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

NCT04635358 | Completed

• 1 other identifier: 19-PP-16
• Study Type: interventional
• Target: 20
• Locations: 1 country
• Sites: 1

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.

Conditions

Smoking Cessation

Keywords

Smoking, hypnosis, nutrition support, psychological support

Outcome Measures

Primary Outcomes (1)

• Number of subjects enrolled in the program who participated in the full range of care offered

  6 months

Study Arms (1)

Intervention

EXPERIMENTAL

Setting up hypnosis sessions, psychological and nutritional assistance.

Behavioral: Hypnosis; Behavioral: Psychological support; Behavioral: Nutrional support

Interventions

Hypnosis BEHAVIORAL

Setting up hypnosis sessions

Intervention

Psychological support BEHAVIORAL

Setting up psychological support

Intervention

Nutrional support BEHAVIORAL

Setting up nutritional support

Intervention

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• 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.

You may not qualify if:

• 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

Sponsors & Collaborators

• Centre Hospitalier Universitaire de Nice: lead

Study Sites (1)

CHU de Nice

Nice, 06003, France

Location

MeSH Terms

Conditions

Smoking Cessation; Smoking

Interventions

Hypnosis

Condition Hierarchy (Ancestors)

Health Behavior; Behavior

Intervention Hierarchy (Ancestors)

Mind-Body Therapies; Complementary Therapies; Therapeutics; Psychotherapy; Behavioral Disciplines and Activities

Study Officials

• Bernard PROUVOST-KELLER, Dr

  Centre Hospitalier Universitaire de Nice

  PRINCIPAL INVESTIGATOR

Study Design

• Study Type: interventional
• Phase: not applicable
• Allocation: NA
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: OTHER
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: November 13, 2020
• First Posted: November 19, 2020
• Study Start: September 21, 2020
• Primary Completion: July 21, 2021
• Study Completion: October 21, 2021
• Last Updated: February 6, 2024

Record last verified: 2024-01

Data Sharing

• IPD Sharing: Will not share

Locations

FR (1)