Effects of Wearable Devices Initiates Behavioral Change Intervention on Body Composition, Physical Activity, Sleep Quality and Stress of Nurses in Hospital Working Place

Официальное название

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

Обзор

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.

Вмешательства

• Поведенческое 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.
• Поведенческое 12 week wearable devices monitor
  12 week wearable devices monitor physical activity and sleep quality only

Первичные конечные точки

• Physical activity (subjective) [Срок оценки: From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up]
• Physical activity (objective) [Срок оценки: From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up]

Вторичные конечные точки (4)

• Sleep quality (objective) [Срок оценки: From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up]
• sleep quality (subjective) [Срок оценки: From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up]
• Body composition [Срок оценки: From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up]
• Stress [Срок оценки: From enrollment to the end of treatment at 12 weeks, and 24 weeks follow up]

Критерии участия

Критерии включения

• 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.

Критерии исключения

• 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.

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Да

Дизайн исследования

Распределение

Рандомизированное

Модель

Параллельные группы

Маскирование

Тройное слепое

Основная цель

Организация здравоохранения

Центры проведения

Тайвань · 1 центр

• Tri-Service General Hospital — Taipei

Идентификаторы

NCT: NCT06814886 · A202405171

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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