[{"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":29},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,3,0,[8,51,78],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":13,"acronym":14,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":19,"targetDuration":4,"studyType":22,"phases":23,"briefSummary":25,"conditions":26,"keywords":32,"overallStatus":39,"whyStopped":4,"lastUpdateSubmitDate":40,"lastUpdatePostDateStruct":41,"startDateStruct":44,"completionDateStruct":46,"leadSponsor":48,"locationsCount":5},"100652288","evaluating-the-effects-of-reproductive-health-training-on-provider-behavior---aim-3-100652288",false,"NCT07770438","Evaluating the Effects of Reproductive Health Training on Provider Behavior - Aim 3","THP-2 Aim 3","Inclusion Criteria:\n\n* Current pre-final year student at the State University of Zanzibar, Kilimanjaro Christian University, or the University of Dodoma in midwifery, nursing, or medicine\n* Able to attend the full 4-day training\n* Fluent in English and Kiswahili\n* Willing to volunteer to complete all evaluation procedures\n\nExclusion Criteria:\n\n* Unable to attend all days of the seminar at SUZA, KCMC, or UDOM\n* Unable to be on the SUZA, KCMC, or UDOM campus for the follow-up dates\n* Expresses reservations about attending, including religious objections\n* Expresses fear of violence due to attending, including fear from a spouse or relative\n* Prior exposure to the Training for Health Professionals curriculum or either of the previous pilots\n* Younger than 18 years of age\n* Non-English speaker\n* Unable to read\n* Employee of the researcher\n* Prisoner\n* Adult lacking capacity to consent or with diminished capacity to consent\n* Active member of the military or DoD personnel",true,"ALL","18 Years",{"count":20,"type":21},650,"ESTIMATED","INTERVENTIONAL",[24],"NA","This study will evaluate the real-world effectiveness of a four-day Afrocentric sexual and reproductive health curriculum for health professional students in Tanzania.\n\nMedical, nursing, and midwifery students from the State University of Zanzibar, Kilimanjaro Christian University, and the University of Dodoma will receive the curriculum. The curriculum covers sexual health across the lifespan, sexual dysfunctions, key populations, sexual violence, clinical skills training, ethics, policy writing, community resources, and cultural considerations.\n\nStudent outcomes will be assessed using surveys at baseline, immediately after the curriculum, and at 3-month and 12-month follow-up to examine changes in sexual health knowledge, attitudes, and sexual history and counseling skills.",[27,28,29,30,31],"Sexual and Reproductive Health","Health Knowledge, Attitudes, Practice","Provider Behavior","Health Education","Sexual Health",[33,34,35,36,37,38],"THP-2","Sexual and reproductive health","Training for Health Professionals","Medical students","Afrocentric curriculum","Sexual health curriculum","NOT_YET_RECRUITING","2026-08-12",{"date":42,"type":43},"2026-08-18","ACTUAL",{"date":45,"type":21},"2026-08-17",{"date":47,"type":21},"2027-08-17",{"name":49,"class":50},"University of Minnesota","OTHER",{"id":52,"slug":53,"hasResults":11,"nctId":54,"briefTitle":55,"officialTitle":56,"acronym":4,"eligibilityCriteria":57,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":58,"targetDuration":4,"studyType":22,"phases":60,"briefSummary":61,"conditions":62,"keywords":64,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":68,"lastUpdatePostDateStruct":69,"startDateStruct":71,"completionDateStruct":73,"leadSponsor":75,"locationsCount":77},"100594869","multilevel-community-centered-intervention-to-reduce-pregnancy-related-and-associated-morbidity-and-mortality-pramm-disparities-100594869","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",{"count":59,"type":21},480,[24],"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.",[63,29],"Provider Confidence",[65,66],"Maternal mortality","Maternal morbidity","RECRUITING","2026-07-02",{"date":70,"type":43},"2026-07-07",{"date":72,"type":43},"2025-02-03",{"date":74,"type":21},"2030-08-15",{"name":76,"class":50},"Michigan State University",1,{"id":79,"slug":80,"hasResults":11,"nctId":81,"briefTitle":82,"officialTitle":83,"acronym":84,"eligibilityCriteria":85,"healthyVolunteers":11,"sex":17,"minAge":18,"maxAge":4,"enrollmentInfo":86,"targetDuration":4,"studyType":22,"phases":88,"briefSummary":89,"conditions":90,"keywords":95,"overallStatus":67,"whyStopped":4,"lastUpdateSubmitDate":102,"lastUpdatePostDateStruct":103,"startDateStruct":105,"completionDateStruct":106,"leadSponsor":108,"locationsCount":110},"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":87,"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.",[91,92,93,29,94],"Vital Sign Evaluation","Vital Sign Monitoring","Sleep Quality","Patient Satisfaction",[96,97,98,99,100,101],"time motion study","vital signs","sleep quality","inpatient sleep","wireless device","patient satisfaction","2025-06-02",{"date":104,"type":43},"2025-06-05",{"date":102,"type":43},{"date":107,"type":21},"2026-07-31",{"name":109,"class":50},"Northwestern University",2]