Objective: We would like to differentiate *normative mood swings*. in adolescence from early signs of depression. A comparison between low-risk adolescents and an at risk and a clinically referred sample is needed to detect an unrecognized subsample…
ID
Source
Brief title
Condition
- Mood disorders and disturbances NEC
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Main study parameters/endpoints: The primary focus of our study is to
recognized a subsample of adolescents at risk for depression among the general
population: clinical patients and at risk adolescents (this study), are
therefore compared to healthy controls (data collected).
Secondary outcome
n/a
Background summary
Rationale: Early signs of depression resemble prototypical behaviors of
teenagers, such as irritability, sadness, and grumpiness. Therefore, youths who
suffer from early depression are often not detected, and, therefore, receive
insufficient treatment. We hypothesize that adolescents at risk for depression
have an atypical rigid negative mood patterns across social contexts (e.g.,
school, home, peer group), that resembles the mood pattern of clinically
referred depressed youth and youth at risk for depression due to family load
(first degree family member affected). These mood patterns can be detected by
combining the methodological strengths of monitoring daily mood swings with
powerful cutting-edge Bayesian statistics.
Study objective
Objective: We would like to differentiate *normative mood swings*. in
adolescence from early signs of depression. A comparison between low-risk
adolescents and an at risk and a clinically referred sample is needed to detect
an unrecognized subsample of adolescents at risk for depression among the
normal population.,
Study design
Study design: Adolescents will use a cell-phone app to monitor their mood over
the course of a week. State-of-the-art analyses will identify underlying mood
patterns and their unique predictive value for adolescent depression, compared
to multi-informant questionnaire data (i.e., adolescent and parent).
Study burden and risks
Nature and extent of the burden and risks associated with participation,
benefit and group relatedness: Adolescent participants are asked to fill in
questionnaires at the beginning of the study (total duration 30 min). The
ecological momentary assessment (EMA) period is 7 days with 8 measurements a
day. In total 56 measurements of 1 min during 7 days. Also parents are asked to
fill in a questionnaire about general functioning and parenting styles, mood
and behavior problems of their child (see schedule of measurements in method
section). Parents are also asked to give information about their own
psychological functioning.
EMA is a non-invasive technique, so there is no need for special preparation
for the subject. There are no known risks associated with the EMA and the data
are solely used for research purposes. Adolescents might benefit from this
study, by experiencing the effect of monitoring their mood and get insight in
their own mood profile.
If the results point out severe psychopathology (e.g. suicidality), the child
and adolescent psychiatrist involved (MH) will discuss the findings with the
treating psychiatrist of the participating adolescent.
Heidelberglaan 100
Utrecht 3584 CX
NL
Heidelberglaan 100
Utrecht 3584 CX
NL
Listed location countries
Age
Inclusion criteria
Between 12 and 18 years old
Depressive symptoms or selective mutism or an affected first degree family member
Children and parents provide written informed consent
Dutch speaking and reading
Own a smartphone
Exclusion criteria
Not able to speak or read Dutch
No smartphone to install the ESM app (Mypanel)
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 | NL52304.041.15 |