SERENE Low-Intensity Focused Ultrasound for Cognitive Control
Suicide-related Experience Reduction Via Enhancement of Neuroplasticity
SERENE is an experimental study evaluating low-intensity focused ultrasound neuromodulation of cognitive control circuitry in adults with a lifetime history of suicide attempt or suicidal ideation, but without current suicidality.
Participants will complete screening, cognitive control tasks, MRI/fMRI, ecological momentary assessments, and low-intensity focused ultrasound neuromodulation using the DIADEM system. The study will examine whether low-intensity focused ultrasound (LIFU) neuromodulation changes cognitive control performance measured by the Multi-Source Interference Task (MSIT) and EEG event-related spectral power in the alpha and theta frequency bands.
The study will also examine the time course of LIFU effects and explore whether changes in cognitive control circuitry relate to self-reported experiences, including mood, anxiety, psychosis symptoms, suicidal ideation, and emotion regulation.
Przegląd badań
Status
Interwencja / Leczenie
Szczegółowy opis
SERENE is an experimental study designed to test a personalized, non-invasive neuromodulation technique to investigate the neural basis of cognitive control.
The study will enroll adults with a lifetime history of suicide attempt or suicidal ideation, but without current suicidal ideation or behavior. Participants will be screened using the Columbia-Suicide Severity Rating Scale to confirm suicide history and exclude current suicidality. Participants will also complete MRI/fMRI-based cognitive control screening to identify cognitive control circuit function.
Participants will complete baseline cognitive and self-report assessments, including computerized cognitive tasks and clinical/self-report measures. Ecological momentary assessments will be completed before and after neuromodulation to assess symptoms and daily-life experiences related to cognitive control, including mood, anxiety, psychosis-related symptoms, suicidal ideation, and emotion regulation.
The study intervention is low-intensity focused ultrasound neuromodulation delivered using the DIADEM system. LIFU will be applied to deep brain regions involved in cognitive control, including subregions of the internal capsule and connected brain regions. During LIFU visits, participants will complete the Multi-Source Interference Task to assess cognitive control. EEG and fMRI may also be collected to evaluate neurocircuitry changes associated with LIFU.
The primary objective is to evaluate the effect of LIFU on cognitive control and associated circuitry. The study will also examine the time course of this effect, whether responses differ by baseline cognitive control circuit function, and whether changes in circuitry relate to self-reported experiences.
Typ studiów
Zapisy (Szacowany)
Faza
- Nie dotyczy
Kontakty i lokalizacje
Kontakt w sprawie studiów
- Nazwa: Michael V Bronstein, PhD
- Numer telefonu: 781-492-5644
- E-mail: brons139@umn.edu
Lokalizacje studiów
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Minnesota
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Minneapolis, Minnesota, Stany Zjednoczone, 55455
- Masonic Institute for the Developing Brain
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Kontakt:
- Michael V Bronstein, PhD
- Numer telefonu: 781-492-5644
- E-mail: brons139@umn.edu
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Kryteria uczestnictwa
Kryteria kwalifikacji
Wiek uprawniający do nauki
Akceptuje zdrowych ochotników
Płeć kwalifikująca się do nauki
Opis
Inclusion Criteria:
- Lifetime history of suicide attempt or suicidal ideation, as determined by the Columbia-Suicide Severity Rating Scale
- Score in specified ranges on measures of cognitive control behavior and/or cognitive control circuit function
- No current suicide ideation or behavior within the past 3 months, as determined by the Columbia-Suicide Severity Rating Scale
- Age 18 to 65 years
- Speaks and understands English
- Primary user of a smartphone
Exclusion Criteria:
- Under age 18
- Neurological disorder that may affect fMRI scan results or cause reaction to LIFU to differ from healthy adults
- Regular use of psychoactive medication, except PRN use if the participant is willing and able to abstain during the study period
- Psychiatric hospitalization within the past 3 months
- Contraindication to fMRI scanning, including claustrophobia, unremovable piercings, pregnancy, medical devices such as pacemakers, or a movement or sleep disorder
- Pregnant or may have reason to believe they are pregnant
- Diagnosis of certain psychiatric conditions, such as schizophrenia, bipolar disorder, or a developmental disorder other than ADHD
- Any other neurological, autoimmune, or medical disorder that may inhibit participation
- Children
- Pregnant women/persons
- Fetuses
- Neonates
- Prisoners
- Adults lacking capacity to consent or adults with diminished or fluctuating capacity to consent
- Non-English speakers
- Individuals unable to read
- Employees of the researcher
- Students of the researcher
- Individuals approached during a stressful situation, such as an emergency room setting or childbirth
- Individuals with fear of negative consequences for not participating
- Any other circumstance that could increase vulnerability to coercion or exploitation
Plan studiów
Jak projektuje się badanie?
