STAMPP-HTN in a High-risk Rural Population of Women

NACompletedINTERVENTIONAL
Enrollment

250

Participants

Timeline

Start Date

December 14, 2020

Primary Completion Date

September 30, 2021

Study Completion Date

April 30, 2022

Conditions
Hypertension in Pregnancy
Interventions
DEVICE

Home Blood Pressure Telemonitoring

Women will complete a 9-question survey (pre-education) prior to discharge and will go over an education video a study team member. Once discharged, women will be asked to measure their blood pressure daily for the first postpartum week, and then weekly until postpartum week 6. Women who have a doctor's visit scheduled during the first 10 days, a member of the study team will meet them there to assess blood pressure and answer any questions. Women who do not have a visit scheduled they will have a telehealth visit during days 8-10 to complete the same assessments. At the final visit, participants will measure their blood pressure via HBPT, prior to returning the unit, complete a post-education questionnaire, a post-study questionnaire and have any questions or concerns addressed.

Trial Locations (1)

39216

University of MS Medical Center, Jackson

All Listed Sponsors
collaborator

University of Chicago

OTHER

lead

University of Mississippi Medical Center

OTHER

NCT04570124 - STAMPP-HTN in a High-risk Rural Population of Women | Biotech Hunter | Biotech Hunter