Actively Recruiting
Implementation of Online Advance Care Planning Tool for (Hemato-)Oncological Patients Within the Cancer Network CONCORD
Led by Erasmus Medical Center · Updated on 2024-04-08
30
Participants Needed
1
Research Sites
26 weeks
Total Duration
On this page
Sponsors
E
Erasmus Medical Center
Lead Sponsor
M
Maasstad Hospital
Collaborating Sponsor
AI-Summary
What this Trial Is About
Researchers are evaluating how an online advance care planning module is implemented and used for patients with blood cancers and other cancers within the oncology network CONCORD. The study aims to understand how early integration of advance care planning in cancer care can help discuss patient preferences and improve treatment planning. This mixed-methods research includes both qualitative interviews and quantitative data analysis. The study involves oncology patients treated in hospitals within the CONCORD network during their palliative phase, as well as healthcare providers and implementation staff. Qualitative research gathers experiences through interviews with patients, relatives, medical staff, and project leaders before and after implementation. Quantitative research uses anonymized electronic health record data from patients who have died to analyze the use and outcomes of the advance care planning module. Participants share their experiences with the module while the researchers collect data on medical care and costs in the last three months of life. The study measures how well the module is implemented and its effects over three years. Data includes demographics, healthcare use such as ICU admissions and emergency visits, and economic analysis of care costs. The goal is to improve advance care planning integration in daily oncological care.
CONDITIONS
Brief Title
Implementation of Online Advance Care Planning Tool for (Hemato-)Oncological Patients Within the Cancer Network Concord
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Adults aged 18 years or older
- Diagnosed with cancer
- Treated at a hospital within the CONCORD oncology network
You will not qualify if you...
- None specified
AI-Screening
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Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
Duration - Up to 3 years
Participants who undergo routine care are observed to assess the implementation and use of an online advance care planning tool within the oncology network. Data on medical care in the last three months of life and advance care plans are collected and analyzed.
Trial Site Locations
Total: 1 location
1
Joica Benschop
Rotterdam, Netherlands, 3023TB
Actively Recruiting
Research Team
J
Joica A.M. Benschop, MSc
E
Erasmus Medical Center Oldenmenger, PhD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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