Exploring the Effect of Discharge Education, Blood Pressure Cuffs, and Postpartum Bracelets to Improve Health Among Newly Diagnosed Gestational Hypertension and Preeclampsia Patients During the Postpartum Period.

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
AgeNot listed
SponsorMemorial Hermann Health System

About this trial

This pilot, exploratory qualitative, descriptive study will examine whether standard postpartum discharge education, a free home blood pressure cuff, and an "At-Risk Postpartum" bracelet support self-management among postpartum patients newly diagnosed with preeclampsia or gestational hypertension at Memorial Hermann Memorial City Medical Center. Up to 40 eligible patients will receive standard postpartum education supplemented with blood pressure monitoring instruction, the Preeclampsia Foundation's blood pressure guidance sheet, and a bracelet intended to serve as a visual reminder of postpartum risk. Participants will complete virtual interviews at 6 and 10 weeks post-discharge to assess home blood pressure monitoring, knowledge retention, perceived usefulness of the bracelet, self-advocacy, and barriers to following recommended self-management behaviors. Findings will help determine whether these low-burden educational and practical tools can improve postpartum awareness, engagement, and safety, and will inform the design of a larger future study.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Patients with a preexisting diagnosis of chronic hypertension or PE, or are currently on antihypertensive medications (as these factors may influence self-management behaviors and outcomes).

Trial design

Design model

Single group

Treatments tested in this trial

  • Education, Blood Pressure Cuff, and Visual Cue Bracelet

    Other intervention

    In Family Life Center the intervention will be to provide standard education, at-risk bracelet, and BP cuff on discharge day. We are combining these practical tools to enhance self-management, knowledge, and engagement.

Treatment groups

40 Participants
are divided into 1 treatment group
Group A: Blood Pressure Cuff, At-Risk Postpartum Bracelet, and In Hospital Preeclampsia EducationOther 1 intervention

Trial outcomes

Primary outcomes

1

Evidence of Blood Pressure Self-Management

The primary outcome measure assesses whether the intervention supports postpartum blood pressure self-management among participants newly diagnosed with gestational hypertension or preeclampsia. This outcome is evaluated through the 6-week and 10-week semi-structured interview by asking participants if they are using tools to measure their blood pressure, and what action they are taking to manage their blood pressure and what barriers they face.

Time frame
6-10 weeks

Secondary outcomes

1

Postpartum Bracelet Stimulates Self-Management Behaviors

The secondary outcome measure evaluates whether the "At-Risk Postpartum" bracelet serves as a visual reminder that reinforces self-management of preeclampsia and gestational hypertension. The semi-structure interviews address this outcome by asking participants at 6 and 10 weeks whether they wear the postpartum bracelet, why or why not, what value the bracelet adds if they wear it, and whether something else inspires them to take care of themselves if they do not wear it.

Time frame
6-10 weeks

Other outcomes

1

In Hospital Preeclampsia Education on Self-Management

The tertiary outcome measure determines whether participants retain the in-hospital education they received about preeclampsia signs and symptoms, blood pressure management, and appropriate follow-up actions. This is assessed through the semi-structured interviews by asking participants, in their own words, to describe signs and symptoms associated with preeclampsia, what they would do if they recognized those symptoms, and whether they remember any education about preeclampsia and blood pressure management if they are unable to identify the signs and symptoms.

Time frame
6-10 weeks

Locations

This trial has no locations.

Sponsors and contacts

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