| Literature DB >> 29422873 |
Sandra Fielenbach1,2, Franc C L Donkers3, Marinus Spreen1, Harmke A Visser1, Stefan Bogaerts2,4.
Abstract
BACKGROUND: Effective treatment interventions for criminal offenders are necessary to reduce risk of criminal recidivism. Evidence about deviant electroencephalographic (EEG)-frequencies underlying disorders found in criminal offenders is accumulating. Yet, treatment modalities, such as neurofeedback, are rarely applied in the forensic psychiatric domain. Since offenders usually have multiple disorders, difficulties adhering to long-term treatment modalities, and are highly vulnerable for psychiatric decompensation, more information about neurofeedback training protocols, number of sessions, and expected symptom reduction is necessary before it can be successfully used in offender populations.Entities:
Keywords: criminal offending; electroencephalographic learning; impulsivity; neurofeedback; neurofeedback-learning
Year: 2018 PMID: 29422873 PMCID: PMC5788905 DOI: 10.3389/fpsyt.2017.00313
Source DB: PubMed Journal: Front Psychiatry ISSN: 1664-0640 Impact factor: 4.157
Figure 1Preferred Reporting Items for Systematic Reviews and Meta-Analyses flow diagram of selection of studies. Two articles included in the search results (44, 45) refer to the same study, so the flow chart does not count them twice.
Characteristics of the included studies (N = 10).
| Reference, | Protocol, electrode position, number of sessions | Control group (yes/no), moment of measurement | Change in EEG-parameters investigated by | Behavioral change investigated by | Criterion established for EEG-learning (yes/no) | Results |
|---|---|---|---|---|---|---|
| Arns et al. ( | QEEG-Informed protocols: beta ↑/theta ↓/alpha ↓; or beta ↓; or SMR ↑/theta ↓ (+possibly alpha ↑); or SMR ↑; individual electrode position; mean number of sessions 33.62 | No, pre-training, mid-training and post-training | Changes in power in IAF, SMR, beta frequency bands and ERP measures | MINI PLUS/MINI PLUS KID, BDI (inattention, hyperactivity/impulsivity, depression scores) | No | Inattention ↑, hyperactivity/impulsivity ↑, depressive symptoms ↑. Response rate was 76% (16 out of 21) on behavioral measures SMR power ↓, alpha, beta <> |
| Mayer et al. ( | SCP ↓↑; Cz; 30 sessions | No, pre-, mid-, post-training and 6 months follow-up | Changes in CNV mean amplitude with Go/NoGo ERP task | ADHD-SB, WRI, FEA, FERT | Yes: learners/non-learners based on ability to differentiate between negativation/positivation in transfer condition of last 3 sessions | Self-rated ADHD symptoms ↑, third-party rated ADHD symptoms ↑, depressive symptoms ↑, state and trait anxiety ↑, reaction time and reaction time variability ↑ CNV showed a trend of increase over time 13 learners vs 11 non-learners. Trend toward larger improvements of self-rated ADHD symptoms in learners. Higher improvements of self-rated symptoms for learners at follow-up |
| Schönenberg et al. ( | Theta (4–8 Hz) ↓; beta (13–21 Hz) ↑; 30 sessions | Yes: sham-NFB/meta-cognitive group therapy (MCT), pre-training, mid-training, post-training and follow-up | Changes in mean theta/beta ratio | CAARS, BDI-II, STAI-state, FPTM-23, TAP, Stroop, CPT, INKA | No | Inattention ↑, hyperactivity ↑, impulsivity ↑, anxiety symptoms ↑, depression ↑, TAP flexibility ↑, reaction time <>, no superiority of NFB as compared to control groups Theta/Beta ratio <> |
| Arani et al. ( | Alpha (8–11 Hz) ↓/theta (5–8 Hz) ↑, after crossover alpha + theta ↑ while delta (2–5 Hz) ↓ at Pz; SMR (12–15 Hz) ↑ at Cz; 30 sessions | Yes: control group, no NFB, pre- and post-training | Changes in power of delta, theta, alpha, SMR, and high beta | SCL-90, HCQ | No | SCL-90: somatization, obsession, interpersonal sensitivity, psychosis, hostility, total score ↑, Delta ↓ (central and frontal), theta ↓ (central area), alpha ↓ (parietal and frontal areas), SMR ↑ (frontal, central area) |
| Horrell et al. ( | SMR (12–15 Hz) ↑ at C3/theta (4–7 Hz) ↓ at F3; 12 sessions | No, pre- and post-training | Changes in mean amplitude of theta, SMR frequency and ERP measures | BDI-II (PTSS and depressions scores), PSS-R, cue reactivity test, drug testing | No | Cue reactivity test: reaction time <>, accuracy <>, depression/stress ↑, drug testing: positive drug testing ↑ SMR ↑ (mean increase 17%), theta <> Cue reactivity test: gamma responses to drug cues ↓ |