Szczegóły projektu
- Główny cel: Podstawowa nauka
- Przydział: Nie dotyczy
- Model interwencyjny: Zadanie dla jednej grupy
- Maskowanie: Brak (otwarta etykieta)
Broń i interwencje
Grupa uczestników / Arm |
Interwencja / Leczenie |
|---|---|
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Eksperymentalny: DIADEM LIFU Neuromodulation
Participants will receive low-intensity focused ultrasound neuromodulation using the DIADEM device while completing cognitive control tasks. Stimulation may be applied to subregions of the internal capsule and connected brain regions to identify targets that modulate cognitive control performance or circuitry. |
Low-intensity focused ultrasound neuromodulation will be delivered using the SPIRE DIADEM device. LIFU will be applied to subregions of deep brain circuitry involved in cognitive control, including regions within the dorsal or ventral internal capsule, surrounding striatal nuclei, and/or connected brain areas. Stimulation will be delivered by trained study staff according to device safety and screening procedures.
Inne nazwy:
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Co mierzy badanie?
Podstawowe miary wyniku
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Mean Reaction Time During the Multi-Source Interference Task Following LIFU at Different Internal Capsule Sites
Ramy czasowe: Baseline and during MSIT task blocks corresponding to each internal capsule LIFU sonication site
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Cognitive control performance will be assessed using the Multi-Source Interference Task (MSIT), a computerized cognitive control task. Reaction time will be measured in milliseconds. The MSIT will be administered in blocks, with one block corresponding to each internal capsule sonication site. Mean reaction time will be calculated separately for each block and compared with baseline MSIT mean reaction time. Lower reaction times indicate faster task performance. |
Baseline and during MSIT task blocks corresponding to each internal capsule LIFU sonication site
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Event-Related EEG Alpha-Band Spectral Power Following LIFU
Ramy czasowe: During post-LIFU MSIT assessment at each internal capsule sonication site
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EEG alpha-band activity will be assessed using event-related spectral power during the Multi-Source Interference Task (MSIT) following LIFU. Spectral power will be baseline-normalized using a pre-stimulus reference interval from -500 to -100 milliseconds relative to the target event. Baseline normalization will be performed in the linear power domain, with results expressed in decibels (dB). |
During post-LIFU MSIT assessment at each internal capsule sonication site
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Event-Related EEG Theta-Band Spectral Power Following LIFU
Ramy czasowe: During post-LIFU MSIT assessment at each internal capsule sonication site
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EEG theta-band activity will be assessed using event-related spectral power during the Multi-Source Interference Task (MSIT) following LIFU. Spectral power will be baseline-normalized using a pre-stimulus reference interval from -500 to -100 milliseconds relative to the target event. Baseline normalization will be performed in the linear power domain, with results expressed in decibels (dB). |
During post-LIFU MSIT assessment at each internal capsule sonication site
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Time Course of Mean Reaction Time During the Multi-Source Interference Task Following LIFU
Ramy czasowe: During repeated MSIT assessments across LIFU sonication sessions and through post-treatment follow-up within 2 weeks
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The time course of LIFU effects on cognitive control will be evaluated using repeated mean reaction time measurements obtained during the Multi-Source Interference Task (MSIT). Reaction time will be measured in milliseconds and summarized for each assessment block. Mean reaction time will be compared across the repeated assessments to evaluate changes in cognitive control performance over time. Lower values indicate faster task performance. |
During repeated MSIT assessments across LIFU sonication sessions and through post-treatment follow-up within 2 weeks
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Miary wyników drugorzędnych
Miara wyniku |
Opis środka |
Ramy czasowe |
|---|---|---|
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Change in MSIT Mean Reaction Time From Baseline Following LIFU at Different Internal Capsule Sites
Ramy czasowe: Baseline and during MSIT task blocks corresponding to each internal capsule LIFU sonication site
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Differential response to LIFU across internal capsule stimulation sites will be assessed using mean reaction time during the Multi-Source Interference Task (MSIT), measured in milliseconds. Mean reaction time will be calculated separately for the MSIT block corresponding to each sonication site. Change will be calculated as the mean reaction time following sonication at each site minus the baseline mean reaction time. Negative change values indicate faster responses relative to baseline. Changes will be compared across sonication sites. |
