RecruitingPhase 4NCT06004115

Processes and Circuitry Underlying Threat Sensitivity as a Treatment Target for Co-morbid Anxiety and Depression


Sponsor

Laureate Institute for Brain Research, Inc.

Enrollment

165 participants

Start Date

Nov 8, 2023

Study Type

INTERVENTIONAL

Conditions

Summary

This mechanistic study uses an anti anxiety drug and brain imaging to study the threat processing system and associated brain circuits in people with depression, anxiety disorders and comorbid depression and anxiety disorders. In a double blind, placebo controlled crossover design, up to 65 individuals will be recruited who will have a diagnosis of major depressive disorder (MDD) and at least one anxiety disorder (AD) (AD-MDD group), up to 65 participants will have a diagnosis of MDD and no diagnosis of an AD and up to 65 participants will have no diagnosis of MDD and a diagnosis of at least one AD will be enrolled to participate in an two session study to obtain 150 completers (50 per group). All participants will receive a single dose of Lorazepam and placebo (order randomized) taken orally. After the \~2.5 hr screening session, participants will complete two identical \~5 hr experimental sessions, each of which include a 30 min eyeblink startle session and a 1.5 hr functional magnetic resonance imaging (MRI) brain scan session. The total time involved in the study is approximately 10.5 hours. The main questions the study seeks to answer are: * are people with comorbid depression and anxiety different than those with depression alone in terms of their eyeblink startle response to threat? * are people with comorbid depression and anxiety different than those with depression alone in terms of their brain activation in response to threat? * are people with comorbid depression and anxiety different than those with depression alone in terms of their responses to anxiety drugs?


Eligibility

Min Age: 18 YearsMax Age: 65 Years

Plain Language Summary

Simplified for easier understanding

This brain imaging study is looking at how anxiety and depression affect threat sensitivity in the brain, and whether this can be a target for future treatments. Researchers are recruiting people with depression, anxiety, or both — as well as healthy volunteers. **You may be eligible if:** - You are between 18 and 65 years old - You have a current diagnosis of major depression and/or an anxiety disorder (such as generalized anxiety, panic disorder, or social phobia) - You have normal or corrected-to-normal vision and hearing - You speak fluent English **You may NOT be eligible if:** - You have bipolar disorder, schizophrenia, psychosis, PTSD, or an eating disorder - You have a history of moderate or severe traumatic brain injury - You currently use benzodiazepines or opioids - You have a BMI over 40 - You have a moderate-to-severe substance use disorder - You have MRI contraindications (such as a metal implant) - You are pregnant or planning to become pregnant - Your medication dose has changed in the past 6 weeks Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGLorazepam

1mg of Lorazepam will be prepared by pharmacy (Barnes, Tulsa) in capsule form

OTHERPlacebo

placebo will be prepared by pharmacy (Barnes, Tulsa) in capsule form


Locations(1)

Laureate Institute for Brain Research

Tulsa, Oklahoma, United States

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NCT06004115


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