The purpose of this study is to assess the effect of commercially available genital vibrator use on sexual health, female pelvic floor disorders, and overall quality of life among a diverse population of women.
Age range
18 Years – 99 Years
Sex
FEMALE
See this in plain English?
AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.
Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.
The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.
A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.
To assess the change from baseline sexual function at 3 month
Timeframe: baseline, post intervention at 3 months
To assess the change from baseline sexual function at 3 month
Timeframe: baseline, post intervention at 3 months
To assess the change from baseline degree of pelvic organ prolapse at 3 month
Timeframe: baseline, post intervention at 3 months
To assess the change from baseline overall health and quality of life at 3 month
Timeframe: baseline, post intervention at 3 months
To assess the change from baseline overall health and quality of life at 3 month
Timeframe: baseline, post intervention at 3 months
To assess the change from baseline overall health and quality of life at 3 month
Timeframe: baseline, post intervention at 3 months