- ICH GCP
- US-Register für klinische Studien
- Klinische Studie NCT07620288
Comparing Outcomes of Theta Burst Stimulation in Depression Using Advanced PET Imaging
Measuring Neuroplasticity Outcomes of Theta Burst Stimulation in Depression Using Advanced PET Imaging
Studienübersicht
Status
Intervention / Behandlung
Detaillierte Beschreibung
Major depressive disorder (MDD) is one of the most prevalent and disabling disorders worldwide, affecting approximately one in 20 Canadians at any given time and ranking among the leading causes of lost productivity, poor quality of life, and suicide. Despite major advances in pharmacological and psychotherapeutic interventions, only 40-60% of patients respond to first-line treatments. Theta Burst Stimulation (TBS) represents the next generation of rTMS technology: by delivering patterned bursts of magnetic pulses that mimic intrinsic theta-gamma coupling, TBS is thought to more efficiently engage synaptic plasticity mechanisms that underlie mood regulation. Clinically, iTBS achieves antidepressant efficacy comparable to conventional 10 Hz rTMS in one-tenth of the stimulation time, enabling faster, more accessible treatments. Yet, despite its growing clinical use and regulatory approval in multiple countries, the fundamental mechanisms by which iTBS modulates limbic-cortical networks to alleviate depressive symptoms remain poorly understood. Addressing this knowledge gap is essential to optimizing treatment protocols and advancing precision neuromodulation strategies.
Understanding how iTBS drives recovery thus requires moving beyond traditional symptom-based approaches toward multi-level indices of brain plasticity that capture functional, neurochemical, and microstructural change. Current evidence remains largely descriptive, with limited direct insight into the underlying synaptic or cellular mechanisms of iTBS-induced modulation. Integrating PET with high-resolution MRI techniques provides a unique window on these processes. We now have full capacity for in-house synthesis and imaging with [F18]SynVesT-1. Thus, this tracer quantifies synaptic density in vivo, providing a direct molecular measure of plasticity. The ability to pair [F18]SynVesT-1 PET simultaneously with MRI represents a transformative advance for mechanistic neuromodulation research.
Clinical trials show that accelerated TBS, individually targeted to the DLPFC region most anti-correlated to sgACC, can produce rapid symptom relief within days rather than weeks. However, the neurobiological mechanisms underlying these effects remain unknown. It is hypothesized that repeated stimulation sessions promote cumulative synaptic potentiation and large-scale network reorganization. Elucidating these processes is crucial to optimize dosing parameters, understand inter-individual variability in response, and guide the next generation of biologically informed treatment strategies.
The proposed project will investigate the neurobiological mechanisms of accelerated TBS in MDD using an advanced multimodal imaging approach. In this single-arm, within-subject study, participants will undergo one week of accelerated iTBS treatment while completing pre- and post-treatment positron emission tomography (PET) and magnetic resonance imaging (MRI). PET imaging with the synaptic vesicle tracer [¹⁸F]SynVesT-1 will quantify changes in synaptic density, while MRI sequences such as resting-state functional MRI, magnetic resonance spectroscopy, and neurite orientation dispersion and density imaging (NODDI) will assess functional connectivity and microstructural plasticity. By integrating molecular, functional, and structural measures of brain plasticity, the study will provide new insight into how accelerated iTBS alters brain circuits implicated in depression and how these changes relate to clinical improvement.
Studientyp
Einschreibung (Geschätzt)
Phase
- Unzutreffend
Kontakte und Standorte
Studienkontakt
- Name: Stacey Shim
- Telefonnummer: 6356 613-722-6521
- E-Mail: rtms@theroyal.ca
Studieren Sie die Kontaktsicherung
- Name: Emma Cummings
- Telefonnummer: 6586 613-722-6521
Studienorte
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Ontario
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Ottawa, Ontario, Kanada, K1Z 7K4
- The Royal's Institute of Mental Health Research
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Kontakt:
- Sara Tremblay, PhD
- Telefonnummer: 6227 613-722-6521
- E-Mail: Sara.Tremblay@theroyal.ca
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Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
- Erwachsene
Akzeptiert gesunde Freiwillige
Beschreibung
Inclusion Criteria
For inclusion in the study, participants must fulfill all the following criteria:
- 18 to 55 years old.
