Young Vulvodynia: Effect and Efficacy of Multimodal Treatment.

Recruiting N/A Interventional Study
Vulvodynia
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
15 – 23
Sex
Female
Study type
Interventional
Purpose
Treatment
Participants needed
15 (estimated)
Sponsor
Region Örebro County · Other
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About This Trial
The aim of this SCED-study is to evaluate a multimodal treatment for vulvodynia in young women. The main questions it aims to answer are: Is multimodal treatment effective for provoked vulvodynia in young women? How is multimodal treatment experienced by young women with vulvodynia? Participants will respond to frequent questionnaires (two times a week) during a baseline period of 4,5 or 6 weeks…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Biological sex female * 15-23 years of age * Diagnosed with Provoked vulvodynia Exclusion Criteria: * Severe psychological issues that should be prioritized before vulvodynia treatment (e.g., substance abuse, psychosis) * Ongoing pregnancy * Childbirth within the last year *…
Contacts

Rebecca Lennartsson, MSc

+46733690524

rebecca.lennartsson@regionorebrolan.se

CONTACT

Ida Flink, Professor

+46721564449

ida.flink@kau.se

CONTACT