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Search / Trial NCT06926153

Interventional Study on Smoking Reduction in Psychiatry

Launched by GCS-CCOMS · Apr 7, 2025

Trial Information

Current as of September 09, 2025

Recruiting

Keywords

Smoking Reduction People With Mental Disorders Psychiatry

ClinConnect Summary

This clinical trial, called the "Interventional Study on Smoking Reduction in Psychiatry," is focused on helping people with mental health conditions who smoke. Research shows that people with mental disorders tend to smoke more than others, which can lead to serious health issues and significantly shorter lifespans. The study aims to test an intervention called 'Tabapsy,' designed to support adults who are regular smokers and receiving care from mental health services. The main goal is to see if this program can help participants quit smoking for at least 7 days within three months.

To take part in the study, participants need to be adults aged 18 or older who smoke at least one cigarette a day and are being treated in outpatient psychiatric care. Those interested will need to give their consent and must be covered by health insurance. The trial is currently recruiting participants and will also look into how well the program works and its overall costs. Participants will have the opportunity to share their experiences through interviews, which will help improve the program's implementation.

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Regular smokers (at least one cigarette per day)
  • Followed in psychiatric ambulatory care at one of the participating sectors' CMPs
  • Adults (18 years or older)
  • Covered by the statuary health insurance
  • Who gave their informed consent to participate to the study
  • Exclusion Criteria:
  • Users under guardianship or legal protection,
  • Psychological state incompatible with completing the questionnaire,
  • Persons with no command or understanding of the French language

About Gcs Ccoms

GCS-CCOMS is a leading clinical trial sponsor dedicated to advancing innovative therapies through rigorous research and development. With a strong commitment to enhancing patient outcomes, the organization specializes in the design, implementation, and management of clinical trials across various therapeutic areas. GCS-CCOMS collaborates with academic institutions, healthcare providers, and pharmaceutical companies to ensure the highest standards of scientific integrity and regulatory compliance. Through a patient-centered approach and a focus on ethical practices, GCS-CCOMS strives to contribute to the advancement of medical knowledge and improve the quality of care available to patients worldwide.

Locations

Armentières, France

Armentières, France

Bailleul, France

Etampes, France

Laxou, France

Lille, France

Nanterre, France

Paris, France

Rouffach, France

Rouffach, France

Rouffach, France

Saint Maurice, France

Saint Maurice, France

Saint Maurice, France

Saint Maurice, France

Saint Maurice, France

Saint Venant, France

Saint Venant, France

Saint Venant, France

Saint Claude, Guadeloupe

Saint Claude, Guadeloupe

Saint Paul, Réunion

Patients applied

0 patients applied

Trial Officials

Jean-Luc ROELANDT, MD

Principal Investigator

GCS-CCOMS & INSERM ECEVE 1123

Karine CHEVREUL, MD and Pr of public health

Study Director

Evaluation and research in health services and policies for vulnerable populations, French National Institute for Health and Medical Research (INSERM ECEVE 11 23)

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported