Diamond Health Care Centre, Vancouver Hospital
Vancouver, British Columbia, V5Z 1M9, Canada
NCT Number: NCT01731288
The main purpose of this study is to assess conception, pregnancy, childbirth, and pain experiences among women who have been diagnosed with vulvodynia. Specifically, this study aims to examine the following among women who have been diagnosed with vulvodynia: 1) rates of pregnancy/childbirth and desire for children; 2) fear of pregnancy and childbirth; 3) potential difficulties experienced while attempting to become pregnant and during pregnancy/childbirth; 4) methods used to become pregnant and deliver; 5) methods used to manage vulvodynia symptoms during pregnancy; and 6) pain outcomes associated with pregnancy.
Very little research has examined pregnancy/childbirth experiences among women with vulvodynia, or the natural history of vulvodynia. As such this is a preliminary investigation that will provide descriptive information regarding many of the proposed research questions. Based on the clinical experience of the investigators, it is expected that women with vulvodynia will report lower rates of pregnancy and higher levels of fear about pregnancy and childbirth in comparison to women without such pain. It is also expected that women with vulvodynia will report more difficulties becoming pregnant as compared to women without such pain, and that women with vulvodynia will report more elective nonvaginal births in comparison to vaginal births.
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Notify Me19 year and older
Female
Observational
Vancouver, British Columbia, V5Z 1M9, Canada
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: data is collected at a single time point
We will assess if women with vulvodynia experience different rates of pregnancy in comparison to women without such pain
Time frame: data is collected at a single time point
We will assess how many women with vulvodynia wish to have children in their lifetime.
Time frame: data is collected at a single time point
We will assess if women with vulvodynia report higher levels of fear about pregnancy and childbirth in comparison to women without such pain.
Time frame: data is collected at a single time point
We will assess if women with vulvodynia experience more difficulties becoming pregnant in comparison to women without such pain.
Time frame: data is collected at a single time point.
We will assess if women with vulvodynia experience more complications during pregnancy and delivery in comparison to women without such pain.
Time frame: data is collected at a single time point
We will assess what methods women with vulvodynia use to become pregnant and deliver.
Time frame: data is collected at a single time point
We will assess how women manage their vulvodynia symptoms during pregnancy.
Time frame: data is collected at a single time point
We will assess if vulvodynia-related pain symptoms change during and after pregnancy.
Time frame: data is collected at a single time point
We will assess the course of vulvodynia after treatment is received from health care workers specializing in vulvar pain.
University of British Columbia
Other
Acronym: PRECIOUS
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