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SCOPE-Kinesisk kvinnestudie (SCOPE)

6. november 2026 oppdatert av: University of California, San Francisco

Det smarttelefonbaserte utdanningsprogrammet for kreft og fedmeforebygging for kinesiske kvinner (SCOPE-kinesiske kvinner)

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.

Studieoversikt

Status

Fullført

Intervensjon / Behandling

Detaljert beskrivelse

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.

Studietype

Intervensjonell

Registrering (Faktiske)

102

Fase

  • Ikke aktuelt

Kontakter og plasseringer

Denne delen inneholder kontaktinformasjon for de som utfører studien, og informasjon om hvor denne studien blir utført.

Studiesteder

    • California
      • San Francisco, California, Forente stater, 94143
        • University of California, San Francisco
    • Changsha, Hunan
      • Yuelucun, Changsha, Hunan, Kina, 410083
        • Central South University

Deltakelseskriterier

Forskere ser etter personer som passer til en bestemt beskrivelse, kalt kvalifikasjonskriterier. Noen eksempler på disse kriteriene er en persons generelle helsetilstand eller tidligere behandlinger.

Kvalifikasjonskriterier

Alder som er kvalifisert for studier

18 år og eldre (Voksen, Eldre voksen)

Tar imot friske frivillige

Ja

Kjønn som er kvalifisert for studier

Hunn

Beskrivelse

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).

Studieplan

Denne delen gir detaljer om studieplanen, inkludert hvordan studien er utformet og hva studien måler.

Hvordan er studiet utformet?

Designdetaljer

  • Primært formål: Forebygging
  • Tildeling: Randomisert
  • Intervensjonsmodell: Parallell tildeling
  • Masking: Dobbelt

Våpen og intervensjoner

Deltakergruppe / Arm
Intervensjon / Behandling
Ingen inngripen: Control

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.

Eksperimentell: SCOPE-Chinese Women Intervention

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.

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.

Hva måler studien?

Primære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mean Change in Waist Circumference Over Time
Tidsramme: Baseline, 3 months, and 6 months

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

Baseline, 3 months, and 6 months

Sekundære resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Mean Change in Body Mass Index (BMI) Over Time
Tidsramme: Baseline, 3 months, and 6 months

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.

Baseline, 3 months, and 6 months
Mean Change in Scores on the Self-Rated Abilities for Health Practices Scale Over Time
Tidsramme: Baseline, 3 months, and 6 months

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.

Baseline, 3 months, and 6 months
Mean Changes in China Food Frequency Questionnaire (FFQ) over time.
Tidsramme: Baseline, 3 months, and 6 months

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.

Baseline, 3 months, and 6 months
Mean Changes in Overall Physical Activity
Tidsramme: Baseline, 3 months, and 6 months

Change in overall Physical activity over time will be measured using the Fitbit Alta-HR device for 10 hours while participants are awake.

Baseline, 3 months, and 6 months
Mean Change in Blood Pressure Over Time
Tidsramme: Baseline, 3 months, and 6 months

Changes in blood pressure will be measured using the YuWell YE690A monitor for each participant over time.

Baseline, 3 months, and 6 months
Mean Change in Hemoglobin A1C (HbA1C) Over Time
Tidsramme: Baseline and 6 months

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%.

Baseline and 6 months
Mean Change in Serum Lipid Levels Over Time
Tidsramme: Baseline and 6 months

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

Baseline and 6 months
Mean Change in Cortisol over time
Tidsramme: Baseline and 6 months

A blood sample will be collected to measure change in total cortisol levels over time for each participant.

Baseline and 6 months
Relative telomere length (RTL)
Tidsramme: baseline and 6 months follow-up.

A blood sample will be collected to measure relative telomere length (RTL), assessed using the real-time quantitative polymerase chain reaction (qPCR) technique, adhering to the protocol specified by Cawthon.

baseline and 6 months follow-up.

Andre resultatmål

Resultatmål
Tiltaksbeskrivelse
Tidsramme
Percentage of Eligible participants Who Agree To Be Screened
Tidsramme: At Baseline

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.

At Baseline
Number of Uses of The Tracking App Over Time
Tidsramme: Baseline to 6 months

The number of uses of the tracking app and frequency of accessing the 12 modules, to measure change in usability over time

Baseline to 6 months
Percentage of Participants who completed assessments
Tidsramme: Up to 6 months

The percentage of completed assessments by participants at each visit will be used to measure adherence over time

Up to 6 months

Samarbeidspartnere og etterforskere

Det er her du vil finne personer og organisasjoner som er involvert i denne studien.

Samarbeidspartnere

Etterforskere

  • Hovedetterforsker: Jyu-Lin Chen, RN, PhD, University of California, San Francisco
  • Hovedetterforsker: Jia Guo, RN, PhD, Central South Univeristy

Publikasjoner og nyttige lenker

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Generelle publikasjoner

Studierekorddatoer

Disse datoene sporer fremdriften for innsending av studieposter og sammendragsresultater til ClinicalTrials.gov. Studieposter og rapporterte resultater gjennomgås av National Library of Medicine (NLM) for å sikre at de oppfyller spesifikke kvalitetskontrollstandarder før de legges ut på det offentlige nettstedet.

Studer hoveddatoer

Studiestart (Faktiske)

20. juli 2020

Primær fullføring (Faktiske)

30. desember 2022

Studiet fullført (Faktiske)

30. desember 2022

Datoer for studieregistrering

Først innsendt

23. mars 2020

Først innsendt som oppfylte QC-kriteriene

26. mars 2020

Først lagt ut (Faktiske)

30. mars 2020

Oppdateringer av studieposter

Sist oppdatering lagt ut (Faktiske)

10. november 2026

Siste oppdatering sendt inn som oppfylte QC-kriteriene

6. november 2026

Sist bekreftet

1. november 2026

Mer informasjon

Begreper knyttet til denne studien

Plan for individuelle deltakerdata (IPD)

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NEI

Legemiddel- og utstyrsinformasjon, studiedokumenter

Studerer et amerikansk FDA-regulert medikamentprodukt

Nei

Studerer et amerikansk FDA-regulert enhetsprodukt

Nei

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