Behavioral Health Collaborative Care Model in an ICU Recovery Clinic
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- The protocol lists: Behavioral Health Collaborative Care Model.
- Who it may be relevant to
- Registry conditions: PICS, Anxiety, Depression - Major Depressive Disorder, Post-Traumatic Stress. Basic parameters: from 18 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Integration of a Behavioral Health Collaborative Care Model Into an ICU Recovery Clinic
Overview
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.
Detailed description
Patients seen in the MUSC ICU Recovery Clinic will be approached for consent for enrollment. Patients that consent will be randomized to an attention control group or an intervention group.
The intervention group receive BH CoCM. They 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. A behavioral manager will monitor their needs and provide behavioral health coaching and psychiatric support as needed.
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.
Interventions
- Behavioral Behavioral Health Collaborative Care Model
behavioral health collaborative care model in ICU recovery patients and families
Primary outcome measures
- Depression [Time frame: Enrollment to 6 months]
- Anxiety [Time frame: enrollment to six months]
- Post-Traumatic Stress [Time frame: enrollment to six months]
Eligibility criteria
Inclusion criteria
\- Attendance at the MUSC ICU Recovery Clinic within 180 days of discharge from the hospital
Exclusion criteria
- ICU Admission was due to a primary addiction diagnosis (eg alcohol withdrawal or delirium tremens requiring ICU care)
- Serious Mental Illness such as Schizophrenia, psychotic disorder, acute mania
- Late Stage Dementia or Cognitive Impairment
- Limited English or Spanish Proficiency
- Lack of regular access to a computer, tablet or mobile device with internet access
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Allocation
- Randomized
- Model
- Parallel assignment
- Masking
- Open label
- Primary purpose
- Supportive care
Study locations
United States · 1 center
- Medical University of South Carolina — Charleston
Identifiers
NCT: NCT07372586 · Pro00145295