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CMN LIFU for Enhanced Amyloid Reduction (CLEART Study)
Safety and Feasibility Study of ATTN201 Centromedian Nucleus of the Thalamus Focused Ultrasound Stimulation for Enhanced Glymphatic Clearance in Amyloid Positive Patients With Mild Cognitive Impairment
The goal of this clinical trial is to learn if a wearable ultrasound device, called ATTN201, is safe and easy to use. The study is for adults ages 65 and older who have mild cognitive impairment (MCI) and a buildup of a protein called amyloid in the brain. Amyloid buildup is an early sign of Alzheimer's disease. The ATTN201 device sends low-intensity sound waves to a deep area of the brain that helps control sleep. The aim is to boost deep-sleep brain waves. These brain waves may help the brain clear away waste, including amyloid.
The main questions it aims to answer are:
- What, if any, issues do participants have when using the ATTN201 device?
- Can participants complete the full study schedule?
Researchers will compare focused ultrasound to unfocused ultrasound. Unfocused ultrasound is a look-alike treatment. It feels and sounds the same but is not aimed at the brain target. The comparison will show if the focused treatment changes sleep brain waves, blood markers of Alzheimer's disease, or memory and thinking.
Participants will:
- Visit the study site for memory and thinking tests, blood draws, a health check, and MRI scans of the brain
- Record their sleep at home for at least 5 days with a sleep diary, a watch-like sensor, and a headband that measures brain waves
- Be assigned by chance to focused or unfocused ultrasound
- Take part in 10 nap sessions over 2 weeks while wearing the device, at the study site or at home
- Return for a final visit to repeat the first tests, and may return for an optional visit 3 months later
Studie Overzicht
Toestand
Conditie
Interventie / Behandeling
Gedetailleerde beschrijving
This pilot study is a randomized, double-blind, parallel-group trial of repeated low-intensity focused ultrasound (LIFU) stimulation of the centromedian nucleus of the thalamus (CMN) in amyloid-positive older adults with mild cognitive impairment (MCI).
Background and rationale: Poor sleep both predicts and accelerates Alzheimer's disease (AD) pathology, in part by impairing glymphatic clearance of metabolites including soluble amyloid-beta and tau. Slow waves during sleep generate metabolic signals that alter neurovascular tone and cerebrospinal fluid (CSF) volume, creating pulsatile fluid flow thought to support clearance. Slow waves can be entrained by stimulating seed regions of the brain at a slow rate, but existing approaches (transcranial magnetic stimulation, optogenetic or electrical stimulation of the CMN) are too invasive, cumbersome, or costly for regular home use in a broad aging population. Low-Intensity focused ultrasound can both elicit neural activity in the CMN and directly produce fluid flow, non-invasively and with lightweight hardware. In a prior single-session study targeting the CMN in 10 patients with chronic pain, sonication improved subjective sleep for several days. This study extends that preliminary work to a clinical population for which the effects are likely to be therapeutically relevant.
Investigational device: ATTN201 is a head-worn LIFU system that delivers MRI-guided stimulation offline, without real-time imaging or clinician aid. Bilateral 64-element sparse ultrasound arrays operating at 500 kHz are positioned over the temporal windows and deliver cross-beam focused stimulation to deep brain targets. Targeting is participant-specific: before first use, each participant undergoes a 3.0T MRI for personalized targeting. Automated brain segmentation, transducer spatial mapping, and acoustic simulation are used to compute the per-element phase delays required to focus energy at the target. All stimulation remains within International Transcranial Ultrasonic Stimulation Safety and Standards (ITRUSST) consortium recommendations, with sessions lasting up to 60 minutes.
Control condition: Unfocused ultrasound is used as the comparator to maintain participant and study-administrator blinding. It mimics the auditory and peripheral sensations of focused stimulation without creating substantive pressure at the focal target relative to surrounding tissue.
