- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04994691
Effect of Varied Outreach Methods on Appointment Scheduling and Appointment Completion Using MyChart
August 8, 2024 updated by: Children's Hospital Medical Center, Cincinnati
Our objective is to determine the effectiveness of varied outreach methods (e.g. standard versus tailored MyChart messaging) to children age 6-17 years old who are due for a WCC visit and don't have one scheduled in the next 45 days on the outcomes of appointment scheduling and appointment completion.
Study Overview
Status
Completed
Conditions
Intervention / Treatment
Study Type
Interventional
Enrollment (Actual)
945
Phase
- Not Applicable
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Ohio
-
Cincinnati, Ohio, United States, 45229
- Cincinnati Children's Hospital Medical Center
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
6 years to 17 years (Child)
Accepts Healthy Volunteers
No
Description
Inclusion Criteria:
- age 6-17 years
- has not had a well child check in past 365 days
- no future well child check visit scheduled
- parent preferred language = English or Spanish
Exclusion Criteria:
- no active MyChart account
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Triple
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Placebo Comparator: No message
No message sent
|
No messages are sent
|
|
Active Comparator: Standard message
2 MyChart reminders that child is overdue for well child check visit
|
2 MyChart reminders that child is overdue for well child check visit
|
|
Active Comparator: Tailored message
2 MyChart reminders that child is overdue for well child check visit with date of last WCC and age
|
2 MyChart reminders that child is overdue for well child check visit with date of last WCC and age
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants Who Completed Well Child Check Visit
Time Frame: Within 8 weeks of the date of intervention or the date of randomization for the control group
|
Participants completed well child check visit as determined by presence of a well visit billing code documentation in the electronic health record.
|
Within 8 weeks of the date of intervention or the date of randomization for the control group
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Number of Participants Who Scheduled an Appointment for a Well Child Check Visit.
Time Frame: Within 8 weeks of the date of intervention or the date of randomization for the control group
|
Participant scheduled a well child check visit as determined by electronic health record documentation.
|
Within 8 weeks of the date of intervention or the date of randomization for the control group
|
|
Number of Participants Who Received Their First COVID-19 Vaccination
Time Frame: Within 8 weeks of the date of the intervention or the date of randomization for the control group
|
Participant receipt of their first COVID-19 vaccination as determined by presence of documentation of vaccine administration in the electronic health record.
|
Within 8 weeks of the date of the intervention or the date of randomization for the control group
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Investigators
- Principal Investigator: William Brinkman, MD, Cincinnati Children's
Publications and helpful links
The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
July 30, 2021
Primary Completion (Actual)
October 7, 2021
Study Completion (Actual)
February 28, 2022
Study Registration Dates
First Submitted
July 29, 2021
First Submitted That Met QC Criteria
July 29, 2021
First Posted (Actual)
August 6, 2021
Study Record Updates
Last Update Posted (Actual)
August 28, 2024
Last Update Submitted That Met QC Criteria
August 8, 2024
Last Verified
August 1, 2024
More Information
Terms related to this study
Other Study ID Numbers
- 2020-0769-2
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
product manufactured in and exported from the U.S.
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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