The primary objective of the proposed study is to gain insight in the underlying neural mechanisms by which frontal cortical activation patterns are established, and its implications for human aggressive behaviour. The proposed approach aims to…
ID
Source
Brief title
Condition
- Personality disorders and disturbances in behaviour
Synonym
Research involving
Sponsors and support
Intervention
Outcome measures
Primary outcome
Main study parameters in the proposed study are the inter-individual
differences in relations between cortico-cortical functional connectivity,
behavioural measures and personality characteristics. In two of the four
proposed substudies the collected endocrine measures will also be related to
cortico-cortical functional connectivity, behavioural measures and personality
characteristics.
Secondary outcome
Subject's demographics, motorthreshold values (part of the transcranial
magnetic stimulation procedure).
Background summary
Social aggression poses a major threat for individuals and society. The
investigation of the psychobiological underpinnings of this destructive
phenomenon is thus of critical importance. Recent evidence suggests that
hormonal imbalances in steroid hormones
and aberrant forms of cortical brain communication are associated with social
aggression.
Study objective
The primary objective of the proposed study is to gain insight in the
underlying neural mechanisms by which frontal cortical activation patterns are
established, and its implications for human aggressive behaviour. The proposed
approach aims to integrate hormonal and physiological properties of
cortico-cortcal and cortico-subcortical brain communication, and relate these
properties to human aggressive behaviour.
Study design
As the proposed study aims to compare inter individual differences in
relations in hormonal, physiological and behavioural properties, this
observational study employs a between subjects design.
Study burden and risks
In order to alleviate experimental demands posed upon the participants, all
participants will perform not all tasks. Therefore, candidate participants will
be asked to perform only a subset of tasks in each of the proposed sub
experiments. The study will consist of four sub experiments, each of which will
last approximately one and a half hour. In 2 of the four proposed sub
experiments, an additional time investment of the participant will be asked
because of the collection of saliva directly after awakening, and the
collection of a saliva sample directly preceding the experimental session. The
experimental sessions will consist of the administration of two questionnaires,
a Transcranial Magnetic Stimulation session and a behavioural task. The
parameters used in the Transcranial Magnetic Stimulation session are well
within internationally accepted stimulation parameters, and bear a negligible
health risk.
Heidelberglaan 2
3584 CS Utrecht
Nederland
Heidelberglaan 2
3584 CS Utrecht
Nederland
Listed location countries
Age
Inclusion criteria
Good health
Right-handedness
Non-smoking
Aged between 18-40 years
Normal or corrected-to-normal vision
Signed informed consent
Exclusion criteria
Metal in cranium
15 alcoholic beverages per week
Use of psychotropic drugs, including cannabis, XTC, amphetamines and cocaine
Epilepsy or family history of epilepsy (1st degree relatives)
History of closed-head injury
History of neurological or psychiatric disorders and/or treatment
Current neurological or psychiatric treatment
History of endocrinological disorders and/or treatment
Current endocrinological treatment
Medication: Benzodiazepines, antidepressants & neuroleptica
Cardiac pacemaker
Implanted medication pump
Intra-cardiac lines
Habitual smoking
Pregnancy
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 | NL27425.041.09 |