Virtual Reality for Urinary Incontinence in Women
NCT07070063
Female Urogenital Diseases, Female Urogenital Diseases and Pregnancy Complications
Wroclaw, Lower Silesian Voivodeship, Poland
View Trial DetailsNCT Number: NCT00178334
The purpose of this study is to:
* Assess the rate of screening for urinary incontinence (UI) in women by their primary care providers * Identify the type of screening used by primary care providers * Identify barriers to screening for UI * Identify differences in screening rates between specialties * Assess whether primary care providers view UI as a serious medical problem * Assess the comfort level of primary care providers in the diagnosis and treatment of UI * Identify primary care providers' preferred mode of learning more about UI
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Notify Me21 year and older
All sexes
Observational
UI is a very common condition whose prevalence can be expected to increase dramatically in the coming decades. Treatment options are available to improve women's health and quality of life. However, inadequate communication between physicians and patients leads to decreased diagnosis and treatment. Past studies evaluating the use of screening by primary care providers, who act as gatekeepers in our healthcare system, clearly demonstrate that improvements must be made in the screening system. We propose a survey of local primary care providers to quantify screening rates for UI and identify barriers to successful screening. The information collected in this survey will allow us to identify methods such as targeted education opportunities and patient literature or questionnaires that will assist providers and their patients in initiating discussion and evaluation of UI.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Time frame: Response to mailing
University of Rochester
Other
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