Overactive Bladder Clinical Trial
Official title:
Yoga for Treatment of Overactive Bladder in Pediatric Patients
NCT number | NCT05895045 |
Other study ID # | Pro00112833 |
Secondary ID | |
Status | Recruiting |
Phase | N/A |
First received | |
Last updated | |
Start date | July 2024 |
Est. completion date | September 2024 |
Verified date | June 2024 |
Source | Duke University |
Contact | Rafael Tua-Caraccia, MD |
Phone | 7865546150 |
rdt25[@]duke.edu | |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The goal of this pilot study is to assess the impact of yoga as a treatment modality in pediatric patients age 8-18 diagnosed with idiopathic overactive bladder as measured by validated questionnaires and urinary biomarkers. The main question it aims to answer is: Does yoga help improve overactive bladder symptoms in this patient population? Participants will take part in a weekly yoga session for a total of 6 weeks with validated questionnaires and urinary samples for biomarkers to be completed at the beginning, middle and end of the study. This study will follow a cross-over study design and patients will receive standard of care while not in the active treatment arm.
Status | Recruiting |
Enrollment | 40 |
Est. completion date | September 2024 |
Est. primary completion date | September 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 8 Years to 18 Years |
Eligibility | Inclusion Criteria: - 8-18 years of age - History of non-neurogenic overactive bladder or detrusor overactivity and/or urinary incontinence (ICD 10 codes respectively - N32.81, N39.498) - Obtained legally effective informed consent and Health Insurance Portability and Accountability Act (HIPPA) authorization from the participant or the participant's parent/legal guardian - Minor participant is willing and able to provide assent (as applicable) - Vancouver Dysfunctional Elimination Syndrome[15] score of =11 and a positive modified bother score within 30 days of consent Exclusion Criteria: - Known or apparent untreated anatomical abnormality of lower urinary tract (i.e. untreated ureterocele) - Known neurogenic bladder (e.g., spina bifida, history of spinal cord injury, tethered cord) - Nerve damage that may impact pelvic floor function - History of chemodenervation of the bladder (e.g., via intravesical instillation or intradetrusor injection of botulinum toxin) - Active, untreated UTI at the time of enrollment (UTI undergoing active treatment is allowable) - Current or previous pregnancy at screening or planned pregnancy during the duration of the study, for females of childbearing potential - Any condition that, in the judgment of the investigator or treating clinician, precludes participation because it could affect participant safety |
Country | Name | City | State |
---|---|---|---|
United States | Duke University Hospital | Durham | North Carolina |
Lead Sponsor | Collaborator |
---|---|
Duke University |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in overactive bladder symptoms | Measured via Vancouver symptom score for Dysfunctional Elimination Syndrome with modified bother score (both parts of same survey assessment to be filled out). VDES score ranging from 5-65 with higher number representing worse symptoms; modified bother score ranges from 1-4 with 1= never bothered and 4= always bothered | 0, 6 and 12 weeks | |
Primary | Change in expression of nerve growth factor | nerve growth factor urinary biomarker via urine specimen collection | 0, 6 and 12 weeks | |
Primary | Change in expression of interleukin - 1B | Interleukin-1B urinary biomarker via urine specimen collection | 0, 6 and 12 weeks | |
Primary | Change in expression of tumor necrosis factor-alpha | tumor necrosis factor-alpha urinary biomarker via urine specimen collection | 0, 6 and 12 weeks |
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