Evaluation of the Added Value of Sophrology on the Intensity of Craving During Smoking Withdrawal

Centre Hospitalier Intercommunal Creteil17 enrolled

Overview

To evaluate the added value of Sophrology on the intensity of craving during cigarette withdrawal.

Pilot study to evaluate the impact of sophrology on the intensity of craving and on certain determinants of cigarette consumption: number of cigarettes, anxiety, degree of dependence, motivation, confidence, fatigue, irritability, quality of sleep. This pilot study could serve as a basis for the development of research on a larger cohort.

Study Type

INTERVENTIONAL

Allocation

RANDOMIZED

Purpose

SUPPORTIVE_CARE

Masking

NONE

Enrollment

Conditions

Craving Cigarette Smoking

Interventions

SophrologyBEHAVIORAL

Patient must make 8 visits with interviews and questionnaires, including 7 visits with a session of sophrology.

Eligibility

Sex: ALLMin age: 18 YearsMax age: 75 Years

Medical Language ↔ Plain English

Inclusion Criteria: * First outpatient consultation in tobacco addiction department * Consumption greater than or equal to 35 cigarettes per week * Minimum age: 18 years old / Maximum age: 75 years old * Absence of co-addiction of alcohol, other products and behavioural addictions (except if withdrawal for more than 1 year) * Commitment by the patient not to practice hypnosis or mindfulness while participating in the study * Mastering reading and writing skills * Acceptance to participate in the protocol * Affiliated to a social security system Exclusion Criteria: * Patient-reported psychosis * Pregnant women * Participation in other intervention research * Patient under guardianship or curatorship * Refusal to participate in the study

Locations (2)

CHI Créteil Equipe de liaison et de soins en addictologie (ELSA)

Créteil, France

CHU Henri Mondor Service d'addictologie

Créteil, France

Outcomes

Primary Outcomes

FTCQ-12 questionnaire (French Tobacco Craving Questionnaire - 12 items) (0 to 84)

Comparison of the inte craving between the sophrology group and the control group at nsity of 6 months after the end of consultations, using the FTCQ-12 questionnaire.