跳至主要内容
临床试验/NCT02333396
NCT02333396已完成不适用

Improving Communication in the Pediatric Intensive Care Unit for Patients Facing Life-Changing Decisions: The Navigate Study

Ann & Robert H Lurie Children's Hospital of Chicago4 个研究点 分布在 1 个国家目标入组 442 人开始时间: 2015年4月6日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
442
试验地点
4
主要终点
Satisfaction With Decision Making (Percentage of "Excellent" Scores in the Decision Making Domain of the Pediatric Family Satisfaction in the Intensive Care Unit (pFS-ICU) Questionnaire)

研究概览

简要总结

The project seeks to study the use of an navigator-based intervention called "PICU Supports." The study will test the impact of PICU Supports during and after PICU discharge on parent outcomes (satisfaction with decision making, decision regret, anxiety, depression, post-traumatic stress, health-related quality of life, and complicated bereavement) and on parent and healthcare team member assessments of communication and team collaboration.

详细描述

Parents of children admitted to the PICU often face challenging decisions. Research demonstrates deficiencies in communication in the PICU which could impact decision making. This study team has developed a navigator-based intervention call PICU Supports. PICU Supports aims to provide the following types of support to parents of patients in the PICU: emotional; communication (between healthcare team members and parents/families as well as among healthcare team members ); decision making; transitions out of the PICU (i.e. discharge transitions to a non-PICU hospital bed, a long term care facility, or home); and information. Support is accomplished by navigator engagement with parents and healthcare team members and the guided use of navigator supported ancillary tools provided to parents and healthcare team members as needed. During the patient's PICU stay, the navigator activities and use of ancillary tools is directed by the family's needs. Thus PICU Supports uses a predefined framework of activities and tools to provide individualized support directed by the needs of the parent and the patient situation. This research will test PICU Supports in the clinical setting. This will be accomplished by conducting a pilot study of PICU Supports at Ann & Robert H. Lurie Children's Hospital of Chicago (Lurie Children's Hospital), followed by a randomized controlled trial (RCT) comparing the intervention, PICU Supports, to a control, parental receipt of an educational brochure. The RCT will be conducted at Lurie Children's Hospital and at University of Chicago Medicine Comer Children's Hospital (Comer Children's Hospital).

研究设计

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

入排标准

性别
All
接受健康志愿者

入选标准

  • Case Patients
  • patients < 18 years of age admitted to the PICU
  • parents are English or Spanish-speakers and who:
  • are likely to require PICU care for at least 24 hours (as determined by the PICU attending physician) or
  • have a Pediatric Index of Mortality 2 (PIM2) score ≥ 4% (a PIM2 score predicts risk of mortality based on clinical data collected at the time of admission to the PICU)
  • Case patients will be included in the study if one of his/her parents agrees to participate in the study and signs a written consent form.
  • Parents of case patients
  • Parent of an eligible case patient.
  • PICU attending gives permission to approach the parent about the study.
  • Parent is an English or Spanish speaker.
  • Parent provides written consent for participation.
  • Healthcare Team Members for the pre-post assessment of team communication and focus group:
  • This group will include as many clinicians in the following groups as possible (identified by the site principal investigator): PICU physicians (attendings and fellows); PICU bedside nurses; PICU Advance Practice Nurses (APNs); hospitalists; subspecialty physicians who consult on PICU patients; subspecialty APNs who consult on PICU patients; PICU respiratory therapist; PICU physical/occupational/speech therapists; and social workers (SWs), chaplains, and case managers who follow PICU patients.
  • Healthcare team members for the written feedback/assessment of the intervention:
  • HTMs caring for the case patient at the time of PICU discharge: (PICU attending; PICU fellow; social worker (if involved); chaplain (if involved); bedside nurse; PICU resident, APN or hospitalist; and one to two subspecialty attendings)

排除标准

  • Exclusion criteria for parents of case patients:
  • PICU attending does not give permission to approach the parent about the study.
  • Parent is not an English or Spanish speaker.
  • Parent does not provide written consent to participate.
  • The case patient does not provide assent (if able to provide assent).
  • Exclusion criteria for Healthcare Team members:
  • Healthcare team member that does not regularly care for patients in the PICU.

结局指标

主要结局

Satisfaction With Decision Making (Percentage of "Excellent" Scores in the Decision Making Domain of the Pediatric Family Satisfaction in the Intensive Care Unit (pFS-ICU) Questionnaire)

时间窗: 3-5 weeks following PICU discharge

Percentage of "excellent" scores in the decision making domain of the Pediatric Family Satisfaction in the Intensive Care Unit (pFS-ICU) questionnaire; minimum=0, maximum=100, higher score is better outcome

次要结局

  • Pediatric Family Decision Making Satisfaction in the Intensive Care Unit (pFS-ICU)(3-5 weeks following PICU discharge)
  • Parental Satisfaction in the PICU (Score on the Pediatric Family Satisfaction in the Intensive Care Unit (pFS-ICU) Questionnaire)(3-5 weeks after PICU Discharge)
  • Parental Decision Regret (Decision Regret Scale)(3-5 weeks after PICU discharge)
  • Parental Anxiety (Anxiety SF8a)(3-5 weeks after PICU discharge)
  • Parental Depression (Depression SF8a)(3-5 weeks after PICU discharge)
  • Parental Impact of Event/Post-Traumatic Distress (Impact of Event Scale-revised)(3-5 weeks after PICU discharge)
  • Parental Health-related Quality of Life (Global Health Scale) Physical(3-5 weeks after PICU discharge)
  • Parental Health-related Quality of Life (Global Health Scale) Mental(3-5 weeks after PICU discharge)
  • Parental Complicated Bereavement (Grief Scale)(3-5 weeks after PICU discharge)
  • Parent Report of Healthcare Team Satisfaction (Collaboration and Satisfaction About Care Decisions Scale)(3-5 weeks after PICU Discharge)
  • Parent Report of Healthcare Team Collaboration (Collaboration and Satisfaction About Care Decisions Scale)(3-5 weeks after PICU Discharge)
  • Parental Report of Acceptability and Perceived Effectiveness of PICU Supports (Likert-scale)(3-5 weeks after PICU Discharge)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Kelly Michelson

Kelly Michelson, MD

Ann & Robert H Lurie Children's Hospital of Chicago

研究点 (4)

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