Social Media Chatbot on Physical Activity Education for Older Adults

March 5, 2025 updated by: Taipei Medical University

Exploring the Effectiveness of Applying Social Media Chatbot for Providing Real-Time Feedback on Physical Activity Education for Older Adults

In this study, a social media chatbot was used to provide a continuous and real-time multimedia health education program on physical activity for the older adults, as well as supportive messages and feedbacks, to improve physical activity and exercise self-efficacy among the older adults. This study was a cluster randomized trial, and participants were recruited from community care stations and activity centers in Taipei City. The experimental group was involved in an 8-week, 5-day-a-week intervention with a total of 40 multimedia physical activity education programs, and users were provided with real-time feedback interactions and regular physical activity education guidelines, and self-administered questionnaires were used for data collection. The research instruments include basic personal information, International Physical Activity Questionnaire, Exercise Self-Efficacy Scale, Behavioral regulation in exercise questionnaire-2, Exercise Benefits/Barriers Scale, and the statistical methods will be descriptive statistics, independent sample t-test, paired sample t-test, and one-way analysis of covariance.

Study Overview

Study Type

Interventional

Enrollment (Estimated)

104

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

  • Name: Hsin-Yen Dr. Yen, PhD
  • Phone Number: 6326 886-2736-1661
  • Email: kenji@tmu.edu.tw

Study Locations

      • Taipei City, Taiwan, 110
        • Recruiting
        • Taipei Medical University
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult
  • Older Adult

Accepts Healthy Volunteers

Yes

Description

Inclusion Criteria:

  1. Persons aged 60 to 85 years old living in Taipei City, healthy or with chronic conditions
  2. Those who can listen, read and write Chinese
  3. Those who have used smartphones in the past month and can use Line social software
  4. Those who voluntarily participate in this study, can understand the research content after explanation and explanation, and sign the subject consent form

Exclusion Criteria:

  1. Those who are advised by a doctor not to exercise
  2. Those who must exercise under the supervision of medical personnel
  3. Patients with severe cardiovascular disease
  4. Anyone with disability or cognitive impairment
  5. Persons living in long-term care institutions

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: Single

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
No Intervention: Control
Experimental: Experiment
a social media chatbot was used to provide a continuous and real-time multimedia health education program on physical activity for the older adults, as well as supportive messages and feedbacks.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Physical activity
Time Frame: up to 8 weeks
International Physical Activity Questionnaire
up to 8 weeks
Self-Efficacy
Time Frame: up to 8 weeks
Exercise Self-Efficacy Scale
up to 8 weeks
Behavioral regulation
Time Frame: up to 8 weeks
Behavioral regulation in exercise questionnaire-2
up to 8 weeks
Benefits/Barriers
Time Frame: up to 8 weeks
Exercise Benefits/Barriers Scale
up to 8 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

August 30, 2024

Primary Completion (Estimated)

July 1, 2025

Study Completion (Estimated)

July 1, 2025

Study Registration Dates

First Submitted

May 8, 2024

First Submitted That Met QC Criteria

May 15, 2024

First Posted (Actual)

May 21, 2024

Study Record Updates

Last Update Posted (Actual)

March 25, 2025

Last Update Submitted That Met QC Criteria

March 5, 2025

Last Verified

April 1, 2024

More Information

Terms related to this study

Other Study ID Numbers

  • N202403043

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

NO

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

product manufactured in and exported from the U.S.

No

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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