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Biofeedback in treatment of aggression

The additive effect of biofeedback to regular aggression regulation treatment in a forensic outpatient population

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
NL-OMON
Registry ID
NL-OMON21893
Enrollment
24
Registered
2019-11-27
Start date
2019-11-01
Completion date
Unknown
Last updated
2024-02-28

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

Conditions

This research project will be performed among forensic outpatients with a proven lack of anger management skills

Interventions

In our study, real-time biofeedback will be added to regular aggression regulation treatment for two weeks (during the intervention phase).

Sponsors

None listed

Eligibility

Inclusion criteria

Inclusion criteria: 1. Proven lack of anger management skills, indicated by either a recently committed violent crime and/or a high risk of committing one; 2. Assigned to individual outpatient Aggression Regulation Treatment after multidisciplinary consultation; 3. Basic understanding of mobile applications; 4. Aged 16 years or above.

Exclusion criteria

Exclusion criteria: 1. Acute manic or psychotic symptoms according to the clinician and/or DSM-V criteria as measured with the (revised) Mini International Neuropsychiatric Interview (MINI), indicated by a score of 3 (or higher) on item 6 or addendum item 1 of the Health of the Nations Outcome Scales (HoNOS); 2. Current high risk of suicide requiring immediate intervention according to the clinician and/or DSM-V criteria as measured with the MINI, indicated by a score of 3 (or higher) on item 2 of the HoNOS; 3. Severe addiction problems, indicated by a score of 4 on the HoNOS, or severe conditions requiring immediate intervention or hospitalisation; 4. Insufficient understanding of the spoken and written Dutch language.

Design outcomes

Primary

MeasureTime frame
Psychophysiological awareness and aggression-related concepts during the ABA-design (baseline, intervention, and follow-up phase using Ecological Momentary Assesment) and at T1 by use of the Agression Questionnaire (AQ) and Anger Bodily Sensations Questionnaire (ABSQ). Also, physiological measures (heart rate) are measured during the ABA-design (baseline, intervention and follow-up).

Secondary

MeasureTime frame
Secondary measures, such as anger and aggression (e.g. STAXI-2), emotion regulation (DERS), psychiatric functioning (HoNOS), will be assessed before and after the four-week ABA-period (T1); and some also at 1 month follow-up (Tf). Also, the system usability of the biofeedback will be evaluated at T1, both quantitatively and qualitatively. At T0, several other outcomes will be assessed to describe the sample, such as aggression type (RPQ), psychopathy (YPI-s) and demographic information.

Contacts

Public ContactAnnemieke ter Harmsel

Inforsa / Arkin

annemieke.ter.harmsel@inforsa.nl020-5904578

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)