Healthy, Major Depressive Disorder
Conditions
Brief summary
Current first-line treatments for major depression (antidepressants and psychotherapy) show a long latency to response, and less than half of all patients experience full remission with optimized treatment, indicating the need for new developments. The aim of this study is to extend and further develop a longstanding line of research of using sleep neurophysiology as a 'window to the brain' and treatment development in major depression. Particularly, this project is designed to test the feasibility, efficacy and mechanisms of action of a new sleep-based treatment technology.
Detailed description
The planned study is a single-centre, doubled-blind, randomized, sham controlled, repeated measures within-subject (stimulation and sham) study including patients with major depression and healthy controls, across four sleep laboratory nights (adaptation, baseline, stimulation and sham in counterbalanced order). The investigators will test the primary hypothesis that auditory-closed loop suppression of slow wave sleep will improve depressive clinical symptomatology compared to sham stimulation.
Interventions
DEVICEAuditory closed-loop stimulation
Auditory closed-loop suppression of slow wave sleep
DEVICESham stimulation
No auditory stimulation
Sponsors
Christoph Nissen
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
30 Years to 60 Years
Healthy volunteers
Yes
Inclusion criteria
* Written informed consent * MDD according to ICD-10 criteria (F32.1/2, F33.1/2; i.e. unipolar depression) for patient group
Exclusion criteria
* Relevant psychiatric disorders (other than MDD for the patient group), such as organic psychiatric disorders, lifetime history of substance dependency or current substance abuse (smoking will be allowed for recruitment reasons), schizophrenia or other psychotic disorders, affective disorders including bipolar disorder, borderline personality disorder, autism or other severe psychiatric disorders * Known pregnancy * Unstable medical conditions, such as unstable cardiovascular or metabolic disorders, etc. * Relevant neurological disorders, including epilepsy, stroke, etc. * Organic sleep disorders including relevant sleep apnea (AHI\>15/h), periodic limb movement disorder (PLMS index\>5/h), Restless-Legs-Syndrome (RLS), narcolepsy, circadian rhythm disorder or shift work/ jet lag * Intake of medication affecting the central nervous system (other than antidepressants and lithium in patients); patients receiving benzodiazepines or (es)ketamine will not be included * Current brain stimulation treatment, such as electroconvulsive therapy (ECT), TMS or deep brain stimulation * Contraindications for tDCS or TMS studies, including but not limited to metal in the head/ brain or epilepsy * Hearing impairment or tinnitus (auditory stimulation study) * Inability to follow the procedures of the study (for example due to language problems) * Left-handedness
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Montgomery Åsberg Depression Rating Scale | Up to three weeks | Measure of the severity of depressive symptomatology The scores range between 0 to 60. The higher the score, the more symptamology of depression the subjects presents. |
Countries
Switzerland
Contacts
Primary ContactChristoph Nissen, Prof. Dr. med.
Outcome results
None listed