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Be Healthy, So Easy: FAMILY Education Project

10 juillet 2018 mis à jour par: Dr. Agnes Yuen-Kwan Lai, The University of Hong Kong

The goal of the study is to evaluate the effectiveness of a family-focused, interactive, and theory-based intervention to reduce the sedentary behavior and increase physical activity, family communication and well-being of the participants.

The intervention is to use Zero-time Exercise, the positive psychology theme "Appreciation and Gratitude" [23, 24], and role modelling approach to get sedentary people to start exercising, increase levels of physical activity, family communication and well-being of the participants and their family members.

The intervention aims to encourage positive and sustainable health actions among participants and their family members.

Aperçu de l'étude

Statut

Complété

Les conditions

Description détaillée

Lack of physical activity is a behavioural risk for non-communicable diseases. The World Health Organization (WHO) reported that physical inactivity and unhealthy diets are two of the four main behavioural risk factors that contribute to non-communicable diseases. Globally, people who are overweight and obese, particularly if these people are physically inactive. They are at risk for morbidity and mortality.

Hong Kong-specific data demonstrates that many people cannot meet World Health Organization targets for physical activity. The Hong Kong Behavioural Risk Factor Survey reported that, for the seven days prior to the survey, about half (52.0%) of adults aged 18-64 had not done any moderate physical activity. Overall, only 37.5% of the respondents met the WHO's recommended physical activity level of at least 150 minutes of moderate or 75 minutes of vigorous physical activity a week for adults.

There is emerging evidence of effective behavioral interventions to decrease sedentary behavior. Some studies focused on reducing screen time or active workstations that encourage standing at the computer. Others focus on increased use of stairs instead of lifts. These interventions used behaviour change techniques such as goal-setting and behavioural self-monitoring. As previous approaches have not shown promising results, new approaches are needed to reduce sedentary behaviour and increase exercise or physical activity.

The goal of the study is to evaluate the effectiveness of a family-focused, interactive, and theory-based intervention to reduce the sedentary behavior and increase physical activity of the participants.

The intervention is to use Zero-time Exercise, the positive psychology theme "Appreciation and Gratitude", and role modelling approach to get sedentary people to start exercising, increase levels of physical activity, family communication and well-being of the participants and their family members. The intervention aims to encourage positive and sustainable health actions among participants and their family members.

Needs assessment and focus group interview will be conducted before program design and after conducting the training, respectively. Process evaluation will be performed to evaluate the process of each component of the program. Qualitative and quantitative assessments will be used to evaluate the effectiveness of this Zero-time Exercise intervention.

Type d'étude

Interventionnel

Inscription (Réel)

673

Phase

  • N'est pas applicable

Contacts et emplacements

Cette section fournit les coordonnées de ceux qui mènent l'étude et des informations sur le lieu où cette étude est menée.

Lieux d'étude

      • Hong Kong, Hong Kong, 852
        • Caritas integrated Family Service Centre

Critères de participation

Les chercheurs recherchent des personnes qui correspondent à une certaine description, appelée critères d'éligibilité. Certains exemples de ces critères sont l'état de santé général d'une personne ou des traitements antérieurs.

Critère d'éligibilité

Âges éligibles pour étudier

18 ans à 100 ans (Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  1. Parents with at least on child between 3 and 18;
  2. Parents with at least primary school educational level:
  3. Parents who can read and write Chinese.

Exclusion Criteria:

  1. People with a serious health condition that might prevent them from participating in physical activity;
  2. Parents who do not have a child between 3 and 18.

Plan d'étude

Cette section fournit des détails sur le plan d'étude, y compris la façon dont l'étude est conçue et ce que l'étude mesure.

Comment l'étude est-elle conçue ?

Détails de conception

  • Objectif principal: La prévention
  • Répartition: Randomisé
  • Modèle interventionnel: Affectation parallèle
  • Masquage: Aucun (étiquette ouverte)

Armes et Interventions

Groupe de participants / Bras
Intervention / Traitement
Expérimental: Zero-time Exercise (PA) group

The intervention arm (PA group) aims to improve family communication and well-being, reduce sedentary behavior and increase physical activity. The programme includes a knowledge and motivation enhancement session at baseline, an experience sharing session at 3 months, a family gathering session at 6 months, and a holistic health session at 12 months after the first session as well as biweekly/monthly mobile messages.

