NCT06901037

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

57
Monitor

Trial Health Score

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

Trial has exceeded expected completion date
Enrollment
84

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started May 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
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

March 23, 2025

Completed
5 days until next milestone

First Posted

Study publicly available on registry

March 28, 2025

Completed
1 month until next milestone

Study Start

First participant enrolled

May 1, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 30, 2025

Completed
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

December 31, 2025

Completed
Last Updated

September 15, 2025

Status Verified

September 1, 2025

Enrollment Period

6 months

First QC Date

March 23, 2025

Last Update Submit

September 8, 2025

Conditions

Keywords

Chatbot, older adults

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

EXPERIMENTAL

Participants will immediately receive access to a 2-month chatbot-based intervention

Other: A chatbot-based intervention

Waitlist

OTHER

Participants will be placed on a waiting list before accessing the intervention

Other: A chatbot-based intervention

Interventions

A smartphone-delivered AI-based chatbot program designed to provide personalized physical activity and dietary recommendations

Chatbot-based interventionWaitlist

Eligibility Criteria

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

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

RECRUITING

Study Officials

  • Arkers Wong, PhD

    The Hong Kong Polytechnic University

    PRINCIPAL INVESTIGATOR

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.

Locations