Integration of a Behavioral Health Collaborative Care Model Into an ICU Recovery Clinic-Pilot for Families

What this Trial Is About

Researchers are evaluating the feasibility and acceptability of a Behavioral Health Collaborative Care Model (BH CoCM) for family members of patients who survived intensive care. This pilot study aims to support family members' behavioral health by using telehealth assessments and the NeuroFlow platform. The study compares outcomes between an intervention group and an attention control group over six months. Participants in the intervention group will use the NeuroFlow platform designed to support BH CoCM for six months, undergoing assessments for anxiety, depression, and post-traumatic stress. The control group will receive attention and assessments for these symptoms but will not have access to NeuroFlow. Some participants will also take part in qualitative interviews to provide feedback on the intervention. During the study, participants will complete regular assessments including the Patient Health Questionnaire 9 (PHQ-9), General Anxiety Disorder 7 (GAD-7), and PTSD Checklist for DSM-5 (PCL-5). Researchers will monitor consent rates, study completion rates, adherence to the intervention, and the type and amount of content accessed on NeuroFlow. The total participation duration is six months, with ongoing evaluation of behavioral health symptoms and intervention experiences.

Behavioral Health Collaborative Care Model in Post-ICU Clinic Family Pilot