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NCT06615349Recruiting

DigiPall; a Trial of Digital Patient Reported Outcome and Biomarker Monitoring in Palliative Care

Summary

The aim of this study is to test if a system consisting of a wearable device measuring heartbeats and steps, together with daily communication with a chatbot on the smartphone asking the patients about their symptoms and giving tips, can reduce unplanned hospital readmissions and improve well-being in advanced cancer and severely ill patients.

Inclusion criteria

• Patients with established diagnosis of a metastatic cancer/severe illness with limited life expectancy receiving palliative care services • Estimated life expectancy \<24 months (physician's guess)/ \>3 months • Karnofsky Index ≥ 50% / ECOG≤ 2 • Aged \>18 years • Owns and uses a smartphone • Give written informed consent

Exclusion criteria

• Patients under curative treatment • Relevant cognitive impairment

Contacts

The trial team's contact details are shown on request.

See the official trial record
Status
Recruiting
Phase
No phase (N/A)
Study type
Interventional
Countries
Switzerland
Sponsor
David Blum(Other)
Protocol no.
digiPall
Conditions
Terminal Illness, Terminal Cancer
Interventions
Behavioral

Treatments studied

  • DigiPall

Collaborators

Zurich University of Applied Sciences

Locations · 1

  • Zurich, SwitzerlandUniversity Hospital ZurichRecruiting at this site

In total, worldwide, the only site listed in the registry is recruiting.

Site status per the ClinicalTrials.gov registry (last update posted: July 10, 2025).

This status may have changed and says nothing about your eligibility: before taking any step, check with your oncologist or the site.

See also

Other versions

These results are indicative and do not replace medical advice — discuss them with your doctor.