Not yet recruitingNCT07851038VANTUSUpdated Oct 1, 2026

Focused Ultrasound for Behavioral Health

An interventional study of ATTN201 head-worn focused ultrasound in Depression, Anxiety and Obsessive Compulsive Disorder (OCD), sponsored by Attune Neurosciences Inc. Not yet recruiting at 1 site in United States. Open to participants aged 22 Years to 80 Years. Per ClinicalTrials.gov, last updated 2026-10-01.

Sponsored by Attune Neurosciences Inc · Not applicable, Interventional, and Treatment

Updated Oct 1, 2026Newly registeredGo to Updates ↓

Phase: Not applicable
Study type: Interventional
Enrollment: 300
Allocation: Non-randomized
Ages: 22 Years to 80 Years
Sex: All

Study summary

This is a double-blind, within-participant crossover, multi-site dose-finding study evaluating the safety, feasibility, and preliminary efficacy of repeated low-intensity focused ultrasound (LIFU) stimulation using the ATTN201 device across seven candidate deep-brain targets in adults with subsyndromal-to-moderate depression, anxiety, or obsessive-compulsive disorder. Every session delivers active ATTN201 stimulation; there is no sham or placebo condition. Participants and the on-site study staff who deliver stimulation and administer the clinical scales are blinded to the brain target and to the stimulation parameters assigned for each session by a constrained Bayesian optimization algorithm.

Read the detailed description

Following a remote pre-screen and an in-person screening/baseline visit (Visit 0), at which informed consent is obtained, eligibility is confirmed, baseline clinical scales are administered, optional biospecimens are collected from participants who consent to them, a multi-sequence brain MRI is acquired for targeting, and monitoring devices are fitted, each participant receives between 3 and 10 ATTN201 stimulation sessions spaced approximately 7 days apart. Each stimulation visit serves as the pre-stimulation baseline for that session, the 1-week post-stimulation measurement for the prior session, and the 2-week post-stimulation measurement for the session before that. A platform-administered scale battery at day 7 after the last stimulation captures the 1-week measurement for the final session; a remote final treatment-period follow-up approximately 2 weeks after the last stimulation captures the 2-week measurement. A remote 3-month post-treatment check-in captures durability and any delayed adverse events.

The trial uses a two-stage architecture. In Stage 1, visits are allocated across all seven candidate targets. After approximately 300 visits, the Sponsor and ARPA-H convene a joint review and select 3-5 targets for continued Bayesian optimization in Stage 2.

Monitoring during enrollment includes validated clinical scales (PHQ-9, GAD-7, OCI-R) at baseline, before each stimulation visit, at the final treatment-period follow-up, and at the 3-month follow-up; transdiagnostic visual analog scales, a morning sleep diary, and brief voice recordings prompted through the Attune platform during monitoring blocks; optional nightly ambulatory EEG; and a smart watch worn from Visit 0 through device return. All scheduled platform prompts are voluntary at the individual-prompt level.

Blinding: A single on-site research associate positions the device, runs the stimulation session, and administers participant-facing assessments, and is blinded to the brain target and parameter combination; this individual occupies both the care provider and the outcomes assessor role. The stimulation condition is selected by the Bayesian optimization algorithm and pushed to the device as a sealed session. The Lead Principal Investigator and the optimization team are unblinded as required to operate the adaptive design and do not deliver stimulation or administer participant-facing assessments. The independent Medical Monitors and the Data Safety and Monitoring Board receive unblinded safety data.

Conditions studied

Depression
Anxiety
Obsessive Compulsive Disorder (OCD)

Browse trials for

In context

Depression

8,055 studies on the registry are indexed under Depression; 1,643 are open to participants now.

This study's planned enrollment of 300 is above the median of 84 across 6,718 interventional studies indexed under Depression.

Browse Depression studies →

Lead sponsor

This is the only study on the registry with Attune Neurosciences Inc as lead sponsor.

Counted across the registry records on this site, refreshed daily.

Who can participate

Ages eligible: 22 Years to 80 Years
Sexes eligible: All
Accepts healthy volunteers: No

