Living lab field test Amsta and Sevagram Use of the IncoSense Smart

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

NL-OMON

Registry ID

NL-OMON24594

Enrollment

Registered

2016-01-14

Start date

2016-01-18

Completion date

Unknown

Last updated

2024-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

incontinence, incontinentie, incontinence care, proces of incontinence care, proces incontinentiezorg, quality of life, kwaliteit van leven, field test, IncoSense Smart

Interventions

Incontinent clients are provided with the IncoSense Smart device for two weeks. In the first week client receive usual incontinence care. In the second week care takes place when the IncoSense Smart d

Eligibility

Inclusion criteria

Inclusion criteria: clients with incontinence who wear incontinence material, who are not able to change incontinence pads independently living in a health facility

Exclusion criteria

Exclusion criteria: clients who are able to change incontinence pads independently

Design outcomes

Primary

Measure	Time frame
Does the IncoSense Smart device indicate the exact right moment of exchanging the incotinense material.	—

Secondary

Measure	Time frame
Increase Quality of Life Decrease costs	—

Contacts

Public ContactJeanne Heijkers

Centre of Expertise for Innovative Care and Technology

Jeanne.heijkers@zuyd.nl

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)