Stress Urinary Incontinence
Conditions
Brief summary
A virtual prospective randomized controlled study to evaluate the efficacy of using the leva® Pelvic Digital Health System (PDHS) to perform PFMT compared to a standard home exercise home program for the treatment of SUI/SMUI. The treatment part of the study lasts eight weeks and has two arms. One group will receive routine care consisting of at-home Kegel exercises, and the other will be provided with a leva® device and instructions for use. Subjects in both groups will be assessed at baseline, then at 4 and 8 weeks for change and improvement of their symptoms. They will also be assessed at 6 and12 months after study completion.
Detailed description
This trial is entirely virtual. No office visits, specific locations, or physical examination will be required. Enrollment may occur from any location in the United States * A virtual prospective randomized controlled study to evaluate the efficacy of using the leva® PDHS to perform PFMT (leva arm) compared to standard care of a PFM exercise home program (Kegel arm) for the treatment of SUI or SMUI. * Following completion of e-consent and screening, including an initial bladder diary and introductory phone call to review the study requirements, subjects are considered officially enrolled. * A series of baseline assessments will be administered to all subjects to evaluate symptom severity, frequency and impact. * Subjects will then be randomized to either the leva® arm or Kegel arm on a 1 to 1 ratio using block randomization. Prior to initiation of the trial, a randomization sequence will be generated by the ObvioHealth system. Participants will be automatically allocated the next available slot in the sequence at the time of their randomization and assigned to the leva® or Kegel group accordingly. * Prior to beginning the program, subjects in the Kegel arm will receive printed instructions for PFMT with Kegel exercises. Subjects in the leva® arm will be shipped the leva® digital device, along with instructions for use and how to download the corresponding digital app. Day 1 of the study begins the day following receipt of materials. * Study population: women with SUI or SMUI. * The study requires no office visits. All participant data will be entered in the subject's smartphone using a custom designed mobile application. Participants will be able to interact with the app throughout the study period and will be presented with surveys and a voiding diary on a specified schedule during an 8-week treatment period. There will also be expected post-intervention follow up surveys at 6- and 12-months * Using virtual recruiting, a total of up to 350 subjects will be enrolled in the trial. * Subjects in both arms will have three scheduled phone calls with study staff during the first two weeks of treatment. * Subjects can speak to the study staff at any time via an in-app chat function, the phone, or videoconference.
Interventions
DEVICELeva Pelvic Digital Health System
Pelvic floor muscle training using the pelvic digital health system to treat pelvic floor disorders, specifically stress urinary incontinence.
OTHERKegel exercises
Pelvic floor muscle training (PFMT), commonly referred to as Kegel exercises, is a first line conservative treatment for pelvic floor disorders, specifically stress urinary incontinence (SUI) or stress-predominant mixed urinary incontinence (SMUI).
Sponsors
OBVIO HEALTH USA, Inc.
University of Alabama at Birmingham
Renovia, Inc.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Investigator, Outcomes Assessor)
Masking description
Subjects will be randomized to either the leva® arm or Kegel arm on a 1 to 1 ratio using block randomization. Prior to initiation of the trial, a randomization sequence will be generated by the ObvioHealth system. Participants will be automatically allocated the next available slot in the sequence at the time of their randomization and assigned to the leva® or Kegel group accordingly
Intervention model description
A virtual prospective randomized controlled study to evaluate the efficacy of using the leva® PDHS to perform PFMT (leva arm) compared to standard care of a PFM exercise home program (Kegel arm) for the treatment of SUI or SMUI.
