Online Radical Acceptance Intervention for Social Anxiety Disorder
RA-SAD-001
1 other identifier
interventional
100
1 country
1
Brief 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 few months later.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started Dec 2025
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
December 2, 2025
CompletedStudy Start
First participant enrolled
December 16, 2025
CompletedFirst Posted
Study publicly available on registry
January 8, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2027
May 6, 2026
December 1, 2025
1 year
December 2, 2025
April 30, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Liebowitz Social Anxiety Scale
Change in social anxiety symptoms using the self-report Liebowitz Social Anxiety Scale (LSAS). In this questionnaire, participants are asked to respond to 24 social situations by marking how much they feel fear in each situation (anxiety subscale) and to which extent they will avoid this situation (avoidance subscale) on a 0-3 Likert scale. This measure ranges 0-144; higher scores indicate greater social anxiety severity.
baseline, after session 4 (~1 week), 2 weeks (end of treatment), 3-week follow-up, 3-month follow-up
Secondary Outcomes (2)
Generalized Anxiety Disorder-7
baseline, after session 4 (~1 week), 2 weeks (end of treatment), 3-week follow-up, 3-month follow-up
Patient Health Questionnaire-9
Time Frame: baseline, after session 4 (~1 week), 2 weeks (end of treatment), 3-week follow-up, 3-month follow-up
Other Outcomes (6)
Word-sentence association task
baseline, after session 4 (~1 week)
Emotional faces task
baseline, after session 4 (~1 week)
Emotion regulation flexibility task
baseline, after session 4 (~1 week)
- +3 more other outcomes
Study Arms (2)
Radical Acceptance
EXPERIMENTALParticipants will receive an online radical acceptance training based on DBT principles. The intervention consists of six guided exercises delivered over a two-week period, designed to enhance acceptance of distressing internal experiences.
Relaxation Skills
ACTIVE COMPARATORParticipants will receive an online training in DBT TIPP relaxation skills (Temperature, Intense Exercise, Paced Breathing/Progressive Muscle Relaxation). The intervention includes six guided exercises over two weeks, aiming to rapidly decrease physiological arousal and support emotion regulation under stress.
Interventions
Online DBT-based program focusing on implementing radical acceptance in daily life and coping with socially anxious situations.
Online DBT-based program teaching relaxation techniques to achieve rapid physiological down-regulation and improve emotional control.
Eligibility Criteria
You may qualify if:
- 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.
You may not qualify if:
- 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
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
University of Haifa
Haifa, 3498838, Israel
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Noam Weinbach, PhD
School of Psychological Sciences, University of Haifa
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 2, 2025
First Posted
January 8, 2026
Study Start
December 16, 2025
Primary Completion (Estimated)
January 1, 2027
Study Completion (Estimated)
April 1, 2027
Last Updated
May 6, 2026
Record last verified: 2025-12