Actively Recruiting
Effects of Wearable Devices Initiates Behavioral Change Intervention on Body Composition, Physical Activity, Sleep Quality and Stress of Nurses in Hospital Working Place: A Randomized Controlled Trial
Led by Tri-Service General Hospital · Updated on 2025-06-24
120
Participants Needed
1
Research Sites
4 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Physically inactive nurses with poor sleep quality face a higher risk of developing non-communicable diseases. Nurses are especially vulnerable due to their demanding shift work and heavy workloads, which may prevent them from meeting recommended physical activity levels. This trial evaluates the effects of a behavioral intervention initiated by wearable devices on body composition, physical activity, sleep quality, and stress among nurses working in a hospital setting. The study randomly assigns 120 nurses into two groups. One group receives a 12-week behavioral intervention using wearable devices combined with a LINE app that provides behavior change advice and weekly 15-minute motivational interviewing sessions through an app. The comparison group receives wearable devices for 12 weeks that only monitor physical activity and sleep quality without additional behavioral support. Data collection occurs at baseline, 12 weeks, and 24 weeks follow-up. Participants will be monitored for physical activity and sleep quality using Fitbit wearable devices and applications. Body composition is assessed by bioelectrical impedance analysis, and stress levels are measured by salivary amylase activity. Researchers will track the effects over time and between groups, assess treatment quality, identify barriers to implementation, and evaluate participant satisfaction. The primary outcomes focus on subjective and objective physical activity, measured from enrollment through 24 weeks.
CONDITIONS
Brief Title
Effects of Wearable Devices Initiates Behavioral Change Intervention on Body Composition, Physical Activity, Sleep Quality and Stress of Nurses in Hospital Working Place
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Individuals who provide informed consent and are 20 years old or older
- Own a smartphone and are willing to join the study's LINE group
- Have a mobile app that can sync with the Fitbit Charge 6 wearable device
- Hold a nursing license and work as a nurse in a clinical setting
You will not qualify if you...
- Unable to provide informed consent or younger than 20 years old
- Do not own a smartphone
- Do not have a nursing license or are not employed as a nurse in a clinical setting
- Currently participating in other health promotion or exercise training studies
- Nurses who are pregnant
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 screening and enrollment visit (in-person or virtual)
Duration - 12 weeks
Participants use wearable devices to either initiate behavioral interventions with weekly motivational interviewing or to monitor physical activity and sleep quality only.
Weekly motivational interviewing sessions for 15 minutes (intervention group); continuous device monitoring for both groups
Duration - 12 weeks
Participants are followed for continued assessment of physical activity, sleep quality, body composition, and stress after the treatment period ends.
1 follow-up visit at 24 weeks after enrollment
Trial Site Locations
Total: 1 location
1
Tri-Service General Hospital
Taipei, Taiwan, Taiwan, 114
Actively Recruiting
Research Team
Y
YIPANG LO, PhD candidate
How is the study designed?
Study Type
INTERVENTIONAL
Masking
TRIPLE
Allocation
RANDOMIZED
Model
PARALLEL
Primary Purpose
HEALTH_SERVICES_RESEARCH
Number of Arms
2
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