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NCT05506189 Clinical Trial

Life Style Modification for Breast Canccer Survivors Using Mobile App-based Human Coaching Program

Breast Cancer Survivors Clinical Trial

Official title:
A Prospective Study on the Effect of Quality of Life and Life Style Modification for Breast Cancer Survivors Using Mobile App-based Human Coaching Program

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT05506189
Other study ID # NCC 2019-0098
Secondary ID
Status Completed
Phase
First received
Last updated
Start date May 14, 2019
Est. completion date June 30, 2022

Study information
Verified date August 2022
Source National Cancer Center, Korea
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

This study is aimed to investigate whether mobile app-based human coaching program for 6 months is effective for reducing BMI in breast cancer survivors with overweight and obesity.

Recruitment information / eligibility
Status Completed
Enrollment 130
Est. completion date June 30, 2022
Est. primary completion date December 31, 2021
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 70 Years
Eligibility Inclusion Criteria: 1. breast cancer survivors who have completed acute treatment of breast cancer 2. Age: 18 ~ 70 year old 3. stage: I, II, III 4. BMI=25.0 Kg/m2 5. breast cancer survovrs who can use mobile application program 6. breast cancer survovrs who agree with this study's consent Exclusion Criteria: 1. Stage IV, carcinoma in situ 2. breast cancer survivors who don't use smartphone 3. breast cancer survivors with previous other malignant disease 4. breast cancer survivors with multiple malignancies 5. breast cancer survivors with uncontrolled chronic comorbid disease 6. breast cancer survovrs who disagree with this study's consent

Study Design

Related Conditions & MeSH terms

Intervention

Other:
• mobile application program with human coach
6-months mobile application program with human coach for life-style modifiation including diet and exercise

Locations
Country Name City State
Korea, Republic of National Cancer Center Goyang-si Gyeonggi-do

Sponsors (1)
Lead Sponsor Collaborator
National Cancer Center, Korea

Country where clinical trial is conducted

Korea, Republic of, 

Outcome
Type Measure Description Time frame Safety issue
Primary reduction of body mass index (BMI) whether the 6-month mobile program can be effective for reducing BMI Baseline and 6 month
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