- Competent to provide voluntary informed consent.
- English comprehension and verbal communication (participants must be able to both understand and speak English sufficiently to follow study procedures and be understood by study personnel
- Referred by their treating physician.
- Mini-International Neuropsychiatric Interview-confirmed diagnosis of MDD, as a single or recurring episode.
- Symptoms of MDD have not improved after ≥ 1 adequate antidepressant medication trial in the current depressive episode29.
- Baseline score of ≥18 on the 17-item Hamilton Rating Scale for Depression (HRSD-17).
- Maintained a stable treatment regimen for at least four weeks prior to entering the study, defined as being on a stable antidepressant regimen, a stable psychotherapy regimen, both, or neither (i.e., no treatment), with no changes during this period.
Exclusion Criteria
Participants fulfilling any of the following criteria will be excluded from the study:
- Any comorbid mental health disorders (including, but not limited to lifetime history of psychotic disorders, OCD, and/or bipolar I or II disorder) with the exception of anxiety/panic disorders, posttraumatic stress disorder and ADHD
- Current or past (< 3 months) substance (including nicotine) or alcohol abuse/dependence, as defined in DSM-5 criteria.
- Positive urine test for illegal substances, cannabis, or cotinine.
- Significant unstable medical or neurologic illness confirmed by medical history (e.g. uncontrolled diabetes, or renal dysfunction).
- Breastfeeding or pregnant (confirmed via urine test).
- BMI > 30 or BMI < 18.
- Contraindication for TMS (e.g., personal history of epilepsy or convulsion, metallic head implant, pacemaker).
- Contraindication for MRI (e.g. metallic implant, claustrophobia).
- Have received a cumulative radioactivity dose > 15.2mSv during the last 12 months.
- Have active malignancies (due to high chance of undergoing radiation therapy).
- Suicide attempt in the past three months and/or active suicidal intent.
- Failed (non-response) course of ECT or rTMS treatment in the current depressive episode.
- Benzodiazepine or lithium use. Other psychotropic medications (e.g. ADHD medications) are permitted, if stable in the 4 weeks prior to and during the treatment course)
- Any other condition that, in the opinion of the investigators, would adversely affect the participant's ability to complete the study.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: N / A
- Interventionsmodell: Einzelgruppenzuweisung
- Maskierung: Keine (Offenes Etikett)
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
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Experimental: Accelerated iTBS
One week of accelerated iTBS and use pre-/post-treatment PET/MRI to quantify changes in synaptic density, functional connectivity, and microstructural integrity.
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Die repetitive transkranielle Magnetstimulation (rTMS) ist eine von Health Canada zugelassene Behandlung für schwere Depressionen.
Typische Behandlungen umfassen tägliche Sitzungen von 30 bis 45 Minuten, die über einen Zeitraum von 4 bis 6 Wochen durchgeführt werden.
Jüngste technische Fortschritte ermöglichten die Entwicklung der Theta-Burst-Stimulation (TBS), eines neuartigen rTMS-Paradigmas, das die täglichen Sitzungen auf 3 bis 4 Minuten reduziert und gleichzeitig die gleiche klinische Wirksamkeit beibehält.
In dieser Studie wird speziell intermittierendes TBS (iTBS) verabreicht, eine neuartige Verfeinerung des herkömmlichen rTMS, die aus Bursts von 3 Stimulationen bei 50 Hz und der Theta-Frequenz (5 Hz) besteht.
Andere Namen:
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Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Change in Synaptic Density Following iTBS Measured by [¹⁸F]SynVesT-1 PET
Zeitfenster: Administered at baseline (prior to first iTBS treatment), and after the iTBS treatment course (i.e. one week later).
