Does a Virtual Program for Pelvic Pain Improve Pain and Sexual Outcomes in Individuals With Provoked Vestibulodynia?
Recruiting
N/A
Interventional Study
Vulvodynia (Chronic Vulvar Pain)
Vulvar Vestibulitis
Vestibulodynia
Provoked Vestibulodynia
Provoked Localized Vulvodynia
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 and older
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 250 (estimated)
- Sponsor
- Queen's University · Other
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About This Trial
The goal of this clinical trial is to learn if a 3-month online pelvic health program works to improve pain and sexual wellbeing in adult women with chronic genital pain. The main research questions it aims to answer are:
* How well does the program work to improve pain and sexual wellbeing?
* How well does the program work to improve pain anxiety and pain interference?
* How do participants rate…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
* Self-reported physician diagnosis of provoked vestibulodynia (PVD)
* PVD duration of at least 3 months
* PVD pain intensity rating of at least 3 on a scale from 0 (no pain) to 10 (extreme pain)
* Resides in North America (Canada or the United States)
* Fluent in English
Exclu…
Contacts