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
Name Time Method Deep Brain Targets Reached Hour 1 MRI-based readouts testing whether LIFU neuromodulation can successfully engage targets in deep brain
Multi-Source Interference Test (MSIT) Performance Hour 1 Behavioral readouts of successful LIFU neuromodulation of our target regions
28/Posit Science Performance Hour 1 Behavioral readouts of successful LIFU neuromodulation of our target regions
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
University of Minnesota
πΊπΈMinneapolis, Minnesota, United States
University of MinnesotaπΊπΈMinneapolis, Minnesota, United StatesMiriam FreedmanContact612-625-3330mfreedma@umn.edu
