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Trials / Not Yet Recruiting

Not Yet RecruitingNCT06679647

Acceptability, Usability and Preliminary Effectiveness of ChatGPT in Increasing Seasonal Influenza Vaccination Uptake Among Older Adults in Hong Kong

Status
Not Yet Recruiting
Phase
N/A
Study type
Interventional
Enrollment
50 (estimated)
Sponsor
Chinese University of Hong Kong · Academic / Other
Sex
All
Age
65 Years
Healthy volunteers
Accepted

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.

Conditions

Interventions

TypeNameDescription
BEHAVIORALAccess to a trained ChatGPTParticipants 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.

Timeline

Start date
2024-12-01
Primary completion
2025-03-31
Completion
2025-03-31
First posted
2024-11-07
Last updated
2024-11-07

Source: ClinicalTrials.gov record NCT06679647. Inclusion in this directory is not an endorsement.