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

Smoking Cessation Clinical Trial

— Je_Respire  

Official title:

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.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04635358
• Other study ID #: 19-PP-16
• Status: Completed
• Phase: N/A
• Start date: September 21, 2020
• Est. completion date: October 21, 2021

Study information

• Verified date: January 2024
• Source: Centre Hospitalier Universitaire de Nice
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 20
• Est. completion date: October 21, 2021
• Est. primary completion date: July 21, 2021
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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

Related Conditions & MeSH terms

• Smoking Cessation

Intervention

Behavioral:
• Hypnosis
Setting up hypnosis sessions
• Psychological support
Setting up psychological support
• Nutrional support
Setting up nutritional support

Locations

Country	Name	City	State
France	CHU de Nice	Nice

Sponsors (1)

Lead Sponsor	Collaborator
Centre Hospitalier Universitaire de Nice

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Number of subjects enrolled in the program who participated in the full range of care offered		6 months