UCLA tests if naltrexone cancels the Fear-Busting power of a hug
NCT ID NCT04166071
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
Researchers at UCLA are studying whether naltrexone, a drug that blocks opioid receptors, can stop reminders of a social support figure from helping people overcome fear. Sixty healthy adults aged 18-35 will receive either naltrexone or a placebo, then undergo a fear extinction procedure where threatening cues are paired with images of a loved one. The goal is to see if the drug disrupts the brain's natural safety-signal mechanism, shedding light on how social bonds protect against fear.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- naltrexone
- What this could lead to
- If it works, this could reveal how social support helps reduce fear, potentially guiding future treatments for anxiety disorders.
- What could go wrong
- This is a very early, small study (60 healthy people) testing a single dose. It may not translate to real-world fear or anxiety conditions.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Early phase 1
The earliest testing in people: a first look at safety, in a very small group.
- Participants
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About 60 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Dec 2021
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 35 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * healthy adults 18 and 35 * fluent in English * no history of mental illness (including anxiety, depression, phobia, or any other mental health related disorder diagnosed by a mental health professional) Exclusion Criteria: * pregnant or planning to become pregnant during the experiment period * presence of chronic mental illness (as determined by the report of a past diagnosis of mental illness by a physician or psychologist and/or the prescription of medication related to mental health disorder; including anxiety, depression, phobia, or any other diagnosed psychological disorder) * chronic physical illness (as determined by past diagnosis and/or treatment by a physician) * history of liver disease or abnormal liver function * current and regular use of prescription medications related to mental health disorders or liver function * previous history of fainting during blood draws * difficulty or discomfort swallowing pills * history of substance abuse or addiction (especially alcohol or opiate abuse) Other exclusion criteria may apply.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
2 sites. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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UCLA
Los Angeles, California, 90095, United States
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UCLA Department of Psychology, 5514 Pritzker Hall
Los Angeles, California, 90095-1563, United States
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