Evaluating an Adverse Childhood Experience-Targeting Advocate Model of a Substance Use Prevention Program

Официальное название

Evaluating an Adverse Childhood Experience-Targeting Advocate Model of a Substance Use Prevention Program: A Hybrid Type 1 Effectiveness-Implementation Trial

Обзор

Primary Objective: Conduct a rigorous evaluation of a prevention-based intervention designed to mitigate the harms of adverse childhood experiences (ACEs) exposure and prevent future ACEs, substance use, and overdose within 36 communities experiencing a disproportionate burden of substance use and ACEs. The study has three aims: (1) use a cluster randomized controlled trial to test effectiveness of the Strengthening Families Program (SFP) + Family Advocate (FA) intervention on substance use, overdose, and ACEs in 18 communities compared with SFP-only in 18 communities; (2) conduct a robust process evaluation informed by the Consolidated Framework for Implementation Research (CFIR) to explore implementation barriers and facilitators; and (3) conduct a cost evaluation to accurately estimate the costs required to implement SFP and SFP+FA and assess the cost-effectiveness of SFP+FA relative to SFP alone. Findings will provide a roadmap about the best ways to help disproportionately affected communities prevent substance use, overdose, and ACEs.

Подробное описание

Early exposure to Adverse Childhood Experiences (ACEs), such as parental substance use, increases the likelihood of future substance use and drug overdose, resulting in an intergenerational cycle of substance-related ACEs that can continue indefinitely if left uninterrupted. Community-level interventions may moderate the relationship between ACEs and substance use by providing an array of family support services and treatments to reduce disparities and improve reach and service linkages in the community. Although research suggests that effectively decreasing the prevalence and impact of ACEs and substance use requires addressing both family- and community-level factors in tandem, there is a critical gap within the evidence base pertaining to interventions that effectively integrate the two factors to prevent substance use and ACEs. RTI International and its partners, the New Jersey Prevention Network and RWJBarnabas Health, will evaluate an intervention integrating New Jersey's established, evidence-based Strengthening Families Program (SFP) with clinically trained, trauma-informed Family Advocates (FAs) who will assist families (i.e., parents/caregivers and youth between the ages of 12 and17) in accessing community resources. Specifically, this study will use a Hybrid Type 1 effectiveness-implementation design across 36 New Jersey communities experiencing a disproportionate burden of substance use and ACEs.

Вмешательства

• Поведенческое Strengthening Families Program + Family Advocate
  This intervention will integrate clinically trained, trauma-informed Family Advocates (FA) into the established, evidence-based Strengthening Families Program (SFP). Families will participate in the SFP7-17 curriculum, which consists of 11 sessions over 10-14 weeks. FAs will assist families in accessing community resources for substance use and Adverse Childhood Experiences (ACE) prevention and treatment.
• Поведенческое Strengthening Families Program
  This intervention consists of the SFP7-17 Group Class Curriculum. Families will participate in the SFP7-17 curriculum, which consists of 11 sessions over 10-14 weeks.

Первичные конечные точки

• Substance use prevalence [Срок оценки: Baseline, intervention completion (ranging from 10 to 14 weeks), and 6-month post-intervention follow-up]
• Substance use perceptions of harm [Срок оценки: Baseline, intervention completion (ranging from 10 to 14 weeks), and 6-month post-intervention follow-up]
• Referrals to clinical services [Срок оценки: Baseline, intervention completion (ranging from 10 to 14 weeks), and 6-month post-intervention follow-up]
• Referrals to non-clinical services [Срок оценки: Baseline, intervention completion (ranging from 10 to 14 weeks), and 6-month post-intervention follow-up]

Вторичные конечные точки (7)

• ACEs prevalence [Срок оценки: Baseline and 6-month post-intervention follow-up]
• Social needs prevalence [Срок оценки: Baseline and 6-month post-intervention follow-up]
• Substance use risk [Срок оценки: Baseline, intervention completion (ranging from 10 to 14 weeks), and 6-month post-intervention follow-up]
• System linkages [Срок оценки: Baseline and 6-month post-intervention follow-up]
• Average start-up cost [Срок оценки: Pre-implementation]
• Intervention cost [Срок оценки: Intervention start to intervention completion (ranging from 10 to 14 weeks)]
• Cost per service referral [Срок оценки: Intervention start to intervention completion (ranging from 10 to 14 weeks)]

Критерии участия

Inclusion Criteria: To be eligible to participate in this study, a family must meet all of the following criteria:

• Either reside in, or attend SFP meetings, within one of the 36 New Jersey communities with disproportionate levels of ACEs and substance use disorder (SUD) issues that are assigned to either the treatment or control conditions via the study's cluster randomized controlled trial design
• Meet family eligibility requirements:

• One or more adult caregivers
• One or more adolescents, ages 7 to 17
• Caregiver provision of signed and dated informed consent form
• For children, informed assent and parental permission via the informed consent to participate in the study
• Stated willingness to comply with all study procedures and lifestyle considerations and availability for the duration of the study
• Willingness to adhere to the regimens of the SFP and FA interventions
• Access to necessary resources for participating in a technology-based intervention (i.e., computer, smart phone, internet access)

Exclusion Criteria: A family who meets any of the following criteria will be excluded from participation in this study:

• Caregiver has previously completed SFP with one or more children, ages 7 to 17
• Intellectual disabilities (i.e., cognitive impairments that would prohibit the completion of the SFP curriculum or data collection instruments)
• Language difficulties (caregivers and children must read and understand spoken English)

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

Простое слепое

Основная цель

Профилактика

Центры проведения

США · 1 центр

• New Jersey Prevention Network — Tinton Falls

Идентификаторы

NCT: NCT06236100 · 0218779

Первоисточники (государственные реестры)

• ClinicalTrials.gov (NIH, США)

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