Family Support Intervention in Intensive Care Units (The Four Supports Study)

University of Pittsburgh159 enrolled

Overview

The purpose of this study is to test the effectiveness of a multi-faceted communication intervention for family members of critically ill patients to reduce the family members' long-term symptoms of depression and anxiety.

One in four elderly Americans die in or shortly after discharge from an intensive care unit. An expanding body of literature documents that physician-family communication and end-of-life care is poor in intensive care units. These deficiencies are associated with high rates of adverse psychological outcomes among surrogates, physician-family conflict, and life support decisions that may be inconsistent with patients' goals and preferences. There is a lack on information on practical, generalizable interventions that effectively improve this important aspect of care for elderly patients and their families. The primary aim of this study is to evaluate the effectiveness of a multifaceted communication intervention to improve psychological outcomes among family members of critically ill patients, using a randomized, controlled trial design.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

159

Conditions

Physician-Family Communication in Intensive Care Units Surrogate Decision-making for Critically Ill Patients

Interventions

Family Support InterventionBEHAVIORAL

Multifaceted family support intervention

Eligibility

Sex: ALLMin age: 50 Years

Medical Language ↔ Plain English

Inclusion Criteria for ICU Patients: * must be unable to make treatment decisions for him/herself, as determined by the patient's physicians. * must have have either an APACHE II score of ≥ 25 or, for patients with a primary neurologic diagnosis (e.g. intracranial hemorrhage, subdural hemorrhage, or subarachnoid hemorrhage), physician estimate that the patient has at least a 50% risk of long term, severe functional impairment * must be 50 years old or greater. Exclusion Criteria for ICU Patients: * Patients who do not have surrogates or at least one family member who is willing to participate in the study. * Patients awaiting organ transplantation.

Locations (1)

University of Pittsburgh Medical Center (UPMC)

Pittsburgh, Pennsylvania, United States

Outcomes

Primary Outcomes

Family Outcome: Family members' depressive symptoms

Time frame: Three months following patient death or discharge from the ICU.

Patient Outcome: Patient centeredness of care

Time frame: Three months following patient death or discharge from the ICU.

Data from ClinicalTrials.gov

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