Behavioral Therapy to Treat Urinary Symptoms in Parkinson Disease (BETTUR PD)
Primary Purpose
Urinary Incontinence, Nocturia
Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Exercise-based behavioral therapy
Behavioral control
Sponsored by
About this trial
This is an interventional treatment trial for Urinary Incontinence focused on measuring Parkinson disease, Incontinence
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of Parkinson's disease determined by a board-certified neurologist with specialty training in movement disorders
- ≥ 4 weekly episodes of UI and at least one episode per week associated with feelings of urgency, where urgency is defined as the complaint of a sudden compelling desire to void which is difficult to defer
- Willingness to attend clinic visits
- Willingness to keep 7-day bladder diaries throughout the study period
Exclusion Criteria:
- Significant cognitive impairment, as indicated by a Montreal Cognitive Assessment (MoCA) score of < 18.
- Inability to produce an interpretable 7-day bladder diary at baseline
- Previous intensive PFME training
- Clinically significant depression as measured by a Geriatric Depression Scale-Short Form score ≥ 10 which could affect motivation to fully engage in the intervention
- Use of an indwelling urinary catheter
- Bladder outlet obstruction defined as having been prescribed in-and-out catheterization in the past 12 months, having a post-void residual urine volume by bladder ultrasound of ≥ 200 mL or a peak voiding flow rate of ≤ 4 mL/min on a void ≥ 125 mL in volume
- Severe uterine prolapse past the vaginal introitus
- Poorly controlled diabetes defined by a hemoglobin A1c (HgbA1c) of >8.0%
- Chronic renal failure and on hemodialysis
- Poorly controlled congestive heart failure or poorly controlled chronic obstructive pulmonary disease on physical exam
- Genitourinary cancer with ongoing surgical or external beam radiation treatment
- Any unstable health condition expected to result in hospitalization or death within in the next 3 months as determined by principal investigator.
Sites / Locations
- Birmingham VAMC
- Atlanta VA Medical Center
Arms of the Study
Arm 1
Arm 2
Arm Type
Experimental
Placebo Comparator
Arm Label
Exercise-based behavioral therapy
Behavioral control
Arm Description
Pelvic floor muscle exercise-based behavioral therapy
Mirrored Star Drawing
Outcomes
Primary Outcome Measures
Bladder diary
Secondary Outcome Measures
Quality of Life Questionnaire
Full Information
NCT ID
NCT01520948
First Posted
January 26, 2012
Last Updated
January 8, 2018
Sponsor
Atlanta VA Medical Center
1. Study Identification
Unique Protocol Identification Number
NCT01520948
Brief Title
Behavioral Therapy to Treat Urinary Symptoms in Parkinson Disease
Acronym
BETTUR PD
Official Title
Behavioral Therapy to Treat Urinary Symptoms in Parkinson Disease
Study Type
Interventional
2. Study Status
Record Verification Date
January 2018
Overall Recruitment Status
Completed
Study Start Date
September 2012 (undefined)
Primary Completion Date
August 2017 (Actual)
Study Completion Date
August 2017 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Atlanta VA Medical Center
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
Parkinson's disease (PD) is a neurodegenerative disorder characterized by motor symptoms of tremor, slowness of movement, and stiffness, leading to progressive disability and loss of independence. Lower urinary tract symptoms (LUTS), including urinary incontinence (UI), urgency, and/or nocturia, are common non-motor symptoms that further diminish the already compromised quality of life for adults living with PD. Behavioral interventions for UI - including pelvic floor muscle exercise (PFME) therapy - have proven efficacy in randomized controlled trials and are free of side effects. Exercise-based behavioral therapy for UI requires individuals to learn a motor skill (PFME) and implement an adaptive behavioral strategy that incorporates the PFME to suppress urinary urgency and prevent UI.
We will conduct a two-site, randomized controlled trial to assess the efficacy of PFME-based behavioral therapy to treat urinary symptoms in adults with PD. After stratification by UI severity, PD severity, and gender, a group of 60 subjects (30 in each group) will be randomized to receive behavioral therapy or a behavioral control over 8 weeks in order to achieve a sample size of 50 individuals (25 in each group) who complete the study. A 6-month follow-up is planned in the treatment group.
We hypothesize that:
PD participants who are randomized to the exercise-based behavioral therapy group (Group A) will report a significant reduction in weekly frequency of UI episodes compared to PD participants in the behavioral control group (Group B). The primary outcome, frequency of UI, will be measured using a seven-day bladder diary.
Compared to PD participants in Group B, the reduction in UI frequency in Group A will be clinically meaningful as measured by a corresponding improvement on questionnaires of satisfaction and quality of life as well as a decline in other urinary symptoms including urgency and nocturia.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Urinary Incontinence, Nocturia
Keywords
Parkinson disease, Incontinence
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
53 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Exercise-based behavioral therapy
Arm Type
Experimental
Arm Description
Pelvic floor muscle exercise-based behavioral therapy
Arm Title
Behavioral control
Arm Type
Placebo Comparator
Arm Description
Mirrored Star Drawing
Intervention Type
Behavioral
Intervention Name(s)
Exercise-based behavioral therapy
Intervention Description
Pelvic floor muscle exercise training, bladder training, fluid management, constipation management
Intervention Type
Behavioral
Intervention Name(s)
Behavioral control
Intervention Description
Mirrored star drawing
Primary Outcome Measure Information:
Title
Bladder diary
Time Frame
1 week
Secondary Outcome Measure Information:
Title
Quality of Life Questionnaire
Time Frame
4 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Clinical diagnosis of Parkinson's disease determined by a board-certified neurologist with specialty training in movement disorders
≥ 4 weekly episodes of UI and at least one episode per week associated with feelings of urgency, where urgency is defined as the complaint of a sudden compelling desire to void which is difficult to defer
Willingness to attend clinic visits
Willingness to keep 7-day bladder diaries throughout the study period
Exclusion Criteria:
Significant cognitive impairment, as indicated by a Montreal Cognitive Assessment (MoCA) score of < 18.
Inability to produce an interpretable 7-day bladder diary at baseline
Previous intensive PFME training
Clinically significant depression as measured by a Geriatric Depression Scale-Short Form score ≥ 10 which could affect motivation to fully engage in the intervention
Use of an indwelling urinary catheter
Bladder outlet obstruction defined as having been prescribed in-and-out catheterization in the past 12 months, having a post-void residual urine volume by bladder ultrasound of ≥ 200 mL or a peak voiding flow rate of ≤ 4 mL/min on a void ≥ 125 mL in volume
Severe uterine prolapse past the vaginal introitus
Poorly controlled diabetes defined by a hemoglobin A1c (HgbA1c) of >8.0%
Chronic renal failure and on hemodialysis
Poorly controlled congestive heart failure or poorly controlled chronic obstructive pulmonary disease on physical exam
Genitourinary cancer with ongoing surgical or external beam radiation treatment
Any unstable health condition expected to result in hospitalization or death within in the next 3 months as determined by principal investigator.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
E. Camille Vaughan, MD, MS
Organizational Affiliation
Atlanta VAMC/Emory University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Birmingham VAMC
City
Birmingham
State/Province
Alabama
ZIP/Postal Code
35233
Country
United States
Facility Name
Atlanta VA Medical Center
City
Decatur
State/Province
Georgia
ZIP/Postal Code
30033
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Behavioral Therapy to Treat Urinary Symptoms in Parkinson Disease
We'll reach out to this number within 24 hrs