search
Back to results

Conservative Treatment of Postprostatectomy Incontinence

Primary Purpose

Urinary Incontinence

Status
Completed
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Behavioral Therapy
Pelvic Floor Electrical Stimulation
Biofeedback
No Treatment
Sponsored by
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Urinary Incontinence focused on measuring urinary incontinence, therapy, prostatectomy, prostate cancer

Eligibility Criteria

undefined - undefined (Child, Adult, Older Adult)MaleAccepts Healthy Volunteers

Inclusion Criteria: Involuntary loss of urine that started immediately after radical prostatectomy and has persisted for at least one year. One-week bladder diary with interpretable data and at least two incontinence episodes Exclusion Criteria: Any unstable medical condition, particularly decompensated congestive heart failure, history of malignant arrhythmias, or unstable angina Cardiac pacemaker or implanted cardiac defibrillator Current use of anticholinergic agents for detrusor instability Folstein's Mini-Mental State Exam score below 24 (impaired mental status) One-week bladder diary with continual leakage - defined as always being damp or wet or unable to quantitate individual accidents. Poorly controlled diabetes, defined as (glycosylated hemoglobin > 9 within last 3 months). Hematuria on microscopic examination. Enrollment will be permitted after urologic evaluation. Urodynamic evaluation: Post-void residual volume greater than 200 mL

Sites / Locations

  • University of Alabama at Birmingham

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Placebo Comparator

Arm Label

Behavioral Therapy

Behavioral Therapy Plus Technologies

Placebo Comparator

Arm Description

Behavioral Therapy (Pelvic floor muscle training, bladder control strategies)

Behavioral therapy plus technologies (home pelvic floor electrical stimulation and biofeedback)

No treatment control

Outcomes

Primary Outcome Measures

Percent Change in Incontinence Episodes on Bladder Diary
[(Baseline incontinence episodes minus 2-month incontinence episodes)/baseline incontinence episodes] x 100%
Percent Change in Incontinence Episodes Per Week on Bladder Diary
[(Baseline incontinence episodes minus 12-month incontinence episodes)/baseline incontinence episodes] x 100%

Secondary Outcome Measures

Full Information

First Posted
September 13, 2005
Last Updated
March 21, 2016
Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)
search

1. Study Identification

Unique Protocol Identification Number
NCT00212264
Brief Title
Conservative Treatment of Postprostatectomy Incontinence
Official Title
Conservative Treatment of Postprostatectomy Incontinence
Study Type
Interventional

2. Study Status

Record Verification Date
March 2016
Overall Recruitment Status
Completed
Study Start Date
August 2003 (undefined)
Primary Completion Date
September 2008 (Actual)
Study Completion Date
August 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
National Institute of Diabetes and Digestive and Kidney Diseases (NIDDK)

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary purpose of this study is to test the effectiveness, impact on quality of life, and durability of non-surgical therapies for incontinence persisting at least one year after surgery. The study is a a prospective, controlled, randomized trial comparing an 8-week, multi-component behavioral training program (pelvic floor muscle exercises, self-monitoring with bladder diaries, regular office visits, bladder control techniques, and fluid management) to the same program with the addition of biofeedback and pelvic muscle electrical stimulation.
Detailed Description
The primary purpose of this project is to test the effectiveness, impact on quality of life, and durability of conservative therapies for persistent post-prostatectomy urinary incontinence in a prospective, controlled, randomized trial comparing an 8-week, multi-component behavioral training program (pelvic floor muscle exercises, self-monitoring with bladder diaries, regular office visits, bladder control techniques, and fluid management) to the same program with the addition of biofeedback and pelvic muscle electrical stimulation. The second purpose of the study is to examine and compare the cost-effectiveness of the 8-week, multi-component behavioral training program to the same program with the addition of biofeedback and pelvic floor electrical stimulation. Prostate cancer is the most common internal cancer in men in the United States. The most common treatment for early disease is radical prostatectomy, the removal of the prostate gland. The two most common sequelae of prostatectomy are incontinence and erectile dysfunction. The incontinence improves and often resolves in the first year after prostatectomy, but surveys of patients show that 40% of men have incontinence severe enough to require pads 1 and 2 years after their surgery. There are currently no randomized, controlled studies of non-surgical treatments for persistent post-prostatectomy incontinence.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence
Keywords
urinary incontinence, therapy, prostatectomy, prostate cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
208 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Behavioral Therapy
Arm Type
Experimental
Arm Description
Behavioral Therapy (Pelvic floor muscle training, bladder control strategies)
Arm Title
Behavioral Therapy Plus Technologies
Arm Type
Experimental
Arm Description
Behavioral therapy plus technologies (home pelvic floor electrical stimulation and biofeedback)
Arm Title
Placebo Comparator
Arm Type
Placebo Comparator
Arm Description
No treatment control
Intervention Type
Behavioral
Intervention Name(s)
Behavioral Therapy
Intervention Description
Pelvic Floor Muscle Exercises and Bladder control strategies
Intervention Type
Device
Intervention Name(s)
Pelvic Floor Electrical Stimulation
Intervention Description
Pelvic Floor Electrical Stimulation daily for 8 weeks
Intervention Type
Behavioral
Intervention Name(s)
Biofeedback
Intervention Description
Pelvic Floor Muscle training via biofeedback
Intervention Type
Other
Intervention Name(s)
No Treatment
Intervention Description
No treatment
Primary Outcome Measure Information:
Title
Percent Change in Incontinence Episodes on Bladder Diary
Description
[(Baseline incontinence episodes minus 2-month incontinence episodes)/baseline incontinence episodes] x 100%
Time Frame
2 months
Title
Percent Change in Incontinence Episodes Per Week on Bladder Diary
Description
[(Baseline incontinence episodes minus 12-month incontinence episodes)/baseline incontinence episodes] x 100%
Time Frame
1 year

10. Eligibility

Sex
Male
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Involuntary loss of urine that started immediately after radical prostatectomy and has persisted for at least one year. One-week bladder diary with interpretable data and at least two incontinence episodes Exclusion Criteria: Any unstable medical condition, particularly decompensated congestive heart failure, history of malignant arrhythmias, or unstable angina Cardiac pacemaker or implanted cardiac defibrillator Current use of anticholinergic agents for detrusor instability Folstein's Mini-Mental State Exam score below 24 (impaired mental status) One-week bladder diary with continual leakage - defined as always being damp or wet or unable to quantitate individual accidents. Poorly controlled diabetes, defined as (glycosylated hemoglobin > 9 within last 3 months). Hematuria on microscopic examination. Enrollment will be permitted after urologic evaluation. Urodynamic evaluation: Post-void residual volume greater than 200 mL
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patricia S Goode, MD
Organizational Affiliation
University of Alabama at Birmingham
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of Alabama at Birmingham
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35294
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
21224456
Citation
Goode PS, Burgio KL, Johnson TM 2nd, Clay OJ, Roth DL, Markland AD, Burkhardt JH, Issa MM, Lloyd LK. Behavioral therapy with or without biofeedback and pelvic floor electrical stimulation for persistent postprostatectomy incontinence: a randomized controlled trial. JAMA. 2011 Jan 12;305(2):151-9. doi: 10.1001/jama.2010.1972.
Results Reference
result

Learn more about this trial

Conservative Treatment of Postprostatectomy Incontinence

We'll reach out to this number within 24 hrs