[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100650840":3},{"organization":4,"armGroups":7,"interventions":19,"overallOfficials":25,"centralContacts":29,"locations":25,"responsibleParty":35,"collaborators":37,"id":41,"slug":42,"hasResults":43,"nctId":44,"briefTitle":45,"officialTitle":46,"acronym":47,"eligibilityCriteria":48,"healthyVolunteers":43,"sex":49,"minAge":50,"maxAge":25,"enrollmentInfo":51,"targetDuration":25,"studyType":54,"phases":55,"briefSummary":57,"conditions":58,"keywords":60,"overallStatus":65,"whyStopped":25,"lastUpdateSubmitDate":66,"lastUpdatePostDateStruct":67,"startDateStruct":70,"completionDateStruct":72,"leadSponsor":74,"locationsCount":25},{"fullName":5,"class":6},"Glasgow Caledonian University","OTHER",[8,15],{"label":9,"type":10,"description":11,"interventionNames":12},"Eye movement training + usual care","EXPERIMENTAL","Usual post-stroke care, plus eye movement training (VISIOcoach)",[13,14],"Device: NeuroEyeCoach eye movement training","Other: Usual Care",{"label":16,"type":6,"description":17,"interventionNames":18},"usual care","Usual post-stroke care",[14],[20,26],{"type":21,"name":22,"description":23,"armGroupLabels":24,"otherNames":25},"DEVICE","NeuroEyeCoach eye movement training","computer based eye movement training for visual field loss in stroke",[9],null,{"type":6,"name":27,"description":17,"armGroupLabels":28,"otherNames":25},"Usual Care",[9,16],[30],{"name":31,"role":32,"phone":33,"phoneExt":25,"email":34},"Christine Hazelton, PhD","CONTACT","0141 331 8181","christine.hazelton@gcu.ac.uk",{"type":36,"investigatorFullName":25,"investigatorTitle":25,"investigatorAffiliation":25,"oldNameTitle":25,"oldOrganization":25},"SPONSOR",[38],{"name":39,"class":40},"National Health Service, United Kingdom","OTHER_GOV","100650840","pilot-rct-of-computer-based-eye-movement-training-100650840",false,"NCT07752563","Pilot RCT of Computer-based Eye Movement Training","Computer-based Eye Movement Training for Stroke-related Visual Field Loss: a Pilot Randomised Controlled Trial","CRYSTAL","Inclusion Criteria:\n\n* adult (\\>18 years)\n* stroke survivor\n* stroke-related homonymous VFL (minimum quadrantanopia)\n* sufficient language, cognitive, and upper limb ability to participate in trial activities.\n\nExclusion Criteria:\n\n* pre-existing (ie pre-stroke) registration as sight impaired (partially sighted) or severely sight impaired (blind)\n* • history of seizure disorders, especially those of a photosensitive nature","ALL","18 Years",{"count":52,"type":53},60,"ESTIMATED","INTERVENTIONAL",[56],"NA","The goal of this study is to learn whether NeuroEyeCoach, a computer-based eye movement training programme, can help stroke survivors with visual field loss. The study will also assess whether a larger clinical trial is feasible. The main questions it aims to answer are:\n\n* Can stroke survivors be successfully recruited, randomised and followed up in a larger trial?\n* Is NeuroEyeCoach acceptable and practical to use?\n* Is there early evidence that NeuroEyeCoach improves vision-related functioning and wellbeing? Researchers will compare NeuroEyeCoach plus usual care with usual care alone.\n\nParticipants will:\n\n* Be randomly assigned to receive NeuroEyeCoach plus usual care or usual care alone\n* Complete six weeks of training if allocated to NeuroEyeCoach\n* Complete questionnaires and tests of vision, daily activities, quality of life, confidence and wellbeing\n* Take part in follow-up assessments over six months This pilot trial will include 60 stroke survivors living with visual field loss after stroke. Findings will be used to inform the design of a larger study.",[59],"Stroke",[61,62,63,64],"visual field loss","rehabilitation","pilot RCT","process evaluation","NOT_YET_RECRUITING","2026-08-03",{"date":68,"type":69},"2026-08-07","ACTUAL",{"date":71,"type":53},"2026-10-01",{"date":73,"type":53},"2027-07-31",{"name":5,"class":6}]