← Back to all trials
Active Not Recruiting
NCT07092332
Young Vulvodynia: Effect and Efficacy of Multimodal Treatment.
Conditions: Vulvodynia
Sex: Female
Ages: 15 Years – 23 Years
Healthy volunteers: No
Phase: NA
Enrollment: 15
Sponsor: Region Örebro County
Location: Ungdomsmottagningen Örebro
Summary
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
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
* Post-traumatic stress disorder (PTSD) related to sexual trauma
* Insufficient mastery of the Swedish language
* No experience of vaginal sex, as vaginismus might be suspected, which requires different treatment
Source: ClinicalTrials.gov (NCT07092332). StuddyBuddy aggregates publicly available trial information.