- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05052190
Patient Portal Flu Vaccine Reminders_RCT 4
Improving Influenza Vaccination Delivery Across a Health System by the Electronic Health Records Patient Portal RCT 4
This trial is taking place in Los Angeles, CA at clinics within the UCLA Health System.
The study design is a 2x2 nested factorial design. Patients will be randomized into 1) receiving text based reminder messages, 2) portal-based reminder messages or 3) the control group. Patients randomized to the intervention arms will receive reminders if they are due for influenza vaccine.
Nested within the reminder arms (text or portal), we will have 2 additional components for which patients will be randomized separately:
- A direct scheduling link within the reminder letter enabling the patient to schedule an influenza vaccine only visit (direct scheduling link vs. no direct scheduling link).
- A pre-appointment reminder, encouraging patients to ask for their influenza vaccine at their upcoming appointment (pre-appointment reminder encouraging influenza vaccination vs. standard pre-appointment reminder not mentioning influenza vaccination)
Despite the Advisory Committee on Immunization Practices (ACIP) recommendation in 2010 that all people above 6 months of age should receive an annual flu vaccine, vaccination rates remain low: at 6m-4.9 yrs. (70%), 5-17.9 yrs. (56%), 18-64.9 yrs. (38%), and >65 yrs. (63%). The investigators will assess the effectiveness of MyChart R/R messages and text R/R messages as compared to the standard of care control (no messages).
Study Overview
Status
Conditions
Intervention / Treatment
- Behavioral: Text Message R/R with Direct Appointment Schedule Link
- Behavioral: Text Message R/R without Direct Appointment Schedule Link
- Behavioral: Text Pre-Appointment Reminder
- Behavioral: Portal Message R/R with Direct Appointment Schedule Link
- Behavioral: Portal Message R/R without Direct Appointment Schedule Link
- Behavioral: Portal Pre-Appointment Reminder
Detailed Description
Sub-optimal vaccination rates are a significant problem in the U.S., despite their effectiveness in preventing morbidity and mortality from vaccine-preventable illness. For influenza specifically, annual epidemics of influenza cause substantial morbidity in the U.S. with up to 40,00-80,000 deaths/year and many hospitalizations, emergency and outpatient visits, and significant costs.
Reminder/recall (R/R), sent by phone, mail or other modality, can improve child and adult influenza vaccination rates. However, the majority of pediatric or adult primary care practices do not conduct R/R. Barriers are lack of finances, personnel, and algorithms to identify eligible patients.
A technological breakthrough that might overcome these barriers involves patient portals-- secure, web-based communication systems, embedded within electronic health records (EHRs), for patients and providers to communicate with each other via email and the internet. Portals are used by about half of Americans and half of UCLA patients. Another is text messaging at the health system level.
This randomized controlled trial will assess the effectiveness of reminders messages sent to portal users, encouraging influenza vaccination, on increasing influenza vaccination rates within a health system. Patients will be randomized into three groups: 1) one-third of patients will receive reminder letters via the portal, 2) one-third will receive reminders via text messages sent by the health system and 3) one-third will not receive reminders.
Patients in the reminder arms will be further randomized (separately) for two additional components: 1) direct appointment scheduling and 2) pre-appointment reminders.
Direct scheduling: The convenience of scheduling an appointment for influenza vaccination may increase the likelihood that patients receive an influenza vaccination. Patients receiving reminders will be randomized to receive one of two types of reminder letters: 1) one half will receive flu vaccine reminder letters with a link to the MyChart direct appointment scheduling page and 2) one half will receive flu vaccine reminder message without the direct appointment scheduling link.
Pre-appointment flu reminders: Finally, a missed opportunities for vaccination occurs when patients are eligible for vaccination but are not offered a vaccine at their medical appointment. Pre-appointment reminders, sent in advance of an upcoming appointment, encouraging the patient talk to their doctor about influenza vaccination, may increase the likelihood of that patient receiving a vaccine. Patients will be randomized to one of two groups: 1) one half will receive modified pre-appointment reminders that mention influenza vaccination and 2) one half will receive the standard pre-appointment reminders for an upcoming appointment (no mention of influenza vaccination).
Interventions that apply Behavioral Economics principles in vaccine promotion messaging can increase vaccine receipt. We will include ownership language in the pre-appointment messages. Additionally, the convenience of reminders sent via text and with a Direct Appointment Schedule link included enables patients to self-schedule a flu vaccine only visit, reducing friction for vaccine receipt.
For the primary analysis, the primary outcome will be the patient's end of flu season vaccination status. Intervention effects will be assessed using mixed effects log-binomial models. Models will contain terms for messaging modality (text v. portal v. none), pre-appointment reminders (sent v. not sent), and direct scheduling link (included v. not included).
