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The primary purpose of this project is to evaluate the effectiveness of behavioral treatment compared to standard drug therapy for symptoms of OAB in male veterans.
Overactive bladder (OAB) is a very common and bothersome condition manifested by urgency, frequent urination, urge urinary incontinence, and nocturia. Drug therapy with oxybutynin or tolterodine is the most common approach to treatment of OAB in VA Medical Center clinics and is the standard of care nationally. Although it improves symptoms of OAB for many patients, drug therapy often has side effects, which cause a significant number of patients to discontinue therapy. Further, many symptoms are not completely controlled, even while patients are on the medication. Therefore, there is a need to improve interventions for this common problem. Although behavioral treatment is a well-established treatment for urge urinary incontinence and frequency in women, there are no controlled trials of behavioral treatment for symptoms of OAB in men. The primary purpose of this project is to evaluate the effectiveness of behavioral treatment for symptoms of OAB in male veterans.
The study is a two-site (Birmingham and Atlanta) randomized clinical trial to evaluate the effects of behavioral training compared to a standard (drug) treatment control condition. Subjects are 143 men with OAB as manifested by urgency and frequent urination (>8 voids per day), with or without incontinence, and without significant bladder outlet obstruction. Following a run-in period in which all patients are treated with an alpha blocker to empirically treat any undetected obstruction, they are stratified on severity and presence of urge incontinence and randomized to 8 weeks of behavioral treatment or drug therapy. The behavioral treatment is a comprehensive, behavioral training program, which includes pelvic floor muscle rehabilitation, self monitoring with bladder diaries, and teaching urge suppression and other skills to inhibit detrusor contraction, thus reducing urgency, frequency, incontinence, and nocturia. Patients in the control group receive standard therapy consisting of individually titrated, extended-release oxybutynin, a well-established pharmacologic agent with a state of the art drug delivery system that has the lowest rates of side effects. Bladder diaries completed by subjects prior to randomization and following the last treatment session are used to calculate changes in frequency of urination, as well as other symptoms of overactive bladder, including reports of urgency, incontinence, and nocturia. Secondary outcome measures include patient global ratings of satisfaction and improvement, impact of incontinence, and the American Urological Association (AUA) Symptom Index.
The second purpose of the study is to examine combined behavioral and drug therapy. Following post-treatment assessment, patients who do not achieve satisfactory outcomes with either behavioral or drug therapy alone are crossed over into a second phase, in which they receive combined treatment to improve outcome as much as possible.
This study will yield important information related to alternative treatment of OAB in male veterans. Though many clinicians use drug therapy routinely in the treatment of OAB, most do not offer behavioral treatments such as pelvic floor muscle training for this problem. Thus, this study has potential to alter standards of care for OAB in men.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Behavioral Training | Experimental | Behavioral training using delayed voiding, urge suppression techniques, and pelvic floor muscle training |
|
| Drug Therapy | Active Comparator | Oxybutynin chloride, extended-release, individually-titrated, 5-30 mg |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Behavioral training | Behavioral | Comprehensive behavioral training program using delayed voiding, urge suppression techniques, pelvic floor muscle training, and monitoring with bladder diaries. Treatment is implemented by a nurse practitioner in 4 clinic visits over 8 weeks. |
| Measure | Description | Time Frame |
|---|---|---|
| 24-hour Voiding Frequency | Mean voiding frequency per 24 hours derived from 7-day bladder dairy | post-treatment (week 8) |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Nocturia Frequency | Change in frequency of nocturia episodes based on 7-day bladder diary | baseline to post-treatment (week 8) |
| Change in Urgency Severity | Indevus Urgency Severity Scale incorporated into the 7-day bladder diary. Scores for urgency severity ranged from 0 to 3: 0: None-no urgency
|
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Inclusion Criteria:
Exclusion Criteria:
Urologic surgery in the past 6 months
Nonambulatory (unless has independent transfer skills)
Flow rate < 5mL at baseline and < 10mL/sec after run-in (on simple uroflowmetry)
Post-void residual urine volume > 250mL at baseline and > 150mL after run-in (on bladder ultrasound)
Continual leakage
Urinary tract infection (growth of > 100,000 colonies per ml of a urinary pathogen on urine culture). May be reconsidered after treatment and negative culture.
Fecal impaction
Poorly controlled diabetes (glycosylated hemoglobin >9 within last 3 months)
Hematuria on microscopic examination in the absence of infection
Any unstable medical condition (particularly: decompensated congestive heart failure, malignant arrhythmias, unstable angina)
-- Impaired mental status (< 24 on Folstein's Mini-Mental State Exam)
Narrow angle glaucoma
Gastric retention (by medical history)
Hypersensitivity to tamsulosin or oxybutynin
Current use of anticholinergic agents for detrusor instability. May be reconsidered after 2-week wash-out.
