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Behavioral Health Collaborative Care Model in Post-ICU Clinic Family Pilot
NCT07390786 · Medical University of South Carolina
In plain English
Click the button to translate this study into plain language — what it is, who qualifies, and what participation looks like.
Official title
Integration of a Behavioral Health Collaborative Care Model Into an ICU Recovery Clinic-Pilot for Families
About this study
Patients seen in the MUSC ICU Recovery Clinic will be approached for consent for care through our Behavioral Health Collaborative Care Model. Patients and their families that consent will be randomized to an attention control group or an intervention group.
The intervention group will have access to NeuroFlow platform, which has been specifically designed to support delivery of a BH CoCM. They will utilize Neuroflow for 6 months. They will undergo assessments for anxiety, depression, post-traumatic stress The attention control group will undergo assessments for anxiety, depression, post-traumatic stress.
Investigators will look at changes over six months in intervention group compared to attention control group for patients in terms of symptoms of depression, anxiety, post-traumatic stress. Investigators will also look at adherence, BH CoCM implementation metrics, type and amount of guided content accessed in NeuroFlow. Investigators will perform qualitative surveys to understand better what patients thought about the intervention and ways in which it could be improved.
Eligibility criteria
Inclusion Criteria:
\- Family member of ICU Recovery Clinic patient enrolled in parent BH CoCM study
Exclusion Criteria:
* Serious mental illness (e.g., schizophrenia, mania)
* Late-stage dementia or cognitive impairment
* Limited English proficiency
* No internet-enabled device
* Prisoners
Study design
Enrollment target: 150 participants
Allocation: randomized
Masking: none
Age groups: adult, older_adult
Timeline
Starts: 2026-01-30
Estimated completion: 2028-06-30
Last updated: 2026-03-12
Interventions
Behavioral: Behavioral Treatment
Primary outcomes
- • Consent Rate (Baseline)
- • Study Completion Rate (enrollment to 6 months)
Sponsor
Medical University of South Carolina · other
With: Health Resources and Services Administration (HRSA)
Contacts & investigators
ContactRita Bakhru, MD · contact · recruitment@musc.edu · 8437920965
InvestigatorRita Bakhru, MD · principal_investigator, Medical University of South Carolina
All locations (1)
Medical University of South CarolinaRecruiting
Charleston, South Carolina, United States