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SCOPE-Chinese Women Study (SCOPE)

Primary Purpose

Cancer, Breast, Obesity, Abdominal

Status
Completed
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
SCOPE-Chinese Women
Sponsored by
University of California, San Francisco
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Cancer, Breast focused on measuring Obesity, Abdominal, Cancer Prevention

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)FemaleAccepts Healthy Volunteers

Inclusion Criteria:

Participants must:

  • Be female
  • Be at least 18 years old
  • Have a waist circumference great than 80 cm
  • Own a smartphone
  • Be able to read Chinese and speak Mandarin
  • Be premenopausal
  • Have a child between the age of 1 and 18 years old

Exclusion Criteria:

Women are excluded from the study if they:

  • Are pregnant
  • Gave birth less than 12 months prior to enrollment date
  • Have an acute or life-threatening disease (e.g., renal failure).

Sites / Locations

  • University of California, San Francisco
  • Central South University

Arms of the Study

Arm 1

Arm 2

Arm Type

No Intervention

Experimental

Arm Label

Control

SCOPE-Chinese Women Intervention

Arm Description

Participants in the control group will receive a Fitbit Alta-Heart Rate (HR) and 12 weekly non-tailored educational modules via WeChat on general health topics that are important to 20-45 year-old women in China. Topics include intimate partner violence, anxiety, depression, sexually transmitted infections, HIV, unintended pregnancy, hepatitis B, and general cancer prevention.

SCOPE-Chinese Women intervention content and methods: SCOPE-Chinese Women is a smartphone- based intervention. Component 1. All study participants will receive a Fitbit Alta-HR tracking device to wear daily. Each participant will receive in-person, training on how to access the app and their tracking data. If a participant has not used the fitness device and app for more than one week, a WeChat reminder message will be sent to the participant. Component 2. Participants will receive 12 weekly culturally appropriate and evidence-based SCOPE-Chinese Women educational modules along with tailored tips and messages via WeChat. Each module will include three educational sessions that last less than 45 minutes total. Component 3. Six bi-weekly messages will be sent to participants via WeChat to encourage positive behavioral changes. Each participant's message content will be based on the participant's tracker information, personal goals, and preferences.

Outcomes

Primary Outcome Measures

Mean Change in Waist Circumference Over Time
The National Institutes of Health (NIH) waist circumference measurement protocol will be used to measure change in waist circumference for each participant over time.

Secondary Outcome Measures

Mean Change in Body Mass Index (BMI) Over Time
Weight and height will be used to compute the BMI with the formula=weight (kilograms(kg)) / height in (meters squared (m2). Changes in BMI will be collected for each participant over time.
Mean Change in Scores on the Self-Rated Abilities for Health Practices Scale Over Time
The Self Rated Abilities for Health Practices Scale (SRAHP) is a 28-item survey, with each item scored on a 5-point scale, with item scores ranging from 0=Not at all to 4=Completely. The survey is designed to measure self-perceived ability to implement health-promoting behaviors across four subscales: Exercise, Nutrition, Responsible Health Practice, and Psychological Well Being, and overall. The total score ranges from 0 - 112, with higher scores indicating greater abilities for health practices. Changes in scores will be collected for each participant over time.
Mean Changes in China Food Frequency Questionnaire (FFQ) over time.
Food intake using the China food frequency questionnaire (FFQ), which includes a list of 118 food items will be used to measure aggregate changes in food intake over time.
Mean Changes in Overall Physical Activity
Change in overall Physical activity over time will be measured using the Fitbit Alta-HR device for 10 hours while participants are awake.
Mean Change in Blood Pressure Over Time
Changes in blood pressure will be measured using the YuWell YE690A monitor for each participant over time.
Mean Change in Hemoglobin A1C (HbA1C) Over Time
A blood sample will be collected to measure change in HbA1C over time for each participant, using an established cut off value at 6.4%.
Mean Change in Serum Lipid Levels Over Time
A blood sample will be collected to measure change in total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides (all measured in milligrams per deciliter (mg/dL)) over time for each participant
Mean Change in Cortisol over time
A blood sample will be collected to measure change in total cortisol levels over time for each participant.