If on diuretic, dose has not been stable for at least three months
Sleep apnea, unless surgically corrected
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| Name | Affiliation | Role |
|---|---|---|
| Kathryn L. Burgio, PhD MA BA | Birmingham, Alabama VA Medical Center | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Birmingham VA Medical Center | Birmingham | Alabama | 35233 | United States | ||
| Atlanta VA Medical and Rehab Center, Decatur |
| PubMed Identifier | Type | Citation | Retractions |
|---|---|---|---|
| 22092152 | Result | Burgio KL, Goode PS, Johnson TM, Hammontree L, Ouslander JG, Markland AD, Colli J, Vaughan CP, Redden DT. Behavioral versus drug treatment for overactive bladder in men: the Male Overactive Bladder Treatment in Veterans (MOTIVE) Trial. J Am Geriatr Soc. 2011 Dec;59(12):2209-16. doi: 10.1111/j.1532-5415.2011.03724.x. Epub 2011 Nov 7. | |
| 37811598 |
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To minimize possible effect of undetected obstruction we used a 4-week alpha-blocker run-in (tamsulosin 0.4 mg/d or alternative). Participants who continued to meet inclusion criteria after run-in were randomized. Alpha-blocker therapy was continued throughout the trial, unless not tolerated.
Participants were recruited through mailed surveys about bladder symptoms and through clinics at two Veterans Affairs Medical Centers(2005-2009).
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| ID | Title | Description |
|---|---|---|
| FG000 | Behavioral Training | Delayed voiding, urge suppression techniques, pelvic floor muscle training |
| FG001 | Drug Therapy | Individually titrated, extended-release oxybutynin chloride, 5-30mg |
| Title | Milestones | Reasons Not Completed | ||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Overall Study |
|
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| ID | Title | Description |
|---|---|---|
| BG000 | Behavioral Training | Delayed voiding, urge suppression techniques, pelvic floor muscle training |
| BG001 | Drug Therapy | Individually titrated, extended release oxybutynin chloride |
| Units | Counts |
|---|---|
| Participants |
|
| Title | Description | Population Description | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Denominator Units Selected | Denominators | Classes |
|---|---|---|---|---|---|---|---|---|---|
| Age, Continuous | Mean |
| Type | Title | Description | Population Description | Reporting Status | Anticipated Posting Date | Parameter Type | Dispersion Type | Unit of Measure | Calculate Percentage | Time Frame | Units Analyzed | Denominator Units Selected | Arm/Group Information | Denominators | Classes | Analyses | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Primary | 24-hour Voiding Frequency | Mean voiding frequency per 24 hours derived from 7-day bladder dairy | Treatment completers | Posted | Mean | Standard Deviation | voids per 24-hour day | post-treatment (week 8) |
|
8-week treatment period
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| ID | Title | Description | Deaths (Affected) | Deaths (At Risk) | Serious Events (Affected) | Serious Events (At Risk) | Other Events (Affected) | Other Events (At Risk) |
|---|---|---|---|---|---|---|---|---|
| EG000 | Behavioral Training | Delayed voiding, urge suppression techniques, pelvic floor muscle training |
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Results can only be generalized to men without evidence of obstruction as determined by uroflowmetry, post-void residual urine (PVR) volume, and a trial of an alpha-blocker.
| Title | Organization | Phone | Extension | |
|---|---|---|---|---|
| Kathryn L. Burgio, PhD | Birmingham VA Medical Center | 205-558-7064 | kburgio@uabmc.edu |
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| ID | Term |
|---|---|
| D053201 | Urinary Bladder, Overactive |
| D059411 | Lower Urinary Tract Symptoms |
| D014549 | Urinary Incontinence |
| ID | Term |
|---|---|
| D001745 | Urinary Bladder Diseases |
| D014570 | Urologic Diseases |
| D052776 | Female Urogenital Diseases |
| D005261 | Female Urogenital Diseases and Pregnancy Complications |
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| ID | Term |
|---|---|
| D001521 | Behavior Therapy |
| C005419 | oxybutynin |
| ID | Term |
|---|---|
| D011613 | Psychotherapy |
| D004191 | Behavioral Disciplines and Activities |
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|
| Oxybutynin chloride, extended-release | Drug | Individually titrated, extended-release oxybutynin chloride, initiated at 10 mg, fluid management handout, and monitoring with bladder diaries. Treatment is implemented by a nurse practitioner in 4 clinic visits over 8 weeks. |
|
|
| baseline to post-treatment (week 8) |
| Percent Change in Frequency of Urge Incontinence | Percent change in frequency of urge incontinence episodes based on 7-day bladder diary. Percent change was calculated as ([frequency at baseline] - [frequency at 8 weeks]) / (frequency at baseline). | baseline to post-treatment (week 8) |
| Change on American Urological Association (AUA) Symptom Index | Change in score on American Urological Association (AUA) Symptom Index (baseline to week 8). The index measures lower urinary tract symptoms. Scores range from 0 to 35, with higher scores indicating worse symptoms. | baseline to post-treatment (week 8) |
