B3 Buddy for Securing Urinary Drainage Bag to Patient While Walking

Not Applicable

Recruiting

• Conditions: Urinary System Disorder

• Registration Number: NCT06571058
• Lead Sponsor: Ohio State University Comprehensive Cancer Center

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Study Start: 2024-6-27
• Last Update Posted: 2 September 2024

Recruitment & Eligibility

• Status: Recruiting
• Sex: All
• Target Recruitment: 40

Inclusion Criteria

Inclusion Criteria:<br><br> - PATIENT PARTICIPANT: Must be English-speaking<br><br> - PATIENT PARTICIPANT: Able to comprehend and agree to consent<br><br> - PATIENT PARTICIPANT: Able to read and complete the Acceptability of Implementation<br> Measure (AIM) survey<br><br> - PATIENT PARTICIPANT: Be willing to participate using the B3 Buddy device<br><br> - PATIENT PARTICIPANT: Have an indwelling urinary catheter or urostomy device<br> connected to a drainage bag<br><br> - PATIENT PARTICIPANT: Have no restrictions in ambulation<br><br> - CLINICIAN PARTICIPANT: Must be English-speaking<br><br> - CLINICIAN PARTICIPANT: Able to comprehend and agree to consent<br><br> - CLINICIAN PARTICIPANT: Able to read and complete the System Usability Scale (SUS)<br> survey<br><br> - CLINICIAN PARTICIPANT: Be willing to participate using the B3 Buddy device<br><br> - CLINICIAN PARTICIPANT: Have a professional role in assisting patients in ambulation<br> in normal workday activities<br><br>Exclusion Criteria:<br><br> - Those patient participants that have more than one urinary-like drainage bags will<br> be excluded. This exclusion is due to the limited prototype samples available to the<br> research team. Limiting one device for one patient with multiple drainage bags may<br> not allow for accurate assessment of the B3 Buddy device

Exclusion Criteria

Not provided

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
Acceptability of device;Usability of device