- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT06423040
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
Status
Recruiting
Conditions
Intervention / Treatment
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:
- Hsin-Yen Yen
- Phone Number: 6326 886-27361661
- Email: kenji@tmu.edu.tw
-
-
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:
- Persons aged 60 to 85 years old living in Taipei City, healthy or with chronic conditions
- Those who can listen, read and write Chinese
- Those who have used smartphones in the past month and can use Line social software
- Those who voluntarily participate in this study, can understand the research content after explanation and explanation, and sign the subject consent form
Exclusion Criteria:
- Those who are advised by a doctor not to exercise
- Those who must exercise under the supervision of medical personnel
- Patients with severe cardiovascular disease
- Anyone with disability or cognitive impairment
- 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.
Sponsor
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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