The goal of this study is the assess the use of remote monitoring of vital signs using commercially available medical devices in patients with advanced cancer admitted to a hospice inpatient unit for end-of-life care.
The objectives of the study are:
1. could remote monitoring of vital signs improve patient care through the earlier identification of infections and other (potentially reversible) problems;
2. could remote monitoring of vital signs improve the accuracy of our estimates about how long a person has to live; and c) determine the relationship between complaints of pain / other symptoms and vital signs.
Eligibility
Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria:
* Age ≥ 18 years old
* Primary diagnosis of malignant disease
* Admitted for end-of-life care (or focus of care changed to end-of-life care)
* Estimated prognosis \< 14 days
Exclusion Criteria:
* Primary diagnosis of non-malignant disease
* Inability to provide informed consent
* Contraindications to use of biosensor adhesive patch (e.g. chest wall skin problem, allergy to adhesive)
Primary outcome measure(s)
Mean, standard deviation, median, and range of heart rate variability (HRV) at predefined time intervals prior to death — From device initiation until death (up to 14 days), with analysis conducted across predefined time intervals prior to death Summary statistics (mean, standard deviation, median, and range) of heart rate variability defined as the Root Mean Square of Successive Differences (RMSSD), measured using a wearable ECG patch at predefined time intervals prior to death (0-24 hours, 24-48 hours, 48-72 hours, 72 hours-7 days, and 7-14 days).
Trial sites (1)
Facility
City
Region
Status
Our Lady's Hospice and Care Services
Dublin
Ireland
Recruiting
Official registry record
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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