[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-study-detail:100542048":3},{"organization":4,"armGroups":7,"interventions":14,"overallOfficials":21,"centralContacts":25,"locations":20,"responsibleParty":34,"collaborators":20,"id":37,"slug":38,"hasResults":39,"nctId":40,"briefTitle":41,"officialTitle":42,"acronym":20,"eligibilityCriteria":43,"healthyVolunteers":39,"sex":44,"minAge":45,"maxAge":46,"enrollmentInfo":47,"targetDuration":20,"studyType":50,"phases":51,"briefSummary":53,"conditions":54,"keywords":20,"overallStatus":56,"whyStopped":20,"lastUpdateSubmitDate":57,"lastUpdatePostDateStruct":58,"startDateStruct":61,"completionDateStruct":63,"leadSponsor":65,"locationsCount":20},{"fullName":5,"class":6},"University of Iowa","OTHER",[8],{"label":9,"type":10,"description":11,"interventionNames":12},"Research Pharmacist Monitoring","EXPERIMENTAL","The research pharmacist will help the mother find a primary care physician if she doesn't have one and discuss strategies to lower blood pressure, if needed. The pharmacist interactions will occur 7 days after enrollment and then approximately every 2 weeks to 2 months during 12 months of follow up, depending on blood pressure control. They may recommend medications to the participant's physician. The pharmacist will have access to the participant's electronic medical record to obtain any blood pressure-related medications that the mother is prescribed as well as throughout the follow up to ensure any health-related conditions can be discussed.",[13],"Behavioral: Research Pharmacist",[15],{"type":16,"name":17,"description":18,"armGroupLabels":19,"otherNames":20},"BEHAVIORAL","Research Pharmacist","The goal of this intervention is to determine if allied health professionals will improve blood pressure in new mothers.",[9],null,[22],{"name":23,"affiliation":5,"role":24},"Philip M Polgreen, MD","PRINCIPAL_INVESTIGATOR",[26,30],{"name":23,"role":27,"phone":28,"phoneExt":20,"email":29},"CONTACT","319-384-6194","philip-polgreen@uiowa.edu",{"name":31,"role":27,"phone":32,"phoneExt":20,"email":33},"Shelby L Francis, PhD","319-678-8037","shelby-francis@uiowa.edu",{"type":24,"investigatorFullName":35,"investigatorTitle":36,"investigatorAffiliation":5,"oldNameTitle":20,"oldOrganization":20},"Philip Polgreen","Professor","100542048","use-of-allied-health-professionals-to-improve-treatment-of-disease-100542048",false,"NCT06337799","Use of Allied-health Professionals to Improve Treatment of Disease","Use of Non-physician Allied-health Professionals to Recruit (and Follow) Research Participants, Sustain Engagement, and Improve and Diagnose Treatment of Diseases by Facilitating Transitions of Care","Inclusion Criteria:\n\n* Biological mothers delivering at UIHC or attending a well-child visit for an infant between 1 month and 9 months\n* Preeclampsia during pregnancy\n* Preceived prenatal care at UIHC\n* Owns a smartphone\n\nExclusion Criteria:\n\n* Arm circumference greater than 17 inches\n* Prisoner status\n* Unable to provide own written informed consent","FEMALE","18 Years","55 Years",{"count":48,"type":49},200,"ESTIMATED","INTERVENTIONAL",[52],"NA","The goal of this clinical trial is to learn if allied-health professionals can recruit and follow research participants, sustain engagement, and improve and diagnose treatment of diseases by facilitating transitions of care.\n\nParticipants will:\n\nTake their blood pressure at home and return it to the research team; Follow up with a research pharmacist for 12 months; Return for a follow up visit after 12 months.",[55],"Preeclampsia","NOT_YET_RECRUITING","2026-06-02",{"date":59,"type":60},"2026-06-04","ACTUAL",{"date":62,"type":49},"2026-10",{"date":64,"type":49},"2030-03",{"name":5,"class":6}]