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Идёт набор NCT07661550

Prevention of Postpartum Smoking Relapse and Related Health Consequences by Breastfeeding Promotion

Без фазы С лечением Smoking ( Cigarette) Breastfeeding

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: Breastfeeding promotion, Attention placebo control.
Кому может быть актуально
Состояния в реестре: Smoking ( Cigarette), Breastfeeding. Базовые параметры: от 18 лет · Женщины.
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 →

Обзор

The objective of this randomized controlled trial is to examine the efficacy of a new intervention to prevent postpartum smoking relapse and related health consequences through breastfeeding promotion. After the pre-test, ex-smokers who are still abstinent from smoking will be randomized into either the breastfeeding intervention or the attention placebo control group. The outcomes are postpartum smoking relapse, breastfeeding practices, and maternal and child health.

Подробное описание

We propose a randomized controlled trial to reduce postpartum smoking relapse by breastfeeding promotion from late pregnancy to 12 months postpartum. We will enroll 280 pregnant mothers who successfully quit smoking during this pregnancy (≤28 weeks). After the pre-test, participants who are still smoking abstinent will be randomized into either the breastfeeding intervention group (N=140) or the attention control group (N=140). The intervention group will receive a multicomponent intervention consisting of breastfeeding education, lactation counseling, social support, contingent financial incentives, and early limited formula milk via syringe feeding (optional for at-risk infants). The control group will receive counseling and support focusing on general infant care, with attention and monetary earnings similar to the intervention group. Both groups will receive usual care (i.e., information, education, and Quitline) for postpartum smoking relapse. The outcomes are postpartum smoking relapse, breastfeeding practices, and maternal and child health.

Aim 1 is to examine the efficacy of breastfeeding promotion intervention on postpartum smoking relapse. Aim 2 is to examine potential mediating mechanisms: reductions in stress and negative affect, enhancing mother-infant bonding and maternal sensitivity, and maternal weight retention. Aim 3 is to assess the effects of breastfeeding promotion intervention on maternal and infant health among ex-smoking mothers. This innovative study can yield promising data to support a new intervention to prevent postpartum smoking relapse. It has the potential to reduce smoking-related harms to both the mother and the infant, maximize the protective effects of breastfeeding on infant health and development, and narrow health disparities.

Вмешательства

  • Поведенческое Breastfeeding promotion
    The intervention group will receive a multicomponent intervention promoting breastfeeding, including education, lactation counseling, social support, breastfeeding-contingent financial incentives, and early limited formula milk via syringe feeding (optional for at-risk infants).
  • Поведенческое Attention placebo control
    The control group will receive instructions on general pregnancy and infant care from this project

Первичные конечные точки

  • Number of participants reporting to smoke [Срок оценки: 12 months postpartum]
Вторичные конечные точки (8)
  • Number of participants reporting to breastfeed [Срок оценки: 12months postpartum]
  • Systolic blood pressure level [Срок оценки: 12 months postpartum]
  • Diastolic blood pressure level [Срок оценки: 12 months postpartum]
  • Infant weight-for-length z-score [Срок оценки: 12 months of age]
  • Infant length-for-age z-score [Срок оценки: 12 months of age]
  • Infant head circumference [Срок оценки: 12 months of age]
  • Infant arm circumference [Срок оценки: 12 months of age]
  • Number of infants with bronchiolitis [Срок оценки: 12 months of age]

Критерии участия

Критерии включения

  • Be pregnant
  • Be 18 years or older
  • Have quit smoking cigarettes during this pregnancy
  • Be willing to receive infant care and breastfeeding education
  • Be able to read, listen, and talk in English

Критерии исключения

  • Medical conditions contraindicating breastfeeding, such as HIV infection, active tuberculosis, and breast removal
  • Current heavy drinking (≥4 standard drinks on any day or ≥8 standard drinks per week)

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
  • Division of Behavioral Medicine Department of Pediatrics Jacobs School of Medicine and Bio — Buffalo

Идентификаторы

NCT: NCT07661550 · STUDY00002632 · R01HD117113

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