跳至主要内容
临床试验/NCT04635358
NCT04635358已完成不适用

Feasibility Study of Smoking Cessation for the Staff of a Hospital Center Through a Treatment Proposal Combining Nicotine Substitutes, Psychological Support, Nutritional Assistance and Hypnosis.

Centre Hospitalier Universitaire de Nice2 个研究点 分布在 1 个国家目标入组 20 人开始时间: 2020年9月21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
20
试验地点
2
主要终点
Number of subjects enrolled in the program who participated in the full range of care offered

研究概览

简要总结

The recorded prevalence of daily smoking among health professionals (doctors, nurses, midwives, etc.), regardless of their mode of practice (salaried or self-employed, etc.) varies between 14 and 23%. In health care institutions, according to the studies, the prevalence of daily smoking among staff, caregivers and non-caregivers ranges from 17% to 27%. These professionals who continue to smoke, although they are particularly well informed about the risks they run, probably constitute a group with specific withdrawal difficulties. Beyond the impact on their own health, the smoking status of caregivers could also have an impact on the management of tobacco patients. There are very few studies of the impact of interventions on the smoking status of caregivers in health care facilities. The combination of several intervention modalities can facilitate the participation of target professionals and generate efficiency synergies.

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
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Professionals employed at the Nice hospital who are volunteers and have :
  • an initial Fagerstrom test > 3
  • associated with expired carbone monoxide > 10 ppm at least 60' after the last cigarette.

排除标准

  • Reported associated addiction (cannabis, alcohol or any other psychoactive product)
  • Professionals likely to no longer work at the Nice Hospital in the year following the start of the study
  • Pregnant or breastfeeding woman

结局指标

主要结局

Number of subjects enrolled in the program who participated in the full range of care offered

时间窗: 6 months

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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