Depression Clinical Trial
Official title:
The Antidepressant Effect of Right Prefrontal Low Frequency rTMS in an Accelerated Treatment Model ( rTMS). An Open Controlled, Randomized Study
Repetitive transcranial magnetic stimulation has appeared a new non-invasive antidepressant method, which implies non-convulsive focal stimulation of the prefrontal cortex of the brain through a time varying magnetic field. The method is associated with minimal side effects limited to local discomfort and especially no impact on cognitive function. The method has been approved for the treatment of depression in Canada, USA and a couple of European countries. The department for Affective Disorders, Aarhus University Hospital has used rTMS as add-on to conventional antidepressant treatment in the outpatient clinic since 2015. A single treatment course covers 20 sessions given on 20 consecutive days. The demand for daily treatment and attendance for 20 days is resource demanding for both the patient and the clinic. In consequence the investigators want to examine the antidepressant effect of an accelerated stimulus model comparing the outcome of the standard model ( 20 days) with a treatment model covering the same number of stimuli given within one week.
rTMS has appeared a potential new non-invasive antidepressant method, which implies
nonconvulsive focal stimulation of the brain through a time varying magnetic field. RTMS is
based on the principle of electromagnetism. An electromagnetic coil placed on the scalp
produces a time-varying magnetic field that penetrates the scalp and skull unattenuated and
gives rise to a current in the proximity of the cerebral cortex as well as functionally
connected parts of the brain. Research on rTMS reports of minimal side effects of the method.
Previous research indicates that the antidepressant effect of rTMS is associated with
specific stimulation of the dorsolateral prefrontal cortex. The stimulus frequency has shown
to play a key role in the mechanisms of action of rTMS. Previous animal studies have shown
that low frequency rTMS is associated with long term inhibition of neuronal activity (long
term depression), while high frequency stimulation is followed by prolonged activation (long
term potentiation). The majority of clinically controlled studies have used high frequency
stimulation of the left frontal cortex, which has been approved by the USA and later in the
European Union for the treatment of depression. Fewer studies have used right prefrontal low
frequency rTMS, which has less side effects, such as local discomfort and a lower risk of
releasing epileptic seizures, than high frequency stimulation. Randomized controlled trials
and meta-analysis have shown that both stimulus models have a clinically, significant
antidepressant effect at the same level as antidepressant drugs, and recent research clearly
indicates that low frequency rTMS of the right prefrontal cortex is associated with an
antidepressant effect at the same level as the high frequency model. The issue indicates that
low frequency due to the more advantageous side effect profile should be the stimulus model
of choice in a clinical setting.
The Department for Affective Disorders, Aarhus University Hospital has taken part in rTMS
research since 1999, and the outpatient clinic has used low frequency rTMS as add-on to
conventional antidepressant treatment since 2015. A single treatment course covers 20
treatment sessions given on 20 consecutive days. The demand for daily treatment and
attendance in the outpatient clinic for 20 days is resource demanding both for the patient
and the clinic. In consequence the investigators want to examine the antidepressant effect of
an accelerated stimulus model comparing the antidepressant efficacy of conventional treatment
(20 days) with a treatment model covering the same number of stimuli given within one
week.The study is lightening the significance of the association between the number of
stimulus pulses, the length of the total treatment period and the antidepressant effect.
Patients suffering for depression may benefit from the outcome of the study by obtaining an
accelerated antidepressant effect from a less time consuming stimulus model. The outcome of
the study may be implemented in clinical practice from day one.
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