Effects of Wearable Devices Initiates Behavioral Change Intervention on Body Composition, Physical Activity, Sleep Quality and Stress of Nurses in Hospital Working Place
NCT ID: NCT06814886
Last Updated: 2025-06-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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RECRUITING
NA
120 participants
INTERVENTIONAL
2025-05-01
2027-03-01
Brief Summary
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Objectives: To evaluate the effects of wearable devices initiate behavioral intervention on body composition, physical activity, sleep quality and stress of nurses in hospital working place.
Method: This is a randomized controlled trial that will recruit 120 nurses and randomly assign them into two groups from a hospital working place. The nurses in the intervention group will receive 12-week wearable devices to initiate behavioral intervention. The nurses in the comparison group will only receive 12-week wearable devices monitoring. Data will be collected at baseline and 12-week and 24-week follow-up. The body composition will be measured by bioelectrical impedance analysis (BIA). The physical activity and sleep quality will be monitored by the Fitbit wearable device and application. The mediator parameter of the stress will be measured by salivary amylase activity (SAA). We will control the internal validity to assure the quality of training, treatment fidelity, identify barriers and facilitators of implementation, and assess participants' satisfaction. General estimating equations (GEE) will be applied to examine the effects of time and group interaction.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
HEALTH_SERVICES_RESEARCH
TRIPLE
Study Groups
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Intervention group(wearable devices to initiate behavioral intervention)
12 week wearable devices to initiate behavioral intervention including line APP recruited participants and give some behavior change advises, also give a APP-based motivational interviewing 15 minutes per week.
wearable devices to initiate behavioral intervention
12 week wearable devices to initiate behavioral intervention including line APP recruited participants and give some behavior change advises, also give a APP-based motivational interviewing 15 minutes per week.
comparison group (wearable devices monitor only)
12 week wearable devices just monitor
12 week wearable devices monitor
12 week wearable devices monitor physical activity and sleep quality only
Interventions
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wearable devices to initiate behavioral intervention
12 week wearable devices to initiate behavioral intervention including line APP recruited participants and give some behavior change advises, also give a APP-based motivational interviewing 15 minutes per week.
12 week wearable devices monitor
12 week wearable devices monitor physical activity and sleep quality only
Eligibility Criteria
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Inclusion Criteria
* Those who own a smartphone and are willing to join the study's LINE group.
* Individuals whose mobile application (APP) can synchronize with the Fitbit Charge 6 wearable device.
* Nurses who hold a nursing license and are working in a clinical setting.
Exclusion Criteria
* Those who do not own a smartphone.
* Individuals who do not have a nursing license or are not employed in a clinical setting as a nurse.
* Participants who are already involved in other health promotion or exercise training studies.
* Nurses who are currently pregnant.
20 Years
ALL
Yes
Sponsors
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Tri-Service General Hospital
OTHER
Responsible Party
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LO, YIPANG
Head Nurse in emergency department, SongShan Branch
Locations
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Tri-Service General Hospital
Taipei, Taiwan, Taiwan
Countries
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Central Contacts
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Facility Contacts
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Other Identifiers
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A202405171
Identifier Type: -
Identifier Source: org_study_id
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