Inclusion criteria

Be between 22 and 80 years of age (inclusive) on the day of signing informed consent.
Have at least one of the following at screening: PHQ-9 total score 5-16 (depression), GAD-7 total score 5-14 (anxiety), or OCI-R total score 14-27 (obsessive-compulsive disorder).
If currently taking psychiatric medication, have been on the same stable dose(s) for at least 4 weeks prior to screening and be willing to maintain the regimen throughout the treatment period.
Be able and willing to undergo a multi-sequence cranial MRI.
Be willing to use the ATTN201 device during stimulation visits and to attempt use of monitoring devices (optional ambulatory EEG system, smart watch) during the pre- and post-stimulation monitoring blocks; use of the optional ambulatory EEG system does not affect eligibility.
Sign the informed consent form, in accordance with local requirements, after the scope and nature of the investigation have been explained to the participant, and before any screening assessments.
Be able to speak, read, and understand English.
Be able to use a smartphone and the Attune platform.
Possess the ability to respond verbally to questions, follow instructions, and complete study assessments.
Be able to adhere to the treatment protocol and visit schedules through the 3-month post-treatment follow-up.
Be judged by the investigator as likely to comply with study procedures and willing to participate in the entirety of the study.
Be determined by the investigator to be medically stable at baseline as assessed by medical history and non-significant clinical results of a vital signs examination.
Male participants must ensure a condom is used for all sexual intercourse and follow acceptable methods of contraception for their female partner for the entire duration of the study and for 90 days after the final study visit. Male participants should not father a child or donate sperm during this same period.
Female participants who are sexually active agree to use two methods of contraception for the duration of the study and for 30 days after the final study visit, or not be of childbearing potential as indicated by natural menopause (≥12 consecutive months of spontaneous amenorrhea), hysterectomy, bilateral tubal ligation, bilateral oophorectomy (with or without hysterectomy) more than 6 weeks prior to screening, or a vasectomized partner with documented absence of sperm.

Exclusion criteria

Exclusion Criteria:

Columbia Suicide Severity Rating Scale (C-SSRS) score ≥ 3 (ideation with intent, with or without plan) at screening.
Any suicide attempt within the past 12 months.
Any change in psychiatric medication (start, stop, or dose change) within 4 weeks prior to screening.
Has an unstable or severe medical or psychiatric condition that, in the investigator's judgment, would pose a safety risk to the participant or prevent completion of study procedures. Stable comorbid conditions (e.g., treated depression, anxiety, OCD, insomnia) within the protocol-specified score windows are permitted.
Has an active, unstable substance use disorder including alcohol use disorder in the past 6 months (except for caffeine and nicotine). Participants on stable medication-assisted treatment (e.g., buprenorphine, methadone, naltrexone) for at least 6 months are eligible.
Has a history of moderate-to-severe traumatic brain injury, or mild traumatic brain injury within the past 12 months.
Has a history of seizure disorder or epilepsy, or any structural CNS lesion known to lower seizure threshold.
Has any contraindications for completing a brain MRI scan (e.g., pacemaker, ferromagnetic implants).
Body mass index (BMI) greater than 40 kg/m².
Is pregnant, is attempting to become pregnant, or is nursing.
Is or has an immediate family member (e.g., spouse, parent/legal guardian, sibling, or child) who is an investigational site or Sponsor staff member directly involved with this trial.
Has a known allergy or sensitivity to ultrasound gel, silicone, or adhesive materials used in monitoring devices.
Has an active skin condition at sensor placement sites that would prevent device wear.
Has received an investigational drug or device in another clinical study within 30 days before screening

Study design

Phase: Not applicable
Primary purpose: Treatment
Allocation: Non-randomized
Intervention model: Crossover assignment
Masking: Triple (Participant, Care provider, Outcomes assessor)
Enrollment: 300 participants (estimated)

Study arms

Experimental
Basolateral amygdala (BLA)
ATTN201 head-worn low-intensity focused ultrasound delivered to the basolateral amygdala (BLA). Sessions at which the constrained Bayesian optimization algorithm assigns this target; stimulation parameters (pulse repetition frequency, duty cycle, target pressure) vary within the ITRUSST-bounded search space. Participants may cross over to other target arms at subsequent sessions.
Device: ATTN201 head-worn focused ultrasound
Experimental
Dorsal anterior cingulate cortex (dACC)
ATTN201 head-worn low-intensity focused ultrasound delivered to the dorsal anterior cingulate cortex (dACC). Sessions at which the constrained Bayesian optimization algorithm assigns this target; stimulation parameters (pulse repetition frequency, duty cycle, target pressure) vary within the ITRUSST-bounded search space. Participants may cross over to other target arms at subsequent sessions.
Device: ATTN201 head-worn focused ultrasound
Experimental
Anterior limb of internal capsule (ALIC)
ATTN201 head-worn low-intensity focused ultrasound delivered to the anterior limb of the internal capsule (ALIC). Sessions at which the constrained Bayesian optimization algorithm assigns this target; stimulation parameters (pulse repetition frequency, duty cycle, target pressure) vary within the ITRUSST-bounded search space. Participants may cross over to other target arms at subsequent sessions.
Device: ATTN201 head-worn focused ultrasound
Experimental
Centromedian nucleus of thalamus (CMN)
ATTN201 head-worn low-intensity focused ultrasound delivered to the centromedian nucleus of the thalamus (CMN). Sessions at which the constrained Bayesian optimization algorithm assigns this target; stimulation parameters (pulse repetition frequency, duty cycle, target pressure) vary within the ITRUSST-bounded search space. Participants may cross over to other target arms at subsequent sessions.
Device: ATTN201 head-worn focused ultrasound
Experimental
Rostral zona incerta (rZi)
ATTN201 head-worn low-intensity focused ultrasound delivered to the rostral zona incerta (rZi). Sessions at which the constrained Bayesian optimization algorithm assigns this target; stimulation parameters (pulse repetition frequency, duty cycle, target pressure) vary within the ITRUSST-bounded search space. Participants may cross over to other target arms at subsequent sessions.
Device: ATTN201 head-worn focused ultrasound
Experimental
Subthalamic nucleus (STN)
ATTN201 head-worn low-intensity focused ultrasound delivered to the subthalamic nucleus (STN). Sessions at which the constrained Bayesian optimization algorithm assigns this target; stimulation parameters (pulse repetition frequency, duty cycle, target pressure) vary within the ITRUSST-bounded search space. Participants may cross over to other target arms at subsequent sessions.
Device: ATTN201 head-worn focused ultrasound
Experimental
Anterior nucleus of thalamus (ANT)
ATTN201 head-worn low-intensity focused ultrasound delivered to the anterior nucleus of the thalamus (ANT). Sessions at which the constrained Bayesian optimization algorithm assigns this target; stimulation parameters (pulse repetition frequency, duty cycle, target pressure) vary within the ITRUSST-bounded search space. Participants may cross over to other target arms at subsequent sessions.
Device: ATTN201 head-worn focused ultrasound

