Post-Hospital Case Management to Improve Clinical Outcomes in Individuals Requiring Mechanical Ventilation
Primary Purpose
Acute Respiratory Distress Syndrome
Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Targeted Case Management
Usual care
Sponsored by
About this trial
This is an interventional treatment trial for Acute Respiratory Distress Syndrome
Eligibility Criteria
Inclusion Criteria: On a ventilator for 5 or more days Expected to survive the 6 months post-hospital discharge period Lives in the SOS zip code area (King, Pierce and Snohomish counties) Exclusion Criteria: Severe pre-hospital health conditions Lack of availability for follow-up (e.g. homeless, chronic substance abuse) Non-English speakers Severe psychiatric issues Need for special rehabilitation services not available in the intervention Predicted survival of less than 6 months
Sites / Locations
- University of Washington
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Active Comparator
Arm Label
1
2
Arm Description
Targeted nurse case management
Usual Care
Outcomes
Primary Outcome Measures
Scores for quality of life measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00149513
First Posted
September 6, 2005
Last Updated
December 21, 2017
Sponsor
University of Washington
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT00149513
Brief Title
Post-Hospital Case Management to Improve Clinical Outcomes in Individuals Requiring Mechanical Ventilation
Official Title
King County Lung Injury Project: Survivor Outcome Study (KCLIP:SOS)
Study Type
Interventional
2. Study Status
Record Verification Date
December 2017
Overall Recruitment Status
Completed
Study Start Date
September 2003 (undefined)
Primary Completion Date
February 2009 (Actual)
Study Completion Date
February 2009 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Washington
Collaborators
National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
King County Lung Injury Project: Survivor Outcome Study (KCLIP:SOS) is a randomized trial for individuals who have survived prolonged mechanical ventilation (5 days or more). The objective is to enroll individuals who are likely to have impaired health status resulting from prolonged critical illness but whose long term prognosis is good. Such individuals are most likely to benefit from the study intervention of case management targeted at post intensive care complications.
KCLIP:SOS will test whether an outpatient intervention based on a nurse using a targeted case management tool can reduce patient morbidity and improve quality of life in the 6 months following hospital discharge. This intervention will be compared to usual post-hospital care.
Detailed Description
BACKGROUND:
The purpose of this study is to understand individuals' physical and emotional conditions and concerns after being ventilated in the hospital. Modern hospital care helps many people survive even if they are on ventilators for long periods of time. Some individuals who leave the hospital after this kind of intensive care suffer from depression, post-traumatic stress disorder, muscle weakness, tiredness or breathing difficulties that may decrease their quality of life. Doctors know little about finding and treating these problems in survivors of mechanical ventilation.
DESIGN NARRATIVE:
Participants will be randomly assigned in blocks of 10 (5 participants to usual care and 5 participants to case management) for home or skilled nursing facility discharges. The Outcome Assessors (the interviewers collecting outcomes data) will be blinded to group assignment.
Primary outcome: All participants will have a baseline interview soon after hospital discharge and a final interview at the end of the 6-month intervention period (outcome assessments). All subjects will be asked to keep a diary/journal of their medical appointments, health services, and medications. Participants will be called once a month to collect this information.
Key secondary outcomes: Case management participants will be contacted by the nurse case manager who will provide follow-up care for 6 months. At the end of the study, interview results will be sent to the personal physician of the usual care participants so that appropriate care can follow.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Respiratory Distress Syndrome
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
600 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Experimental
Arm Description
Targeted nurse case management
Arm Title
2
Arm Type
Active Comparator
Arm Description
Usual Care
Intervention Type
Behavioral
Intervention Name(s)
Targeted Case Management
Intervention Description
A nurse case manager will assess and follow intervention arm subjects for six months. Nurse case manager will help subjects acquire needed community health services.
Intervention Type
Behavioral
Intervention Name(s)
Usual care
Intervention Description
Participants will receive usual care.
Primary Outcome Measure Information:
Title
Scores for quality of life measures
Time Frame
6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
On a ventilator for 5 or more days
Expected to survive the 6 months post-hospital discharge period
Lives in the SOS zip code area (King, Pierce and Snohomish counties)
Exclusion Criteria:
Severe pre-hospital health conditions
Lack of availability for follow-up (e.g. homeless, chronic substance abuse)
Non-English speakers
Severe psychiatric issues
Need for special rehabilitation services not available in the intervention
Predicted survival of less than 6 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gordon Rubenfeld, MD
Organizational Affiliation
University of Washington
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Washington
City
Seattle
State/Province
Washington
ZIP/Postal Code
98104
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Post-Hospital Case Management to Improve Clinical Outcomes in Individuals Requiring Mechanical Ventilation
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