Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05989308

MyChart Proxy Outreach to Parents (MyPOP)

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

Status
Recruiting
Phase
N/A
Study type
Interventional
Enrollment
5,200 (estimated)
Sponsor
Yale University · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

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.

Detailed description

This study aims to evaluate the feasibility and impact of contacting parents/guardians of children seen in pediatric primary care practices to establish their proxy access to the EHR patient portal, called "MyChart." The primary objective of the study is to determine if directly messaging a guardian results in activation of proxy access to a child's MyChart at a higher rate compared with no specific messaging (usual care). A secondary objective of the study is to compare messaging strategies, with one arm being a message to the guardian's patient portal, and the other text messaging. Another secondary objective of the study is to ascertain whether sending information about activation to a guardian via text or email (as preferred) will result in self-activating their own Electronic Health Record (EHR) patient portal access. At the conclusion of the study, the investigators will determine best-method for activation and utilize this method to invite guardians initially randomized to the usual-care arm of the study.

Conditions

Interventions

TypeNameDescription
BEHAVIORALEmailEmail message sent to guardian with proxy information.
BEHAVIORALTextText message sent to guardian with proxy information.
BEHAVIORALPatient Portal MessagePatient portal message (MyChart) to guardian with proxy information.

Timeline

Start date
2024-10-15
Primary completion
2026-09-01
Completion
2026-09-01
First posted
2023-08-14
Last updated
2026-02-13

Locations

4 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT05989308. Inclusion in this directory is not an endorsement.