[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"trial:NCT07715695":3,"trial-entities:NCT07715695":90,"trial-summary:NCT07715695":94},{"id":4,"nct_id":4,"org_study_id":5,"brief_title":6,"official_title":6,"overall_status":7,"completion_date":8,"status_verified_date":9,"last_update_date":10,"start_date":10,"sponsor_name":11,"lead_sponsor_class":12,"has_dmc":13,"brief_summary":14,"detailed_description":15,"conditions":16,"keywords":18,"study_type":19,"primary_purpose":12,"phases":20,"enrollment_info":22,"interventions":25,"primary_outcomes":31,"secondary_outcomes":36,"sex":42,"minimum_age":43,"maximum_age":44,"healthy_volunteers":13,"eligibility_criteria":45,"std_ages":52,"locations":55,"central_contacts":80,"overall_officials":86,"references":88,"see_also_links":89},"NCT07715695","2026P001151","Evaluation of a Scalable Educational Intervention for Adjustment and Coping to Vision Loss","NOT_YET_RECRUITING","2027-06-30","2026-07","2026-07-20","Brigham and Women's Hospital","OTHER",false,"The goal of this interventional study is to learn if an educational intervention improves awareness in people experiencing visual loss. The main question it aim to answer is:\n\n* Will participants have an improved awareness of shared experiences regarding themes such as grief and isolation?\n\nParticipants will be asked to answer questions, engage with an audiovisual educational intervention, and then answer additional questions.",null,[17],"Visual Loss",[],"INTERVENTIONAL",[21],"NA",{"count":23,"type":24},300,"ESTIMATED",[26],{"type":12,"name":27,"description":28,"armGroupLabels":29},"audiovisual educational intervention","A brief audiovisual educational intervention.",[30],"Educational Intervention Arm",[32],{"measure":33,"description":34,"timeFrame":35},"Change from Baseline in Educational Awareness of Shared Themes as Measured by Likert-scale Questions","Higher values (or increases relative to baseline) correspond to better outcomes, with each question having a minimum value of 1 and a maximum value of 5.","From baseline to completion of post-intervention questions (e.g., within 1 week).",[37,40],{"measure":38,"description":39,"timeFrame":35},"Change from Baseline in Screening Measures of Depression and Anxiety as Measured by the Patient Health Questionnaire 4 (PHQ-4)","Lower values (or decreases relative to baseline) correspond to better outcomes, with each question having a minimum value of 0 and a maximum value of 3.",{"measure":41,"timeFrame":35},"Change from Baseline of Vision-Related Wellbeing as Measured by the Visual Function Questionnaire 25 (VFQ-25) Socioemotional Wellbeing Subscale","ALL","18 Years","89 Years",{"inclusion":46,"exclusion":49,"raw_text":51},[47,48],"have capacity to provide informed consent","have had a visit within a low-vision rehabilitation clinic",[50],"are unable to engage with the audiovisual educational intervention","Inclusion Criteria:\n\n* have capacity to provide informed consent\n* have had a visit within a low-vision rehabilitation clinic\n\nExclusion Criteria:\n\n* are unable to engage with the audiovisual educational intervention",[53,54],"ADULT","OLDER_ADULT",[56,72],{"facility":57,"city":58,"state":59,"zip":60,"country":61,"contacts":62,"geoPoint":69},"Brigham and Women's Hospital, Mass General Brigham","Boston","Massachusetts","02115","United States",[63,66],{"name":64,"role":65},"Ali S Raza, MD, PhD","PRINCIPAL_INVESTIGATOR",{"name":67,"role":68},"Pamela B Mahon, PhD","SUB_INVESTIGATOR",{"lat":70,"lon":71},42.35843,-71.05977,{"facility":73,"city":58,"state":59,"zip":60,"country":61,"contacts":74,"geoPoint":79},"New England College of Optometry",[75,77],{"name":76,"role":65},"Micaela Gobeille, OD, MS, FAAO, Dipl AAO LV",{"name":78,"role":68},"Nicole Ross, OD, MSc, FAAO, Dipl AAO LV",{"lat":70,"lon":71},[81],{"name":82,"role":83,"phone":84,"email":85},"Research Coordinator","CONTACT","617-732-6753","ophthalmic-psychiatry-recruitment@massgeneralbrigham.org",[87],{"name":64,"affiliation":57,"role":65},[],[],{"nct_id":4,"conditions":91,"biomarkers":93},[92],"Loss of Vision",[],{"nct_id":4,"found":95,"summary":96,"prompt_version":106},true,{"design":97,"status":98,"heading":99,"summary":100,"follow_up":101,"word_count":102,"commitments":103,"compensation":104,"drugs_mentioned":105},"This is an interventional study, meaning participants will receive a specific intervention. It plans to enroll 300 participants.","completed","Educational Intervention for Coping with Vision Loss","This study is looking at whether a brief audiovisual educational intervention can help people who are experiencing visual loss. The goal is to see if this intervention improves your awareness of shared experiences, like feelings of grief and isolation, that can come with vision loss. You would answer some questions, watch the educational material, and then answer more questions. The study aims to enroll 300 adults aged 18 to 89 who have recently visited a low-vision rehabilitation clinic. The study's status is currently unclear, so it's not known if they are actively recruiting.","Your awareness will be measured from before the intervention to within one week after completing the post-intervention questions.",93,"You will be asked to answer questions, engage with an audiovisual educational intervention, and then answer additional questions. This will take place within about one week.","Not stated in the trial record.",[27],"v2"]