160
Participants
Start Date
July 28, 2021
Primary Completion Date
February 28, 2023
Study Completion Date
February 28, 2023
Continence material with sensor
"Healthcare organizations are prepared for the use of smart continence care (for the intervention condition) using specially developed implementation guideline. They receive training, including how to apply continence material (only provided to intervention condition).~Each participating location will use the product for 12 weeks. Correct size and absorption level will be determined for each participant. The optimize the result, this can change. Evaluation meetings with the caregivers, supplier and researcher will be held. Resulting in suggestions for alterations in continence care provided or products used, or giving indications that a team needs support in any way to foster the implementation.~After 12 weeks, the implementation guidance from the research group will be phased out.~The waiting list group will continue their continence care as usual during data collection period. Thereafter they will receive support for implementing smart continence care."
's Heeren Loo, Amersfoort
Siza, Arnhem
Lunet, Eindhoven
Esdégé-Reigersdaal, Heerhugowaard
Zozijn, Wilp
Collaborators (1)
Tilburg University
OTHER
Stichting Trimbos-Instituut
OTHER
Maastricht University
OTHER
s Heeren Loo Zorggroep
UNKNOWN
Esdégé-Reigersdaal
UNKNOWN
Lunet
UNKNOWN
Siza
UNKNOWN
Zozijn
UNKNOWN
Academy Het Dorp
OTHER