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Electronic Health Record Strategies to Promote Diverse Participation in Research

NCT05348603 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 726199

Last updated 2023-12-11

No results posted yet for this study

Summary

The purpose of this study is to determine the effectiveness of enhanced features in an online patient portal including banners, a chatbot, and direct to patient message and traditional mailed letters on increasing interest in research among online patient portal users.

Conditions

  • Patient Participation

Interventions

OTHER

Traditional Letter

Patients receive a traditional letter.

OTHER

Direct to Patient Message

Patients receive a direct to patient message via the portal.

OTHER

Chatbot

Patients are contacted by a chatbot via the portal.

OTHER

Banner

Patients are exposed to a banner ad via the portal.

Sponsors & Collaborators

  • Food and Drug Administration (FDA)

    collaborator FED

  • Yale University

    lead OTHER

Principal Investigators

  • Brian Smith, MD · Yale University

Study Design

Allocation
RANDOMIZED
Purpose
OTHER
Masking
DOUBLE
Model
FACTORIAL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-09-13
Primary Completion
2023-05-15
Completion
2023-11-14

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05348603 on ClinicalTrials.gov