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Screening for Urinary Incontinence by Primary Care Providers

Screening for Urinary Incontinence by Primary Care Providers

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT00178334
Enrollment
554
Registered
2005-09-15
Start date
2006-03-31
Completion date
2006-07-31
Last updated
2013-01-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Urinary Incontinence

Brief summary

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

Detailed description

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.

Interventions

None listed

Sponsors

Pfizer
CollaboratorINDUSTRY
University of Rochester
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
21 Years to No maximum
Healthy volunteers
Yes

Inclusion criteria

* All primary care providers in the Greater Rochester metropolitan area, including: Primary care Medical Doctors (MD), Doctors of Osteopathy (DO), Primary care Nurse Practitioners (NP), and Physician Assistants (PA)

Exclusion criteria

* Physicians in the Greater Rochester metropolitan area who are not primary care providers

Design outcomes

Primary

MeasureTime frame
QuestionnaireResponse to mailing

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026