Patient-Centered Decision Support for Eosinophilic Esophagitis
This study is looking at how people with Eosinophilic Esophagitis (EoE), a chronic allergic inflammatory disease of the esophagus, prefer to receive and use educational materials about their treatment options. Researchers are comparing two approaches: a "General education control" where you review standard online materials, and a "Decision support tool" where you review tailored online materials. Both groups will complete surveys before and after reviewing the materials, around the time of a regular doctor's appointment. The study aims to enroll 40 participants aged 18 or older who are new EoE patients at the University of Michigan and can read English. The main goals are to see if these educational tools are practical to use and well-liked by patients.
- Study design
- This interventional study plans to enroll 40 participants. It compares two behavioral interventions: general education materials versus a tailored decision support tool.
- What's involved
- You would complete an online survey before reviewing educational materials and then a follow-up survey approximately 3 months later. These activities are timed around a standard doctor's appointment.
- Compensation
- Not stated in the trial record.
- Follow-up
- Participants will complete a follow-up survey approximately 3 months after their clinic visit. Acceptability will be measured at approximately 4 months.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Patient-Centered Decision Support for Eosinophilic Esophagitis
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Joy Chang, MD, MS · PRINCIPAL_INVESTIGATOR · University of Michigan
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Feasibility: measured as the proportion of eligible patients that consent to participate in the studyRecruitment period approximately 18 months
The study aims to achieve at least 20% consented for eligible patients.
- Acceptability: measured on a 4-point Likert scaleApproximately 4 months
Measured on a 4-point Likert-scale (1) Very Unhelpful to (4) Very Helpful. Analyzed as high scores indicate more helpful.