The Effect of Footwear Generated Biomechanical Manipulation on Symptoms of Stress Urinary Incontinence (SUI)
Primary Purpose
Pelvic Floor Disorders, Stress Urinary Incontinence
Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Footwear Generated Bio-Mechanical Manipulation (using shoes with pertupods) along with Traditional Pelvic Floor Therapy
Traditional Pelvic Floor Therapy
Sponsored by
About this trial
This is an interventional treatment trial for Pelvic Floor Disorders focused on measuring FGBMM, LPSE, UDI - 6, UIQ - 7
Eligibility Criteria
Inclusion Criteria:
- Stress or Mixed Urinary Incontinence, based on UDI-6.
- Females between the ages of 18-75 years.
- Weight less than 350 lbs.
- Ambulatory and active patients that can participate in a rehabilitation program that includes daily walking
- Able to walk at least 50 meters and scored positive on the STEADI test
- Able to understand, read and sign the informed consent form
- English or Spanish speaking
Exclusion Criteria:
- Prior surgery for incontinence
- Pelvic Floor Therapy within past 6 months.
- Currently pregnant
- Predominantly Urge Incontinence.
- Patients with more than 3 falls in the last 52 weeks, OR any balance related fall with an injury in the last 52 weeks.
- Patients exhibiting a lack of physical or mental ability to perform or comply with the study procedure.
- Patients with a history of pathological osteoporotic fracture
- Any major cardiovascular comorbidities prohibiting enrollment in an active exercise program
- Active heart disease (ischemia or heart failure admissions within 24 weeks) and Active COPD (exacerbation within 24 weeks)
- Active malignancies on ongoing treatment
- Patient with neurological gait pattern.
- Patient requiring assistive device during gait analysis.
Sites / Locations
- Montefiore Medical Center - Medical Park CampusesRecruiting
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Experimental
Arm Label
Traditional Pelvic Floor Therapy
FGBMM plus Traditional pelvic floor therapy
Arm Description
up to six sessions, with one session every alternate week.
Treatment with FGBMM using shoes with pertupods daily at home along with traditional pelvic floor therapy sessions.
Outcomes
Primary Outcome Measures
Severity of Stress Urinary Incontinence
Improvement in symptoms of Stress Urinary Incontinence (SUI) measured by Urinary Distress Inventory) UDI - 6 questionnaire
Secondary Outcome Measures
Quality of life
Assessed with a questionnaire Urinary Impact Questionnaire (UIQ-7)
Pelvic Floor Muscle Activity
Assessment of Pelvic Floor Muscle Activity by surface EMG (electromyography)
Gait assessment
Objective assessment of patient's gait measured by gait analysis equipment.
Adherence to treatment
Compliance to FGBMM and PFT using questionnaire.
6 minute walk test
objective assessment using maximum distance comfortably walked in 6 minutes on a 100 foot closed course
Medication costs
changes in medication costs assessed by patient interview
Healthcare utilization
Changes in healthcare facility utilization assessed by patient interview
Full Information
NCT ID
NCT03194789
First Posted
June 19, 2017
Last Updated
January 9, 2023
Sponsor
Montefiore Medical Center
Collaborators
Apos Medical and Sports Technology Ltd.
1. Study Identification
Unique Protocol Identification Number
NCT03194789
Brief Title
The Effect of Footwear Generated Biomechanical Manipulation on Symptoms of Stress Urinary Incontinence
Acronym
SUI
Official Title
The Effect of Footwear Generated Biomechanical Manipulation on Symptoms of Stress Urinary Incontinence
Study Type
Interventional
2. Study Status
Record Verification Date
January 2023
Overall Recruitment Status
Recruiting
Study Start Date
November 29, 2017 (Actual)
Primary Completion Date
January 9, 2024 (Anticipated)
Study Completion Date
January 9, 2024 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Montefiore Medical Center
Collaborators
Apos Medical and Sports Technology Ltd.
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
FGBMM (footwear generated biomechanical manipulation) effects neuromuscular patterns of pelvic muscles. While there have been no published studies to our knowledge investigating the effect of FGBMM on urinary incontinence, FGBMM causes perturbations in balance and gait that create dynamics similar to dynamic lumbosacral stabilization exercises. The investigators propose that FGBMM induces the same bio-mechanical improvements as LPSE (lumbopelvic stabilization exercises) which have shown benefit for incontinence. Instead of instructing patients to co-contract the lower trunk and pelvic floor muscles as commonly done for LPSE, the shoes used in FGBMM can be calibrated in a way that causes this co-contraction to occur without the patient realizing. Beneficial pelvis and spine positioning can also be accomplished by strategic placement of the pods without having to instruct the patient on complicated maneuvers. Capitalizing on the excellent adherence and clinical benefits of FGBMM on related conditions, the investigators propose to evaluate the effects of FGBMM in addition to pelvic floor therapy for improving the symptoms of stress urinary incontinence in an urban inner city population.
Detailed Description
FGBMM (footwear generated biomechanical manipulation) effects neuromuscular patterns of pelvic muscles. While there have been no published studies to our knowledge investigating the effect of FGBMM on urinary incontinence, FGBMM has been shown to cause perturbations in balance and gait that create dynamics similar to dynamic lumbosacral stabilization exercises. In support of this theory, although not published, one of the founders of the technique, Avi Elbaz, has noted anecdotal evidence that patients who had SUI (stress urinary incontinence) and underwent FGBMM for knee or low back pain reported improvement of incontinence. The investigators propose that FGBMM induces the same bio-mechanical improvements as LPSE (lumbopelvic stabilization exercises) which have shown benefit for incontinence. The pods on the footwear can be positioned to challenge the patients balance in a manner similar to the way trampolines are utilized in LPSE. Instead of instructing patients to co-contract the lower trunk and pelvic floor muscles as commonly done for LPSE, the shoes used in FGBMM can be calibrated in a way that causes this co-contraction to occur without the patient realizing. Beneficial pelvis and spine positioning can also be accomplished by strategic placement of the pods without having to instruct the patient on complicated maneuvers. An additional advantage of FGBMM is that this exercise is done with increased intra-abdominal pressure mimicking the condition and the setting when incontinence occurs rather than static exercise that is used in PFT. While performing regular activities, people are naturally squatting and doing other activities that increase intra-abdominal pressure. Furthermore, FGBMM is more practical for people with busy schedules because it can be accomplished with a much smaller time commitment from the patient than traditional PFT since it is done during normal activity. Capitalizing on the excellent adherence and clinical benefits of FGBMM on related conditions, the investigators propose to evaluate the effects of FGBMM in addition to pelvic floor therapy for improving the symptoms of stress urinary incontinence in an urban inner city population.
A potential use of FGBMM using shoes as a addition to traditional pelvic floor therapy may yield a more effective therapy with better adherence. Problems with traditional therapy include poor patient adherence (patients often do not complete the sessions and have poor adherence (about 50%), lack of the continuation in an ongoing program, leading to relapse and need for re treatment or even little clinical benefit. Additionally, access to pelvic floor therapy is limited for many patients since there are not enough available outpatient therapy services to meet the needs of all patients. Finding an additional exercise program that will increase adherence and improve patient outcomes with better clinical benefits is a high priority from both patient care and cost management perspectives.
FGBMM using shoes potentially overcomes many of these issues with improving/modifying abnormal biomechanics of pelvic floor muscles (therefore decreasing incontinence), and a home based exercise program utilizing footwear that causes exercise with normal activity by promoting perturbation. This bio-mechanical approach may significantly improve the symptoms of urinary incontinence in patients with Stress SUI or Mixed urinary incontinence. Capitalizing on the reported excellent adherence and clinical benefit of FGBMM in patients with related conditions, the investigators propose to evaluate the bio-mechanical exercise (wearing an appropriately calibrated shoe at home for a prescribed amount of time each day) as a conservative treatment that may supplement traditional pelvic floor therapy, medications and even surgical intervention for the same in an inner urban city population.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Pelvic Floor Disorders, Stress Urinary Incontinence
Keywords
FGBMM, LPSE, UDI - 6, UIQ - 7
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Single blinded (evaluator), single-center, randomized controlled trial Interventional and Control group.
Masking
Outcomes Assessor
Masking Description
Randomized single blinded (evaluator) controlled trial. The outcomes assessor will be masked in the study. Assessor will be independent of randomization, trial coordination and care providers.
Allocation
Randomized
Enrollment
64 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
Traditional Pelvic Floor Therapy
Arm Type
Active Comparator
Arm Description
up to six sessions, with one session every alternate week.
Arm Title
FGBMM plus Traditional pelvic floor therapy
Arm Type
Experimental
Arm Description
Treatment with FGBMM using shoes with pertupods daily at home along with traditional pelvic floor therapy sessions.
