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Feasibility Study of Smoking Cessation for the Staff of a Hospital Center (Je_Respire)

C

Centre Hospitalier Universitaire de Nice

Status

Completed

Conditions

Smoking Cessation

Treatments

Behavioral: Nutrional support
Behavioral: Psychological support
Behavioral: Hypnosis

Study type

Interventional

Funder types

Other

Identifiers

NCT04635358
19-PP-16

Details and patient eligibility

About

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.

Enrollment

20 patients

Sex

All

Ages

18+ years old

Volunteers

No 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

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Intervention
Experimental group
Description:
Setting up hypnosis sessions, psychological and nutritional assistance.
Treatment:
Behavioral: Psychological support
Behavioral: Nutrional support
Behavioral: Hypnosis

Trial contacts and locations

1

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Central trial contact

Bernard PROUVOST-KELLER, Dr

Data sourced from clinicaltrials.gov

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