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Набор скоро начнётся NCT07303062

Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement

Без фазы С лечением Adolescent Behavior

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: Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement (AMP-CARE).
Кому может быть актуально
Состояния в реестре: Adolescent Behavior. 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

Evaluating the Impact of Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement (AMP-CARE)

Обзор

The purpose of this research study is to learn if a parenting program called Adolescent Mental Health Parenting Program for Child Adult Relationship Enhancement (AMP-CARE) can help parents have more confidence in parenting their teen and improve their knowledge about normal teen development and teen mental health. The main questions it aims to answer are: * Does the AMP-CARE parenting program improve confidence in teen parenting and positive parenting? * Does the AMP-CARE parenting program improve parent knowledge about mental health? Researchers will compare participants who complete the parenting program to those who do not. Participants will: * Complete 2 surveys, one at the start of the study and one 6 -12 weeks later * Half of the participants will be randomly picked to attend the 6 virtual AMP-CARE sessions right away. * The other half will have the opportunity to attend AMP-CARE after they complete the second survey.

Подробное описание

In this randomized controlled trial, 60 parents of teens, ages 11-14 years, will be randomized to either AMP-CARE or wait-list control to achieve the following aims:

AIM 1. To measure the impact of AMP-CARE on parent mental health literacy as measured by the Parental Child Mental Health Literacy Questionnaire (PCMHLQ).

AIM 2: To measure the impact of AMP-CARE on parenting self-efficacy as measured by the Parenting Self Efficacy Scale.

AIM 3: To measure the impact of AMP-CARE on promotive parenting practices assessed by the Positive Parenting and Parental Involvement subscales of the Alabama Parenting Questionnaire.

Вмешательства

  • Поведенческое Adolescent Mental Health Parenting Program for Child-Adult Relationship Enhancement (AMP-CARE)
    The goals of AMP-CARE are to teach parents how to form a positive relationship with their teen and to teach about typical adolescent development and mental health. Each AMP-CARE session will be led by 1 or 2 trainers. About 4 to 13 parents will attend each virtual session lasting approximately 1.5 hours. Sessions will be weekly for 6 weeks. Participants are encouraged to practice the skills learned at AMP-CARE between the sessions.

Первичные конечные точки

  • Parent Mental Health Literacy [Срок оценки: From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.]
Вторичные конечные точки (2)
  • Parent Self Efficacy [Срок оценки: From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.]
  • Promotive Parenting Practices [Срок оценки: From enrollment to completion of AMP-CARE program or 6-12 weeks after enrollment.]

Критерии участия

Критерии включения

  • Parent or guardian of teen age 11-14 years
  • Receiving primary care at selected study sites
  • English speaking

Критерии исключения

  • Parents of children with severe mental illness (indicated by psychiatric hospitalization in the last 12 months or previous diagnosis of psychosis)
  • Parents of children with severe developmental delay (indicated by prior diagnosis of severe neurodevelopmental impairment, global developmental delay, severe expressive language delay)
  • Not available at time group is scheduled

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
Профилактика

Центры проведения

США · 2 центра
  • UNC Pediatrics at Panther Creek — Cary
  • UNC Children's Primary and Specialty Care at Carolina Pointe II — Chapel Hill

Идентификаторы

NCT: NCT07303062 · 20-3652

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