Post-Intensive Care Transitional Care, Rehabilitation, and Family-Support RCT
Overview
- Phase
- N/A
- Intervention
- Post Intensive Care Transitions Rehabilitation and Family Support (PIC-TRFS)
- Conditions
- Intensive Care Unit Syndrome
- Sponsor
- University of Pittsburgh
- Enrollment
- 320
- Locations
- 1
- Primary Endpoint
- Between-group difference in mean patient PROMIS-Preferences at the end of the intervention period
- Status
- Suspended
- Last Updated
- 3 months ago
Overview
Brief Summary
The goal of this randomized control trial is to test an intervention designed to improve patient and family outcomes after critical illness compared to usual care. The intervention, called Post-Intensive Care Transitions, Rehabilitation and Family Support (PIC-TRFS) combines four elements: (1) health management; (2) rehabilitation; (3) social support; (4) care coordination. All patients and families enrolled in this study will have spent at least 48 hours in an ICU, be at risk for long-term functional impairment, and be discharged home. Although age of the patients will be restricted to those who are at least 50 years old and caregivers must be adults over 18 and all participants must speak English, the study will enroll all sexes, genders, races, and ethnicities. The main questions the study aims to answer are:
- Compared to usual care, does PIC-TRFS improve patient quality of life at the end of the 6-month intervention period measured via PROMIS-Preferences (PROPr) score?
- Compared to usual care, does PIC-TRFS improve patient physical, cognitive, and psychological functioning measured via PROMIS Physical, Cognitive, and Depression Computer Adaptive Test (CAT) at 6 and 12 months after discharge? Does it increase the number of days survivors spend alive at home in the 6 and 12 months after discharge? Does it improve patient and family trauma scores and dyadic quality of life, measured via the Impact of Events Scale-Revised and dyadic PROPr score?
Participants will:
- Complete Run-In assessments of symptoms and function in the hospital;
- Be randomized to intervention or control;
- Complete assessments of their function and quality of life at 0, 3, 6 and 12 months
- Control participants will get a brochure on the Post-Intensive Care syndrome and complete the assessments on the same schedule as those receiving the intervention
- Intervention participants will complete tele-health based check-ins providing health management, social support, and care coordination; and telehealth-based rehabilitation sessions focusing on patient functioning.
Detailed Description
Each year in the United States, over 3 million people survive critical illness only to experience long-term physical, cognitive, and psychological functional impairments that contribute to ongoing health problems, high healthcare costs, and early death. Gaps in care delivery contribute to poor outcomes and preventable rehospitalizations for both patients and families. In response to these gaps, the study team used community engagement to design an intervention with 4 elements: (1) rehabilitation; (2) health and symptom management; (3) social support; (4) healthcare coordination. The result is the PIC-TRFS, which stands for Post-Intensive Care Transitional care, Rehabilitation, and Family Support (PIC-TRFS). PIC-TRFS combines in-person and telehealth support delivered by an interdisciplinary team to nimbly address health, rehabilitation, social, and care coordination needs in collaboration with existing hospital, home health, and primary care providers. The PIC-TRFS team follows participants across transitions from hospital to home in the six months following a critical illness hospitalization. This single center randomized control trial will test whether PIC-TRFS improves outcomes compared to Enhanced Usual Care. Specifically, this research will test whether PIC-TRFS improves survivor quality of life, days alive at home, function, trauma symptoms, and family care partner quality of life. It will also test whether PIC-TRFS reduces healthcare utilization, measured as a combination of days in a healthcare facility, Emergency Department visits, and outpatient visits. At the same time, this research will assess how consistently the intervention is delivered to make sure that differences between groups really reflect the impact of the intervention. Finally, the study will explore whether the intervention may reduce health disparities between people with higher health and social needs. Successful conduct of this trial will test whether PIC-TRFS works, generate insight into how it works, and identify its impact on health equity.
