NCT06679647

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. 1.Self-reported uptake of SIV in the past month.
  2. 2.Changes in behavioural intention to receive SIV for the approaching flu season.
  3. 3.Changes in knowledge and attitudes related to SIV.

Trial Health

35
At Risk

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
50

participants targeted

Target at P25-P50 for not_applicable

Timeline
Completed

Started Dec 2024

Shorter than P25 for not_applicable

Status
not yet recruiting

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

November 6, 2024

Completed
1 day until next milestone

First Posted

Study publicly available on registry

November 7, 2024

Completed
24 days until next milestone

Study Start

First participant enrolled

December 1, 2024

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

March 31, 2025

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

March 31, 2025

Completed
Last Updated

November 7, 2024

Status Verified

November 1, 2024

Enrollment Period

4 months

First QC Date

November 6, 2024

Last Update Submit

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

EXPERIMENTAL

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.

Behavioral: Access to a trained ChatGPT

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.

ChatGPT group

Eligibility Criteria

Age65 Years+
Sexall
Healthy VolunteersYes
Age GroupsOlder Adult (65+)

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.

Study Officials

  • Zixin Wang, PhD

    Chinese University of Hong Kong

    PRINCIPAL INVESTIGATOR

Central Study Contacts

Zixin Wang, PhD

CONTACT

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