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Home-Based Randomized Trial of Spaced Transcranial Direct Current Stimulation for Treatment-Resistant Depression

16. september 2026 oppdatert av: Jean-Philippe Miron, University of California, San Diego

Spaced Transcranial Direct Current Stimulation for Treatment-Resistant Depression: A Home-Based Randomized Sham-Controlled Trial and Mechanistic Exploration

This study aims to evaluate the clinical efficacy and neurophysiological mechanisms of home-based spaced tDCS in TRD through a randomized, double-blind, sham-controlled trial conducted under remote supervision. Specifically, this trial will: (1) compare the efficacy of active versus sham spaced tDCS on depressive symptom severity in individuals with TRD and (2) characterize neurophysiological changes associated with spaced tDCS using TMS-EEG, TMS-EMG and resting state EEG.

Studieoversikt

Studietype

Intervensjonell

Registrering (Antatt)

74

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiekontakt

Studiesteder

    • California
      • San Diego, California, Forente stater, 92127
        • UCSD Interventional Psychiatry
        • Ta kontakt med:
        • Ta kontakt med:
          • UCSD Interventional Psychiatry Clinic
          • Telefonnummer: 858-207-0938

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år til 70 år (Voksen, Eldre voksen)

Tar imot friske frivillige

Nei

Kjønn som er kvalifisert for studier

Alle

Beskrivelse

Inclusion Criteria:

  • People between the ages of 18 and 70 at the time of screening.
  • Able to read, understand, and provide written, dated informed consent prior to screening. Proficiency in English sufficient to complete questionnaires / follow instructions during interventions. Stated willingness to comply with all study procedures, including availability for the duration of the study, and to communicate with study personnel about adverse events and other clinically important information.
  • Currently diagnosed with Major Depressive Disorder (MDD) and meets criteria for a Major Depressive Episode, according to the criteria defined in the Diagnosis and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5).
  • Medical records confirming a history of at least moderate treatment-resistance as defined on Antidepressant Treatment History Form (ATHF) score for that antidepressant trial of > 2 in the current episode OR have been unable to tolerate at least 2 separate trials of antidepressants of inadequate dose and duration (ATHF score of 1 or 2 on those 2 separate antidepressants) OR have a combination of one failed trial and one not tolerated trial, per the definitions above.
  • MADRS score of ≥20 at screening.
  • Existing relationship with mental health provider and access to ongoing psychiatric care before and after completion of the study.
  • Must be on a stable antidepressant therapeutic regimen for at least 4 weeks prior to study enrollment and agree to continue this regimen throughout the study period. Participants who are not currently on antidepressant treatment are eligible, provided that no discontinuation occurred within the 4 weeks preceding study enrollment.
  • For persons of child-bearing potential: use of highly effective contraception for at least 1 month prior to screening and agreement to use such a method during study participation.
  • Agreement to adhere to Lifestyle Considerations (i.e. must continue with any existing treatments) throughout study duration.
  • For persons of childbearing potential: must take a pregnancy test prior to initiating treatment, with results confirmed as negative by study staff
  • Participants will need to have a stable internet connection and a device compatible with UCSD Microsoft Teams or UCSD Zoom to facilitate remote communication and engagement in study activities.

Exclusion Criteria:

  • Pregnancy this includes breastfeeding or trying to becoming pregnant.
  • History of psychotic or bipolar disorder or depression with psychotic features.
  • Significant borderline personality disorder.
  • Significant comorbid obsessive-compulsive or post-traumatic stress disorder.
  • Previously diagnosed Intellectual Disability or Autism Spectrum Disorder.
  • Current moderate or severe substance use disorder or demonstrating signs of acute substance withdrawal.
  • Clinically significant suicidality.
  • Any history of tDCS.
  • Any history of ECT.
  • History of TMS (greater than 15 sessions) without a clinically meaningful response.
  • History of ketamine (greater than 4 sessions) without a clinically meaningful response.
  • History of significant neurologic disease, including dementia, Parkinson's or Huntington's disease, brain tumor, seizure disorder, subdural hematoma, multiple sclerosis, or history of significant head trauma with persistent symptoms.
  • Untreated or insufficiently treated endocrine disorder.
  • Contraindication to receiving tDCS (e.g., ferromagnetic implant, history of seizure, known brain lesion).
  • Treatment with an investigational drug or other intervention within the study period.
  • Unstable symptoms between screening and baseline as defined by a ≥ 30% change in MADRS score.
  • Require a benzodiazepine with a dose > lorazepam 2 mg/day
  • Has started a new psychotherapeutic process in the past 3 months from screening.
  • Use of potentially irritant topical treatments (ex: retinoids, alpha hydroxy acids).

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Behandling
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Trippel

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Aktiv komparator: Active spaced-tDCS

Active tDCS applies low-intensity electrical current to the scalp to modulate cortical excitability through subthreshold shifts in neuronal membrane potentials, influencing synaptic plasticity

Spaced-tDCS will be self-administered at home under the supervision of a trained clinical research coordinator using the Soterix Medical mini-CT device with remote monitoring via a secure videoconferencing platform (e.g., Microsoft Teams).

Sham-komparator: Sham spaced-tDCS

Sham tDCS is a placebo control that simulates the physical sensations of tDCS but does not deliver any actual, prolonged electrical current to the brain.

