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Completed
NCT07810348
Effectiveness of an AI-Integrated Proactive Thought Control Intervention for Young Adults With Social Anxiety Disorder
Conditions: Social Anxiety Disorder (SAD)
Sex: All
Ages: 18 Years – 26 Years
Healthy volunteers: No
Phase: NA
Enrollment: 75
Sponsor: Farah Shahzadi
Location: Farah Shahzadi Gujranwala Punjab Province
Summary
Participants with Social Anxiety Disorder will be recruited from educational settings . After screening and informed consent, participants will be randomly assigned to PTC , ACG or CBT .The therapy session will be 8 session once a week, and data will be collected through psychological questionnaires in two phases at start and end of intervention.
Eligibility Criteria
Inclusion Criteria:
* Were between 18 and 26 years of age, corresponding to the developmental period of emerging adulthood (Arnett, 2000).
* Met DSM-5 diagnostic criteria for Social Anxiety Disorder on the SCID-5-RV (First et al., 2015).
* Scored at or above the clinical cutoff of 30 on the LSAS-SR, indicating clinically significant social anxiety (Mennin et al., 2002).
* Were not receiving any other form of psychological intervention at the time of the study.
* Had sufficient English proficiency to understand instructions and complete the assessments (Flores, 2006).
* Provided written informed consent.
* Possessed basic computer literacy and typing skills required for the digital tasks.
Exclusion Criteria:
* Were younger than 18 or older than 26 years.
* Did not meet DSM-5 diagnostic criteria for Social Anxiety Disorder on the SCID-5-RV.
* Scored in the clinically significant range for general anxiety (BAI ≥ 16; Beck et al., 1988) or at or above the threshold for moderate depression (BDI-II ≥ 20; Beck et al., 1996).
* Were currently receiving psychological treatment for any psychiatric condition.
* Had a lifetime history of a severe psychiatric disorder other than Social Anxiety Disorder (e.g., psychosis, bipolar disorder).
* Had a medical or neurological condition that could interfere with task completion or valid responding.
* Were unable to complete the study procedures or assessments.
* Had no prior experience using a computer.
Source: ClinicalTrials.gov (NCT07810348). StuddyBuddy aggregates publicly available trial information.