Community-Based Digital and Behavioral Management for Nocturia in Older Adults
Led by National Taiwan University Hospital · Updated on 2026-07-29
50
Participants Needed
1
Research Sites
26 weeks
Total Duration
AI-Summary
What this Trial Is About
Nocturia, a common and troubling condition among older adults in Taiwan, often disrupts sleep quality and affects mental health while increasing the risk of falls. This research evaluates a new community-based approach that combines digital health technology and behavioral therapy to manage nocturia in people aged 55 and older who experience two or more nighttime voids. The goal is to reduce nocturnal voiding frequency, improve quality of life, and explore reducing medication reliance.
Participants are divided into two groups. The intervention group uses a non-contact home uroflowmetry device and a voiding diary to track urinary patterns, receiving real-time feedback. They also get personalized lifestyle advice such as fluid restriction and leg elevation, alongside psychiatric screening for sleep and mood disorders. The control group receives general health education and follow-up without these devices or personalized interventions.
Throughout the study, participants record their voiding habits for 2-3 consecutive days monthly over six months. Researchers assess nocturnal void frequency, sleep quality, mental health, anxiety, quality of life, and fall or emergency events at the start, three months, and six months after randomization. This comprehensive monitoring helps evaluate the effectiveness of the community-based management model integrating digital tools and behavioral support.
CONDITIONS
Brief Title
A Community-based Solution for Nocturia: Integrating Digital Technology and Behavioral Interventions
Research Team
S
Shuai-Wen Wang
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Baseline nocturia frequency of 2 or more times per night (confirmed by report or questionnaire)
Ability to operate a smartphone app or have caregiver assistance with electronic urinary diary
Age 55 years or older
You will not qualify if you...
Acute urinary tract infection
Uncontrolled heart failure
Serum sodium level below 130 mEq/L
Urological surgery within the past three months
Active major psychiatric or neurological disorder (GDS-15 score above 5)
Participation in other nocturia-related clinical trials
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person or remote)
Treatment
Duration - 6 months
Participants are randomly assigned to either the intervention group using digital tracking devices and personalized lifestyle guidance or the control group receiving general health education and follow-up.
Monthly visits for diary recording and assessments at baseline, 3 months, and 6 months
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
TREATMENT
Number of Arms
2
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Published Research Related To This Trial
An Emerging Trend of At-Home Uroflowmetry-Designing a New Vibration-Based Uroflowmeter with Artificial Intelligence Pattern Recognition of Uroflow Curves and Comparing with Other Technologies.
Vincent F S Tsai, Yao-Chou Tsai, Stephen S D Yang...