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
试验速览
- 阶段
- 不适用
- 状态
- 招募中
- 入组人数
- 120
- 试验地点
- 1
- 主要终点
- Physical activity (subjective)
研究概览
简要总结
Background: Physically inactive and poor sleep quality are at increased risk for non-communicable diseases. Nurses were the most vulnerable inactive healthcare personnel who may not meet global physical activity recommendations because of complicated rotation shifts and heavy working loading. Wearable devices initiate behavior intervention combined with smartphone applications could offer new opportunities for social connection by a convenient way for nurses to improve physical activity and sleep quality.
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.
研究设计
- 研究类型
- Interventional
- 分配方式
- Randomized
- 干预模型
- Parallel
- 主要目的
- Health Services Research
- 盲法
- Triple (Participant, Investigator, Outcomes Assessor)
入排标准
- 年龄范围
- 20 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 是
入选标准
- •Individuals who give informed consent for this study and are 20 years old or older.
- •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.
排除标准
- •Individuals unable to provide informed consent for this study and are younger than 20 years old.
- •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.
研究组 & 干预措施
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.
干预措施: wearable devices to initiate behavioral intervention (Behavioral)
comparison group (wearable devices monitor only)
12 week wearable devices just monitor
干预措施: 12 week wearable devices monitor (Behavioral)
结局指标
主要结局
Physical activity (subjective)
时间窗: From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up
Measurement Tool: International Physical Activity Questionnaire short form - Taiwan version
Physical activity (objective)
时间窗: From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up
Measurement Tool: Wearing Fitbit Charge 6 HR to collect physical activity and sleep quality related data.
次要结局
- Body composition(From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up)
- Sleep quality (objective)(From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up)
- sleep quality (subjective)(From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up)
- Stress(From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up)
研究者
LO, YIPANG
Head Nurse in emergency department, SongShan Branch
Tri-Service General Hospital