Status:
NOT_YET_RECRUITING
Does a Virtual Program for Pelvic Pain Improve Pain and Sexual Outcomes in Individuals With Provoked Vestibulodynia?
Lead Sponsor:
Queen's University
Conditions:
Vulvodynia (Chronic Vulvar Pain)
Vulvar Vestibulitis
Eligibility:
FEMALE
18+ years
Phase:
NA
Brief Summary
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 i...
Detailed Description
The primary aim of the proposed single-centre randomized controlled trial is to examine the efficacy of a virtual multimodal 12-week program for individuals with provoked vestibulodynia (PVD, diagnose...
Eligibility Criteria
Inclusion
- 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
Exclusion
- Less than 18 years old
- Pregnancy or suspected pregnancy
- Breastfeeding
- Up to one year postpartum
- Physical or mental health conditions that significantly interfere with activities of daily living
Key Trial Info
Start Date :
July 1 2025
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2028
Estimated Enrollment :
250 Patients enrolled
Trial Details
Trial ID
NCT06999395
Start Date
July 1 2025
End Date
December 1 2028
Last Update
May 31 2025
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