We would like to test the system in a pilot study with vulonteers with mild depressive symptoms. The goals of this pilot are twofold:1) We want to know how easy to use the system is and how content the volunteers are with this form of treatment en…
ID
Source
Brief title
Condition
- Mood disorders and disturbances NEC
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
The primary outcome of this study is the number of depressive symptoms measured
by the CES-D questionnaire.
Secondary outcome
Secundary outcome measures are:
- anxiety (HADS)
- cognition (ATQ)
- mastery (Pearlin mastery scale)
- activities (PES)
- neuroticism (NEO-FFI)
- contentment with course (own design)
Background summary
Most depressive disorders are treated by general practitioners and
psychologists in primary care. Although internet-based self-help has been
proven to be an effective alternative for face-to-face treatment, several
studies have shown that these interventions are only effective when
professional therapists help patients to work through the treatment. However,
in the current project, a collaboration between clinical psychological and
artificial intelligence researchers, we are developing an internet intervention
which is supported by an internet-connected smart-phone, which will guide the
patient through the intervention, instead of a therapist. The type of
intervention we will use (activity scheduling, also called behavioral
activation treatment) has been shown to be effective in many earlier studies,
and can also be expected to be effective as an unguided internet + smart-phone
intervention.
Study objective
We would like to test the system in a pilot study with vulonteers with mild
depressive symptoms. The goals of this pilot are twofold:
1) We want to know how easy to use the system is and how content the volunteers
are with this form of treatment en support.
2) We would like to get an idea of the effects of the intervention, mostly
whether the volunteers show less symptoms of depression after undergoing the
intervention.
Study design
In this pilot we want to perform a randomised controlled trial. The
participants will be randomly distributed over an intervention group and a
control group that will be put on a waiting list. This last group will undergo
the intervention after three months.
Intervention
The intervention group will follow the course which is based on behavioral
activation therapy. The course consists of 5 parts that can be executed via a
webiste and a mobile phone application. During the intervention, the
participants learn techniques to monitor their mood and daily activities and to
learn the relationship between these two. Then, the participants learn to make
a plan to increase the number of pleasant activities and with that to have more
social interation with their environment.
Study burden and risks
Participants will fill out a questionnaire three time. The burden of the course
is very low: the course consists mainly of planning more pleasant activities.
There are no risks involved.
De Boelelaan 1081a
1081 HV Amsterdam
NL
De Boelelaan 1081a
1081 HV Amsterdam
NL
Listed location countries
Age
Inclusion criteria
Score of ><= 20 with the K10, mild to moderate depression diagnoses with CIDI interview
Exclusion criteria
No or heavy depressive complaints
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 |
---|---|
CCMO | NL32709.029.10 |