| Lackner et al. ( | Alpha (8–12 Hz) ↑ at Pz; theta (4–7 Hz) ↑ at Fz; 12 sessions | Yes: TAU, pre- and post-training and 6 months-follow-up | Changes in absolute and relative band power for theta, alpha and beta frequency band | ACQ-R, BDI-V, BSI, FKV-lis, FPTM-23, PPR, SOC, perceived control over EEG, belief in efficacy of training | No | No significant results for behavioral outcome measures posttreatment, perceived control of EEG ↑, belief in efficacy of training ↑ Trend towards higher alpha, theta power ↑, beta <> No significant effects found at follow-up |
| Gruzelier et al. ( | SCP ↑↓; C3/C4; 10 sessions | No, improvements within and between sessions | Changes in self- regulation of interhemispheric negativity over course of training | Yes: good vs average performers based on visual inspection of performance in NFB-sessions, first 5 sessions vs last 5 sessions | Ability of patients to learn self-regulation of interhemispheric negativity Good performers had lateral shifts about twice as large as average performers ( | |
| Nan et al. ( | IAF ↑, beta 2 (20–30 Hz) ↓, 12.5 h in 4 days | No, pre and post-training | Mean relative amplitude in individual theta, alpha, sigma band, beta 1 (16–20 Hz) | Short-term memory test | Memory↑ Trend to increased IAB amplitude, trend toward decrease in relative beta 2 amplitude | |
| Schneider et al. ( | SCP ↑↓; Cz; 20 sessions for patients, 5 for health controls | Yes: two groups, both receiving NFB: schizophrenic patients Healthy controls, pre and post-training | Changes in mean differentiation of SCP over course of training | Yes: learning success defined as mean difference between required negativity increase and negative suppression | Patients were less efficient in SCP self-regulation than controls, patients were only able achieve differentiation of feedback trials comparable to controls in the last three sessions of training | |
| Konicar et al. ( | SCP ↑↓; Fcz; 25 sessions | No, pre- and post-training | Changes in mean differentiation of SCP for first 6 sessions vs last 6 sessions | FAF, BPAQ, BIS/BAS, Flanker Test | Learning investigated, but no criteria as to group patients | Physical aggression ↑, behavioral approach ↑, reaction time ↑, commission errors ↑ Increase in SCP differentiation, but not for transfer conditions Learning progress over the whole 25 training sessions showed a significant increase of SCP differentiation for the feedback condition as well as for the transfer condition over time |
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N, number of participants based on initial inclusion; IAF, individual alpha frequency; MINI/MINI KID, structured ADHD interview; BDI-(II–V), German version of Beck Depression Interview; ADHD-SB, Current ADHD questionnaire as part of HASE; WRI, ADHD Wender–Reimherr Interview; FEA, ADHD symptom questionnaire; FERT, questionnaire to assess expectancy with regard to treatment; CAARS, Conners’ Adult Rating Scale; STAI, Anxiety questionnaire; FPTM-23, Therapy Motivation Questionnaire; CPT, continuous performance test; INKA, inventory for complex attention; SCL-90, Symptom Checklist-90; HCQ-45, Heroin Craving Questionnaire; PSS-R, Posttraumatic Symptom Scale—Self Report; ACQ-R, Alcohol Craving Questionnaire Revised Form; BSI, Brief Symptom Inventory; PPR, Posttraumatic Growth Inventory; SOC, Sense of Coherence Scale; FAF, Assessment of aggressiveness factors; BPAQ, Buss–Perry Aggression Questionnaire; BIS/BAS, Behavior-Inhibition/Behavior-Activation System Questionnaire; ADHD, attention-deficit hyperactivity disorder; SCP, slow cortical potential; EEG, electroencephalographic; ERP, event-related potential; CNV, contingent negative variation; SMR, sensori motor rhythm.
Figure 2Risk for bias is assessed according to the Cochrane Handbook for Systemtic Review Intervention (52). The risk for bias is defined as ‘bias of sufficient magnitude to have a notable impact on the results or conclusions of the trial’.
Figure 3Risk of bias graph according to the Cochrane Handbook for Systemtic Review Intervention (52). Authors’ judgements about each risk of bias item presented as percentages across all included studies.