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The (Cost)Effect of Smart Diaper Continence Care for People With Profound Intellectual and Multiple Disabilities

A

Academy Het Dorp

Status

Invitation-only

Conditions

Incontinence

Treatments

Device: Continence material with sensor

Study type

Interventional

Funder types

Other

Identifiers

NCT05481840
80-85300-98-19110 (Other Grant/Funding Number)
AHD19.022
NL72751.091.20 (Other Identifier)

Details and patient eligibility

About

Background and study aims

Most people with profound intellectual and multiple disabilities (PIMD) use diapers. When living in a long-term care facilities, most changes of diapers are scheduled. Leading to leakages, unnecessary changes and burden to people with PIMD and their caregivers.

With the use of continence material with sensor (smart diapers) caregivers give more client-based continence care. The smart diaper (product name: Abena Nova) informs the caregivers about the saturation level of the diaper and gives a notification when change is needed or a leakage might occur. This can result in less leakages compared to regular continence care. And we will research the effect on quality of life and number of pad changes and cost effectiveness. The study also investigates the effect on the care givers.

Who can participate?

People with profound intellectual and multiple disabilities, of 18 years and older, who use diapers and live in one of the participating disability care organizations.

What does the study involve?

To investigate the effect, the disability care organization will be assigned to one of the two groups. In one group we will research the use of the smart diaper, the other group will continue their regular continence care.

Data collection started September 2021 and will continue roughly till February 2023. Research period for each location is 12 weeks, with 3 points for data collection. For the first two organization who are using the smart diaper, there is also data collection after 9 months.

Caregivers will fill out questionnaires about the quality of life, received healthcare of the participant, and keep a one week diary about the diaper changes and leakages.

To use the smart diaper, caregivers will receive training, there are meetings to optimize usage and the disability care organization will receive help from the researchers.

Possible benefits and risk of participating?

The potential benefit of participating lays within the organization itself, optimizing continence care and investigating whether this is cost effective. Any negative effect is the cost of the product and the additional time and effort it takes to start using smart diapers. For the patients the benefit is getting more optimized continence care. Any potential discomfort or risk (such as removing of swallowing the sensor) will be evaluated before the start. Any negative advice will result in not implementing the smart diaper for this person showing risk behavior. However, any of these adverse events cannot be complete diminished.

Where does the study run from?

Study is run by Academy Het Dorp, one of the researcher is also affiliated with Tranzo, Tilburg University

Who is funding the study?

ZonMW is funding the research activities. Disability care organization are themselves paying for the smart diapers.

Who is the main contact?

Vivette van Cooten, MSc Vivette.van.cooten@academyhetdorp.nl

Enrollment

160 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion:

  • Age: ≥18 years
  • Gender: male of female
  • People with PIMD
  • Living in a long-term care facility
  • Using continence pads
  • Not able to indicate the need for change of continence pads
  • Caregivers see added value for use of smart continence pads

Exclusion:

  • No informed consent of legal representative
  • Risk of harmful behavior such as pica disorder

Trial design

Primary purpose

Supportive Care

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

160 participants in 2 patient groups

Intervention group
Experimental group
Description:
Receiving smart continence care by the use of continence material with sensor, in which their care professionals receive a notification when change is needed.
Treatment:
Device: Continence material with sensor
Waiting list group
No Intervention group
Description:
Will continue regular continence care as received by their care professionals. After data collection is finalized, they will receive smart continence care.

Trial contacts and locations

5

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Data sourced from clinicaltrials.gov

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