The holistic health session is not a part of the cRCT, it aims to collect one-year feedback from participants and provides additional health information to improve dietary habits.

a knowledge and motivation enhancement session at baseline, an experience sharing session at 3 months, a family gathering session at 6 months, and a holistic health session at 12 months (not a part of cRCT, for the collection of feedback only) as well as biweekly/monthly mobile messages to improve physical activity habit.
Comparateur placebo: Healthy Eating (HE) group

The control arm (HE group) aims to improve family communication and well-being and enhance healthy eating habits. Participants are required to engage their family members in their activities. The programme includes a knowledge and motivation enhancement session at baseline, an experience sharing session at 3 months, a family gathering session at 6 months, and a holistic health session at 12 months after the first session as well as biweekly/monthly mobile messages.

The holistic health session is not a part of the cRCT, it aims to collect one-year feedback from participants and provides additional health information to improve physical activity habit.

a knowledge and motivation enhancement session at baseline, an experience sharing session at 3 months, a family gathering session at 6 months, and a holistic health session at 12 months (not a part of cRCT, for the collection of feedback only) as well as biweekly/monthly mobile messages to improve dietary habit.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Change in behavior on performing physical activity in relation to Zero-time Exercise, moderate and vigorous exercises
Délai: baseline, 3 months
Behaviors on performing physical activity will be assessed by outcome-based questionnaire
baseline, 3 months

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Change in behavior on performing physical activity in relation to Zero-time Exercise, moderate and vigorous exercises
Délai: baseline, 3 months, 6 months, 1 year
Behavior on performing physical activity will be assessed by outcome-based and physical activity questionnaire
baseline, 3 months, 6 months, 1 year
Change in behavior on taking healthy diet
Délai: baseline, 3 months, 6 months, 1 year
Behavior on taking healthy diet will be assessed by outcome-based healthy diet questionnaire
baseline, 3 months, 6 months, 1 year
Attitude on performing Zero-time Exercise,
Délai: immediate after training session, 3 months, 6 months, 1 year
Attitude on performing physical activity in relation to Zero-time Exercise will be assessed by outcome-based questionnaire
immediate after training session, 3 months, 6 months, 1 year
Perceived ability and intention to motivate participants themselves and their family to increase Zero-time Exercise
Délai: baseline, 3 months, 6 months, 1 year
Perceived ability and intention to motivate participants themselves and their family members on performing Zero-time Exercise will be assessed by outcome-based questionnaire
baseline, 3 months, 6 months, 1 year
Change in participants' own health and happiness
Délai: baseline, 3 months, 6 months, 1 year
Personal health and happiness will be assessed by outcome-based questionnaire
baseline, 3 months, 6 months, 1 year
Change in participants' family harmony
Délai: baseline, 3 months, 6 months, 1 year
Family harmony will be assessed by outcome-based questionnaire
baseline, 3 months, 6 months, 1 year
Change in physical fitness performance (Endurance)
Délai: baseline, 3 months,6 months, 1 year
Endurance will be assessed through a simple fitness test called foot pedaling
baseline, 3 months,6 months, 1 year
Family members' behavior on performing physical activity in relation to Zero-time Exercise,
Délai: 6 months
Family members' behavior on performing physical activity in relation to Zero-time Exercise will be assessed by outcome-based questionnaire
6 months

Collaborateurs et enquêteurs

C'est ici que vous trouverez les personnes et les organisations impliquées dans cette étude.

Les enquêteurs

  • Chercheur principal: Agnes YK Lai, DN, The University of Hong Kong

Publications et liens utiles

La personne responsable de la saisie des informations sur l'étude fournit volontairement ces publications. Il peut s'agir de tout ce qui concerne l'étude.

Dates d'enregistrement des études

Ces dates suivent la progression des dossiers d'étude et des soumissions de résultats sommaires à ClinicalTrials.gov. Les dossiers d'étude et les résultats rapportés sont examinés par la Bibliothèque nationale de médecine (NLM) pour s'assurer qu'ils répondent à des normes de contrôle de qualité spécifiques avant d'être publiés sur le site Web public.

Dates principales de l'étude

Début de l'étude (Réel)

1 juillet 2015

Achèvement primaire (Réel)

1 juin 2017

Achèvement de l'étude (Réel)

1 juin 2017

Dates d'inscription aux études

Première soumission

5 novembre 2015

Première soumission répondant aux critères de contrôle qualité

8 novembre 2015

Première publication (Estimation)

10 novembre 2015

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

12 juillet 2018

Dernière mise à jour soumise répondant aux critères de contrôle qualité

10 juillet 2018

Dernière vérification

1 juillet 2018

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • UW 15-330

Ces informations ont été extraites directement du site Web clinicaltrials.gov sans aucune modification. Si vous avez des demandes de modification, de suppression ou de mise à jour des détails de votre étude, veuillez contacter register@clinicaltrials.gov. Dès qu'un changement est mis en œuvre sur clinicaltrials.gov, il sera également mis à jour automatiquement sur notre site Web .

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