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NCT Number: NCT07027618

AI-Driven Personalization of End-of-Life Care for the Elderly

This study aims to evaluate the effectiveness of an artificial intelligence (AI)-based software in personalizing high-quality end-of-life care for elderly patients. As the elderly population grows, providing tailored and quality care during the final stages of life becomes increasingly important. This AI software continuously monitors vital signs and behaviors through wearable sensors, offers smart medication reminders, alerts the care team to potential risks, and provides personalized care plans along with psychological and social support.

The study is designed as a randomized controlled trial comparing two groups: one receiving standard end-of-life care and the other using the AI software. Key outcomes include improving quality of life, reducing adverse events like falls and emergency hospitalizations, increasing patient and family satisfaction, improving medication management, and reducing caregiver burden. Data will be collected over six months to assess these effects. The results will help determine whether AI technology can enhance end-of-life care for seniors and support families and healthcare providers.

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Key information

Age range

60 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

About this study

This section provides a comprehensive overview of the study design, objectives, population, interventions, and methods without repeating information already included in other sections of the record. It elaborates on the rationale for using AI-based software to personalize end-of-life care for elderly patients, details the randomized controlled trial setup, explains inclusion and exclusion criteria, intervention specifics, outcome measures, data collection methods, and planned statistical analyses. This description ensures a clear understanding of the study's scope and methodology.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

Age ≥ 60 years

Clinical diagnosis of being in the end-of-life stage, based on criteria such as the Karnofsky Performance Scale or Palliative Performance Scale

Informed consent obtained from the participant or legal representative

Ability to use technology independently or with support provided by the research team

Access to necessary equipment for the intervention (e.g., wearable sensors, smartphone/tablet)

Exclusion criteria

Presence of severe cognitive impairment preventing software use

Voluntary withdrawal from the study at any stage

Critical medical deterioration or death during the study

Poor adherence or insufficient engagement with the intervention software in the intervention group

Treatment and study plan

AI-based Software for Personalized End-of-Life Care

Behavioral

This intervention involves the use of an AI-powered software system designed to personalize end-of-life care for elderly patients. The software continuously monitors vital signs and behavior through wearable sensors, sends smart medication reminders, issues preventive alerts to care providers, delivers customized care plans, and provides psychological and social support through communication features.

Primary outcomes

  1. Change in Quality of Life Score

    Time frame: Up to 3 months after intervention start

    Assessed using a validated instrument such as the Quality of Life at the End of Life (QUAL-E) scale to measure overall well-being, comfort, and satisfaction with care during end-of-life.

Sponsors and collaborators

Lead sponsor

Baqiyatallah Medical Sciences University

Other

Registry information

Official study title

"Evaluating the Effectiveness of an AI-Based Software in Personalizing High-Quality End-of-Life Care for the Elderly: A Randomized Controlled Clinical Trial"

Acronym: PEACE-AI

Important dates

Study start
2025
Primary completion
2026
Study completion
2026
First posted
Jun 18, 2025
Registry last updated
Jun 18, 2025

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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