Molecular Analysis for Gastro-Esophageal Cancer: Multicenter Discrete Choice Experiment
MAGECmultiDiCE
1 other identifier
interventional
2,200
1 country
1
Brief Summary
The goal of this survey is to investigate the participants' preference for a specific screening/diagnostic tool to detect and assess gastro-esophageal cancer. The main question it aims to answer are:
- Which diagnostic modality is preferred by patients and the general population?
- Which features of the diagnostic test are most detrimental in the decision-making for one or the other modality?
- Are geographical differences present in regard to the preference for a diagnostic modality? Participants will be asked to complete a survey of 20-25min, including a brief intake regarding their socio-economic status. This approach will allow us to correct for confounding factors.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Aug 2024
Typical duration for not_applicable
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 23, 2024
CompletedFirst Posted
Study publicly available on registry
April 3, 2024
CompletedStudy Start
First participant enrolled
August 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 1, 2026
ExpectedStudy Completion
Last participant's last visit for all outcomes
August 1, 2026
February 18, 2026
February 1, 2026
2 years
March 23, 2024
February 14, 2026
Conditions
Keywords
Outcome Measures
Primary Outcomes (2)
The rate of contribution of diagnostic features to the preference of participants
A part-worth analysis, expressed as percentage, from a discrete choice experiment (questionnaire) will assess the features that are most important to the participants
2 years
The percentage differences in preference of participants between geographical regions
Differences in preferences will be compared between different geographical regions using chi-squared or McNemar's test
2 years
Secondary Outcomes (2)
Assess the rate patient-level demographics influence the importance of a test feature, expressed as an odds ratio
2 years
Assess the rate of trade-off demonstrated as odds ratio between cancer-related mortality reduction and costs
2 years
Study Arms (1)
Survey participants
EXPERIMENTALParticipants who will complete a survey investigating their preference for diagnosis and assessment of gastro-esophageal cancer
Interventions
Eligibility Criteria
You may qualify if:
- Individuals \>18yo to 75yo (upper age limit of Barrett's surveillance)
- Access to computer or smartphone
- Clear understanding of available languages of the experiment (English, French, Dutch, Spanish, German, Chinese, Japanese)
You may not qualify if:
- Individuals less than 18yo and more than 75yo
- Incarcerated individuals
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- KU Leuvenlead
Study Sites (1)
University Hospitals Leuven
Leuven, 3000, Belgium
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Stijn Vanstraelen, MD
UZ Leuven
- PRINCIPAL INVESTIGATOR
Philippe Nafteux, MD, PhD
UZ Leuven
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- OTHER
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal investigator
Study Record Dates
First Submitted
March 23, 2024
First Posted
April 3, 2024
Study Start
August 1, 2024
Primary Completion (Estimated)
August 1, 2026
Study Completion (Estimated)
August 1, 2026
Last Updated
February 18, 2026
Record last verified: 2026-02
Data Sharing
- IPD Sharing
- Will share
- Shared Documents
- STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE
Data will be made available upon reasonable request with the principal investigator