Vulvodynia Intervention: the Effect of Multimodal Treatment for Provoked Vulvodynia
Recruiting
N/A
Interventional Study
Vulvodynia (Chronic Vulvar Pain)
No Placebo Group
Every participant receives an active treatment — no one gets a placebo.
At a Glance
- Age
- 18 – 40
- Sex
- Female
- Study type
- Interventional
- Purpose
- Treatment
- Participants needed
- 50 (estimated)
- Sponsor
- Karlstad University · Other
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About This Trial
The purpose of this project is to develop and evaluate a multimodal treatment for provoked vulvodynia, by addressing the following specific research questions:
1. What is the feasibility and acceptability of this multimodal treatment protocol?
2. What are the effects on pain and psychosexual health?
3. How is the treatment perceived by patients, clinicians and stakeholders in the health care sett…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
Biological sex: Female 18-40 years old 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 …
Contacts
No contact information available.