Intervention Type
Device
Intervention Name(s)
Footwear Generated Bio-Mechanical Manipulation (using shoes with pertupods) along with Traditional Pelvic Floor Therapy
Intervention Description
Participants will have FGBMM using shoes with pertupods along with traditional pelvic floor therapy over the course of six months. This will include five sessions of gait assessment and re-calibration with daily at home exercise with the device (shoes) over the course of six months. Along with that, participant will receive traditional pelvic floor therapy of six sessions, up-to one sessions every alternate week. This will involve exercise and modalities as decided by medical providers and therapists. Participants will also have a home exercise program prescribed along with each session and for the remainder of six months.
Intervention Type
Other
Intervention Name(s)
Traditional Pelvic Floor Therapy
Intervention Description
Participant will receive traditional pelvic floor therapy of six sessions, up-to one sessions every alternate week. This will involve exercise and modalities as decided by medical providers and therapists. Participants will also have a home exercise program prescribed along with each session and for the remainder of six months.
Primary Outcome Measure Information:
Title
Severity of Stress Urinary Incontinence
Description
Improvement in symptoms of Stress Urinary Incontinence (SUI) measured by Urinary Distress Inventory) UDI - 6 questionnaire
Time Frame
Six months
Secondary Outcome Measure Information:
Title
Quality of life
Description
Assessed with a questionnaire Urinary Impact Questionnaire (UIQ-7)
Time Frame
Six months
Title
Pelvic Floor Muscle Activity
Description
Assessment of Pelvic Floor Muscle Activity by surface EMG (electromyography)
Time Frame
Six months
Title
Gait assessment
Description
Objective assessment of patient's gait measured by gait analysis equipment.
Time Frame
Six months
Title
Adherence to treatment
Description
Compliance to FGBMM and PFT using questionnaire.
Time Frame
Six months
Title
6 minute walk test
Description
objective assessment using maximum distance comfortably walked in 6 minutes on a 100 foot closed course
Time Frame
Six months
Title
Medication costs
Description
changes in medication costs assessed by patient interview
Time Frame
six months
Title
Healthcare utilization
Description
Changes in healthcare facility utilization assessed by patient interview
Time Frame
six months
10. Eligibility
Sex
Female
Gender Based
Yes
Gender Eligibility Description
The investigators traditionally see stress urinary incontinence patients, most commonly females, in our clinics everyday. The investigators only have about one patient visit per month in our clinics as 'males with same disorder.' To get a significant number of male patients in our study with the same condition will need at least 7-10 years approximately.
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Stress or Mixed Urinary Incontinence, based on UDI-6.
Females between the ages of 18-75 years.
Weight less than 350 lbs.
Ambulatory and active patients that can participate in a rehabilitation program that includes daily walking
Able to walk at least 50 meters and scored positive on the STEADI test
Able to understand, read and sign the informed consent form
English or Spanish speaking
Exclusion Criteria:
Prior surgery for incontinence
Pelvic Floor Therapy within past 6 months.
Currently pregnant
Predominantly Urge Incontinence.
Patients with more than 3 falls in the last 52 weeks, OR any balance related fall with an injury in the last 52 weeks.
Patients exhibiting a lack of physical or mental ability to perform or comply with the study procedure.
Patients with a history of pathological osteoporotic fracture
Any major cardiovascular comorbidities prohibiting enrollment in an active exercise program
Active heart disease (ischemia or heart failure admissions within 24 weeks) and Active COPD (exacerbation within 24 weeks)
Active malignancies on ongoing treatment
Patient with neurological gait pattern.
Patient requiring assistive device during gait analysis.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Atira H. Kaplan, MD
Phone
917-331-0611
Email
akaplan@montefiore.org
First Name & Middle Initial & Last Name or Official Title & Degree
Anna M. Lasak, MD
Phone
718-920-9171
Email
alasak@montefiore.org
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Anna M. Lasak, MD
Organizational Affiliation
Montefiore Medical Center
Official's Role
Principal Investigator
Facility Information:
Facility Name
Montefiore Medical Center - Medical Park Campuses
City
Bronx
State/Province
New York
ZIP/Postal Code
10461
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Atira H. Kaplan, MD
Phone
917-331-0611
Email
akaplan@montefiore.org
First Name & Middle Initial & Last Name & Degree
Anna M. Lasak, MD
Phone
718-920-9171
Email
alasak@montefiore.org
12. IPD Sharing Statement
Plan to Share IPD
No
IPD Sharing Plan Description
Undecided about sharing the data.
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The Effect of Footwear Generated Biomechanical Manipulation on Symptoms of Stress Urinary Incontinence
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