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Идёт набор NCT06999382

Place Activation in Urban Peripheries: the 'Comunidades y Espacios Activos" Project (CEA)

Без фазы С лечением Uptake of Systematic Review Evidence

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: Active Dissemination and Implementation, Passive Dissemination.
Кому может быть актуально
Состояния в реестре: Uptake of Systematic Review Evidence. 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
Мексика
Следующий шаг
Сохраните исследование, покажите его лечащему врачу и уточните актуальный статус у исследовательского центра. Расходы, документы и поездка →
Официальное название

Contextually Responsive Implementation of Place-Activation Interventions for Promoting Physical Activity in Low-Income Urban Communities

Обзор

This study will use a Hybrid III Cluster-Randomized Controlled Trial to test an 'active dissemination and implementation' intervention in peripheral urban neighborhoods, designed to accelerate the uptake of evidence-based place-based activations that are known to be effective in increasing physical activity among local residents. The study will use a parallel design with eligible neighborhoods randomized to one of two arms: the (1) "Active Dissemination and Implementation" intervention arm (n=15 neighborhoods); and (2) the comparison arm (n=15 neighborhoods). Participants will be "implementation partners" in each of the participating neighborhoods (n=510 total participants, n=17 per neighborhood), comprised of a mix of local government representatives, representatives of non-governmental organizations working in the area, and community leaders. Intervention components to be delivered to implementation partners of neighborhoods randomized to the "Active Dissemination and Implementation" Intervention Arm include participation in 2 workshops, facilitation of coalition building activities, newsletters, targeted messaging, and access to a knowledge broker, and implementation support for 1 year (12 months).

Подробное описание

A group-randomized hybrid III trial (Aim 2) testing the effectiveness of a 1-year 'active dissemination and implementation' intervention in increasing the reach, adoption, and implementation fidelity (primary outcomes); and the real-world effectiveness (secondary outcome) of contextually relevant place-activation evidence-based interventions. 30 urban peripheral neighborhoods with recently completed open public space improvements will be selected and randomized within pairs to the intervention vs. comparison condition (15 in each arm). Participants (n=510 total, n=17 per neighborhood) will be community leaders and local-level stakeholders with authority over or engagement with the public open space being assessed. Intervention conditions include capacity-building activities for participants, and intervention implementation support for 1-year, which are hypothesized to improve adoption, reach, and implementation fidelity of place-activation evidence-based interventions.

Вмешательства

  • Поведенческое Active Dissemination and Implementation
    This intervention is designed to accelerate the uptake of evidence-based interventions that help maximize the impact of the addition or renovation of public open spaces on their utilization for active recreation among community members, ultimately effective physical activity levels in communities. The intervention targets implementation partners: local stakeholders/decision makers and community leaders, to increase their awareness of these evidence-based approaches for place-activation, and thei
  • Поведенческое Passive Dissemination
    Delivery of booklet with menu of evidence-based interventions for place-activation; and of pamphlet summarizing importance of healthy lifestyle promotion.

Первичные конечные точки

  • Reach [Срок оценки: Measured at baseline, 6-months (interim effects), 12-months (post-intervention), 24-months (maintenance)]
  • Adoption (self-reported by implementation partners) [Срок оценки: Measured at baseline, 6-months (interim effects), 12-months (post-intervention), 24-months (maintenance)]
  • Implementation (self-reported) [Срок оценки: Measured at baseline, 6-months (interim effects), 12-months (post-intervention), 24-months (maintenance)]
Вторичные конечные точки (3)
  • Adoption (group-level) [Срок оценки: Measured at baseline, 6-months (interim effects), 12-months (post-intervention), 24-months (maintenance)]
  • Implementation (group-level) [Срок оценки: Measured at baseline, 6-months (interim effects), 12-months (post-intervention), 24-months (maintenance)]
  • Real world effectiveness (physical activity) [Срок оценки: Measured at baseline, 6-months (interim effects), 12-months (post-intervention), 24-months (maintenance)]

Критерии участия

Inclusion Criteria for Implementation Partners (main sample for primary Outcomes):

  • Adults 18 years of age or older
  • Stakeholders (government or nongovernmental organization representatives in sectors such as health, education, air quality, economic development, urban planning, transportation, parks and recreation, public safety, etc.) or community leaders of peripheral urban neighborhoods of study cities (10 possible cities in Mexico: Colima, Merida, Monterrey, Toluca, Mexico City, Guadalajara, Tijuana, Leon, Cuernavaca, Tapachula).

Exclusion Criteria for Implementation Partners (main sample of primary outcomes):

  • Not meeting any of the inclusion criteria.

Inclusion Criteria for Intercept Survey Participants (for secondary outcomes):

  • 18 years or older
  • Located within the confines of the public open space being assessed in a study neighborhood at time of direct observation assessments.

Exclusion Criteria for Intercept Survey Participants (for secondary outcomes):

  • Not meeting any of the inclusion criteria.

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

Мексика · 1 центр
  • Instituto Nacional de Salud Publica — Cuernavaca

Идентификаторы

NCT: NCT06999382 · UTexasAustin-STUDY00005076 · R01MD019155

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