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

Endometriosis

This study will examine the effectiveness of the PelvicSense 3-month online program on pain and other outcomes in those with endometriosis. 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 endometriosis 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, and have a formal diagnosis of endometriosis for at least 3 months.

Exclusion Criteria:

* Younger than 18 years of age, nonfluency in English, self-identified diagnosis, endometriosis 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

Backup Contact

Shannon Coyle, MA

[email protected]
613 533 3276
Primary Contact

Caroline Pukall, PhD

[email protected]
613 533 3200
Study Sponsored By
Queen's University
Participants Required
More Information
Study ID: NCT05909579