Understanding patient preferences for screening tests for Barrett's esophagus and esophageal cancer
Official title: Patient Preferences for Barrett's Esophagus and Esophageal Cancer Screening Tests: A Discrete Choice-Based Conjoint Analysis
Run by University of Colorado, Denver · NCT06693622 · Data updated 2026-11-12
This study is trying to understand what patients prefer when it comes to screening tests for Barrett's esophagus and esophageal cancer to help improve current practices.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 89 Years |
| Sex | All |
| Enrollment | 556 (estimated) |
| Sponsor | University of Colorado, Denver Academic / other |
| Locations | 1 site (Aurora, Colorado) |
| Status | Recruiting |
| Started | November 1, 2024 |
| Main results expected | March 1, 2029 |
| Study ends | March 1, 2029 |
| Registry record updated | November 18, 2024 |
| Trial ID | NCT06693622 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include individuals over 50 years old with three or more risk factors for Barrett's esophagus, such as chronic GERD, male gender, and obesity.
✕Probably not a fit
Patients who have already been diagnosed with Barrett's esophagus or esophageal cancer will not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study aims to gather insights into patient preferences regarding screening for Barrett's esophagus and esophageal cancer. Through a multicenter discrete choice-based conjoint survey, patients will evaluate various screening test attributes, including sensitivity, convenience, procedural discomfort, and financial implications. The findings will help identify barriers and preferences that could inform modifications to current screening practices in the United States, ultimately aiming to reduce esophageal cancer mortality rates.
Why it matters
Potential benefit: If successful, this study could lead to more patient-centered screening practices that improve early detection of esophageal cancer.
How similar studies have gone: While there have been studies on screening preferences, this specific approach using discrete choice modeling for Barrett's esophagus and esophageal cancer is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Provision to sign and date the consent form. * Stated willingness to comply with all study procedures and be available for the duration of the study. * Individual has 3 or more established risk factors for BE (age \> 50 years, chronic GERD, male, white race, smoking, obesity, family history of BE/EAC). Exclusion Criteria: * Unable to consent. * Prior diagnosis of BE/EAC. * Life limiting comorbidity/ disability. * Active dementia/ cognitive impairment. * Incarcerated.
Where it's running
-
University of Colorado Anschutz Medical Campus
Aurora, Colorado, United States Recruiting
Study contacts
- Principal investigator: Sachin Wani, MD — University of Colorado, Denver
- Study coordinator: Alexa DeBord, MS
- Email: alexa.debord@cuanschutz.edu
- Phone: 303-724-0432
Similar studies
Other studies for the same condition or treatment. Recruiting studies are listed first.
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This study is testing a new capsule device that collects cells from the esophagus to see if it can effectively detect Barrett's Esophagus in people at high risk, without needing an endoscopy.
-
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This project will try stopping routine endoscopies in people with low-risk, non-dysplastic Barrett's esophagus to see if it remains safe.
-
Non-endoscopic test to find Barrett's esophagus in veterans without chronic reflux.
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.