Young Vulvodynia: Effect and Efficacy of Multimodal Treatment.
ConditionVulvodynia
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexFemale
Age15-23
SponsorRegion Örebro County
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, as well as during their treatment period ( a total of 25 weeks). In addition they will respond to pre-, post-treatment and 6 month follow-up questionnaires.
Eligibility criteria
Qualifiers
Biological sex female
15-23 years of age
Diagnosed with Provoked vulvodynia
Disqualifiers
Severe psychological issues that should be prioritized before vulvodynia treatment (e.g., substance abuse, psychosis)
Ongoing pregnancy
Childbirth within the last year
Post-traumatic stress disorder (PTSD) related to sexual trauma
Trial design
Treatments tested in this trial
- Multimodal treatment
Treatment groups
15 Participants
are divided into 2 treatment groupsSponsors and collaborators
Region Örebro County
Lead sponsor
Örebro University, Sweden
Collaborator
Source ClinicalTrials.gov