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NCT06289322 | NOT YET RECRUITING | Dementia


AI4HOPE Dementia Pain Assessment Pilot Study 1
Sponsor:

University of Bonn

Information provided by (Responsible Party):

Lukas Radbruch

Brief Summary:

The pilot study will develop and test a standardized assessment toolkit that will provide conclusive information with a tolerable burden for cognitively impaired patients with dementia.

Condition or disease

Dementia

Intervention/treatment

Digital toolkit for assessment

Phase

NA

Detailed Description:

The clinical study is part of an EU-funded project on the use of artificial intelligence for patients with dementia. This study will test a digital toolkit fo assessment and monitoring of patients with mild or moderate dementia and pilot-test this toolkit for feasibility and acceptability. Patients with mild to moderate dementia will be recruited for the pilot study in the six participating countries. The study population includes all types of dementia without stratification, as the aim of the study is to construct a digital assessment and intervention toolkit for clinical practice in any patient with cognitive impairment from any type of dementia. Even though the final assessment and intervention toolkit could also be useful for patients with advanced dementia and more severe cognitive impairment, the pilot study will recruit only patients with mild or moderate dementia, who will still be able to provide informed consent, and who will be able to self-assess at least minimum patient-related outcome or patient-related experience measures to validate the behavioural and observational scales and biomarkers used in the toolkit. Patients with dementia treated in the participating study centers will be screened for inclusion criteria and, if suitable will be invited to participate. The study will be performed for seven days, with optional extension to 30 days according to patients' preferences. Patients with baseline data and at least one intervention performed from the digital toolkit and data completed before and after that intervention will be included in the evaluation.

Study Type : INTERVENTIONAL
Estimated Enrollment : 150 participants
Masking : NONE
Primary Purpose : SUPPORTIVE_CARE
Official Title : AI4HOPE - Artificial Intelligence Based Health, Optimism, Purpose and Endurance in Palliative Care for Dementia: Pilot Study 1 Digital Toolkit Assessment
Actual Study Start Date : 2025-07
Estimated Primary Completion Date : 2026-12
Estimated Study Completion Date : 2026-12

Information not available for Arms and Intervention/treatment

Ages Eligible for Study:
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Mild or moderate dementia of any type
  • * Able to provide informed consent, or consent from surrogate decision maker
  • * Able to self-assess patient-related outcome (PROM) or experience (PREM) measures
Exclusion Criteria
  • * Ongoing delir
  • * Severe cognitive impairment (MMSE \< 10 \[22\])
  • * Unable to provide informed consent
  • * Life expectancy estimated less than 3 months

AI4HOPE Dementia Pain Assessment Pilot Study 1

Location Details

NCT06289322


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