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Follow-Up Study to the parent study "Comparison of CBASP versus Escitalopram for chronic depression"

Follow-Up Study to the parent study "Comparison of CBASP versus Escitalopram for chronic depression" - CBASP1_FUP

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00008935
Enrollment
60
Registered
2015-08-06
Start date
2015-06-19
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

chronic depression, double depression F34.1

Interventions

Group 1: patients receiving CBASP in the mother study now fill out questionnaires concerning current depr. symptomatology and general health Group 2: patients receiving Escitalopram and clinical manag

Sponsors

Universitätsklinikum FreiburgKlinik für Psychiatrie und Psychotherapie
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: This is a follow-up investigation. Thus only participants of the mother-study were included. The inclusion criteria were as follows: eligible subjects were between 18 and 65 years old and met the DSM-IV criteria for a current episode of chronic major depressive disorder (with the modification of at least 1 year of depressive symptomatology) or recurrent major depressive episodes ( = 3 episodes with the preceding episode no more than 2.5 years before the onset of the current episode). A score of = 18 on the Montgomery-Asberg Depression Scale (MADRS, [24] ) was required. The patients had to be medication free for a minimum of 2 weeks before baseline. Furthermore, the subjects needed to be fluent in German and able to provide written informed consent.

Exclusion criteria

Exclusion criteria: The exclusion criteria were as follows: patients were not eligible for the study if they had an acute risk for suicide (as opposed to suicidal thoughts or chronic suicidality) assessed according to clinical practice guidelines. Further exclusion criteria were: a history of psychotic symptoms, bipolar disorder, or dementia; severe substance- related abuse or dependence disorder; schizotypal, antisocial, or borderline personality disorder; serious medical conditions; severe cognitive impairment, and absence of a response to a previous adequate trial of CBASP or ESC.

Design outcomes

Primary

MeasureTime frame
depressive symptomatology after minimum of 2 years after treatment measured via IDS

Secondary

MeasureTime frame
General Health as measured by the WHOWoL-BREF a minimum of 2 years after the mother-study

Countries

Germany

Contacts

Public ContactPaul Bausch

Uniklinikum FreiburgKlinik für Psychiatrie und Psychotherapie

paul.bausch@uniklinik-freiburg.de0049 761 270 69420

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Feb 4, 2026