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Evidence-based Internet Cognitive-behavioral Therapy for Social Anxiety

Social Anxiety

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.

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Participation Requirements

  • Sex:

    ALL
  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* Aged ≥18 years; and
* Speak and write in French or English; and
* Have access to the internet and a digital device; and
* Screen for social anxiety using the 17-item Social Phobia Inventory (SPIN) questionnaire (\> 20).

Exclusion Criteria:

* Self-report severe symptoms of depressions (PHQ-9 score ≥ 23); or
* Thoughts they would be better off dead or hurting themselves on the 9th item of PHQ-9 in the past two weeks or thoughts or wishes to kill themselves on the 9th item of the Beck Depression Inventory-II; or
* A diagnosis of schizophrenia, bipolar disorder or problems related to active substance use or dependence; or
* Current use of benzodiazepines.

Study Location

CISSS de la Montérégie-Centre
CISSS de la Montérégie-Centre
Greenfield Park, Quebec
Canada

Contact Study Team

Primary Contact

Helen-Maria Vasiliadis, Ph.D.

[email protected]
450 466-5000
CIUSSS de l'Estrie - CHUS
CIUSSS de l'Estrie - CHUS
Sherbrooke, Quebec
Canada

Contact Study Team

Primary Contact

Helen-Maria Vasiliadis, Ph.D.

[email protected]
450 466-5000
Study Sponsored By
Université de Sherbrooke
Participants Required
More Information
Study ID: NCT06403995