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OpenTrials
Completed

NCT Number: NCT03733405

Postpartum Care Timing: A Randomized Trial

The purpose of this study is to determine if shortening the time to initial postpartum visit from six weeks to two weeks can improve clinic visit attendance and decrease usage of the emergency department.

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Key information

Age range

18 year–50 year

Sex eligibility

Female

Study type

Interventional

Phase

Not applicable

Primary location

University of California Los Angeles

Los Angeles, California, 90095, United States

About this study

Postpartum care is an integral component to completing the maternal peripartum experience and transitioning the patient to well-women care. The American Congress of Obstetrics and Gynecology has recently highlighted the importance of this "fourth stage" of pregnancy suggesting earlier and more comprehensive visits compared to the standard 6-week postpartum visit. Specifically they describe that "all women should ideally have contact with a maternal care provider within the first three weeks postpartum" however this is largely derived from expect opinion and retrospective data. The current rate of postpartum visit attendance is as low as 66%, especially in women with scant prenatal care. In the investigators government-funded clinic, the postpartum clinic attendance in 2017 was 69% and many of the patients have co-morbidities, notably a 25% rate of psychiatric illness. Additionally, in this population, the investigators have identified a high rate of Emergency Department (ED) usage (8.7%) within 30 days of delivery suggesting that perhaps an earlier routine visit is ideal and can prevent the use of the ED. The aim therefore is to evaluate the utility of an early postpartum visit at two weeks in addition to a standard six-week visit with a randomized control trial.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • At least 18 years of age
  • Receives antepartum, intrapartum and postpartum care at UCLA
  • Speaks English or Spanish
  • Provides informed consent for study participation
  • Vaginal, cesarean delivery or operative vaginal delivery

Exclusion criteria

  • Cognitive impairment, psychiatric instability, or language barriers that limit her ability to provide informed consent
  • Plans to received postpartum care at other institution

Treatment and study plan

Postpartum Visit at 6 Weeks

Behavioral

The patient will be scheduled for a routine postpartum visit at the standard time interval. Each postpartum visit will consist of the standard interview and physical examination. The purpose of this visit is for routine postpartum care. If she has a medical complication during delivery, she may be recommended to schedule an additional earlier visit.

Postpartum Visit at 2 Weeks

Behavioral

The patient will be scheduled for an earlier postpartum visit in addition to the standard time interval. Each postpartum visit will consist of the standard interview and physical examination. The purpose of this visit is for routine postpartum care. If she has a medical complication during delivery, she may be recommended to schedule an additional earlier visit.

Primary outcomes

  1. Attendance at one or more routine postpartum visits

    Time frame: 8 weeks postpartum

    The primary outcome will be the attendance at one or more scheduled postpartum visits at the clinic where the patient received her prenatal care.

Secondary outcomes

  1. Rate of Emergency Department usage within 30 days of delivery

    Time frame: 30 days postpartum

    The secondary outcome will be the presentation and usage of an Emergency Department during the 30 days since delivery of the baby.

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Registry information

Official study title

Randomized Control Trial of Postpartum Visits at Two or Six Weeks to Evaluate Clinic Attendance and Emergency Department Usage

Acronym: PUnCTuAL

Important dates

Study start
2018
Primary completion
2020
Study completion
2020
First posted
Nov 7, 2018
Registry last updated
Nov 4, 2020

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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