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临床试验/NCT06483022
NCT06483022Enrolling By Invitation不适用

Building Equitable Linkages With Interprofessional Education Valuing Everyone

University of North Carolina, Chapel Hill2 个研究点 分布在 1 个国家目标入组 32,000 人开始时间: 2024年7月1日最近更新:
适应症

试验速览

阶段
不适用
状态
Enrolling By Invitation
入组人数
32,000
试验地点
2
主要终点
Severe Postpartum Pain

研究概览

简要总结

This is a step-wedge design implementation protocol of an interprofessional education curriculum intervention that is delivered through virtual reality and designed to reduce disparities and improve patient experiences in receiving maternal healthcare.

研究设计

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

入排标准

年龄范围
18 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Healthcare Team Participants
  • Employed as one of the following roles: maternity care provider, nurse, lactation consultant or doula.
  • Primary inpatient clinical assignment is maternity care.
  • If Per Diem: Employed for a minimum of 4 shifts/month at a participating site.
  • Birthing Parent Data Extraction Participants
  • Had a live birth at a participating site from the start of the study through the last Data Retrieval timepoint.
  • Birthing Parent Interview Participants
  • Had a live birth at a participating site from the start of the study through the last Data Retrieval timepoint.
  • Black race or Limited English Proficiency with preferred language of Spanish.
  • Age ≥ 18.

排除标准

  • Healthcare Team Participants
  • Birthing Parent Data Extraction Participants
  • Baby with birth gestational age < 24 weeks.
  • Birthing Parent Interview Participants
  • Baby with birth gestational age < 24 weeks.
  • Baby is no longer alive at time of Data Retrieval (regardless of gestational age).
  • Currently incarcerated.
  • Previously completed a birthing parent interview for the BELIEVE study.
  • Previously enrolled as a Healthcare Team Participant.

结局指标

主要结局

Severe Postpartum Pain

时间窗: 0 to <24 and 24 to <48 hours postpartum

Proportion of individuals with severe pain postpartum. Severe pain will be defined as pain score \>4 on postpartum day 1 following vaginal birth, or pain score \>7 on postpartum day 2 following cesarean birth, as documented in the electronic health record using the Numerical Rating Scale (NRS) of patient-reported pain from 0-10.

次要结局

  • Birthing parent-reported experiences of the respectful care (Qualitative)(2-8 weeks postpartum)
  • Patient-reported examples of respectful and equitable health care team member practices (Qualitative)(2-8 weeks postpartum)
  • Patient-reported examples of supportive health team member practices for pain management (Qualitative)(2-8 weeks postpartum)
  • Pain assessments(0 to <24 and 24 to <48 hours postpartum)
  • NSAID doses administered(0 to <24 and 24 to <48 hours postpartum)
  • MMEs administered(0 to <24 and 24 to <48 hours postpartum)
  • Acetaminophen doses administered(0 to <24 and 24 to <48 hours postpartum)
  • Healthcare team members' perceptions of interprofessional collaboration(Baseline (pre-intervention) and after completing the IPC training intervention, a total of up to 4 months)
  • Quality of interprofessional teamwork(Baseline (pre-intervention) and after completing the IPC training intervention, a total of up to 4 months)
  • Feasibility of the IPC training(2-8 weeks after health care team members' completion of the IPC training)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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