Depressive Disorder
Conditions
Interventions
Cognitive-Behavioral Group Therapy
Treatment as usual
Sponsors
Keio University, School of Medicine
1. Ichigaya Himorogi Clinic 2. Shinjuku Yoyogi Kokoro no Labo Clinic 3. Hamadayama Metal Clinic
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Subjects with DSM-V Depression Disorder 2. Subjects with CGIS(Clinical Global Impression)score is 3(mildly ill ), 4(Moderately ill), or 5(Markedly ill) 3. Subjects between the ages of 18 and 70 at the time of screening 4. Subjects ca obtain written consent
Exclusion criteria
Exclusion criteria: 1. No alcohol or substance use disorder in 24 months prior to the screening. 2. No history of concurrent manic, or psychotic episodes. 3. No other primary Axis I Disorders in 6 months prior to the screening. 4. No comorbid antisocial personality disorder. 5. No serious suicidal ideation at screening. 6. Unlikely to attend more than 4 visits during the 8-week trial phase. 7. No treatment of CBT or CBGT within the last year prior to the screening. 8. No organic brain lesions or major cognitive deficits. 9. No severe or unstable medical illness at screening. 10. Other relevant reasons decided by the CogGrout study principal investigator.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Depressive symptom: PHQ-9(Patient Health Questionnaire | — |
Secondary
| Measure | Time frame |
|---|---|
| -Anxiety symptom: GAD-7(Generalized Anxiety Disorder) -Self-Efficacy: GSES(General Self-Efficacy Scale) -Personal Recovery: QPR-J(Japanese version of the Questionnaire about the Process of Recovery) -Coping stress: CISS(Coping Inventory for Stressful Situation) -QOL: WHO-QOL -Disability: SDS(Sheehan Disability Scale) -Others: Questionnaire on the use of CBT skills after participating in the group. | — |
Countries
Japan
Contacts
Public ContactMiyuki Tajima
Keio University School of Medicine Department of Neuropsychiatry
Outcome results
None listed