Baseline and during MSIT task blocks corresponding to each internal capsule LIFU sonication site
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Change in Momentary Active Suicidal Ideation Rating Measured by Ecological Momentary Assessment
Ramy czasowe: Twice daily for 3 days before and 3 days after LIFU
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Momentary active suicidal ideation will be assessed using a study-adapted ecological momentary assessment (EMA) item delivered through participants' smartphones. Responses are rated on a 5-point Likert scale from 1 to 5. |
Twice daily for 3 days before and 3 days after LIFU
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Change in Momentary Passive Suicidal Ideation Rating Measured by Ecological Momentary Assessment
Ramy czasowe: Twice daily for 3 days before and 3 days after LIFU
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Momentary passive suicidal ideation will be assessed using a study-adapted ecological momentary assessment (EMA) item delivered through participants' smartphones. Responses are rated on a 5-point Likert scale from 1 to 5. |
Twice daily for 3 days before and 3 days after LIFU
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Change in Momentary Depression Rating Measured by Ecological Momentary Assessment
Ramy czasowe: Twice daily for 3 days before and 3 days after LIFU
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Momentary depressive symptoms will be assessed using a study-adapted ecological momentary assessment (EMA) item delivered through participants' smartphones. Responses are rated on a 5-point Likert scale from 1 to 5. |
Twice daily for 3 days before and 3 days after LIFU
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Change in Momentary Rumination Rating Measured by Ecological Momentary Assessment
Ramy czasowe: Twice daily for 3 days before and 3 days after LIFU
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Momentary rumination will be assessed using a study-adapted ecological momentary assessment (EMA) item delivered through participants' smartphones. Responses are rated on a 5-point Likert scale from 1 to 5. |
Twice daily for 3 days before and 3 days after LIFU
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Change in Momentary Physical Pain Rating Measured by Ecological Momentary Assessment
Ramy czasowe: Twice daily for 3 days before and 3 days after LIFU
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Momentary physical pain will be assessed using a study-adapted ecological momentary assessment (EMA) item delivered through participants' smartphones. Responses are rated on a 5-point Likert scale from 1 to 5. |
Twice daily for 3 days before and 3 days after LIFU
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Change in Momentary Co-dampening Rating Measured by Ecological Momentary Assessment
Ramy czasowe: Twice daily for 3 days before and 3 days after LIFU
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Momentary co-dampening will be assessed using a study-adapted ecological momentary assessment (EMA) item delivered through participants' smartphones. Responses are rated on a 5-point Likert scale from 1 to 5. |
Twice daily for 3 days before and 3 days after LIFU
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Change in Momentary Hallucination Rating Measured by Ecological Momentary Assessment
Ramy czasowe: Twice daily for 3 days before and 3 days after LIFU
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Momentary experiences of hallucinations will be assessed using a study-adapted ecological momentary assessment (EMA) item delivered through participants' smartphones. Responses are rated on a 5-point Likert scale from 1 to 5. |
Twice daily for 3 days before and 3 days after LIFU
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Change in Momentary Persecutory Experience Rating Measured by Ecological Momentary Assessment
Ramy czasowe: Twice daily for 3 days before and 3 days after LIFU
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Momentary persecutory experiences will be assessed using a study-adapted ecological momentary assessment (EMA) item delivered through participants' smartphones. Responses are rated on a 5-point Likert scale from 1 to 5. |
Twice daily for 3 days before and 3 days after LIFU
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Współpracownicy i badacze
Sponsor
Śledczy
- Główny śledczy: Michael V Bronstein, PhD, University of Minnesota
- Dyrektor Studium: Alik S Widge, MD,PhD, University of Minnesota
Daty zapisu na studia
Główne daty studiów
Rozpoczęcie studiów (Szacowany)
Zakończenie podstawowe (Szacowany)
Ukończenie studiów (Szacowany)
Daty rejestracji na studia
Pierwszy przesłany
Pierwszy przesłany, który spełnia kryteria kontroli jakości
Pierwszy wysłany (Rzeczywisty)
Aktualizacje rekordów badań
Ostatnia wysłana aktualizacja (Rzeczywisty)
Ostatnia przesłana aktualizacja, która spełniała kryteria kontroli jakości
Ostatnia weryfikacja
Więcej informacji
Terminy związane z tym badaniem
Słowa kluczowe
Dodatkowe istotne warunki MeSH
Inne numery identyfikacyjne badania
- STUDY00028755
Informacje o lekach i urządzeniach, dokumenty badawcze
Bada produkt leczniczy regulowany przez amerykańską FDA
Bada produkt urządzenia regulowany przez amerykańską FDA
produkt wyprodukowany i wyeksportowany z USA
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