Terminal cancer
Conditions
Interventions
From the day consent is obtained until the day of discharge, a wearable heart rate sensor device will be attached to the left anterior chest of each study participant, and heart rate data will be coll
Sponsors
Murofushi Keiko
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1. Prognosis predicted by the Palliative Prognostic Index is likely to be 21 days or less 2. Written informed consent is obtained
Exclusion criteria
Exclusion criteria: 1. With arrhythmias affecting the R-R interval 2. Cardiac pacemaker being fitted 3. Other conditions judged as inappropriate for the study by the investigator
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Correlation between prognosis and autonomic nervous activity measured by heart rate variability | — |
Contacts
Public ContactTetsushi Tsuruga
Tokyo Metropolitan Komagome Hospital
Outcome results
None listed