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

ConditionsCritical Illness RecoveryBehavioral Health ConcernsAnxietyDepression - Major Depressive DisorderPTSDCritical Care, Intensive CarePICS-F
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorMedical University of South Carolina

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

None

Disqualifiers

Serious mental illness (e.g., schizophrenia, mania)

Late-stage dementia or cognitive impairment

Limited English proficiency

No internet-enabled device

Trial design

Design model

Parallel

Treatments tested in this trial

  • Behavioral Treatment

    Behavioral

    behavioral health collaborative care model in ICU recovery patients and families

Treatment groups

150 Participants
are divided into 2 treatment groups
Group A: ControlNo intervention 0 interventions
Group B: InterventionalExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Consent Rate

Investigators will assess the consent rate

Time frame
Baseline
2

Study Completion Rate

We will assess the completion rate of all enrolled family members

Time frame
enrollment to 6 months

Secondary outcomes

1

Monthly Completion Rate of PHQ9 (Patient Health Questionnaire 9)

Rate of completion of scheduled monthly assessment: PHQ9

Time frame
Enrollment to 6 months
2

Monthly Completion Rate of GAD 7 (General Anxiety Disorder 7)

Rate of completion of scheduled monthly assessment: GAD7

Time frame
baseline to 6 months
3

Monthly Completion Rate of PCL 5 (PTSD Checklist for DSM-5)

Rate of Completion of scheduled monthly assessment: PCL5

Time frame
baseline to 6 months

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Medical University of South Carolina

Lead sponsor

Health Resources and Services Administration (HRSA)

Collaborator

Source ClinicalTrials.gov
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