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Low Intensity Focused Ultrasound for Learning and Memory and Emotion Regulation (LIFUPMEMEMOT)

University of California, Los Angeles (UCLA) logo

University of California, Los Angeles (UCLA)

Status

Completed

Conditions

Learning Disabilities
Cognitive Impairment
Memory Disorders
Brain Diseases

Treatments

Device: Low Intensity Focused Ultrasound Pulsation to Entorhinal Cortex
Device: Low Intensity Focused Ultrasound Pulsation to Amygdala

Study type

Interventional

Funder types

Other

Identifiers

NCT03717922
IRB#18-000104 / IRB#18-000978

Details and patient eligibility

About

The goal of this clinical trial is to investigate the impact of low intensity focused ultrasound pulsation (LIFUP) to two different brain regions, the amygdala and entorhinal cortex, in older adults. The main questions it aims to answer are:

  1. Will LIFUP change brain activity in the targeted regions?
  2. Will LIFUP to the amygdala have an impact on anxiety and emotion regulation?
  3. Will LIFUP to the entorhinal cortex have an impact on memory performance?

Participants will complete two in-person visits including neuropsychological testing, MRI of the brain, and LIFUP to the brain.

Full description

Medial temporal lobe (MTL)-dependent memory is impacted by a wide range of psychiatric and neurologic conditions. These cognitive limitations often result in limited functional abilities for patients. Currently available pharmacologic and behavioral treatments are somewhat controversial and have minimal evidence-based effectiveness. Recently, deep brain stimulation was used to modulate MTL activity and subsequently improve memory performance. However, such implantable devices require neurosurgery with major associated health risk. At present, there are no publications reporting non-invasive neurostimulation targeting MTL regions to improve memory. The central hypothesis of this project is that non-invasive, low intensity focused ultrasound pulsation (LIFUP) can selectively increase regional MTL activity and thus be used as a cognitive neural prosthetic capable of improving memory performance. The aims of this portion of the study focus on whether LIFUP can increase blood oxygen level dependent (BOLD) activation and perfusion (measured by arterial spin labeling) in the entorhinal cortex and functionally associated regions, and whether LIFUP to the entorhinal cortex will result in improved memory.

The Amygdala is highly involved in emotional response, emotional reactivity and anxiety. Amygdala functions are therefore involved in a wide range of psychiatric disorders including generalized and social anxiety, specific phobia, obsessive compulsive disorder and posttraumatic stress disorder. Therefore, potential clinical implications of amygdala stimulation are great. However, to date, such efforts have been limited by the inability of non-invasive neuromodulation techniques (e.g. transcranial magnetic stimulation - TMS) to reach the amygdala and the highly invasive (i.e. neurosurgical) nature of methods (e.g. deep brain stimulation - DBS) which can, but to our knowledge has rarely been used, target these areas. In order to overcome these current limitations, study investigators propose the use of low intensity focused ultrasound pulsation (LIFUP) to affect amygdala activity to improve emotion regulation. The aim of this portion of the study focuses on whether LIFUP can modulate blood oxygen level dependent (BOLD) activation and perfusion (measured by arterial spin labeling) in the amygdala and functionally associated regions, and whether LIFUP to the amygdala will result in changes to anxiety levels and emotion regulation.

This study will be conducted using a crossover design in which each participant will complete two visits spaced two weeks apart. At one visit, they will receive LIFUP sonication (with parameters hypothesized to be inhibitory) to the right amygdala, and at the other, they will receive sonication (with parameters hypothesized to be excitatory) to the left entorhinal cortex. The order of conditions will be randomized and counterbalanced across participants. Participants will be blinded to condition order, and all other testing will be conducted the same at both visits. This design will allow us to test the effects of two potentially clinically-relevant targets for LIFUP, and will allow us to determine whether observed effects on brain activity, learning and memory, and emotion regulation are target-specific by comparing results between the two LIFUP paradigms.

Enrollment

21 patients

Sex

All

Ages

35 to 90 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Must be right handed
  • English must be the dominant language

Exclusion criteria

  • contraindications for MRI (e.g. metal implants, pregnancy)
  • history of head injury sufficient to warrant medical attention
  • history of alcohol abuse or dependence
  • history of substance abuse or dependence
  • history of major psychiatric illness requiring treatment
  • history of cancer or other neoplastic syndromes
  • history of major neurologic illness (e.g. epilepsy).

Trial design

Primary purpose

Other

Allocation

Randomized

Interventional model

Crossover Assignment

Masking

Double Blind

21 participants in 2 patient groups

Amygdala first, then Entorhinal Cortex
Experimental group
Description:
Low Intensity focused ultrasound pulsation (LIFUP) will be administered to the amygdala while participants are in the MRI scanner. Then, 2 weeks later, entorhinal cortex LIFUP will be administered.
Treatment:
Device: Low Intensity Focused Ultrasound Pulsation to Entorhinal Cortex
Device: Low Intensity Focused Ultrasound Pulsation to Amygdala
Entorhinal Cortex first, then Amygdala
Experimental group
Description:
Low Intensity focused ultrasound pulsation (LIFUP) will be administered to the entorhinal cortex while participants are in the MRI scanner. Then, 2 weeks later, amygdala LIFUP will be administered.
Treatment:
Device: Low Intensity Focused Ultrasound Pulsation to Entorhinal Cortex
Device: Low Intensity Focused Ultrasound Pulsation to Amygdala

Trial documents
1

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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