Brief CBT for the Treatment of Depression During Inpatient Hospitalization

NYU Langone Health

Status: Withdrawn

Conditions: Depression

Treatments: Behavioral: Cognitive Behavioral Therapy Condition (CBT); Behavioral: Usual Standard of Care

Study type: Interventional

Funder types: Other

Identifiers

NCT03011619

16-01404

Details and patient eligibility

About

Moderately to severely depressed subjects will be randomized to the "Control Group," who will receive care as usual, or the "CBT Group," who will receive care as usual in addition to the manualized course of Cognitive Behavioral Therapy (CBT).

Full description

Participants assigned to the CBT condition will receive the usual standard of care during an inpatient psychiatric hospitalization. This includes but is not limited to medication management, group therapy, and individual therapy. If a patient is randomly assigned to the enhanced CBT group, manualized CBT, including a sequence of sessions that builds upon prior sessions and planned exercises, including worksheets and journal entries.The training M.D., who is a treating physician on HCC-10, will also intermittently and randomly observe the CBT sessions to ensure the manual properly is being followed. Although the control condition may contain elements of CBT as per the clinician completing the therapy, it is not manualized, does not include specific exercises to be completed between sessions, and is not a course that builds upon skills from the previous day, as in the CBT condition. Participants assigned to the control condition will receive the usual standard of care during an inpatient psychiatric hospitalization. This includes but is not limited to medication management, group therapy, and individual therapy.

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosed with depression according to Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition (DSM-V) criteria on initial assessment on the unit.
• Demonstrates at least moderate degree of depressive symptoms on MADRS, HAM-D, and CGI-S.
• Provides written informed consent.

Exclusion criteria

• A mental illness other than depression that is the primary cause of treatment, as determined by the Principal Investigator.
• A cognitive or neurologic disorder that inhibits ability to engage in CBT.

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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0 participants in 2 patient groups

Control Condition

Active Comparator group

Description:

usual standard of care during an inpatient psychiatric hospitalization; medication management, group therapy, and individual therapy.

Treatment:

Behavioral: Usual Standard of Care

CBT Condition

Experimental group

Description:

If a patient is randomly assigned to the enhanced CBT group, they will participate in manualized CBT, including a sequence of sessions that builds upon prior sessions and planned exercises, including worksheets and journal entries.

Treatment:

Behavioral: Cognitive Behavioral Therapy Condition (CBT)

Behavioral: Usual Standard of Care