[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"als-frontotemporal-dementia\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:als-frontotemporal-dementia":41},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,1,0,[8],{"id":9,"slug":4,"hasResults":10,"nctId":11,"briefTitle":12,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":10,"sex":16,"minAge":17,"maxAge":4,"enrollmentInfo":18,"targetDuration":4,"studyType":21,"phases":4,"briefSummary":22,"conditions":23,"keywords":4,"overallStatus":28,"whyStopped":4,"lastUpdateSubmitDate":29,"lastUpdatePostDateStruct":30,"startDateStruct":33,"completionDateStruct":35,"leadSponsor":37,"locationsCount":40},"100323309",false,"NCT03489278","Clinical Procedures to Support Research in ALS","Clinical Procedures to Support Research in ALS (CAPTURE-ALS)","CAPTURE-ALS","Inclusion Criteria:\n\n* Diagnosis of ALS or a related disorder (e.g. primary lateral sclerosis, progressive muscular atrophy).\n* Receiving care at a clinical center that uses Epic as its EHR.\n* Able and willing to provide informed consent (or informed consent obtainable from a designated proxy).\n\nExclusion Criteria:\n\n* Inability to understand English and\u002For Spanish","ALL","18 Years",{"count":19,"type":20},1200,"ESTIMATED","OBSERVATIONAL","The purpose of the Clinical Procedures To Support Research (CAPTURE) study is to utilize information collected in the medical record to learn more about a disease called amyotrophic lateral sclerosis (ALS) and related disorders.",[24,25,26,27],"Amyotrophic Lateral Sclerosis","ALS-Frontotemporal Dementia","Primary Lateral Sclerosis","Progressive Muscular Atrophy","RECRUITING","2026-06-11",{"date":31,"type":32},"2026-06-15","ACTUAL",{"date":34,"type":32},"2018-02-15",{"date":36,"type":20},"2034-06",{"name":38,"class":39},"University of Miami","OTHER",11,""]