이 페이지는 자동 번역되었으며 번역의 정확성을 보장하지 않습니다. 참조하십시오 영문판 원본 텍스트의 경우.

SERENE Low-Intensity Focused Ultrasound for Cognitive Control

2026년 11월 2일 업데이트: University of Minnesota

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.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

100

단계

  • 해당 없음

연락처 및 위치

이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.

연구 연락처

  • 이름: Michael V Bronstein, PhD
  • 전화번호: 781-492-5644
  • 이메일: brons139@umn.edu

연구 장소

    • Minnesota
      • Minneapolis, Minnesota, 미국, 55455
        • Masonic Institute for the Developing Brain
        • 연락하다:
          • Michael V Bronstein, PhD
          • 전화번호: 781-492-5644
          • 이메일: brons139@umn.edu

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

공부할 수 있는 나이

18년 (성인, 고령자)

건강한 자원 봉사자를 받아들입니다

아니

연구 대상 성별

모두

설명

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

공부 계획

이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.

연구는 어떻게 설계됩니까?

디자인 세부사항

  • 주 목적: 기초 과학
  • 할당: 해당 없음
  • 중재 모델: 단일 그룹 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.

다른 이름들:
  • SPIRE DIADEM System
  • LIFU Neuromodulation

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Mean Reaction Time During the Multi-Source Interference Task Following LIFU at Different Internal Capsule Sites
기간: Baseline and during MSIT task blocks corresponding to each internal capsule LIFU sonication site

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
Event-Related EEG Alpha-Band Spectral Power Following LIFU
기간: During post-LIFU MSIT assessment at each internal capsule sonication site

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
Event-Related EEG Theta-Band Spectral Power Following LIFU
기간: During post-LIFU MSIT assessment at each internal capsule sonication site

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
Time Course of Mean Reaction Time During the Multi-Source Interference Task Following LIFU
기간: During repeated MSIT assessments across LIFU sonication sessions and through post-treatment follow-up within 2 weeks

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

2차 결과 측정

결과 측정
측정값 설명
기간
Change in MSIT Mean Reaction Time From Baseline Following LIFU at Different Internal Capsule Sites
기간: Baseline and during MSIT task blocks corresponding to each internal capsule LIFU sonication site

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
Change in Momentary Active Suicidal Ideation Rating Measured by Ecological Momentary Assessment
기간: Twice daily for 3 days before and 3 days after LIFU

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
Change in Momentary Passive Suicidal Ideation Rating Measured by Ecological Momentary Assessment
기간: Twice daily for 3 days before and 3 days after LIFU

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
Change in Momentary Depression Rating Measured by Ecological Momentary Assessment
기간: Twice daily for 3 days before and 3 days after LIFU

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
Change in Momentary Rumination Rating Measured by Ecological Momentary Assessment
기간: Twice daily for 3 days before and 3 days after LIFU

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
Change in Momentary Physical Pain Rating Measured by Ecological Momentary Assessment
기간: Twice daily for 3 days before and 3 days after LIFU

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
Change in Momentary Co-dampening Rating Measured by Ecological Momentary Assessment
기간: Twice daily for 3 days before and 3 days after LIFU

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
Change in Momentary Hallucination Rating Measured by Ecological Momentary Assessment
기간: Twice daily for 3 days before and 3 days after LIFU

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
Change in Momentary Persecutory Experience Rating Measured by Ecological Momentary Assessment
기간: Twice daily for 3 days before and 3 days after LIFU

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

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 수석 연구원: Michael V Bronstein, PhD, University of Minnesota
  • 연구 책임자: Alik S Widge, MD,PhD, University of Minnesota

연구 기록 날짜

이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.

연구 주요 날짜

연구 시작 (추정된)

2027년 1월 1일

기본 완료 (추정된)

2028년 9월 20일

연구 완료 (추정된)

2028년 9월 20일

연구 등록 날짜

최초 제출

2026년 10월 13일

QC 기준을 충족하는 최초 제출

2026년 11월 2일

처음 게시됨 (실제)

2026년 11월 6일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 11월 6일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 11월 2일

마지막으로 확인됨

2026년 11월 1일

추가 정보

이 연구와 관련된 용어

약물 및 장치 정보, 연구 문서

미국 FDA 규제 의약품 연구

아니

미국 FDA 규제 기기 제품 연구

예

미국에서 제조되어 미국에서 수출되는 제품

아니

이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .

구독하다