Optimizing Cardiovascular Preventive Care for Women Following Hypertensive Disorders of Pregnancy
Part of paid clinical trials in Salt Lake City, Utah.
- Sponsor
- University of Utah
- Study ID
- NCT05826925
- Status
- Recruiting
Conditions
- Cardiovascular Diseases
- Hypertension Complicating Pregnancy
- Hypertension, Pregnancy Induced
- Patient Engagement
- Preeclampsia
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - N/A
- Healthy Volunteers
- Accepted
Interventions
- Decision aid — OTHERA decision aid will be developed based on qualitative data from Aim 1 and iterative refinement with input from stakeholders from Aim 2. Anticipated content includes: 1) information about cardiovascular risk following hypertensive disorders of pregnancy; 2) goal-setting exercises for blood pressure, weight management, glucose control, physical activity, and smoking cessation; 3) self-care steps to achieve management targets; 4) values clarification exercises to identify values related to cardiovascular risk management and identify priority areas for focus and improvement; and 5) discussion of how to communicate questions and goals of treatment to their provider.
Study Details
Cardiovascular disease is the leading cause of death among women in the United States, and women with hypertensive disorders of pregnancy have a 2-fold higher risk for cardiovascular disease later in life compared to women with uncomplicated pregnancies. This research investigates a patient-centered intervention during the postpartum period to promote engagement in cardiovascular preventive care.
Key Dates
- Start date
- Feb 27, 2025
- Status verified
- Jun 2025
- Primary completion
- Aug 31, 2027
- Completion
- Aug 31, 2027
Study Design
- Enrollment
- 30 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- OTHER
Arms
- Experimental: Decision aidParticipants will use the decision aid in the postpartum period
- No Intervention: Usual careParticipants will receive standard postpartum care
Primary Outcome Measure
Decisional conflict [ Time Frame: 6-8 weeks postpartum ]
Central Contacts
- Lauren Theilen, MD801-581-8425
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| University of Utah Hospital | Salt Lake City | Utah | 84132 |
Find similar trials in Salt Lake City, UT
By research site
Related Studies
- The EMPOWER Trial - The Carillon Mitral Contour System® in Treating Heart Failure With FMRRecruiting · Cardiac Dimensions, Inc. · Gilbert, Arizona
- Continuous Positive Airway Pressure (CPAP) for Sleep Apnea in PregnancyRecruiting · The George Washington University Biostatistics Center · Birmingham, Alabama
- Pragmatic Evaluation of Events And Benefits of Lipid-lowering in Older AdultsPHASE4 · Recruiting · Duke University · Birmingham, Alabama
- Continuation of the nuMoM2b Heart Health StudyEnrolling By Invitation · RTI International · Orange, California