Accompaniment study:Effect study of the treatment as usual group of the randomized controlled trial (UMIN00002998) of the remote personal cognitive-behavioral therapy for panic disorder patients

Accompaniment study:Effect study of the treatment as usual group of the randomized controlled trial (UMIN00002998) of the remote personal cognitive-behavioral therapy for panic disorder patients - Effect study of the TAU group in RCT of the remote personal cognitive-behavioral therapy for panic disorder patients

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000033680

Enrollment

Registered

2018-08-08

Start date

2018-08-24

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

panic disorder

Interventions

videoconference cognitive behavioral therapy(vCBT)(16weeks)

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Primary diagnosis of Panic Disorder refractory to medicine(Taking antidepressant or anti-anxiety drugs treatment and had done so for at least 8 weeks at an adequate dose while remaining at least moderately ill(PDSS >=8)).

Exclusion criteria

Exclusion criteria: psychosis, major depression, bipolar, active suicidality, organic brain disorder, substance abuse or dependence, antisocial personality disorder, other severe mental / physical condition

Design outcomes

Primary

Measure	Time frame
Panic Disorder Severity Scale(PDSS)(assessor-rated)	—

Secondary

Measure	Time frame
PAS(Panic and Agoraphobia Scale) PHQ-9(Patient Health Questionnare-9) GHQ-7(Generalized anxiety disorder-7) EQ-5D-5L(EuroQol5-Dimension-5Levels)	—

Countries

Japan

Contacts

Public ContactYoichi Seki

Chiba University Hospital Cognitive Behavioral Therapy Center

yoichi-seki@chiba-u.jp043-226-2027

Outcome results

None listed

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