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Идёт набор NCT06995924

Improving Uptake of Surveillance in Colorectal Cancer Survivors Through Navigation and Web Education

Без фазы С лечением Stage I Colorectal Cancer AJCC v8 Stage II Colorectal Cancer AJCC v8 Stage III Colorectal Cancer AJCC v8

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: Educational Intervention, Electronic Health Record Review, Internet-Based Intervention, Patient Navigation.
Кому может быть актуально
Состояния в реестре: Stage I Colorectal Cancer AJCC v8, Stage II Colorectal Cancer AJCC v8, Stage III Colorectal Cancer AJCC v8. 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 →

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Официальное название

A Pilot Trial to Evaluate the Effectiveness of Navigation, Interactive Web Education, or the Combination of Both to Promote Guideline-Concordant Colorectal Cancer Surveillance Care

Обзор

This pilot clinical trial looks at whether patient navigation services, an interactive web education intervention, called Current Together After Cancer (CTAC), or both navigation and CTAC works to improve the uptake of surveillance in patients with stage I-III colorectal cancer (CRC). Post-treatment surveillance is critical to detect recurrence early, yet many CRC survivors do not receive recommended surveillance care. Surveillance is a complex process that includes laboratory tests, cross-sectional imaging, and endoscopic procedures. Patient navigation services, interactive web education, or a combination of both may improve surveillance care for patients with stage I-III colorectal cancer.

Подробное описание

OUTLINE:

Patients are assigned to 1 of 3 arms based on the clinic location they receive cancer care at.

ARM A (VIRGINIA MASON): Patients receive access to navigation services, including education on surveillance care, reminders to complete care and assistance in scheduling surveillance, within 3 months of standard of care surgical resection for stage I-III CRC.

ARM B (FRED HUTCH \[SOUTH LAKE UNION\]): Patients receive access to the CTAC intervention, which includes self-directed, interactive web-based education about surveillance and a checklist of care, within 3 months of standard of care surgical resection for stage I-III CRC.

ARM C (FRED HUTCH \[OVERLAKE + EVERGREEN\]): Patients receive access to navigation services, including education on surveillance care, reminders to complete care and assistance in scheduling surveillance, and access to the CTAC intervention, which includes self-directed, interactive web-based education about surveillance and a checklist of care, within 3 months of standard of care surgical resection for stage I-III CRC.

Patients are followed up at 3 months post study-enrollment and 12-18 months after surgical resection.

Вмешательства

  • Другое Educational Intervention
    Complete self-directed interactive education
  • Другое Electronic Health Record Review
    Ancillary studies
  • Другое Internet-Based Intervention
    Receive access to CTAC
  • Поведенческое Patient Navigation
    Receive patient navigation services
  • Другое Survey Administration
    Ancillary studies

Первичные конечные точки

  • Completion of colonoscopy (stage I colorectal carcinoma patients) [Срок оценки: Up to 18 months post-surgical resection]
  • Completing any colonoscopy, carcinoembryonic antigen tumor marker (CEA), and cross-sectional imaging (stage II-III colorectal carcinoma patients) [Срок оценки: Up to 18 months post-surgical resection]
Вторичные конечные точки (5)
  • Knowledge of colorectal cancer (CRC) surveillance [Срок оценки: At baseline, and 3 months post enrollment]
  • Self-efficacy to complete CRC surveillance [Срок оценки: At baseline, and 3 months post enrollment]
  • Acceptability of the intervention [Срок оценки: At 3 months post enrollment]
  • Intervention appropriateness [Срок оценки: At 3 months post enrollment]
  • Feasibility of the intervention [Срок оценки: At 3 months post enrollment]

Критерии участия

Критерии включения

  • Age ≥ 18 due to disease and clinic population
  • Stage I-III CRC survivor within 3 months post-surgical resection
  • Being seen at a participating clinic
  • Ability to understand and complete surveys in English

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Нерандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Организация здравоохранения

Центры проведения

США · 2 центра
  • Benaroya Research Institute at Virginia Mason — Seattle
  • Fred Hutch/University of Washington Cancer Consortium — Seattle

Идентификаторы

NCT: NCT06995924 · RG1125283 · NCI-2025-03304 · 20875

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