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Идёт набор NCT07455513

A Novel Tobacco Cessation Resource for Smokers With a Diagnosed or Suspected Thoracic Cancer

Без фазы С лечением Cigarette Smoking-Related Carcinoma Malignant Thoracic Neoplasm

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: Electronic Health Record Review, Informational Intervention, Interview, Referral.
Кому может быть актуально
Состояния в реестре: Cigarette Smoking-Related Carcinoma, Malignant Thoracic Neoplasm. Базовые параметры: от 21 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
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Официальное название

A Pilot/Feasibility Study of the Buckeye Quit Stick: A Novel Resource for Successful Tobacco Cessation

Обзор

This clinical trial evaluates the feasibility of a novel tobacco cessation resource called a Buckeye Quit Stick among smokers with a diagnosed or suspected thoracic cancer. Tobacco use is the single most preventable cause of disease, disability, and death in the United States. While the benefits of quitting smoking are numerous, rates of persistent smoking after cancer diagnosis remain high. Research has found that patients who quit smoking but subsequently relapse frequently report the hand/oral habit as a barrier to sustained smoking cessation. The Buckeye Quit Stick is an innovative cessation aid designed to directly address patients' hand/oral habit by substituting the cessation aid for cigarettes without integrating pharmacologic intervention, which is typically managed by their medical provider and may require direct supervision due to the patient's health status. The Buckeye Quit Stick is designed to satisfy the repeated hand/oral pattern or ritual, thereby avoiding the physical loss of holding a cigarette in the hand or mouth and the action of smoking. It may also help occupy fidgeting hands and potentially reduce stress and cravings. This novel cessation resource may address key factors that influence smoking abstinence and improve patients' health outcomes.

Подробное описание

PRIMARY OBJECTIVE:

I. To evaluate the feasibility and acceptability of the Buckeye Quit Stick among 30 patients seen in the Ohio State University (OSU) thoracic clinic(s) and to characterize frequency of use among the accrued sample.

EXPLORATORY OBJECTIVES:

I. Characterizing the population. II. Determining communication preferences, acceptance of the Buckeye Quit Stick, abstinence estimates.

III. Assessing the quality of subjective measures (e.g., anxiety, quality of life, etc.).

IV. Gathering qualitative data to elicit participant feedback regarding the device, The James Comprehensive Cancer Center (CCC) smoking cessation clinic, and overall study design.

OUTLINE:

Patients receive a Buckeye Quit Stick and a smoking cessation informational packet on study. Patients also receive a referral to the James CCC smoking cessation clinic on study.

After completion of study intervention, patients are followed up at 2 weeks, 3 and 6 months, and then up to 24 months.

Вмешательства

  • Другое Electronic Health Record Review
    Ancillary studies
  • Другое Informational Intervention
    Receive smoking cessation information
  • Другое Interview
    Ancillary studies
  • Другое Referral
    Receive referral
  • Устройство Smoking Cessation Intervention
    Receive Buckeye Quit Stick
  • Другое Survey Administration
    Ancillary studies

Первичные конечные точки

  • Recruitment rates (feasibility) [Срок оценки: Up to 1 year]
  • Adherence (feasibility) [Срок оценки: at baseline, 2 weeks, 3 months and 6 months]
  • Retention rates (feasibility) [Срок оценки: At 2 weeks, 3 months, and 6 months]

Критерии участия

Критерии включения

  • >= 21 years old
  • Speak and understand English
  • Established patient of the OSU thoracic clinics
  • Diagnosed with a thoracic malignancy or has a clinically suspected thoracic malignancy as documented by treating provider
  • Willing and able to participate in the study protocol (e.g., complete the survey and related study documents and provide informed consent)
  • Current self-reported smoker
  • Willingness to change = score of above 1 on the Stages of Change measure

Критерии исключения

  • < 21 years old (Ohio is a tobacco 21 state.)
  • Patient outside of the OSU clinics (This intervention targets patients who may benefit the most from cessation.)
  • Unwilling or unable to provide consent or complete study components
  • Prisoners will be excluded from participation

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

Здоровые добровольцы: Нет

Дизайн исследования

Распределение
Не применимо
Модель
Одна группа
Маскирование
Открытое
Основная цель
Профилактика

Центры проведения

США · 1 центр
  • Ohio State University Comprehensive Cancer Center — Columbus

Идентификаторы

NCT: NCT07455513 · OSU-25129 · NCI-2026-00966

Первоисточники (государственные реестры)

Открыть это исследование на ClinicalTrials.gov ↗