Collaborative Care for Post Intensive Care Syndrome
(BeColM Trial)
What You Need to Know Before You Apply
What is the purpose of this trial?
Survivors of critical illness are at high risk for mental health issues such as anxiety, depression, and PTSD. This single-site, randomized controlled trial at the Medical University of South Carolina will enroll 150 patients to compare outcomes between a behavioral health Collaborative Care Model (BH CoCM) and usual care (attention control). The intervention includes digital tools (Neuroflow), behavioral health coaching, and psychiatric support.
Who Is on the Research Team?
Rita Bakhru, MD
Principal Investigator
Medical University of South Carolina
Are You a Good Fit for This Trial?
This trial is for survivors of critical illness who visit the MUSC ICU Recovery Clinic within 6 months after leaving the hospital. It's designed to help those at high risk for mental health issues like anxiety, depression, and PTSD.Inclusion Criteria
Timeline for a Trial Participant
Screening
Participants are screened for eligibility to participate in the trial
Treatment
Participants receive the Behavioral Health Collaborative Care Model intervention, including access to the NeuroFlow platform, behavioral health coaching, and psychiatric support
Follow-up
Participants are monitored for changes in symptoms of depression, anxiety, and post-traumatic stress
What Are the Treatments Tested in This Trial?
Interventions
- Behavioral Health Collaborative Care Model
Trial Overview
The study compares a Behavioral Health Collaborative Care Model (BH CoCM) with usual care. BH CoCM includes digital tools, behavioral coaching, and psychiatric support to improve mental health in ICU survivors.
How Is the Trial Designed?
2
Treatment groups
Experimental Treatment
Active Control
Attention Control
Find a Clinic Near You
Who Is Running the Clinical Trial?
Medical University of South Carolina
Lead Sponsor
Health Resources and Services Administration (HRSA)
Collaborator
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