跳至主要内容
临床试验/NCT03777527
NCT03777527Unknown不适用

My PICU Diary: a Patient Diary for Critically Ill Children

McMaster University1 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2019年10月30日最近更新:
适应症

试验速览

阶段
不适用
入组人数
20
试验地点
1
主要终点
Patient Diary Acceptability

研究概览

简要总结

The PICU-Diary study is a prospective single centre pilot study in the Pediatric Critical Care Unit at McMaster Children's Hospital. We will evaluate the impressions of family caregivers and healthcare providers on the PICU Patient Diary, and its acceptability for use in the PICU, using mixed methods. We will assess the feasibility of assessing the impact of a patient diary on PICU outcomes and psychological distress in critically ill children, 1 month following PICU discharge.

详细描述

There is considerable need for research dedicated to exploring interventions to improve the psychological and functional effects of critical care admission on patients and families. Patient diaries are one approach that has been used in several adult critical care groups and has been shown to positively impact patient care by helping patients better understand their illness, acting as a therapeutic tool and debriefing aid, and providing an outlet for caregivers to participate in care plans. However, to date, there is minimal research available in the pediatric population.

The specific objectives of this study are to evaluate the acceptability and impressions of a patient diary as a supportive measure for critically ill children in the PICU. Our secondary objective is to evaluate the feasibility of measuring the impact of a patient diary on psychological distress in critically ill children, following discharge from the PICU.

The purpose of this diary is to support the recovery of critically ill children and their family members by:

  1. Helping patients understand visually and in written form as age appropriate, what has happened to them during their PICU stay, how ill they were, and in so doing, reduce anxiety and post-traumatic stress symptoms; AND
  2. Serving as an engagement tool to help families take on an informed, active role in their child's care plan.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

入排标准

性别
All
接受健康志愿者

入选标准

  • Consecutive patients admitted to the PICU will be screened for eligibility to participate in the evaluation component of the PICU Diary study
  • We will offer a PICU Diary to families of any critically ill children admitted to the PICU for at least 72 hours and who are fluent in the English language
  • Eligible patients and their families will be approached for consent to participate, by a member of the investigator team (MB, KC, SB or CC). For those who consent to participate, they will be oriented to the diary and its use.

排除标准

  • Stay less than 72 hours
  • Not fluent in the English language

结局指标

主要结局

Patient Diary Acceptability

时间窗: 1 day

Acceptability of the diary to family members, patients, and healthcare providers in the PICU to determine the perception of impact of the diary on patient recovery. Information collected with surveys and qualitative interviews.

Feasability of measuring psychological well-being

时间窗: 1 day

Patient reported outcome measure of psychological well-being after critical illness with Children's Critical Illness Impact Scale

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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