Study conduct: Because the study enrolls people with MCI, capacity to consent is assessed before enrollment using a teach-back method, and only individuals who can demonstrate adequate understanding of the study are enrolled. After screening and informed consent, participants complete screening and baseline visits that include a blood draw for plasma biomarkers, cognitive and functional assessment, safety assessments, and an MRI. Participants then complete at least 5 days of at-home baseline sleep recording using actigraphy, sleep diaries, and wearable EEG. They are subsequently randomized to CMN-focused or unfocused stimulation, delivered during 10 nap opportunities over 2 weeks at the study site or the participant's home, per participant preference. Treatment visits include continuous EEG monitoring, adverse event assessment, and visual analog scales for memory and related psychiatric symptoms; home sleep monitoring continues throughout the treatment period. A post-treatment visit repeats the baseline measures, including cognitive testing, neurological exam, blood draw, and an MRI. An optional follow-up visit 3 months later repeats the same measures to assess durability of effects. The study is conducted in conformance with Good Clinical Practice (GCP).
Studietype
Inschrijving (Geschat)
Fase
- Niet toepasbaar
Contacten en locaties
Studiecontact
- Naam: Andrew D Krystal, MD
- Telefoonnummer: 415-514-0446
- E-mail: clear@ucsf.edu
Studie Locaties
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California
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San Francisco, California, Verenigde Staten, 94107
- Werving
- University of California San Francisco
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Contact:
- Andrew D Krystal, MD
- Telefoonnummer: 415-476-7702
- E-mail: andrew.krystal@ucsf.edu
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Hoofdonderzoeker:
- Andrew D Krystal, MD
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Deelname Criteria
Geschiktheidscriteria
Leeftijden die in aanmerking komen voor studie
Accepteert gezonde vrijwilligers
Geslachten die in aanmerking komen voor studie
Beschrijving
Inclusion Criteria:
- 65+ years old, male or female
- Amyloid positivity as assessed by either PET, CSF, or plasma.
- Qualify for an MCI Diagnosis.
- Study partner available for informant measures.
- Willing and able to undergo a brain MRI.
- If currently on AD or sleep medications, must be at the same stable dose(s) for at least 3 weeks prior to screening and throughout the course of the study, and must continue to be under the care of their treating neurologist through the duration of the study.
- Be able and willing to wear an Attune device during treatments
- Able to sign informed consent in accordance with local regulations.
- Be able to speak, read, and understand the language of the trial staff and the informed consent form.
- Possess the ability to respond verbally to questions, follow instructions, and complete study assessments.
- Be able to adhere to the stimulation protocol and visit schedules.
- Be medically stable at baseline/randomization as assessed by medical history and non-significant clinical results of safety labs and vital signs examination.
Exclusion Criteria:
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Early-onset Alzheimer's disease, as defined by a diagnosis occurring prior to age 65.
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Clinically significant depression, as defined by a score of >10 on the Geriatric Depression Scale
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Moderate to severe untreated obstructive sleep apnea, as defined by an Apnea-Hypopnea Index (AHI) ≥ 15.
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Has other medical or psychiatric symptoms or conditions that, in the opinion of the investigator, will interfere with study activities or confound interpretation of study results.
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Is on medication which, in the opinion of the investigator, will confound study results.
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Has a history of deep brain stimulation or ablative surgery
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Has a history of substance abuse including alcohol use disorder in the past 6 months
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Has a history of traumatic brain injury
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Has any contraindications for completing a brain MRI scan.
a. The subject's head must fit within the head coil.
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Has an uncontrolled medical condition which may impact study results.
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Is or has an immediate family member of staff directly involved with this trial.
Studie plan
Hoe is de studie opgezet?
Ontwerpdetails
- Primair doel: Behandeling
- Toewijzing: Gerandomiseerd
- Interventioneel model: Parallelle opdracht
- Masker: Verviervoudigen
Wapens en interventies
Deelnemersgroep / Arm |
Interventie / Behandeling |
|---|---|
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Experimenteel: Low-Intensity Focused Ultrasound to the CMN
Participants will receive low-intensity focused ultrasound (LIFU) stimulation targeted to the centromedian nucleus of the thalamus (CMN), delivered by the head-worn ATTN201 device. Targeting is individualized for each participant's brain and skull anatomy using a spatial-mapping MRI acquired at baseline. |
Low-intensity focused ultrasound delivered to the centromedian nucleus of the thalamus by the investigational ATTN201 head-worn device.
