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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06130423
Other study ID # MUSMOKHEALTH
Secondary ID
Status Recruiting
Phase N/A
First received
Last updated
Start date February 28, 2024
Est. completion date January 10, 2026

Study information

Verified date September 2023
Source Poitiers University Hospital
Contact Claire LAFAY-CHEBASSIER, Dr
Phone 05 49 44 38 36
Email claire.lafay-chebassier@chu-poitiers.fr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

The study is a randomized, controlled trial comparing music therapy associated to NRT versus NRT alone to evaluate the value of music therapy in improving the management of craving among 50 health staff smokers. This pilot multi-method study will combine the methodology of clinical trial with qualitative techniques used in social sciences to show the interest of a digital music therapy tool, adapted to a health staff audience.


Description:

The participants will be recruited at the Clinical Investigation Center (CIC) of the University Hospital of Poitiers. At baseline visit, they will be randomly 1:1 assigned to receive either music therapy and NRT or NRT alone for 3 months. During the 3 months after Target Quit Date (TQD) , 3 visits will be performed by practitioners and nurses at the CIC. They will register smoking status of the participant, exhaled carbon monoxide concentration, body weight and all adverse events. Participants will answer questionnaires (FTCQ-12,Hospital Anxiety and Depression Scale ( HAD), Minnesota Nicotine Withdrawal Scale (MNWS), Impulsive Behavior Scale (UPPS), State-trait Anxiety Inventory Forme Y (STAI-Y)).


Recruitment information / eligibility

Status Recruiting
Enrollment 50
Est. completion date January 10, 2026
Est. primary completion date January 10, 2025
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Health staff, - Age >= 18 years - Smoking more than 10 cigarettes per day for at least 6 months - motivated to quit smoking - without legal tutors or subordination - affiliated to a health insurance system as required by the French law on biomedical research - written informed consent for participation in the study Exclusion Criteria: - Roommates and couples - NRT contraindication - unstabilised depression - psychosis and/or cognitive disorder and/or mental retardation - substance misuse or alcohol dependence - smoking-cessation medication (NRT, bupropion) or undergoing cognitive-behavioral therapy or hypnotherapy for smoking cessation in the last 3 months - electronic cigarette for smoking cessation in the last 3 months - participating in a study up to visit 4 - Persons benefiting from enhanced protection, i.e.persons deprived of their liberty by a judicial or administrative decision, adults under legal and finally patients in a vital emergency situation.

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Music intervention
Music therapy carried out with Music Care
Nicotine replacement
NRT: Nicotine Patch, Nicotine Gum

Locations

Country Name City State
France CHU Poitiers / CIC Poitiers

Sponsors (1)

Lead Sponsor Collaborator
Poitiers University Hospital

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary Assess if Music therapy associated to NRT decrease tabacco craving compared to NRT alone Score of French Version of the Tabacco Craving Questionnaire-12 (FTCQ-12). It consist of 12 questions, each rated on a likert-type scale with 7 response options. Lower scores mean a better outcome Month 1
Secondary Test the feasibility of such a program in smoking cessation Music therapy sessions compliance. Number and reasons for non attending music therapy sessions Month 3
Secondary Evaluate the evolution of tabacco craving Score of French Version of the Tabacco Craving Questionnaire-12 (FTCQ-12). It consist of 12 questions, each rated on a likert-type scale with 7 response options. Lower scores mean a better outcome Month [2;3]
Secondary Evaluate the evolution of Anxiety HAD (Hospital Anxiety and Depression Scale) score. Maximum score for each score (total A, total D) =21. Score over 10 definite state of anxiety. Lower scores mean a better outcome Month [1;2;3]
Secondary Evaluate the evolution of nicotine withdrawal symptoms MNWS (Minnesota Nicotine Withdrawal Scale) score. It consist of 8 questions, each rated on a likert-type scale with 0-4 response options. Lower scores mean a better outcome. Month [1;2;3]
Secondary Evaluate the evolution of impulsivity UPPS (Impulsive Behavior Scale) score. It consist of 20 questions, each rated on a likert-type scale with 1-4 response options. Lower scores mean a better outcome. Month [1;2;3]
Secondary Evaluate the efficacy of the intervention on smoking cessation Self reported abstinence or smoking reduction > or = 50% Month [1;2;3]
Secondary Evaluate the efficacy of the intervention on smoking cessation Self reported abstinence or smoking reduction > or = 50% Month [6;12]
Secondary Evaluate the evolution of Anxiety STAI-Y (Form-Y of the State-Trait Anxiety Inventory) score. It consist of two 20-item scales providing separate measures of state and trait anxiety (S-Anxiety and T-Anxiety, respectively). On a 4-point Likert scale (1-4), a score equal to 4 indicates the presence of a higher level of anxiety. Month [1;2;3]
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