Идёт набор NCT07390435

Feasibility and Acceptability of Collecting Sociodemographic Data in CCTG Trials

— Наблюдательное 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: Social Determinants of Health Questionnaire.
Кому может быть актуально: Состояния в реестре: 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: Канада
Следующий шаг: Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →

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Обзор

This study is being done to answer the following question: Are patients on a clinical trial willing to provide answers to questions about their social, economic, and environmental factors-sometimes called social determinants of health-which affect people's health experiences and access to care. These factors may include income, education, employment, housing, social supports, and experiences with discrimination or stress. Participation will help researchers better understand barriers to participating in clinical trials and access to health care.

Подробное описание

It is anticipated that 1000 people will take part in this study. Participation in this study will only take about 10 minutes or less. Participants who choose to take part in this study will be asked to fill out a form with questions in English or French about the non-medical factors that influence health. This includes asking about the conditions and places in which the participant lives, learns, works, and plays. Participants will also be asked how they feel about answering these questions. Researchers will use this information to better understand who participates in clinical trials.

Вмешательства

Другое Social Determinants of Health Questionnaire
This study will use a standardized SDoH Questionnaire to collect the required sociodemographic data

Первичные конечные точки

To evaluate the feasibility of collecting comprehensive sociodemographic data via a standardized SDoH Questionnaire among participants being screened and consented to a CCTG trial and participants already enrolled in a CCTG trial [Срок оценки: 12 months]

Вторичные конечные точки (1)

To assess the acceptability of this SDoH questionnaire to participants. [Срок оценки: 12 months]

Критерии участия

Критерии включения

Adults (≥18 years) who are either:

Currently being screened and consented to a CCTG trial (prospective).
Already enrolled in an ongoing CCTG trial and still under follow-up (retrospective).