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We will quantify changes in synaptic density (expressed as non-displaceable binding potential (BPND)) within (a) the sgACC (primary ROI) and (b) the stimulated DLPFC (secondary ROI), with exploratory analyses in frontal, parietal and cerebellar regions identified in the seed dataset.
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Administered at baseline (prior to first iTBS treatment), and after the iTBS treatment course (i.e. one week later).
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Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Change in Resting-State Functional Connectivity Following accelerated iTBS
Zeitfenster: Administered at baseline (prior to first iTBS treatment) and after the iTBS treatment course (i.e. one week later).
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Resting-state functional MRI (rs-fMRI) will be used to assess changes in functional connectivity (Fisher z-transformed correlation coefficients) within fronto-limbic networks following accelerated iTBS.
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Administered at baseline (prior to first iTBS treatment) and after the iTBS treatment course (i.e. one week later).
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Correlation Between Changes in [18F]SynVesT-1 Binding and Depressive Symptom Improvement Following iTBS
Zeitfenster: Administered at screening, before the first iTBS, mid-treatment course (i.e. treatment day 3, following treatment #15), after the iTBS treatment course (i.e. treatment day 5, following treatment #30), and 1-month post treatment course.
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This outcome will assess the correlation between pre-post changes in synaptic density, measured using [18F]SynVesT-1 positron emission tomography (PET) standardized uptake value ratio (SUVR), and changes in depressive symptom severity, measured using the 17-item Hamilton Rating Scale for Depression (HRSD-17) total score, following accelerated iTBS, with the outcome metric defined as the correlation coefficient between changes in [18F]SynVesT-1 PET SUVR values and HRSD-17 total scores.
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Administered at screening, before the first iTBS, mid-treatment course (i.e. treatment day 3, following treatment #15), after the iTBS treatment course (i.e. treatment day 5, following treatment #30), and 1-month post treatment course.
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Change in Cortical Neurochemistry Following iTBS
Zeitfenster: Administered at baseline (prior to first iTBS treatment) and after the iTBS treatment course (i.e. one week later).
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Magnetic resonance spectroscopy (MRS) will be used to assess changes in cortical neurochemical metabolite concentrations or metabolite ratios (e.g., Glx, GABA+/Cr) following accelerated iTBS.
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Administered at baseline (prior to first iTBS treatment) and after the iTBS treatment course (i.e. one week later).
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Change in Cerebral Perfusion Following iTBS
Zeitfenster: Administered at baseline (prior to first iTBS treatment) and after the iTBS treatment course (i.e. one week later).
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Arterial spin labelling (ASL) MRI will be used to assess changes in regional cerebral blood flow levels following accelerated iTBS.
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Administered at baseline (prior to first iTBS treatment) and after the iTBS treatment course (i.e. one week later).
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Change in Neurite Microstructure Following iTBS
Zeitfenster: Administered at baseline (prior to first iTBS treatment) and after the iTBS treatment course (i.e. one week later).
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Neurite Orientation Dispersion and Density Imaging (NODDI) will be used to assess changes in neurite microstructure following accelerated iTBS, as measured by changes in neurite density index (NDI) and orientation dispersion index (ODI).
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Administered at baseline (prior to first iTBS treatment) and after the iTBS treatment course (i.e. one week later).
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Andere Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
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Incidence of Treatment-Emergent Adverse Events
Zeitfenster: Daily Monday-Friday throughout treatment course (1 week).
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Adverse events will be tracked and recorded.
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Daily Monday-Friday throughout treatment course (1 week).
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Side Effects
Zeitfenster: Daily Monday-Friday throughout study (1 week).
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Side effects will be tracked and recorded on any TMS visits, using the TMS side effects questionnaire.
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Daily Monday-Friday throughout study (1 week).
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Mitarbeiter und Ermittler
Ermittler
- Hauptermittler: Sara Tremblay, The Royal's Institute of Mental Health Research
- Hauptermittler: Lauri Tuominen, The Royal's Institute of Mental Health Research
Publikationen und hilfreiche Links
Allgemeine Veröffentlichungen
- Disner SG, Beevers CG, Haigh EA, Beck AT. Neural mechanisms of the cognitive model of depression. Nat Rev Neurosci. 2011 Jul 6;12(8):467-77. doi: 10.1038/nrn3027.
