Young Vulvodynia: Effect and Efficacy of a Multimodal Treatment for Young Women With Vulvar Pain
Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
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
Participation Requirements
Sex: Female
Minimum Age: 15
Maximum Age: 23
Healthy Volunteers: f
View:
• Biological sex female
• 15-23 years of age
• Diagnosed with Provoked vulvodynia
Locations
Other Locations
Sweden
Ungdomsmottagningen
RECRUITING
Örebro
Contact Information
Primary
Rebecca Lennartsson, MSc
rebecca.lennartsson@regionorebrolan.se
+46733690524
Backup
Ida Flink, Professor
ida.flink@kau.se
+46721564449
Time Frame
Start Date: 2025-06-10
Estimated Completion Date: 2026-12-31
Participants
Target number of participants: 15
Treatments
No_intervention: Baseline period
During a 4, 5 or 6 week waiting period, participants respond to a short questionnaire twice a week.
Experimental: Multimodal Treatment
Multimodal Treatment.
Related Therapeutic Areas
Sponsors
Leads: Region Örebro County
Collaborators: Örebro University, Sweden