CClinicalTrials.gg
TerminatedNCT00731315UTI-KioskUpdated Mar 6, 2015

Computer-Assisted Treatment of Urinary Tract Infection in Emergency Departments and Community Health Centers

An interventional study of Computer-assisted treatment group and Usual care group in Urinary Tract Infections, sponsored by University of California, San Francisco. Terminated at 5 sites in United States. Open to female participants aged 18 Years to 64 Years. Per ClinicalTrials.gov, last updated 2015-03-06.

Sponsored by University of California, San Francisco · Not applicable, Interventional, and Health services research

Why this study was terminated
Funding Period ended, did not reach full sample size due to limited numbers of eligible patients
Phase
Not applicable
Study type
Interventional
Enrollment
200
Allocation
Randomized
Ages
18 Years to 64 Years
Sex
Female
01

Study summary

Our study aims to test the utility of computer-assisted treatment for uncomplicated, recurrent urinary tract infections (UTIs) for women receiving care in safety net health care facilities. As of November 2009, we are also testing the utility of computer-assisted treatment for certain types of complicated cystitis (i.e. women with voiding symptoms and one of the following complicating symptoms: fever, flank pain, or symptoms greater than 7 days).

Read the detailed description

An English version of the UTI Kiosk module was validated at UCSF urgent care clinic in 2005, and has been successfully integrated into the clinical work flow at this clinic for over 2 years. The computer-based module is housed in a freestanding kiosk with a touch-screen monitor and audio handset to allow patients with low literacy and minimum computer skills to complete the module. A printer in the kiosk provides a summary of the patient's responses to each question in the module, as well as a prescription for the clinic physician to sign and return to the patient.

It's important to emphasize that the computer only "fast-tracks" women who will be treated with antibiotics. All other women see the provider as usual. Also, all women who are eligible for computer treatment may opt to see a provider instead.

02

Conditions studied

  • Urinary Tract Infections

Keywords

  • UTI
  • Kiosk
  • Computer Assisted Care
  • cystitis
03

In context

Infections

6,687 studies on the registry are indexed under Infections; 807 are open to participants now.

This study's enrollment of 200 is above the median of 120 across 4,200 interventional studies indexed under Infections.

Browse Infections studies →

Lead sponsor

University of California, San Francisco is the lead sponsor of 2,132 studies on the registry; 375 are open to participants now.

Of its 262 completed or terminated interventional studies of FDA-regulated products, 196 (75%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 64 Years
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  • Female
  • 18-64 years old

Exclusion criteria

Exclusion Criteria:

  • Below 18 or Above 64
  • Male
  • New flank pain
  • severe vomiting
  • High blood sugar or diabetes
  • surgery on kidneys
  • chronic kidney disease
  • Previous cancer or chemotherapy
  • HIV or AIDS
  • pregnant or suspected pregnancy
05

Study design

Phase
Not applicable
Primary purpose
Health services research
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Double (Participant, Outcomes assessor)
Enrollment
200 participants (actual)

Study arms

  • Experimental
    Treatment Group 1 - uncomplicated UTI

    Would receive computer-assisted treatment for a uncomplicated UTI.

    Other: Computer-assisted treatment group

  • Active comparator
    Control Group 1

    Qualified for expedited treatment for uncomplicated cystitis but would receive usual care in the Emergency Department of Community Health Center.

    Other: Usual care group

  • Experimental
    Treatment Group 2 - Complicated Cystitis

    Would receive expedited treatment for complicated cystitis with longer antibiotic course than the simple UTI patients.

    Other: Computer-assisted treatment group

  • Active comparator
    Control Group 2

    Qualified for expedited treatment for complicated cystitis treatment but would receive usual care in the clinic or emergency department.

    Other: Usual care group

Interventions

  • OtherComputer-assisted treatment group

    This group will receive computer-assisted expedited treatment for uncomplicated UTI or complicated cystitis based on their symptoms and past medical history reported on the computer.

  • OtherUsual care group

    This group will receive usual care for an uncomplicated UTI or complicated cystitis in the Emergency Department or Community Health Center.

06

What researchers measure

Primary outcomes

  1. The proportion of subjects with treatment failure or relapse

    Time frame: 21 days

Secondary outcomes

  1. Patient acceptability of treatment by computer

    Time frame: 21 days

07

Study locations

5 sites
  • CMC Fresno Emergency Department
    Fresno, California 93701, United States
  • La Clinica
    Oakland, California 94601, United States
  • Highland Hospital Emergency Department
    Oakland, California 94602, United States
  • San Francisco General Hospital - Emergency Department
    San Francisco, California 94110, United States
  • UCSF Emergency Deparmtent
    San Francisco, California 94143, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 6, 2015, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00731315
Lead sponsor
University of California, San Francisco
Responsible party
Sponsor
First posted
Aug 11, 2008
Start date
Aug 2008
Primary completion
Jul 2011
Completion
Jul 2011
Last update
Mar 6, 2015

Study contacts

Ralph Gonzales, MD
principal investigator · University of California, San Francsico
John Stein, MD
principal investigator · University of California, San Francisco
Bradley Frazee, MD
principal investigator · Alameda County Medical Centers, Highland Hospital

Oversight

Data monitoring committee
Yes
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is terminated, as verified in Mar 2015. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion