Baseline Knowledge of Stress Urinary Incontinence Among Urogynecology Patients

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexFemale
Age18+
SponsorSunnybrook Health Sciences Centre

About this trial

The goal of this prospective study is to assess whether a standardized educational flyer (pamphlet) improves knowledge about stress urinary incontinence (SUI) in adult females attending a urogynecology clinic. It will also explore how participant characteristics relate to treatment preferences.

The main questions it aims to answer are:

Does reading a standardized SUI patient information flyer improve participants' knowledge of SUI? How do patient characteristics influence treatment preferences for SUI?

Participants will:

Complete a self-administered questionnaire assessing knowledge of SUI, including its definition, pathophysiology, risk factors, natural history, and treatment options (this questionnaire is not part of standard care).

Review a standardized SUI educational flyer during their clinic visit. Complete the same questionnaire again after reading the pamphlet to assess any change in knowledge.

Questionnaire scores before and after reading the flyer will be compared. Secondary outcomes include participant characteristics and reported treatment preferences.

Eligibility criteria

Qualifiers

Participants are patients referred to Sunnybrook Health Sciences Centre Urogynecology Clinics with the condition of SUI.

≥ 18 years old

Female

Able to provide informed consent and communicate in English

Disqualifiers

Under the age of 18 years

Urge-predominant mixed urinary incontinence or pure urinary urge incontinence

Inability to respond to research questionnaires in English

Unable to provide informed consent

Trial design

Treatments tested in this trial

  • 15 Item Questionnaire

Treatment groups

90 Participants
are divided into 1 treatment group