Full Information

First Posted
March 23, 2020
Last Updated
December 21, 2022
Sponsor
University of California, San Francisco
Collaborators
Central South University
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1. Study Identification

Unique Protocol Identification Number
NCT04326660
Brief Title
SCOPE-Chinese Women Study
Acronym
SCOPE
Official Title
The Smartphone-Based Cancer and Obesity Prevention Education Program for Chinese Women (SCOPE-Chinese Women)
Study Type
Interventional

2. Study Status

Record Verification Date
December 2022
Overall Recruitment Status
Completed
Study Start Date
July 20, 2020 (Actual)
Primary Completion Date
December 30, 2021 (Actual)
Study Completion Date
December 30, 2021 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University of California, San Francisco
Collaborators
Central South University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This project examines the feasibility of a smartphone-based intervention to reduce obesity and breast cancer risk among Chinese women in China. The proposed intervention is to use the mobile application and an activity tracker device to promote a healthier lifestyle and physical activity. The intervention will be tailored to the participants' behaviors, personal needs, and preferences. The aim is to reduce abdominal obesity and improve healthy lifestyle behaviors in premenopausal women with children in order to reduce the growing cancer burden in China.
Detailed Description
Cancer presents a major disease burden across the globe. The incidence and mortality of gynecologic cancers have increased significantly in China over the last two decades with breast and endometrial cancer as leading causes of death in women in China. Obesity, especially abdominal obesity, and unhealthy lifestyles are major risk factors for breast and endometrial cancer. A high risk group for obesity is mothers with dependent children as they have high levels of stress and family responsibilities that prevent regular engagement in a healthy lifestyle and early screening activities. Because reducing postmenopausal abdominal obesity is very difficult and because of the significant increased risk for gynecologic cancers in obese postmenopausal women, interventions that aim to reduce abdominal obesity and improve healthy lifestyle behaviors in premenopausal women with children are critical to reducing the growing cancer burden in China. A smartphone-based intervention provides a promising platform for obesity and cancer prevention. In this proposed study, the research team will modify the Healthy Mothers Healthy Children: Technology-Based Intervention to Prevent Obesity, which was developed by the principal investigator. The proposed intervention (titled "The Smartphone-Based Cancer and Obesity Prevention Education Program for Chinese Women: SCOPE-Chinese Women") is a smartphone-based, data-driven, and individually tailored intervention. It includes 12 weekly educational modules and six bi-weekly tailored messages delivered via WeChat, a popular communication app in China. The intervention will also be tailored to the participants' behaviors, personal needs, and preferences. The overall goal of this proposed study is to assess the feasibility and estimate the preliminary efficacy of the SCOPE-Chinese Women intervention using a randomized control study design (RCT). The following aims will be addressed. Aim 1: To assess the feasibility of the smartphone-based lifestyle intervention (i.e., SCOPE-Chinese Women). Aim 2: To estimate the preliminary efficacy of the SCOPE-Chinese Women intervention on the primary outcome (waist circumference) and secondary outcomes (body mass index, self-efficacy, food intake, physical activity, and metabolic risk) between the intervention and control groups at baseline, 3 months, and 6 months. Aim 3: To understand participants' acceptance, barriers to adherence, and recommendations for intervention.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Cancer, Breast, Obesity, Abdominal
Keywords
Obesity, Abdominal, Cancer Prevention

