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

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.

Status

Completed

Phases

Study type

Interventional

Source

ClinicalTrials.gov

Registry ID

NCT04635358

Acronym

Je_Respire

Enrollment

Registered

2020-11-19

Start date

2020-09-21

Completion date

2021-10-21

Last updated

2024-02-06

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smoking Cessation

Keywords

Smoking, hypnosis, nutrition support, psychological support

Brief summary

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.

Interventions

BEHAVIORALHypnosis

Setting up hypnosis sessions

BEHAVIORALPsychological support

Setting up psychological support

BEHAVIORALNutrional support

Setting up nutritional support

Study design

Allocation

Intervention model

SINGLE_GROUP

Primary purpose

TREATMENT

Masking

NONE

Eligibility

Sex/Gender

ALL

Age

18 Years to No maximum

Healthy volunteers

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

Design outcomes

Primary

Measure	Time frame
Number of subjects enrolled in the program who participated in the full range of care offered	6 months

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026