[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100585883":3},{"organization":4,"armGroups":7,"interventions":7,"overallOfficials":8,"centralContacts":12,"locations":21,"responsibleParty":35,"collaborators":7,"id":37,"slug":38,"hasResults":39,"nctId":40,"briefTitle":41,"officialTitle":42,"acronym":7,"eligibilityCriteria":43,"healthyVolunteers":39,"sex":44,"minAge":45,"maxAge":7,"enrollmentInfo":46,"targetDuration":7,"studyType":49,"phases":7,"briefSummary":50,"conditions":51,"keywords":7,"overallStatus":57,"whyStopped":7,"lastUpdateSubmitDate":58,"lastUpdatePostDateStruct":59,"startDateStruct":62,"completionDateStruct":64,"leadSponsor":66,"locationsCount":67},{"fullName":5,"class":6},"Center for Eye Research Australia","OTHER",null,[9],{"name":10,"affiliation":5,"role":11},"Penelope J Allen, FRACO, FRACS","PRINCIPAL_INVESTIGATOR",[13,18],{"name":14,"role":15,"phone":16,"phoneExt":7,"email":17},"Lisa Lombardi, BOptom","CONTACT","+61 3 9959 0119","llombardi@cera.org.au",{"name":19,"role":15,"phone":7,"phoneExt":7,"email":20},"Lauren Moussallem, BAppSc MOrth","lmoussallem@unimelb.edu.au",[22],{"facility":23,"status":7,"city":24,"state":25,"zip":26,"country":27,"countryCode":28,"cosmosGeoPoint":29,"geoPoint":34,"contacts":7},"Centre for Eye Research Australia","Melbourne","Victoria","3002","Australia","AU",{"type":30,"coordinates":31},"Point",[32,33],144.96332,-37.814,{"lat":33,"lon":32},{"type":36,"investigatorFullName":7,"investigatorTitle":7,"investigatorAffiliation":7,"oldNameTitle":7,"oldOrganization":7},"SPONSOR","100585883","functional-assessments-in-vision-impairment-100585883",false,"NCT06908161","Functional Assessments in Vision Impairment","A Novel Approach for Capturing Real-world Functional Assessment Outcomes in Participants With a Vision Impairment","Inclusion Criteria:\n\n1. Willing to provide signed informed consent.\n2. Be available for study visits.\n3. Willing to comply with study assessments.\n4. In good general health and ambulant.\n5. Aged over 18 years of age.\n6. Have a vision impairment caused by any ocular condition which affects independent mobility.\n7. Agree to allow the research team into their home and local environments.\n8. Participate in assessments in public settings\n\nExclusion Criteria:\n\n1. Significant co-morbidities which prohibit involvement in study visits.\n2. Anything that would place the individual at increased risk or preclude the individual's full compliance with or completion of the study.\n3. Cognitive deficiencies, including dementia or progressive neurological disease.\n4. Have a psychiatric condition that, in the investigator's opinion, precludes compliance with the protocol including past or present psychoses and bipolar disorder.\n5. Deafness or significant hearing loss.\n6. Inability to converse in English.","ALL","18 Years",{"count":47,"type":48},45,"ESTIMATED","OBSERVATIONAL","The aim of the research project is to validate the use of a novel functional assessment tool designed to document how participants with a vision impairment complete activities of daily living in a real world environment.",[52,53,54,55,56],"Retinitis Pigmentosa (RP)","Diabetic Retinopathy (DR)","Age Related Macular Degeneration (AMD)","Glaucoma","Retinal Dystrophy","NOT_YET_RECRUITING","2025-03-26",{"date":60,"type":61},"2025-04-03","ACTUAL",{"date":63,"type":48},"2025-04-01",{"date":65,"type":48},"2027-12-31",{"name":5,"class":6},1]