[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100510604":3},{"organization":4,"armGroups":7,"interventions":24,"overallOfficials":39,"centralContacts":43,"locations":49,"responsibleParty":66,"collaborators":69,"id":73,"slug":74,"hasResults":75,"nctId":76,"briefTitle":77,"officialTitle":78,"acronym":30,"eligibilityCriteria":79,"healthyVolunteers":75,"sex":80,"minAge":81,"maxAge":30,"enrollmentInfo":82,"targetDuration":30,"studyType":85,"phases":86,"briefSummary":88,"conditions":89,"keywords":91,"overallStatus":51,"whyStopped":30,"lastUpdateSubmitDate":96,"lastUpdatePostDateStruct":97,"startDateStruct":100,"completionDateStruct":102,"leadSponsor":104,"locationsCount":105},{"fullName":5,"class":6},"University of Michigan","OTHER",[8,13,19],{"label":9,"type":6,"description":10,"interventionNames":11},"Standard care arm - patient participants","This group will be enrolled first.",[12],"Behavioral: Survey questionnaires",{"label":14,"type":15,"description":16,"interventionNames":17},"Intervention arm (Epilepsy Visit Planner) - patient participants","EXPERIMENTAL","This group will be enrolled after the standard care arm enrollment is completed.",[12,18],"Behavioral: Epilepsy Visit Planner",{"label":20,"type":6,"description":21,"interventionNames":22},"Intervention arm (Epilepsy Visit Planner) - provider participants","Epilepsy providers will be recruited from the University of Michigan (approximately 10 providers).",[23],"Behavioral: Questionnaires for Providers",[25,31,35],{"type":26,"name":27,"description":28,"armGroupLabels":29,"otherNames":30},"BEHAVIORAL","Survey questionnaires","Participants will be enrolled before a scheduled clinic appointment. Following the clinic visit, the research staff will ask the patient to complete questionnaires electronically (or by phone if patient prefers) within three days after the baseline clinic visit and then at three months following this visit. Additionally, some data will be obtained from the participant's medical record.",[14,9],null,{"type":26,"name":32,"description":33,"armGroupLabels":34,"otherNames":30},"Epilepsy Visit Planner","Participants will be identified before a scheduled clinic appointment. Prior to the clinic visit (at the site) the participants will meet with a research staff to obtain written informed consent and then present the Epilepsy Visit Planner to the patient. Participants will be encouraged to use the Planner and share the Planner's output with the provider during the clinic visit. In some cases, there could be an option for the participants to consent prior to the visit and have a virtual presentation of the Planner.\n\nFollowing the clinic visit, the research staff will ask the participants to complete questionnaires electronically (or by phone if patient prefers) within three days after the baseline clinic visit and then at three months following this visit. Additionally, some data will be obtained from the participant's medical record.",[14],{"type":26,"name":36,"description":37,"armGroupLabels":38,"otherNames":30},"Questionnaires for Providers","Providers will be asked to complete a survey after the clinic visit for the intervention group.",[20],[40],{"name":41,"affiliation":5,"role":42},"Chloe Hill, MD","PRINCIPAL_INVESTIGATOR",[44],{"name":45,"role":46,"phone":47,"phoneExt":30,"email":48},"Queen Bolden","CONTACT","734-615-5495","qmbolden@umich.edu",[50],{"facility":5,"status":51,"city":52,"state":53,"zip":54,"country":55,"countryCode":56,"cosmosGeoPoint":57,"geoPoint":62,"contacts":63},"RECRUITING","Ann Arbor","Michigan","48109","United States","US",{"type":58,"coordinates":59},"Point",[60,61],-83.74088,42.27756,{"lat":61,"lon":60},[64,65],{"name":45,"role":46,"phone":30,"phoneExt":30,"email":48},{"name":41,"role":42,"phone":30,"phoneExt":30,"email":30},{"type":42,"investigatorFullName":67,"investigatorTitle":68,"investigatorAffiliation":5,"oldNameTitle":30,"oldOrganization":30},"Chloe Hill","Assistant Professor of Neurology",[70],{"name":71,"class":72},"National Institute of Neurological Disorders and Stroke (NINDS)","NIH","100510604","goals-for-epilepsy-clinic-visits-trial-100510604",false,"NCT05928598","Goals for Epilepsy Clinic Visits Trial","Drug-Resistant Epilepsy (DRE) Goals for Epilepsy Clinical Visits mHealth Epilepsy Visit Planner Trial","Inclusion Criteria - Patient Participants:\n\n* Adults with drug-resistant epilepsy\n* Participants receiving care through the Epilepsy clinics at the University of Michigan\n\nExclusion Criteria - Patient Participants:\n\n* \\\u003C18 years old\n* Non-English speaking\n* Do not clearly have drug-resistant epilepsy\n* Moderate-to-severe cognitive impairment that precludes study questionnaire completion\n\nInclusion Criteria - Provider Participants:\n\n-University of Michigan epilepsy providers\n\nExclusion Criteria - Provider Participants:\n\n-Not University of Michigan epilepsy providers","ALL","18 Years",{"count":83,"type":84},152,"ESTIMATED","INTERVENTIONAL",[87],"NA","The purpose of this project is to conduct a trial to assess whether patients that receive a tablet-based waiting room priority communication tool (the \"Epilepsy Visit Planner\") have improved outcomes compared to patients that do not receive the tool.\n\nThe project's hypotheses are:\n\n* Patients that receive the Epilepsy Visit Planner will have improved patient-provider communication compared to the non-planner group.\n* Patients that receive the Epilepsy Visit Planner will have improved quality of life scores.\n* The Epilepsy Visit Planner will score highly on process measures of feasibility and acceptability, demonstrating suitability for future larger scale study.\n\nAdditionally, there is a related survey project that is not part of the clinical trial and will not be included in this registration information.",[90],"Drug Resistant Epilepsy",[92,93,94,95],"Survey","Quality of life","Communication tool","Patient-provider communication","2025-10-15",{"date":98,"type":99},"2025-10-20","ACTUAL",{"date":101,"type":99},"2023-09-27",{"date":103,"type":84},"2027-01-01",{"name":5,"class":6},1]