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Cognitive Determinants of Psychoeducation and Information in Psychoses

Psychoeducation in Patients With Schizophrenia: Neuropsychological Performance and Cognitive Training as Determinants of Outcome

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00646256
Acronym
COGPIP
Enrollment
120
Registered
2008-03-28
Start date
2006-02-28
Completion date
Unknown
Last updated
2008-03-28

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

Conditions

Delusional Disorders (ICD-10), Schizophrenia

Keywords

schizoaffective, schizotypal

Brief summary

The aim of the study is to examine whether the efficacy of psychoeducation in patients with schizophrenia or schizoaffective disorders is dependent on their cognitive performance level and if a preceding cognitive training can enhance the therapeutic effects of psychoeducation

Detailed description

Schizophrenic inpatients are examined shortly after admission with a broad battery of clinical and neurological rating scales and neuropsychological tests. They are then randomized to either standard treatment (including antipsychotic medications, art and occupational therapy, psychotherapy) or to standard treatment plus daily computerbased cognitive training (COGPACK; ten 1-hour sessions over two weeks). After repetition of the broad assessment battery all patients (and some of their family members) take part in a bifocal psychoeducation group program (eight 1-hour sessions over four weeks). Specific pre-post measures are illness knowledge, self and expert ratings of adherence to treatment, insight to the illness, treatment satisfaction. The study also includes a 9-month follow-up, with number of rehospitalizations, days in hospital and psychopathology as the primary outcome measures.

Interventions

BEHAVIORALCOGPACK training, psychoeducation

Bifocal psychoeducation group program (Munich Psychoses Information Program - PIP) with preceding computerbased cognitive training program (COGPACK)

Sponsors

German Research Foundation
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 60 Years
Healthy volunteers
No

Inclusion criteria

* Inpatients * Informed consent * German as first language or very good knowledge of German

Exclusion criteria

* Mental retardation * Any serious somatic illness

Design outcomes

Primary

MeasureTime frame
illness knowledge, adherence to treatment, insight to the illness, satisfaction with treatment. 9-month follow-up: number of rehospitalizations, days in hospitalBaseline, after cognitive training, after psychoeducation, 9-month after end of psychoeducation

Secondary

MeasureTime frame
Psychopathological status
Psychosocial rehabilitation

Countries

Germany

Contacts

Primary ContactThomas Jahn, Prof. Dr. phil. Dipl.-Psych.
th.jahn@lrz.tum.de+49 (0)89-4140 4278

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026