Evaluating the AI-Supporter Robot to Reduce Urinary Tract Infections, Skin Problems, and Caregiver Burden in Women with Incontinence
Led by China Medical University Hospital · Updated on 2024-09-26
60
Participants Needed
1
Research Sites
N/A
Total Duration
AI-Summary
What this Trial Is About
Researchers are evaluating the effectiveness of the AI Supporter, an intelligent robot designed to manage excretion for incontinent patients. This study focuses on female patients who have been bedridden for more than three months and have urinary andor fecal incontinence. The goal is to determine if using this AI-driven device can reduce the rates of urinary tract infections and incontinence-associated dermatitis while also exploring cost savings and caregiver burden reduction.
The AI Supporter uses artificial intelligence-based vision recognition to detect urine and feces autonomously, then cleanses, dries, and changes the diaper without the need for caregiver intervention. Participants are randomly assigned to either the AI Supporter group or the traditional diaper care group. The intervention lasts for 14 days during which participants intermittently use the AI Supporter. Data such as excretion timing, frequency, and weight are recorded for analysis.
During the study, participants will undergo routine urine analysis and assessments of incontinence-associated dermatitis, pressure sores, and skin pH. Researchers will also track caregiver hours and costs related to both diapers and the AI Supporter device. The primary outcomes measured are white blood cell count and bacterial count in urine 14 days after intervention. The study is conducted under single masking and uses statistical methods to evaluate outcomes with significance set at p < 0.05.
CONDITIONS
Brief Title
Effectiveness of the AI-Supporter in Reducing Urinary Tract Infections
Research Team
K
Kwo-Chen Lee, ph.D
J
Jing-ya Fu
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Participants with urinary and/or fecal incontinence
Participants able to wear the AI-supporter device during the study period
You will not qualify if you...
Participants with severe skin conditions unrelated to incontinence
Participants with current urinary tract infections or incontinence-associated dermatitis at enrollment
Participants unable to provide informed consent or without a legal representative to do so
Your Study Journey
Screening
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Implementation
Duration - 14 days
Participants use the AI-supporter device which autonomously detects and cleanses affected areas to reduce urinary tract infections and incontinence-associated dermatitis.
Intermittent use over 14 days
How is the study designed?
Study Type
INTERVENTIONAL
Masking
SINGLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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