MedPath

Cognition and Ultrasound

Not Applicable
Recruiting
Conditions
Healthy Participants
Registration Number
NCT07220655
Lead Sponsor
University of Minnesota
Brief Summary

Our primary goal is to investigate the role of Low-Intensity Focused Ultrasound (LIFU) neuromodulation on deep brain targets, and its potential to improve cognition

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
100
Inclusion Criteria
  • 18 years of age or older
  • Speak English (as assessed by their ability to read/answer survey questions)
  • May be required to score in the appropriate range on self-report measures
Exclusion Criteria
  • They have a neurological disorder which may impact their fMRI scan or cause their reaction to LIFU to differ from that of healthy adults.
  • They take any psychoactive medication.
  • They are unable to undergo fMRI scanning due to a contraindication such as claustrophobia, unremovable piercings, pregnancy, the presence of medical devices such as pacemakers, or a movement or sleep disorder.
  • Are pregnant, or may have reason to believe that they are pregnant.
  • They have a diagnosis of a psychiatric condition other than depression or anxiety

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Primary Outcome Measures
NameTimeMethod
Deep Brain Targets ReachedHour 1

MRI-based readouts testing whether LIFU neuromodulation can successfully engage targets in deep brain

Multi-Source Interference Test (MSIT) PerformanceHour 1

Behavioral readouts of successful LIFU neuromodulation of our target regions

28/Posit Science PerformanceHour 1

Behavioral readouts of successful LIFU neuromodulation of our target regions

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Minnesota

πŸ‡ΊπŸ‡Έ

Minneapolis, Minnesota, United States

University of Minnesota
πŸ‡ΊπŸ‡ΈMinneapolis, Minnesota, United States
Miriam Freedman
Contact
612-625-3330
mfreedma@umn.edu

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