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临床试验/NCT03733405
NCT03733405已完成不适用

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

University of California, Los Angeles1 个研究点 分布在 1 个国家目标入组 256 人开始时间: 2018年10月31日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
256
试验地点
1
主要终点
Attendance at one or more routine postpartum visits

研究概览

简要总结

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.

详细描述

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.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Prevention
盲法
None

入排标准

年龄范围
18 Years 至 50 Years(Adult)
性别
Female
接受健康志愿者
是

入选标准

  • •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

排除标准

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

研究组 & 干预措施

Postpartum Visit 6 Weeks

Experimental

Participants will have a postpartum visit scheduled 6 weeks after birth

干预措施: Postpartum Visit at 6 Weeks (Behavioral)

Postpartum Visit 2 and 6 Weeks

Experimental

Participants will have postpartum visits scheduled 2 and 6 weeks after birth

干预措施: Postpartum Visit at 6 Weeks (Behavioral)

Postpartum Visit 2 and 6 Weeks

Experimental

Participants will have postpartum visits scheduled 2 and 6 weeks after birth

干预措施: Postpartum Visit at 2 Weeks (Behavioral)

结局指标

主要结局

Attendance at one or more routine postpartum visits

时间窗: 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.

次要结局

  • Rate of Emergency Department usage within 30 days of delivery(30 days postpartum)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Ilina Datkhaeva

Co-principal investigator

University of California, Los Angeles

研究点 (1)

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