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Smart mHealth Strategy for Physical Activity and Health Promotion

Smart mHealth Strategy in the Delivery of Behavior Change Techniques for Physical Activity and Health Promotion

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06423014
Enrollment
360
Registered
2024-05-21
Start date
2023-05-01
Completion date
2026-12-31
Last updated
2024-05-21

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chatbot, Health Behavior Change, Sedentary Lifestyle, Social Media, Wearable Technology

Brief summary

The purpose of this study is to develop a Smart mHealth Strategy that delivers behavior change techniques through wearable physical activity trackers and social media chatbots, including self-monitoring, real-time feedback and reminders, goal-setting, competition and rewards, social support, and health coaching. This study also aims to explore the effect of the Smart mHealth Strategy on the behavioral outcomes and psychological factors of physical activity, and physical and mental health. The study design is a three-stage randomized controlled trial. In each stage, 120 are recruited and randomly assigned to control and experimental groups. Participants are adults with insufficient physical activity and a sedentary lifestyle. The Smart mHealth Strategy uses smartwatches and self-developed chatbots. The constrained dialogue content is designed to finally deliver the six behavior change techniques. Data are collected in the pre-, mid-, and post-tests. The measurement includes self-administered questionnaires, Actigraphy GT9X, Inbody 270S, OMRON HEM-7130, and heart rate variability monitors.

Interventions

BEHAVIORALWearable devices only

self-monitoring

BEHAVIORALWearable devices with the 1st behavior change technique

reminder

BEHAVIORALWearable devices with the 2nd behavior change technique

social support

BEHAVIORALWearable devices with the 3rd behavior change technique

Competition

BEHAVIORALWearable devices with the 4th behavior change technique

Goal-setting

BEHAVIORALWearable devices with the 5th behavior change technique

health coach

BEHAVIORALWearable devices with all behavior change techniques

Self-monitoring, health coach, goal-setting, competition, social support, and reminder

Sponsors

Taipei Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
PREVENTION
Masking
SINGLE (Subject)

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
Yes

Inclusion criteria

Adults who is the age of majority, with insufficient physical activity, and a sedentary lifestyle who have smartphones

Exclusion criteria

* Individuals' health conditions may affect physical activity in daily living and the experiment, such as disability, serious health problems * There are unconventional life plans during the experiment, such as going abroad for vacation, pregnancy, and surgery. * Individuals have using experiences in any wearable physical activity trackers in the past six months ④ People who have ever had severe allergies to any wearable device ⑤ Professional athletes or student-athletes

Design outcomes

Primary

MeasureTime frameDescription
Behavioural Regulation in Exercise Questionnaire (BREQ-3)up to 12 weeksHigher score higher Behavioural Regulation
Subjective physical activityup to 12 weeksInternational Physical Activity Questionnaire (IPAQ-SF, MET-minute/week)
Objective physical activityup to 12 weeksActigraphy GT9X and GT3X (MET-minute/week)
Exercise Benefits/Barriers Scale-Concise (EBBS-C)up to 12 weeksHigher score higher benefits and barriers
Exercise self-efficacy scale (EXSE)up to 12 weeksHigher score higher self-efficacy
Physical Activity Self-Regulation Scale (PASR)up to 12 weeksHigher score higher Self-Regulation

Secondary

MeasureTime frameDescription
blood pressureup to 12 weeksSystolic and diastolic blood pressure (mmHg)
heart rate variabilityup to 12 weeksTotal power (TP, 0-0.5 Hz), low-frequency power (LF, 0.04-0.15 Hz), high-frequency power (HF, 0.15-0.40 Hz), the ratio of low frequency to high frequency (LF/HF), and the standard deviation of all normal-to-normal intervals (SDNN)
Depression Anxiety Stress Scale (DASS)up to 12 weeksHigher score worse mental health
World Health Organization Quality of Life Scale (WHOQOL-BREF)up to 12 weeksHigher score higher Quality of Life
body composition (Inbody)up to 12 weeksBody mass index (BMI, kg/m\^2), skeletal muscle index (SMI, kg/m\^2), body fat percentage (%), body fat mass (kg), and fat-free mass (kg)

Countries

Taiwan

Contacts

Primary ContactHsin-Yen Yen, PhD
kenji@tmu.edu.tw886-2-2736-1661

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026