Aggression Replacement Training for adults.
- Registration Number
- NL-OMON25956
- Lead Sponsor
- Radboud University Nijmegen Medical Centre
- Brief Summary
/A
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Pending
- Sex
- Not specified
- Target Recruitment
- 66
Inclusion Criteria
1. Age 18-55 years;
2. Men and women;
Exclusion Criteria
1. IQ < 84;
2. Lifetime history of (hypo)mania, schizophrenia, or delusional disorder;
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The main outcome of aggressive behavior will be the score on the Overt Aggression Scale-Modified for Outpatient Use (MOAS) and Social Dysfunction and Aggression Scale (SDAS). The MOAS and SDAS will be completed by different relevant informants.
- Secondary Outcome Measures
Name Time Method During the pre-screening, the MOAS will be completed to examine if the participant meets the inclusion criteria. To examine if the participant does meet the inclusion and does not meet the exclusion criteria the M.I.N.I., SCID-II, CIDI, PPI, Mate-Crimi and NLV will be completed during the screening. For the baseline and follow-up measure of the interventions, the IOA will be conducted to measure social skills. The IPAS, RPQ, AQ, ZAV, HIT and PSAP will be used to measure the effect of the Anger Control Training. To assess psychomotor training, heart rate and skin conductance will be measured. In addition, neurocognitive tasks will be conducted to examine how responders and non-responders profiles relate to forms and correlates of aggressive behaviour.