Interventions

DeviceATTN201 head-worn focused ultrasound
ATTN201 head-worn focused ultrasound

What researchers measure

Primary outcomes

Patient-specific transdiagnostic score (TDx) at 1 week after stimulation
TDx measured 1 week after each stimulation session. The TDx is a severity-weighted composite of normalized improvement on PHQ-9, GAD-7, and OCI-R; higher TDx indicates greater improvement.
Time frame: 1 week after each stimulation session

Secondary outcomes

Patient-specific transdiagnostic score (TDx) at 2 weeks after stimulation
TDx measured 2 weeks after each stimulation session. The TDx is a severity-weighted composite of normalized improvement on PHQ-9, GAD-7, and OCI-R; higher TDx indicates greater improvement.
Time frame: 2 weeks after each stimulation session
Posterior mean transdiagnostic score (TDx) at the best stimulation parameter set for each brain target
Posterior mean TDx, from a Gaussian process model fit for each brain target, at the stimulation parameter set that maximizes it. TDx is a severity-weighted composite of normalized improvement on PHQ-9, GAD-7, and OCI-R; higher TDx indicates greater improvement.
Time frame: At study completion, up to 19 months
Change from pre-stimulation baseline in PHQ-9 total score
Change from the local pre-stimulation baseline in Patient Health Questionnaire-9 (PHQ-9) total score. The PHQ-9 is a 9-item self-report measure of depression severity over the preceding 2 weeks. Total score range is 0 to 27; higher scores indicate greater depression severity. A negative change score indicates improvement.
Time frame: Pre-stimulation baseline, 1 week after stimulation, and 2 weeks after stimulation
Change from pre-stimulation baseline in GAD-7 total score
Change from the local pre-stimulation baseline in Generalized Anxiety Disorder-7 (GAD-7) total score. The GAD-7 is a 7-item self-report measure of anxiety severity over the preceding 2 weeks. Total score range is 0 to 21; higher scores indicate greater anxiety severity. A negative change score indicates improvement.
Time frame: Pre-stimulation baseline, 1 week after stimulation, and 2 weeks after stimulation
Change from pre-stimulation baseline in OCI-R total score
Change from the local pre-stimulation baseline in Obsessive-Compulsive Inventory-Revised (OCI-R) total score. The OCI-R is an 18-item self-report measure of distress associated with obsessive-compulsive symptoms. Total score range is 0 to 72; higher scores indicate greater symptom severity. A negative change score indicates improvement.
Time frame: Pre-stimulation baseline, 1 week after stimulation, and 2 weeks after stimulation
Mood visual analog scale (VAS) score
Self-rated mood on a 0-100 continuous VAS administered through the Attune platform; higher scores indicate better mood.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Arousal visual analog scale (VAS) score
Self-rated arousal on a 0-100 continuous VAS administered through the Attune platform; higher scores indicate greater arousal.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Sleepiness visual analog scale (VAS) score
Self-rated sleepiness on a 0-100 continuous VAS administered through the Attune platform; higher scores indicate greater sleepiness.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Anxiety symptom visual analog scale (VAS) score
Self-rated current anxiety symptoms on a 0-100 continuous VAS administered through the Attune platform; higher scores indicate greater anxiety.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Obsessive-compulsive symptom visual analog scale (VAS) score
Self-rated current obsessive-compulsive symptoms on a 0-100 continuous VAS administered through the Attune platform; higher scores indicate greater symptom severity.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Depression symptom visual analog scale (VAS) score
Self-rated current depression symptoms on a 0-100 continuous VAS administered through the Attune platform; higher scores indicate greater symptom severity.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Prefrontal EEG delta band spectral power
Absolute spectral power in the delta band from nightly two-channel prefrontal ambulatory EEG recordings, among participants who elect optional EEG monitoring.
Time frame: Nightly from Day 1 through Day 7 after each stimulation session
Prefrontal EEG theta band spectral power
Absolute spectral power in the theta band from nightly two-channel prefrontal ambulatory EEG recordings, among participants who elect optional EEG monitoring.
