Feasibility Study of Smoking Cessation for the Staff of a Hospital Center

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

COMPLETED

Clinical Phase

NA

Total Enrollment

20 participants

Study Classification

INTERVENTIONAL

Study Start Date

2020-09-21

Study Completion Date

2021-10-21

Brief Summary

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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.

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Detailed Description

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Conditions

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Smoking Cessation

Study Design

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Allocation Method

NA

Intervention Model

SINGLE_GROUP

Primary Study Purpose

TREATMENT

Blinding Strategy

NONE

Study Groups

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Intervention

Setting up hypnosis sessions, psychological and nutritional assistance.

Group Type EXPERIMENTAL

Hypnosis

Intervention Type BEHAVIORAL

Setting up hypnosis sessions

Psychological support

Intervention Type BEHAVIORAL

Setting up psychological support

Nutrional support

Intervention Type BEHAVIORAL

Setting up nutritional support

Interventions

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Hypnosis

Setting up hypnosis sessions

Intervention Type BEHAVIORAL

Psychological support

Setting up psychological support

Intervention Type BEHAVIORAL

Nutrional support

Setting up nutritional support

Intervention Type BEHAVIORAL

Eligibility Criteria

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Inclusion Criteria

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.

Exclusion Criteria

* 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

Minimum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No