[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"low-vision-digital-assistance\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:low-vision-digital-assistance":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":11,"sex":16,"minAge":17,"maxAge":18,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":30,"overallStatus":34,"whyStopped":4,"lastUpdateSubmitDate":35,"lastUpdatePostDateStruct":36,"startDateStruct":39,"completionDateStruct":41,"leadSponsor":43,"locationsCount":5},"100656534","effectiveness-of-a-multi-disciplinary-vision-rehabilitation-programme-in-improving-the-overall-quality-of-life-of-visually-impaired-adults-100656534",false,"NCT07827040","Effectiveness of a Multi-disciplinary Vision Rehabilitation Programme in Improving the Overall Quality of Life of Visually Impaired Adults","Effectiveness of a Multi-disciplinary Vision Rehabilitation Programme in Improving Function and Quality of Life of Visually Impaired Patients: a Randomized Controlled Trial","Inclusion Criteria:\n\n* Aged 18 and 80 years\n* Community-dwelling in Hong Kong\n* Cantonese Speaker\n* Clinical diagnosis of low vision (best-corrected visual acuity \\\u003C6\u002F18; and\u002For field loss of \\\u003C 20 degree)\n* Stable ocular condition for ≥ 3 months\n* Owns a smartphone\n* Not currently participating in any vision rehabilitation programme\n* Willing to participate and commit for at least 6 months to 12 months\n* Provides informed consent\n\nExclusion Criteria:\n\n* Living in a nursing home\u002F institutionalized\n* Self-reported severe cognitive impairment or HK-MoCA-VI cut off score of 12\n* Self-reported severe hearing impairment\n* Uncontrolled systemic ocular diseases\u002F neurological or psychiatric conditions\n* Immobility caused by physical impairment\n* Refuse to provide written informed consent\n* Participating in another vision rehabilitation programme during the trial period","ALL","18 Years","80 Years",{"count":20,"type":21},1000,"ESTIMATED","INTERVENTIONAL",[24],"NA","This trial compares multidisciplinary vision rehabilitation and vision rehabilitation services to determine which service works better at improving overall quality of life for adults with visual impairment. Before receiving the intervention, participants will complete baseline measurements, including an eye examination, cognitive and hearing screenings, mobility and balance assessments, questionnaires on basic demographics and health, and a home environment assessment. This randomised controlled trial includes three arms: 1) control-waitlist (wait for 3 months before joining either intervention arm), 2) vision rehabilitation with low vision training only, and 3) multidisciplinary vision rehabilitation arm.\n\nThe intervention period lasts for eight weeks, comprising of four on-site training sessions.\n\n* During the intervention period, all participants will receive low-vision training on the use of advanced assistive technology.\n* Those in the multidisciplinary group will also receive counselling, exercise training, and home assessment with home modifications (if needed).",[27,28,29],"Visual Impairments","Low Vision Digital Assistance","Adults",[31,32,33],"low vision","advanced assistive technology","vision rehabilitation","RECRUITING","2026-09-12",{"date":37,"type":38},"2026-09-18","ACTUAL",{"date":40,"type":21},"2026-09-29",{"date":42,"type":21},"2029-09-30",{"name":44,"class":45},"The Hong Kong Polytechnic University","OTHER"]