Nurses' readiness key to adopting new female urinary device
NCT ID NCT07656701
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study surveys 200 nurses in resource-limited hospitals to understand what makes it easier or harder to adopt female external urinary collection devices. Nurses will answer questionnaires after a brief explanation of the device. The goal is to identify barriers and facilitators to improve patient care.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this study could identify key factors that help hospitals adopt female external urinary collection devices, improving patient comfort and reducing infections.
- What could go wrong
- This is an observational study with no intervention, so it will not directly test the device's effectiveness. Results may not apply to well-resourced 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.
- Participants
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About 200 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Jun 2026
An estimate. Start dates often move.
- Expected to finish
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Jul 2026
An estimate. End dates often move.
- 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.
Who is studied
The study population includes registered nurses, staff nurses, and head nurses working in clinical settings across participating healthcare facilities. Participants are involved in direct patient care in units such as intensive care, medical, and surgical wards.
- Ages
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18 years and older
- Sex
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Anyone
- 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: * Registered nurses, staff nurses, or head nurses * Currently working in clinical settings (e.g., ICU, medical, or surgical units) * Direct involvement in patient care * Willing to participate and provide informed consent Exclusion Criteria: * Nurses on extended leave during the data collection period * Incomplete questionnaire responses
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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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Faculty of Nursing, Alexandria University
Alexandria, 21511, Egypt