Evaluation of the Effectiveness of Routine Nurse Education in Prescribing Nicotine Replacement Therapy for Hospitalized Smokers in a University Hospital

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

The goal of this study is to determine whether training nurses to prescribe nicotine replacement therapy (NRT) can increase the proportion of smoking cessation at one month after hospital discharge among active smokers (daily or occasional tobacco use) hospitalized at the European Hospital Georges Pompidou in the following departments: Hypertension/Vascular Medicine, Nephrology, Pulmonology, and the Cardiac Intensive Care Unit.

The main questions it aims to answer are :

Does training nursing teams in the prescription and adjustment of nicotine replacement therapy increase the proportion of smoking cessation at one month after hospital discharge, defined as a total absence of tobacco consumption for at least seven days prior to the consultation, based on self-report and confirmed by an exhaled carbon monoxide (CO) level of ≤10 ppm? We will compare the usual care provided in the targeted departments with the care provided after all nurses in these departments receive training. The training will involve teaching the prescription of nicotine replacement therapy, dose adjustment, and communication with general practitioners and/or community nurses through a referral letter to facilitate continued care. Nurses will also have access to a dose adjustment document to provide to patients.

Participants will be followed up at discharge and at 1, 3, and 6 months post-discharge. At each visit, they will complete questionnaires on smoking behavior, quality of life, anxiety, and depression symptoms, and an exhaled CO measurement will be performed.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

An active smoking patient (daily or occasional tobacco use) hospitalized in the following departments: hypertension/vascular medicine, nephrology, pulmonology, or the coronary care unit (CCU).

Patient residing in the Île-de-France region.

Proficient in the French language.

Has signed informed consent.

Disqualifiers

Patient not affiliated with social security;

Patient under State Medical Aid (AME);

Patient under legal protection measures;

Pregnant or breastfeeding patient;

Trial design

Design model

Sequential

Treatments tested in this trial

  • training nurses to prescribe nicotine substitutes, to adapt doses and to transmit to the outpatient physician and/or nurse nurse to facilitate the continuation of treatment

    Other intervention

    Nurses will undergo training sessions provided by the smoking cessation team to learn how to prescribe nicotine replacement therapy, adjust dosages, and forward a referral letter to the patient's primary care physician and/or community nurse for continuity of care. They will receive a dosage adjustment guide to share with patients. Upon completing the training, nurses will be authorized to prescribe nicotine replacement therapy using the hospital's prescription software.

Treatment groups

442 Participants
are divided into 2 treatment groups
Group A: Trained nursesExperimental treatment 1 intervention
Group B: No trained nursesNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

smoking cessation one month after hospital discharge

The primary outcome is smoking cessation one month after hospital discharge, defined as a total absence of tobacco use for at least 7 days prior to the consultation day, based on self-reported data and confirmed by an exhaled carbon monoxide measurement of 10 ppm or less.

Time frame
1 month after enrollment

Secondary outcomes

1

The average number of cigarettes smoked per day at 1, 3, and 6 months after hospital discharge

The average number of cigarettes smoked per day at 1, 3, and 6 months after hospital discharge based on self-reported data

Time frame
1, 3 and 6 months after enrollment
2

The proportion of patients who reduced their consumption by at least 50% compared to their initial consumption

The proportion of patients who reduced their consumption by at least 50% compared to their initial consumption at 1, 3, and 6 months after hospital discharge, based on self-reported consumption.

Time frame
1, 3, and 6 months after enrollment
3

The proportion of patients who achieved smoking cessation at 3 and 6 months after hospital discharge

The proportion of patients who achieved smoking cessation at 3 and 6 months after hospital discharge, defined as a total absence of tobacco consumption for at least 7 days prior to the consultation day, based on self-reported data and confirmed by an exhaled carbon monoxide measurement of 10 ppm or less.

Time frame
3 and 6 months after enrollment
4

The patients' quality of life score

The patients' quality of life score measured using the 12-Item Short Form Survey (SF-12) quality of life scale available in the national smoking cessation consultation file published by Santé publique France, at 1, 3, and 6 months after hospital discharge. Minimum value of SF-12 is: 0, Maximum value is: 100 (representing the best possible health)

Time frame
1, 3, and 6 months after enrollment

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Assistance Publique - Hôpitaux de Paris

Lead sponsor

National Cancer Institute, France

Collaborator

Institut de Recherche en Santé Publique, France

Collaborator

This trial is not recruiting at the moment. You can still explore other options: