Brief CBT for the Treatment of Depression During Inpatient Hospitalization

Withdrawn before enrolling · Not applicable

Conditions studied: Depression

In brief

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).

Key facts

Study ID

NCT03011619

Run by

NYU Langone Health

People needed

0

Starts

2017-04-06

Expected to finish

2018-04-05

Last updated by the study team

2019-03-26

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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.

You may not qualify if…

• 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.

Where it is running

• New York University School of Medicine — New York, New York, United States

Full record on ClinicalTrials.gov

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