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NCT04635358 Clinical Trial

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
Secondary ID
Status Completed
Phase N/A
First received
Last updated
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
Health authority
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

Study Design

Related Conditions & MeSH terms

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
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