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Идёт набор NCT05386719

Cardiometabolic Screening Program

Без фазы С лечением Breast Cancer Early-stage Breast Cancer

Ориентир для пациента и семьи

Простыми словами

Автоматическая сводка по структурированным данным реестра. Она помогает сориентироваться, но не заменяет официальный протокол или оценку врача.

Что изучают
В протоколе указаны: Prescreening, Screening and Enrollment, Baseline, Interpret BMI.
Кому может быть актуально
Состояния в реестре: Breast Cancer, Early-stage Breast Cancer. Базовые параметры: от 18 лет · Все.
Что важно проверить
Возраст, диагноз и пол — только базовые ориентиры. Предыдущее лечение, анализы и другие обязательные условия указаны ниже в критериях участия.
Где проводится
США
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

A Cardiometabolic Screening Program for Breast Cancer Survivors

Обзор

This research study is being done to implement a screening program for prediabetes, diabetes, dyslipidemia and/or hyperlipidemia, and higher risk of cardiovascular disease in breast cancer survivors. This program will also help to direct individuals with risk factors to community and institutional resources for management.

Подробное описание

The investigators propose a prospective cardiometabolic screening program for breast cancer survivors. A formalized screening program may ensure that all patients are receiving these routine screening tests. This program could not only serve to detect prediabetes, diabetes, dyslipidemia and/or hyperlipidemia, but also direct individuals with other risk factors to community and institutional resources for management.

HYPOTHESIS

* Prediabetes, diabetes, dyslipidemia and overweight/obesity are prevalent in women with early stage breast cancer. * Participants that continue to participate in the study will have lower HbA1c, lower LDL, percent weight loss, and change in patient-reported outcomes (quality of life, function and symptoms) at 6 and 12 months compared to baseline. * Risk factors for cardiovascular disease (such as tobacco use, family history, hypertension) are common in breast cancer patients. * The screening program will refer patients to established institutional programs and resources (Cardiovascular Disease prevention program, Healthful Weight Eating Activity Program and Endocrinology). * The prevalence of prediabetes, diabetes and dyslipidemia in women with breast cancer will be significantly higher than healthy controls from a national database, matched for age and other comorbidities.

OBJECTIVES

Primary Objectives

1. To estimate the prevalence of prediabetes, diabetes, dyslipidemia and overweight/obesity in women with early stage breast cancer 2. To estimate the proportion of participants with lower HbA1c, lower LDL, percent weight loss, and change in patient-reported outcomes (quality of life, function and symptoms) at 6 and 12 months compared to baseline.

Secondary Objectives

1. To estimate the prevalence of other risk factors for cardiovascular disease (tobacco use, family history, hypertension) in breast cancer patients 2. To report the number of referrals of individuals with diabetes or prediabetes or risk factors for cardiovascular disease (CVD) to established institutional programs and resources. 3. To compare the prevalence of prediabetes, diabetes and dyslipidemia in women with breast cancer with healthy controls from a national database, matched for age and other comorbidities.

Exploratory

1. To assess change in HbA1c from baseline 6 and 12 months, and use of antidiabetes pharmacotherapy for patients referred to Endocrinology for diabetes management 2. To assess change in total cholesterol and LDL from baseline to 6 and 12 months, and use of statins, aspirin or antihypertensives for patients referred to CVD prevention program 3. To assess percent weight loss, and use of pharmacotherapy in patients referred to institutional weight loss program

Вмешательства

  • Другое Prescreening
    Eligible patients (history of early stage breast cancer and at least 3 months from completion of local and systemic therapy at Johns Hopkins, reads and speaks English) complete survey for demographics, smoking status \& questions about cardiovascular disease.
  • Другое Screening and Enrollment
    Consent
  • Поведенческое Baseline
    Behavioral Battery and Patient Reported Outcome Quality of Life questionnaires (EORTC QLQ-C30 and QLQ-BR23) Labs (Hba1c + lipid panel if not done within 12 months or if abnormal within 1 year) Abstract vitals from chart review
  • Поведенческое Interpret BMI
    Refer to Healthful Eating, Activity and Weight Program (HEAWP) if BMI ≥25 and not already on lifestyle intervention
  • Другое Interpret HbA1c
    HbA1c results categorized as follows: HbA1c \<5.7%; HbA1c 5.7-6.4%; HbA1c 6.5%+; or Known diabetic on medication
  • Другое Interpret lipid panel and assess other risk factors
    Based on above categories: HbA1c \<5.7%: Any of these cardiovascular disease risk factors: current/former tobacco use, total cholesterol \>200, family history of Coronary Artery Disease/Heart Attack in first degree family \<55 year old male or \<65 year old female, systolic blood pressure \>130 HbA1c 5.7-6.4%: Refer to Primary Care Provider and consider Healthful Eating, Activity and Weight Program (HEAWP) HbA1c 6.5%+: Refer to Endocrinology if HbA1c ≥8% Known diabetic on medication: Refer to E
  • Поведенческое Assess 10 year risk of cardiovascular event
    If risk factors are present - refer to Cardiovascular Disease Prevention Program
  • Поведенческое Recommendations
    Provide individual patient handout based on all above interventions
  • Поведенческое Follow-Up
    6 and 12 month labs (if prior abnormal) and Patient Reported Outcome questionnaires

Первичные конечные точки

  • Prevalence of prediabetes [Срок оценки: 3 years]
  • Prevalence of diabetes [Срок оценки: 3 years]
  • Prevalence of hyperlipidemia [Срок оценки: 3 years]
  • Change in HbA1c [Срок оценки: Baseline, 6 months, 12 months]
  • Change in LDL cholesterol [Срок оценки: Baseline, 6 months, 12 months]
  • Prevalence of obesity/ overweight [Срок оценки: Baseline, 6 months, 12 months]
  • Quality of Life Questionnaire The European Organisation for Research and Treatment Cancer C30 [Срок оценки: Baseline, 6 months, 12 months]
  • Breast-specific symptoms assessed by the of The European Organisation for Research and Treatment Cancer Quality of Life Questionnaire BR-23 [Срок оценки: Baseline, 6 months, 12 months]
Вторичные конечные точки (9)
  • Cardiovascular risk factors (tobacco use) [Срок оценки: 3 years]
  • Cardiovascular risk factors (family history) [Срок оценки: 3 years]
  • Cardiovascular risk factors (hypertension) [Срок оценки: 3 years]
  • Referrals for individuals with pre-diabetes [Срок оценки: 3 years]
  • Referrals for individuals with diabetes [Срок оценки: 3 years]
  • Referrals for individuals with risk of cardiovascular disease [Срок оценки: 3 years]
  • Prevalence of prediabetes in women with breast cancer versus healthy individuals [Срок оценки: 3 years]
  • Prevalence of diabetes in women with breast cancer versus healthy individuals [Срок оценки: 3 years]
  • Prevalence of hyperlipidemia in women with breast cancer versus healthy individuals [Срок оценки: 3 years]

Критерии участия

Критерии включения

  • Diagnosis of early stage breast cancer
  • Completed local and/or systemic therapy at least 3 months ago
  • Receiving medical oncology care at through the breast cancer clinics at Johns Hopkins Medical Institute, including the Sidney Kimmel Comprehensive Cancer Center in Baltimore MD and Green Spring Station in Lutherville-Timonium MD, and Sibley Memorial Hospital in Washington D.C.
  • Read and speak English

Критерии исключения

  • Metastatic breast cancer

Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Скрининг

Центры проведения

США · 1 центр
  • Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins — Baltimore

Идентификаторы

NCT: NCT05386719 · J21125 · IRB00285627

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