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NCT00885716 Clinical Trial

A Shared Decision Making Training for Inpatients With Schizophrenia

Schizophrenia Clinical Trial

Official title:
Shared Decision Making: Ein Kommunikationstraining für Patienten Mit Schizophrenie

Clinical Trial Details — Status: Recruiting

Administrative data
NCT number NCT00885716
Other study ID # GIF2168-1764.1
Secondary ID
Status Recruiting
Phase N/A
First received April 20, 2009
Last updated April 7, 2010
Start date May 2009

Study information
Verified date April 2010
Source Technische Universität München
Contact Johannes Hamann, MD
Phone +49894140
Email j.hamann@lrz.tum.de
Is FDA regulated No
Health authority Germany: Federal Ministry of Education and Research
Study type Interventional

Clinical Trial Summary

Patients suffering from schizophrenia who attend the communication skills program engage more deeply in therapeutic reasoning and treatment decisions. This results in stronger preferences to participate, greater perceived involvement and better long term adherence compared to patients who do not attend the training.

Recruitment information / eligibility
Status Recruiting
Enrollment 80
Est. completion date
Est. primary completion date
Accepts healthy volunteers No
Gender Both
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria:

- Male and female inpatients with a diagnosis of schizophrenia/schizoaffective disorder according to ICD 10

- between 18 and 60 years of age are eligible for the study

- informed consent

- inpatients

Exclusion Criteria:

- poor German language skills

Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Open Label, Primary Purpose: Health Services Research

Related Conditions & MeSH terms

Intervention

Behavioral:
• patient training in shared decision making

• cognitive training

Locations
Country Name City State
Germany Klinik und Poliklinik für Psychiatrie und Psychotherapie, Technische Universität München München

Sponsors (2)
Lead Sponsor Collaborator
Technische Universität München The German-Israeli Foundation for Scientific Research and Development

Country where clinical trial is conducted

Germany, 

Outcome
Type Measure Description Time frame Safety issue
Primary Decision Self Efficacy post intervention No
Secondary Adherence to medication 6 months post intervention No
Secondary Participation preferences post intervention No
Secondary Treatment satisfaction post intervention No
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