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Идёт набор NCT07059078

Brief Motivational Interviewing +/- Mindfulness Training for Adolescent Alcohol Use in Pediatric Primary Care

Без фазы С лечением Adolescent Alcohol Use

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: Brief Motivational Interviewing-based Alcohol Intervention, Smartphone App-delivered Mindfulness Training.
Кому может быть актуально
Состояния в реестре: Adolescent Alcohol Use. Базовые параметры: 12 лет — 17 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

PCORI Comparative Effectiveness Study: Comparative Effectiveness of Brief Motivational Interviewing +/- Adjunctive Smartphone App-delivered Mindfulness Training for Reducing Alcohol Use in Adolescents in Pediatric Primary Care Settings

Обзор

Alcohol use is prevalent in U.S. adolescents and contributes to adverse health outcomes in this population. Care for adolescent alcohol use is lacking in most pediatric primary care settings (PPC). This project is a pragmatic comparative effectiveness and implementation study that employs a superiority, two-arm, randomized, prospective, observer-blinded, controlled trial design to compare the effectiveness of a patient-centered brief motivational interviewing-based alcohol intervention (BMAI) alone to the same BMAI augmented with adjunctive smartphone app-delivered mindfulness training (MT) for alcohol use in adolescents receiving primary care in PPC clinics across a regional health network. Main effectiveness outcomes will be alcohol use and alcohol related problems assessed over a one-year follow-up period. Implementation outcomes and mediators and moderators of intervention response will also be examined as part of the study.

Подробное описание

Alcohol use is prevalent in U.S. adolescents and contributes to adverse health outcomes in this population. Over the past decade, screening, brief intervention, and referral to treatment (SBIRT) has become the primary model for addressing alcohol problems in US adolescents in pediatric healthcare settings. However, uptake and fidelity of SBIRT vary widely in real world settings and barriers to implementing effective brief interventions are common. Standard brief alcohol interventions (BAIs) have predominantly applied motivational interviewing (MI) and feedback techniques to target alcohol and other drug use in adolescents. There is a need to expand BAI options for youth who do not respond to these standard approaches. One intervention approach with growing societal interest and emerging evidence for efficacy in adolescent alcohol and other drug use is mindfulness training (MT). This project will compare two types of evidenced-based care for alcohol use in adolescents recruited from 13 pediatric primary care clinics in a regional health system. The interventions will be a patient-centered brief motivational interviewing-based alcohol intervention (BMAI) delivered by PPC clinicians as part of routine care, and BMAI in combination with smartphone app-delivered mindfulness training (BMAI+ MT).

The project is a pragmatic effectiveness and implementation study that employs a superiority, two-arm, randomized, prospective, observer-blinded, controlled trial design to compare the effectiveness of BMAI alone vs. BMAI augmented with adjunctive smartphone app-delivered MT on alcohol outcomes over a one-year follow-up period. The investigators will use the well-established standard BMAI adapted from the Provider Guide: Adolescent SBIRT Using the Screening to Brief Intervention Car, Relax, Alone, Forget, Friends, Trouble (S2BI-CRAFFT) Screening Tool, an evidence-based brief intervention for alcohol use in youth, and the widely disseminated Healthy Minds Program (HMP) smartphone meditation/mindfulness app which is freely available, science-based, and has shown feasibility and efficacy for reducing stress in youth populations. These interventions which combine elements of face-to-face +/- digital delivery and MI +/- MT will be tested in PPC clinics throughout the Johns Hopkins Medical Institute (JHMI) healthcare network which primarily serves racially/ethnically diverse population of urban and suburban youth in the greater Baltimore/Washington region that has a high proportion of minoritized youth.

The project seeks to answer the following three research questions:

Comparative effectiveness outcomes: What is the relative effectiveness of face-to-face clinician-administered BMAI with vs. without adjunctive app-delivered MT with the HMP app for alcohol using youth in PPC settings? Does supplementing clinician-administered BMAI with app-delivered MT result in superior outcomes in the form of reduced alcohol use and problems for this population or subgroups of the population?

Implementation outcomes: What are the patient and stakeholder perspectives, experiences, and preferences related to delivering BAI with these different components? What are the barriers and facilitators to delivering these BAI in PPC settings and for the diverse patient population served?

Heterogeneity of treatment effect (HTE) outcomes: How do baseline factors such as clinical severity, comorbid psychiatric symptoms and conditions, Socio-economic status (SES), sex, race, ethnicity, caregiver involvement, treatment preference, organization and clinical site readiness, and level of SBIRT integration at PPC clinic sites moderate outcomes across comparator interventions? How do changes in factors that may be mechanism of behavioral change (MOBC) for the different interventions (e.g. 'intrinsic' motivation to quit/reduce drinking, self-efficacy, and goal commitment for MI and mindfulness, anxiety, depression, impulsivity, and self-regulation for MT) and degree of engagement with intervention components (e.g., no. of sessions attended, time spent and no. of MT exercises completed, application of mindfulness in real-life settings) mediate outcomes across comparator interventions? Which patient subgroups benefit the most from which specific mindfulness and motivational BAI components?

