Organization of Smoking Cessation in Pregnant Women With the Implementation of the 5A Strategy in New Aquitaine.

Smoking Cessation Clinical Trial

— 5A-QUIT-N  

Official title:

Organization of Smoking Cessation in Pregnant Women: Study of the Effectiveness, Transferability, Barriers and Facilitators of the Implementation of the 5A Strategy in French Context. A Cluster Randomized Controlled Trial in New Aquitaine.

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT05355012
• Other study ID #: CHUBX 2019/61
• Status: Recruiting
• Phase: N/A
• Start date: October 3, 2022
• Est. completion date: May 31, 2026

Study information

• Verified date: October 2023
• Source: University Hospital, Bordeaux
• Contact: François Alla, Prof
• Phone: +335 57 82 26 50
• Email: francois.alla[@]u-bordeaux.fr
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The investigators are conducting a pragmatic cluster randomized trial in stepped-wedge of which objectives are to evaluate the effectiveness and the conditions of effectiveness of an organizational strategy for smoking cessation - 5A-QUIT-N - among pregnant women in New Aquitaine (NA), by using and optimizing existing resources

Description:

In France, in 2016, 16.6% of pregnant women were smokers, the highest levels among European countries. Pregnancy is considered a teachable moment for smoking cessation. There are many tools, interventions and programs to reduce the smoking habits of pregnant women. The challenge is therefore not to propose new interventions but to understand what is hindering the implementation of existing interventions and proposing corrective measures. In this context, the scientific literature shows that interventions for smoking pregnant women only seem effective when based on a comprehensive approach that combines multiple interventions. In particular, interventions based on the 5A's model (Ask, Advise, Assess, Assist, Arrange) are largely recommended and have shown their effectiveness abroad. Factors facilitating or hindering the implementation of such strategies are mainly organizational. As organizations are context-dependent by nature, considering the generalization of such strategies in France therefore requires adapting them to the French health system and evaluating them in context, in a pragmatic approach, inserted into routine care and using the tools, procedures and existing organizations in the territories.

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 4505
• Est. completion date: May 31, 2026
• Est. primary completion date: May 31, 2025
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

In this research, there are 4 categories of research participants:

• Healthcare professionals: the target of the 5A-QUIT-N intervention from whom data will be collected to meet the secondary objective of the effectiveness conditions.

• Stakeholders: individuals involved in the implementation of the research and intervention from whom data will be collected to meet the secondary objective of the effectiveness conditions.

• Women who have just given birth and who smoke tobacco in early pregnancy: indirect beneficiaries of the intervention, from whom data will be collected to meet the primary objective of effectiveness.

• Co-parent (partner) of the new-born child of the woman who has just given birth included in the study

Inclusion criteria for the intervention

The inclusion criteria for the clusters are :

• Territory of maternity attractiveness in New Aquitaine

The inclusion criteria for care providers within the clusters are:

• All institutions, structures and organizations and health professionals likely to participate in the follow-up of pregnant women

• All institutions, structures and organizations and health professionals specializing in addictology or tobaccoology

The inclusion criteria for pregnant women within the clusters are :

• All pregnant women who have smoked tobacco (at least 2 times a week, for at least 1 week) during the pregnancy (including the period when she was unaware of the pregnancy)

Inclusion criteria for the primary objective measures:

The inclusion criteria for women are (for data collection):

• Have given birth in a New Aquitaine maternity hospital,

• Reside in New Aquitaine

• To have been followed for the pregnancy in the territory of the maternity of delivery

• To have used tobacco during (at least 2 times a week, for at least 1 week) the pregnancy (including the period when she was unaware of the pregnancy)

• Be over 18

• Have given free, informed and express consent

• Exclusion criteria:

Non-inclusion criteria for the intervention

Cluster non-inclusion criteria:

• Pilot territory (territory of attractiveness of the Arcachon maternity hospital)

• Impossibility of collecting the main judgment criterion in the cluster Within these clusters, the health care providers and the pregnant women are all concerned and therefore do not have any non-inclusion criteria.

