A RCT Evaluating a Chatbot in Increasing Physical Activity Among Older Adults
A Randomized Controlled Trial Evaluating a Trans-Theoretical-Model-based Online Intervention Delivered by Fully-automated Chatbot in Increasing Physical Activity Among Inactive Community-dwelling People Aged ≥65 Years
1 other identifier
interventional
278
1 country
1
Brief Summary
This study will compare the efficacy of a Chatbot-delivered stage of changes (SOC)-tailored online intervention (intervention group) versus a Chatbot-delivered non-SOC-tailored online intervention in increasing the prevalence of meeting WHO recommended physical activity level six months after completion of the intervention among inactive community-dwelling individuals aged ≥65 yeas. In the intervention group, the Chatbot will assess participants' physical activity level and SOC regarding PA and automatically deliver interventions tailor to their SOC every week for 12 weeks. In the control group, the Chatbot will not assess participants' SOC. It will assess participants' physical activity level and provides a standard intervention covering general information about physical activity for older adults, which is not tailoring to participants'SOC every week for 12 weeks. All participants will be followed up after completion of the interventions (T1) and six months after T1 (T2).
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for not_applicable
Started Nov 2024
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
October 12, 2024
CompletedFirst Posted
Study publicly available on registry
October 15, 2024
CompletedStudy Start
First participant enrolled
November 1, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 31, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
December 31, 2025
CompletedOctober 15, 2024
October 1, 2024
1.2 years
October 12, 2024
October 12, 2024
Conditions
Outcome Measures
Primary Outcomes (1)
Meeting WHO recommended level of physical activity
Prevalence of meeting WHO recommended level of physical activity (at least 150 minutes moderate-intensity aerobic physical activity every week) at T1 (after completion of intervention) and T2 (6 months after T1). Physical activity will be measured by self-reported data and using an accelerometer.
9 months
Study Arms (2)
Intervention
EXPERIMENTALThe Chatbot will assess participants' physical activity level and stage of changes regarding physical activity and automatically deliver interventions tailor to their stage of changes every week for 12 weeks. The Chatbot will address questions related to physical activity raised by the participants.
Control
ACTIVE COMPARATORThe Chatbot will not assess participants' stage of changes. It will assess participants' physical activity level and provides a standard intervention covering general information about physical activity for older adults, which is not tailoring to participants' stage of changes every week for 12 weeks. The Chatbot will address questions related to physical activity raised by the participants.
Interventions
The Chatbot will assess participants' physical activity level and stage of changes regarding physical activity and automatically deliver interventions tailor to their stage of changes every week for 12 weeks. The Chatbot will address questions related to physical activity raised by the participants.
The Chatbot will not assess participants' stage of changes. It will assess participants' physical activity level and provides a standard intervention covering general information about physical activity for older adults, which is not tailoring to participants' stage of changes every week for 12 weeks. The Chatbot will address questions related to physical activity raised by the participants.
Eligibility Criteria
You may qualify if:
- Aged ≥65 years,
- Having a Hong Kong ID,
- Chinese speaking,
- Not meet the WHO recommended level of MVPA
- Willing to be followed by telephone at 3 and 9 months,
- Having a smartphone
- Able to send and read text/voice message via smartphone.
- Willing to wear an accelerometer for a week at T0, T1 and T2.
You may not qualify if:
- Blindness or deafness,
- Having been diagnosed with major psychiatric illness (schizophrenia or bipolar disorder) or dementia,
- Score ≥1 in the Chinese version of the Physical Activity Readiness Questionnaire (PAR-Q)
- Score ≤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)
Liang X, Sun F, Zhang Q, Fang Y, Yu FY, Ye D, Zhang B, Liao Q, Mo PK, Wang Z. Chatbot-Delivered Stage of Change-Tailored Web-Based Intervention to Promote Physical Activity Among Inactive Community-Dwelling People Aged 65 years or More: Protocol for a Randomized Controlled Trial. JMIR Res Protoc. 2025 Jun 20;14:e68796. doi: 10.2196/68796.
PMID: 40540737DERIVED
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Zixin Wang, Dr.
Centre for Health Behaviours Research, the Chinese University of Hong Kong
Central Study Contacts
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- SINGLE
- Who Masked
- OUTCOMES ASSESSOR
- Purpose
- HEALTH SERVICES RESEARCH
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Assistant Professor
Study Record Dates
First Submitted
October 12, 2024
First Posted
October 15, 2024
Study Start
November 1, 2024
Primary Completion
December 31, 2025
Study Completion
December 31, 2025
Last Updated
October 15, 2024
Record last verified: 2024-10
Data Sharing
- IPD Sharing
- Will not share