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Informing Decisions in Chronic Critical Illness: A Randomized Control Trial (RCT)

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT01230099
Recruitment Status : Completed
First Posted : October 28, 2010
Last Update Posted : October 29, 2015
Sponsor:
Collaborators:
National Institute of Nursing Research (NINR)
University of North Carolina
Duke University
Information provided by (Responsible Party):
Icahn School of Medicine at Mount Sinai

Brief Summary:
The purpose of this study is to test a communication intervention to support family decision-making for patients with chronic critical illness.

Condition or disease Intervention/treatment Phase
Chronic Critical Illness Prolonged Mechanical Ventilation Behavioral: Supportive Information Team Group Not Applicable

Detailed Description:
Increasing use of intensive care therapies by an aging population has created a new medical syndrome - "chronic critical illness" - encompassing multi-system derangements, recurrent complications, and protracted/permanent dependence on mechanical ventilation and other life-supports. Numbering >100,000 at any point in time, the chronically critically ill are a growing population of older adults and a serious national health problem. Annual expenditures for these patients are estimated at $24 billion, mostly for patients ≥ 65 years old. Yet 6-month mortality rates exceed those for most malignancies, impairments are severe among survivors, and return to the community is rare. Descriptive research has identified domains of information that are important for decision-making by patients/families about continuation of treatment in the chronic phase of critical illness, but has also revealed that decisions are often made without this information or patient goals of care as a context. In acute critical illness, scheduled, structured meetings and printed informational aids are effective for Intensive Care Unit (ICU) families, but no study has tested an intervention to inform and support decision-making about chronic critical illness. This study is a randomized, controlled, multi-center clinical trial of such an intervention. Specific Aims are: (1) To evaluate the impact on family- and patient-focused outcomes of a proactive program of protocolized, interdisciplinary, informational support meetings led by a palliative care physician, plus a printed informational aid, for families of chronically critically ill patients; and (2) To evaluate the impact of this intervention on utilization of critical care resources for the chronically critically ill. We hypothesize that as compared to usual care plus the printed aid, this intervention will effectively inform decision-making, improve family well-being, promote discussion of preferences for patient goals of care, and optimize critical care resource utilization, without increasing patient mortality.

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Study Type : Interventional  (Clinical Trial)
Actual Enrollment : 622 participants
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: Single (Outcomes Assessor)
Primary Purpose: Supportive Care
Official Title: Informing Decisions in Chronic Critical Illness: A Randomized Control Trial (RCT)
Study Start Date : October 2010
Actual Primary Completion Date : October 2014
Actual Study Completion Date : October 2014

Resource links provided by the National Library of Medicine


Arm Intervention/treatment
Experimental: Supportive Information Team Group
Protocolized information and support meetings led by palliative care clinicians
Behavioral: Supportive Information Team Group
A minimum of two protocolized, interdisciplinary, informational support meetings led by palliative care clinicians will be arranged with family members or other patient surrogates who participate in decision-making for individual chronically critically ill patients.
Other Name: SIT

No Intervention: Usual Care Group



Primary Outcome Measures :
  1. Hospital Anxiety and Depression Scale [ Time Frame: Day 90 ]

Secondary Outcome Measures :
  1. Hospital Anxiety and Depression Scale [ Time Frame: Day 18-20 ]
  2. Impact of Events Scale-Revised [ Time Frame: Day 90 ]
  3. Discussion of Preferences for Patients Goals of Care [ Time Frame: Day 18-20 ]
    Subscale of Center for Gerontology and Health Care Research Toolkit

  4. Quality of Communication [ Time Frame: Day 18-20 ]
    Curtis Measure

  5. Family Satisfaction in the Intensive Care Unit (ICU) Survey [ Time Frame: Day 90 ]
  6. Modified Center for Gerontology and Health Care Research (CHCR) Tool [ Time Frame: Day 90 ]
  7. Limitation of Intensive Care Unit (ICU) Therapy [ Time Frame: Average of 60 days ]
    Percent of patients with mechanical ventilation, renal replacement, vasopressors, or artificial nutrition withheld or withdrawn

  8. Hospital Length of Stay [ Time Frame: Average of 60 days ]
    Days since randomization

  9. Mortality [ Time Frame: Day 90 ]
  10. Physician-Surrogate Discordance Score [ Time Frame: day 18-20 ]
  11. Discussion of Preferences for Patients Goals of Care [ Time Frame: Day 90 ]
    Subscale of Center for Gerontology and Health Care Research Toolkit



Information from the National Library of Medicine

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Ages Eligible for Study:   21 Years and older   (Adult, Older Adult)
Sexes Eligible for Study:   All
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Mechanically ventilated ≥ 7 days
  • Mechanically ventilated without > 96 hour interruption
  • Age ≥ 21 years
  • ICU MD does not expect patient will die within 72 hours
  • ICU MD does not expect patient will be liberated from the ventilator within 72 hours.

Exclusion Criteria:

  • Previous admission to study ICU this hospitalization Mechanically ventilated at outside hospital for > 7 days before transfer
  • Chronic Neuromuscular (NM) Disease
  • Trauma
  • Burn
  • Previous palliative care consultation in this hospitalization
  • No family or other surrogate decision-maker
  • Family not available
  • Surrogate lacks English proficiency
  • Physician refused permission for research staff to approach the family

Information from the National Library of Medicine

To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.

Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01230099


Locations
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United States, New York
Icahn School of Medicine at Mount Sinai
New York, New York, United States, 10029
United States, North Carolina
University of North Carolina School of Medicine
Chapel Hill, North Carolina, United States, 27599
Durham Regional Medical Center
Durham, North Carolina, United States, 27704
Duke University School of Medicine
Durham, North Carolina, United States, 27710
Sponsors and Collaborators
Icahn School of Medicine at Mount Sinai
National Institute of Nursing Research (NINR)
University of North Carolina
Duke University
Investigators
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Principal Investigator: Judith Nelson, MD, JD Icahn School of Medicine at Mount Sinai
Principal Investigator: Shannon Carson, MD University of North Carolina, Chapel Hill
Publications automatically indexed to this study by ClinicalTrials.gov Identifier (NCT Number):
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Responsible Party: Icahn School of Medicine at Mount Sinai
ClinicalTrials.gov Identifier: NCT01230099    
Other Study ID Numbers: 08-0601 0001 01 ME
R01NR012413-01A1 ( U.S. NIH Grant/Contract )
First Posted: October 28, 2010    Key Record Dates
Last Update Posted: October 29, 2015
Last Verified: October 2015
Keywords provided by Icahn School of Medicine at Mount Sinai:
Critical Illness
Mechanical Ventilation
Palliative Care
Caregivers
Additional relevant MeSH terms:
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Critical Illness
Disease Attributes
Pathologic Processes