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NCT06926153: TABAPSY
Interventional Study on Smoking Reduction in Psychiatry
NA trial testing TABAPSY in Tobacco Addiction in 6,500 participants. Currently enrolling.
14 May 2026
Quick facts
| Lead sponsor | GCS-CCOMS |
|---|---|
| Phase | NA |
| Status | Recruiting now |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | none |
| Primary purpose | prevention |
| Enrollment | 6,500 |
| Start date | 15 January 2025 |
| Primary completion | 14 May 2026 |
| Estimated completion | 14 November 2026 |
| Sites | 22 locations across Guadeloupe, France, Reunion |
Drugs / interventions tested
- TABAPSY
- Usual Care
Conditions studied
- Tobacco Addiction — all drugs for Tobacco Addiction →
Sponsor
GCS-CCOMS
Who can join
18 and older, any sex, with Tobacco Addiction. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
The smoking rate among people with mental disorders is higher than in the general population. Greater exposure to the harmful effects of tobacco partly explains the major inequality in life expectancy observed among people with mental disorders who, depending on the disorder and the study, live 10 to 25 years less than the general population, a gap mainly due to the occurrence of cardiovascular and respiratory pathologies, notably bronchial cancers. However, tobacco reduction actions specifically targeting these people remain insufficiently developed, particularly in psychiatry where this addiction is often banalized and its treatment neglected. The objective of this study is to evaluate an intervention ('Tabapsy') co-constructed with mental health services users, mental health professionals, and general practitioners and targeting adult patients followed in ambulatory psychiatry. The main objective is to evaluate the effectiveness of the intervention on short-term smoking cessation (cessation for at least 7 days) among regular smokers at 3 months. Secondary objectives include evaluation of its cost-effectiveness and implementation. To this end, a national cluster-randomized controlled study will be carried out, supplemented by qualitative interviews to study the implementation of the intervention.
Publications & conference data
No peer-reviewed publications indexed yet for this trial.
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- PubMed search for NCT06926153
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Related trials
Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT06926153 (US National Library of Medicine, public domain)
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by GCS-CCOMS
- Last refreshed: 2 February 2026
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