Actively Recruiting

Phase Not Applicable
Age: 18Years - 55Years
All Genders
Healthy Volunteers
NCT04564976

Social Support and Reduced Fear Acquisition

Led by University of California, Los Angeles · Updated on 2026-03-18

100

Participants Needed

1

Research Sites

229 weeks

Total Duration

On this page

Sponsors

U

University of California, Los Angeles

Lead Sponsor

N

National Institute of Mental Health (NIMH)

Collaborating Sponsor

AI-Summary

What this Trial Is About

University of California, Los Angeles researchers will recruit healthy participants and anxious participants (those diagnosed with social anxiety disorder) age 18-55 years old to participate in a study examining whether the ability of social support figure reminders to prevent the acquisition of fear in healthy participants extends to those with anxiety disorders. After being recruited from the UCLA community (healthy participants, n = 50) or referred by treatment providers at the Anxiety and Depression Research Center at UCLA (anxious participants, n =50) and undergoing a telephone screening and in-person screening, 100 participants will be enrolled in the study. During the experiment, all participants will undergo the same procedures: undergoing fear acquisition procedures--the repeated pairing of a neutral image with a mild electric shock that ultimately leads to the association of threat of shock with the image--in the presence of an image of a social support figure (provided by participants) and an image of a smiling stranger.

CONDITIONS

Official Title

Social Support and Reduced Fear Acquisition

Who Can Participate

Age: 18Years - 55Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults aged 18 to 35 years
  • Fluent in English
  • No history of mental illness for healthy participants
  • Diagnosis of social anxiety disorder for anxious participants, including allowed co-morbid disorders such as depression, other anxiety disorders, and PTSD
Not Eligible

You will not qualify if you...

  • Pregnant or planning to become pregnant during the study period
  • Chronic mental illness for healthy participants as determined by past diagnosis or related medication use
  • Non-allowed co-morbid disorders for anxious participants, including bipolar disorder, psychosis, substance use disorder, neurological disorder, and obsessive-compulsive disorder
  • Current and regular use of prescription medications related to mental health disorders

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

UCLA Department of Psychology

Los Angeles, California, United States, 90095-1563

Actively Recruiting

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Research Team

E

Erica Hornstein, PhD

CONTACT

N

Naomi Eisenberger, PhD

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NA

Model

SINGLE_GROUP

Primary Purpose

BASIC_SCIENCE

Number of Arms

1

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