Идёт набор NCT06648278

Patient Care Outreach, Navigation, Technology and Support 2.0

Без фазы С лечением Breast Cancer Cardiovascular Diseases

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: Patient Navigation Program, Quality-of-Life (QOL) Assessment, Survey Administration.
Кому может быть актуально: Состояния в реестре: Breast Cancer, Cardiovascular Diseases. 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

The Patient Care Outreach, Navigation, Technology and Support 2.0 Study

Обзор

This is a feasibility study employing virtual patient navigation for underserved individuals who speak English, Chinese or Spanish and were diagnosed with breast cancer or cardiovascular disease to determine the extent of usability for a virtual patient navigation portal serving people in underserved communities. While not able to entirely replace in-person interactions, virtual patient navigation may be used to expand reach and availability of navigation services to a much greater segment of the population.

Подробное описание

Patient COUNTS 2.0 aims to improve and scale up the current Patient COUNTS program.

PRIMARY OBJECTIVES:

I. Identify underserved individuals who speak English, Chinese or Spanish and were diagnosed with breast cancer or cardiovascular disease through collaboration with Zuckerberg San Francisco General Hospital (ZSFG), University of California, San Francisco clinics (Athena), University of California, San Francisco registries (via medical chart review), San Francisco State University, and other community organization collaborators.

II. Conduct outreach to potential participants to let them know about the availability of virtual patient navigation via the Patient Care Outreach, Navigation, Technology and Support (COUNTS) web portal, and the Patient COUNTS patient navigation program (NCT03867916).

III. Provide patient navigation virtually.

OUTLINE:

The patient COUNTS portal will be available in English and expanded to include content in Chinese and Spanish. An initial cohort of focus group of 15 breast cancer patients, 5 navigators, social workers, caregivers or other person involved in breast cancer care will help develop the culturally and language specific components of the COUNTS program. Following implementation, breast cancer participants and cardiovascular participants will participate in an online navigation program along with family members of the patient community will be enrolled. Participants will use the online COUNTS portal to access navigation program and may choose to have online/virtual navigation support or in-person navigation support. Participants also complete data collection and surveys over 15 minutes via web portal at baseline and 6 months and user experience survey at end of program participation.

Вмешательства

Поведенческое Patient Navigation Program
Online health tool
Другое Quality-of-Life (QOL) Assessment
Online surveys to assess QOL
Другое Survey Administration
Ancillary studies

Первичные конечные точки

Proportion of participants who reported satisfaction with COUNTS program [Срок оценки: Up to 6 months]
Rate of Participation [Срок оценки: Up to 6 months]
Utilization rate [Срок оценки: Up to 6 months]

Вторичные конечные точки (1)

Mean scores on the Functional Assessment of Cancer Therapy- Breast (FACT-B) [Срок оценки: Up to 6 months]

Критерии участия

Критерии включения

For Focus groups:

Breast cancer patients: Diagnosed with breast cancer, ages 18 or older, speaks English, Mandarin/Cantonese, or Spanish
Navigators: any patient navigator who has provided care to underserved populations diagnosed with cancer

For Portal Implementation phase:

Ages 18 or older
Speaks English, Mandarin/Cantonese, Spanish,
Has any stage breast cancer
Has access to a phone that is able to receive text messages, is willing to stay in the study for six-seven months.

Family User experience survey:

Family member or friend who may have assisted breast cancer participant with registration, accessing or otherwise assisting breast cancer family member or friend participant with the online portal.