New program empowers veterans to skip unneeded antibiotics
NCT ID NCT07430904
First seen Jun 27, 2026 · Last updated Aug 20, 2026 · Updated 4 times
Summary
This study tests a patient empowerment program for veterans with spinal cord injury and neurogenic bladder who have had at least one urinary tract infection in the past year. The program provides training and tools to help them recognize when antibiotics are not needed and advocate for themselves with their healthcare providers. The goal is to reduce unnecessary antibiotic use and improve quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Empowerment Program (behavioral intervention)
- What this could lead to
- If it works, this program could help veterans with spinal cord injury avoid unnecessary antibiotics and improve their quality of life.
- What could go wrong
- This is a very small, early-stage study with only 30 participants, so results may not apply widely. The program relies on patient engagement, which may vary.
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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About 30 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2027
An estimate. Start dates often move.
- Expected to finish
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Jun 2032
An estimate. End dates often move.
- Lead sponsor
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A government agency
The lead sponsor is a US federal agency other than the NIH.
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 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Veterans with SCI/D and neurogenic bladders who have been treated for at least one UTI in the past year * Have access to a telephone * Have not been involved in the development phase of the program Exclusion Criteria: * Non-Veterans * Veterans without SCI/D or neurogenic bladder * Patients with dementia who would not be able to provide consent or respond to interview prompts * Patients who do not receive primary care at the MEDVAMC * Veterans who participated in the development of the empowerment program
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Get notified about this study
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Michael E. DeBakey VA Medical Center, Houston, TX
Houston, Texas, 77030-4211, United States
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