RecruitingNot ApplicableNCT05989308

MyChart Proxy Outreach to Parents (MyPOP)

MyChart Proxy Outreach to Parents (MyPOP): Mode of Outreach to Parents for Proxy Patient Portal Enrollment


Sponsor

Yale University

Enrollment

5,200 participants

Start Date

Oct 15, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

The goal of this randomized controlled trial is to assess the extent to which different modes of contacting parents who have not yet enabled to access to their children's medical records will result in greater proxy access. The main questions the study aims to answer are: * will outreach via text or patient portal message result in more parents having access than usual care (which is in-office suggestions to get access). * which mode - text or portal - will get more parents access. Participants will get a text message, or a portal message through their own patient portal, or no message. The investigators will check access to see which group has increased more during the study period.


Eligibility

Min Age: 18 Years

Inclusion Criteria1

  • Guardian of a child aged ≤12 years seen in one of the two identified health centers within the last 3 years with guardian status and contact information documented in the child's EHR

Exclusion Criteria2

  • Preferred method of contact for guardians with no MyChart is telephone or physical letter to home
  • Guardians with EHR proxy access already activated for all children in their care.

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Interventions

BEHAVIORALEmail

Email message sent to guardian with proxy information.

BEHAVIORALText

Text message sent to guardian with proxy information.

BEHAVIORALPatient Portal Message

Patient portal message (MyChart) to guardian with proxy information.


Locations(4)

Cornell Scott Hill Health Center

New Haven, Connecticut, United States

Fair Haven Community Health Center

New Haven, Connecticut, United States

Yale New Haven Health

New Haven, Connecticut, United States

Yale School of Medicine

New Haven, Connecticut, United States

View Full Details on ClinicalTrials.gov

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NCT05989308