This study aims at gathering conclusive information about the effectiveness and efficiency of the secondDepression Breakthrough Collaborative and to make the results useful to other implementationprograms.This study aims to answer the following…
ID
Source
Brief title
Condition
- Mood disorders and disturbances NEC
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Outcomes are on the professional, organisational and on the patient level.
The primary outcome measure of professional performance is:
• a reduction of antidepressants prescription for patients with non-severe
depression (reduction of overtreatment)
The primary outcome measure of organisational performance is:
•a reduction of the waiting time to specialised depression treatment for
patients with severe or long term depression (reduction of undertreatment)
The primary outcome measures on the patient level are:
•a reduction in depressive symptoms and an improvement in disability status
(effectiveness).
Secondary outcome
Secondary measures are:
Professional performance: satisfaction with collaboration, patient education
delivered
Organisational level: monitoring system in use
Patient level outcomes: care consumption, satisfaction with care
Background summary
Depression is a growing problem in terms of suffering and care utilization. Two
depression guidelines contain recommendations about the use of effective
interventions in Dutch mental health. There is a gap between guidelines and
daily practice. One of the problems is the prescription of antidepressants to a
broad group of patients, unrelated to the severeness of symptoms. The
Breakthrough method is a promising guideline implementation strategy, but has
not been evaluated in Dutch mental health. Some lessons can be learned from a
pilot project actually being effectuated by the Trimbos-institute and the CBO.
A second large scale Depression Collaborative will start in december 2006. This
study is and evaluation of the break through method in Dutch mental health.
Results are of interest to implementation experts and researchers within and
outside mental health, as well as to policy makers and financers of this type
of projects. Results will be spread from 2008 onwards during an invitational
conference and in the scientific literature, as part of a PhD programme.
Study objective
This study aims at gathering conclusive information about the effectiveness and
efficiency of the second
Depression Breakthrough Collaborative and to make the results useful to other
implementation
programs.
This study aims to answer the following central questions:
1 .Does a Depression Breakthrough Collaborative lead to better adherence to
guidelines with better outcomes for patients compared to care as usual?
2.Does implementing guidelines with the Breakthrough Method lead to more
efficient health care compared to care as usual?
3. What are the implementation activities and experiences of the improvement
teams and what barriers and facilitators for successful implementation can be
identified?
Study design
The design is a quasi-experimental trial, consisting of a systematic
measurement of patient outcomes (depression symptoms and functional status) and
care provided by practitioners (antidepressant prescription, monitoring) of the
new Depression Collaborative. Outcomes are compared to care as usual
delivered by a control group of primary and specialty mental health
practitioners from the NESDA cohort study (ZonMw/GeestKracht consortium
Depression). The design of the economic evaluation is a cost-effectiveness
study. (In-)direct health care cost as well as implementation costs are
included. Additional information about the implementation processes is gathered
using mainly qualitative methods.
Study burden and risks
The additional burden in this reasearch caused to patients is limited and
consist of 1 interview and 1 questionaire at inclusion and 1 questionaire at
follow-up after 1 year.
The burden for health care providers is limited to some questionaires during
the course of the project, and participation in a group and/or individual
interview.
Postbus 725
3500 AS Utrecht
Nederland
Postbus 725
3500 AS Utrecht
Nederland
Listed location countries
Age
Inclusion criteria
down or depressive symptoms (according to general practitioner)
aged 18-65
Exclusion criteria
already receiving care, insufficient Dutch language skills, aged under 18 or above 65
Design
Recruitment
Followed up by the following (possibly more current) registration
No registrations found.
Other (possibly less up-to-date) registrations in this register
No registrations found.
In other registers
Register | ID |
---|---|
ISRCTN | ISRCTN99634826 |
CCMO | NL14942.097.06 |