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Clinical Trials/NCT06039501
NCT06039501
Recruiting
N/A

The Family Perspectives Project Pilot Trial

Matthew Modes1 site in 1 country70 target enrollmentOctober 13, 2023

Overview

Phase
N/A
Intervention
Not specified
Conditions
Respiratory Failure
Sponsor
Matthew Modes
Enrollment
70
Locations
1
Primary Endpoint
Feasibility of implementing the program for families of patients with acute respiratory failure.
Status
Recruiting
Last Updated
10 months ago

Overview

Brief Summary

The purpose of the study is to conduct a pilot randomized trial of a program designed to enhance equitable communication and emotional support for families of critically ill patients in order to determine feasibility, acceptability, and participant experience with the program.

The primary study procedures include: chart abstraction, questionnaires, meetings with ICU support counselors, meetings with ICU physicians and care team, audio recordings of these meetings (optional), and interviews with study participants (optional).

Study participants include: 70 critically ill patients with acute respiratory failure (enrolled with the consent of their Legally Authorized Representative) and their primary surrogate decision makers as well as ICU support counselors and ICU care teams (physicians, nurses, social workers).

Registry
clinicaltrials.gov
Start Date
October 13, 2023
End Date
October 2026
Last Updated
10 months ago
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Sponsor
Matthew Modes
Responsible Party
Sponsor Investigator
Principal Investigator

Matthew Modes

Assistant Professor

Cedars-Sinai Medical Center

Eligibility Criteria

Inclusion Criteria

  • Patient inclusion criteria:
  • Individuals 18 years old or older.
  • Individuals admitted to the medical intensive care unit (MICU) at Cedars-Sinai Medical Center.
  • Individuals with acute respiratory failure, defined as \>24 hours of invasive mechanical ventilation.
  • Individuals who received invasive mechanical ventilation within 24 hours of admission to the MICU.
  • Individuals expected to need invasive mechanical ventilation for \>72 hours total, as determined by the patient's intensivist physician (fellow or attending).
  • Primary surrogate decision maker inclusion criteria:
  • o Individuals 18 years old or older.
  • Individual who self-identifies as the most responsible for making decisions for the enrolled patient (can be either family member or close friend).
  • Proficiency in English language.

Exclusion Criteria

  • Patient exclusion criteria:
  • o Any records flagged "break the glass" or "research opt out."
  • o Individuals expected to die within 24 hours of potential enrollment, as determined by the patient's intensivist physician (fellow or attending).
  • o Individuals on comfort care protocol or with clear preference for comfort care, as determined by the patient's intensivist physician (fellow or attending).
  • Individuals who are chronically dependent on a ventilator prior to admission.
  • Individuals with acute on chronic neuromuscular disease-related respiratory failure (e.g., Guillain Barre, Muscular Dystrophy, Myasthenia Gravis, etc.).
  • Individuals imminently awaiting organ transplant, as determined by the patient's intensivist physician (fellow or attending).
  • Individuals with decisional capacity, as determined by the patient's intensivist physician (fellow or attending).
  • Individuals who are unrepresented (i.e., patient has no surrogate decision maker).
  • Individuals whose potential enrolled family member (primary surrogate decision maker) is not proficient in English.

Outcomes

Primary Outcomes

Feasibility of implementing the program for families of patients with acute respiratory failure.

Time Frame: 6 months

The proportion of enrolled primary surrogate decision makers randomized to the program who receive all program components. The study will be declared "feasible" if at least 70% of primary surrogate decision makers receive all program components (meeting with ICU support counselors, ICU support counselors generating standardized reports, reports being reviewed by ICU care team members prior to meeting with families).

Secondary Outcomes

  • Feasibility of collecting data from families(6 months)
  • Feasibility of collecting data from ICU support counselors(6 months)
  • ICU care team member perception of feasibility of implementing the program(6 months)
  • Feasibility of collecting data from ICU care team members(6 months)
  • ICU support counselor perception of feasibility of implementing the program(6 months)

Study Sites (1)

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