Andere namen:
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Sham-vergelijker: Unfocused Ultrasound
Participants will receive unfocused ultrasound from the same head-worn ATTN201 device on the same schedule. Unfocused ultrasound mimics the auditory and peripheral sensations of focused stimulation but does not generate substantive acoustic pressure at the CMN target relative to surrounding tissue. |
Unfocused ultrasound delivered by the same device, serving as the control condition. |
Wat meet het onderzoek?
Primaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Incidence, Severity, and Relatedness of Adverse Events and Serious Adverse Events
Tijdsspanne: From informed consent through the 3-month follow-up visit (up to ~5 months)
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Safety and tolerability of repeated ATTN201 stimulation, assessed by the incidence, severity, and relatedness of AEs and SAEs. |
From informed consent through the 3-month follow-up visit (up to ~5 months)
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Incidence of New Clinically Significant Findings on Post-Treatment Safety MRI
Tijdsspanne: From baseline through the post-treatment (~Week 5)
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Post-treatment brain MRI compared with the baseline MRI and reviewed for new clinically significant findings. |
From baseline through the post-treatment (~Week 5)
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Study completion rate and adherence to scheduled study procedures
Tijdsspanne: From baseline through the post-treatment (~Week 5)
|
Proportion of randomized participants who complete all scheduled study procedures with acceptable adherence. |
From baseline through the post-treatment (~Week 5)
|
Secundaire uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
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Change From Baseline in Clinical Dementia Rating - Sum of Boxes (CDR-SB)
Tijdsspanne: Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
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CDR-SB scores range from 0 to 18, with higher scores indicating greater cognitive and functional impairment. |
Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
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Change From Baseline in Alzheimer's Disease Assessment Scale - Cognitive Subscale (ADAS-Cog)
Tijdsspanne: Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
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ADAS-Cog scores range from 0-85 with higher scores indicating greater cognitive impairment. |
Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
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Change From Baseline in the NULISASeq™ CNS Disease Panel 120
Tijdsspanne: Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
|
Blood samples will be collected using EDTA vials, minimally preprocessed, and stored for the duration of the study. Upon completion of the study, all samples will be analyzed using the NULISASeq™ CNS Disease Panel 120 for changes in Alzheimer's Disease biomarkers from baseline to post-treatment and follow-up. |
Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
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Change From Baseline in Alzheimer's Disease Cooperative Study Activities of Daily Living for MCI (ADCS-MCI-ADL)
Tijdsspanne: Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
|
Scores range from 0 to 53, with higher scores indicating better daily function. |
Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
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Change From Baseline in Slow-Wave Activity During Nap Opportunities
Tijdsspanne: Baseline through the 2-week treatment period and post-treatment (~Week 5)
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EEG-derived slow-wave activity (SWA) recorded during nap sessions. |
Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change From Baseline in Objective Nocturnal Sleep: TST
Tijdsspanne: Baseline through the 2-week treatment period and post-treatment (~Week 5)
|
Change from baseline in total sleep time derived from limited-channel home PSG. |
Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change From Baseline in Objective Nocturnal Sleep: Rate of Delta Decline
Tijdsspanne: Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change from baseline in rate of delta decline derived from limited-channel home PSG. |
Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change From Baseline in Objective Nocturnal Sleep: WASO
Tijdsspanne: Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change from baseline in sleep quality as measured by Wake After Sleep Onset derived from limited-channel home PSG. |
Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change From Baseline in Objective Nocturnal Sleep: Percentage of Time Spent in Each Sleep Stage
Tijdsspanne: Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change from baseline in percentage of total sleep time spent in each sleep stage derived from limited-channel home PSG. |
Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change From Baseline in Objective Nocturnal Sleep: SWA/SWS
