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Идёт набор NCT06187077

Techquity by FAITH!

Без фазы С лечением Health Equity 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: DHA-Enhanced FAITH! App, FAITH! App.
Кому может быть актуально
Состояния в реестре: Health Equity, 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 →
Официальное название

Techquity by FAITH!: A Cluster Randomized Controlled Trial To Assess the Efficacy of a Community-informed, Cardiovascular Health Promotion Mobile Intervention With Digital Health Advocate Support

Обзор

The goal of this clinical trial is to engage African-American churches via an established community-academic partnership (FAITH! Program) to build capacity to promote cardiovascular health and digital health equity in African-American faith communities. There are 3 study aims: Aim 1: Co-design a culturally tailored digital health equity toolkit with community members Aim 2: Train a network of Digital Health Advocates (DHAs) in digital health equity and cardiovascular health promotion Aim 3: Test the impact of a DHA-enhanced mobile health intervention (the FAITH! App) on cardiovascular health and digital health readiness among participants In Aim 1, participants will attend a series of focus groups to share their input on a digital health equity curriculum that will be condensed into a toolkit. In Aim 2, DHAs will be trained using this toolkit as well as a community health advocacy curriculum to learn how to promote digital health readiness and cardiovascular health in their communities. Finally, Aim 3 will be a randomized controlled trial where participants will use the FAITH! App to improve their cardiovascular health. Some participants will have the added support of a DHA, and the control group participants will use the app with no additional support to test whether the DHA support is associated with a more significant improvement in cardiovascular health.

Подробное описание

This study addresses cardiovascular health and digital health disparities faced by African-Americans (AAs). We propose three aims to engage with the AA community and build capacity for a digital literacy and cardiovascular health promotion. Aim 1 will engage AA churches to co-design a culturally relevant digital health equity toolkit through an iterative focus group process. In aim 1, we will recruit 20 AAs to represent their churches and be trained as digital health advocates (DHAs) by completing digital health readiness education (using the toolkit developed in aim 1) and cardiovascular health promotion. This advocacy program will be integrated into an existing mobile health intervention, the FAITH! App, in Aim 3. The impact of the community-informed, mHealth intervention, enhanced with DHA support, on AA adults' cardiovascular health will be assessed in a cluster randomized controlled trial. 150 participants will be be randomized to utilize the FAITH! App alone or with the support of the DHA at their church. Cardiovascular health will be assessed at baseline, approximately 3 months, 6 months, and 12 months post-randomization using the American Heart Association's Life's Essential 8 metric for cardiovascular health.

Вмешательства

  • Поведенческое DHA-Enhanced FAITH! App
    This group of participants will follow an 11-week guided intervention with the FAITH! App. Weekly educational modules provide information on components of cardiovascular health (CVH). Participants are given a Fitbit to track physical activity, which will automatically synch to the app and will be asked to track their daily fruit and vegetable intake on the app. DHAs will promote CVH and digital health readiness as peer mentors by guiding participants through the educational modules and encouragi
  • Поведенческое FAITH! App
    This group of participants will follow an 11-week guided intervention with the FAITH! App. Each week, an educational module is completed in the app, which provides information on a component of cardiovascular health. Participants will be given a Fitbit to track their physical activity, which will automatically synch to the app, and will be asked to track their daily fruit and vegetable intake on the app as well. Following the 11-week guided intervention, participants will have a 12-month mainten

Первичные конечные точки

  • Life's Essential 8 Composite Score change [Срок оценки: Baseline, 6-months and 12-months post-randomization]
  • Blood Pressure Score Change (Life's Essential 8 Component) [Срок оценки: Baseline, 6-months and 12-months post-randomization]
  • Fasting Glucose/Hemoglobin A1c Score Change (Life's Essential 8 Component) [Срок оценки: Baseline, 6-months and 12-months post-randomization]
  • Fasting Blood Lipids Score Change (non-HDL cholesterol) (Life's Essential 8 Component) [Срок оценки: Baseline, 6-months and 12-months post-randomization]
  • Body Mass Index (BMI) Score Change (Life's Essential 8 Component) [Срок оценки: Baseline, 6-months and 12-months post-randomization]
  • Tobacco/Nicotine Exposure Score Change (Life's Essential 8 Component) [Срок оценки: Baseline, 6-months and 12-months post-randomization]
  • Dietary Quality Score Change (Life's Essential 8 Component) [Срок оценки: Baseline, 6-months and 12-months post-randomization]
  • Physical Activity Score Change (Life's Essential 8 Component) [Срок оценки: Baseline, 6-months and 12-months post-randomization]
  • Sleep Health Score Change (Life's Essential 8 Component) [Срок оценки: Baseline, 6-months and 12-months post-randomization]
Вторичные конечные точки (9)
  • Digital Health Readiness [Срок оценки: Baseline, 3 months post-randomization]
  • Social Support - Diet [Срок оценки: Baseline, 3 months, 6 months, and 12 months post-randomization]
  • Self Regulation - Diet [Срок оценки: Baseline, 3 months, 6 months, and 12 months post-randomization]
  • Perceived Barriers - Diet [Срок оценки: Baseline, 3 months, 6 months, and 12 months post-randomization]
  • Social Support - Physical Activity [Срок оценки: Baseline, 3 months, 6 months, and 12 months post-randomization]
  • Self Regulation - Physical Activity [Срок оценки: Baseline, 3 months, 6 months, and 12 months post-randomization]
  • Perceived Barriers - Physical Activity [Срок оценки: Baseline, 3 months, 6 months, and 12 months post-randomization]
  • Artificial Intelligence (AI)-Electrocardiogram (ECG) [Срок оценки: Baseline, 6 months and 12 months post-randomization]
  • Cardio-ankle vascular index (CAVI) [Срок оценки: Baseline, 6 months and 12 months post-randomization]

Критерии участия

Aim 1- Inclusion Criteria: African/American race/ethnicity, age ≥ 18 years, basic Internet navigation skills, active email address

Aim 2- Inclusion Criteria: African/American race/ethnicity, age ≥ 18 years, ownership of smartphone (supporting iOS or Android systems), moderate to high digital health literacy (by eHealth literacy scale \[eHEALS\], score ≥26)

Aim 3- Inclusion Criteria: African/American race/ethnicity, age ≥ 18 years, ownership of smartphone (supporting iOS or Android systems), low digital health literacy (by eHEALS, score ≤26), basic Internet navigation skills, at least weekly Internet access, active email address, fruit/vegetable intake ≤5 servings/day, no regular physical activity, able to engage in moderate physical activity and willingness to participate in all aspects of the study.

Exclusion Criteria: Unable to walk up ≥2 flights of stairs or walk ≥1 city block without assistance or stopping, pregnant (at time of study enrollment), visual/hearing impairment or mental disability that would preclude independent app use.

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

Здоровые добровольцы: Да

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Открытое
Основная цель
Профилактика

Центры проведения

США · 1 центр
  • Mayo Clinic in Rochester — Rochester

Идентификаторы

NCT: NCT06187077 · 23-011118 · 3P50MD017342-03S3

Первоисточники (государственные реестры)

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