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NCT05655936 · ClinicalTrials.gov registry record · NA

Eliminating Severe Maternal Morbidity With Heart Health Doulas Trial

A NA study of Obesity and Hypertension, sponsored by University of Pittsburgh.

Recruiting
Registry status
NA
Development phase
454
Enrollment target
1
Study location

NCT05655936 is a NA study of Obesity and Hypertension that is actively recruiting participants, run by University of Pittsburgh. The registered enrollment target is 454 participants, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (45% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05655936, a NA study of Obesity and Hypertension, is actively recruiting participants, sponsored by University of Pittsburgh.

RECRUITING
Registry status
NA
Development phase
454 participants
Enrollment target
1
Study location

Study Summary

This is a single site, single-blinded parallel randomized control trial that investigates a multi-level intervention to improve postpartum blood pressure in women with hypertensive disorder pregnancy. The investigators will recruit women diagnosed with a hypertensive disorder of pregnancy, identified between 3rd trimester and 2 weeks post-delivery. The investigators will randomize participants to receive usual care home blood pressure monitoring for 6 weeks versus an intervention of usual care + blood pressure and weight monitoring + a doula trained in heart health. This trial will be conducted in partnership with a local community-based organization, Healthy Start Inc.

Interventions

  • BEHAVIORAL Usual Care
  • BEHAVIORAL Heart Health Doula Intervention Program

Study Locations (1)

Pennsylvania

  • Magee Women's Hospital of UPMC - Pittsburgh

Trial Details

FieldValue
Enrollment Target 454 participants
Start Date 2023-06-29
Est. Completion 2027-07-01
Phase NA

Sponsor

University of Pittsburgh

1,238 total trials

What the Registry Record Tells You About NCT05655936

The ClinicalTrials.gov registry entry for NCT05655936 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 454 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 819-participant average among 1,053 other Obesity trials with a reported enrollment target (45% lower). The listed sponsor is University of Pittsburgh, which has 1,238 total studies on file at ClinicalTrials.gov.

The record links to 10 conditions, with Obesity appearing as the primary indexed condition, and to 2 interventions - of which Usual Care is the first listed.

NCT05655936 reports 1 study location spanning 1 distinct geographic area - top geographies include Pennsylvania.

Frequently Asked Questions

What is clinical trial NCT05655936 about?

NCT05655936 is a clinical study titled "Eliminating Severe Maternal Morbidity With Heart Health Doulas Trial". This is a single site, single-blinded parallel randomized control trial that investigates a multi-level intervention to improve postpartum blood pressure in women with hypertensive disorder pregnancy. The investigators will recruit women diagnosed with a hypertensive disorder of pregnancy, identifie...

What is the current status of trial NCT05655936?

This trial is currently recruiting. It is a NA study. The enrollment target is 454 participants. The study started on 2023-06-29. Estimated completion is 2027-07-01.

What conditions does trial NCT05655936 study?

This clinical trial studies the following conditions: Obesity, Hypertension, Overweight, Vascular Diseases, Preeclampsia.

What interventions are being tested in trial NCT05655936?

The interventions under investigation include: Usual Care (BEHAVIORAL), Heart Health Doula Intervention Program (BEHAVIORAL).

Who is sponsoring clinical trial NCT05655936?

This trial is sponsored by University of Pittsburgh, which has 1,238 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05655936 being conducted?

This trial has 1 study location across Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.