Investigators
Leslie Scheunemann
Assistant Professor
University of Pittsburgh
Eligibility Criteria
Inclusion Criteria
- •In order to be eligible to participate in this study, a patient must meet all of the following criteria:
- •All genders; Age ≥ 50
- •Admission to the hospital from home/independent living
- •Receive treatment in an ICU for ≥ 48 hours
- •At least some risk of ongoing functional impairment, measured as Activity Measures for Post-Acute Care (AMPAC) \< 24, Highest Level Mobility (HLM) \< 8, Intensive Care Delirium Screening Checklist (ICDSC) \> 2, Significant mental health impairment (major depression, generalized anxiety, PTSD, substance use disorder)
- •Provider or e-prognosis that they are reasonably likely to be alive in 12 months (answers no to "Would you be surprised if this person were alive in 12 months?' or eprognosis risk of 1-year mortality \<= 35%
- •Willingness to adhere to the PIC-TRFS regimen.
- •Provision of signed and dated informed consent form
- •In order to be eligible to participate in this study, a family caregiver must meet all of the following criteria:
- •All genders; Age ≥ 18 years old
Exclusion Criteria
- •Survivors will be excluded if any of the following apply:
- •They lack a family caregiver willing to participate;
- •They have a chronic condition for which they are already receiving dedicated transitional care services (e.g., post-cardiac arrest, transplant, TAVR, etc)
- •They have chronic functional dependency without potential to increase participation in meaningful activity
- •They reside outside of Pennsylvania (interventionists are only licensed to practice here)
- •They are unable to participate in English
- •A family caregiver who meets any of the following criteria will be excluded from participation in this study:
- •1\. They are unable to participate in English
Arms & Interventions
PIC-TRFS Intervention
Post-Intensive Care Transitions, Rehabilitation and Family Support (PIC-TRFS) is a complex dyadic intervention consisting of 4 essential elements: (1) rehabilitation; (2) health and symptom management; (3) social support; (4) healthcare coordination. It is delivered by an interventionist team. One trained interventionist leads the healthcare coordination, health and symptom management, and social support. An occupational therapist interventionist leads the rehabilitation. Following a Run-In period in the hospital, the interventionists deliver PIC-TRFS via telehealth from the time of randomization at discharge until 6 months after discharge. This Team partners with survivors, families, and the usual care team to deliver the active ingredients of PIC-TRFS.
Intervention: Post Intensive Care Transitions Rehabilitation and Family Support (PIC-TRFS)
Enhanced Usual Care Control
After receiving the Run-In and being randomized to control, this group will receive a brochure on critical illness survivorship, outcome ascertainment on the same schedule as the intervention group, and intervention for serious adverse events (e.g., suicidal ideation) identified during study conduct. This design limits exposure of the control group to the hypothesized essential elements of the PIC-TRFS intervention, while maintaining regular contact to enhance retention and outcomes ascertainment, and addressing safety concerns among participants.
Intervention: Enhanced Usual Care Control
Outcomes
Primary Outcomes
Between-group difference in mean patient PROMIS-Preferences at the end of the intervention period
Time Frame: 6 months
Patients will report health-related quality of life using Patient Reported Outcomes Measurement Information System (PROMIS) surveys in 7 domains: physical, cognitive, mental health, social role satisfaction, pain, fatigue, and sleep. The statistician will use the surveys to calculate a PROMIS-Preferences (PROPr) score using the code available here https://www.proprscore.com/code-and-data/ . This yields a T-score with a minimum of -0.022 (worse than dead) and a maximum score of 1 (maximum quality of life). These scores will be aggregated by calculating the mean for each study group.
Secondary Outcomes
- Between-group difference in patient PROMIS-Preferences scores at the end of the study period(12 months)
- Between group differences in survivor physical function(6 and 12 months)
- Between group differences in survivor cognitive function(6 and 12 months)
- Between group differences in survivor mood(6 and 12 months)
- Between-group differences in mean dyadic PROMIS-Preferences (PROPr) Scores(6 and 12 months)
- Between group differences in dyadic trauma symptoms(6 and 12 months)
- Between group differences in survivor days alive at home.(6 and 12 months)
- Between group differences in survivor Healthcare Utilization(6 and 12 months)