Chinese Herbal Medicine for Incontinence

JY
Overseen ByJohn Yang, Dr.
Age: 65+
Sex: Any
Trial Phase: Academic
Sponsor: Kwantlen Polytechnic University

What You Need to Know Before You Apply

What is the purpose of this trial?

This study aims to evaluate the effectiveness and safety of Chinese herbal medicine in improving urinary incontinence symptoms among older adults. Urinary incontinence is a common condition in aging populations that can significantly impact quality of life, yet existing treatments are often limited by side effects or insufficient efficacy.

The primary research question is whether a standardized Chinese herbal formula can reduce the frequency and severity of urinary incontinence compared to a placebo. We hypothesize that participants receiving the herbal intervention will demonstrate greater improvement in urinary symptoms and quality of life measures than those receiving placebo, without significant adverse effects.

To test this hypothesis, a randomized, double-blind, placebo-controlled clinical trial will be conducted. Eligible older adults will be randomly assigned to receive either the herbal treatment or a matched placebo over a defined study period. Outcomes will include validated measures of urinary incontinence severity, frequency of episodes, and patient-reported quality of life.

Potential benefits of this research include generating high-quality evidence on the effectiveness and safety of Chinese herbal medicine for urinary incontinence, which may inform clinical practice and expand treatment options for older adults. If effective, this intervention could offer a complementary or alternative approach with fewer side effects, contributing to improved symptom management and overall well-being in this population.

Are You a Good Fit for This Trial?

This trial is for older adults who have symptoms of urinary incontinence (leakage with coughing, sneezing, or urge), are able to understand and follow study instructions, can attend visits and fill out questionnaires, have stable health overall, and are not in another similar clinical trial.

Inclusion Criteria

I have symptoms of urinary incontinence confirmed by a doctor or screening test.
I understand the study and can give my consent to participate.
* Willing and able to comply with study requirements, including attending study visits, and completing questionnaires.
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Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Treatment

Participants receive either the Chinese herbal medicine or a placebo

4 weeks
Weekly visits (in-person)

Follow-up

Participants are monitored for safety and effectiveness after treatment

4 weeks

What Are the Treatments Tested in This Trial?

Interventions

  • Chinese Herbal Medicine (CHM) supplement

Trial Overview

The study compares a standardized Chinese herbal medicine supplement to a placebo. Participants are randomly assigned to one group without knowing which they receive. The goal is to see if the herbal treatment helps reduce urine leakage more than placebo.

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Placebo Group

Group I: Chinese Herbal InterventionExperimental Treatment1 Intervention
Group II: Control GroupPlacebo Group1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Kwantlen Polytechnic University

Lead Sponsor

Trials
3
Recruited
150+