A Pilot Randomized Controlled Trial of Chatbot Use in Older Adults for Lifestyle Change
The Acceptability and Preliminary Effectiveness of Using A Smartphone-delivered AI-Based Chatbot in Older Adults for Lifestyle Modification: A Pilot Randomized Controlled Trial
1 other identifier
interventional
84
1 country
1
Brief Summary
The purpose of this study is to evaluate the acceptability and preliminary effectiveness of a smartphone-delivered AI-based chatbot in promoting healthy dietary behavior and physical activity participation among older adults.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for not_applicable
Started May 2025
Shorter than P25 for not_applicable
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 23, 2025
CompletedFirst Posted
Study publicly available on registry
March 28, 2025
CompletedStudy Start
First participant enrolled
May 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
October 30, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedSeptember 15, 2025
September 1, 2025
6 months
March 23, 2025
September 8, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (3)
The acceptance of the chatbot among older adults, as measured by a 14-item simplified version of the Senior Technology Acceptance Model questionnaire
The 14-item questionnaire uses a 10-point Likert scale, ranging from 0 (strongly disagree, very poor, very uneasy, and very unsatisfied) to 10 (strongly agree, very good, very easy, and very satisfied)
End of study (2 months)
The Usability of the chatbot, as measured by the System Usability Scale
The System Usability Scale (SUS) is a 10-item Likert scale questionnaire. The result of this survey is called SUS score, which ranges from 0 to 100 and provides information about overall customer satisfaction and usability. A higher score indicates better usability, while a lower score may suggest usability issues.
End of study (2 months)
The user experience, as measured by 10 open-ended questions
A qualitative interview will be provided to the participants for asking their experience in using chatbot.
End of study (2 months)
Secondary Outcomes (4)
Change of dietary behavior, as measured by the intake of fruits and vegetables over the last seven days
Baseline, end of study (2 months)
Change of walking, as measured by the Community Health Activities Model Program for Seniors questionnaire
Baseline, end of study (2 months)
Change of total activity and moderate and more vigorous physical activity variables, as measured by the CHAMPS-Q
Baseline, end of study (2 months)
Change of quality of life, as measured by the Hong Kong Quality of Life for Older Persons Scale
Baseline, end of study (2 months)
Study Arms (2)
Chatbot-based intervention
EXPERIMENTALParticipants will immediately receive access to a 2-month chatbot-based intervention
Waitlist
OTHERParticipants will be placed on a waiting list before accessing the intervention
Interventions
A smartphone-delivered AI-based chatbot program designed to provide personalized physical activity and dietary recommendations
Eligibility Criteria
You may qualify if:
- aged 65 or above.
- are community-dwelling.
- are proficient in Mandarin.
- have an Internet connection.
- have at least one instant messaging app on the smartphone or agree to download one.
You may not qualify if:
- have any neurocognitive disorders.
- are unable to engage in moderate-intensity level of physical activity due to a preexisting medical condition.
- live with another participant who will participate in this study.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
The Hong Kong Polytechnic University
Hong Kong, Hong Kong
Study Officials
- PRINCIPAL INVESTIGATOR
Arkers Wong, PhD
The Hong Kong Polytechnic University
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, OUTCOMES ASSESSOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Associate Professor in the School of Nursing
Study Record Dates
First Submitted
March 23, 2025
First Posted
March 28, 2025
Study Start
May 1, 2025
Primary Completion
October 30, 2025
Study Completion
December 31, 2025
Last Updated
September 15, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share
No sharing of data except reasonable request.