The Family Perspectives Project Pilot Trial

NCT06039501 | Recruiting

• 1 other identifier: Study00002813
• Study Type: interventional
• Target: 70
• Locations: 1 country
• Sites: 1

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).

Conditions

Respiratory Failure; Family Support; Physician-Patient Relations; Critical Illness

Outcome Measures

Primary Outcomes (1)

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

  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).

  6 months

Secondary Outcomes (5)

• Feasibility of collecting data from families

  6 months

• Feasibility of collecting data from ICU support counselors

  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

• ICU care team member perception of feasibility of implementing the program

  6 months

Study Arms (2)

Family Perspective Program

EXPERIMENTAL

Families of critically ill patients will receive a program designed to enhance equitable communication and emotional support. Questionnaires will be completed by primary surrogate decision makers, ICU support counselors, and ICU care team members (physicians, nurses, social workers). Meetings between families and ICU support counselors will be audio recorded (optional). Meetings between families and ICU care teams will be audio recorded (optional). Interviews with participants will be completed (optional).

Behavioral: Family Perspective Program

Usual Care

NO INTERVENTION

Families of critically ill patients will receive usual care, which involves regular and routine meetings between families and the ICU care team. Questionnaires will be completed by primary surrogate decision makers and ICU care team members (physicians, nurses, social workers). Meetings between families and ICU care teams will be audio recorded (optional). Interviews with participants will be completed (optional).

Interventions

Family Perspective Program BEHAVIORAL

The program involves regular meetings between families and an ICU support counselor. The ICU support counselor is a trained expert in providing culturally competent emotional and/or spiritual support. The ICU support counselor will support families and also learn and summarize family perspectives in a standardized report. ICU care team members will be prompted to perspective take as they review reports prior to regular routine meetings between families and the ICU care team.

Family Perspective Program

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: Yes
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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).
• 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.
• Individuals 18 years old or older.
• Individuals who work as hospital chaplains in the MICU.
• Individuals 18 years old or older.
• Individuals who work as critical care physicians in the MICU (fellow or attending).
• Individuals 18 years old or older.
• Individuals who work as bedside nurses in the MICU.
• Individuals 18 years old or older.

You may not qualify if:

• 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.
• Individuals whose attending physician is the PI on this study at the time of potential enrollment.
• Individuals who are cared for by intensivist physicians (fellow and attending) who do not agree to participate in the study.
• Individuals who have a pre-existing relationship with a hospital chaplain who does not agree to participate in the study, as determined by that chaplain.
• o Not proficient in English language. (Rationale: materials and intervention are not adapted in other languages.)
• o None
• o None

Sponsors & Collaborators

• Matthew Modes: lead
• National Palliative Care Research Center: collaborator

Study Sites (1)

Cedars-Sinai Medical Center

Los Angeles, California, 90048, United States

RECRUITING

MeSH Terms

Conditions

Respiratory Insufficiency; Critical Illness

Condition Hierarchy (Ancestors)

Respiration Disorders; Respiratory Tract Diseases; Disease Attributes; Pathologic Processes; Pathological Conditions, Signs and Symptoms

Study Officials

• Matthew Modes, MD, MPP, MS

  Cedars-Sinai Medical Center

  PRINCIPAL INVESTIGATOR

Central Study Contacts

Matthew Modes, MD, MPP, MS

CONTACT

310-423-9017; matthew.modes@cshs.org

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: RANDOMIZED
• Masking: NONE
• Purpose: OTHER
• Intervention Model: PARALLEL
• Sponsor Type: OTHER
• Responsible Party: SPONSOR INVESTIGATOR
• PI Title: Assistant Professor

Study Record Dates

• First Submitted: September 9, 2023
• First Posted: September 15, 2023
• Study Start: October 13, 2023
• Primary Completion (Estimated): October 1, 2026
• Study Completion (Estimated): October 1, 2026
• Last Updated: June 15, 2025

Record last verified: 2025-06

Data Sharing

• IPD Sharing: Will not share

Locations

US (1)