Online Radical Acceptance Intervention for Social Anxiety Disorder
The goal of this clinical trial is to learn if a self-guided online Radical Acceptance program helps reduce symptoms of Social Anxiety Disorder. The study will also compare this program to an online relaxation skills program. The main questions are: * Does the Radical Acceptance program lower symptoms of Social Anxiety
| Condition(s) | Social Anxiety Disorder (SAD) |
|---|---|
| Status | Recruiting |
| Phase | NA |
| Study type | Interventional |
| Summary | The goal of this clinical trial is to learn if a self-guided online Radical Acceptance program helps reduce symptoms of Social Anxiety Disorder. The study will also compare this program to an online relaxation skills program. The main questions are: * Does the Radical Acceptance program lower symptoms of Social Anxiety Disorder? * Is the Radical Acceptance program more helpful than relaxation skills? Adults with Social Anxiety Disorder will be randomly assigned to one of two online programs. They will complete a baseline learning session and six short home practice sessions over two weeks. Participants will answer surveys about their symptoms and complete brief computer tasks. Researchers will measure changes in social anxiety at several points during the study and again a few weeks and a |
| Who can participate | Inclusion Criteria: * Aged 18-45 * Score \> 9 on Mini-SPIN * Positive responses in brief phone screening * Eligibility confirmed in Zoom interview using ADIS * Native Hebrew speakers * Having regular access to a computer. Exclusion Criteria: * Changes in psychiatric medication in the past 3 months * Current or past diagnosis of bipolar disorder * Current or past diagnosis of schizophrenia * Current or past diagnosis of PTSD * Current or past diagnosis of substance use disorder * History of traumatic brain injury (TBI) * Previous experience with Dialectical Behavior Therapy (DBT) * Currently receiving psychotherapy specifically targeting social anxiety |
| Ages | 18 Years to 45 Years |
| Sex | All |
| Lead sponsor | University of Haifa |
| Locations | Haifa, Israel |
| Start date | 2025-12-16 |
| NCT ID | NCT07325929 |
| Official listing | https://clinicaltrials.gov/study/NCT07325929 |