Evidence-Based Intervention for Rumination in Clinical Settings

Effectiveness of a face-to-face rumination-focused cognitive-behavioral therapy for depression and anxiety - RFCBT-NARA

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000046216

Enrollment

Registered

2021-11-30

Start date

2021-12-01

Completion date

Unknown

Last updated

2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

depression, anxiety

Interventions

Patients receive 12 to 20 individual face-to-face RFCBT sessions (50m per session) weekly or once in several weeks.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Aged 18 or over, with diagnosis of depression and/or anxiety (GAD), or showing risks or residual symptoms of either or both. Participation will follow doctor's consultation.

Exclusion criteria

Exclusion criteria: Age younger than 18; when the patient's doctor considers participation unsuitable, e.g., diagnosed with schizophrenia, manic episode etc.; those who requires intensive care e.g., showing risk to harm self or others

Design outcomes

Primary

Measure	Time frame
Rumination: RRS Depression: PHQ-9 Assessed at pre- and post-intervention and at each session	—

Secondary

Measure	Time frame
Worry: PSWQ Anxiety: GAD-7 Assessed at pre- and post-intervention	—

Countries

Japan

Contacts

Public ContactYusuke Umegaki

Nara Women's University Faculty of Human Life and Environment

y.umegaki@cc.nara-wu.ac.jp0742203577

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026