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Military Aggression Regulation Study

Military Aggression Regulation Study - MARS

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON39980
Enrollment
100
Registered
2013-03-14
Start date
2013-05-14
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

agressieregulatie problematiek aggression anger

Interventions

None listed

Sponsors

Universitair Medisch Centrum Utrecht
Lead Sponsor

Eligibility

Age
18 Years to 99 Years

Inclusion criteria

Inclusion criteria: For participants with impulsive aggression, the following inclusion criteria: - Soldiers and veterans (men) who participated in a military deployment (minimum 4 months) - Age between 18 and 50 years - Presence of problems with aggression as evidenced by either (I): the A1 or A2 criterion of the research diagnostic criteria for impulsive aggression "(Coccaro, 2012), or (II) evidence for problems with pent-up anger as revealed by answers to the screening questionnaire. - Written informed consent;  For control participants, the following inclusion criteria: - Healthy men - Age between 18 and 50 years - Written informed consent - No (current) DSM-IV Axis-I disorder - No evidence of problems with aggression

Exclusion criteria

Exclusion criteria: - Alcohol / substance abuse and / or dependence - Severe neurological diseases (eg Parkinson's disease, stroke, MS);Exclusion for MRI procedure: - Claustrophobia, pacemaker (or other implants), or metal objects in the body causing an MRI scan is not possible. - Current use of psychotropic drugs (benzodiazepines, antidepressants, antipsychotics, anticonvulsants)

Design outcomes

Primary

MeasureTime frame
Differences in amygdala and prefrontal cortex activity, differences in startle response, differences in blood parameters as neuropeptide Y, vasopressin and testosterone, differences in performance on neuropsychological tasks between veterans with aggression regulation problems and healthy control participants.

Secondary

MeasureTime frame
n.a.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)