| Patient Global Perception of Improvement (GPI) | Patient global perception of improvement ("much better" to "much worse") | post-treatment (week 8) |
| Patient Satisfaction | Patient global rating of satisfaction with progress in treatment ("completely satisfied" to "very dissatisfied") | post-treatment (week 8) |
| Patient Global Rating of Activity Restriction | Patient global rating of activity restriction ("not at all" to "all the time") | post-treatment (week 8) |
| Patient Report of Symptom Distress | Patient report of how disturbed they were by symptoms ("not at all" to "extremely") | post-treatment (week 8) |
| Patient Global Rating of Bothersomeness of Side Effects | Patient global rating of how bothersome their side effects were ("no side effects" to "extremely bothersome") | post-treatment (week 8) |
| Patient Desire for Alternate Treatment | Patient response to "Do you wish to receive another form of treatment?" (yes) | post-treatment (week 8) |
| Decatur |
| Georgia |
| 30033 |
| United States |
| Funada S, Yoshioka T, Luo Y, Sato A, Akamatsu S, Watanabe N. Bladder training for treating overactive bladder in adults. Cochrane Database Syst Rev. 2023 Oct 9;10(10):CD013571. doi: 10.1002/14651858.CD013571.pub2. |
| 23448285 | Derived | Johnson TM 2nd, Markland AD, Goode PS, Vaughan CP, Colli JL, Ouslander JG, Redden DT, McGwin G, Burgio KL. Efficacy of adding behavioural treatment or antimuscarinic drug therapy to alpha-blocker therapy in men with nocturia. BJU Int. 2013 Jul;112(1):100-8. doi: 10.1111/j.1464-410X.2012.11736.x. Epub 2013 Feb 28. |
| BG002 | Total | Total of all reporting groups |
| years |
|
| Sex: Female, Male | Count of Participants | Participants |
|
| Region of Enrollment | Number | participants |
|
| Units |
|---|
| Counts |
|---|
| Participants |
|
|
|
| Secondary | Change in Nocturia Frequency | Change in frequency of nocturia episodes based on 7-day bladder diary | Posted | Mean | Standard Deviation | nocturia episodes per night | baseline to post-treatment (week 8) |
|
|
|
|
| Secondary | Change in Urgency Severity | Indevus Urgency Severity Scale incorporated into the 7-day bladder diary. Scores for urgency severity ranged from 0 to 3: 0: None-no urgency
| Participants who completed treatment and returned bladder diary with useable urgency scores | Posted | Mean | Standard Deviation | Score on scale | baseline to post-treatment (week 8) |
|
|
|
|
| Secondary | Percent Change in Frequency of Urge Incontinence | Percent change in frequency of urge incontinence episodes based on 7-day bladder diary. Percent change was calculated as ([frequency at baseline] - [frequency at 8 weeks]) / (frequency at baseline). | Included participants who experienced incontinence at baseline only | Posted | Mean | Standard Deviation | Percent change in episodes per week | baseline to post-treatment (week 8) |
|
|
|
|
| Secondary | Change on American Urological Association (AUA) Symptom Index | Change in score on American Urological Association (AUA) Symptom Index (baseline to week 8). The index measures lower urinary tract symptoms. Scores range from 0 to 35, with higher scores indicating worse symptoms. | Completers | Posted | Mean | Standard Deviation | Scores on the scale | baseline to post-treatment (week 8) |
|
|
|
|
| Secondary | Patient Global Perception of Improvement (GPI) | Patient global perception of improvement ("much better" to "much worse") | Completers minus one missing value | Posted | Number | participants | post-treatment (week 8) |
|
|
|
|
| Secondary | Patient Satisfaction | Patient global rating of satisfaction with progress in treatment ("completely satisfied" to "very dissatisfied") | Completers minus one missing value | Posted | Number | participants | post-treatment (week 8) |
|
|
|
|
| Secondary | Patient Global Rating of Activity Restriction | Patient global rating of activity restriction ("not at all" to "all the time") | Com0leters minus one missing value | Posted | Number | participants | post-treatment (week 8) |
|
|
|
|
| Secondary | Patient Report of Symptom Distress | Patient report of how disturbed they were by symptoms ("not at all" to "extremely") | Completers minos one missing value | Posted | Number | participants | post-treatment (week 8) |
|
|
|
|
| Secondary | Patient Global Rating of Bothersomeness of Side Effects | Patient global rating of how bothersome their side effects were ("no side effects" to "extremely bothersome") | Completers minus one missing value | Posted | Number | participants | post-treatment (week 8) |
|
|
|
|
| Secondary | Patient Desire for Alternate Treatment | Patient response to "Do you wish to receive another form of treatment?" (yes) | Completers minus one missing value | Posted | Number | participants | post-treatment (week 8) |
|
|
|
|
| 0 |
| 73 |
| 0 |
| 73 |
| EG001 | Drug Therapy | Individually titrated, extended release oxybutynin chloride | 0 | 70 | 0 | 70 |
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| D000091642 | Urogenital Diseases |
| D052801 | Male Urogenital Diseases |
| D020924 | Urological Manifestations |
| D012816 | Signs and Symptoms |
| D013568 | Pathological Conditions, Signs and Symptoms |
| D014555 | Urination Disorders |
| About the same |
|
| Worse |
|
| Much worse |
|
| Somewhat dissatisfied |
|
| Very Dissatisfied |
|
| Some of the time |
|
| All the time |
|
| Somewhat |
|
| All the time |
|
| A Little |
|
| Somewhat |
|
| Extremely |
|