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A single case experimental design of combined program of compassion focused therapy with family psychoeducation for depression and anxiety.

A single case experimental design of combined program of compassion focused therapy with family psychoeducation for depression and anxiety. - A single case experimental design of combined program of compassion focused therapy with family psychoeducation for depression and anxiety.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000054304
Enrollment
6
Registered
2024-05-02
Start date
2023-08-01
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

Major Depressive Disorder and Anxiety Disorders.

Interventions

Compassion Focused Therapy and Psycho-education for Family or Partner

Sponsors

National Center of Neurology and Psychiatry
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Have major depressive disorder, panic disorder, square phobia, social anxiety, or generalized anxiety on the MINI 2)Have mild or severe depressive symptoms (more than 10 points on the PHQ-9) 3)Aged between 18 and 65 years at screening 4)Have given written consent for significant others to participate in online psychoeducation 5)Understand the purpose and content of this study and have given written consent to participate in the study of their own free will

Exclusion criteria

Exclusion criteria: 5) Those with alcohol or substance dependence present within 6 months of the time of screening 6) Manic episodes, schizophrenia and other psychotic disorders at the time of pre-intervention evaluation. 5 and 6 above will be evaluated by MINI. 7) Patients with significant suicidal ideation (B. module of MINI, B10-14, 16) at the time of pre-intervention evaluation. 8)Significant others must not have a history of psychiatric disorders within the past year. 9)Persons with physical illness or severe cognitive impairment that would make it difficult to implement CFT at the time of pre-intervention evaluation. 10)Patients who are known in advance at the time of pre-intervention evaluation to have difficulty in coming to the hospital for at least 50% of the CFT implementation period. 11) Patients receiving other psychotherapy or counseling at the time of the pre-intervention evaluation. 12) Other subjects deemed inappropriate for this study by the principal investigator.

Design outcomes

Primary

MeasureTime frame
Depressive symptoms as measured by PHQ-9

Countries

Japan

Contacts

Public ContactKenichi Asano

National Center of Neurology and Psychiatry CBT Center

kenichi-asano@ncnp.go.jp042-341-2711

Outcome results

None listed

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