Tijdsspanne: Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change from baseline in slow wave activity/slow-wave sleep derived from limited-channel home PSG. |
Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change From Baseline in Objective Nocturnal Sleep: Onset Latency
Tijdsspanne: Baseline through the 2-week treatment period and post-treatment (~Week 5)
|
Change from baseline in sleep onset latency derived from limited-channel home PSG. |
Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Change From Baseline in Subjective Sleep Quality and Daytime Alertness
Tijdsspanne: Baseline through the 2-week treatment period and post-treatment (~Week 5)
|
Self-reported sleep quality and daytime alertness measured by visual analog scales (range 1-100). |
Baseline through the 2-week treatment period and post-treatment (~Week 5)
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Incidence and Severity of Adverse Events Associated With the Unfocused Control Procedure
Tijdsspanne: From the first control session through the 3-month follow-up visit (up to approximately 4 months)
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Safety and tolerability of the unfocused control condition, assessed by adverse event reporting. |
From the first control session through the 3-month follow-up visit (up to approximately 4 months)
|
Andere uitkomstmaten
Uitkomstmaat |
Maatregel Beschrijving |
Tijdsspanne |
|---|---|---|
|
Change From Baseline in Functional Connectivity of the Centromedian Nucleus of the Thalamus
Tijdsspanne: Baseline to post-treatment (~Week 5)
|
Resting-state fMRI-derived functional connectivity between the centromedian nucleus of the thalamus (CMN) and known brain networks. |
Baseline to post-treatment (~Week 5)
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Change From Baseline in Self-Reported Memory Complaints and Neurodegeneration-Related Psychiatric Symptoms
Tijdsspanne: Baseline, during the 2-week treatment period, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
|
Measured by visual analog scales (range 1-100); higher scores indicate greater symptom burden. |
Baseline, during the 2-week treatment period, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
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Change From Baseline in NULISAseq Inflammation Panel 250
Tijdsspanne: Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
|
Samples will be collected via EDTA vials, minimally preprocessed, and stored for the duration of the study. Upon study completetion, samples will be analyzed for changes from baseline to post-treatment and follow-up in inflammatory biomarkers using the NULISAseq Inflammation Panel 250. |
Baseline, post-treatment (~Week 5), and 3-month follow-up (~Week 17)
|
Medewerkers en onderzoekers
Onderzoekers
- Hoofdonderzoeker: Andrew Krystal, MD, University of California, San Francisco
Studie record data
Bestudeer belangrijke data
Studie start (Geschat)
Primaire voltooiing (Geschat)
Studie voltooiing (Geschat)
Studieregistratiedata
Eerst ingediend
Eerst ingediend dat voldeed aan de QC-criteria
Eerst geplaatst (Werkelijk)
Updates van studierecords
Laatste update geplaatst (Werkelijk)
Laatste update ingediend die voldeed aan QC-criteria
Laatst geverifieerd
Meer informatie
Termen gerelateerd aan deze studie
Trefwoorden
Aanvullende relevante MeSH-voorwaarden
Andere studie-ID-nummers
- 23-39270
Plan Individuele Deelnemersgegevens (IPD)
Bent u van plan om gegevens van individuele deelnemers (IPD) te delen?
Beschrijving IPD-plan
De-identified individual participant data that support the results will be shared, provided the investigator who proposes to use the data has approval from an Institutional Review Board (IRB), Independent Ethics Committee (IEC), or Research Ethics Board (REB), as applicable, and executes a data use/sharing agreement with UCSF and Attune Neurosciences. Shared data will include participant-level clinical, cognitive, sleep, EEG, actigraphy, and fluid biomarker data underlying published results, together with a data dictionary. Direct identifiers will be removed and dates offset prior to release. Access is controlled rather than open because this study enrolls a small, deeply phenotyped cohort in which the combination of demographic, longitudinal physiological, and biomarker variables carries a residual risk of re-identification that open deposition would not adequately mitigate.
IPD-tijdsbestek voor delen
9 to 60 months following publication of the primary results manuscript.
IPD-toegangscriteria voor delen
Requests should be directed to the Principal Investigator at andrew.krystal@ucsf.edu. Requesters must submit a written proposal stating the scientific question, the proposed analysis plan, and the variables required. Proposals will be reviewed by the study team and Attune Neurosciences, and a response provided within 60 days of receipt. The data use/sharing agreement will prohibit attempts at re-identification, prohibit onward transfer to third parties, restrict use to the approved analysis, and require acknowledgment of the source study and its funder.
IPD delen Ondersteunend informatietype
- LEERPROTOCOOL
- SAP
- ICF
- ANALYTIC_CODE
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