NCT06346080

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

77
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
2,200

participants targeted

Target at P75+ for not_applicable

Timeline
2mo left

Started Aug 2024

Typical duration for not_applicable

Geographic Reach
1 country

1 active site

Status
recruiting

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

Study Progress90%
Aug 2024Aug 2026

First Submitted

Initial submission to the registry

March 23, 2024

Completed
11 days until next milestone

First Posted

Study publicly available on registry

April 3, 2024

Completed
4 months until next milestone

Study Start

First participant enrolled

August 1, 2024

Completed
2 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Expected
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Last Updated

February 18, 2026

Status Verified

February 1, 2026

Enrollment Period

2 years

First QC Date

March 23, 2024

Last Update Submit

February 14, 2026

Conditions

Keywords

Esophageal cancerSurveyGastric cancer

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

EXPERIMENTAL

Participants who will complete a survey investigating their preference for diagnosis and assessment of gastro-esophageal cancer

Other: Survey

Interventions

SurveyOTHER

Discrete choice survey

Survey participants

Eligibility Criteria

Age18 Years - 85 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)

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

Study Sites (1)

University Hospitals Leuven

Leuven, 3000, Belgium

RECRUITING

MeSH Terms

Conditions

Esophageal NeoplasmsStomach Neoplasms

Interventions

Surveys and Questionnaires

Condition Hierarchy (Ancestors)

Gastrointestinal NeoplasmsDigestive System NeoplasmsNeoplasms by SiteNeoplasmsHead and Neck NeoplasmsDigestive System DiseasesEsophageal DiseasesGastrointestinal DiseasesStomach Diseases

Intervention Hierarchy (Ancestors)

Data CollectionEpidemiologic MethodsInvestigative TechniquesHealth Care Evaluation MechanismsQuality of Health CareHealth Care Quality, Access, and EvaluationPublic HealthEnvironment and Public Health

Study Officials

  • Stijn Vanstraelen, MD

    UZ Leuven

    PRINCIPAL INVESTIGATOR
  • Philippe Nafteux, MD, PhD

    UZ Leuven

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Stijn Vanstraelen, MD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
OTHER
Intervention Model
SINGLE GROUP
Model Details: A survey will be conducted in a single group of participants from different geographical regions and backgrounds
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

Data will be made available upon reasonable request with the principal investigator

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR, ANALYTIC CODE

Locations