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Reshaping Postpartum Follow-up

Reshaping Postpartum Follow-up in Women With High Risk Pregnancies

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06054841
Enrollment
157
Registered
2023-09-26
Start date
2023-05-22
Completion date
2025-03-01
Last updated
2025-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cervical Dysplasia, Gestational Diabetes, Hypertension in Pregnancy

Keywords

Postpartum followup, hypertensive disorders of pregnancy, eclampsia, pre-eclampsia, pap smear, gestational diabetes

Brief summary

The aim of this study is to evaluate the impact of personalized postpartum follow-up cards on completion of postpartum health related tasks. The intervention will consist of a card given to patients at time of discharge. One side of the card will list the patient's name and a list of recommended postpartum follow-up appointments based on their diagnoses at the time of discharge. Participants will be randomized to this intervention or the control group, which will consist of standard education routinely given at discharge. The primary endpoint will be the rate of completion of a postpartum blood pressure check or two hour glucose tolerance test, or both, depending on the patient's discharge diagnosis within the first year after discharge. The secondary endpoints will include establishing care with a primary care provider within the first year after delivery, or completion of postpartum pap smear or colposcopy, as indicated.

Interventions

BEHAVIORALPostpartum follow up card

The intervention will consist of a card given to patients at time of discharge. One side of the card will list the patient's name and a list of recommended postpartum follow-up appointments based on their diagnoses at the time of discharge. The back of the card will list relevant phone numbers to assist patients with scheduling.

OTHERControl

No deviation from standard discharge education

Sponsors

Medstar Health Research Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
NONE

Eligibility

Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* Subjects \>=18 years of age * Ability to read English or Spanish * Delivered via vaginal delivery or c-section within the past 48 hours * Able to consent for themselves

Exclusion criteria

* Received antepartum care at a facility outside of the Medstar system or plans to continue care with a facility outside of the Medstar system

Design outcomes

Primary

MeasureTime frameDescription
Blood pressure check6 monthsRate of attendance at a blood pressure check one week postpartum
Two hour glucose tolerance test6 monthsRate of completion of two hour glucose tolerance test at six weeks postpartum

Secondary

MeasureTime frameDescription
Cervical cancer screening6 monthsRate of completion of postpartum pap smear or colposcopy as indication
Primary care6 monthsRate of attendance at visit with primary care provider for annual exam

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026