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Pilot study to understand the impact of a digital health system, including a phone app and a vaginal probe to treat fecal incontinence in women
Subjects meeting inclusion/exclusion criteria at screening will complete training in behavioral therapy for the treatment of fecal incontinence and training in the use of the Leva pelvic digital health system.
Subjects will then participate in 10 weeks of at home pelvic floor muscle training using the leva device twice daily for 2 ½ minutes of training.
Adherence to the training protocol will be observed digitally, and subjects will receive phone calls every other week from research assistants reviewing their adherence.
Subjects are expected to participate in at least 80% of the weekly exercises (11 weekly).
Subjects will return to clinic at 5- and 10-weeks during the study to complete questionnaires. At 5-weeks, subjects will review the use of the device with the study assistant, who will answer any questions and repeat training if the subject desires additional training.
Following 10 weeks of training, subjects will be free to pursue any additional therapies, but will also retain the leva device and may continue its use if desired. Adherence will be monitored for one additional year, with follow up surveys to be completed by mail or digitally at 6- and 12-months
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Leva Arm | Experimental | Subjects will undergo training in the use of a vaginal device and its associated app, to be used twice daily to perform pelvic floor muscle exercises guided by the device/app for 10 weeks. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| leva | Device | Vaginal device used for pelvic floor muscle exercises |
|
| Measure | Description | Time Frame |
|---|---|---|
| St. Mark's Incontinence Score | Validated survey of fecal incontinence severity, score ranges from 0-24, Higher scores indicate more severe symptoms | Baseline to 10 weeks |
| Measure | Description | Time Frame |
|---|---|---|
| Change in Fecal incontinence episodes | Percent improvement= number of fecal incontinence episodes at 10 weeks divided by the number of incontinence epsiodes at baseline. | Baseline to 10 weeks |
| Fecal Incontinence Quality of Life Scale (FIQoL) |
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Inclusion Criteria:
Exclusion Criteria:
Subject must have a vagina
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| Name | Affiliation | Role |
|---|---|---|
| Holly Richter, MD PhD | University of Alabama at Birmingham | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Alabama | Birmingham | Alabama | 35233 | United States |
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| ID | Term |
|---|---|
| D005242 | Fecal Incontinence |
| ID | Term |
|---|---|
| D012002 | Rectal Diseases |
| D007410 | Intestinal Diseases |
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
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Validated Survey evaluates four areas- coping, depression, lifestyle and embarrassment. Each area is scored from 1-5. Higher numbers indicate more severe symptoms. Area scores are not combined
| Change in score from baseline to 10 weeks |
| Cumulative adherence correlation with change in St. Mark's score | Adherence as a percentage of all expected exercise sessions (140) correlation with change in St Mark's Incontinence Score (1-24) | baseline to 10 weeks |