Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT07408102 · ClinicalTrials.gov registry record · NA
Online Study on the Impact of a Self-Help Tool for Social Anxiety
A NA study, sponsored by Trustees of Princeton University.
- Not yet
- Registry status
- NA
- Development phase
- 200
- Enrollment target
NCT07408102: Clinical Trial NA study, sponsored by Trustees of Princeton University.
NCT07408102 is a NA study that has not yet begun recruiting, run by Trustees of Princeton University. The registered enrollment target is 200 participants, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower). According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07408102, a NA study, has not yet begun recruiting, sponsored by Trustees of Princeton University.
- NOT YET RECRUITING
- Registry status
- NA
- Development phase
- 200 participants
- Enrollment target
Study 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 changes in symptom scores from the intervention.
Primary Outcome
Social anxiety symptom severity will be assessed using the Liebowitz Social Anxiety Scale (LSAS), a validated self-report questionnaire measuring fear and avoidance across social interaction and performance situations. The LSAS total score ranges from 0 to 144, with higher scores indicating greater social anxiety symptom severity. LSAS total scores will be collected at baseline (pre-intervention) and at the end of the 5-week e-couch intervention period. The outcome metric is the individual-leve
Interventions
- BEHAVIORAL Internet-delivered self-help for social anxiety based on principles of cognitive behavioral therapy
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2026-06 |
| Est. Completion | 2027-04 |
| Phase | NA |
What is known before NCT07408102 opens enrollment
NCT07408102 is an interventional study that assigns participants to a tested intervention. The registered 200 participants enrollment target is mid-sized for trials with a published cap, below the 1,404-participant average among 58,714 other NA trials with a reported enrollment target (86% lower).
The record links to 0 conditions, and to 1 intervention - of which Internet-delivered self-help for social anxiety based on principles of cognitive behavioral therapy is the first listed.
NCT07408102 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT07408102 about?
NCT07408102 is a clinical study titled "Online Study on the Impact of a Self-Help Tool for Social Anxiety". 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 s...
What is the current status of trial NCT07408102?
This trial is currently not yet recruiting. It is a NA study. The enrollment target is 200 participants. The study started on 2026-06. Estimated completion is 2027-04.
What interventions are being tested in trial NCT07408102?
The interventions under investigation include: Internet-delivered self-help for social anxiety based on principles of cognitive behavioral therapy (BEHAVIORAL).
Who is sponsoring clinical trial NCT07408102?
This trial is sponsored by Trustees of Princeton University, which has 4 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT07408102's enrollment target sits among peer trials
200 506th of 2000 higher than 1,434 of 2,000 other NA trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other NA trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
Nationwide trials with similar profiles
Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.
Similar enrollment target
- NCT00107289 · 200 participants · Phase 2
Iodine I 131 Metaiodobenzylguanidine in Treating Patients With Recurrent, Progressive, or Refractory Neuroblastoma or Malignant Pheochromocytoma or Paraganglioma
- NCT00109174 · 200 participants · NA
MRS Measurement of Glutamate and GABA Metabolism in Brain
- NCT00177268 · 200 participants
Blood, Urine, and Tissue Collection for Cutaneous Lymphoma, Eczema, and Atopic Dermatitis Research
- NCT00493688 · 200 participants
A Study to Determine Whether Perioperative Energy Dynamics Correlates With Postoperative Outcomes
Similar registry start date
- NCT05988463 · started 2027-01-01 · Phase 1
Dose-Escalation Study of Artesunate Patients With IPF
- NCT07219706 · started 2026-12-10 · NA
Dietary Fiber and Time Restricted Eating
- NCT02831335 · started 2026-12-01
Technical Development of Multi-Parametric Renocerebral MRI
- NCT05962346 · started 2026-12 · NA
Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia