- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02670486
Audiovisual Stimulus During Urodynamics (AVUDE)
May 9, 2017 updated by: Vivian Sung, Women and Infants Hospital of Rhode Island
Audiovisual Stimulus During Urodynamics to Provoke Detrusor Overactivity
Many women have the need to run to the restroom frequently during the night and day, a condition called "overactive bladder".
Embarrassing urinary leakage is also commonly associated with these symptoms.
The investigators believe the primary cause in most cases is the bladder muscle contracting too frequently but are still not sure exactly why this happens and if it is triggered by factors in the environment.
When bladder testing using pressure catheters ("urodynamics") is done these bladder contractions are often not picked up, even in women with overactive bladder.
This may be partly due to the unnatural environment in which the testing is done without the presence of the usual visual or audible triggers, such as running water or seeing a toilet.
The investigators propose adding an audiovisual stimulant to the usual bladder testing to see if this makes it more likely for bladder contractions to happen.
One group of patients would have the usual bladder testing as part of their normal care.
The other group would receive the normal care in addition to hearing a water fountain in the room and watching a video of things that may trigger overactive bladder symptoms; seeing public restroom signs in a mall, a toilet bowl being lowered and a kitchen sink with water running over dishes.
The suspicion is that the proportion of patients in whom bladder contractions are seen will be higher for those with audiovisual triggers compared to those with the usual care.
Women with overactive bladder or leakage with urge who are sent for urodynamics by their doctor will be asked if they wish to participate in the study.
Study Overview
Detailed Description
Detrusor overactivity (DO), defined as a rise in detrusor pressure during bladder filling on urodynamic evaluation (UDE), is presumed to be involved in the pathophysiology of overactive bladder syndrome (OAB) and urge urinary incontinence (UUI).
However, the mechanism of DO is not fully understood and the detection rate of DO on UDE is low.
Currently there is limited data in the literature investigating audiovisual stimulation of DO.
To improve the understanding of the neural regulation of micturition, the investigators propose adding an audiovisual stimulant to standard UDE.
Methods: 218 women with OAB and/or UUI undergoing UDE will be recruited.
Subjects will be randomized to standard care versus standard care with the addition of an audiovisual stimulant, involving the patient listening to running water and watching a video of several well-known triggers.
The primary outcome will be proportion of patients in whom detrusor contractions are seen.
Secondary outcomes will include number, amplitude and length of contractions and presence of incontinence associated with a contraction.
The objective of this study is to estimate the effect of adding audiovisual cues during UDE on the proportion of patients in whom DO is detected compared to standard clinical care.
The hypothesis is that the proportion of patients in whom detrusor contractions are seen will be higher in female patients with OAB symptoms and/or UUI using an audiovisual stimulant.
Data obtained will be analyzed by chi square, t-tests, and multivariable logistic regression analysis as appropriate.
Study Type
Interventional
Enrollment (Actual)
218
Phase
- Not Applicable
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
14 years and older (Adult, Older Adult)
Accepts Healthy Volunteers
No
Genders Eligible for Study
Female
Description
Inclusion Criteria:
- women 18 years and older undergoing UDE with clinical diagnosis of OAB and/or UUI
Exclusion Criteria:
- urinary tract infection
- pregnancy
- current treatment for OAB or UUI
- stage 3 and 4 pelvic organ prolapse
- undergone major pelvic reconstructive surgery or incontinence surgery in the last 6 months
- neurogenic bladder
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Basic Science
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
No Intervention: standard of care
Usual urodynamics with no intervention.
|
|
|
Active Comparator: Audiovisual intervention
Audiovisual stimulus during urodynamic testing.
|
Water fountain and a video (including scenes of some common triggers for OAB) played on continuous loop throughout the test on a laptop
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Proportion of patients in whom detrusor contractions are seen
Time Frame: 30 minutes
|
30 minutes
|
Secondary Outcome Measures
Outcome Measure |
Time Frame |
|---|---|
|
Presence of incontinence associated with a contraction
Time Frame: 30 minutes
|
30 minutes
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Study Chair: Alexandra Caffrey, BS, Women & Infants Hospital IRB
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start
August 1, 2014
Primary Completion (Actual)
May 1, 2016
Study Completion (Actual)
June 1, 2016
Study Registration Dates
First Submitted
October 9, 2015
First Submitted That Met QC Criteria
January 28, 2016
First Posted (Estimate)
February 1, 2016
Study Record Updates
Last Update Posted (Actual)
May 10, 2017
Last Update Submitted That Met QC Criteria
May 9, 2017
Last Verified
May 1, 2017
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 14-0034
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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