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NCT Number: NCT04557891

Low-Intensity Focused Ultrasound Pulsation (LIFUP) for the Treatment of Generalized Anxiety Disorder (GAD)

There are few treatment options available for patients once they have failed standard psychopharmacological therapy for generalized anxiety disorder. Existing brain stimulation methods such as rTMS fail to target deep brain structures associated with anxiety disorders; structures such as the amygdala. In this double-blind sham-controlled clinical trial, the investigators propose to establish baseline severity of anxiety in 48 patients, then deliver eight treatments over four sessions of focused ultrasound stimulation to the amygdala. Anxiety severity will be assessed using standard psychometric scales after each session, and at follow-ups.

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Key information

Age range

18 year–65 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of California, Los Angeles, Los Angeles, California, United States

Loading trial locations.

About this study

Anxiety disorders have tremendous disease burden in the United States. Up to 1 in 3 Americans will be diagnosed with an anxiety disorder in their lifetimes. Anxiety treatment is typically consisting of psychotherapy (e.g. cognitive behavioral therapy) and medication management (e.g. benzodiazepines, selective serotonin reuptake inhibitors, etc). With major depressive disorder, rTMS is a suitable alternative treatment for refractory depression, rTMS is not approved for treatment of anxiety, nor can rTMS stimulate deep enough to reach those brain circuits involved in anxiety (e.g. the amygdala). Focused ultrasound is a new treatment modality being developed for several different neuropsychiatric conditions. In this study, the investigators propose to randomize 48 individuals to either active or sham treatment. Each participant will be evaluated to establish a baseline diagnose of generalized anxiety disorder, and then will be reassessed after each treatment session (of which there are four). One week and one month after the last treatment session, the investigators will conduct follow-up evaluations.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male or female
  • Age 18-65
  • Normal or corrected-to normal vision and hearing
  • Primary diagnosis of generalized anxiety disorder, moderate/severe per DSM-5. (HAM-A>17) 4a) The duration of the illness must exceed one year.
  • Must be medically stable as determined by investigator
  • Patient must have attempted and failed treatment with at least 2 SSRI and 1 augmentation
  • History of rTMS is permitted, but not required.

Exclusion criteria

  • Diagnosis of primary DSM-5 anxiety disorder other than GAD 1a) Affective disorders such as unipolar or bipolar depression are permitted as long as GAD is primary
  • Current use of any non-prescribed psychoactive medications or drugs (aside from medications for treatment of GAD)
  • Contraindication to enter the MRI environment
  • Pregnancy (or suspected/possible pregnancy or plan to become pregnant in the short-term)
  • Inability to adhere to treatment schedule
  • Initiation of new anxiolytic treatment at the time of study randomization

Treatment and study plan

Active LIFUP Treatment

Device

8 LIFUP Treatments

Other names: BX Pulsar 1002

Sham LIFUP Treatment

Device

8 sham LIFUP treatments

Primary outcomes

  1. Hamilton Anxiety Rating Scale (HAM-A)

    Time frame: 1 week after the fourth LIFUP treatment

    HAM-A is a rating scale for measuring the severity of anxiety symptoms.

Study contacts

Contact information is provided by the study sponsor or research team.

Andrew Bishay, BS

CONTACT

[email protected]

4243719869

Margaret G Distler, MD,PhD

CONTACT

[email protected]

(310) 794-1553

Sponsors and collaborators

Lead sponsor

University of California, Los Angeles

Other

Collaborators

  • Massachusetts General Hospital
  • Medical University of South Carolina

Registry information

Official study title

Feasibility of Low-Intensity Focused Ultrasound Pulsation (LIFUP) for the Treatment of Generalized Anxiety Disorder (GAD)

Important dates

Study start
2021
Primary completion
2026
Study completion
2027
First posted
Sep 22, 2020
Registry last updated
Feb 10, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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