A RCT Evaluating an Online Intervention in Increasing Pneumococcal Vaccination Among Older Adults
A Randomized Controlled Trial Evaluating a Theory-based Online Intervention Via Fully Automated Chatbot in Increasing Pneumococcal Vaccination Among Community Dwelling Individuals Aged ≥65 Years
1 other identifier
interventional
374
1 country
1
Brief Summary
To evaluate the relative efficacy of an online intervention based on the Trans-theoretical Model delivered by a fully-automated Chatbot with natural language processing functions versus a control in promoting pneumococcal vaccination uptake among Hong Kong people aged ≥65 years. A total of 374 participants will be randomized evenly to either the intervention group or the control group. Participants in the intervention group will receive Chatbot-delivered interventions tailored to their stage of change regarding PV uptake in a conversational way at Month 0, 1, 2, and 3. Participants in the control group will receive Chatbot-delivered general information related to PV at Month 0, 1, 2, and 3. All participants will be followed up 6 and 12 months after completion of the intervention.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Mar 2023
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 6, 2023
CompletedStudy Start
First participant enrolled
March 13, 2023
CompletedFirst Posted
Study publicly available on registry
March 16, 2023
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2024
CompletedStudy Completion
Last participant's last visit for all outcomes
August 31, 2024
CompletedApril 6, 2023
April 1, 2023
1.5 years
March 6, 2023
April 4, 2023
Conditions
Outcome Measures
Primary Outcomes (1)
Pneumococcal vaccination uptake
Self-reported uptake of pneumococcal vaccination within the 12-month follow-up period
12 months
Study Arms (2)
Intervention
EXPERIMENTALParticipants receive Chatbot-delivered interventions tailored to their stage of change regarding PV uptake in a conversational way at Month 0, 1, 2, and 3.
Control
ACTIVE COMPARATORParticipants receive Chatbot-delivered general information related to PV at Month 0, 1, 2, and 3.
Interventions
Participants receive Chatbot-delivered interventions tailored to their stage of change regarding PV uptake in a conversational way at Month 0, 1, 2, and 3.
Participants receive Chatbot-delivered general information related to PV at Month 0, 1, 2, and 3.
Eligibility Criteria
You may qualify if:
- aged ≥65 years
- having Hong Kong ID
- Chinese speaking
- have not received any penumococcal vaccination
- willing to be followed up by telephone
- having a smartphone
- able to send and read text/voice messages via smartphone.
You may not qualify if:
- blindness or deafness
- not able to communicate with others effectively
- with known contradictions of pneumococcal vaccination
- having been diagnosed with major psychiatric illness
- scored ≤16 in the validated telephone version of the Cantonese Mini-mental State Examination (T-CMMSE).
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Centre for Health Behaviours Research, the Chinese University of Hong Kong
Hong Kong, 666888, Hong Kong
Related Publications (1)
Wang Z, Chen S, Poon J, Han SC, Ye D, Yu FY, Fang Y, Ni Z, Wong MCS, Mo PKH. A Hybrid Chatbot to Promote Pneumococcal Vaccination Among Older Adults: A Randomized Clinical Trial. JAMA Netw Open. 2025 Oct 1;8(10):e2535813. doi: 10.1001/jamanetworkopen.2025.35813.
PMID: 41060654DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
March 6, 2023
First Posted
March 16, 2023
Study Start
March 13, 2023
Primary Completion
August 31, 2024
Study Completion
August 31, 2024
Last Updated
April 6, 2023
Record last verified: 2023-04
Data Sharing
- IPD Sharing
- Will not share