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Study identifier: NCT06403995 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Evidence-based Internet Cognitive-behavioral Therapy for Social Anxiety

Condition: Social Anxiety  ·  Sponsor: Université de Sherbrooke

PhaseNA
Planned participants252
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNo

About this study

The objectives of the study are to 1) to translate and adapt iCBT Shyness Program to the Canadian context; 2) to examine the completion and effectiveness of the Canadian adapted, including the French translated and English iCBT Shyness Program, in improving SAD symptoms; 3) to explore barriers and facilitating factors to the program's implementation. The overall study design is a hybrid effectiveness-implementation study of a quasi-experimental parallel group trial reflecting real world pathways (recommended and self-referrals). The project will be conducted in two Canadian provinces: Quebec (Montérégie) and Ontario. Prior to implementing the iCBT Shyness Program, it will undergo an initial adaptation to the Canadian context and focus groups will be conducted with key actor groups to discuss the adaptations to the graphics, narration of the modules, and this to better reflect varying sociocultural context among Canadian French- and English-speaking populations. We will then evaluate the outcomes associated with the implementation of the program in a three-pathway parallel trial. As a last step to this trial, semi-structured interviews will be conducted with study participants and health care providers to explore facilitating factors and barriers to the implementation of the iCBT adapted program.

This description comes directly from the study's public registry record.

Talk to the study team

Helen-Maria Vasiliadis, PhD  ·  (450) 466-5000  ·  helen-maria.vasiliadis@usherbrooke.ca

Always discuss trial participation with your own doctor first.

Locations (2)

CISSS de la Montérégie-CentreGreenfield Park, Quebec, CanadaRecruiting
CIUSSS de l'Estrie - CHUSSherbrooke, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT06403995