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

Medical University of South Carolina (MUSC)

Status: Not yet enrolling

Conditions: PTSD; PICS-F; Behavioral Health Concerns; Critical Care, Intensive Care; Anxiety; Critical Illness Recovery; Depression - Major Depressive Disorder

Treatments: Behavioral: Behavioral Treatment

Study type: Interventional

Funder types: Other; Other U.S. Federal agency

Identifiers

NCT07390786

Pro00145594

Details and patient eligibility

About

This pilot study evaluates the feasibility and acceptability of implementing a Behavioral Health Collaborative Care Model (BH CoCM) for family members of ICU survivors. The intervention includes telehealth-enabled behavioral health assessments and access to the NeuroFlow platform. A subset of participants will undergo qualitative interviews.

Full description

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.

Enrollment: 150 estimated patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

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

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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150 participants in 2 patient groups

Control

No Intervention group

Description:

Attention Control.

Interventional

Experimental group

Treatment:

Behavioral: Behavioral Treatment