An explorative study to assess the potential impact of the Incosense Smart in Envida

Completed

• Conditions: urine incontinentie; incontinence; loss of control of the bladder; accidental release of urine

• Registration Number: NL-OMON44181
• Lead Sponsor: Zuyd Hogeschool

Brief Summary

Not available

Detailed Description

Not available

Study Timeline

• Last Update Posted: 11 June 2024

Recruitment & Eligibility

• Status: Completed
• Sex: Not specified
• Target Recruitment: 40

Inclusion Criteria

Urine incontinence
Use of incontinence material
Willing to let incontinence changes occur on the basis of the incosense smart notifications

Exclusion Criteria

There are no exclusion criteria

Study & Design

• Study Type: Interventional
• Study Design: Not specified

Primary Outcome Measures

Name	Time	Method
<p>Outcome measures include:<br /><br><br /><br>- client: experiences, comfort<br /><br>- care: saturation levels of the incontinence material when changed,<br /><br>appropriate use of material (size), appropriate time of change (too early,<br /><br>late, on time).<br /><br>- Professionals: problems experienced during use of the Incosense Smart,<br /><br>experiences<br /><br>- Organisation: use (amount) of incontinence material</p><br>

Secondary Outcome Measures

Name	Time	Method
<p>NA</p><br>