Feasibility Study of Unified Protocol for Anxiety and Depressive Disorders

Phase 1

• Conditions: Anxiety Disorders, Depressive Disorders

• Registration Number: JPRN-UMIN000008322
• Lead Sponsor: ational Center of Neurology and Psychiatry, National Center for Cognitive Behavior Therapy and Research

Brief Summary

The severity of anxiety symptoms decreased significantly after the intervention and remained low for 3 months.

Detailed Description

Not available

Study Timeline

• Study Start: 2012-07-12
• Study Completion: 2014-07-31
• Results First Posted: 2016-02-24
• Last Update Posted: 17 October 2023

Recruitment & Eligibility

• Status: Complete: follow-up complete
• Sex: All
• Target Recruitment: 17

Inclusion Criteria

Not provided

Exclusion Criteria

1. No alcohol or substance use disorder in 6 months prior to the screening. 2. No history or concurrent manic or psychotic episode. 3. No other primary DSM-IV Axis I Disorders in six months prior to the screening. 4. No comorbid of antisocial personality disorder. 5. No serious suicidal ideation at screening. 6. Evidence of unable to participate half or more of the intervention phase. 7. No past treatment of CBT. 8. No structured psychotherapy (except supportive therapy) during the intervention. 9. No major cognitive deficits at screening. 10. No life-threatening, severe or unstable physical disorders at screening. 11. Other relevant reason decided by the investigators.

Study & Design

• Study Type: Interventional
• Study Design: Not specified