跳至主要内容
临床试验/NCT06586541
NCT06586541招募中不适用

Family Participation in Intensive Care Unit Rounds (The Family-ICU Trial)

Lady Davis Institute2 个研究点 分布在 1 个国家目标入组 194 人开始时间: 2024年11月18日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
194
试验地点
2
主要终点
FAMily Engagement (FAME) score within 1 week of ICU discharge

研究概览

简要总结

Family inclusion in adult intensive care unit (ICU) rounds is recommended by critical care professional societies, yet widespread uptake of this practice is limited. A key barrier cited by ICU clinicians is insufficient evidence to support this practice. There is a need for robust evidence to support family participation in adult ICU rounds and influence change to routine clinical care. The primary purpose of this study is to assess whether family participation in adult ICU rounds improves family engagement in care. The secondary objectives are to assess family satisfaction, and anxiety and depression, to explore user experiences of family participation in ICU rounds, and to evaluate strategies to improve family member recruitment and retention rates. This is a stepped-wedge cluster randomized trial (n=194) at 6 Canadian ICUs. The stepped wedge cluster randomized trial is a pragmatic study design that overcomes methodological limitations in evaluating a healthcare service delivery intervention. In the stepped-wedge cluster design, there is random and sequential crossover of clusters from control (phase 1) to intervention (phase 2) until all clusters are exposed. The stepped-wedge design also allows each site to function as its own control. The stepped-wedge design is more powerful than a parallel design when substantial cluster level effects are present.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Crossover
主要目的
Health Services Research
盲法
Double (Investigator, Outcomes Assessor)

入排标准

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

入选标准

  • •Adult family members (age ≥ 18 years) of ICU patients
  • •Expected ICU stay ≥ 48 hours

排除标准

  • •Family members who do not wish to participate in care
  • •Repeat admissions within the study period
  • •Another family member has already participated in the study

研究组 & 干预措施

Phase 1 (Control group)

No Intervention

Participants will be able to engage in care as per current family engagement practices. Family members in the usual care group will not participate in daily ICU rounds. In-person family participation in rounds is not routinely performed at any of the trial sites.

Phase 2 (Intervention)

Experimental

Participants in the Intervention group will be invited to participate in attending team rounds.

干预措施: Participation in attending team rounds (Other)

结局指标

主要结局

FAMily Engagement (FAME) score within 1 week of ICU discharge

时间窗: 1-week post-hospital discharge

The FAMily Engagement (FAME) tool is a self-administered 12-item questionnaire that assesses an individual's current engagement practice. FAME uses a five-point Likert scale ranging from 1 (strongly agree) to 5 (strongly disagree), and scale results are changed to a 0-100 scoring system, with higher scores indicating greater engagement in care. The following subdomains are evaluated: engagement perception, family presence, communication, education, decision-making, care contribution, and family needs. FAME includes the following engagement domains: family presence, family needs, communication and education, decision making, and direct care. FAME also captures the following family-centered care principles: dignity and respect, information sharing, participation, and collaboration.

Quality of communication (QOC score)

时间窗: 1-week post-hospital discharge

The Quality of Communication tool is a 13-item questionnaire that was developed and validated in an ICU setting to measure the perceived quality of communication. Scores range from 0 to 100, with higher scores indicating better clinician-family communication.

次要结局

  • Anxiety and depression (HADS)(1-week post-hospital discharge)
  • Post-traumatic stress (IES-Revised)(6 months post-hospital discharge)
  • Family satisfaction in the ICU (FS-ICU)(1-week post-hospital discharge)
  • Quality of life (EuroQOL-5D-5L score)(6 months post-hospital discharge)
  • Anxiety and depression (HADS)(6 months post-hospital discharge)

研究者

发起方
Lady Davis Institute
申办方类型
Other
责任方
Principal Investigator
主要研究者

Michael Goldfarb

Attending Staff, Division of Cardiology

Lady Davis Institute

研究点 (2)

Loading locations...

相似试验