Vulvar Pain Survey Seeks Participants

Female participants needed for an online questionnaire study on women’s health and genital pain. The purpose of this study is to develop a questionnaire (the Vulvar Pain Assessment Questionnaire) that will help health care professionals assess symptoms of chronic vulvar pain. Participants must be 18 years of age or older, be able to read and write in English and currently experience genital pain.

This confidential study is conducted entirely online by researchers at Queen’s University in Kingston, Ontario, Canada. For more information visit: https://surveys.psyc.queensu.ca/Checkbox/VPAQ.aspx, or e-mail sex.lab@queensu.ca and ask for information about the Online Women’s Health and Genital Pain study. Compensation provided; participation typically takes 30-45 minutes per part of the study.

Sincerely,

Emma Dargie [MSc., Dr. Caroline Pukall, and Dr. Susan Chamberlain]

By Jill Osborne|2015-01-30T16:02:16-08:00January 30th, 2015|Our Blog, Research|Comments Off

About the Author: Jill Osborne

My Google Profile+ Jill Heidi Osborne is the president and founder of the Interstitial Cystitis Network, a health education company dedicated to interstitial cystitis, bladder pain syndrome and other pelvic pain disorders. As the editor and lead author of the ICN and the IC Optimist magazine, Jill is proud of the academic recognition that her website has achieved. The University of London rated the ICN as the top IC website for accuracy, credibility, readability and quality. (Int Urogynecol J - April 2013). Harvard Medical School rated both Medscape and the ICN as the top two websites dedicated to IC. (Urology - Sept 11). For many years, Jill served on the Congressionally Directed Medical Research Panel (US Army) where she collaborated with researchers to evaluate new IC research studies for possible funding. Jill has conducted and/or collaborates on a variety of IC research studies on new therapeutics, pain care, sexuality, the use of medical marijuana, menopause and the cost of treatments, shining a light on issues that influence patient quality of life. An IC support group leader and national spokesperson for the past 20 years, she has represented the IC community on radio, TV shows, at medical conferences. She has written hundreds of articles on IC and its related conditions. Jill has a Bachelors Degree in Pharmacology and a Masters in Psychology, Jill was named Presidential Management Intern (aka Fellowship) while in graduate school. (She was unable to earn her PhD due to the onset of her IC.) She spends the majority of her time providing WELLNESS COACHING for patients in need and developing new, internet based educational and support tools for IC patients, including new live IC Support Group Meetings via Youtube and the “Living with IC” video series. Jill was diagnosed with IC at the age of 32 but first showed symptoms at the age of 12.