Contact information
Type
Scientific
Primary contact
Dr Lieselotte Mahler
ORCID ID
Contact details
Große Hamburger Strasse 5-11
Berlin
10115
Germany
lieselotte.mahler@charite.de
Additional identifiers
EudraCT number
ClinicalTrials.gov number
Protocol/serial number
Version I 31.05.2010
Study information
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")
Acronym
Weddinger Modell
Study hypothesis
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
Ethics Committee of the Charité-University Medicine Berlin (Ethikkommission der Charité -Universitätsmedizin) approved on 29th June 2010, ref: EA4/074/10
Study design
Controlled parallel group observational study
Primary study design
Observational
Secondary study design
Non randomised controlled trial
Trial setting
GP practices
Trial type
Quality of life
Patient information sheet
Not available in web format, please use the contact details below to request a patient information sheet
Condition
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
Phase
Not Applicable
Drug names
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 trial start date
01/09/2010
Overall trial end date
31/12/2013
Reason abandoned (if study stopped)
Eligibility
Participant 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
Participant type
Patient
Age group
Adult
Gender
Both
Target number of participants
1200
Participant exclusion criteria
1. Duration of stay in hospital less than 24 hours
2. Suicidal indication and severe aggression
3. Serious organic brain disease
Recruitment start date
01/09/2010
Recruitment end date
31/12/2013
Locations
Countries of recruitment
Germany
Trial participating centre
Große Hamburger Strasse 5-11
Berlin
10115
Germany
Sponsor information
Organisation
Charité - University Medicine Berlin (Charité - Universitätsmedizin Berlin) (Germany)
Sponsor details
c/o Dr. Lieselotte Mahler
Department of Psychiatry and Psychotherapy
Campus Mitte
Berlin
10115
Germany
lieselotte.mahler@charite.de
Sponsor type
Hospital/treatment centre
Website
Funders
Funder type
Hospital/treatment centre
Funder name
Charité University Medicine (Germany)
Alternative name(s)
Funding Body Type
Funding Body Subtype
Location
Results and Publications
Publication and dissemination plan
Not provided at time of registration
Intention to publish date
Participant level data
Not provided at time of registration
Basic results (scientific)
Publication list