Not Yet RecruitingNot Applicable

Implementation Models for Blood Pressure Monitoring in Pregnancy and Postpartum: Connected MOM Plus

United States2,000 participantsStarted 2026-07

Plain-language summary

Quality improvement (QI) initiative to improve uptake and utilization of Connected MOM, particularly among those with limited access to health care

Who can participate

Age range

18 Years – 80 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Access to a smartphone * Understanding of English or Spanish in oral and written discourses * Have a participating Ochsner-employed provider * Plan to deliver at a participating Ochsner hospital * Reside in a zip code served by the participating clinics Exclusion Criteria: * Provider feels that study participation is not in patient's best interest * Does not understand English or Spanish well enough to follow recommendations * Plans to move from the study area served by the participating clinics

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

Successful use of the intervention and control programs measured by enrollment aggregate

Timeframe: 6-9 months

Successful use of the intervention and control programs as determined by the systolic and diastolic blood pressure measurements

Timeframe: 6-9 months

Successful use of the intervention and control programs as determined by postpartum blood pressure measurement

Timeframe: 6-9 months

Adequacy of prenatal care

Timeframe: 6-9 months

Adverse composite maternal outcome

Timeframe: 6-9 months

Trial details

NCT IDNCT07691541

SponsorTulane University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2029-07

Contact for this trial

Emily W Harville, PhD

504-988-7327 harville@tulane.edu

View on ClinicalTrials.gov More Maternal Health Care trials

Who can participate

Age range

18 Years – 80 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

What they're measuring

Successful use of the intervention and control programs measured by enrollment aggregate

Timeframe: 6-9 months

Successful use of the intervention and control programs as determined by the systolic and diastolic blood pressure measurements

Timeframe: 6-9 months

Successful use of the intervention and control programs as determined by postpartum blood pressure measurement

Timeframe: 6-9 months

Adequacy of prenatal care

Timeframe: 6-9 months

Adverse composite maternal outcome

Timeframe: 6-9 months