Вмешательства

  • Поведенческое Brief Motivational Interviewing-based Alcohol Intervention
    Participants in both arms (BMAI and BMAI + MT) will receive a brief motivational interviewing-based alcohol intervention (BMAI) delivered by a pediatric clinician in the primary care setting. BMAI is adapted from the Provider Guide: Adolescent SBIRT Using the S2BI-CRAFFT Screening Tool, grounded in the stages of change model and motivational interviewing (MI). It consists of one or more brief sessions involving structured feedback, advice, and goal setting to help adolescents recognize links be
  • Поведенческое Smartphone App-delivered Mindfulness Training
    In addition to BMAI, participants in the BMAI + MT arm will receive 8 weeks of smartphone-delivered mindfulness training using the Healthy Minds Program (HMP) app. The HMP app provides self-guided, self-paced mindfulness and meditation training designed to improve psychological well-being, reduce stress/anxiety, and enhance self-regulation. It includes podcast-style teachings and guided meditations. The app features four modules-Awareness, Insight, Connection, and Purpose-based on neuroscience

Первичные конечные точки

  • Alcohol Use (total standard drinks) in the past 30 days [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Acceptability of intervention (adolescent report) assessed by the Client Satisfaction Questionnaire-Patient Report [Срок оценки: Month 2]
  • Acceptability of intervention (caregiver report) assessed by the Client Satisfaction Questionnaire-Caregiver Report [Срок оценки: Month 2]
  • Acceptability of intervention (provider report) assessed by the Provider Satisfaction Questionnaire [Срок оценки: month 3, and month 12]
  • Intervention experiences, perspectives, and preferences (adolescent report) assessed by qualitative interview [Срок оценки: Month 2]
  • Intervention experiences, perspectives, and preferences (caregiver report) assessed by qualitative interview [Срок оценки: Month 2]
  • Intervention experiences, perspectives, and preferences (provider report) assessed by qualitative interview [Срок оценки: month 3, and month 12]
  • Implementation barriers and facilitators for SBIRT and BMAI (provider report) [Срок оценки: Baseline, month 3, and month 12]
  • Percentage of providers reporting barriers and facilitators (provider report) [Срок оценки: Baseline, month 3, and month 12]
Вторичные конечные точки (9)
  • Heavy episodic drinking (HED) days in the past 30 days [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Cannabis use days in the past 30 days [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Tobacco/nicotine use days in the past 30 days [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Other drug use days in the past 30 days [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Alcohol-related problem severity assessed by the Alcohol Use Disorders Identification Test [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Recent Alcohol Consumption (past 7 days) [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Alcohol-related consequences assessed by the Short Index of Problems [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Emergency health service utilization [Срок оценки: Baseline, 1, 3, 6, and 12 months]
  • Quality of Life (QOL) as assessed by the Patient Reported Outcomes Measurement Information System (PROMIS) [Срок оценки: Baseline, 1, 3, 6, and 12 months]

Критерии участия

Критерии включения

  • 12-17 years old
  • Receiving pediatric primary care (PPC) services through the Johns Hopkins Medical Institute healthcare network
  • Screening positive for moderate or high alcohol use risk as indicated by a S2BI score (i.e., showing any monthly alcohol use in the past 12 months)
  • Able to speak, understand, and read in English or Spanish
  • Able to provide assent, and receiving parental consent/permission to participate.

Критерии исключения

  • Severe medical or psychiatric condition (e.g., behavioral dysregulation, psychopathology, or cognitive impairment that in the judgement of study or PPC provider may make participation hazardous \[e.g., psychosis, homicidality, active suicidality, mania\])
  • Intellectual Disability (self-, caregiver-, or PPC-reported, or PPC-documented)
  • Current or recent specialty substance use disorder treatment in the past 6 months
  • Demonstrated current physiological alcohol withdrawal requiring urgent inpatient referral in the judgement of study or PPC physician
  • Reported regular opioid, benzodiazepine, or cocaine use (> weekly) or history of opioid, benzodiazepine, or cocaine overdose in the past 6 months
  • Previous experience with a mindfulness-based intervention in the past 12 months
  • Current regular meditation practice (> 30 min/day for > 5 days avg. over 30 days prior to screening).

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Рандомизированное
Модель
Параллельные группы
Маскирование
Двойное слепое
Основная цель
Лечение

Центры проведения

США · 13 центров
  • Johns Hopkins Community Physicians, Remington — Baltimore
  • Johns Hopkins Bayview Pediatrics (Baltimore Medical System, Yard 56) — Baltimore
  • Johns Hopkins Community Physicians, Canton Crossing — Baltimore
  • Harriet Lane Clinic — Baltimore
  • Johns Hopkins University Center for Adolescent and Young Adult Health — Baltimore
  • Johns Hopkins Community Physicians, Water's Edge — Belcamp
  • Johns Hopkins Community Physicians, Bowie — Bowie
  • Johns Hopkins Community Physicians, Howard County Pediatrics — Columbia
  • … и ещё 5 центров

Идентификаторы

NCT: NCT07059078 · IRB00452272

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