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FamilyLink Family-Centered Rounds

2021年3月3日更新者：University of California, Davis

FamilyLink Family-Centered Rounds Pilot Study

This study will be a pilot test of using FamilyLink software to bring parents of patients in the neonatal intensive care unit (NICU) virtually to the bedside during Family Centered Rounds.

研究概览

地位

完全的

条件

Family Centered Rounds

干预/治疗

研究类型

介入性

注册 (实际的)

110

阶段

不适用

联系人和位置

本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。

学习地点

美国
- California
  - Sacramento、California、美国、95817
    - University of California-Davis

参与标准

研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

孩子
成人
年长者

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

Patients admitted to the Blue Team in the NICU aged 0-365 days
Parents/guardians of patients admitted to the Blue Team in the NICU aged ≥ 18 years
Medical team members (physicians, nurse practitioners, fellows, residents, medical students, nurses) of patients admitted to the Blue Team in the NICU aged ≥ 18 years

Exclusion Criteria:

Patients who are not discharged home from the NICU (e.g., transferred to another inpatient unit or another hospital)
Parents/guardians of patients admitted to the Blue Team in the NICU who do not speak English, as a translator will not reliability be available to participate in rounds when the parent/guardian is not physically present
Patients who have more than one admission to the Blue Team during our study period will only be included on their first admission

学习计划

本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。

研究是如何设计的？

设计细节

主要用途：卫生服务研究
分配：随机化
介入模型：并行分配
屏蔽：无（打开标签）

手臂数量

武器和干预

参与者组/臂	干预/治疗
实验性的：Telemedicine FCR These patients will be eligible to use telemedicine for Family Centered Rounds	其他：Telemedicine FCR Parents/guardians will be able to join family centered rounds using telemedicine (audio and visual)
安慰剂比较：Control These patients will not be eligible to use telemedicine for Family Centered Rounds (standard of care)	其他：Standard of care Parents/guardians will not be able to join family centered rounds using telemedicine (audio and visual)

研究衡量的是什么？

主要结果指标

结果测量	措施说明	大体时间
CAHPS Communication with Parent Subscale 大体时间：Through study completion, approximately 3 months	19 questions from the Communication with Parent Subscale of the Consumer Assessment of Healthcare Providers and Systems Child Hospital Survey; specifically, we will report the following measures: Communication between you and your child's nurses (composite measure); Communication between you and your child's doctors (composite measure); Communication about your child's medicines (composite measure); Keeping you informed about your child's care (composite measure) Privacy when talking with doctors, nurses, and other providers (single-item measure); Preparing you and your child to leave the hospital (composite measure); Keeping you informed about your child's care in the Emergency Room (single-item measure). Higher scores are better; 0 (minimum) - 100 (maximum)	Through study completion, approximately 3 months

次要结果测量

结果测量	措施说明	大体时间
Rates of adverse events 大体时间：Up to 6 months	Rates of adverse events reported by parents, providers, or nurses	Up to 6 months
Hospital Length of Stay 大体时间：Through study completion, approximately 3 months	Hospital length of stay of the patient measured in days	Through study completion, approximately 3 months
Breastmilk at discharge 大体时间：Through study completion, approximately 3 months	If the patient was receiving all, some or no breastmilk	Through study completion, approximately 3 months

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

University of California, Davis

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2020年4月1日

初级完成 (实际的)

2020年11月23日

研究完成 (实际的)

2021年2月2日

研究注册日期

首次提交

2020年2月7日

首先提交符合 QC 标准的

2020年2月10日

首次发布 (实际的)

2020年2月11日

研究记录更新

最后更新发布 (实际的)

2021年3月5日

上次提交的符合 QC 标准的更新

2021年3月3日

最后验证

2021年3月1日

FamilyLink Family-Centered Rounds