Texting away UTIs: could a phone platform cut unnecessary antibiotics?
NCT ID NCT06035601
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This trial tests whether an EHR-integrated texting platform, called Urotrust, can help women with recurrent urinary tract infections (UTIs) manage their condition better than usual care. The platform provides symptom triage, clinical guidance, and prevention education via text messages, along with standing orders for urine tests. The main goal is to see if it reduces unnecessary antibiotic prescriptions, while also improving patients' confidence in managing their UTIs. Participants are women aged 18 and older who receive care at Penn Urogynecology or Penn Urology and own a mobile phone with texting.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- EHR-integrated texting platform (Urotrust) providing symptom triage, prevention education, and standing orders for urine tests
- What this could lead to
- If effective, this platform could reduce unnecessary antibiotic use and empower women to better manage recurrent UTIs, potentially lowering healthcare costs and antibiotic resistance.
- What could go wrong
- This is a relatively small trial, and the platform's success depends on user engagement and adherence. It may not generalize to all populations or healthcare settings.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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102 people
The number who actually took part.
- Started
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Mar 2024
- Finished
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May 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 100 years
- Sex
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Female participants only
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Provision of signed and dated informed consent form 2. Stated willingness to comply with all study procedures and availability for the duration of the study 3. Females who currently meet the criteria for recurrent UTIs 4. Age 18 years or older 5. Owns a mobile device with text messaging capability 6. Ability to read and write English 7. Currently receiving care from a provider in Penn Urogynecology or Penn Urology Exclusion criteria: 1. History of known multidrug resistant UTIs 2. History of interstitial cystitis/bladder pain syndrome or current diagnosis of chronic pelvic pain 3. On continuous suppressive antibiotics currently 4. Currently pregnant or within 6 weeks of pregnancy 5. Transplant patient on immunosuppressive medication currently 6. Practice of chronic self-catheterization
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
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