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NCT Number: NCT07563764

Low-Energy Shock Wave Therapy for Overactive Bladder in Women With Metabolic Syndrome

Overactive bladder (OAB) is a common condition that causes urinary urgency, frequent urination, and nocturia, which can significantly affect quality of life. Women with metabolic syndrome may have a higher risk of OAB due to vascular and metabolic abnormalities.

This study aims to evaluate the effectiveness and safety of low-energy extracorporeal shock wave therapy (LiESWT), a non-invasive treatment, in women with metabolic syndrome-associated OAB. Participants will be randomly assigned to receive either active LiESWT treatment or a sham (inactive) procedure.

Symptoms and treatment outcomes will be assessed using validated questionnaires, including the Overactive Bladder Symptom Score (OABSS), International Consultation on Incontinence Questionnaire (ICIQ-SF), Urinary Distress Inventory (UDI-6), and Incontinence Impact Questionnaire (IIQ-7), as well as a voiding diary and uroflow measurements.

The results of this study may help determine whether LiESWT is an effective treatment option for improving OAB symptoms in this patient population.

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Key information

About this study

Overactive bladder (OAB) is a prevalent urological condition characterized by urinary urgency, frequency, and nocturia, which significantly impairs quality of life. Emerging evidence suggests a strong association between OAB and metabolic syndrome, which is characterized by insulin resistance, hypertension, dyslipidemia, and central obesity. These metabolic abnormalities may contribute to endothelial dysfunction, chronic inflammation, and autonomic dysregulation, potentially affecting bladder function.

Low-energy extracorporeal shock wave therapy (LiESWT) is a novel, non-invasive therapeutic modality that has been shown to promote angiogenesis, improve tissue perfusion, and modulate inflammatory responses. Previous studies have demonstrated its potential benefits in various urological conditions.

This study is designed as a randomized, double-blind, sham-controlled trial to evaluate the efficacy and safety of LiESWT in women with metabolic syndrome-associated OAB. Participants are randomly assigned to receive either LiESWT treatment or a sham procedure.

Clinical outcomes are assessed using validated patient-reported outcome measures, including OABSS, ICIQ-SF, UDI-6, and IIQ-7, along with objective parameters such as uroflowmetry and post-void residual volume. Assessments are performed at baseline and at multiple follow-up time points after treatment.

This study aims to provide clinical evidence on the therapeutic role of LiESWT in improving symptoms and quality of life in this specific patient population.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion:

  • Female participants aged 20 to 75 years
  • Diagnosed with overactive bladder (OAB), defined as urinary frequency (≥8 times/day), nocturia (≥2 times/night), and urgency (≥2 episodes/week) for at least 3 months
  • Diagnosed with metabolic syndrome, defined by the presence of at least three of the following criteria:
  • Waist circumference ≥80 cm
  • Blood pressure ≥130/85 mmHg or receiving antihypertensive treatment
  • Fasting glucose ≥100 mg/dL or receiving treatment for diabetes
  • Triglycerides ≥150 mg/dL or receiving lipid-lowering treatment
  • High-density lipoprotein cholesterol <50 mg/dL
  • No pharmacological or injection treatment for OAB within 3 months prior to enrollment
  • Able to understand and comply with study procedures and questionnaires
  • Willing to provide informed consent

Exclusion:

  • History of kidney stones or bladder stones
  • Urinary tract infection within 3 months prior to enrollment or recurrent urinary tract infections (≥3 episodes)
  • Lower urinary tract surgery within 6 months prior to enrollment
  • Known or suspected malignancy of the urinary tract
  • Significant bladder outlet obstruction
  • Severe coagulopathy, liver failure, or renal failure
  • Prior pelvic malignancy or pelvic radiation therapy
  • Intravesical injection or electrical stimulation therapy within the past year
  • Substance abuse (drug or alcohol) within the past year
  • Chronic pelvic pain due to other causes
  • Inability to complete study questionnaires or procedures

Treatment and study plan

Low-Energy Extracorporeal Shock Wave Therapy (LiESWT)

Device

LiESWT is delivered using a focused shock wave device at an energy flux density of 0.25 mJ/mm², frequency of 3 Hz, and 3,000 pulses per session.

Sham Shock Wave Therapy

Device

The device is applied in the same manner as the active treatment but does not emit therapeutic shock wave energy.

Primary outcomes

  1. Change in Overactive Bladder Symptom Score (OABSS)

    Time frame: Baseline to 24 weeks

    The Overactive Bladder Symptom Score (OABSS; range 0-15, with higher scores indicating more severe symptoms) will be used. The primary outcome is the change in OABSS from baseline to 4, 8, 12, 16, 20, 24 weeks after treatment. Lower scores indicate improvement in symptoms.

Secondary outcomes

  1. Change in International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF)

    Time frame: Baseline to 24 weeks

    The International Consultation on Incontinence Questionnaire-Short Form (ICIQ-SF; range 0-21, higher scores indicate worse symptoms).

  2. Change in Urinary Distress Inventory (UDI-6)

    Time frame: Baseline to 24 weeks

    The Urinary Distress Inventory-6 (UDI-6; range 0-100, higher scores indicate greater symptom distress).

  3. Change in maximum urinary flow rate measured by uroflowmetry (Qmax)

    Time frame: Baseline to 24 weeks

    Maximum urinary flow rate (Qmax, mL/s) will be assessed using standard uroflowmetry. Higher values indicate improved urinary flow function.

  4. Change in post-void residual volume measured by bladder ultrasound (PVR)

    Time frame: Baseline to 24 weeks

    Post-void residual (PVR, mL) will be measured using bladder ultrasound immediately after voiding. Lower values indicate improved bladder emptying.

  5. Change in voided volume per micturition assessed by 3-day voiding diary

    Time frame: Baseline to 24 weeks

    Voided volume (mL) will be calculated from a 3-day voiding diary. Higher values indicate improved bladder capacity.

  6. Change in total daily urine volume assessed by 3-day voiding diary

    Time frame: Baseline to 24 weeks

    Total urine volume (mL/day) will be calculated from a 3-day voiding diary.

  7. change in Incontinence Impact Questionnaire short version (IIQ-7)

    Time frame: Baseline to 24 weeks

    The IIQ-7 uses a 0-3 scale to measure how urinary incontinence impacts household chores, physical recreation, entertainment, travel, social activities, emotional health, and feelings of frustration to determine an overall quality-of-life score.

Other outcomes

  1. Incidence of treatment-related adverse events

    Time frame: Baseline to 24 weeks

    Adverse events will be recorded throughout the study period and classified according to severity and relationship to treatment.

Study contacts

Contact information is provided by the study sponsor or research team.

JIUNHUNG GENG, MD

CONTACT

[email protected]

+88673121101 ext.6694

Yung-Chin Lee, MD, PHD

CONTACT

[email protected]

+88673121101 ext.6694

Sponsors and collaborators

Lead sponsor

KMUHIRB-F(I)-20230051

Other

Registry information

Official study title

A Randomized, Double-Blind, Sham-Controlled Trial of Low-Energy Extracorporeal Shock Wave Therapy for Overactive Bladder in Women With Metabolic Syndrome

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
May 4, 2026
Registry last updated
May 4, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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