🇮🇪Ireland
16°C Partly Cloudy · Dublin
Live Updates
--:--:-- IST
Contributor sign in
Latest
Clinical Trials in Canada / NCT07427693
Active, not recruiting Not applicable

Usability, Acceptability and Effect of a Mobile Application and Connected Object for Older Women With UI

NCT07427693 · tracked via the Priya Life Science Canada tracker
Phase
Not applicable
Started
2025-01-13
Last updated
2026-02-23

Condition(s) studied

Urinary Incontinence (UI)Urinary Stress IncontinenceTelehealth

Investigational drug(s) / intervention(s)

Physiotherapy through mobile app and connected device

Physiotherapy through mobile app and connected device: Multimodal physiotherapy through the Oups! mobile app and connected device including pelvic floor muscle exercises 5x/week, an educational video 1x/week, and a motivational video 1x/week. The connected device allows instant feedback about the quality of their contractions and adjusts the goals for each exercise.

Study summary

This project aims to evaluate the usability, acceptability, and impact of the Oups! mobile app and a connected Bluetooth dynamometer for at-home PFM training to treat UI. The study will:

1. assess usability and participant feedback on the Oups! app, identifying improvements;
2. evaluate the usability and acceptability of the dynamometer during assessment and home practice, noting potential enhancements; and
3. measure the effects of the app and device on UI symptoms, quality of life, and PFM function post-treatment.

Eligibility

Sex
FEMALE
Min age
55 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Women * 55 years + * Stress or mixed UI symptoms with predominantly stress UI symptoms * At least 3 or more urinary leaks/week * Able to ambulate safely * Understand simple instruction in French, written and verbally * Basic understanding of how to use a tablet or mobile phone * Willing to participate in a gynecological exam * Able to properly contract the PFM * Provide informed consent. Exclusion Criteria: * Urge UI symptoms or mixed incontinence with primarily urgency * Neurological condition * Grade 3 or 4 of pelvic organ prolapse (POP) * Any other acute or chronic condition likely to interfere with the mobile app and/or connected object * Risk factors likely to interfere with the mobile app and/or connected object (i.e.: chronic constipation, chronic cough) * Medications that can interfere with the mobile app and/or connected object * Received UI treatments in the last year.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Women's Health and Aging Laboratory - CRIUGM Montreal Quebec

More Centre de Recherche de l'Institut Universitaire de Geriatrie de Montreal trials in Canada

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07427693 on ClinicalTrials.gov ↗ ← All trials in Canada