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Идёт набор NCT07021885

NLit and Outcomes in HNC Survivor-Caregiver Dyads

— Наблюдательное Head and Neck Cancer Caregiver Burden Health Knowledge, Attitudes, Practice

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
Это наблюдательное исследование: исследуемое лечение участникам по протоколу не назначают.
Кому может быть актуально
Состояния в реестре: Head and Neck Cancer, Caregiver Burden, Health Knowledge, Attitudes, Practice. 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

Nutrition Literacy and Associated Outcomes in Head and Neck Cancer Survivor-caregiver Dyads

Обзор

The goal of this observational (cross-sectional) study is to better understand nutrition literacy in survivor-caregiver dyads and its impact on nutrition related outcomes and quality of life. We're interested in finding out how much they know about nutrition and how this might relate to their overall health, body composition, functional status, and overall well-being. We will target post-treatment head and neck cancer survivors and a paired informal caregiver. The main questions we aim to answer are: * How does the nutrition literacy of both the survivor and caregiver relate to their sociodemographic, behavioral, and clinical characteristics? * How dyadic nutrition literacy influence individual nutrition outcomes like skin carotenoid levels, body composition, and functional status? * Does the shared nutrition knowledge (nutrition literacy) of both the survivor and caregiver impact their quality of life together? Participants will: Answer questions about their knowledge of nutrition. Have their nutritional health status checked. Use a non-invasive device to measure skin carotenoid content to validate self-reports of fruit and vegetable intake. Have a simple and painless test to measure their body composition - like how much muscle and fat they have. Do some physical tests like grip strength and walking to measure their physical ability. Answer questions about their general well-being and lifestyle, like exercise and diet. (For the survivor) Share details about their cancer, its treatment, and their overall well-being. (For the caregiver) Answer questions about their role in taking care of the survivor, and their involvement in care routine such as food shopping and cooking.

Первичные конечные точки

  • Nutrition Literacy [Срок оценки: at a single time point between 6 months and 5 years post-treatment]
  • Nutrition Status [Срок оценки: at a single time point between 6 months and 5 years post-treatment]
  • Skin Carotenoid [Срок оценки: at a single time point between 6 months and 5 years post-treatment]
  • Body composition [Срок оценки: at a single time point between 6 months and 5 years post-treatment]
  • Functional status [Срок оценки: at a single time point between 6 months and 5 years post-treatment]
  • Sociodemographics. [Срок оценки: at a single time point between 6 months and 5 years post-treatment]
  • Fruit & Vegetable Intake [Срок оценки: at a single time point between 6 months and 5 years post-treatment]
  • Exercise [Срок оценки: at a single time point between 6 months and 5 years post-treatment]
  • Food Security [Срок оценки: At a single time point between 6 months and 5 years post-treatment]
  • Caregiving characteristics [Срок оценки: between 6 months and 5 years post-treatment]

Критерии участия

Критерии включения

  • Survivors and their caregivers will be eligible to participate if the survivor 1) has a history of oral cavity, pharyngeal, or laryngeal cancer, 2) is between 6 months - 4 years post-primary oncology treatment, 3) has no evidence of disease, 4) has an informal caregiver living in or out of the home who has a shared or primary role in food procurement and/or preparation, 5) no current use of feeding tube as the primary source of nutrition and can consume food orally, 6) age 18+, 7) English-speaking. Survivors and their caregivers will not be eligible to participate if either has 1) dementia or organic brain syndrome; 2) severe emotional distress; 3) active schizophrenia, 4) another diagnosis of cancer in the past five years (not including skin or cervical cancer in situ).

Критерии исключения

  • Adults unable to consent
  • Individuals who are not yet adults (infants, children, teenagers)
  • Pregnant women
  • Prisoners

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

Дизайн исследования

Модель наблюдения
Другое

Центры проведения

США · 1 центр
  • University of Kansas Medical Center — Kansas City

Идентификаторы

NCT: NCT07021885 · COE Pilot 2023

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