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Effects of Mindfulness Meditation in Virtual Reality on Craving and Smoking Cessation

Not Applicable
Recruiting
Conditions
Tobacco Use Disorder
Interventions
Other: Virtual reality pod
Other: nicotine patches and chewing gum
Registration Number
NCT05766553
Lead Sponsor
Centre Hospitalier Henri Laborit
Brief Summary

Investigators seek to propose a non-drug therapeutic alternative, namely a mindfulness meditation protocol based on virtual reality training in order to induce progressive modifications of various indicators of craving.

The study hypothesis is that the practice of mindfulness meditation in a virtual reality environment reduces the craving induced by cues and stress and therefore ultimately smoking relapse.

The main objective of the protocol will be to demonstrate that mindfulness meditation can reduce long-term relapse (continuous cessation (\> 30 days) of smoking cessation).

The participants will be randomized into two groups: the experimental group will perform six virtual reality sessions in a multisensory cabin at the rate of one session per week; the control group will be prescribed the gold standard treatment (nicotine patches and chewing gum).

Participants will be seen again at three and six months to assess whether or not there has been a smoking relapse.

Detailed Description

Not available

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria
  • Any patient consuming 10 to 40 cigarettes per day
  • Woman or man aged 18 to 75 inclusive
  • Substance use disorder according to the DSM5 classification
  • Benefit from social security or benefit from it through a third party in accordance with French law on research involving the human person
  • Having signed the informed consent form after having received written information.
Exclusion Criteria
  • Disabling cognitive disorders
  • Patient under 18 or over 75 years old.
  • Patient with a psychological disorder or a psychiatric pathology requiring specialized follow-up
  • Patient with addiction to another product.
  • Cardiological pathologies that could compromise the participation of patients, detected by an ECG (only for patients who will be randomized in the experimental group).
  • Advanced pulmonary, renal, and hepatic diseases, or any unstable and serious medical conditions that could compromise the patient's participation in the study, subject to the judgment of the doctor
  • Pregnant or breastfeeding woman
  • Simultaneous participation in another trial
  • Employee of the investigator or of the clinical trial site
  • Patients protected by law
  • Patients who do not speak the French language
  • People not covered by state health insurance
  • Patients who in the opinion of the investigator are unable to complete the questionnaires
  • Patient claustrophobic or anxious about using the cabin
  • Patient allergic to a molecule present in nicotine substitutes

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Interventional GroupVirtual reality podPatients in this arm will have 6 sessions of virtual reality in a pod (1 session per week). Patients will then have a visit at day 90 and day 180.
Control groupnicotine patches and chewing gumPatients in this arm will receive the gold standard of treatment for tobacco cessation (nicotine patches and chewing gum) from day 0 (inclusion visit) to day 90. Patients will then have a visit at day 90 and day 180.
Primary Outcome Measures
NameTimeMethod
Relapse at 3 months3 months

Relapse of patients by declaring their consumption at 3 months.

Relapse at 6 months6 months

Relapse of patients by declaring their consumption at 6 months.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (3)

Cabinet Médical

🇫🇷

Iteuil, France

Centre Hospitalier Henri Laborit

🇫🇷

Poitiers, France

Cabinet médical des Couronneries

🇫🇷

Poitiers, France

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