Clinical Utility of Methylation-based Prognostic Assay for Barrett's Esophagus

Sponsor
Capsulomics, Inc. (Industry)
Overall Status
Active, not recruiting
CT.gov ID
NCT05846971
Collaborator
(none)
100
1
2
35.1
2.8

Study Details

Study Description

Brief Summary

Capsulomics has developed a prognostic assay for patients with diagnosed Barrett's esophagus (BE). This study will measure how gastroenterologists make surveillance and treatment management decisions when presented with different clinical and prognostic assay information.

Condition or Disease Intervention/Treatment Phase
  • Other: Educational materials on validated methylation assay
N/A

Detailed Description

Capsulomics has developed a prognostic assay for patients with diagnosed Barrett's esophagus (BE). This study will measure how gastroenterologists make surveillance and treatment management decisions for virtual patient cases when presented with different clinical and prognostic assay information. The data from this study will be published in a peer-review scientific journal.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
100 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Care Provider)
Primary Purpose:
Diagnostic
Official Title:
Clinical Utility of Methylation-based Prognostic Assay for Barrett's Esophagus
Actual Study Start Date :
Jan 26, 2021
Anticipated Primary Completion Date :
Dec 31, 2023
Anticipated Study Completion Date :
Dec 31, 2023

Arms and Interventions

Arm Intervention/Treatment
No Intervention: Control Group

The control group will receive standard-of-care clinical data for their virtual patient cases. No educational material on the methylation assay will be provided.

Experimental: Intervention Group

The intervention group will receive standard-of-care clinical data for their virtual cases along with educational materials about the methylation assay. This group will then be provided with methylation assay data to be used in addition to clinical data.

Other: Educational materials on validated methylation assay
Educational materials include overall information on the assay including what the test does, how to use the test and report, and performance metrics on the test.

Outcome Measures

Primary Outcome Measures

  1. Clinical performance change in physician behavior. [1 year]

    Change in the overall and the diagnostic and treatment in patient simulations: difference-in-differences regression analysis between the control and the intervention groups' diagnosis and treatment of risk progression in patients with Barrett's esophagus, as measured by the participants' diagnostic and treatment scores. In each category, participants' care recommendations are evaluated, ranging from 0 to a high potential score of up to 10, where higher scores mean increased intensity in surveillance and treatment, to measure the impact of the methylation assay on care decision making.

  2. The impact of methylation assay on physician confidence in clinical care decision-making. [1 year]

    Measure the confidence in care decisions based on patient's methylation test result: Once the intervention group is exposed to the intervention, education materials on the methylation assay (a validated molecular test for risk stratifying patients with Barrett's esophagus), the scores are measured, on a scale of 0 to 10 from round 1 (pre-exposure) to round 2 (post-exposure) and observe how the assay impacts confidence in the physician following evidence-based patient care.

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  1. Be currently practicing board-certified gastroenterologist practicing in the United States

  2. Have practiced (as a board-certified gastroenterologist) for greater than 2

  3. Be English-speaking

  4. Have ≥ 50 Barrett's esophagus patients under care annually

  5. Have Internet access

  6. Have no prior experience with the methylation assay test

  7. Provide voluntary informed consent to participate in the study.

Exclusion Criteria:
  1. Non-practicing gastroenterologists

  2. Less than two years of gastroenterology practice

  3. Non-English speaking

  4. Does not have access to the internet

  5. Does not consent to participate in study

Contacts and Locations

Locations

Site City State Country Postal Code
1 Capsulomics, Inc. Baltimore Maryland United States 21215

Sponsors and Collaborators

  • Capsulomics, Inc.

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Capsulomics, Inc.
ClinicalTrials.gov Identifier:
NCT05846971
Other Study ID Numbers:
  • 23-001
First Posted:
May 6, 2023
Last Update Posted:
May 6, 2023
Last Verified:
Apr 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Additional relevant MeSH terms:

Study Results

No Results Posted as of May 6, 2023