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临床试验/NCT06410287
NCT06410287
已完成
不适用

Feasibility of an Art-based Intervention to Address Clinician Stigma and Improve Care for Neonatal Opioid Withdrawal Syndrome

University of Michigan2 个研究点 分布在 1 个国家目标入组 99 人2024年7月1日

概览

阶段
不适用
干预措施
ArtSpective
疾病 / 适应症
Nurse's Role
发起方
University of Michigan
入组人数
99
试验地点
2
主要终点
Nurse Stigma Toward Perinatal Substance Use
状态
已完成
最后更新
上个月

概览

简要总结

The goal of this pilot clinical trial is to evaluate the feasibility and limited effectiveness of a digital, arts-based educational intervention addressing nurse stigma towards perinatal substance use. The main questions it aims to answer are:

  • What is the the feasibility of delivering the training through an asynchronous, web-based platform?
  • What is the limited effectiveness of the program on nurse stigma towards perinatal substance use?

Participants will access and complete the training, including completion of a perinatal substance use stigma scale at baseline, immediately post, and 1-2 months month later. Participants will also be invited to participate in an interview.

Researchers will compare the intervention and control groups to see if the training reduces nurse stigma towards perinatal substance use.

注册库
clinicaltrials.gov
开始日期
2024年7月1日
结束日期
2024年11月30日
最后更新
上个月
研究类型
Interventional
研究设计
Parallel
性别
All

研究者

责任方
Principal Investigator
主要研究者

Clayton John Shuman

Assistant Professor

University of Michigan

入排标准

入选标准

  • Age 18 years or older
  • Licensed as a registered nurse
  • Works at least part time
  • Works on a labor, postpartum, nursery, neonatal intensive care, or pediatric unit in one of the participating hospitals

排除标准

  • Works as per diem or agency nurse
  • Not employed by a participating hospital
  • Not a perinatal/pediatric nurse

研究组 & 干预措施

Site 1

Participants from the hospital randomized to the experimental group will be first to receive an invitation to complete the web-based educational program. The program will be open for one month. Thirty days after a participant completes the program, they will be sent a link to a follow up survey (web-based). At 60 days, participants who completed the program and the first follow up survey will be randomized to complete a second follow up survey or participate in a 1:1 interview.

干预措施: ArtSpective

Site 2

Participants from the hospital randomized to the control setting will receive an invitation to complete a survey that collects baseline data for the outcome (stigma toward perinatal substance use) and demographic information. After thirty days, participants will be invited to complete the web-based educational program. Thirty days after completion, they will receive a link to a web-based follow up survey.

干预措施: ArtSpective

结局指标

主要结局

Nurse Stigma Toward Perinatal Substance Use

时间窗: Baseline (Phase 1a); immediately post intervention (Site 1) or 7-30 days post baseline (Site 2) (Phase 1b); immediately post (Site 2) or 30 days post intervention (Site 1) (Phase 2); 30 days post (Site 2) or 60 days post intervention (Site 1) (Phase 3)

Negative or stigmatizing attitudes and/or beliefs registered nurses have towards perinatal substance use; measured using the Modified Attitudes About Drug Use in Pregnancy Scale. Total scores range between 1 and 5, with scores closer to 1 associated with a more positive outcome.

次要结局

  • Acceptability(immediately post intervention (Site 1= Phase 1b; Site 2 = Phase 2))

研究点 (2)

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