AI4HOPE Pilot Study 2 Digital Dementia Care Planning

ConditionDementia
Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
AgeNot listed
SponsorUniversity of Bonn

About this trial

This pilot study will test a digital care planning decision support system for patients with dementia.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Mild or moderate dementia of any type

Montreal Cognitive Assessment (MoCA) score of 16-25

Living at home, or in residential or nursing home care

Receiving adequate social support

Disqualifiers

Moderate/severe cognitive impairment (MoCA < 16)

No cognitive impairment (MoCA >25)

Inpatient or acute hospital treatment

Infectious diseases or lokal skin conditions preventing the use of wearable body sensors

Trial design

Design model

Single group

Treatments tested in this trial

  • Advance Care Planning Toolkit

    Other intervention

    Participants or their caregivers will access the digital platform for advance care planning

Treatment groups

150 Participants
are divided into 1 treatment group
Group A: Advance Care Planning toolkitOther 1 intervention

Trial outcomes

Primary outcomes

1

Feasibility and acceptability of digital ACP-platform, the Dementia Journey Companion (DJC)

Participant feedback on feasibility, usefulness and burden of ACP-platform; acceptability of content included in the ACP-platform for participantd, user satisfaction with conversational support and suc-cess rate in achieving communicative goals, answering questions and providing guidance.

Time frame
30 days

Secondary outcomes

1

Effect of DJC on documentation of ACP

Rating of benefit by health care professionals.

Time frame
30 days
2

Completion rate of preference documentation

Completion rate of preference documentation across domains (daily living, medical, end-of-life) and frequency of use; frequency of chatbot interactions; number of memories, stories, and preferences documented.

Time frame
30 days
3

Assessment of pain, distress and anxiety

Assessment of pain, distress and anxiety (PROM as part of assessment toolkit).

Time frame
30 days

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University of Bonn

Lead sponsor

University Hospital, Bonn

Sponsor institution

University College Cork

Collaborator

University of Leeds

Collaborator

Fundacion Intras

Collaborator

Universidade do Porto

Collaborator

University Medical Centre Maribor

Collaborator

This trial is not recruiting at the moment. You can still explore other options: