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Investigating the Effectiveness of PelvicSense(R) on Pain and Sexual Outcomes in Provoked Vestibulodynia

Provoked Vestibulodynia

This study will examine the effectiveness of the PelvicSense 3-month online program on pain and other outcomes in those with provoked vestibulodynia. This study is prospective in nature and will involve several assessment points: baseline, immediately post-treatment (at the end of the 3 month program), and 3-month follow up. All aspects of the study will be conducted remotely (e.g., online, email, video calls), and participants will be at least 18 years of age, fluent in English, and experience pain due to provoked vestibulodynia for at least 3 months with a physician diagnosis. Participants are expected to continue their treatment as usual and this information will be documented throughout the study.

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Participation Requirements

  • Sex:

    FEMALE

  • Eligible Ages:

    18 and up

Participation Criteria

Inclusion Criteria:

* 18 years or older
* fluent in English
* have a formal diagnosis of PVD for at least 3 months

Exclusion Criteria:

* younger than 18 years of age
* nonfluent in English
* self-identified diagnosis
* PVD duration of less than 3 months

Study Location

Sexual Health Research Laboratory, Department of Psychology, Queen's University
Sexual Health Research Laboratory, Department of Psychology, Queen's University
Kingston, Ontario
Canada

Contact Study Team

Primary Contact

Caroline Pukall, PhD

[email protected]
613 533 3200
Backup Contact

Shannon Coyle, MA

[email protected]
613 533 3276
Study Sponsored By
Queen's University
Participants Required
More Information
Study ID: NCT05909514