Treatment Programme
Cross-source consensus on Treatment Programme from 1 sources and 5 claims.
1 sources · 5 claims
Dosage & preparation
Interactions
Other
Highlighted claims
- Participants are randomised equally to CBASP or BA after baseline assessment. — Efficacy, moderators and mediators of cognitive behavioural analysis system of psychotherapy (CBASP) versus behavioural activation (BA) in persistently depressed treatment-resistant inpatients: study protocol for the multicentre, randomised controlled changePDD trial
- Both interventions last 16 weeks and combine 10 weeks of inpatient or day clinic treatment with 6 weeks of outpatient continuation group therapy. — Efficacy, moderators and mediators of cognitive behavioural analysis system of psychotherapy (CBASP) versus behavioural activation (BA) in persistently depressed treatment-resistant inpatients: study protocol for the multicentre, randomised controlled changePDD trial
- Across the full programme, each participant is scheduled for 20 individual therapy sessions, 26 group therapy sessions, 10 nurse contacts, and 10 exercise therapy sessions. — Efficacy, moderators and mediators of cognitive behavioural analysis system of psychotherapy (CBASP) versus behavioural activation (BA) in persistently depressed treatment-resistant inpatients: study protocol for the multicentre, randomised controlled changePDD trial
- Both trial arms receive the same weekly amount of treatment during the acute phase. — Efficacy, moderators and mediators of cognitive behavioural analysis system of psychotherapy (CBASP) versus behavioural activation (BA) in persistently depressed treatment-resistant inpatients: study protocol for the multicentre, randomised controlled changePDD trial
- Both arms receive standardised guideline-based pharmacotherapy in addition to psychotherapy. — Efficacy, moderators and mediators of cognitive behavioural analysis system of psychotherapy (CBASP) versus behavioural activation (BA) in persistently depressed treatment-resistant inpatients: study protocol for the multicentre, randomised controlled changePDD trial