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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.
Participants are asked to try a novel first-void urine collection device and give feedback on the instructions and usability of the device through a questionnaire. Further, only the volume of the collected sample is measured. A first group of 30 participants (15 men and 15 women) will be asked for a one-time visit. If any substantial changes need to be made based on the results of the questionnaire, a second group of 30 participants will be asked to evaluate the adapted version.
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| First-void urine collection | Experimental | Use of first-void urine device and filling out questionnaire on the instructions for use and the usability after collection. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| First-void urine collection device | Device | Use of a first-void urine collection device |
|
| Measure | Description | Time Frame |
|---|---|---|
| Feedback usability | Collected data on the usability through questionnaire | Immediately after use of the first-void urine collection device by participants |
| Feedback instructions for use | Data collected on the instructions for use through questionnaire | Immediately after use of the first-void urine collection device by participants |
| Measure | Description | Time Frame |
|---|---|---|
| Volume first-void urine collected | Volume (in mL) of first-void urine sample collected by using the device | Baseline (single visit) |
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Inclusion Criteria:
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| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Alex Vorsters | Contact | +32 3 265 91 30 | alex.vorsters@uantwerpen.be |
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| University of Antwerp - Centre for the Evaluation of Vaccination | Recruiting | Edegem | 2650 | Belgium |
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Primary purpose: Usability study (device feasibility with 30 participants and, if necessary, another cohort of 30 participants if substantial adaptations are needed to be made between cohorts)
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