Cognition and Ultrasound
ConditionHealthy Participants
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity of Minnesota
About this trial
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
Eligibility criteria
Qualifiers
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
Disqualifiers
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.
Trial design
Treatments tested in this trial
- Low-Intensity Focused Ultrasound (FUS or LIFU)
Treatment groups
100 Participants
are divided into 1 treatment groupSponsors and collaborators
Source ClinicalTrials.gov