- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT03153176
"Escola em Ação" (School in Action) (EA)
"Escola em Ação": School Based Interventions of Incentive to the Practice Physical and Life Habits of Healthy Promotion
Background: The health promotion actions carried out in the school environment have positive effects on reducing risk factors for chronic diseases in adolescents. Interdisciplinary strategies involving school and family to increase the level of physical activity among adolescents, inside and outside the school, are essential to encourage healthier lifestyles.
Aim: To determine whether a 24-weeks interdisciplinary intervention program promotes improvement in the level of physical activity, physical fitness, sleep quality, life satisfaction, eating habits and reduce the sedentary behavior of schoolchildren aged 10 to 13 years of public schools in the city of Presidente Prudente, São Paulo, Brazil.
The intervention: Includes training of teacher Physical Education in the principles of self-determination theory and ecological theory at practical applications for motivating adolescents in physical activities and sports. The students will be given information on the benefits of a physically active lifestyle and will be encouraged to participated the new opportunities for physical activity in their school and community. The program will offer physical activity strategies over the 24-weeks during class Physical Education, afternoon recess and active lesson breaks in theoretical classes. Nutritional guidelines and gardening experience will be developed to encourage healthy eating habits among schoolchildren and to reduce salt, oil and sugar in the preparation of school lunch.
Methods/design: The project, which being conducted as cluster randomized trial, is to evaluated whit in a mixed methods, including qualitative and quantitative approach will be used for the construction of the actions integrated to the school physical education curriculum and evaluation of the program by the participants and supporters. The RE-AIM evaluation metric (Reach, Effectiveness, Adoption, Implementation, and Maintenance) is used to guide the validation this program.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
-
-
São Paulo
-
Presidente Prudente, São Paulo, Brésil, 19060-900
- Sueyla Ferreira da Silva dos Santos
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- Students enrolled in 2017, in the 6th and 7th year of Elementary School in the full-time schools participating in the study
Exclusion Criteria:
- Students with physical or motor impairment that prevents the performance of physical fitness assessments or with mental or cognitive impairment that prevents them from responding with clarity to the questionnaires and instruments of data collection
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Autre
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: intervention
Training program for Physical Education teacher.
Individual level: moderate to vigorous physical activity.
Organizational level: school health policy for healthy lifestyle
|
Training program 30 hours accumulated before, during and after intervention
Autres noms:
7 to 10 minutes in Physical Education in class time, 3 sections for week during lunch break
Autres noms:
Inclusion of actions in the school curriculum: counseling sections with health for parents and adolescent, active lesson breaks during theoretical class, gardening experience in school, nutrition guidance for school lunch professionals.
Autres noms:
|
|
Aucune intervention: no intervention
Physical Education and school curriculum as usual
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change from baseline in weekly time in moderate-to-vigorous physical activity at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with accelerometers for tenn days and supplemented with a questionnaire
|
Baseline, end of intervention (6 months), 1 year after baseline
|
|
Change from baseline in weekly time in sedentary activity at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with accelerometers for tenn days and supplemented with a questionnaire
|
Baseline, end of intervention (6 months), 1 year after baseline
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change from baseline in Physical Education class time in moderate-to-vigorous physical activity at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with accelerometers in Physical Education class
|
Baseline, end of intervention (6 months), 1 year after baseline
|
|
Change from baseline in level physical fitness at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with physical fitness test (abdominal resistance, palmar grip, horizontal jump, Wells bench, beep test)
|
Baseline, end of intervention (6 months), 1 year after baseline
|
|
Change from baseline in body composition at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with Dual-energy X-ray absorptiometry (DXA) and anthropometric measurements (body height, body weight, waist circumference, hip circumference, arm circumference, triceps skin fold and puberty status (self- assessed)
|
Baseline, end of intervention (6 months), 1 year after baseline
|
|
Change from baseline in caloric intake at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with food register at 3 days and supplemented with a questionnaire
|
Baseline, end of intervention (6 months), 1 year after baseline
|
Autres mesures de résultats
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Change from baseline in the time and quality sleep at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with accelerometers for tenn days and supplemented with a questionnaire (Pittsburgh sleep quality index)
|
Baseline, end of intervention (6 months), 1 year after baseline
|
|
Change from baseline in performance academic at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with school scores and state education performance exam
|
Baseline, end of intervention (6 months), 1 year after baseline
|
|
Change from baseline in satisfaction with life at six months
Délai: Baseline, end of intervention (6 months), 1 year after baseline
|
Measured with standardized questionnaire
|
Baseline, end of intervention (6 months), 1 year after baseline
|
Collaborateurs et enquêteurs
Collaborateurs
Les enquêteurs
- Directeur d'études: Ismael Freitas Junior, Phd, CELAPAM
Publications et liens utiles
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Réel)
Achèvement de l'étude (Réel)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Autres numéros d'identification d'étude
- UNESP Presidente Prudente
Plan pour les données individuelles des participants (IPD)
Prévoyez-vous de partager les données individuelles des participants (DPI) ?
Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
Étudie un produit pharmaceutique réglementé par la FDA américaine
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