Yoga for Treatment of Overactive Bladder in Pediatric Patients

NCT ID: NCT05895045

Last Updated: 2025-05-06

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Clinical Phase

NA

Total Enrollment

40 participants

Study Classification

INTERVENTIONAL

Study Start Date

2025-06-30

Study Completion Date

2025-09-30

Brief Summary

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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.

Detailed Description

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Detrusor overactivity, otherwise known as overactive bladder (OAB) is the most common disease of voiding dysfunction in children and is characterized by urgency with or without incontinence. Current understanding of OAB suggests that it is a component of central sensitization whereby the central nervous system is in a persistent state of high reactivity. In this state, patients have lower thresholds for pain and for normal physiologic signals such as the sensation of bladder fullness. Yoga has been shown to favor parasympathetic output and appears to be effective in reversing central sensitization for patients with chronic pain. Further, both central sensitization and OAB have been associated with inflammation and so observation of urinary markers of inflammation allow an objective measurement, along with subjective symptom reporting, to measure treatment effects. Children with OAB are likely to become adults with similar urinary complaints and are also more likely to have anxiety, depression and other problems throughout development and maturation. Treatment for OAB in children is comprised of first conservative management with behavioral therapies including biofeedback, subsequent addition of pharmacologic treatment options and finally more invasive therapies including intradetrusor botulinum toxin injections and neuromodulation.

Yoga has been shown to have some positive health benefits in pediatric patients with pulmonary dysfunction, epilepsy, anxiety/depression and even in pediatric oncology patients with regards to quality of life during treatment. Additionally, yoga has been assessed as an adjunctive therapy for the treatment of urinary incontinence and overactive bladder in predominantly adult female populations. That said, to date there have been no studies assessing the impact of yoga on detrusor overactivity in pediatric patient populations (\< 19 years old). This is a pilot study in which the investigators hypothesize that yoga will lead to improved quality of life, reduced urinary symptoms and reduced expression of inflammatory urinary biomarkers.

Conditions

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Overactive Bladder Overactive Bladder Syndrome Overactive Detrusor

Study Design

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Allocation Method

NON_RANDOMIZED

Intervention Model

CROSSOVER

The study will start with two treatment arms. Arm 1 will receive standard behavioral modification and possible pharmacologic intervention for six weeks without other intervention. Arm 2 will receive the same therapies in addition to participating in a weekly yoga session for six weeks. At six weeks, arms 1 and 2 we will switch intervention - Arm 1 will then initiate a weekly yoga session for six weeks with emphasis on the pelvic floor relaxation while Arm 2 will continue with standard behavioral / pharmacologic therapy.

Patients will be divided into two separate yoga groups based on age. The first group will be comprised of 8-12-year-old and the second group will be comprised of 13 - 18-year-old. These will be divided within each treatment arm (i.e Arm 1.1 and 1.2) and the interventions will remain the same.
Primary Study Purpose

TREATMENT

Blinding Strategy

SINGLE

Caregivers

Study Groups

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1.1: 8-12 yoga first

Group Type EXPERIMENTAL

Yoga

Intervention Type BEHAVIORAL

Restorative Vinyasa Yoga

1.2: 13-18 yoga first

Group Type EXPERIMENTAL

Yoga

Intervention Type BEHAVIORAL

Restorative Vinyasa Yoga

2.1: 8-12 yoga second

Group Type EXPERIMENTAL

Yoga

Intervention Type BEHAVIORAL

Restorative Vinyasa Yoga

2.2: 13-18 yoga second

Group Type EXPERIMENTAL

Yoga

Intervention Type BEHAVIORAL

Restorative Vinyasa Yoga

Interventions

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Yoga

Restorative Vinyasa Yoga

Intervention Type BEHAVIORAL

Eligibility Criteria

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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
Minimum Eligible Age

8 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Duke University

OTHER

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Locations

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Duke University Hospital

Durham, North Carolina, United States

Site Status RECRUITING

Countries

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United States

Central Contacts

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Rafael Tua-Caraccia, MD

Role: CONTACT

7865546150

Jonathan Routh, MD, MPH

Role: CONTACT

(919) 684-6994

Facility Contacts

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Jonathan Routh, MD, MPH

Role: primary

919-684-6994

Other Identifiers

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Pro00112833

Identifier Type: -

Identifier Source: org_study_id

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