This study examines a the role of four key ultra-high-risk criteria for personality disorders: interpersonal trauma, personality functioning, quality of social support system and subclinical features of borderline personality disorder. For two of…
ID
Source
Brief title
Condition
- Personality disorders and disturbances in behaviour
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
De primaire uitkomstmaten zijn de scores op elk van de instrumenten voor
UHR-criteria. We verwachten op alle criteria hogere gemiddeldes in de
risicosteekproef dan in de samenlevingssteekproef.
The primary outcome is the score on each of the instruments meant to assess the
UHR-criteria. We predict higher mean scores in the risk sample then in the
cohort sample for all criteria.
Secondary outcome
not applicable
Background summary
For optimal indication for indicated prevention, it is necessary to predict the
onset of a mental disorder. This is especially true for severe and potentially
chronic (mental) disorders, such as personality disorders. Recent models of
personality disorders imply the existence of four ultra high risk criteria for
the development of personality disorders. In this study we aim to develop and
validate assessment tools for these four UHR-criteria.
Study objective
This study examines a the role of four key ultra-high-risk criteria for
personality disorders: interpersonal trauma, personality functioning, quality
of social support system and subclinical features of borderline personality
disorder. For two of these four UHR-criteria, there a not yet validated
assessment tools. In this study we aim to develop and validate those tools in a
risk sample.
Study design
In across-sectional design the instrument to assess UHR-criteria are developed
and validated in a risk and cohort sample.
Study burden and risks
Interviews and questionnaires are conducted. The baseline measurement takes a
little over 1,5 hours with the child/adolescent and 75 minutes with a parent.
The risks are minimal. Development of a reliable and valid instrument requires
extensive assessment of the identified UHR criteria.
Warandelaan 2
Tilburg 5037 AB
NL
Warandelaan 2
Tilburg 5037 AB
NL
Listed location countries
Age
Inclusion criteria
The clinical sample consists of children and adolescents (and their parents)
enrolled in MST-CAN, a treatment programme for families where there is
objectified maltreatment. The control sample is a community sample.
Participants are both children/adolescents and their parent(s). Children must
be between 10 and 15 years old.
Exclusion criteria
Inability to participate in interviews or questionnaires due to insufficient
command of language, intelligence or for other reasons
Design
Recruitment
Medical products/devices used
Followed up by the following (possibly more current) registration
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Other (possibly less up-to-date) registrations in this register
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In other registers
| Register | ID |
|---|---|
| CCMO | NL84463.028.23 |