Tabacco Cessation in Hospital Services
ConditionTobacco Use Cessation
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorCentre Hospitalier Universitaire de Nice
About this trial
Tobacco poses a health risk, whatever the method of consumption. According to the baro cancer 2021 : Only 23% of smokers say they have discussed smoking with a healthcare professional in the last 12 months. Studies in France on the practitioner's point of view have mainly been carried out in private practice, and at least 2 years ago. Few studies have looked at the patient's point of view. To date, no studies have been carried out in France on the patient's point of view. This is why the aim of our study is to: current state of smoking cessation in a hospital services: knowledge, attitudes and practices, from the point of view of the practitioner and the patient. Evaluation via a questionnaire.
Eligibility criteria
This trial accepts healthy volunteersQualifiers
Patients: Female male non gendered.
Over 18 years old
Whatever their state of healthRegular smoker: According to the Institut national de prévention et d'éducation pour la santé (INPES), a regular smoker is someone who reports smoking at least one cigarette (or equivalent) a day.
Whether or not they use any other form of 'drug'.
Disqualifiers
Patients: Ex-smoker patients
Non-smokers
Patients under guardianship
Patients with language difficulties
Trial population
Smoking patients attending the Nice Institute of Oral Medicine. Practitioners, interns and 4th, 5th and 6th year students.
Trial design
Design model
Other
Time perspective
Cross-sectional
Treatments tested in this trial
Not listed
Trial groups
300 Participants
are grouped into 2 trial groupsGroup A: Patients
Group B: Hospital practitioner
Trial outcomes
Primary outcomes
1
Description of the participant's group
Participant's questionnaire: 16 questions without score
Time frame
At the inclusionSecondary outcomes
1
Identify the factors that influence responses to questions (Demographic characteristics)
Demographic characteristics of participants: gender and age.
Time frame
At the inclusion2
Identify the factors that influence responses to questions (the knowledge particiapnts)
Questionnaire:the knowledge participants without score
Time frame
At the inclusion3
Identify the factors that influence responses to questions (patients prejudices)
Questionnaire:the patients prejudices without score
Time frame
At the inclusion4
Identify the factors that influence responses to questions ( Practionner status)
Questionnaire: Professionnal status of practionners without score
Time frame
At the inclusionSponsors and contacts
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Source ClinicalTrials.gov