The R/R text and portal messages (with and without direct scheduling links) and pre-appointment reminders and will all begin in October of 2021.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
California
-
Los Angeles, California, United States, 99095
- University of California LA
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Active Portal Users A patient within the UCLA Health System identified as a primary care patient per an internal algorithm
Exclusion Criteria:
- A patient within the UCLA Health System not identified as a primary care patient per an internal algorithm
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Health Services Research
- Allocation: Randomized
- Interventional Model: Factorial Assignment
- Masking: Single
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
No Intervention: No R/R Message or Pre-Appointment Reminder
Participants do not receive any flu vaccine R/R message or Pre-Appointment Reminder advising them to ask their doctor for the flu vaccine at their upcoming appointment during the specified flu season.
|
|
Active Comparator: Text Message R/R with Direct Appointment Schedule Link
Participants in this arm will receive up to 3 R/R messages by text.
R/R message will be sent with a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
|
Participants in this arm will receive up to 3 R/R messages by text reminding them to get a flu vaccine with a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
|
Active Comparator: Text Message R/R without Direct Appointment Schedule Link
Participants in this arm will receive up to 3 R/R messages by text with no link to schedule an appointment.
|
Participants in this arm will receive up to 3 R/R messages by text reminding them to get a flu vaccine without a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
|
Active Comparator: Text Message R/R with Direct Appointment Schedule Link + text Pre-Appointment Reminder
Participants in this arm will receive up to 3 R/R messages by text.
R/R message will be sent with a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
Participants will receive a Pre-Appointment Reminder via text when they schedule a visit during the study period.
|
Participants in this arm will receive up to 3 R/R messages by text reminding them to get a flu vaccine with a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
Participants will receive a Pre-Appointment Reminder via text when they schedule a visit during the study period advising them to get the flu vaccine at their upcoming appointment.
|
Active Comparator: Text Message R/R without Direct Appointment Schedule Link + Text Pre-Appointment Reminder
Participants in this arm will receive up to 3 R/R messages by text.
R/R message will be sent without a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
Participants will receive a Pre-Appointment Reminder via text when they schedule a visit during the study period.
|
Participants in this arm will receive up to 3 R/R messages by text reminding them to get a flu vaccine without a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
Participants will receive a Pre-Appointment Reminder via text when they schedule a visit during the study period advising them to get the flu vaccine at their upcoming appointment.
|
Active Comparator: Portal Message R/R with Direct Appointment Schedule Link
Participants in this arm will receive up to 3 R/R messages by portal.
R/R message will be sent with a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
|
Participants in this arm will receive up to 3 R/R messages by portal.
R/R message will be sent with a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
|
Active Comparator: Portal Message R/R without Direct Appointment Schedule Link
Participants in this arm will receive up to 3 R/R messages by portal.
R/R message will be sent without a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
|
Participants in this arm will receive up to 3 R/R messages by portal.
R/R message will be sent without a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
|
Active Comparator: Portal Message R/R with Direct Appointment Schedule Link + Portal Pre-Appointment Reminder
Participants in this arm will receive up to 3 R/R messages by portal.
R/R message will be sent with a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
Participants will receive a Pre-Appointment Reminder advising them to ask their doctor for the flu vaccine at their upcoming appointment via portal when they schedule a visit during the study period.
|
Participants in this arm will receive up to 3 R/R messages by portal.
R/R message will be sent with a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
Participants will receive a Pre-Appointment Reminder via the portal advising them to ask their doctor for the flu vaccine at their upcoming appointment via text when they schedule a visit during the study period.
|
Active Comparator: Portal Message R/R without Direct Appointment Schedule Link + Portal Pre-Appointment Reminder
Participants in this arm will receive up to 3 R/R messages by portal.
R/R message will be sent without a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
Participants will receive a Pre-Appointment Reminder advising them to ask their doctor for the flu vaccine at their upcoming appointment via portal when they schedule a visit during the study period.
|
Participants in this arm will receive up to 3 R/R messages by portal.
R/R message will be sent without a Direct Appointment Scheduling link and instructions to make a flu vaccine appointment.
Participants will receive a Pre-Appointment Reminder via the portal advising them to ask their doctor for the flu vaccine at their upcoming appointment via text when they schedule a visit during the study period.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Receipt of the Annual Influenza Vaccine Among Adult Index Patients
Time Frame: 6 months
|
Percent of patients with annual influenza vaccination (between 10/1/21 - 4/1/22) among adult index patients. Outcomes will be assessed via vaccine data extraction from the electronic health record and external claims and pharmacy data. The index patients must also be an active UCLA Health MyChart user (>= 1 login over the last 12 months from 8/1/21, excluding activity on the user's initial profile activation date). Individuals not affiliated with any primary care practice will be excluded from the primary analysis. |
6 months
|
Receipt of the Annual Influenza Vaccine Among Pediatric Index Patients
Time Frame: 6 months
|
Percent of patients with annual influenza vaccination (between 10/1/21 - 4/1/22) among pediatric index patients. Outcomes will be assessed via vaccine data extraction from the electronic health record and external claims and pharmacy data. The index patients must also be an active UCLA Health MyChart user (>= 1 login over the last 12 months from 8/1/21, excluding activity on the user's initial profile activation date). Individuals not affiliated with any primary care practice will be excluded from the primary analysis. |
6 months
|
Collaborators and Investigators
Investigators
- Principal Investigator: Peter Szilagyi, MPH, MD, University of California, Los Angeles
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 17-001889-AM-00015
- R01AI135029-04 (U.S. NIH Grant/Contract)
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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