- Baeken C, Marinazzo D, Everaert H, Wu GR, Van Hove C, Audenaert K, Goethals I, De Vos F, Peremans K, De Raedt R. The Impact of Accelerated HF-rTMS on the Subgenual Anterior Cingulate Cortex in Refractory Unipolar Major Depression: Insights From 18FDG PET Brain Imaging. Brain Stimul. 2015 Jul-Aug;8(4):808-15. doi: 10.1016/j.brs.2015.01.415. Epub 2015 Feb 7.
- Blumberger DM, Vila-Rodriguez F, Thorpe KE, Feffer K, Noda Y, Giacobbe P, Knyahnytska Y, Kennedy SH, Lam RW, Daskalakis ZJ, Downar J. Effectiveness of theta burst versus high-frequency repetitive transcranial magnetic stimulation in patients with depression (THREE-D): a randomised non-inferiority trial. Lancet. 2018 Apr 28;391(10131):1683-1692. doi: 10.1016/S0140-6736(18)30295-2. Epub 2018 Apr 26.
- Cash RFH, Zalesky A, Thomson RH, Tian Y, Cocchi L, Fitzgerald PB. Subgenual Functional Connectivity Predicts Antidepressant Treatment Response to Transcranial Magnetic Stimulation: Independent Validation and Evaluation of Personalization. Biol Psychiatry. 2019 Jul 15;86(2):e5-e7. doi: 10.1016/j.biopsych.2018.12.002. Epub 2019 Jan 19. No abstract available.
- Tremblay S, Tuominen L, Zayed V, Pascual-Leone A, Joutsa J. The study of noninvasive brain stimulation using molecular brain imaging: A systematic review. Neuroimage. 2020 Oct 1;219:117023. doi: 10.1016/j.neuroimage.2020.117023. Epub 2020 Jun 5.
- Kang SG, Cho SE. Neuroimaging Biomarkers for Predicting Treatment Response and Recurrence of Major Depressive Disorder. Int J Mol Sci. 2020 Mar 20;21(6):2148. doi: 10.3390/ijms21062148.
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Geschätzt)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Schlüsselwörter
Zusätzliche relevante MeSH-Bedingungen
Andere Studien-ID-Nummern
- 0383
Plan für individuelle Teilnehmerdaten (IPD)
Planen Sie, individuelle Teilnehmerdaten (IPD) zu teilen?
Beschreibung des IPD-Plans
After participants have completed their participation, we will ask them for informed consent for the storage of their de-identified data on OpenNeuro (an open access database) for the purpose of unspecified research for unspecified future research.
If they do agree to participate, they will be given a unique study code (different from the participant ID used in the previous study) will be assigned to all of the study data instead of personal identifying information (ex. 'John Smith' replaced by the unique study code 'A283422'). This unique study code will be used in the Open Access database to ensure privacy and confidentiality (i.e. de-identified study data cannot be linked to participant in any way).
In addition to an unique study code, their de-identified study data used in the Open Access database will include: age, sex, handedness, education level, medical diagnosis, medication, summary scores from clinical interviews, and MRI scans.
IPD-Sharing-Zeitrahmen
IPD-Sharing-Zugriffskriterien
Art der unterstützenden IPD-Freigabeinformationen
- SAFT
Arzneimittel- und Geräteinformationen, Studienunterlagen
Studiert ein von der US-amerikanischen FDA reguliertes Arzneimittelprodukt
Studiert ein von der US-amerikanischen FDA reguliertes Geräteprodukt
Diese Informationen wurden ohne Änderungen direkt von der Website clinicaltrials.gov abgerufen. Wenn Sie Ihre Studiendaten ändern, entfernen oder aktualisieren möchten, wenden Sie sich bitte an register@clinicaltrials.gov. Sobald eine Änderung auf clinicaltrials.gov implementiert wird, wird diese automatisch auch auf unserer Website aktualisiert .
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