Development of Low-Intensity Focused Ultrasound for Post Traumatic Brain Injury Depression
The goal of this clinical trial is to learn about evaluate the safety, tolerability, and feasibility of MRI-guided LIFU targeting the sgACC in Veterans with post-traumatic brain injury depression. The main questions it aims to answer are:
- the safety, tolerability, and feasibility of MRI-guided LIFU.
- Evaluate preliminary antidepressant efficacy.
- Characterize target engagement using multimodal neuroimaging and electrophysiology.
- Identify imaging and electrophysiological biomarkers that predict treatment response.
- Generate preliminary effect size estimates to support future multicenter clinical trials.
Studienübersicht
Status
Status
Bedingungen
Bedingungen
Intervention / Behandlung
Intervention / Behandlung
Detaillierte Beschreibung
Studientyp
Studientyp
Einschreibung (Geschätzt)
Einschreibung
Phase
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
Studienkontakt
- Name: Masataka Wada, MD
- Telefonnummer: 650-434-7844
- E-Mail: mwada@stanford.edu
Studieren Sie die Kontaktsicherung
- Name: John P Coetzee, PhD
- E-Mail: jpcoetzee@stanford.edu
Studienorte
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California
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Stanford, California, Vereinigte Staaten, 94305
- Department of Psychiatry and Behavioral Sciences, Stanford School of Medicine
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Kontakt:
- Nick Bassano, MSW
- Telefonnummer: 6504973933
- E-Mail: nbassano@stanford.edu
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Hauptermittler:
- Mahendra Bhati, MD
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Teilnahmekriterien
Zulassungskriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria:
- Adult Veteran, male or female, 22 to 55 years of age at the time of screening.
- Able to read, understand, and provide written, dated informed consent before initiation of formal study screening procedures. A brief IRB-approved telephone pre-screen may be conducted prior to written informed consent as described in Section 8.1. Proficiency in English sufficient to complete questionnaires / follow instructions during fMRI assessments and LIFU 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.
- History of non-penetrating mild to moderate TBI confirmed by medical records and adjudicated by the study investigator using established TBI criteria (e.g., ACRM/VA-DoD criteria). If contemporaneous records are incomplete, a structured lifetime TBI interview may be used to support classification.
- The TBI must have occurred at least 3 months before the occurrence of depression
- Current depressive disorder defined in the Diagnosis and Statistical Manual of Mental Disorders, Fifth Edition, Text Revision (DSM-5).
- Medical records confirming a history of moderate to severe treatment-resistance as defined by a score of 7-14 on the Maudsley Staging Method (MSM3).
- MADRS score of ≥20 at screening.
- Total duration of current depressive episode is less than 2 years
- LIFU naive.
- Access to ongoing psychiatric care before and after completion of the study.
- The dose of the primary antidepressant medication must be stable for 6 weeks prior to baseline , and participants must agree to continue at this dose throughout the study period.
- In good general health, as evidenced by medical history.
- For females of reproductive potential: use of highly effective contraception for at least 1 month prior to baseline and agreement to use such a method during study participation.
- Agreement to adhere to Lifestyle Considerations (see section 5.3) throughout study duration.
Exclusion Criteria:
- Any lifetime DSM-5 depressive disorder or clinically significant depressive episode with onset prior to the qualifying index TBI, including major depressive disorder, persistent depressive disorder, or other specified/unspecified depressive disorder, or any antidepressant treatment initiated for depression prior to the index TBI.
- Pregnancy
- Primary psychiatric condition other than MDD requiring treatment except stable comorbid anxiety disorder
- History of or current psychotic disorder or bipolar disorder
- Severe borderline personality disorder.
- Diagnosis of Intellectual Disability or Autism Spectrum Disorder
- Current moderate or severe substance use disorder or demonstrating signs of acute substance withdrawal
- Urine screening test positive for illicit substances
- Active suicidal ideation (defined as an MSSI > 8) or a suicide attempt (as defined by the C-SSRS) within the past one year
- Cognitive impairment (defined as MoCA < 23)
10. Any history of ECT without meeting responder criteria 11. Recent (within 4 weeks of any clinical effect) or concurrent use of rapid acting antidepressant agent (i.e., ketamine or a course of ECT) 12. History of significant neurologic disease, including dementia, Parkinson's or Huntington's disease, brain tumor, seizure disorder, subdural hematoma, or multiple sclerosis 13. Untreated or insufficiently treated endocrine disorder. 14. Contraindication to receiving LIFU 15. Contraindication to MRI (ferromagnetic metal in their body) 16. Treatment with another investigational drug or other intervention within the study period 17. Unstable symptoms between screening and baseline as defined by a > 30% change in MADRS-S score.
