Online Study on the Impact of a Self-Help Tool for Social Anxiety
1 other identifier
interventional
200
1 country
1
Brief Summary
The goal of this clinical trial is to understand which individuals benefit most from an internet-based cognitive behavioral intervention for social anxiety. Adults aged 18-65 will complete a self-guided online program designed to reduce anxiety symptoms. The investigators will use a combination of self-reported clinical information and data from computerized decision-making and cognitive tasks to predict behavioral change due to the intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Oct 2026
Shorter than P25 for not_applicable
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 12, 2025
CompletedFirst Posted
Study publicly available on registry
February 12, 2026
CompletedStudy Start
First participant enrolled
October 1, 2026
CompletedPrimary Completion
Last participant's last visit for primary outcome
February 1, 2027
ExpectedStudy Completion
Last participant's last visit for all outcomes
April 1, 2027
September 17, 2026
February 1, 2026
4 months
December 12, 2025
September 14, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Cumulative Score for Self-Selected Goals Over a 5-Week Intervention
At baseline, participants select three personal goals. At the end of each intervention week, participants rate their progress toward each goal. The primary outcome is cumulative per-goal scores across the 5 intervention weeks.
From baseline (goal selection) to the end of Week 5 of the intervention, assessed weekly at the end of each intervention week.
Secondary Outcomes (1)
Change from Baseline in Liebowitz Social Anxiety Scale (LSAS) Avoidance Subscale Score at End of Week 5
From baseline to the end of Week 5 of the intervention.
Study Arms (1)
Intervention Group
EXPERIMENTALAll participants are assigned to the e-couch social anxiety program. Over a 5-week study period, participants are instructed to complete specific modules on a weekly schedule. They are asked to engage with the program at least once per week for approximately 30 minutes. Participants receive weekly reminders and guidance indicating which modules to complete each week.
Interventions
Participants will be offered the use of a self-help tool, e-couch (https://ecouch.com.au), for 5 weeks. e-couch is an online, self-directed tool that provides interactive self-help and evidence-based information to help users understand and manage common mental health challenges including symptoms of depression and anxiety. The e-couch social anxiety program will be used in this study. It is structured like an interactive self-help book and participants can log back into at any time to learn and review skills. The e-couch social anxiety program includes a comprehensive information module, as well as self-help modules with interactive exercises and workbooks that teach evidence-based strategies. The content will cover topics such as cognitive restructuring and exposure, with an emphasis on learning strategies to reduce social anxiety.
Eligibility Criteria
You may qualify if:
- Age 18 to 65 years
- Live in the United States
- Comfortable reading and writing in English
- Have regular access to the internet and a desktop/laptop computer
- Report wanting to feel more comfortable in social situations, to improve social confidence, and/or to reduce symptoms of social anxiety as primary reason for joining the study
- Have a valid photo ID and be willing to complete a video-based identity verification call if requested
You may not qualify if:
- Lack of attention when completing parts of the study, and/or not completing the study tasks as instructed
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Princeton University, but recruitment and study are conducted completely online and can occur anywhere in the US.
Princeton, New Jersey, 08540, United States
Study Officials
- PRINCIPAL INVESTIGATOR
Yael Niv, PhD
Princeton University
- PRINCIPAL INVESTIGATOR
Jamie C Chiu, PsyD
Princeton University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
December 12, 2025
First Posted
February 12, 2026
Study Start
October 1, 2026
Primary Completion (Estimated)
February 1, 2027
Study Completion (Estimated)
April 1, 2027
Last Updated
September 17, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, ICF, ANALYTIC CODE
- Time Frame
- Within one year after study completion
- Access Criteria
- Upon reasonable request and providing that the requesters will treat the data in line with the researchers' ethical principles. Researchers may also make de-identified data publicly available.
Researchers will share de-identified individual participant data used in the results publication, including questionnaire data and data from computerized cognitive and decision-making tasks, with other researchers upon reasonable request and after publication.