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Идёт набор NCT05978128

Utilizing Advocates and Supporters to Increase Lung Cancer Screening Rates in Eligible Participants

Без фазы С лечением Breast Carcinoma Lung Carcinoma

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: Health Education, Health Promotion and Education, Patient Navigation, Survey Administration.
Кому может быть актуально
Состояния в реестре: Breast Carcinoma, Lung Carcinoma. Базовые параметры: 40 лет — 80 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
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Официальное название

Utilizing Spheres of Influence to Increase Cancer Screening: Empowering Community Health Advocates

Обзор

This clinical trial assesses the use of advocates and supporters of breast and lung cancer screening to increase lung cancer screening rates amongst eligible participants. Imaging-based cancer screening is utilized with variable frequency. Breast cancer screening with mammography has been widely accepted and is commonly used among eligible women. Lung screening with computed tomography scans is poorly used, despite the potential to decrease deaths from lung cancer. There are many reasons lung screening isn't being used when compared to breast screening, such as smoking stigma and fear, along with a lack of awareness of lung screening. By conducting this trial, researchers want to assess the effectiveness of advocates and supporters of breast and lung screening, and to learn about the psychological barriers to cancer screening, identifying those that are unique to lung screening.

Подробное описание

PRIMARY OBJECTIVES:

I. Determine the number of patients undergoing breast screening who are eligible to participate in lung screening.

II. Determine whether patients currently participating in cancer screening (breast OR lung) are successful as "cancer screening advocates." III. Determine whether laypersons who are aware of screening (including those who accompany friends and family members to their screening appointments) are successful as "cancer screening advocates." IV. Identify knowledge base and psychological barriers to screening through surveys of potential screening participants.

OUTLINE:

Participants access an electronic patient portal with educational materials at baseline, 1- and 2-year follow-ups, and also interact with a patient navigator on study. Patients also receive materials to share with their friends/family on benefits of breast and lung cancer screening on study.

After completion of study intervention, participants are followed up yearly for up to 3 years.

Вмешательства

  • Поведенческое Health Education
    Access electronic patient portal with educational material
  • Другое Health Promotion and Education
    Receive materials on breast/lung cancer screening
  • Поведенческое Patient Navigation
    Interact with a patient navigator
  • Другое Survey Administration
    Ancillary studies

Первичные конечные точки

  • Increased rates of lung and breast cancer screening adherence [Срок оценки: Up to 3 years]
Вторичные конечные точки (1)
  • Success of "sphere of influence" model [Срок оценки: Up to 3 years]

Критерии участия

Критерии включения

  • Age:
  • Breast screening > 40
  • Lung screening 50-80
  • Male (M) or Female (F)
  • Current, former, or never smokers
  • Close family or friend with smoking history (in or out of state)

Критерии исключения

  • Age:
  • Breast screening < 40
  • Lung screening < 50 or > 80
  • Persons who had previously received a diagnosis of lung cancer, had hemoptysis, or had an unexplained weight loss of more than 6.8 kg (15 lb) in the preceding year will also be excluded
  • Persons with an active cancer

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Скрининг

Центры проведения

США · 1 центр
  • UCLA / Jonsson Comprehensive Cancer Center — Los Angeles

Идентификаторы

NCT: NCT05978128 · 22-000947 · NCI-2023-04133

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