18. Any other condition deemed by the PD to interfere with the study or increase risk to the participant
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Doppelt
Anzahl der Arme
Waffen und Interventionen
Teilnehmergruppe / ArmTeilnehmergruppe / Arm |
Intervention / BehandlungIntervention / Behandlung |
|---|---|
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Aktiver Komparator: Active Low-Intensity Focused Ultrasound (LIFU)
Participants receive active LIFU over 5 consecutive treatment days, with 5 sessions per day and 20 minutes per session
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MRI-guided Low-Intensity Focused Ultrasound (LIFU) neuromodulation targeting the sgACC delivered over a brief, intensive course (20-minute sessions; 5 sessions/day for 5 consecutive days).
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Schein-Komparator: Sham Low-Intensity Focused Ultrasound (LIFU)
Participants receive sham LIFU over 5 consecutive treatment days, with 5 sessions per day and 20 minutes per session
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Non-active MRI-guided Low-Intensity Focused Ultrasound (LIFU) neuromodulation targeting the sgACC delivered over a brief, intensive course (20-minute sessions; 5 sessions/day for 5 consecutive days).
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Was misst die Studie?
Primäre Ergebnismessungen
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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To evaluate the safety and tolerability of repeated sgACC-targeted LIFU stimulation in adult Veterans with PTD.
Zeitfenster: Baseline, Treatment Days 1 through 5, 1-Week, 1-2:4-week follow up visits.
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Cumulative incidence of treatment-emergent adverse events and serious adverse events.
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Baseline, Treatment Days 1 through 5, 1-Week, 1-2:4-week follow up visits.
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Sekundäre Ergebnismessungen
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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To evaluate the preliminary antidepressant efficacy of repeated sgACC-targeted LIFU in adult Veterans with PTD.
Zeitfenster: Baseline, 1-week follow up, 4-week follow up
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Absolute change from baseline in the MADRS total score.
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Baseline, 1-week follow up, 4-week follow up
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Andere Ergebnismessungen
Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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To characterize changes in neuroimaging measures associated with LIFU.
Zeitfenster: Baseline and 1-week follow-up
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Change from baseline in prespecified resting-state fMRI measures of sgACC-centered functional connectivity and depression-related network connectivity.
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Baseline and 1-week follow-up
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To characterize changes in electrophysiologic measures associated with LIFU.
Zeitfenster: Baseline, treatment days 1 through 5 and 1-week follow-up
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Change from baseline in prespecified resting-state and LIFU-associated EEG measures of neural activity and functional connectivity.
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Baseline, treatment days 1 through 5 and 1-week follow-up
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To evaluate whether baseline fMRI feature predict clinical response to LIFU.
Zeitfenster: Baseline, 1-week follow up and 4-week follow up visits
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Associations between baseline fMRI features and absolute change from baseline in MADRS total score.
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Baseline, 1-week follow up and 4-week follow up visits
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To evaluate whether baseline EEG features predict clinical response to LIFU.
Zeitfenster: Baseline, 1-week follow up and 4-week follow up visits
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Associations between baseline EEG features and absolute change from baseline in MADRS total score.
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Baseline, 1-week follow up and 4-week follow up visits
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Mitarbeiter und Ermittler
Sponsor
Sponsor
Mitarbeiter
Mitarbeiter
Ermittler
Ermittler
- Hauptermittler: Mahendra Bhati, MD, Stanford University
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Studienbeginn
Primärer Abschluss (Geschätzt)
Primärer Abschluss
Studienabschluss (Geschätzt)
Studienabschluss
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Zuerst gepostet
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes Update gepostet
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
Andere Studien-ID-Nummern
- 85834 (Hillman)
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Produkt, das in den USA hergestellt und aus den USA exportiert wird
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