Time frame: Nightly from Day 1 through Day 7 after each stimulation session
Prefrontal EEG alpha band spectral power
Absolute spectral power in the alpha band from nightly two-channel prefrontal ambulatory EEG recordings, among participants who elect optional EEG monitoring.
Time frame: Nightly from Day 1 through Day 7 after each stimulation session
Prefrontal EEG beta band spectral power
Absolute spectral power in the beta band from nightly two-channel prefrontal ambulatory EEG recordings, among participants who elect optional EEG monitoring.
Time frame: Nightly from Day 1 through Day 7 after each stimulation session
Prefrontal EEG gamma band spectral power
Absolute spectral power in the gamma band from nightly two-channel prefrontal ambulatory EEG recordings, among participants who elect optional EEG monitoring.
Time frame: Nightly from Day 1 through Day 7 after each stimulation session
EEG-derived sleep efficiency
Sleep efficiency (percentage of time in bed spent asleep) derived by automated sleep staging of nightly two-channel prefrontal ambulatory EEG recordings, among participants who elect optional EEG monitoring.
Time frame: Nightly from Day 1 through Day 7 after each stimulation session
Smart-watch-derived heart rate variability
Daily heart rate variability (milliseconds) recorded by the study smart watch.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Smart-watch-derived daily step count
Daily step count (actigraphy) recorded by the study smart watch.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Smart-watch-derived sleep duration
Nightly total sleep duration (minutes) recorded by the study smart watch.
Time frame: Nightly from Day 1 through Day 7 after each stimulation session
Life-space mobility
Daily life-space mobility (maximum distance from home, kilometers) derived from de-identified GPS collected by the optional Beiwe research application on the participant's smartphone.
Time frame: Daily from Day 1 through Day 7 after each stimulation session
Patient-specific transdiagnostic score (TDx) at 1 week after stimulation, by primary indication
TDx measured 1 week after each stimulation session, summarized separately for participants whose primary indication is depression, anxiety, obsessive-compulsive disorder, or comorbid. TDx is a severity-weighted composite of normalized improvement on PHQ-9, GAD-7, and OCI-R; higher TDx indicates greater improvement.
Time frame: 1 week after each stimulation session

Study locations

1 site

Attune Neurosciences, Inc.
San Francisco, California 94107, United States

References and documents

Individual participant data

Plan to share: Yes — De-identified individual participant data will be deposited into the ARPA-H designated data repository as required by the funded ARPA-H EVIDENT program. Deposited data include clinical outcome measures (PHQ-9, GAD-7, OCI-R, PROMIS Sleep Disturbance 8a, PROMIS Sleep-Related Impairment 8a, DASS-8, Brief Resilience Scale, Flourishing Scale, and transdiagnostic visual analog scales), delivered stimulation parameters, EEG-derived and wearable-derived biomarker measures, platform-derived measures, relevant metadata, and optional baseline dried blood spot and saliva biospecimens where collected. Participant identifiers are not included in deposited datasets.

Supporting information: Study protocol, Sap

No publications or documents are linked to this record.

Updates

1 registry update since Sep 25, 2026

Registered

First appeared on the registry. No changes since

Oct 1, 2026

Show all 1 update

Oct 1, 2026
First appeared on the registry

From the registry record's own update history. This site started tracking changes on Sep 25, 2026; for anything earlier, see the record history on ClinicalTrials.gov ↗

Registry details

Key details

Study ID: NCT07851038
Lead sponsor: Attune Neurosciences Inc
Collaborators: University of California, San Francisco, University of Pennsylvania
Responsible party: Sponsor
First posted: Oct 1, 2026
Start date: Oct 5, 2026 (estimated)
Primary completion: Apr 5, 2028 (estimated)
Completion: May 17, 2028 (estimated)
Last update: Oct 1, 2026

Study contacts

Keith Murphy, PhD

Contact

keith@attuneneuro.com

415-658-7001

Oversight

Data monitoring committee: Yes
FDA-regulated drug: No
FDA-regulated device: Yes

View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is not yet recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Other studies in this condition

Depression→

Start the discussion