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Behavioral Intervention
PelvicSense Program for Vulvodynia
Recruiting1 award
Kingston, Ontario
This trial will study if an online program helps reduce pain and other outcomes in those with provoked vestibulodynia. Participation will be remote & monitored for 3 months.
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Get in touch with the study teamWe’ll send your responses to the study team and help you to setup your first screening. This is not the start of informed consent. Screening happens between you and the trial.