Multisensory Rehabilitation of Vision Loss After Cortical Damage

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorWake Forest University Health Sciences

About this trial

Damage to visual cortex on one side of the brain frequently produces a profound and permanent blindness in contralesional space (hemianopia), a debilitating condition that causes enormous suffering for patients and their families.

Eligibility criteria

Qualifiers

Patients will be recruited from the local subject population hospitalized/seen by Ophthalmology, Neurosurgery, and Neurology at Atrium Health Wake Forest Baptist

diagnosis of stable homonymous hemianopia (>4 weeks) with absence of hemineglect

a lesion encompassing at least primary visual cortex but sparing parietal cortex, to include lesions caused by an ischemic or hemorrhagic stroke or post-surgical changes due to an oncologic or non-oncologic tumor

normal or correctable auditory and cognitive function

Disqualifiers

diagnosis of an unstable homonymous hemianopia and/or with hemineglect,

Abnormal or uncorrectable auditory and cognitive function

unwillingness to participate in the program

inability to perform the visual testing in their intact field

Trial design

Treatments tested in this trial

  • Multisensory Rehabilitation

Treatment groups

30 Participants
are divided into 1 treatment group