Clinical Trials Directory

Trials / Active Not Recruiting

Active Not RecruitingNCT06373367

Preeclampsia Educational Program Study (PrEPS)

Preeclampsia Educational Program Study

Status
Active Not Recruiting
Phase
N/A
Study type
Interventional
Enrollment
36 (actual)
Sponsor
MemorialCare Health System · Academic / Other
Sex
Female
Age
18 Years
Healthy volunteers
Not accepted

Summary

Preeclampsia complicates approximately 8% of all pregnancies. A critical factor of outpatient monitoring is patient education; specifically, education regarding nature of the disease, ongoing short- and long-term risks, and warning signs and symptoms for worsening of disease. This study aims to compare patient knowledge using a novel illustration based app compared to standard discharge instructions.

Detailed description

Preeclampsia complicates approximately 8% of all pregnancies. While many patients improve following delivery, the disease process remains a leading cause for postpartum morbidity and mortality. A critical factor of outpatient monitoring is patient education; specifically, education regarding nature of the disease, ongoing short- and long-term risks, and warning signs and symptoms for worsening of disease. There is a gap in the literature regarding effective, patient-centered educational tools specifically addressing these elements, especially in the postpartum period. The investigators propose a pilot, randomized controlled trial of postpartum patients with preeclampsia. The intervention of interest is an illustration-based, educational mobile device application (app) focused on the short- and long-term risks associated with preeclampsia and warning signs and symptoms of worsening disease postpartum. The control for this study will be the same information in a text-only format, also accessed through a mobile device app. The investigators central hypothesis is that an illustration-based app will improve knowledge of preeclampsia among postpartum patients compared to text-only educational material. Specific Aim 1: Compare the difference in preeclampsia knowledge score from text-only versus illustration-based education 24 hours post intervention (short-term). The investigators hypothesize that patients who receive illustration-based education will have a) higher preeclampsia knowledge scores at 24 hours post-intervention compared to text-only educational materials and b) a greater increase in preeclampsia knowledge score from baseline (pre-test) compared to text-only education. Specific Aim 2: Compare the difference in preeclampsia knowledge score from text-only versus illustration-based education \>4 weeks post intervention (long-term). The investigators hypothesize that patients who receive illustration-based education will have a) higher preeclampsia knowledge scores at \> 4 weeks post-intervention compared to text-only educational materials and b) a greater increase in preeclampsia knowledge score from baseline (pre-test) compared to text-only education.

Conditions

Interventions

TypeNameDescription
OTHERIllustration based applicationIllustrations regarding the cause, risks, and warning signs of preeclampsia
OTHERText based applicationStandard preeclampsia discharge instructions

Timeline

Start date
2024-10-01
Primary completion
2025-05-29
Completion
2026-05-31
First posted
2024-04-18
Last updated
2025-10-09

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT06373367. Inclusion in this directory is not an endorsement.