Reshaping Postpartum Follow-up

Status Recruiting

Clinical Trial 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.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT06054841
Study type	Interventional
Source	Medstar Health Research Institute
Contact	Rosanna Sobota
Phone	2028778035
Email	rosanna.sobota@medstar.net
Status	Recruiting
Phase	N/A
Start date	May 22, 2023
Completion date	March 1, 2025

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