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
|
- Study Details
- Tabular View
- No Results Posted
- Disclaimer
- How to Read a Study Record
Condition or disease | Intervention/treatment | Phase |
---|---|---|
Chronic Critical Illness Prolonged Mechanical Ventilation | Behavioral: Supportive Information Team Group | Not Applicable |
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 |

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 |
- Hospital Anxiety and Depression Scale [ Time Frame: Day 90 ]
- Hospital Anxiety and Depression Scale [ Time Frame: Day 18-20 ]
- Impact of Events Scale-Revised [ Time Frame: Day 90 ]
- Discussion of Preferences for Patients Goals of Care [ Time Frame: Day 18-20 ]Subscale of Center for Gerontology and Health Care Research Toolkit
- Quality of Communication [ Time Frame: Day 18-20 ]Curtis Measure
- Family Satisfaction in the Intensive Care Unit (ICU) Survey [ Time Frame: Day 90 ]
- Modified Center for Gerontology and Health Care Research (CHCR) Tool [ Time Frame: Day 90 ]
- 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
- Hospital Length of Stay [ Time Frame: Average of 60 days ]Days since randomization
- Mortality [ Time Frame: Day 90 ]
- Physician-Surrogate Discordance Score [ Time Frame: day 18-20 ]
- Discussion of Preferences for Patients Goals of Care [ Time Frame: Day 90 ]Subscale of Center for Gerontology and Health Care Research Toolkit

Choosing to participate in a study is an important personal decision. Talk with your doctor and family members or friends about deciding to join a study. To learn more about this study, you or your doctor may contact the study research staff using the contacts provided below. For general information, Learn About Clinical Studies.
Ages Eligible for Study: | 21 Years and older (Adult, Older Adult) |
Sexes Eligible for Study: | All |
Accepts Healthy Volunteers: | No |
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

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
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 |
Principal Investigator: | Judith Nelson, MD, JD | Icahn School of Medicine at Mount Sinai | |
Principal Investigator: | Shannon Carson, MD | University of North Carolina, Chapel Hill |
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 |
Critical Illness Mechanical Ventilation Palliative Care Caregivers |
Critical Illness Disease Attributes Pathologic Processes |