Sample Collection and Instruction Optimization
Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-65
SponsorUniversiteit Antwerpen
About this trial
The aim of this study is to improve the instructions for use and to evaluate the usability of a novel first-void urine collection device.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Naïve to first-void urine collection (standard urine cup is allowed)
Able to understand the information brochure and what the study is about
Disqualifiers
None
Trial design
Design model
Single group
Treatments tested in this trial
First-void urine collection device
DeviceUse of a first-void urine collection device
Treatment groups
60 Participants
are divided into 1 treatment groupGroup A: First-void urine collectionExperimental treatment 1 intervention
Trial outcomes
Primary outcomes
1
Feedback usability
Collected data on the usability through questionnaire
Time frame
Immediately after use of the first-void urine collection device by participants2
Feedback instructions for use
Data collected on the instructions for use through questionnaire
Time frame
Immediately after use of the first-void urine collection device by participantsSecondary outcomes
1
Volume first-void urine collected
Volume (in mL) of first-void urine sample collected by using the device
Time frame
Baseline (single visit)Sponsors and contacts
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Source ClinicalTrials.gov