[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100641789":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":22,"centralContacts":26,"locations":37,"responsibleParty":53,"collaborators":31,"id":55,"slug":56,"hasResults":57,"nctId":58,"briefTitle":59,"officialTitle":59,"acronym":31,"eligibilityCriteria":60,"healthyVolunteers":57,"sex":61,"minAge":62,"maxAge":63,"enrollmentInfo":64,"targetDuration":31,"studyType":67,"phases":68,"briefSummary":70,"conditions":71,"keywords":73,"overallStatus":76,"whyStopped":31,"lastUpdateSubmitDate":77,"lastUpdatePostDateStruct":78,"startDateStruct":81,"completionDateStruct":83,"leadSponsor":85,"locationsCount":86},{"fullName":5,"class":6},"Wake Forest University Health Sciences","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"multisensory training","EXPERIMENTAL","At the completion of this initial intervention (12 research sessions + clinical visits at the time of the first and last session), participants will receive a second kinetic visual field test and a 30-2 visual field test to measure any changes according to the clinical standard.\n\nTwo additional follow-up procedures are scheduled for participants identified as showing visual recovery after the initial intervention.\n\nThree months after completing the initial treatment, participants will have an additional research visit. If testing during this visit reveals that vision has degraded from the initial series, participants will be scheduled for 2-5 additional research visits (with testing and training) to reinstate recovery with re-intervention.",[13],"Behavioral: Multisensory Rehabilitation",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","Multisensory Rehabilitation","12 research sessions + clinical visits at the time of the first and last session - In each session, there will be a \"training phase\" in which 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. There will also be a \"testing\" phase during which they are presented with visual stimuli in virtual reality (VR) to assess multiple aspects of visual function. This \"visual battery\" consists of innocuous stimuli, e.g., flashes of light or moving bars, presented at intensities consistent with those experienced during daily life. Subjects detect or discriminate the stimuli (e.g., judge whether a stimulus was flashed, or which stimulus is brighter) and report confidence in assessments.",[9],[21],"multisensory training paradigm",[23],{"name":24,"affiliation":5,"role":25},"Benjamin Rowland, PhD","PRINCIPAL_INVESTIGATOR",[27,33],{"name":28,"role":29,"phone":30,"phoneExt":31,"email":32},"Kimberly Hawley, RN","CONTACT","3367164031",null,"Kimberly.Hawley@Advocatehealth.org",{"name":34,"role":29,"phone":35,"phoneExt":31,"email":36},"Wendy Jenkins, BSNRN, CCRC","336.716.3842","Wendy.Jenkins@AdvocateHealth.org",[38],{"facility":5,"status":31,"city":39,"state":40,"zip":41,"country":42,"countryCode":43,"cosmosGeoPoint":44,"geoPoint":49,"contacts":50},"Winston-Salem","North Carolina","27157","United States","US",{"type":45,"coordinates":46},"Point",[47,48],-80.24422,36.09986,{"lat":48,"lon":47},[51],{"name":34,"role":29,"phone":52,"phoneExt":31,"email":36},"336-716-3842",{"type":54,"investigatorFullName":31,"investigatorTitle":31,"investigatorAffiliation":31,"oldNameTitle":31,"oldOrganization":31},"SPONSOR","100641789","multisensory-rehabilitation-of-vision-loss-after-cortical-damage-100641789",false,"NCT07659691","Multisensory Rehabilitation of Vision Loss After Cortical Damage","Inclusion Criteria:\n\n* Patients will be recruited from the local subject population hospitalized\u002Fseen by Ophthalmology, Neurosurgery, and Neurology at Atrium Health Wake Forest Baptist\n* diagnosis of stable homonymous hemianopia (\\>4 weeks) with absence of hemineglect\n* 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\n* normal or correctable auditory and cognitive function\n* willingness to participate in the three-month program\n* ability to perform visual discriminations in their intact field\n* life expectancy ≥12 months\n\nExclusion Criteria:\n\n* diagnosis of an unstable homonymous hemianopia and\u002For with hemineglect,\n* Abnormal or uncorrectable auditory and cognitive function\n* unwillingness to participate in the program\n* inability to perform the visual testing in their intact field\n* life expectancy \\\u003C 12 months\n* Any other condition that would compromise their ability to complete the study.","ALL","18 Years","85 Years",{"count":65,"type":66},30,"ESTIMATED","INTERVENTIONAL",[69],"NA","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.",[72],"Cortical Blindness",[74,75,9],"hemianopia","blindness","NOT_YET_RECRUITING","2026-06-15",{"date":79,"type":80},"2026-06-22","ACTUAL",{"date":82,"type":66},"2026-08",{"date":84,"type":66},"2027-12",{"name":5,"class":6},1]