Actively Recruiting

Phase Not Applicable
Age: 40Years +
All Genders
Healthy Volunteers
ID07598227

Evaluation of the Efficacy and Safety of Acupoint Moxibustion for Nocturia: A Pilot Study

Led by Buddhist Tzu Chi General Hospital · Updated on 2026-05-20

100

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Nocturia, the condition of waking at night to urinate two or more times, can greatly reduce quality of life and emotional well-being. Some patients do not respond well to standard Western treatments or worry about their side effects, so many turn to Traditional Chinese Medicine (TCM) for other options. This research uses a randomized clinical trial to study the effects and safety of acupoint moxibustion as a potential treatment for nocturia. Participants will be randomly assigned to either receive moxibustion applied to specific acupoints or be in a control group with no intervention. The study will assess these groups over several weeks, measuring symptoms and quality of life. The trial aims to offer a cost-effective and practical complementary therapy by also analyzing patient characteristics with the Constitution in Chinese Medicine Questionnaire and abdominal muscle evaluations. During the study, participants will keep voiding diaries and complete several assessments including the International Prostate Symptom Score, Overactive Bladder Symptom Score, and Quality of Life questionnaires at the start, week 3, and week 6. Additionally, sleep quality and abdominal muscle properties will be measured at these times. The main outcomes focus on how often and how much participants urinate at night, with safety and symptom changes monitored throughout the 6-week period.

CONDITIONS

Brief Title

Moxibustion for Nocturia

Who Can Participate

Age: 40Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Patients aged 40 years or older.
  • Experiencing two or more nocturia episodes per night.
Not Eligible

You will not qualify if you...

  • Active urinary tract infection.
  • Poorly controlled diabetes mellitus (HbA1c > 6.5%).
  • Neurogenic bladder caused by multiple sclerosis, Parkinson's disease, stroke, spinal cord injury, or nerve damage from major pelvic surgery.
  • Severe congestive heart failure (NYHA functional class > II).
  • Use of other Traditional Chinese Medicine therapies for nocturia symptoms within the past 30 days.
  • Pregnant women.

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Treatment

Duration - 6 weeks

Participants receive acupoint moxibustion or are assigned to control to evaluate its effect on nocturia symptoms.

Visits at baseline, Week 3, and Week 6 for assessments

Trial Site Locations

Total: 1 location

1

Hualien Tzu Chi Hospital, Buddhist Tzu Chi Medical Foundation

Hualien City, Taiwan

Actively Recruiting

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Research Team

Y

Yen-Lun Kung

How is the study designed?

Study Type

INTERVENTIONAL

Masking

SINGLE

Allocation

RANDOMIZED

Model

PARALLEL

Primary Purpose

TREATMENT

Number of Arms

2

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