Move ARound And Get Active: an Intervention to Optimize 24-hour Movement Behaviours in Preschoolers

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

In 2019, the World Health Organization established new guidelines for physical activity, sedentary screen time, and sleep for children under 5 years old. Unfortunately, only a few (6%) of preschoolers in Flanders, Belgium, adhere to these guidelines. The aim of this study is to test a health program developed to optimize 24-hour behaviors in preschoolers and encourage more children to follow the guidelines. The program was created using the Intervention Mapping Protocol in collaboration with parents. It consists of seven sessions for parents and preschoolers, providing strategies to encourage compliance with the guidelines. The program's effectiveness will be evaluated through a randomized controlled trial, with the intervention group attending the sessions and the control group receiving the intervention materials at the end of the study.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 2
Maximum Age: 6
Healthy Volunteers: t
View:

• Preschoolers between 2,5 to 6 years

• One parent per preschooler

• Parent needs to be able to understand, speak, read and write Dutch

• Child needs to be able to understand Dutch

• Child needs to be able to wear accelerometer

• Child needs to by mentally and physically able to comply with the 24-hour movement behavior guidelines

• Parent needs to be mentally able to complete the testing and intervention

Locations
Other Locations
Belgium
Onze-Lieve-Vrouwenziekenhuis Campus Aalst
RECRUITING
Aalst
AZ Alma
RECRUITING
Eeklo
AZ Jan Palfijn
RECRUITING
Ghent
University Hospital Ghent
RECRUITING
Ghent
Contact Information
Primary
Marga Decraene, MSc
marga.decraene@ugent.be
+32 9 332 26 32
Backup
Marieke De Craemer, PhD
marieke.decraemer@ugent.be
Time Frame
Start Date: 2023-07-27
Estimated Completion Date: 2024-12-31
Participants
Target number of participants: 200
Treatments
Experimental: Intervention group
Intervention group receives intervention between prétest and posttest. Three months after posttest they undergo a follow-up test
Other: Control group
Waiting group. Control group receives intervention after all test (prétest, posttest and follow-up test)
Related Therapeutic Areas
Sponsors
Collaborators: AZ Jan Palfijn Gent, Algemeen Ziekenhuis Maria Middelares, Onze Lieve Vrouwziekenhuis Aalst, AZ Alma
Leads: University Hospital, Ghent

This content was sourced from clinicaltrials.gov