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临床试验/NCT06632756
NCT06632756已完成不适用

Positive Psychotherapy for Smoking Cessation: A Focus on Strengths to Improve Self-efficacy and Enable Successful Quitting Strategies

Dartmouth-Hitchcock Medical Center2 个研究点 分布在 1 个国家目标入组 16 人开始时间: 2024年10月10日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
16
试验地点
2
主要终点
Abstinence from Smoking

研究概览

简要总结

This study will examine how Positive Psychotherapy (PPT) may help people interested in quitting smoking, quit.

详细描述

This project aims to adapt the Positive Psychotherapy (PPT) practice for smoking cessation in adults with severe mental illness (SMI), testing its usability, feasibility, and acceptability in a mixed-methods feasibility pilot study. Qualitative interviews will be conducted to obtain usability and acceptability input on the adapted PPT manual from 4-5 Peer Providers. Then, in partnership with The Mental Health Center of Greater Manchester (MHCGM), 6-8 adult smokers with SMI will be recruited who want to quit smoking in the next month and are willing to use nicotine replacement therapy (NRT). The 16-week PPT adaptation ("Positive Recovery for Smoking") will be tested progress on cessation assessed through interviewer-administered quantitative assessments at baseline, 8, and 16 weeks. Self-reported cigarettes per day (CPD) and carbon monoxide (CO) will be collected prior to each group treatment session. Informed by the weekly group check-in of cessation progress (quitting status), qualitative interviews will be conducted at 16 weeks to obtain a more nuanced description of the uptake of the intervention, successful quitting strategies, and barriers to cessation with this new method. The manual and materials will be adapted based on the feedback from the first group and another group of 6-8 participants will be recruited to receive the refined intervention and protocol. The result of this feasibility pilot will provide data on the adapted PPT's feasibility and acceptability, alongside a deep description of strategies used and why and how the treatment was perceived as useful or not to the enrolled participants.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
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

  • Serious Mental Illness (SMI) diagnosis;
  • smoking ≥10 CPD;
  • breath CO ≥10;
  • desire to quit in the next month;
  • willingness to use NRT daily;
  • English speaking and literate to engage in the treatment.

排除标准

  • legal guardian;
  • active substance use disorder.

结局指标

主要结局

Abstinence from Smoking

时间窗: baseline to 16 weeks

At least 20% of participants will achieve abstinence (0 cigarettes per day and CO less than 6) at 16 weeks.

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

Joelle Ferron

Assistant Professor

Dartmouth-Hitchcock Medical Center

研究点 (2)

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