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Набира участници Не е приложимо NCT07420621

Preliminary Effectiveness of Enhanced Text Message + Incentives

Не е приложима фаза (напр. обсервационно)
Заболявания: Smoking Cessation Pregnancy

Спонсор: University of Kansas Medical Center

Налично на: БГ
Обобщение
This study is a preliminary evaluation of a smoking cessation intervention designed for pregnant women that combines text message support and financial incentives. The aims of this study are to determine the preliminary feasibility and acceptability of text message + incentives (intervention) vs. text message only (control).
Описание
Pregnant women who smoke and their babies are exposed to known carcinogens and smoking is associated with adverse maternal and birth outcomes. Low-income pregnant women are particularly at risk because they have higher smoking rates and are less likely to quit. Despite continued smoking, most pregnant smokers do not receive smoking cessation counseling and only one in 10 receive referrals to cessation services or follow-up care. Incentives for smoking cessation yield the highest effect sizes of any intervention for pregnant women. Most prior studies evaluating incentives for smoking cessation in this population have used time and resource-intensive in-person visits to verify abstinence for contingent reinforcement. The long-term goal of this research is to reduce the burden of tobacco use by developing and evaluating a highly scalable, effective intervention to support smoking cessation during pregnancy.
Кой може да участва
Inclusion Criteria: * Pregnant women aged: 18+ * Enrolled in the Special Supplemental Nutrition Program for women, Infants, and Children (WIC) or Medicaid (or applied/applying) * Self-reported current daily smokers * Able to communicate in English * Access to a mobile phone capable of receiving text messages Exclusion Criteria: * Not at all interested in quitting * Smoke less than 24 days in the past month * Greater than 30 weeks gestation
Интервенции
Text Messages
BEHAVIORAL
Incentives
BEHAVIORAL
Места на провеждане 1
САЩ (1)
University of Kansas Medical Center
Kansas City , Kansas
Taneisha Scheuermann, PhD
Технически детайли
Статус
Набира участници
Фаза
Не е приложимо
Вид изследване
INTERVENTIONAL
Пол
Само жени
Минимална възраст
18 Years
Здрави доброволци
Не
Начална дата
09.04.2026
Крайна дата
01.08.2026
Регистрационен номер
NCT07420621
Източник
clinicaltrials.gov
Запитване за медицински туризъм

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