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Intensive Communication for Chronically Critically Ill

Intensive Communication for Chronically Critically Ill

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01057238
Enrollment
571
Registered
2010-01-27
Start date
2005-11-30
Completion date
2008-05-31
Last updated
2016-07-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Critical Care

Keywords

mechanical ventilation, critical care

Brief summary

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.

Detailed 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.

Interventions

OTHERIntensive Communication System

Regular family meetings once a week, using a standard protocol

Sponsors

Case Western Reserve University
Lead SponsorOTHER

Study design

Allocation
NON_RANDOMIZED
Intervention model
PARALLEL
Primary purpose
SUPPORTIVE_CARE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
length of stay and depressionICU admission, Day 5, discharge, and 2 months

Countries

United States

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 31, 2026