Pelvic Floor Muscle Training With Leva System for Urge Incontinence

Stopped early · Not applicable

Conditions studied: Overactive Bladder, Urge Urinary Incontinence, Mixed Urinary Incontinence

In brief

This is a pilot non-comparative study to assess the effectiveness of pelvic floor muscle training guided by the leva® system for improving change in subject-reported incontinence-related quality of life and urgency urinary incontinence (UUI) episode frequency based on voiding diaries in women at 8 weeks.

Key facts

Study ID

NCT03923348

Run by

The Christ Hospital

People needed

5

Starts

2019-06-06

Expected to finish

2020-05-04

Last updated by the study team

2020-07-01

Who can join

Age: 18 and older, up to 85. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Age 18-85 years old
• Urinary incontinence for ≥ 3 months
• Reporting at least "moderate bother" on Item 2 on the UDI-6, "Do you experience urine leakage in related to the feeling of urgency" (on new patient paperwork)
• If mixed urinary incontinence, Medical Epidemiologic Social Aspect of Aging Urinary Incontinence Questionnaire (MESA) score indicating urge-predominant MUI (Urge subscale % > Stress subscale %)
• Presence of ≥ 1 UUI episode on 3-d bladder diary (see Appendix 2)
• Is the baseline bladder diary consistent with the patient's typical habits?
• Not currently taking anti-muscarinic or beta3 agonist therapy (after at least 2 week wash-out period)
• Brink Score > 3 (see below)
• Access to smartphone technology, including iOS or Android™

You may not qualify if…

• Non-English speakers
• Severely impaired mobility or cognition
• Spinal cord injury or advanced/severe neurologic condition including Multiple Sclerosis, Parkinson's Disease
• Concomitant prolapse beyond the hymen or repair of prolapse in the previous 6 months
• Received intravesical botulinum injection within the previous 12 months
• History of implanted nerve stimulator for incontinence
• History of prior sling or vaginal mesh placement
• Previous diagnosis of Interstitial cystitis
• Active pelvic organ malignancy
• History of pelvic radiation
• Urethral obstruction
• Urinary retention or prolonged catheter use
• Less than 12 months post-partum are currently pregnant, or plan to become pregnant in the following 12 months
• Untreated symptomatic urinary tract infection
• Unevaluated hematuria
• Medical instability
• Not available for follow-up in 6 months
• Participation in other research trials that could influence results of this study

Where it is running

• The Christ Hospital — Cincinnati, Ohio, United States

Full record on ClinicalTrials.gov

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