The overall aim of this project is to demonstrate content validity and usability of the modified Vulvar Pain Assessment Questionnaire (mVPAQ), the modified Female Sexual Function Index (mFSFI), and pain on intercourse Numeric Rating Scale (NRS) for adult patients with Vulvodynia
Study Type
OBSERVATIONAL
Enrollment
20
San Diego Sexual Medicine
San Diego, California, United States
Center for Vulvovaginal Disorders
Washington D.C., District of Columbia, United States
Omaha OB-GYN Associates, PC
Omaha, Nebraska, United States
The Center for Vulvovaginal Disorders
New York, New York, United States
Validation of mVPAQ
Cognitive debrief and usability through interviews and completion of an electronic diary
Time frame: 1 week
Validation of mFSFI
Cognitive debrief and usability through interviews and completion of an electronic diary
Time frame: 1 week
Validation of Pain on Intercourse Numeric Rating Scale (NRS)
Cognitive debrief and usability through interviews and completion of an electronic diary. Pain on Intercourse NRS that describes pain experienced during this sexual intercourse episode by number. The higher is the number the worse is pain.
Time frame: 1 week
Vulvar pain NRS
Assess understanding of the appropriateness of the vulvar pain NRS through interview and completion of an electronic diary
Time frame: 1 week
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