RECRUITING

Attention Bias Modification Training for Social Phobia (ABMSP)

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

Attentional bias has primarily been investigated as a primary cognitive etiology of social anxiety symptoms. Previous research has found that individuals with high social anxiety showed facilitated attentional engagement to threat stimuli or delayed disengagement of attention from threat. Attentional Bias Modification Training (ABMT) was developed through applying the attentional mechanism in social anxiety. During ABMT, participants are deliberately induced to shift their attention away from threat stimuli and toward neutral stimuli. Despite its proven effectiveness, a recent meta-study found that the effect size of ABMT is significant but too small. As a result, the current study focuses on improving the existing ABMT by incorporating integrative factors into attention training. The current study aims to integrate bottom-up and top-down cognitive processes in ABMT. Participants will be randomly assigned to one of two conditions (active or placebo training) and will complete the ABMT for three weeks. The ABMT's efficacy will be assessed by comparing pre- and post-training measures.

Official Title

Mobile-based Attentional Bias Modification Training (ABMT) for Socially Anxious Individuals

Quick Facts

Study Start:2022-04-07
Study Completion:2024-08-31
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06054386

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 60 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Diagnosis of social anxiety disorder (based on the DIAMOND interview - Social anxiety module)
  2. * Moderate or severe symptoms of social anxiety as revealed by the Liebowitz Social Anxiety Scale (LSAS score of ≥ 40) or MINI-SPIN (Score of ≥ 6)
  3. * Ages 18-60
  4. * English as a primary language
  5. * Possession of a mobile device for access to the app (Inquisit 6)
  1. * Self-reported visual impairment that cannot be adjusted and will prevent them from clearly recognizing words and pictures on mobile screen
  2. * Self-reported history of a bipolar disorder or psychotic disorder

Contacts and Locations

Study Contact

Yourim Kim, M.A.
CONTACT
414-251-5124
yourim@uwm.edu
Han-Joo Lee, PhD
CONTACT
414-229-5858
leehj@uwm.edu

Principal Investigator

Han-Joo Lee, PhD
PRINCIPAL_INVESTIGATOR
414-229-5858

Study Locations (Sites)

University of Wisconsin-Milwaukee
Milwaukee, Wisconsin, 53211
United States

Collaborators and Investigators

Sponsor: University of Wisconsin, Milwaukee

  • Han-Joo Lee, PhD, PRINCIPAL_INVESTIGATOR, 414-229-5858

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-04-07
Study Completion Date2024-08-31

Study Record Updates

Study Start Date2022-04-07
Study Completion Date2024-08-31

Terms related to this study

Keywords Provided by Researchers

  • Attentional bias
  • Cognitive process
  • Mobile training

Additional Relevant MeSH Terms

  • Social Anxiety Disorder