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 100 Years
Healthy volunteers
No
Inclusion criteria
* ≥18 years of age * Capable of giving informed consent * Possess a smartphone capable of interacting with the ObvioHealth and Renovia apps * Self-reported SUI/SMUI symptoms of ≥ three months duration * Diagnosis SMUI based on Medical, Epidemiologic and Social Aspects of Aging (MESA) stress symptom score (Percent of total possible stress score) greater than MESA urge symptom score (percent of total possible urge score) * English speaking * Postmenopausal, post hysterectomy, or willing to use an acceptable method of birth control for the duration of the study * Able to complete a bladder diary using the ObvioHealth app * Able to complete electronic surveys and upload data * Willing to provide contact information and respond to remote contact: phone calls, text messages, email * Willing to participate in the 8-week study with follow up at 6-and 12-months, refraining from the pursuit of treatment for Stress UI using other modalities (i.e. will not wear a pessary, participate in pelvic floor Physical Therapy or surgery) during the first 8 weeks
Exclusion criteria
* Absence of a vagina, per patient report * Reports seeing or feeling a vaginal bulge or sensation of vaginal bulge * Diagnosis of any neuromuscular disease that may contribute to UI (i.e., multiple sclerosis, spinal cord injury, Parkinson's Disease, etc.) * Non-ambulatory, per patient report * Currently pregnant or \<6 months post-partum per patient report * Currently (or within the last 1 month) breast feeding * Prior surgery for stress UI * Previous PFMT: 2 visits within the last 3 months under a supervised therapeutic plan of care * Currently taking, or has taken within the last 2 months, medication to treat UI * Prior augmentation cystoplasty or artificial sphincter * Implanted nerve stimulator for urinary symptoms, active within the past 60 days * Participation in another clinical study within 30 days of screening * Impaired cognitive function per patient report and evaluation of medication list * Contraindication to the use of a vaginal probe * Unable to understand instructions on the use of the leva® PDHS * Unable to operate a smartphone app with use of Bluetooth and Wi-Fi connectivity
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Efficacy - Urogenital Distress Inventory (UDI-6) | Baseline, 4 weeks, 8 weeks, 6 months and 12 months | UDI-6 is a validated questionnaire assessing symptom presence and degree of bother. It will be used to compare the degree of symptom change in the leva arm vs the Kegel arm within and between groups. |
| Efficacy - Bladder diaries | Baseline and 8 weeks | Bladder diaries evaluating the average number of stress-incontinence episodes in 3 days will be compared within and between groups |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Self-reported adherence | 4 weeks, 8 weeks | Visual Analog Score for self-reported adherence to the prescribed therapy, 0% = did not adhere to the prescribed treatment regimen/did not perform any Pelvic Floor exercises to 100% = adhered to the prescribed treatment regimen |
| Correlations between self-reported adherence and device reported adherence in the leva group | 4 weeks, 8 weeks | Self-reported adherence and Device-reported adherence in the Leva group will be correlated |
| Incidence of Treatment-Emergent Adverse Events (Safety and tolerability) | Through study completion, an average of 1 year | Monitored for adverse events and serious adverse events |
| Feedback on perception of treatment - likelihood of recommending to a friend | 4 weeks, 8 weeks | Visual Analog Score of likelihood of recommending to a friend Scale from 0-100%. 0%= Will not recommend to a friend to 100%=Will definitely recommend to a friend. |
| Feedback on perception of treatment - interest in surgical treatment | 4 weeks, 8 weeks | Visual Analog Score of interest in surgical treatment for urinary incontinence. Scale from 0-100%. 0%= Not interested at all in surgical treatment to 100%=Extremely interested in surgical treatment. |
| Survey evaluations of incontinence Pelvic Organ Prolapse Distress Inventory (POPDI-6) | Baseline, 4 weeks, 8 weeks, 6 months and 12 months | POPDI-6 to assess the impact that pelvic floor disorders have on the health related quality of life in women |
| Survey evaluations of incontinence Pelvic Floor Distress Inventory (PFDI-20) | Baseline, 4 weeks, 8 weeks, 6 months and 12 months | PFDI-20 to assess the impact that pelvic floor disorders have on the health related quality of life in women |
| Survey evaluations of incontinence Pelvic Organ Prolapse/Urinary Incontinence Sexual Questionnaire (PISQ-IR) | Baseline, 4 weeks, 8 weeks, 6 months and 12 months | PISQ-IR to assess the impact that pelvic floor disorders have on the health related quality of life in women |
| Survey evaluations of incontinence Patient Global Impression of Severity (PGI-S) | Baseline, 4 weeks, 8 weeks, 6 months and 12 months | PGI-S is the participants description of how their urinary tract condition is currently. |
| Survey evaluations of incontinence Patient Global Impression of Improvement (PGI-I) | 4 weeks, 8 weeks, 6 months and 12 months | PGI-I is the participants description on how their urinary symptoms are now, compared with how they were before they began the study. |
| Survey evaluations of incontinence Pelvic Floor Impact Questionnaire (PFIQ) | Baseline, 4 weeks, 8 weeks, 6 months and 12 months | PFIQ to assess the impact that pelvic floor disorders have on the health related quality of life in women |
| Survey evaluations of incontinence Colorectal-Anal Distress Inventory-8 (CRADI-8) | Baseline, 4 weeks, 8 weeks, 6 months and 12 months | CRADI-8 to assess the impact that pelvic floor disorders have on the health related quality of life in women |
| Patient Reported perception of general health Short Form-20 (SF-20) | Baseline, 4 weeks, 8 weeks, 6 months and 12 months | SF-20 survey on the participants perception of their general health. |
Countries
United States
Outcome results
None listed