.6; 95.4 | — |
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.
Eligibility Criteria
Inclusion Criteria
- adults ( 6 months) with absence of hemineglect
- lesion encompassing at least primary visual cortex but sparing parietal cortex
- normal auditory and cognitive function
- willingness to participate in the three month program
- ability to perform the visual discriminations in their intact field
Exclusion Criteria
- adults (>85)
- normal auditory and cognitive function
- unwilling to participate in the three month program
- inability to perform the visual discriminations in their intact field
Data sourced from ClinicalTrials.gov (NCT04963075). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication.