- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT03364933
Primary Intensivists and Primary Nurses to Decrease Pediatric ICU Length of Stay (PIPRNs)
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Long-stay intensive care unit (ICU) patients, or children who require prolonged hospitalization in the pediatric ICU (PICU), represent a minority of PICU patients but have a disproportionate impact on hospital resources and unfavorable outcomes, including morbidity, mortality, and repeated critical illness. These patients and their families have multifaceted needs (eg, tailored communication) that pose unique challenges to PICU providers and the parent-provider relationship. These experiences and needs are compounded and complicated by the transitory care that is typically provided by PICU. This transitory care may contribute to 1) patient/family dissatisfaction; 2) ineffective passing of important information day to day and week to week; and 3) delayed decision-making. These latter two potential consequences may, in turn, contribute to prolonged length of stay (LOS).
For these reasons, the investigators propose a randomized control trial to test whether primary intensivists and primary nurses can decrease PICU LOS for long-stay patients. A primary intensivist is one that remains a consistent physician-presence for the patient/family and PICU team throughout the child's PICU stay, despite changes in the intensivist(s) who orchestrates day-to-day management. Primary nurses are a team of PICU nurses who provide the all/most of the bedside care to the child. The investigators hypothesize that the long-stay PICU patients who are randomized to receive primary intensivists and nurses will have a statistically lower LOS than those patients who do not.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
New York
-
New York, New York, United States, 10032
- Columbia University Medical Center
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
- ADULT
- OLDER_ADULT
- CHILD
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
PICU patients of any age who
- have a complex chronic condition
- have been admitted to the PICU for one week and are predicted by the PICU attending to continue to be admitted for at least another 3 days.
Exclusion Criteria:
-
Study Plan
How is the study designed?
Design Details
- Primary Purpose: HEALTH_SERVICES_RESEARCH
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
EXPERIMENTAL: Primary intensivist and nurses
Patients randomized to the experimental arm will have a primary intensivist and a team of primary nurses assigned to them.
|
Primary intensivist will have no active role in the daily management of patients. The primary intensivist should facilitate decision-making, be a liaison between the patient/family and PICU team, and be a resource of information for all. Responsibilities of primary intensivist:
Primary nurses will be a team of up to 7 ICU nurses who will provide as much of the bedside care as possible. Responsibilities of primary nurses:
|
|
NO_INTERVENTION: Control
Patients who are randomized to the control group will receive usual care and not be assigned a primary intensivist or nurses.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
PICU length of stay
Time Frame: Up to 2 years
|
Total number of days in which an individual stays in the PICU
|
Up to 2 years
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Family satisfaction
Time Frame: Up to 2 years
|
In order to assess family satisfaction, families of all PICU patients (with PICU lengths of stay > 10 days) will be asked to complete a short anonymous questionnaire (Likert Scale) at the time of ICU discharge or within a few days when the patient is still hospitalized, if discharged late at night or over a weekend.
|
Up to 2 years
|
|
Provider satisfaction
Time Frame: Up to 2 years
|
In order assess provider satisfaction, all PICU attendings, fellows, and nurses will be verbally consented and asked to complete a short anonymous questionnaire (Likert Scale) at one of two time points-1) at the end of the study or 2) before the staff member leaves
|
Up to 2 years
|
|
Percentage of family meetings attended by a primary nurse
Time Frame: Up to 2 years
|
Number of meetings a nurse participated in divided by the number of meetings
|
Up to 2 years
|
|
Duration of invasive mechanical ventilation in those patients without chronic respiratory failure and who are on invasive mechanical ventilation from the time of enrollment
Time Frame: Up to 2 years
|
Measured in days.
|
Up to 2 years
|
|
Time to tracheotomy in those who undergo a tracheotomy
Time Frame: Up to 2 years
|
Measured in days.
|
Up to 2 years
|
|
Incidence of nursing-related KEEPSAFE reports recorded after enrollment
Time Frame: Up to 2 years
|
total number of reports that are recorded.
|
Up to 2 years
|
|
Timing of involvement of Patient Care Services
Time Frame: Up to 2 years
|
Measured in days.
|
Up to 2 years
|
|
Incidence of ICU-acquired infections after enrollment
Time Frame: Up to 2 years
|
Total number of ICU-acquired infections
|
Up to 2 years
|
|
Number of documented family meetings
Time Frame: Up to 2 years
|
Total number of family meetings.
|
Up to 2 years
|
|
Incidence of unplanned re-admissions to a PICU within 48 hours of PICU discharge
Time Frame: Up to 2 years
|
Total number of unplanned re-admissions to a PICU.
|
Up to 2 years
|
|
Percentage of primary intensivists who meet with families
Time Frame: Up to 2 years
|
Measured by total number of meeting divided by the number of weeks after enrollment.
|
Up to 2 years
|
|
Total number of shifts that are not being covered by a primary nurse,
Time Frame: Up to 2 years
|
The Bice-Boxerman Continuity of Care Index will be used to measure continuity compliance in terms of the total number of shifts not covered by a primary nurse.
|
Up to 2 years
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Jeffrey Edwards, MD, Columbia University
Study record dates
Study Major Dates
Study Start (ACTUAL)
Primary Completion (ACTUAL)
Study Completion (ACTUAL)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ACTUAL)
Study Record Updates
Last Update Posted (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- AAAR5445
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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