- ICH GCP
- Registro degli studi clinici negli Stati Uniti
- Sperimentazione clinica NCT07834762
Home-Based Randomized Trial of Spaced Transcranial Direct Current Stimulation for Treatment-Resistant Depression
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.
Panoramica dello studio
Stato
Intervento / Trattamento
Tipo di studio
Iscrizione (Stimato)
Fase
- Non applicabile
Contatti e Sedi
Contatto studio
- Nome: Interventional Psychiatry
- Numero di telefono: 858-657-6149
- Email: iptrials@health.ucsd.edu
Luoghi di studio
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California
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San Diego, California, Stati Uniti, 92127
- UCSD Interventional Psychiatry
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Contatto:
- Edith Jimenez
- Numero di telefono: 858-657-6149
- Email: iptrials@health.ucsd.edu
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Contatto:
- UCSD Interventional Psychiatry Clinic
- Numero di telefono: 858-207-0938
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Criteri di partecipazione
Criteri di ammissibilità
Età idonea allo studio
Accetta volontari sani
Sessi ammissibili allo studio
Descrizione
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).
Piano di studio
Come è strutturato lo studio?
Dettagli di progettazione
- Scopo principale: Trattamento
- Assegnazione: Randomizzato
- Modello interventistico: Assegnazione parallela
- Mascheramento: Triplicare
Armi e interventi
Gruppo di partecipanti / Arm |
Intervento / Trattamento |
|---|---|
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Comparatore attivo: 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). |
|
Comparatore fittizio: 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. |
Cosa sta misurando lo studio?
Misure di risultato primarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Active vs Sham spaced tDCS Efficacy as measured by the Montgomery-Åsberg Depression Rating Scale
Lasso di tempo: Baseline to 4-weeks post treatment
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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
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Misure di risultato secondarie
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
|
Changes in MADRS with active versus sham spaced tDCS during all post treatment visits
Lasso di tempo: 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
Lasso di tempo: 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
Lasso di tempo: 1-week post treatment to 10-week post treatment
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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
Lasso di tempo: 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
|
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Changes in The Modified Scale for Suicidal Ideation
Lasso di tempo: 1-week post treatment to 10-week post treatment
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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
|
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Feasibility (Recruitment)
Lasso di tempo: 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.
|
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Feasibility (Retention)
Lasso di tempo: 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.
|
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Feasibility (Adherence)
Lasso di tempo: 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
|
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Safety of at-home spaced tDCS
Lasso di tempo: Baseline clinical assessment to 10 weeks post treatment
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Safety will be measured by the number of serious adverse events (SAEs) |
Baseline clinical assessment to 10 weeks post treatment
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Tolerability to spaced tDCS
Lasso di tempo: Baseline clinical assessment to 10 weeks post treatment.
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Tolerability will be measured by the number of adverse events (AEs). |
Baseline clinical assessment to 10 weeks post treatment.
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Altre misure di risultato
Misura del risultato |
Misura Descrizione |
Lasso di tempo |
|---|---|---|
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Biomarker Discovery: Short-Interval Intracortical Inhibition (SICI) and Long-Interval Intracortical Inhibition (LICI) via TMS-EMG
Lasso di tempo: Baseline to 4-weeks post treatment
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TMS-EMG will be used to evaluate changes in SICI and LICI. |
Baseline to 4-weeks post treatment
|
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Biomarker Discovery: Intracortical Facilitation (ICF) via TMS-EMG
Lasso di tempo: Baseline to 4-weeks post treatment
|
TMS-EMG will be used to evaluate changes in intracortical facilitation |
Baseline to 4-weeks post treatment
|
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Biomarker Discovery: Cortical Silent Period (CSP) via Transcranial Magnetic Stimulation-Electromyography (TMS-EMG)
Lasso di tempo: 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
|
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TMS-Evoked Potential (TEP) Component Amplitudes via TMS-EEG
Lasso di tempo: Baseline to 4-weeks post treatment
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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
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Resting-State Electroencephalography (rsEEG)
Lasso di tempo: Baseline to 4-weeks post treatment
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rsEEG will be used to analyze changes in brain activity patterns at rest. Unit of Measurement: Frequency (Hz) |
Baseline to 4-weeks post treatment
|
Collaboratori e investigatori
Collaboratori
Pubblicazioni e link utili
Pubblicazioni generali
- Tremblay S, Rogasch NC, Premoli I, Blumberger DM, Casarotto S, Chen R, Di Lazzaro V, Farzan F, Ferrarelli F, Fitzgerald PB, Hui J, Ilmoniemi RJ, Kimiskidis VK, Kugiumtzis D, Lioumis P, Pascual-Leone A, Pellicciari MC, Rajji T, Thut G, Zomorrodi R, Ziemann U, Daskalakis ZJ. Clinical utility and prospective of TMS-EEG. Clin Neurophysiol. 2019 May;130(5):802-844. doi: 10.1016/j.clinph.2019.01.001. Epub 2019 Jan 19.
- Woodham RD, Rimmer RM, Young AH, Fu CHY. Adjunctive home-based transcranial direct current stimulation treatment for major depression with real-time remote supervision: An open-label, single-arm feasibility study with long term outcomes. J Psychiatr Res. 2022 Sep;153:197-205. doi: 10.1016/j.jpsychires.2022.07.026. Epub 2022 Jul 8.
- Woodham RD, Selvaraj S, Lajmi N, Hobday H, Sheehan G, Ghazi-Noori AR, Lagerberg PJ, Rizvi M, Kwon SS, Orhii P, Maislin D, Hernandez L, Machado-Vieira R, Soares JC, Young AH, Fu CHY. Home-based transcranial direct current stimulation treatment for major depressive disorder: a fully remote phase 2 randomized sham-controlled trial. Nat Med. 2025 Jan;31(1):87-95. doi: 10.1038/s41591-024-03305-y. Epub 2024 Oct 21.
- Borrione L, Cavendish BA, Aparicio LVM, Luethi MS, Goerigk S, Ramos MRF, Moran NKS, Carneiro AM, Valiengo L, Moura DO, de Souza JP, Batista MP, Aparecida da Silva V, Klein I, Suen P, Gallucci-Neto J, Padberg F, Razza LB, Vanderhasselt MA, Lotufo PA, Bensenor IM, Fregni F, Brunoni AR. Home-Use Transcranial Direct Current Stimulation for the Treatment of a Major Depressive Episode: A Randomized Clinical Trial. JAMA Psychiatry. 2024 Apr 1;81(4):329-337. doi: 10.1001/jamapsychiatry.2023.4948.
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Maggiori informazioni
Termini relativi a questo studio
Parole chiave
Termini MeSH pertinenti aggiuntivi
Altri numeri di identificazione dello studio
- 814732
- 1K23MH144148-01 (Sovvenzione/contratto NIH degli Stati Uniti)
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Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .