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Escitalopram, Placebo and tDCS in Depression: a Non-inferiority Trial

Escitalopram and Transcranial Direct Current Stimulation in Major Depressive Disorder: a Double-blind, Placebo-controlled, Randomized, Non-inferiority Trial

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT01894815
Acronym
ELECT-TDCS
Enrollment
245
Registered
2013-07-10
Start date
2013-10-31
Completion date
2016-11-30
Last updated
2016-12-05

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Major Depressive Disorder, Major Depressive Disorder, Recurrent, Unspecified, Major Depressive Disorder, Single Episode, Unspecified

Keywords

major depressive disorder, major depression, depressive disorder, major depressive episode

Brief summary

Major depressive disorder (MDD) is a common psychiatric condition, mostly treated with antidepressant drugs, which are limited for issues such as refractoriness and adverse effects. In this context, the investigators investigate a non-pharmacological treatment known as transcranial direct current stimulation (tDCS). To prove that tDCS is similarly effective than antidepressants would have a tremendous impact in clinical psychiatry, since tDCS is virtually absent of adverse effects. Its ease of use, portability and low price are also interesting characteristics for using in primary and secondary health care. Thus, our aim is to compare tDCS against a fully dosed, effective antidepressant. The study will be a non-inferiority, randomized, double-blinded, placebo-controlled, three-arm trial comparing active tDCS/placebo pill, sham tDCS/escitalopram 20mg/day and sham tDCS/placebo pill. Our primary aim is to show that tDCS is not inferior to escitalopram 20mg/day with a noninferiority margin of at least 50% of the escitalopram-placebo effect.

Detailed description

Major depressive disorder (MDD) is a common psychiatric condition, mostly treated with antidepressant drugs, which are limited for issues such as refractoriness and adverse effects. In this context, the researchers investigate a non-pharmacological treatment known as transcranial direct current stimulation (tDCS). In a prior clinical trial with 120 patients with MDD, the investigators demonstrated that the combination of tDCS with sertraline 50mg/day had increased, faster effects on depressive symptoms (Brunoni et al., JAMA Psychiatry, 2013). However, although the investigators suggested that tDCS vs. sertraline had similar efficacy, such comparison was compromised due to the low sertraline dose and also because the comparison of sertraline vs. placebo was not significant. To prove that tDCS is similarly effective than antidepressants would have a tremendous impact in clinical psychiatry, since tDCS is virtually absent of adverse effects. Its ease of use, portability and low price are also interesting characteristics for using in primary and secondary health care. Thus, our aim is to compare tDCS against a fully dosed, effective antidepressant. The study will be a non-inferiority, randomized, double-blinded, placebo-controlled, three-arm trial comparing active tDCS/placebo pill, sham tDCS/escitalopram 20mg/day and sham tDCS/placebo pill for ten weeks, randomizing 240 patients with MDD in a 3:3:2 ratio (less to placebo). Our primary aim is to show that tDCS is not inferior to escitalopram 20mg/day with a noninferiority margin of at least 50% of the escitalopram-placebo effect. As secondary aims, the researchers will investigate putative biomarkers for tDCS response. This is important considering the large sample size of this study and also the paucity of tDCS studies - therefore, the identification of such biomarkers could generate new hypothesis for future studies and for tDCS' mechanisms of action. The biomarkers will be: genetic polymorphisms (BDNF, SLC6A4, THP1, 5HT2A); serum markers (BDNF); motor cortical excitability (cortical silent period, intracortical inhibition, intracortical facilitation); heart rate variability; and neuroimaging (structural volume of the dorsolateral prefrontal and anterior cingulate cortex, white matter tracts of the prefrontal cortex and posterior cingulate cortex connectivity). This project represents a novel research line in our Institution, and the investigators thereby propose the onset of a new center denominated C.I.N.A. (Interdisciplinary Center for Applied Neuromodulation) that will foment the use and development of projects using neuromodulation techniques. This new center will also interact with other centers on the fields of clinical research, neurosciences and neuropsychiatry.

Interventions

The investigators will use 10mg and 20mg pills. The investigators will up-titrate escitalopram from 10 to 20mg/day according to the patient tolerability. The maximum dose (20mg/day) is sought to be achieved at week 3.

DEVICEtranscranial direct current stimulation

The anode will be applied over the F3 area and the cathode over the F4 area. The current dose is 2mA, current density is 0.8 A/m2. Electrodes will be 5x5cm in size. The investigators will apply 15 daily, consecutive tDCS sessions (excluding weekends) and after that one session per week until the primary endpoint.

OTHERSham tDCS + Placebo Pill

This group receives sham tDCS and placebo pill.

Sponsors

Fundação de Amparo à Pesquisa do Estado de São Paulo
CollaboratorOTHER_GOV
Brain & Behavior Research Foundation
CollaboratorOTHER
University of Sao Paulo
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

* HAMD17\>=17 * more than 8 years of schooling OR able to read, speak and understand the Portuguese language. * Low suicide risk.

Exclusion criteria

* Bipolar disorders. * Schizophrenia and other psychotic disorders. * Anxiety disorders, if it is the primary diagnosis (comorbidity with depression is not an exclusion disorder) * Substance abuse or dependence. * Depression symptoms better explained by medical conditions. * Neurologic conditions (e.g., stroke, multiple sclerosis, brain tumor). * Severe medical conditions. * Pregnancy/breast-feeding. * Severe suicidal ideation, suicidal planning or recent (\<4 weeks) suicide attempt. * Contra-indications to escitalopram. * Current use of escitalopram in the current depressive episode. * Use of escitalopram in a prior depressive episode that was not effective. * Contra-indications to tDCS. * Previous use of tDCS (current or previous depressive episode).

Design outcomes

Primary

MeasureTime frameDescription
Changes in Hamilton Rating Scale for Depression, 17 items (HAMD17)Weeks 0 and 10Continuous measure (score changes). Non-inferiority assessment: the difference between tDCS to escitalopram should be \>50% of escitalopram to placebo efficacy.

Secondary

MeasureTime frameDescription
Change in Montgomery-Asberg Depression Rating Scale (MADRS)Weeks 0, 3, 6, 10Continuous measure (score changes).
Change in Beck Depression Inventory (BDI)Weeks 0, 3, 6, 10
Change in Positive and Negative Affect Scale (PANAS)Weeks 0, 3, 6, 10
Change in State-Trait Anxiety Inventory (STAI)Weeks 0, 3, 6, 10
Change in HDRSWeeks 0, 3, 6, 8, 10Continuous measure (score changes).
Adverse eventsWeek 3 and Week 10.Assessment and comparisons of tDCS and drug adverse events. We used a tDCS adverse events questionnaire (Brunoni et al., 2011) and the SAFTEE.
Serious adverse eventsUp to Week 10.Serious adverse events include treatment-emergent hypomania/mania (YMRS\>8), suicide, psychiatric hospitalization and others life-threatening or incapacitant events.
Young Manic Rating Scale (YMRS)Week 3 and Week 10.Assessment of treatment-emergent hypomania/mania, defined as YRMS\>8.
Predictor of responseWeek 10Age (years)
Hamilton Rating Scale for Depression, 17 items (HAMD17)Week 10Response (≥50% improvement from week 0 to 10)

Countries

Brazil

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026