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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06000397
Other study ID # 20220678-01H
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date November 7, 2023
Est. completion date June 2024

Study information

Verified date April 2024
Source Ottawa Hospital Research Institute
Contact Kathryn MacDonald
Phone 613-293-1193
Email kathryn@canimmunize.ca
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The goal of this clinical trial is to assess the effectiveness of enhanced email reminders in improving vaccine coverage at the 12-month visit in CANImmunize app users. The main questions it aims to answer are: - Do enhanced email reminders improve coverage of the 12- month dose of the pneumococcal vaccine and the timely completion of its immunization series at the 12-month's visit in CANImmunize app users? - What are the predictors of predictors of timely completion of the 12-month's series of pneumococcal vaccines in the CANImmunize app users? Participants will be randomized to either receive enhanced reminder/recall materials via email or the standard CANImmunize notifications. Researchers will compare the enhanced reminder group to the standard notification group to see if there is a difference in vaccine coverage at the 12-month visit.


Recruitment information / eligibility

Status Recruiting
Enrollment 700
Est. completion date June 2024
Est. primary completion date June 2024
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 10 Months to 11 Months
Eligibility Inclusion Criteria To be included in the study, CANImmunize account holders must have: - Enabled the reception to receive emails from CANImmunize, and - Record(s) for an infant aged between 10- and 11-months, who have already received the earlier doses of the pneumococcal vaccine in accordance with their provincial/territorial routine immunization schedule. Exclusion Criteria - The account holder (parent, or guardian of the child) has an inactive or undelivered email address, or - No record(s) for an infant aged 10- and 11-months, or - The record for the 10- or 11-month-old indicates that he/she has not received the prior pneumococcal vaccine doses.

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Enhanced reminders
The intervention is sending enhanced (modality and frequency) of reminders to CANImmunize App users, in addition to the standard notifications. Specifically: Deliver reminders and recall emails to parents or guardians of infants waiting for their 12-month dose of pneumococcal vaccine, Add additional information about the benefits, safety and effectiveness of the pneumococcal vaccine to support increased uptake, and Provide tips to improve parents' or guardians' self-efficacy in circumventing barriers to timely immunization of children at the 12-month's visit
Standard CANImmunize notifications
Push notifications at two time points: two weeks prior to the immunization due date one week after the immunization due date

Locations

Country Name City State
Canada CANImmunize Ottawa

Sponsors (1)

Lead Sponsor Collaborator
Ottawa Hospital Research Institute

Country where clinical trial is conducted

Canada, 

Outcome

Type Measure Description Time frame Safety issue
Primary Receipt of 12-month pneumococcal vaccine Receipt of the 12-month dose of the pneumococcal vaccine as recorded in the CANImmunize immunization record 12 months of age
Secondary Timeliness of 12-month pneumococcal vaccine Age at receipt of the 12-month dose of the pneumococcal vaccine as recorded in the CANImmunize immunization record 12-13 months of age will be considered as timely, after 13 months considered late
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