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Remote Assessment of Signs and Symptoms in Palliative Care

The ReASSure-PC Study: A Feasibility Study of Remote Assessment of Signs and Symptoms in Palliative Care

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06587321
Acronym
ReASSure-PC
Enrollment
30
Registered
2024-09-19
Start date
2024-04-01
Completion date
2025-08-31
Last updated
2025-06-27

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Palliative Care, Remote Monitoring, Vital Signs

Keywords

Remote monitoring

Brief summary

Digital health interventions, including remote monitoring of patients, have been identified as a possible way to address current problems within the health service, including insufficient numbers of staff, and an increasing number of patients requiring services. The aim of this study is to assess the feasibility of using remote monitoring for patients who are receiving palliative care and to see whether remote monitoring can improve care and outcomes for patients and their families. Participants in this study will complete regular (daily, weekly, monthly) questionnaires online about how they are feeling. They will also be given equipment to measure their vital signs every day. The clinical team will have access to the results and be able to respond to any new problems as they arise. Patients and their carers will then complete a questionnaire at one month to assess satisfaction with the use of remote monitoring.

Interventions

None listed

Sponsors

Our Lady's Hospice and Care Services
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Primary diagnosis of advanced cancer or another life-limiting condition * Estimated prognosis greater than 3 months * Referred for community-based specialist palliative care * Living in own home (or home of family carer) * Living with a family carer

Exclusion criteria

* Estimated prognosis less than 3 months or more than 12 months * Cognitive impairment - unable to provide consent / complete assessments * Non-English speaker * Living in care home / nursing home / hospice / community hospital * Not living with a family carer

Design outcomes

Primary

MeasureTime frameDescription
Completion rates of assessmentsAt the end of 1 monthNumber of assessments completed over the study time-frame

Secondary

MeasureTime frameDescription
Recruitment rate6 monthsThe number of patients approached to take part in the study who then entered the study
Retention rate6 monthsThe number of patients who entered and then completed the study
Acceptability1 monthA patient / carer acceptability questionnaire completed at 1 month into study period
Use of community palliative care resources6 monthsNumber of phone calls / visits / interventions participants receive
Use of GP / hospital resources6 monthsThe number of unplanned GP visits / hospital attendances over the study period

Countries

Ireland

Contacts

Primary ContactGemma O'Keeffe
gokeeffe@olh.ie01 406 8700

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026