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Studying the Modification of Attention Bias Remotely After Trauma — SMART  

Post Traumatic Stress Disorder Clinical Trial

Official title:
Optimizing Attention Bias Modification for Posttraumatic Stress Disorder: An Entirely Remote Study

Clinical Trial Summary

The investigators will complete an entirely remote randomized controlled trial (RCT) comparing 14 sessions of attention bias modification (ABM), attention control training (ACT), placebo neutral attention training, and a final control condition with daily questions in 1,897 individuals with clinically significant Post-traumatic Stress Symptoms (PTSS) (defined as PCL-5 score ≥ 33). To assess effects of the training and control conditions, the investigators will administer tests of threat-related attention bias and variability, and self-report assessments of PTSS, depression, anxiety, and perceived stress at baseline, after one and two weeks of training, and at eight-week follow up. The investigators plan to screen and confirm interest from over 3,000 eligible participants over a period of 24 months to enroll and randomize 1,897 participants with the end goal of 1,232 completers (176 per condition).

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT04888169
Study type Interventional
Source University of California, San Francisco
Contact Aoife O'Donovan, PhD
Phone 415-221-4810
Email Aoife.ODonovan@ucsf.edu
Status Recruiting
Phase N/A
Start date April 20, 2023
Completion date December 30, 2023
View Details
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