- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT02405611
A Multi-component Intervention on Improving Fruit and Vegetable Consumption in Teenagers and Their Mothers
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
This study is a longitudinal controlled trial that is designed to investigate the effectiveness of a multi-component intervention on improving fruit and vegetable consumption in teenagers and their mothers. Participants will be allocated in three groups with a) an intervention group in which mothers and children receive the intervention and questionnaires, b) only the children receive the intervention and mothers and children receive the questionnaires, and c) mothers and children are in active control group and only receive the questionnaires. The intervention package contains behavior change techniques targeting outcome expectancy, self-efficacy, action planning, coping planning, and self-monitoring. The active control group receives an information sheet regarding recommendations on fruit and vegetable intake. There will be 3 assessment points in time, with 1 months in between. All the intervention materials and information sheets will be handed to participants after the baseline assessment. The self-monitoring calendar will be collected at time 2 assessment.
The primary outcome of this study is to estimate the dyadic mechanisms between mothers and their children regarding improving fruit and vegetable intake. Secondary outcome is to investigate whether fruit and vegetable consumption did improve in the intervention groups in general and also to find the psychological mechanism behind the changes during the time of the study.
Type d'étude
Inscription (Réel)
Phase
- N'est pas applicable
Contacts et emplacements
Lieux d'étude
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Qazvin, Iran (République islamique d
- The Organization for Education
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Qazvin, Iran (République islamique d, 3419759811
- Department of Public Health, Qazvin University of Medical Sciences
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Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Enfant
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
Sexes éligibles pour l'étude
La description
Inclusion Criteria:
- They are not involved in the nutritional education
- Ability to understand Persian language Adolescents attending high schools in Qazvin
Exclusion Criteria:
- Does not meet inclusion criteria
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: La prévention
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Double
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
---|---|
Comparateur actif: active control
mothers and children are in active control group and only receive the questionnaires
|
The intervention package contains behavior change techniques targeting outcome expectancy, self-efficacy, action planning, coping planning, and self-monitoring.
The active control group receives an information sheet regarding recommendations on fruit and vegetable intake.
There will be 3 assessment points in time, with 1 1 month and six months in between.
All the intervention materials and information sheets will be handed to participants after the baseline assessment.
The self-monitoring calendar will be collected at time 2 assessment.
|
Expérimental: mother and student
an intervention group in which mothers and children receive the intervention and questionnaires
|
The intervention package contains behavior change techniques targeting outcome expectancy, self-efficacy, action planning, coping planning, and self-monitoring.
The active control group receives an information sheet regarding recommendations on fruit and vegetable intake.
There will be 3 assessment points in time, with 1 month and six months in between.
All the intervention materials and information sheets will be handed to participants after the baseline assessment.
The self-monitoring calendar will be collected at time 2 assessment.
|
Expérimental: children
only the children receive the intervention and mothers and children receive the questionnaires
|
The intervention package contains behavior change techniques targeting outcome expectancy, self-efficacy, action planning, coping planning, and self-monitoring.
The active control group receives an information sheet regarding recommendations on fruit and vegetable intake.
There will be 3 assessment points in time, with 1 month and six months in between.
All the intervention materials and information sheets will be handed to participants after the baseline assessment.
The self-monitoring calendar will be collected at time 2 assessment.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
changes in fruit intake using a self-reported questionnaire
Délai: baseline, 1 Months, 6 months follow-up
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using a self-reported questionnaire
|
baseline, 1 Months, 6 months follow-up
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changes in vegetable intake using a self-reported questionnaire
Délai: baseline, 1 Months, 6 months follow-up
|
using a self-reported questionnaire
|
baseline, 1 Months, 6 months follow-up
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
---|---|---|
changes in self efficacy using a self-reported questionnaire
Délai: baseline, 1 Months, 6 months follow-up
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using a self-reported questionnaire
|
baseline, 1 Months, 6 months follow-up
|
changes in outcome expectancy using a self-reported questionnaire
Délai: baseline, 1 Months, 6 months follow-up
|
using a self-reported questionnaire
|
baseline, 1 Months, 6 months follow-up
|
changes in coping planning using a self-reported questionnaire
Délai: baseline, 1 Months, 6 months follow-up
|
using a self-reported questionnaire
|
baseline, 1 Months, 6 months follow-up
|
changes in action planning using a self-reported questionnaire
Délai: baseline, 1 Months, 6 months follow-up
|
using a self-reported questionnaire
|
baseline, 1 Months, 6 months follow-up
|
changes in self-monitoring using a self-reported questionnaire
Délai: baseline, 1 Months, 6 months follow-up
|
using a self-reported questionnaire
|
baseline, 1 Months, 6 months follow-up
|
Collaborateurs et enquêteurs
Parrainer
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude
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 (Estimation)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Estimation)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Autres numéros d'identification d'étude
- 682
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