Enhancing Protection Against Influenza and COVID-19 for Pregnant Women and Medically at Risk Children
Influenza, COVID-19
About this trial
This is an interventional health services research trial for Influenza
Eligibility Criteria
Inclusion Criteria: Pregnant women (COVID RCT) - those who have received 2 or less doses of a recommended COVID-19 vaccine Pregnant women (influenza RCT) - those who have not received the influenza vaccine during pregnancy Medically at risk children (COVID RCT) - those who have received 1 or no dose of a recommended COVID-19 vaccine Medically at risk children(influenza RCT) - those who have not received the annual influenza vaccine Exclusion Criteria: Pregnant women (COVID RCT) - those who have received 3 or more doses of a recommended COVID-19 vaccine Pregnant women (influenza RCT) - those who have received the influenza vaccine during pregnancy Medically at risk children (COVID RCT) - those who have received 2 or more doses of a recommended COVID-19 vaccine Medically at risk children(influenza RCT) - those who have received the annual influenza vaccine
Sites / Locations
- Women's and Children's HospitalRecruiting
- Flinders Medical CentreRecruiting
- Lyell McEwin Hospital
- Mercy Hospital For Women
- The Royal Children's Hospital
- Perth Children's Hospital
- King Edward Memorial Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm 5
Arm 6
Arm 7
Arm 8
Experimental
No Intervention
Experimental
No Intervention
Experimental
No Intervention
Experimental
No Intervention
Pregnant women-COVID-19 vaccine RCT - intervention group
Pregnant women-COVID-19 vaccine RCT - standard care group
Pregnant women-influenza vaccine RCT - intervention group
Pregnant women-influenza vaccine RCT - standard care group
Medically at risk children-COVID-19 vaccine RCT - intervention group
Medically at risk children-COVID-19 vaccine RCT - standard care group
Medically at risk children-influenza vaccine RCT - intervention group
Medically at risk children-influenza vaccine RCT - standard care group
Women randomized to the intervention group will receive the nudge (three text messages four weeks apart) to remind them to get the COVID-19 booster vaccine
Women randomized to the standard care group will not receive the nudge (three text messages four weeks apart) to remind them to get the COVID-19 booster vaccine. They will receive normal care at the hospital.
Women randomized to the intervention group will receive the nudge (three text messages four weeks apart) to remind them to get the annual influenza vaccine
Women randomized to the standard care group will not receive the nudge (three text messages four weeks apart) to remind them to get the annual influenza vaccine. They will receive normal care at the hospital.
Parents of medically at risk children randomized to the intervention group will receive the nudge (three text messages four weeks apart) to remind them to get their child the COVID-19 vaccine
Parents of medically at risk children randomized to the standard care group will not receive the nudge (three text messages four weeks apart) to remind them to get their child the COVID-19 vaccine. They will receive normal care at the hospital.
Parents of medically at risk children randomized to the intervention group will receive the nudge (three text messages four weeks apart) to remind them to get their child the annual influenza vaccine
Parents of medically at risk children randomized to the standard care group will not receive the nudge (three text messages four weeks apart) to remind them to get their child the annual influenza vaccine. They will receive normal care at the hospital.