Behavior Change
Conditions
Keywords
Seasonal influenza vaccination uptake
Brief summary
This randomized controlled trial will compare the efficacy of a Chatbot-delivered stage-of-change-tailored online intervention versus a Chatbot-delivered non-stage-of-change-tailored online intervention for mothers in increasing seasonal influenza vaccination uptake of their children aged 3-6 years. Mothers of children aged 3-6 years will be randomized evenly into either the intervention or the control group. In the intervention group, the Chatbot will assess mothers' stage of change regarding their children's seasonal influenza vaccination uptake and deliver SOC-tailored interventions through WhatsApp every two weeks for four times. In the control group, the Chatbot will provide a standard and non-stage-of-change-tailored intervention every two weeks for four times. All participants will complete three telephone surveys at baseline (T0), after completion of the intervention (T1) and three months after T1 (T2).
Interventions
BEHAVIORALStage-of-change-tailored intervention
The Chatbot will deliver four intervention sessions tailored to participants' current stage of change regarding their index child's seasonal influenza vaccination uptake at Week 0, 2, 4, and 6. Participants will also have access to real-time Question-and-Answer (QA) function provided by the chatbot to address their questions related to seasonal influenza vaccination during the intervention period (week 0-6), and they are free to spend as much time as they want on such function.
BEHAVIORALNon-stage-of-change-tailored intervention
The Chatbot will automatically send participants a link to access a standard online video at week 0, 2, 4 and 6. Participants will also have access to real-time Question-and-Answer (QA) function provided by the chatbot to address their questions related to seasonal influenza vaccination during the intervention period (week 0-6), and they are free to spend as much time as they want on such function.
Sponsors
Chinese University of Hong Kong
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
SINGLE (Outcomes Assessor)
Eligibility
Sex/Gender
FEMALE
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Mothers aged ≥18 years with at least one child aged 3-6 years studying in kindergarten in Hong Kong * Cantonese speaking * Having smartphone with internet access * Already having WhatsApp on the smartphone
Exclusion criteria
* Blindness or deafness * The index child has known medical contraindications for seasonal influenza vaccination
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| Index child's seasonal influenza vaccination uptake reported by his/her mother with validation | 3 months after completion of the interventions (T2) | The research team will ask the participants whether their index children have taken up seasonal influenza vaccination at T2 (3 months after completion of the interventions) using a validated question through telephone interview. The research team will validate the outcome by requesting participants uploading an image of SIV receipt, while hiding personal identification, via the WhatsApp account used in this project. |
Contacts
CONTACTZixin Wang, PhD
Outcome results
None listed