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Better Understanding Patient Perspectives of an Educational Tool for Postpartum Hypertensive Patients

NCT06996496 · Status: ACTIVE_NOT_RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 150

Last updated 2025-09-23

No results posted yet for this study

Summary

The goal of this clinical trial is to learn if an educational tool helps postpartum patients after having high blood pressure during their pregnancy. The main question it aims to answer is:

Does receiving this educational tool improve patient activation in the postpartum period?

Researchers will compare a group of postpartum patients who get the tool 0-2 weeks after delivery with patients who do not get the tool to see if there is a difference in their activation scores 4-12 weeks later.

Participants will:

Complete a survey at first contact with study staff

Complete a similar follow-up survey 4-12 weeks later

Conditions

  • Hypertension, Pregnancy Induced

Interventions

OTHER

Postpartum educational tool after hypertensive pregnancy

postpartum educational tool for patients having experienced a hypertensive disorder of pregnancy

Sponsors & Collaborators

  • CVS Health Foundation

    collaborator UNKNOWN

  • Brigham and Women's Hospital

    lead OTHER

Principal Investigators

  • Ann Celi, MD, MPH · Brigham and Women's Hospital

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2024-09-18
Primary Completion
2025-09-02
Completion
2026-08-31

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT06996496 on ClinicalTrials.gov