[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"conditionNormalized\":\"provider-behavior\",\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:provider-behavior":28},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,45],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":29,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":33,"lastUpdatePostDateStruct":34,"startDateStruct":37,"completionDateStruct":39,"leadSponsor":41,"locationsCount":44},"100594869","multilevel-community-centered-intervention-to-reduce-pregnancy-related-and-associated-morbidity-and-mortality-pramm-disparities-100594869",false,"NCT07025057","Multilevel Community-Centered Intervention to Reduce Pregnancy Related and Associated Morbidity and Mortality (PRAMM) Disparities","Multilevel Community-centered Intervention to Reduce Pregnancy Related and Associated Morbidity and Mortality (PRAMM) Disparities in Non-Hispanic Black and Hispanic Medicaid-insured Individuals","Inclusion Criteria:\n\n* Providing care to pregnant and postpartum women in Wayne, Kent, and Genesee Counties in MI\n\nExclusion Criteria:\n\n* None",true,"ALL","18 Years",{"count":20,"type":21},480,"ESTIMATED","INTERVENTIONAL",[24],"NA","The goal of the study involving human subjects is to train providers to address patient-provider interactions. The study will survey providers to assess pre-post knowledge, understanding, and behavior changes.",[27,28],"Provider Confidence","Provider Behavior",[30,31],"Maternal mortality","Maternal morbidity","RECRUITING","2025-06-09",{"date":35,"type":36},"2025-06-17","ACTUAL",{"date":38,"type":36},"2025-02-03",{"date":40,"type":21},"2030-08-15",{"name":42,"class":43},"Michigan State University","OTHER",1,{"id":46,"slug":47,"hasResults":11,"nctId":48,"briefTitle":49,"officialTitle":50,"acronym":51,"eligibilityCriteria":52,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":53,"targetDuration":4,"studyType":22,"phases":55,"briefSummary":56,"conditions":57,"keywords":62,"overallStatus":32,"whyStopped":4,"lastUpdateSubmitDate":69,"lastUpdatePostDateStruct":70,"startDateStruct":72,"completionDateStruct":73,"leadSponsor":75,"locationsCount":5},"100592616","effect-of-anne-one-wellue-device-array-use-on-staff-bedside-vital-sign-measurement-activity-100592616","NCT06995742","Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity","Effect of ANNE One-Wellue Device Array Use on Staff Bedside Vital Sign Measurement Activity: A Randomized Controlled Trial","ANNE One TMRCT","Inclusion Criteria:\n\n* Inpatients admitted to Northwestern Memorial Hospital, Feinberg Unit 16 West.\n\nExclusion Criteria:\n\n* Primary language other than English, under isolation status, pregnant patients, prisoners, employees or students of the hospital or Northwestern University.",{"count":54,"type":21},270,[24],"Randomized controlled trial of a time motion study of time spent obtaining and charting vital signs for inpatients, comparing use of a wireless Bluetooth vital sign array as intervention versus routine vital sign obtainment activity on a general medical floor.",[58,59,60,28,61],"Vital Sign Evaluation","Vital Sign Monitoring","Sleep Quality","Patient Satisfaction",[63,64,65,66,67,68],"time motion study","vital signs","sleep quality","inpatient sleep","wireless device","patient satisfaction","2025-06-02",{"date":71,"type":36},"2025-06-05",{"date":69,"type":36},{"date":74,"type":21},"2026-07-31",{"name":76,"class":43},"Northwestern University"]