Health Behaviour Clinical Trial
— HOPPLearningOfficial title:
HOPPLearning - Active Learning in Elementary Schools in Horten Municipality
Verified date | June 2021 |
Source | Kristiania University College |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
HOPP Learning will be implemented in elementary schools in the Horten municipality and will assess the effect of a combined pedagogical approach, active learning, on a large student population. Students are to increase their amount of physical activity with learning, during a school day by one hour.
Status | Active, not recruiting |
Enrollment | 2300 |
Est. completion date | December 2023 |
Est. primary completion date | December 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 6 Years to 12 Years |
Eligibility | Inclusion Criteria: - Students from Grade 1-6 (2015) from all elementary schools in Horten municipality and two schools from Loerenskog and Baerum municipality. Exclusion Criteria: - Students with psychological and physical disabilities preventing them participating in the tests - Students afflicted with sickness/disease during the testing period - Students who do not wish to participate in the test |
Country | Name | City | State |
---|---|---|---|
Norway | Kristiania University College | Oslo |
Lead Sponsor | Collaborator |
---|---|
Kristiania University College | Horten municipality |
Norway,
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* Note: There are 15 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Academic performance | Change in academic performance due to change in the pedagogic technique using standarised national academic tests | 72 months | |
Secondary | Cognitive ability | Measurements of cognitive ability pre- and post intervention using Eriksen Flanker test and Stroop test | 72 months | |
Secondary | Diet changes | Based on diet information to the parents diet change in the children are measured using a questionnaire Ungkost 2000 | 72 months | |
Secondary | Changes in quality of life | The intervention may change QOL. The study is using ILC for parents and children to measure the change | 72 months | |
Secondary | Changes in blood values | Blood values of total cholesterol, HDL, 6-months blood-sugar, Hb, RBC, Haematocrit, ferritin, iron and CRP are measured pre- and post intervention. | 72 months | |
Secondary | General physical capacity | General physical capacity is measured in all participants using Andersen shuttle run test, Jamar handgrip, Balance Y-test and maximal oxygen uptake (1st. grade). Changes are expected due to increased physical activity level. | 72 months | |
Secondary | Cardiovascular risk factors | The change in cardiovascular risk factors during 5 years of intervention is measured using a combination of data from medical tests, physiological tests and questionnaires | 72 months | |
Secondary | Physical activity level | Change in physical activity level due to active learning are measured using Actigraph wGT3X-BT across one week | 12 months |
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