Condition category
Mental and Behavioural Disorders
Date applied
03/02/2011
Date assigned
22/09/2011
Last edited
22/09/2011
Prospective/Retrospective
Retrospectively registered
Overall trial status
Completed
Recruitment status
No longer recruiting

Plain English Summary

Not provided at time of registration

Trial website

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 measures

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

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

Results - basic reporting

Publication summary

Publication citations

Additional files

Editorial Notes