Patient centred work in psychiatric care: the Weddinger Modell

ISRCTN	ISRCTN88784815
DOI	https://doi.org/10.1186/ISRCTN88784815
Secondary identifying numbers	Version I 31.05.2010

Submission date: 03/02/2011
Registration date: 22/09/2011
Last edited: 22/09/2011

Recruitment status: No longer recruiting
Overall study status: Completed
Condition category: Mental and Behavioural Disorders

Prospectively registered

Protocol

Statistical analysis plan

Results

Individual participant data

Record updated in last year

Plain English summary of protocol

Not provided at time of registration

Contact information

Dr Lieselotte Mahler
Scientific

Große Hamburger Strasse 5-11
Berlin
10115
Germany

Email	lieselotte.mahler@charite.de

Study information

Study design	Controlled parallel group observational study
Primary study design	Observational
Secondary study design	Non randomised controlled trial
Study setting(s)	GP practice
Study type	Quality of life
Participant information sheet	Not available in web format, please use the contact details below to request a patient information sheet
Scientific title	Patient centered work-satisfaction and resilience in the Trialogue - an observational study (Weddinger Modell) (Patientenzentriertes Arbeiten- Zufriedenheit und Resilienz im Trialog - eine Beobachtungsstudie (Das "Weddinger Modell")
Study acronym	Weddinger Modell
Study objectives	The aim of the study is a novel patient centred approach (Weddinger Modell) in psychiatric care for problematic urban districts. Improve measures of patient contentedness, resilience, goal-attainment and therapeutic relationship evaluated by patients, relatives and staff.
Ethics approval(s)	Ethics Committee of the Charité-University Medicine Berlin (Ethikkommission der Charité -Universitätsmedizin) approved on 29th June 2010, ref: EA4/074/10
Health condition(s) or problem(s) studied	Psychiatric disorders leading to hospital admission
Intervention	A controlled, clinical, longitudinal trial using trialogical questionnaires including self-rating as well as ratings by relatives and by professionals.
Intervention type	Other
Primary outcome measure	1. WPAZ 2. Resilence-Questionnaire 3. Work Ability Index (WAI) 4. Goal-Attainment-Scale, Global Assessment of Functional Scale (GAF) 5. Staff contentedness Measured before and after the intervention.
Secondary outcome measures	Need for hospital admission and extent of comunity-based care one year prior and one year after inclusion
Overall study start date	01/09/2010
Completion date	31/12/2013

Eligibility

Participant type(s)	Patient
Age group	Adult
Lower age limit	18 Years
Sex	Both
Target number of participants	1200
Key inclusion criteria	1. Age more than 18 years 2. All admitted patients -patients treated in three psychiatric hospitals in Berlin, who give informed consent 3. Relatives of admitted patients 4. Staff
Key exclusion criteria	1. Duration of stay in hospital less than 24 hours 2. Suicidal indication and severe aggression 3. Serious organic brain disease
Date of first enrolment	01/09/2010
Date of final enrolment	31/12/2013

Locations

Countries of recruitment

Germany

Study participating centre

Große Hamburger Strasse 5-11

Berlin
10115
Germany

Sponsor information

Charité - University Medicine Berlin (Charité - Universitätsmedizin Berlin) (Germany)
Hospital/treatment centre

c/o Dr. Lieselotte Mahler
Department of Psychiatry and Psychotherapy
Campus Mitte
Berlin
10115
Germany

Email	lieselotte.mahler@charite.de
"ROR"	https://ror.org/001w7jn25

Funders

Funder type

Hospital/treatment centre

Charité University Medicine (Germany)

No information available

Results and Publications

Intention to publish date
Individual participant data (IPD) Intention to share	No
IPD sharing plan summary	Not provided at time of registration
Publication and dissemination plan	Not provided at time of registration
IPD sharing plan