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Completed NCT07753538

Interpretation Bias Modification Training for Social Anxiety Disorder

Conditions: Social Anxiety Disorder (SAD)

Sex: All
Ages: 18 Years – 60 Years
Healthy volunteers: No
Phase: NA
Enrollment: 50
Sponsor: University of Wisconsin, Milwaukee

Location: University of Wisconsin-Milwaukee Milwaukee Wisconsin

Summary

The overall goal of the current study is to develop and evaluate a computerized interpretation bias modification (IBM) training for treating social anxiety disorder (SAD). A key focus is placed on enhancing accessibility and efficacy of IBM for SAD by delivering it through a mobile platform, with three specific aims outlined. First, the current study aims to examine the efficacy of the IBM training in reducing social anxiety symptoms by comparing the pre-, post-, and follow-up assessments of the IBM group with a control group. Second, the current study aims to examine the effect of IBM on reducing participants' daily social anxiety symptoms using daily diary methodology. Third, the investigators also aim to evaluate the feasibility and acceptability of the IBM training. The investigators expect that at least 70% of participants will complete 4 or more of the six training sessions.

Eligibility Criteria

Inclusion Criteria: * Diagnosis of SAD based on the DIAMOND screening interview * Moderate or severe symptoms of SAD as assessed by the Liebowitz Social Anxiety Scale (LSAS score of \>= 30) * Ages 18-60 * English as a primary language * Possession of a mobile device for access to training and text message for daily diary Exclusion Criteria: * Self-report visual impairment that cannot be adjusted and will prevent them from clearly recognizing words and pictures on mobile screen * Self-reported history of a bipolar disorder or psychotic disorder as measured by Diagnostic History Scale * Current psychotherapy for SAD

Interested in this study? View the official listing for contact and enrollment details.

View on ClinicalTrials.gov

Source: ClinicalTrials.gov (NCT07753538). StuddyBuddy aggregates publicly available trial information.