NCT05214131

Randomized Study Of Novel Enuresis Alarm vs Standard Bedwetting Alarm

Randomized Study Of Novel Enuresis Alarm (GoGoband® )Vs Standard Nocturnal Enuresis Alarm (SNEA)

• Status: Terminated
• Phase: N/A
• Study type: Interventional
• Enrollment: 16 (actual)
• Sponsor: Yale University · Academic / Other
• Sex: All
• Age: 6 Years – 21 Years
• Healthy volunteers: Accepted

Summary

Identify the dry night rate in patients using the GoGoband® nocturnal enuresis device vs a standard Pflaundler bedwetting alarm.

Detailed description

3.1 Problem Statement At the present time, there are no side-by-side comparison studies of GoGoband® vs SNEA. Since many of the prior studies were conducted using variable outcome parameters that makes direct comparisons of studies difficult it would be beneficial to obtain comparable data from the 2 groups and compare dry night rates for the 2 devices. 3.2 Purpose of Study/Potential Impact Our preliminary quality improvement data indicates that the GoGoband® is more efficacious than both medication and SNEA in an uncontrolled environment when deidentified data was analyzed off our servers. Our present database does not allow us to discern if patients are monosymptomatic nocturnal enuresis (MNE) or non monosymptomatic nocturnal enuresis (NMNE). Without this ability as well as for controlling for behavioral and academic problems which are known to affect outcomes in nocturnal enuresis studies, the investigators are not able to compare our results definitively and accurately to other treatment modalities. Hypothesis Our hypothesis is that the GoGoband® is more effective than SNEA and Desmopressin in the treatment of Nocturnal Enuresis Primary Objective The primary objective of this study is to determine whether the GoGoband®\] is as effective or more effective in comparison to children who use SNEA in a population of MNE patients with no underlying Attention deficit hyperactivity disorder (ADHD) in a 3 month period. Secondary Objectives To ascertain if familial incidence of nocturnal enuresis has an effect on outcomes 5.1 General Design Description The investigators propose the following study in patients who have been evaluated for primary nocturnal enuresis in our Yale New Haven Clinics. * All patients to be evaluated for nocturnal enuresis will undergo standard evaluation and initial treatment for nocturnal enuresis which includes: * Assessment Of Bowel Habits, * Fill Out A Questionnaire To Evaluate For Voiding Dysfunction * Treatment with routine bedwetting protocol of: 1. Stopping drinks 1 HR before bedtime, meals at least 3 hrs before bedtime, eliminating milk and ice cream from dinner and on, making sure that bowel movements are occurring 4 times per week and treating appropriately if necessary. 2. On return visit bedwetters and parents will be given the option of using medication , no further treatment, or alarm therapy. 3. If patients choose alarm therapy, they will be asked if they wish to participate in the Randomized study comparing GoGoband® vs SNEA. 4. Alarms will be provided to the patients free of cost to participants 5. Patients in the alarm group will be treated for 3 months continuously. 6. Patients in the SNEA group will record nightly if they wet their clothes and the report will be recorded and reviewed weekly 7. GoGoband® patients' data will be automatically saved on the HIPPA Compliant servers and subsequently reviewed at the end of the week.

Conditions

• Bedwetting
• Nocturnal Enuresis
• Urinary Incontinence

Interventions

Type	Name	Description
DEVICE	gogoband	use of biometric alarm to wake patient prior to wetting
DEVICE	SNEA group	standard bedwetting alarm is used to treat patients, alarm sounds after wetting accident has occurred

Timeline

• Start date: 2022-04-29
• Primary completion: 2025-06-13
• Completion: 2025-06-13
• First posted: 2022-01-28
• Last updated: 2026-03-09
• Results posted: 2026-03-09

Locations

1 site across 1 country: United States

Regulatory

• FDA-regulated device study