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临床试验/NCT07625956
NCT07625956Enrolling By Invitation4 期

Piloting Novel Interventional Strategies to Improve Nicotine Pouches as a Substitute for Smoking

Medical University of South Carolina1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2026年6月26日最近更新:
干预措施

试验速览

阶段
4 期
状态
Enrolling By Invitation
入组人数
10
试验地点
1
主要终点
Acceptability

研究概览

简要总结

Some people who smoke cigarettes try to switch to oral nicotine pouches but are not able to fully stop smoking. This study tests two new strategies for people who previously tried to switch using nicotine pouches. Participants who were unable to fully switch will either be asked to increase the nicotine strength of their pouches or to use a nicotine patch along with pouches. The goal of the study is to see whether these strategies are feasible, acceptable, and helpful, and to inform the design of larger future studies.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
21 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age 21 years or older
  • Currently enrolled in and completed the Pack2Pouch parent study
  • Current combustible tobacco smoking at extension study enrollment
  • Able to attend in-person visits in the Charleston, SC area
  • Access to internet and mobile communication

排除标准

  • Pregnancy, breastfeeding, or nursing
  • Medical contraindications to nicotine replacement therapy
  • Current use of smoking cessation medications
  • Non-English proficiency
  • Use of other combustible tobacco or frequent non-combustible nicotine products outside study protocol

研究组 & 干预措施

Augment

Active Comparator

Add nicotine replacement therapy

干预措施: Nicotine replacement therapy patches (Drug)

Increase

Active Comparator

Increase nicotine content of pouches

干预措施: Oral nicotine pouches (Drug)

Continue

No Intervention

Participants will continue with their treatment from the parent trial.

结局指标

主要结局

Acceptability

时间窗: Day 28

Acceptability endpoints will be measured by the Acceptability of Intervention Measure (AIM). This measure includes 4 items rated on scale of 1 to 5. Scores are created by averaging responses, with values ranging from 1 to 5. Higher values indicate higher acceptability.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Amanda Palmer

Research Assistant Professor-Faculty

Medical University of South Carolina

研究点 (1)

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