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NCT03200223 Clinical Trial

Lifestyle Related Disease Management With Wearable Device and Mobile Application

Obesity Clinical Trial

Official title:
A Study of the Management of the Patient's Disease Based on the Life Log Data of Patient With Lifestyle-related Diseases Through a Wearable Device and Mobile App

Clinical Trial Details — Status: Terminated

Administrative data
NCT number NCT03200223
Other study ID # B-1706/405-301
Secondary ID
Status Terminated
Phase N/A
First received
Last updated
Start date June 22, 2017
Est. completion date August 22, 2018

Study information
Verified date September 2018
Source Seoul National University Hospital
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In order to study the effectiveness of personalized healthcare intervention for lifestyle-related diseases, investigators designed this study using mobile application and clinical feedback coaching.

Recruitment information / eligibility
Status Terminated
Enrollment 60
Est. completion date August 22, 2018
Est. primary completion date June 22, 2018
Accepts healthy volunteers No
Gender All
Age group 18 Years to 80 Years
Eligibility Inclusion Criteria:

- Study participants must agree to support by him/herself at enroll time

- Patient without severe cardiopulmonary disease, cancer, or other acute diseases

- Patient must be over BMI > 23 kg/m2

Exclusion Criteria:

- Patient who did not agree with this study

- Patient with severe cardiopulmonary disease, cancer, or other acute diseases

- Patient who are pregnant

Study Design

Related Conditions & MeSH terms

Intervention

Behavioral:
• Personalized healthcare service
Personalized healthcare service, such as exercise recommendation, lifestyle activity coaching, health data monitoring

Locations
Country Name City State
Korea, Republic of Seoul National University Bundang Hospital Seongnam Gyeonggi-do

Sponsors (1)
Lead Sponsor Collaborator
Seoul National University Hospital

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary Weight change Measuring weight change Baseline and after 2 weeks, 4 weeks of lifestyle modification
Secondary Body composition change Measuring body composition Baseline and after 2 weeks, 4 weeks of lifestyle modification
Secondary Laboratory test result change Obstructive sleep apnea test Baseline and after 2 weeks, 4 weeks of lifestyle modification
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