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Study to Assess Accuracy of Rapid Mood Screener in Adult Participants With Unipolar Major Depressive Disorder or Bipolar 1 Disorder in Real World Setting

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AbbVie

Status

Completed

Conditions

Bipolar I Disorder

Study type

Observational

Funder types

Industry

Identifiers

NCT05956483
H23-890

Details and patient eligibility

About

Bipolar I Disorder (BP1)is a severe chronic mood disorder characterized by manic and depression. BP1 has high probability of being misunderstood as unipolar major depressive disorder (MDD). The purpose of this study is to confirm Rapid Mood Screener (RMS) effectively classifies participants with BP1.

Rapid Mood Screener (RMS) is a brief 6-item clinician-administered checklist, in which a participant's endorsement of four or more questions should trigger further clinical evaluation for BP1. Approximately 404 participants (303 with confirmed unipolar MDD and 101 with confirmed BP1) will be enrolled in the United States.

Participants will be answering RMS questionnaire and accuracy will be measured against Mini-International Neuropsychiatric Interview (MINI) interview.

Enrollment

423 patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Presenting to provider with primary complaint of new or continuing depressive symptoms.

  • May be treatment naïve even if not in their first depressive episode.

  • Meets one of the following criteria:

    • Previously treated and currently off medication.
    • Currently using an antidepressant, atypical antipsychotic for mood disorder, or mood stabilizer.

Exclusion criteria

  • Hospitalized or admitted to the emergency room due to mental health issues in the past 30 days.
  • Currently experiencing a manic episode.
  • History of schizophrenia or depression due to another psychotic disorder or a medical, organic, or drug-induced cause or a neurocognitive disorder (dementia/delirium) (as defined by Diagnostic and Statistical Manual of Mental Disorders [DSM-V] criteria).
  • Participant did not provide informed consent.

Trial design

423 participants in 1 patient group

Rapid Mood Screener (RMS)
Description:
Participants with Unipolar Major Depressive Disorder and Bipolar 1 Depression will be evaluated with RMS questionnaire and MINI interview.

Trial contacts and locations

9

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Central trial contact

Anita Johnson

Data sourced from clinicaltrials.gov

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