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Intensive Communication for Chronically Critically Ill

Case Western Reserve University logo

Case Western Reserve University

Status

Completed

Conditions

Critical Care

Treatments

Other: Intensive Communication System

Study type

Interventional

Funder types

Other

Identifiers

NCT01057238
R01NR008941

Details and patient eligibility

About

This study was a trial of a formal system of family meetings to support family decision makers of chronically critically ill patients in the intensive care unit.

Full description

Formal family meetings have been recommended as a useful approach to assist in goal setting, facilitate decision making, and reduce use of ineffective resources in the ICU. We implemented an "intensive communication system" to test the effect of regular, structured formal family meetings on patient outcomes among long-stay ICU patients

The design was a pre-post, tandem assignment of patients (n=217) receiving usual care and communication, followed by enrollment of intervention patients (n=354), from 5 ICUs. The "intensive communication system" included: (1) family meeting within 5 days of ICU admission and weekly thereafter; (2) each meeting addressed medical update, values and preferences, goals of care; treatment plan, and milestones for judging effectiveness of treatment.

We measured differences between control and intervention patients in indicators of aggressiveness of care or timing of treatment limitation decisions (ICU mortality, LOS, duration of ventilation, treatment limitation orders, or use of tracheostomy or percutaneous gastrostomy). Difference in outcomes among patients who died or who had treatment limitation orders, comparing control and intervention groups, was also examined.

Enrollment

571 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • cognitively impaired mechanical ventilation >3 days not expected to be discharged before 5 days having a family decision maker

Exclusion criteria

  • no family member hospice referral

Trial design

Primary purpose

Supportive Care

Allocation

Non-Randomized

Interventional model

Parallel Assignment

Masking

None (Open label)

571 participants in 2 patient groups

Intensive Communication
Experimental group
Description:
regular family meeting every 5 days.
Treatment:
Other: Intensive Communication System
Control
No Intervention group
Description:
usual care

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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