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Educating Patients on Management of Overactive Bladder: Written Versus Verbal Instructions

Educating Patients on Management of Overactive Bladder: Written Versus Verbal Instructions

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02197533
Enrollment
60
Registered
2014-07-22
Start date
2014-07-31
Completion date
2019-09-01
Last updated
2019-12-04

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

Conditions

Overactive Bladder

Brief summary

Background: Overactive bladder (OAB) is a common condition among postmenopausal women, requiring a multifaceted treatment approach that requires patient retention of information given to them in clinic. Recall of recommendations is a key component of compliance. Supplemental educational tools such as handouts and audiovisual information have been investigated for their ability to improve patients' recall of information and increase satisfaction with the clinical encounter. Objective: To determine if a written list of seven management strategies for overactive bladder leads to improved immediate and delayed recall of these recommendations in postmenopausal women presenting with OAB compared to a traditional verbal discussion. Methods: In this single-blind, randomized controlled trial, patients' immediate and delayed (2-week) recall of seven OAB management strategies will be compared between two groups. The intervention group will receive a handwritten list during their verbal discussion of OAB treatment while the control group will receive standard care (verbal discussion only). Immediate and delayed recall will be assessed by a member of the study team who has been blinded to participants' group assignments. Results: The results of this study may guide clinicians in the most effective mode of providing treatment recommendations to post-menopausal patients with OAB.

Interventions

OTHERWritten List

Written list of seven management strategies for OAB to be produced during verbal discussion about management.

Sponsors

Unity Health Toronto
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
SINGLE (Outcomes Assessor)

Eligibility

Sex/Gender
FEMALE
Healthy volunteers
No

Inclusion criteria

* New diagnosis of overactive bladder * post-menopausal

Exclusion criteria

* Pre-existing diagnosis of dementia or other cognitive disorders * Patients with mixed incontinence * Non-English speaking * Patients with contraindications to taking vaginal estrogen or anticholinergic medications

Design outcomes

Primary

MeasureTime frameDescription
Recall0 and 2 weeksMean number of treatment strategies recalled (scored out of seven) immediately and two weeks after the clinic appointment.

Countries

Canada

Outcome results

None listed

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