Effects of Mindfulness Meditation in Virtual Reality on Craving and Smoking Cessation
Condition(s) studied
Investigational drug(s) / intervention(s)
Virtual reality pod: The first two sessions provide guided training in relaxation and mindfulness through immersion in a virtual forest environment for the first session, and in a virtual beach environment for the second. Sessions 3 and 4 present environments with addiction-related stimuli (Cues). The session 3 consists of a walk through the virtual street environment, buying a bottle of water from the store, and then ordering a coffee from a virtual bar. The session 4 takes place in a virtual party environment in an apartment: people smoke and drink alcohol in the living room, the session consists of sitting with them, then going to the kitchen to get a water bottle. Sessions 5 and 6 present stressful environments. Session 5 consists of a virtual parachute jump. The 6th session takes place in a virtual airplane environment, which will encounter turbulence.
nicotine patches and chewing gum: Participants in this group will be prescribed a Gold Standard smoking cessation treatment with nicotine patches adapted to their consumption and 4mg nicotine chewing gum for a period of 3 months.
Study 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.
Eligibility
Primary outcome measure(s)
- Relapse at 3 months — 3 months
Relapse of patients by declaring their consumption at 3 months. - Relapse at 6 months — 6 months
Relapse of patients by declaring their consumption at 6 months.
Trial sites (3)
| Facility | City | Region | Status |
|---|---|---|---|
| Cabinet Médical | Iteuil | France | Recruiting |
| Cabinet médical des Couronneries | Poitiers | France | Recruiting |
| Centre Hospitalier Henri Laborit | Poitiers | France | Recruiting |
More Centre Hospitalier Henri Laborit trials in France
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT05766553 on ClinicalTrials.gov ↗ ← All trials in France