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How to Reduce Suicidal Thoughts and Impulsivity in Depression
RECRUITINGN/ASponsored by Centre Hospitalier Universitaire de Besancon
Actively Recruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Besancon
Started2023-09-01
Est. completion2025-07
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT05894980
Summary
The study aims at investigating if tDCS applied to left DLPFC or to right OFC to treatment as usual is effective in reducing severe suicidal ideas in major depressive episode.
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria: * Man or woman older than 18 years oldRight-handed * Signed Informed Consent form * Subject affiliated to or beneficiary from a French social security regime * Inpatient or outpatient at the Adult Psychiatry Service * Diagnosis of Major Depressive Disorder according to the 5th edition of Diagnostic and Statistical Manual of Mental Disorders (DSM-5) criteria and confirmation by the MINI Structured Clinical Interview * MADRS score ≥ 18 * Beck Scale for Suicide Ideation (BSS) score ≥8 * Under antidepressant treatment * Absence of severe progressive neurologic and/or somatic pathologies (specially tumors, degenerative diseases) Exclusion Criteria: * tDCS contraindication * Younger than 18 years old * Left-handed * under mood stabilizer and/or antiepileptic * treated by ECT or rTMS or tDCS for the current eposide * Subject under measure of protection or guardianship of justice * Presence of other psychiatric pahtologies * Subject beneficiary from a legal protection regime * Subject unlikely to cooperate or low cooperation stated by investigator * Subject not covered by social security * Pregnant woman * Subject being in the exclusion period of another study or provided for by the "National Volunteer File"
Conditions4
DepressionImpulsive BehaviorSuicidal IdeationUnipolar Depression
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Actively Recruiting
PhaseN/A
SponsorCentre Hospitalier Universitaire de Besancon
Started2023-09-01
Est. completion2025-07
Eligibility
Age18 Years+
Healthy vol.Accepted
View on ClinicalTrials.gov →
NCT05894980