Reducing and Breaking up School-related Sedentary Behaviour Among Adolescents Using Co-creation

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age11-15
SponsorUniversity Ghent

About this trial

Adolescents spend the majority of the day sedentary, especially at school whilst sitting in class and at home when performing school-related tasks. As high levels of sedentary time are associated with adverse health effects, effective interventions are needed. To improve effectiveness, literature recommends a co-creative approach in which adolescents and other key stakeholders (such as teachers) are actively involved in the choice and development of intervention strategies. Therefore, this project aims to co-adapt a previously co-created intervention targeting adolescents' school-related sedentary behaviour. Further, the effect of this co-adapted intervention on adolescents' sedentary behaviour and related determinants, sleep, and mental wellbeing will be evaluated via a three-arm clustered controlled trial, including a co-adaptation intervention arm, a standard intervention arm (including schools that were not involved in co-adapting the intervention) and a control arm (continuing their curriculum as usual). By comparing these three arms, the investigators can evaluate the added value of co-creation compared to not involving adolescents or stakeholders in the development of an intervention. Lastly, the investigators will conduct a process evaluation of (1) the co-adaptation approach used to adapt the co-created intervention and (2) the implementation of both the co-adapted and standard interventions. Studies that evaluate co-created interventions are scarce. However, if such interventions prove to be more effective, this approach could be promising to change adolescents' health behaviour.

Eligibility criteria

This trial accepts healthy volunteers

Qualifiers

Secondary schools need to have at least 150 pupils in the first two grades (Grade 7 and 8).

Disqualifiers

None

Trial design

Design model

Parallel

Treatments tested in this trial

  • Co-adapted intervention

    Behavioral

    An existing co-created intervention will be adapted by researchers and 7th and 8th grade pupils and teachers during 3 to 5 design sessions in both co-adaptation intervention schools.

  • Standard intervention

    Behavioral

    The existing co-created intervention will be implemented in the standard intervention schools. So, adolescents and school staff from the standard intervention schools will not be involved in adapting the intervention.

Treatment groups

600 Participants
are divided into 3 treatment groups
Group A: Co-adaptation intervention groupExperimental treatment 1 intervention
Group B: Standard intervention groupActive comparator 1 intervention
Group C: Control groupNo intervention 0 interventions

Trial outcomes

Primary outcomes

1

Sitting time and patterns of sitting time

Sitting time and patterns of sitting time will be derived from a GENEActiv accelerometer that will be worn on the non-dominant wrist.

Time frame
Assessed at baseline (pre-intervention) and immediately after the intervention period. The GENEActiv will be worn during one week.
2

Determinants of reducing and regularly interrupting sedentary time in general, in the classroom, and while making homework

These determinants will be measured using a questionnaire including items that will be answered on a 5-point Likert scale.

Time frame
Assessed at baseline (pre-intervention) and immediately after the intervention period.

Secondary outcomes

1

Sleeping time

Sleeping time will be derived from a GENEActiv accelerometer that will be worn on the non-dominant wrist.

Time frame
Assessed at baseline (pre-intervention) and immediately after the intervention period. The GENEActiv will be worn during one week.
2

Mental well-being

Mental well-being will be measured using the the World Health Organization-Five Well-Being Index (WHO-5).

Time frame
Assessed at baseline (pre-intervention) and immediately after the intervention period.

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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