Neurofeedback is effective in the treatment of major depressive disorder.
ID
Bron
Verkorte titel
Aandoening
major depressive disorder, depression
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. Hamilton depression rating scale (17-item);<br>
2. Baseline frontal alpha-activity in resting EEG.
Achtergrond van het onderzoek
It is claimed that neurofeedback (NF) is efficacious in the treatment of MDD. So far, no studies have systematically examined such claims. However, basic neurophysiological studies appear to support the premise of NF that depression is associated with frontal alpha-asymmetry in the resting EEG. Reduction of this FA is thought to be related to a decrease in depressive symptomatology. The aim of this pilot-study is to investigate the effectiveness of NF (delivered as a frontal asymmetry protocol) in MDD by (1) decreasing FA, and (2) reducing severity of depressive symptomatology.
In case of positive results in this pilot-study a larger scale RCT will be conducted.
Doel van het onderzoek
Neurofeedback is effective in the treatment of major depressive disorder.
Onderzoeksopzet
1. Premeasure; diagnosis and assessment of clinical variables (like severity of MDD);
2. Measurement of MDD severity before every NF session;
3. Assessment of clinical variables (like severity of MDD) upon completion of the intervention.
1. Premeasure: 6 days ESM;
2. Postmeasure: after 8 weeks of mindfulness training/time control: 6 days ESM;
3. Follow-ups are planned, but were not yet submitted to ethical committee;
4. Follow-up at 6 months;
5. Follow-up at 12 months.
Onderzoeksproduct en/of interventie
Neurofeedback will be administered based by means of frontal alpha-asymmetry (FA) feedback. Baseline resting-EEG signal will be analyzed and individual thresholds will be used to provide real-time visual feedback in order to diminish FA. A maximum of 30 NF sessions will be delivered with a frequency of 3 sessions each week.
Publiek
University Hospital Maastricht
P.O. Box 5800
F.P.M.L. Peeters
Maastricht 6202 AZ
The Netherlands
043-3874130
f.peeters@maastrichtuniversity.nl
Wetenschappelijk
University Hospital Maastricht
P.O. Box 5800
F.P.M.L. Peeters
Maastricht 6202 AZ
The Netherlands
043-3874130
f.peeters@maastrichtuniversity.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. MMD as a primary axis-1 diagnosis according to criteria of the DSM-IV-TR;
2. Informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. History of braintrauma (commotio or contusio cerebri);
2. Current use of antipsychotics, moodstabilizers, benzodiazepines. the use of antidepressants is permitted if type and dosage are not changed during participation in the study;
3. Chronic MDD (>2 years duration of current episode);
4. Dysthymia;
5. Bipolar disorder;
6. Lefthandedness;
7. Severe (HDRS-17 > 25) episode of MDD which indicates prompt effective treatment;
8. Pregnancy;
9. Other psychiatric disorders other than co-morbid anxiety and personality disorders.
Opzet
Deelname
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Register | ID |
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NTR-new | NL1551 |
NTR-old | NTR1629 |
CCMO | NL25291.068.08 |
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OMON | NL-OMON33576 |