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临床试验/NCT05630456
NCT05630456已完成不适用

The Effect of Health Provider's Feedback on Physical Activity Surveillance Using Wearable Device-Smartphone Application for Resolution of Metabolic Syndrome; a 12-Week Randomized Control Study

Pusan National University Hospital1 个研究点 分布在 1 个国家目标入组 67 人开始时间: 2020年8月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
已完成
入组人数
67
试验地点
1
主要终点
Fasting blood tests on baseline and 12th week visits

研究概览

简要总结

The Effect of Health Provider's Feedback on Physical Activity Surveillance using Wearable Device-Smartphone Application for Resolution of Metabolic Syndrome; a 12-Week Randomized Control Study

详细描述

Patients diagnosed with metabolic syndrome were recruited and prescribed to live for 12 weeks using a wrist-wearable device (B.BAND, B Life Inc, Korea). The block randomization method was used to distribute the participants between an intervention group (n=35) and control group (n=32). In the intervention group, an experienced study coordinator provided feedback on physical activity to individuals through telephone counseling every other week.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Single Group
主要目的
Health Services Research
盲法
Double (Participant, Investigator)

入排标准

年龄范围
19 Years 至 99 Years(Adult, Older Adult)
性别
All
接受健康志愿者
是

入选标准

  • •smart phone user

排除标准

  • 未提供

研究组 & 干预措施

Control Group

Placebo Comparator

In the case of the control group, physical activity is monitored by itself through wearable devices and smartphone apps without phone counseling.

干预措施: No regular feedback (Other)

Intervention Group

Experimental

In the intervention group, the researcher gave feedback on the subjects' exercise amount through telephone contact every 2 weeks during the 12-week study period. Through phone consultations, they answered questions about exercise or discussed problems, encouraged to continue exercising, answered questions or discussed problems related to wearable devices and apps, and encouraged continuous data transmission.

干预措施: Receving feedback (Other)

结局指标

主要结局

Fasting blood tests on baseline and 12th week visits

时间窗: Baseline and 12week

Blood samples were collected from the Jeonju vein after fasting for 6 hours and analyzed in our hospital's laboratory. The lipid profile was tested using an automated analyzer (Hitachi 747, Hitachi Corp, Japan) and enzyme colorimetric method. FPG levels were evaluated using glucose oxidase methods and Synchron LX 20 (Beckman Coulter, Fullerton, CA)

Changes in blood pressure (systolic blood pressure, diastolic blood pressure) at baseline and 12 weeks

时间窗: Baseline and 12week

Blood pressure was measured in a sitting position after resting using BP-203 RVII(Colin Corp, Aichi, Japan)

Changes in waist circumference (cm) at baseline and 12 weeks

时间窗: Baseline and 12week

The waist circumference was evaluated by a trained examiner (after normal exhalation) to the nearest millimeter from the midpoint between the lower edge of the rib and the iliac ridge.

Measurement of physical activity through wearable devices

时间窗: For 12 weeks

Investigators provided with wrist-wearable device (B.BAND, B Life Inc, Korea), which allowed them to wear and live for 12 weeks. Subsequently, a compatible app was installed on the participants' mobile phones and connected to a wearable device. Researchers who have been granted access can check and track participants' steps, calorie consumption, and MVPA (moderate- to vigorousintensity physical activity) on a daily basis through a web page.

次要结局

  • Changes in body composition at baseline and 12 weeks(Baseline and 12week)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Young Jin Tak

Principal Investigator

Pusan National University Hospital

研究点 (1)

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