Application of Smart Devices in Adolescent Weight Control

Status Completed

Clinical Trial Summary

Clinical Trial Description

According to the definition of Health Literacy, health literacy means that a person can apply his or her reading, writing, and computing abilities to health-related information and activities. WHO consider Health Literacy is the cognitive and social skills which determine the motivation and ability of individuals to gain access, to understand and use information. The purposes of this study will to understand the relationship between health literacy, weight control behavior and weight control health outcome. According to the purpose, the study will be multi wave longitudinal panel study. The study will apply mobile phone applications and smart watches to understand the relationship between weight control behaviors and weight control health outcome in adolescent. There are two blocks in the mobile phone applications: questionnaire block and Weight status block will be design for the study. Questionnaire block include demography, and health literacy scales and diet diary. Weight status block include height, weight, waist circumference, and hip circumference. After the participant key-in the height and weight, the system will automatically calculate the BMI, also show the results of the BMI. The standard for BMI interpretation was by Dr. Chang's research about New Growth Charts for Taiwanese Adolescents. The data of smart watches will be upload into the NTUH health cloud system (named NTU MED GOD). This is the NTUH health cloud, different kinds of medical materials and data could be sent to the system, such as mobile phone and smart watches data. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT04760587
Study type	Observational
Source	National Taiwan University Hospital
Contact
Status	Completed
Phase
Start date	June 17, 2020
Completion date	January 1, 2023

View Details

See also
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Clinical trials are conducted in a series of steps, called phases - each phase is designed to answer a separate research question.

Phase 1: Researchers test a new drug or treatment in a small group of people for the first time to evaluate its safety, determine a safe dosage range, and identify side effects.
Phase 2: The drug or treatment is given to a larger group of people to see if it is effective and to further evaluate its safety.
Phase 3: The drug or treatment is given to large groups of people to confirm its effectiveness, monitor side effects, compare it to commonly used treatments, and collect information that will allow the drug or treatment to be used safely.
Phase 4: Studies are done after the drug or treatment has been marketed to gather information on the drug's effect in various populations and any side effects associated with long-term use.