ADHAirE : a Randomized Controlled Trial to Improve the Implementation of Tobacco-free School Policies

Université Catholique de Louvain

Status: Invitation-only

Conditions: Adolescent Behavior; Smoking

Treatments: Behavioral: Feedback; Behavioral: Advocacy coalition

Study type: Interventional

Funder types: Other

Identifiers

NCT06655038

ADHAIRE

Details and patient eligibility

About

The goal of this cluster randomized controlled trial is to learn if the set up of an advocacy coalition in secondary schools can improve the implementation of tobacco-free school policies (TFSP) to prevent adolescent smoking.

The main questions it aims to answer are:

1. To what extent is an advocacy coalition related to smoking prevention implementable in school's routine ?
2. Is an advocacy coalition an effective way to prevent smoking among adolescents and shift smoking norms in school?

Schools in the intervention arm will be compared to schools in the control arm, to test the effectiness of the advocacy coalition to improve the implementation of TFSP.

Schools in the intervention arm will put in place an advocacy coalition, that is

• Set up a task force composed of school stakeholders (students, teachers, educators, principle,...)
• Share their good practices regarding implementation with the other schools of the intervention arm
• Be supported to reffer nicotine-dependant students and staff members to smoking cessation programs

Continuous evaluation is planned to assess the effectiveness of this intervention.

Full description

The ADHAirE project is an experimental study to prevent adolescent smoking.

Its objectives are to

1. Improve the implementation of tobacco-free school policies (TFSP, that is, prohibition of smoking for everyone, anytime, anywhere on the school grounds)
2. Make these TFSP part of school's routine practice
3. Decrease adolescents initiating or reporting smoking

To achieve those goals, schools will put an advocacy coalition in place, that is:

• They wil set up a task force composed of school stakeholders (students, teachers, educators, principle,...). These stakeholders will meet 4 times a year to improve the implementation and enforcement of TFSP through rules that are accepted, adopted and to which all school actors adhere.
• They will share their good practices regarding implementation with the other schools of the intervention arm through a sharing platform and two annual meetings.
• They will be supported to reffer nicotine-dependant students and staff members to smoking cessation programs.
• They will also be supported in the implementation of TFSP and in getting all school actors on board, by the research team, but also by local health promotion partners.

The intervention will be carry out during two years in secondary schools in the Hainaut province, Belgium. This province has one of the highest smoking prevalence in the country and the lowest income level.

A cluster randomized controlled trial will test the effectiveness of the advocacy coalition to improve the implementation of TFSP.

Schools (the clusters) are randomly assigned either to the intervention arm (and set up the advocacy coalition) or to the control arm (and try to achieve the objectives without the advocacy coalition). Randomization will be cross-stratified on the basis of their geographical location (to avoid contamination biases) and social-economic status.

The main questions this study aims to answer are:

1. To what extent is an advocacy coalition related to smoking prevention implementable in school's routine ?
2. Is an advocacy coalition an effective way to prevent smoking among adolescents and shift smoking norms in school?

To answer these questions:

1. We will make an audit on the state of the school policy regarding smoking and tobacco products.
2. A survey will be carried out among staff' members of the participating schools on their engagement in the project, their opinion about smoking prevention at school and their smoking status.
3. A survey will be carried out among adolescents from the 3rd and 4th grade, following a repeated cross-sectional design. Questionnaires will focus on epidemiological indicators such as smoking status and initiation, but also on social norm features such as beliefs and perceptions adolescents hold about smoking.

These evaluations will occur at three times: at baseline, at one year of follow-up and at two years of follow-up. Results of these evaluations will serve to give a feedback to the schools on their situation regarding smoking (regardless to treatment arm to which the school is assigned).

Enrollment: 20 estimated patients

Sex: All

Ages: 13 to 19 years old

Volunteers: Accepts Healthy Volunteers

Inclusion and exclusion criteria

These criteria concern adolescents who will take part in the surveys.

Inclusion Criteria:

• student at a secondary school participating in the study
• student of the 3rd and 4th grade

Exclusion Criteria:

• student at a secondary school not participating in the study
• student of another grade than 3rd and 4th grade

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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20 participants in 2 patient groups

Advocacy coalition

Experimental group

Description:

Feedback + advocacy coalition

Treatment:

Behavioral: Advocacy coalition

Behavioral: Feedback

Control

Active Comparator group

Description:

Only feedback

Treatment:

Behavioral: Feedback