7. Study Design

Primary Purpose
Prevention
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
This pilot study will utilize a randomized control trail design with a control group.
Masking
Participant
Masking Description
To decrease cross-contamination of treatment effect, the six study sites will be the units of randomization. A Statistical Package for Social Sciences (SPSS) program will be used to statistically match the groups and to randomly assign each study group.
Allocation
Randomized
Enrollment
40 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Control
Arm Type
No Intervention
Arm Description
Participants in the control group will receive a Fitbit Alta-Heart Rate (HR) and 12 weekly non-tailored educational modules via WeChat on general health topics that are important to 20-45 year-old women in China. Topics include intimate partner violence, anxiety, depression, sexually transmitted infections, HIV, unintended pregnancy, hepatitis B, and general cancer prevention.
Arm Title
SCOPE-Chinese Women Intervention
Arm Type
Experimental
Arm Description
SCOPE-Chinese Women intervention content and methods: SCOPE-Chinese Women is a smartphone- based intervention. Component 1. All study participants will receive a Fitbit Alta-HR tracking device to wear daily. Each participant will receive in-person, training on how to access the app and their tracking data. If a participant has not used the fitness device and app for more than one week, a WeChat reminder message will be sent to the participant. Component 2. Participants will receive 12 weekly culturally appropriate and evidence-based SCOPE-Chinese Women educational modules along with tailored tips and messages via WeChat. Each module will include three educational sessions that last less than 45 minutes total. Component 3. Six bi-weekly messages will be sent to participants via WeChat to encourage positive behavioral changes. Each participant's message content will be based on the participant's tracker information, personal goals, and preferences.
Intervention Type
Other
Intervention Name(s)
SCOPE-Chinese Women
Intervention Description
SCOPE-Chinese Women is a smart-phone based intervention that includes a Fitbit tracking device to monitor daily activity, 12-weeks of educational modules delivered by WeChat, and Bi-weekly messages that encourage positive behavioral change. The data will be examined by the research team to assess efficacy of the intervention.
Primary Outcome Measure Information:
Title
Mean Change in Waist Circumference Over Time
Description
The National Institutes of Health (NIH) waist circumference measurement protocol will be used to measure change in waist circumference for each participant over time.
Time Frame
Baseline, 3 months, and 6 months
Secondary Outcome Measure Information:
Title
Mean Change in Body Mass Index (BMI) Over Time
Description
Weight and height will be used to compute the BMI with the formula=weight (kilograms(kg)) / height in (meters squared (m2). Changes in BMI will be collected for each participant over time.
Time Frame
Baseline, 3 months, and 6 months
Title
Mean Change in Scores on the Self-Rated Abilities for Health Practices Scale Over Time
Description
The Self Rated Abilities for Health Practices Scale (SRAHP) is a 28-item survey, with each item scored on a 5-point scale, with item scores ranging from 0=Not at all to 4=Completely. The survey is designed to measure self-perceived ability to implement health-promoting behaviors across four subscales: Exercise, Nutrition, Responsible Health Practice, and Psychological Well Being, and overall. The total score ranges from 0 - 112, with higher scores indicating greater abilities for health practices. Changes in scores will be collected for each participant over time.
Time Frame
Baseline, 3 months, and 6 months
Title
Mean Changes in China Food Frequency Questionnaire (FFQ) over time.
Description
Food intake using the China food frequency questionnaire (FFQ), which includes a list of 118 food items will be used to measure aggregate changes in food intake over time.
Time Frame
Baseline, 3 months, and 6 months
Title
Mean Changes in Overall Physical Activity
Description
Change in overall Physical activity over time will be measured using the Fitbit Alta-HR device for 10 hours while participants are awake.
Time Frame
Baseline, 3 months, and 6 months
Title
Mean Change in Blood Pressure Over Time
Description
Changes in blood pressure will be measured using the YuWell YE690A monitor for each participant over time.
Time Frame
Baseline, 3 months, and 6 months
Title
Mean Change in Hemoglobin A1C (HbA1C) Over Time
Description
A blood sample will be collected to measure change in HbA1C over time for each participant, using an established cut off value at 6.4%.
Time Frame
Baseline and 6 months
Title
Mean Change in Serum Lipid Levels Over Time
Description
A blood sample will be collected to measure change in total cholesterol, low-density lipoprotein (LDL) cholesterol, high-density lipoprotein (HDL) cholesterol, and triglycerides (all measured in milligrams per deciliter (mg/dL)) over time for each participant
Time Frame
Baseline and 6 months
Title
Mean Change in Cortisol over time
Description
A blood sample will be collected to measure change in total cortisol levels over time for each participant.
Time Frame
Baseline and 6 months
Other Pre-specified Outcome Measures:
Title
Percentage of Eligible participants Who Agree To Be Screened
Description
The number of overall eligible participants and the number of eligible participants who agree to be screened will be used to compute the percentage used for enrollment.
Time Frame
At Baseline
Title
Number of Uses of The Tracking App Over Time
Description
The number of uses of the tracking app and frequency of accessing the 12 modules, to measure change in usability over time
Time Frame
Baseline to 6 months
Title
Percentage of Participants who completed assessments
Description
The percentage of completed assessments by participants at each visit will be used to measure adherence over time
Time Frame
Up to 6 months

10. Eligibility

Sex
Female
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: Participants must: Be female Be at least 18 years old Have a waist circumference great than 80 cm Own a smartphone Be able to read Chinese and speak Mandarin Be premenopausal Have a child between the age of 1 and 18 years old Exclusion Criteria: Women are excluded from the study if they: Are pregnant Gave birth less than 12 months prior to enrollment date Have an acute or life-threatening disease (e.g., renal failure).
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Jyu-Lin Chen, RN, PhD
Organizational Affiliation
University of California, San Francisco
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Jia Guo, RN, PhD
Organizational Affiliation
Central South Univeristy
Official's Role
Principal Investigator
Facility Information:
Facility Name
University of California, San Francisco
City
San Francisco
State/Province
California
ZIP/Postal Code
94143
Country
United States
Facility Name
Central South University
City
Yuelu
State/Province
Changsha, Hunan
ZIP/Postal Code
410083
Country
China

12. IPD Sharing Statement

Plan to Share IPD
No
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SCOPE-Chinese Women Study

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