Patient Satisfaction Survey of Non-surgical Urinary Incontinence Treatment

University of Rochester

Status: Completed

Conditions: Urinary Incontinence

Treatments: Behavioral: patient acceptable symptom state (PASS)

Study type: Observational

Funder types: Other

Identifiers

NCT04064970

RSRB72759

Details and patient eligibility

About

The purpose of this study is to identify self-reported wellness following nonsurgical treatment of stress urinary incontinence. This will be done by correlating the response of "yes" on the patient acceptable symptom state (PASS) question to responses from other questionnaires regarding urinary symptoms.

Enrollment: 125 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Adult women (> 18 years) seeking care for stress urinary incontinence at the URMC in Rochester, NY, DUMC in Durham, NC, Western New York (WNY) Urology Associates in Cheektowaga, NY, or at the UTMB in Galveston, TX.
• English-speaking
• Possess the ability to complete electronic patient reported outcome questionnaires and voiding diaries

Exclusion criteria

• Women who decline to participate in the study
• Women were unable to complete electronic patient reported outcome questionnaires
• Women with greater than stage II uterovaginal prolapse or post-hysterectomy prolapse.
• Women considered citizens of the European Union (EU), including EU citizens living in the United States.

Trial design

125 participants in 1 patient group

PASS Cohort

Treatment:

Behavioral: patient acceptable symptom state (PASS)