Acceptability, Usability and Preliminary Effectiveness of ChatGPT in Increasing Seasonal Influenza Vaccination Uptake Among Older Adults in Hong Kong
1 other identifier
interventional
50
0 countries
N/A
Brief Summary
In this project, we will train a ChatGPT to provide real-time answers to questions related to the SIV for older adults in Hong Kong. This study aims to evaluate the usability, acceptability, and preliminary effectiveness of the ChatGPT among 50 community-living people aged 65 years and above in Hong Kong. The primary objectives are to evaluate the usability and acceptability (including the extent of usage and subjective experiences of behavioural, cognitive, and affective engagement) of the ChatGPT at the end of the 4-week intervention period (T1). The secondary objectives are to evaluate the following conditions measured at T1, as compared to those measured at baseline (T0):
- 1.Self-reported uptake of SIV in the past month.
- 2.Changes in behavioural intention to receive SIV for the approaching flu season.
- 3.Changes in knowledge and attitudes related to SIV.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Dec 2024
Shorter than P25 for not_applicable
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
November 6, 2024
CompletedFirst Posted
Study publicly available on registry
November 7, 2024
CompletedStudy Start
First participant enrolled
December 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
March 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
March 31, 2025
CompletedNovember 7, 2024
November 1, 2024
4 months
November 6, 2024
November 6, 2024
Conditions
Outcome Measures
Primary Outcomes (3)
Perceived usability
Perceived usability assessed by the validated Chinese version of the 10-item Perceived Usability Scale (SUS)
1 month
Extent of usage documented by the ChatGPT
Extent of usage documented by the ChatGPT
1 month
Subjective experiences related to behavioural, cognitive, and affective engagement
Subjective experiences related to behavioural, cognitive, and affective engagement measured by the validated Twente Engagement with eHealth Technologies Scale (TWEETS)
1 month
Study Arms (1)
ChatGPT group
EXPERIMENTALParticipants will be invited to use a trained ChatGPT which answers questions related to seasonal influenza vaccination. The functions can be used repeatedly throughout the intervention period (4 weeks), and participants will be free to spend as much time as they want on such functions.
Interventions
Participants will be invited to use a trained ChatGPT which answers questions related to seasonal influenza vaccination. The functions can be used repeatedly throughout the intervention period (4 weeks), and participants will be free to spend as much time as they want on such functions.
Eligibility Criteria
You may qualify if:
- Aged ≥65 years;
- Possession of a Hong Kong ID;
- Able to speak and comprehend Cantonese;
- Have a smartphone with internet access;
- Have not taken SIV for the approaching flu season.
You may not qualify if:
- With diagnosis of cognitive impairment or dementia;
- Either blindness or deafness;
- With known contraindications to the SIV as indicated by the Hong Kong Centre for Health Protection
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Related Publications (1)
Wang Z, Tsang TH, Yu FY, Fang Y, Chen S, Sun F, Mo PKH, Wong KC. Effectiveness, Usability, and Acceptability of ChatGPT With Retrieval-Augmented Generation (SIV-ChatGPT) in Increasing Seasonal Influenza Vaccination Uptake Among Older Adults: Quasi-Experimental Study. J Med Internet Res. 2025 Sep 8;27:e76849. doi: 10.2196/76849.
PMID: 40921067DERIVED
Study Officials
- PRINCIPAL INVESTIGATOR
Zixin Wang, PhD
Chinese University of Hong Kong
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NA
- Masking
- NONE
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- SINGLE GROUP
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
November 6, 2024
First Posted
November 7, 2024
Study Start
December 1, 2024
Primary Completion
March 31, 2025
Study Completion
March 31, 2025
Last Updated
November 7, 2024
Record last verified: 2024-11
Data Sharing
- IPD Sharing
- Will not share