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Feasibility study of bladder training app and urination prediction device for women having symptoms of urinary urgency or urine leakage

Not Applicable
Conditions
urinary incontinence, Overactive bladder
Registration Number
JPRN-UMIN000051659
Lead Sponsor
Save Medical Corporation
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up continuing
Sex
Female
Target Recruitment
10
Inclusion Criteria

Not provided

Exclusion Criteria

1)Participants who have hematuria 2)Participants who have discomfort or pain associated with urination 3)Participants who have a residual urine 4)Participants who are taking medication for overactive bladder 5)Participants with a history of pelvic surgery or radiation therapy 6)Participants with a history of neurological disease 7)Participants who are using estrogen preparations 8)Participants with the following diseases (diabetes, spina bifida, uterine fibroids, severe constipation, peripheral neuropathy) 9)Pregnant participants 10)Participants who are using implantable medical devices (pacemakers, defibrillators, etc.) 11)Participants whose records of DFree did not reach zero after urinating during the observation period 12)Participants who are considered as inappropriate for this study by the research collaborating physician

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Change from baseline (observation period) in average daily frequency of urination at 8 weeks of treatment period
Secondary Outcome Measures
NameTimeMethod
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