Patient Navigation for Improving Transition Success Among Multiply Disadvantaged Young Adult Survivors of Childhood 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: Navigation, Control.
- Кому может быть актуально
- Состояния в реестре: Cancer Childhood. Базовые параметры: 20 лет — 29 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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Обзор
The goal of this clinical trial is to improve the successful healthcare transition from pediatric to adult-focused care for childhood cancer survivors. The main questions it aims to answer are * Receipt of the intervention (vs. standard of care control) will increase the proportion of CCS achieving transition success to adult-focused survivorship care from 50% to 70%. * Receipt of the intervention (vs. standard of care control) will significantly reduce patients' unmet HRSN. * Intervention effectiveness will be moderated by sociodemographic factors (gender, race/ethnicity, insurance status), medical risk for late effects, HRSN burden, and patient-reported outcomes (quality of life, self-efficacy). Researchers will compare those that receive intervention versus standard of care. Patients are randomized to either an intervention group, receiving structured PN-led sessions and tailored support for care transitions, or a control group receiving standard follow-up by a nurse case manager. High-HRSN patients in the intervention arm get monthly check-ins and coordinated handoffs to adult care providers for continuity.
Вмешательства
- Поведенческое Navigation
Follow Up - Поведенческое Control
Standard of Care
Первичные конечные точки
- Proportion of participants with Transition to Adult-Focused Survivorship Care [Срок оценки: Within 18 months following transition "launch" (study enrollment/baseline)]
Вторичные конечные точки (7)
- Change in HRSN score from baseline to each follow-up time point in each study arm. [Срок оценки: Baseline to 18 months post-enrollment]
- Change in Global Health-Related Quality of Life Score using Likert scale [Срок оценки: Baseline to 18 months post-enrollment]
- Change in General Self-Efficacy using Likert scale [Срок оценки: Baseline to 18 months post-enrollment]
- Change in mean scores for Patient-Reported Access to and Experience with Healthcare as measures by CAHPS (Consumer Assessment of Healthcare Providers and Systems) [Срок оценки: Baseline to 18 months post-enrollment]
- Change in count for barriers to care as measured by Likert scale barriers to care questionnaire [Срок оценки: Baseline to 18 months post-enrollment]
- Change in Emotional Social Support score using a Likert scale. [Срок оценки: Baseline to 18 months post-enrollment]
- Change in Informational Support score using a Likert scale. [Срок оценки: Baseline to 18 months post-enrollment]
Критерии участия
Критерии включения
- diagnosed between the ages of 0-19 years with cancer or with any condition treated with cancer-like therapy.
- currently in follow up at survivorship clinic or had a survivorship launch visit during the 12 months prior to study activation.
- current age 20-29 (>95% of patients will be age 20-21)
- meet LIFE Clinic transition readiness criteria, as clinically applied:
- at least 5 years off treatment
- medically stable
- demonstrate a workable understanding of transition
- have an identified primary care provider
- able to speak and read English or Spanish
- can provide informed consent.
Критерии исключения
- do not meet transition criteria
- speak a language other than English or Spanish
- are significantly impaired and cannot provide informed consent.
Критерии приведены из реестра в оригинале (на английском). Окончательную оценку соответствия проводит исследовательский центр.
Здоровые добровольцы: Нет
Дизайн исследования
- Распределение
- Рандомизированное
- Модель
- Параллельные группы
- Маскирование
- Открытое
- Основная цель
- Лечение
Центры проведения
США · 1 центр
- Children's Hospital Los Angeles — Los Angeles
Идентификаторы
NCT: NCT07630831 · CHLA-25-00386 · R01CA303651 · NCI-2025-09161