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Behavioral Treatment of Overactive Bladder in Men (MOTIVE)

Primary Purpose

Overactive Bladder

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Behavioral training
Oxybutynin chloride, extended-release
Sponsored by
US Department of Veterans Affairs
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Overactive Bladder focused on measuring Overactive bladder, Behavioral treatment, Drug therapy, Lower urinary tract symptoms, Urinary incontinence, Clinical trial

Eligibility Criteria

19 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Male
  • Community-dwelling
  • Veteran
  • Self-reported urgency
  • Self-reported frequent urination
  • Mean of > 8 voids per 24-hour day on bladder diary
  • Able to come to clinic

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

Sites / Locations

  • Birmingham VA Medical Center
  • Atlanta VA Medical and Rehab Center, Decatur

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Behavioral Training

Drug Therapy

Arm Description

Behavioral training using delayed voiding, urge suppression techniques, and pelvic floor muscle training

Oxybutynin chloride, extended-release, individually-titrated, 5-30 mg

Outcomes

Primary Outcome Measures

24-hour Voiding Frequency
Mean voiding frequency per 24 hours derived from 7-day bladder dairy

Secondary Outcome Measures

Change in Nocturia Frequency
Change in frequency of nocturia episodes based on 7-day bladder diary
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 Mild-awareness of urgency, but is easily tolerated. Moderate-enough urgency discomfort that it interferes with or shortens usual activity Severe-extreme urgency discomfort that abruptly stops all activities or tasks.
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).
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.
Patient Global Perception of Improvement (GPI)
Patient global perception of improvement ("much better" to "much worse")
Patient Satisfaction
Patient global rating of satisfaction with progress in treatment ("completely satisfied" to "very dissatisfied")
Patient Global Rating of Activity Restriction
Patient global rating of activity restriction ("not at all" to "all the time")
Patient Report of Symptom Distress
Patient report of how disturbed they were by symptoms ("not at all" to "extremely")
Patient Global Rating of Bothersomeness of Side Effects
Patient global rating of how bothersome their side effects were ("no side effects" to "extremely bothersome")
Patient Desire for Alternate Treatment
Patient response to "Do you wish to receive another form of treatment?" (yes)

Full Information

First Posted
August 20, 2010
Last Updated
April 22, 2014
Sponsor
US Department of Veterans Affairs
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1. Study Identification

Unique Protocol Identification Number
NCT01187498
Brief Title
Behavioral Treatment of Overactive Bladder in Men
Acronym
MOTIVE
Official Title
Behavioral Treatment of Overactive Bladder in Men
Study Type
Interventional

2. Study Status

Record Verification Date
December 2013
Overall Recruitment Status
Completed
Study Start Date
January 2005 (undefined)
Primary Completion Date
October 2009 (Actual)
Study Completion Date
October 2009 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
US Department of Veterans Affairs

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
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.
Detailed Description
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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Overactive Bladder
Keywords
Overactive bladder, Behavioral treatment, Drug therapy, Lower urinary tract symptoms, Urinary incontinence, Clinical trial

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Crossover Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
143 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Behavioral Training
Arm Type
Experimental
Arm Description
Behavioral training using delayed voiding, urge suppression techniques, and pelvic floor muscle training
Arm Title
Drug Therapy
Arm Type
Active Comparator
Arm Description
Oxybutynin chloride, extended-release, individually-titrated, 5-30 mg
Intervention Type
Behavioral
Intervention Name(s)
Behavioral training
Other Intervention Name(s)
Behavioral treatment
Intervention Description
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.
Intervention Type
Drug
Intervention Name(s)
Oxybutynin chloride, extended-release
Other Intervention Name(s)
Antimuscarinic medication
Intervention Description
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.
Primary Outcome Measure Information:
Title
24-hour Voiding Frequency
Description
Mean voiding frequency per 24 hours derived from 7-day bladder dairy
Time Frame
post-treatment (week 8)
Secondary Outcome Measure Information:
Title
Change in Nocturia Frequency
Description
Change in frequency of nocturia episodes based on 7-day bladder diary
Time Frame
baseline to post-treatment (week 8)
Title
Change in Urgency Severity
Description
Indevus Urgency Severity Scale incorporated into the 7-day bladder diary. Scores for urgency severity ranged from 0 to 3: 0: None-no urgency Mild-awareness of urgency, but is easily tolerated. Moderate-enough urgency discomfort that it interferes with or shortens usual activity Severe-extreme urgency discomfort that abruptly stops all activities or tasks.
Time Frame
baseline to post-treatment (week 8)
Title
Percent Change in Frequency of Urge Incontinence
Description
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).
Time Frame
baseline to post-treatment (week 8)
Title
Change on American Urological Association (AUA) Symptom Index
Description
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.
Time Frame
baseline to post-treatment (week 8)
Title
Patient Global Perception of Improvement (GPI)
Description
Patient global perception of improvement ("much better" to "much worse")
Time Frame
post-treatment (week 8)
Title
Patient Satisfaction
Description
Patient global rating of satisfaction with progress in treatment ("completely satisfied" to "very dissatisfied")
Time Frame
post-treatment (week 8)
Title
Patient Global Rating of Activity Restriction
Description
Patient global rating of activity restriction ("not at all" to "all the time")
Time Frame
post-treatment (week 8)
Title
Patient Report of Symptom Distress
Description
Patient report of how disturbed they were by symptoms ("not at all" to "extremely")
Time Frame
post-treatment (week 8)
Title
Patient Global Rating of Bothersomeness of Side Effects
Description
Patient global rating of how bothersome their side effects were ("no side effects" to "extremely bothersome")
Time Frame
post-treatment (week 8)
Title
Patient Desire for Alternate Treatment
Description
Patient response to "Do you wish to receive another form of treatment?" (yes)
Time Frame
post-treatment (week 8)

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
19 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male Community-dwelling Veteran Self-reported urgency Self-reported frequent urination Mean of > 8 voids per 24-hour day on bladder diary Able to come to clinic 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Kathryn L. Burgio, PhD MA BA
Organizational Affiliation
Birmingham, Alabama VA Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Birmingham VA Medical Center
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Atlanta VA Medical and Rehab Center, Decatur
City
Decatur
State/Province
Georgia
ZIP/Postal Code
30033
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
22092152
Citation
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.
Results Reference
result
PubMed Identifier
23448285
Citation
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.
Results Reference
derived

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Behavioral Treatment of Overactive Bladder in Men

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