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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04565041
Other study ID # SSE
Secondary ID R21MH125274
Status Recruiting
Phase N/A
First received
Last updated
Start date February 1, 2022
Est. completion date December 2024

Study information

Verified date September 2023
Source University of California, Los Angeles
Contact Erica Hornstein, PhD
Phone 9175664470
Email ericahornstien@ucla.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

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 enhance the extinction 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, with an expected recruited 150 to reach this number. During the experiment, all participants will undergo the same procedures: undergoing a fear extinction procedure in which threatening cues--cues that predict electric shock--will be paired with either an image of a social support figure (provided by participants) or an image of a smiling stranger. These pairings will be presented repeatedly in the absence of shock in order for fear extinction to occur. Participants will return for a follow-up test to determine if fear extinction was successful.


Recruitment information / eligibility

Status Recruiting
Enrollment 100
Est. completion date December 2024
Est. primary completion date December 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years to 55 Years
Eligibility Inclusion Criteria: - healthy adults 18 to 55 - fluent in English - no history of mental illness (healthy participants: including anxiety, depression, phobia, or any other mental health related disorder diagnosed by a mental health professional) - diagnosis of social anxiety disorder (anxious participants: allowed co-morbid disorders include depression, other anxiety disorders, and PTSD) Exclusion Criteria: - pregnant or planning to become pregnant during the experiment period - presence of chronic mental illness (healthy participants: 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) - presence of non-allowed co-morbid disorders (anxious participants: including, bipolar disorder, psychosis, substance use disorder, neurological disorder, and/or obsessive-compulsive disorder) - current and regular use of prescription medications related to mental health disorders

Study Design


Related Conditions & MeSH terms


Intervention

Behavioral:
Social Support
Presence of an image of a social support figure (provided by participant) during a fear extinction procedure

Locations

Country Name City State
United States UCLA Department of Psychology Los Angeles California

Sponsors (2)

Lead Sponsor Collaborator
University of California, Los Angeles National Institute of Mental Health (NIMH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Fear response directly post-extinction presence of fear response as indicated by significantly higher galvanic skin response (GSR: an index of peripheral stress responding) to a previously learned fearful image (CS+) compared to a baseline comparator (CS-: never learned to be fearful). within experimental session - directly post-extinction procedure
Primary Fear response 24 hours post-extinction presence of fear response as indicated by significantly higher galvanic skin response (GSR: an index of peripheral stress responding) to a previously learned fearful image (CS+) compared to a baseline comparator (CS-: never learned to be fearful). 24 hours following the completion of fear extinction procedures
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