Soterix Medical mini-CT device sham protocol that match real stimulation parameters will be used.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Active vs Sham spaced tDCS Efficacy as measured by the Montgomery-Åsberg Depression Rating Scale
Tidsramme: Baseline to 4-weeks post treatment

To compare the efficacy of active versus sham spaced tDCS in reducing depressive symptom severity in TRD. Symptom severity will be measured using the MADRS score at four weeks post-treatment.

Baseline to 4-weeks post treatment

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Changes in MADRS with active versus sham spaced tDCS during all post treatment visits
Tidsramme: 1-week post treatment to 10-week post treatment

Clinical outcomes associated with active versus sham spaced tDCS as measured by MADRS response (≥50% reduction) and remission (score ≤10) rates.

1-week post treatment to 10-week post treatment
Changes in Hamilton Depression Rating Scale, 17-item version scores
Tidsramme: 1-week post treatment to 10-week post treatment

Reduction in HAMD-17 scores at all follow-up timepoints. Score range from 0 to 52.

1-week post treatment to 10-week post treatment
Changes in Patient Health Questionnaire-9
Tidsramme: 1-week post treatment to 10-week post treatment

Changes in PHQ scores at all follow-up timepoints. With scores ranging from 0-27

1-week post treatment to 10-week post treatment
Changes in General Anxiety Disorder-7
Tidsramme: 1-week post treatment to 10-week post treatment

Changes in GAD-7 scores at all follow-up timepoints. Score range from 0-21

1-week post treatment to 10-week post treatment
Changes in The Modified Scale for Suicidal Ideation
Tidsramme: 1-week post treatment to 10-week post treatment

Changes in the presence and severity of suicidal thoughts at all follow-up timepoints. Scores ranging from 0-54

1-week post treatment to 10-week post treatment
Feasibility (Recruitment)
Tidsramme: Baseline clinical assessment to 10 weeks post treatment.

Recruitment rate will be measured as the number of patients enrolled by the conclusion of the study, reported as a whole number.

Baseline clinical assessment to 10 weeks post treatment.
Feasibility (Retention)
Tidsramme: Baseline clinical assessment to 10 weeks post treatment.

Retention rate will be measured as the percentage of enrolled patients who complete all study visits, reported as a percentage.

Baseline clinical assessment to 10 weeks post treatment.
Feasibility (Adherence)
Tidsramme: Baseline clinical assessment to 10 weeks post treatment

The proportion of completed sessions relative to the total prescribed sessions, expressed as a percentage.

Baseline clinical assessment to 10 weeks post treatment
Safety of at-home spaced tDCS
Tidsramme: Baseline clinical assessment to 10 weeks post treatment

Safety will be measured by the number of serious adverse events (SAEs)

Baseline clinical assessment to 10 weeks post treatment
Tolerability to spaced tDCS
Tidsramme: Baseline clinical assessment to 10 weeks post treatment.

Tolerability will be measured by the number of adverse events (AEs).

Baseline clinical assessment to 10 weeks post treatment.

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Biomarker Discovery: Short-Interval Intracortical Inhibition (SICI) and Long-Interval Intracortical Inhibition (LICI) via TMS-EMG
Tidsramme: Baseline to 4-weeks post treatment

TMS-EMG will be used to evaluate changes in SICI and LICI.

Baseline to 4-weeks post treatment
Biomarker Discovery: Intracortical Facilitation (ICF) via TMS-EMG
Tidsramme: Baseline to 4-weeks post treatment

TMS-EMG will be used to evaluate changes in intracortical facilitation

Baseline to 4-weeks post treatment
Biomarker Discovery: Cortical Silent Period (CSP) via Transcranial Magnetic Stimulation-Electromyography (TMS-EMG)
Tidsramme: Baseline to 4-weeks post treatment

TMS-EMG will be used to assess changes in the cortical silent period (CSP). Unit of Measurement: Duration (milliseconds).

Baseline to 4-weeks post treatment
TMS-Evoked Potential (TEP) Component Amplitudes via TMS-EEG
Tidsramme: Baseline to 4-weeks post treatment

TMS-EEG will be used to evaluate changes in TMS-evoked potential (TEP) component amplitudes.

Unit of Measurement: Voltage (µV).

Baseline to 4-weeks post treatment
Resting-State Electroencephalography (rsEEG)
Tidsramme: Baseline to 4-weeks post treatment

rsEEG will be used to analyze changes in brain activity patterns at rest. Unit of Measurement: Frequency (Hz)

Baseline to 4-weeks post treatment

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Publikasjoner og nyttige lenker

Den som er ansvarlig for å legge inn informasjon om studien leverer frivillig disse publikasjonene. Disse kan handle om alt relatert til studiet.

Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Antatt)

15. oktober 2026

Primær fullføring (Antatt)

15. oktober 2031

Studiet fullført (Antatt)

15. oktober 2031

Datoer for studieregistrering

Først innsendt

10. september 2026

Først innsendt som oppfylte QC-kriteriene

16. september 2026

Først lagt ut (Faktiske)

22. september 2026

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

22. september 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

16. september 2026

Sist bekreftet

1. september 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

Planlegger du å dele individuelle deltakerdata (IPD)?

NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Ja

produkt produsert i og eksportert fra USA

Ja

Denne informasjonen ble hentet direkte fra nettstedet clinicaltrials.gov uten noen endringer. Hvis du har noen forespørsler om å endre, fjerne eller oppdatere studiedetaljene dine, vennligst kontakt register@clinicaltrials.gov. Så snart en endring er implementert på clinicaltrials.gov, vil denne også bli oppdatert automatisk på nettstedet vårt. .

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