Major Depressive Disorder Clinical Trial
Official title:
Trancranial Direct Current Stiimulation as add-on Treatment to Cognitive-Behavior Therapy in People With Major Depression
This is a parallel randomized, double-blinded, sham-controlled clinical trial in which a
total of 72 drug-naïve MDD subjects (36 per arm) are randomized to one of two groups:
Cognitive-Behavior Therapy (CBT) combined with either active or sham tDCS.
The primary outcome is mood improvement, as measured by the Montgomery-Asberg Depression
Rating Scale (MADRS). The secondary outcome is to test whether tDCS combined with CBT can
engage the proposed mechanistic target, of restoring the prefrontal imbalance and
connectivity, by changes over EEG.
Major Depression Disorder (MDD) is widely recognized as a staggering global healthcare
challenge, as well as a potentially lethal illness. In Portugal, 7% of the population is
diagnosed with depression every year, and suicide is responsible for more than a thousand
deaths annually.
The current standard care for MDD involves the use of psychotherapy, antidepressant
medication, or a combination of both. However, approximately 30% of people suffering from MDD
exhibit depressive symptoms despite the appropriate psychological and pharmacological
treatments. One option is to combine several treatments, usually by the use of drug
augmentations and/or combinations of different drugs, which often increases the risk of
adverse effects. Thus, it is important to study non-pharmacological interventions targeting
mechanisms not directly involved with the regulation of neurotransmitters.
Cognitive-behavioral Therapy (CBT) is a well-established, and empirically-supported
non-pharmacological treatment for depression, including for those that have not responded to
antidepressants. However, several patients remain refractory to CBT.
tDCS is a safe, non-invasive, rather inexpensive, easy to administrate, and well-tolerated
neuromodulatory technique. Several studies, including studies from our group, already shown
that tDCS can be effective in MDD. However, tDCS seems to have a better effect when used as
an add-on treatment to other intervention.
What is not known so far are the effects of using tDCS as add-on intervention to CBT on MDD
symptoms.
Therefore, this is a parallel randomized, double-blinded, sham-controlled clinical trial in
which a total of 72 first-episode MDD subjects (36 per arm) will be randomized to one of two
groups: CBT combined with either active or sham tDCS. The design and the tDCS parameters will
be similar to the SELECT trial by Brunoni et al. (2013).
The primary outcome is mood improvement, as measured by the Montgomery-Asberg Depression
Rating Scale (MADRS). The secondary outcome is to test whether tDCS combined with CBT can
engage the proposed mechanistic target, of restoring the prefrontal imbalance and
connectivity, by changes over resting-state EEG and fMRI.
;
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT05537558 -
Precision Medicine for the Prediction of Treatment (PROMPT) Response (PROMPT)
|
||
Terminated |
NCT02192099 -
Open Label Extension for GLYX13-C-202, NCT01684163
|
Phase 2 | |
Completed |
NCT03142919 -
Lipopolysaccharide (LPS) Challenge in Depression
|
Phase 2 | |
Recruiting |
NCT05547035 -
Identification of Physiological Data by a Wearable Monitor in Subjects Suffering From Major Depression Disorders
|
N/A | |
Terminated |
NCT02940769 -
Neurobiological Effects of Light on MDD
|
N/A | |
Recruiting |
NCT05892744 -
Establishing Multimodal Brain Biomarkers for Treatment Selection in Depression
|
Phase 4 | |
Recruiting |
NCT05537584 -
SMART Trial to Predict Anhedonia Response to Antidepressant Treatment
|
Phase 4 | |
Active, not recruiting |
NCT05061706 -
Multicenter Study of Lumateperone as Adjunctive Therapy in the Treatment of Patients With Major Depressive Disorder
|
Phase 3 | |
Completed |
NCT04479852 -
A Study of the Safety and Efficacy of SP-624 in the Treatment of Adults With Major Depressive Disorder
|
Phase 2 | |
Recruiting |
NCT04032301 -
Repeated Ketamine Infusions for Comorbid PTSD and MDD in Veterans
|
Phase 1 | |
Recruiting |
NCT05527951 -
Enhanced Measurement-Based Care Effectiveness for Depression (EMBED) Study
|
N/A | |
Completed |
NCT03511599 -
Cycloserine rTMS Plasticity Augmentation in Depression
|
Phase 1 | |
Recruiting |
NCT04392947 -
Treatment of Major Depressive Disorder With Bilateral Theta Burst Stimulation
|
N/A | |
Recruiting |
NCT05895747 -
5-HTP and Creatine for Depression R33 Phase
|
Phase 2 | |
Recruiting |
NCT05273996 -
Predictors of Cognitive Outcomes in Geriatric Depression
|
Phase 4 | |
Recruiting |
NCT05813093 -
Interleaved TMS-fMRI in Ultra-treatment Resistant Depression
|
N/A | |
Recruiting |
NCT05135897 -
The Neurobiological Fundaments of Depression and Its Relief Through Neurostimulation Treatments
|
||
Enrolling by invitation |
NCT04509102 -
Psychostimulant Augmentation of Repetitive TMS for the Treatment of Major Depressive Disorder
|
Early Phase 1 | |
Recruiting |
NCT06145594 -
EMA-Guided Maintenance TMS for Depression
|
N/A | |
Recruiting |
NCT06026917 -
Assessing Dopamine Transporter Occupancy in the Patients With Depression Brain With Toludesvenlafaxine Hydrochloride Extended-Release Tablets Using 11C-CFT Positron Emission Tomography (PET)
|
Phase 4 |