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Идёт набор NCT07743710

The SMOKE Telehealth Study

Без фазы С лечением Tobacco Smoking

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: Smoking and Health Telehealth Intervention 1, Smoking and Health Telehealth Intervention 2.
Кому может быть актуально
Состояния в реестре: Tobacco Smoking. 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 →

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Обзор

The goal of this clinical trial is to develop two health-focused interventions for tobacco smokers with chronic pain. The main questions it aims to answer are: * Are the interventions feasible for delivery via telehealth? * Are the interventions acceptable to participants? This study has two phases. First, researchers will develop materials and receive feedback through three focus groups, updating the materials iteratively between each group. Next, researchers will compare the feasibility and acceptability of the two interventions. Participants in the second phase will: * Complete the a single-session telehealth intervention online * Complete surveys online before, immediately after, and at 2-weeks, 1-month, and 3-months after the intervention session.

Вмешательства

  • Поведенческое Smoking and Health Telehealth Intervention 1
    The Smoking and Health Telehealth Intervention 1 provides educational information about how smoking is related to health and resources for smoking cessation. The intervention is delivered via live telehealth online in a single (30 minute) session.
  • Поведенческое Smoking and Health Telehealth Intervention 2
    The Smoking and Health Telehealth Intervention 2 provides educational information about how smoking is related to health and resources for smoking cessation. The intervention is delivered via live telehealth online in a single (30 minute) session.

Первичные конечные точки

  • Recruitment Feasibility [Срок оценки: At the participant level, time from screening through enrollment is anticipated to be up to 4 weeks. The total will be calculated at the end of the entire enrollment period of the study, which is anticipated to be approximately 1 year and 9 months.]
  • Intervention Delivery Feasbility [Срок оценки: At the participant level, intervention delivery occurs in the same session as enrollment. Overall feasibility will be assessed at the end of the entire enrollment period, which is anticipated to be 1 year and 9 months.]
  • Acceptability [Срок оценки: Immediately post intervention (at the end of the intervention session).]
Вторичные конечные точки (5)
  • Cessation Motivation [Срок оценки: Assessed immediately before and after the intervention (during the interventions session), and at 2-weeks, 1-month, and 3-months after the intervention session]
  • Motivation for Cessation Treatment [Срок оценки: Assessed immediately before and after the intervention (during the interventions session), and at 2-weeks, 1-month, and 3-months after the intervention session]
  • Cessation Treatment Engagement [Срок оценки: 2-week, 1-month, 3-month follow-up]
  • Pain and Smoking Inventory [Срок оценки: Assessed immediately before and after the intervention (during the interventions session), and at 2-weeks, 1-month, and 3-months after the intervention session]
  • Pain and Smoking Questionnaire [Срок оценки: Assessed immediately before and after the intervention (during the interventions session), and at 2-weeks, 1-month, and 3-months after the intervention session]

Критерии участия

Критерии включения

  • moderate to severe chronic pain
  • current daily tobacco smoking
  • willing and able to complete study components in English
  • adult (age 18 or over)

Критерии исключения

  • planning or currently attempting to quit
  • recent use of cessation treatments or other products to quit smoking

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 · 1 центр
  • Binghamton University — Binghamton

Идентификаторы

NCT: NCT07743710 · STUDY00005796 · R21DA060345-01A1

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