Non-inclusion criteria of measures for the primary objective:

The criteria for non-inclusion of women who have just given birth are:

• Not speaking French,

• Have COVID during delivery

• Use only electronic cigarettes,

• Under legal protection (guardianship, curatorship, safeguard of justice)

• Women giving birth under X

• Women giving birth to a stillborn baby

• Women having made a denial of pregnancy

• Women who have their child in neonatal intensive care

• Women who have been fully monitored for their pregnancy outside of New Aquitaine

Related Conditions & MeSH terms

• Pregnancy Related
• Smoking Cessation

Intervention

Other:
• 5A organizational innovation
This project is based on three strategic axes: A gradation of the care offer allowing to adapt the means and resources mobilized on the territory Personalized care by developing specific treatment paths based on the risk factors and/or vulnerabilities of the pregnant woman Coordination of territorial resources to support pregnant women in quitting smoking These three key elements will make it possible to propose a partnership-based, multi-professional, coordinated and integrated approach to the territory, supported by the technical resources and expertise available in the territory. It invites a majority of non-specialized actors to invest in the process of supporting pregnant women in quitting smoking, multiplying and potentiating their actions with this population.

Locations

Country	Name	City	State
France	CHU de Bordeaux, Hôpital Saint-André	Bordeaux

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Bordeaux

Country where clinical trial is conducted

France, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Tobacco abstinence at delivery	The point prevalence of abstinence at delivery, which is the proportion of women reporting abstinence from smoking for at least 7 days at delivery. This criterion is well documented in the literature assessing tobacco use. It has the advantage of detecting the delayed effects of an intervention and can be easily extrapolated.	At delivery (smoking status of the previous 7 days)
Secondary	Average number of cigarettes smoked at inclusion	Average number of cigarettes smoked per day over the last 30 (or 7) days	At inclusion
Secondary	Average number of cigarettes smoked at postpartum	Average number of cigarettes smoked per day over the last 30 (or 7) days	6 months and 1 year after delivery
Secondary	Attempts to reduce tobacco consumption	The number of attempts to reduce tobacco consumption (at least 1 cigarette)	1 to 3 days after delivery
Secondary	Attempts to quit smoking	Number of attempts to quit smoking (at least 24 hours)	1 to 3 days after delivery
Secondary	Continuous abstinence	Continuous abstinence (in number of days)	1 to 3 days after delivery
Secondary	Birth weight	Birth weight (in kg) of the baby	At baby birth, up to 3 days after delivery
Secondary	Gestational age	Gestational age (in months) of the baby (at birth).	At baby birth, up to 3 days after delivery
Secondary	Sustainability of professional practices	Prevalence of completion of each A of the 5A approach evaluated on a subgroup of women who have just given birth at a distance from the deployment of the intervention (18 months) via the questionnaire	18 months from the deployment of the intervention
Secondary	Sustainability of the impact on health	Prevalence of women smoking tobacco at delivery over the last 7 days via two sources: the computer systems of the maternity units that have this information systematically (non-exhaustive because not all maternity units in the New Aquitaine region have a computer system) and on a sub-group of women who have just given birth	18 months from the deployment of the intervention
Secondary	Postpartum relapse rate at 6 months	Relapse rate among women who quit smoking during pregnancy at 6 and 12 months postpartum defined as a resumption of at least 7 consecutive days of smoking in the past 6 months.	At 6 months postpartum
Secondary	Postpartum relapse rate at 12 months	Relapse rate among women who quit smoking during pregnancy at 6 and 12 months postpartum defined as a resumption of at least 7 consecutive days of smoking in the past 6 months.	At 12 months postpartum
Secondary	Continued abstinence	Continued abstinence (in number of days)	6 months and 1 year after delivery
Secondary	Implementation of intervention	Barriers and levers to implementation in professionals	Through study completion, an average of 3 years
Secondary	Conditions of transferability	Conditions of transferability linked to the characteristics of the stakeholders and the context: contextual conditions for success within the centres, the characteristics of professionals and patients influencing outcomes	Through study completion, an average of 3 years
Secondary	Viability	Assessment of intervention deployment in a real-world setting, using 5 criteria: utility, affordability, evaluability, adaptability and acceptability.; "Utility" dimension (as a complement to the secondary criteria) of viability through the recovery mechanisms identified as successful mental health recovery Affordability for professionals and beneficiaries (financial, geographical, social and cultural levers and brakes of the intervention) Evaluability of 5A-QUIT-N: carrying out this evaluation, the availability of professionals and beneficiaries to answer questionnaires and interviews, missing data in the questionnaires etc.; Adaptability of 5A-QUIT-N: integration of the action into the context and the current organisation of the centres Acceptability of 5A-QUIT-N: by professionals and beneficiaries	Through study completion, an average of 3 years