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Идёт набор NCT07730827

Community-Informed Interventions for Equitable Congestive Heart Failure Management in Primary Care

Наблюдательное Congestive Heart Failure Heart Failure

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: Interviews and group discussion for patients and caregivers, Interviews and group discussion for community health worker and care-team stakeholders.
Кому может быть актуально
Состояния в реестре: Congestive Heart Failure, Heart Failure. 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 →

Обзор

The purpose of this study is to expand subject matter expertise and sustained capacity for equity-oriented care within the Advanced Care Ecosystem (ACE) by engaging patients, caregivers, community health workers (CHW), and care-team stakeholders in development work focused on adults living with congestive heart failure (CHF) and adverse social determinants of health (SDoH).

Вмешательства

  • Другое Interviews and group discussion for patients and caregivers
    Participants will be asked to complete an individual interview or participate in a group discussion lasting approximately 60 to 120 minutes, conducted in person, by telephone, or by Mayo-approved video platform. Interview and discussion guides will include discussion of barriers, facilitators, preferences, priorities, and care gaps related to congestive heart failure self-care, access, transitions of care, community health worker support, caregiver support, social needs, health literacy, languag
  • Другое Interviews and group discussion for community health worker and care-team stakeholders
    Participants will be asked to complete an individual interview or participate in a group discussion lasting approximately 60 to 120 minutes. Interview and discussion guides will focus on development of a community health worker competency-based training module and development of workflows for community health workers to support congestive heart failure patients' self-management and care transitions. Participants will provide feedback on implementation barriers and facilitators, including trainin

Первичные конечные точки

  • Identification of prioritized barriers to self-care [Срок оценки: Through study completion, an average of 2 years]

Критерии участия

Критерии включения

Patients living with congestive heart failure (CHF):

  • Age 18 years or older.
  • Diagnosis or clinical documentation of CHF or heart failure in the Mayo Clinic medical record.
  • Empaneled in Mayo Clinic, Rochester, primary care
  • Evidence in the EHR of one or more adverse SDoH, elevated utilization, medical/social complexity.
  • Able to provide informed consent.
  • Able to participate in study procedures.

Caregivers:

  • Age 18 years or older.
  • Caregiver with relevant lived, caregiving, or community experience related to CHF, and nominated by the patient.
  • Able to provide informed consent
  • Able to participate in study procedures.

Community health worker and care-team stakeholders:

  • Age 18 years or older.
  • Current or recent role relevant to CHF care, transitions of care, SDoH, patient education, or CHW workflows.
  • Able to provide informed consent
  • Able to participate in study procedures.

Критерии исключения

  • Under age 18 years.
  • Unable or unwilling to provide informed consent.

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

Здоровые добровольцы: Нет

Дизайн исследования

Модель наблюдения
Другое

Центры проведения

США · 1 центр
  • Mayo Clinic — Rochester

Идентификаторы

NCT: NCT07730827 · 25-013641

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