An Internet-based Information Platform for Vulvodynia Patients (EMBLA)
Vulvodynia
About this trial
This is an interventional treatment trial for Vulvodynia
Eligibility Criteria
Inclusion Criteria:
- Vulvodynia patients at their initial evaluation visit to a physician providing written informed consent for participation in the study
Exclusion Criteria:
- inability to read and understand Swedish
- severe mental illness
- currently in treatment for vulvodynia
Sites / Locations
- Gynecological Department, Akademiska Hospital
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Internet-based intervention
Control group
Patients randomized to the internet-based intervention will be given access to the information in the internet-based platform directly after randomization. During the first 6 weeks, information will be offered in a structured way, with a "theme" changing weekly. After this time-point, the patients will have the possibility to navigate through all information. The platform encompasses internet-based training including information on the disorder, psycho-education and information of simple self-implemented intervention strategies cope with vulvodynia and ameliorate dyspareunia. The platform will also include videos where team members will describe their role in treating patients with the disorder, but also short videos from former patients willing to share their individual stories.
Patients randomized to the control group through the platform will immediately be informed about the fact that there is available information and resources on the internet and that they will be called for a visit to the physiotherapist-midwife at due time, according to the present guidelines of care followed in the respective clinic (Uppsala, Falun, Gävle).