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Community Health Campaign: Fitter Families Project

2 juillet 2017 mis à jour par: Dr. Steven C. Shen, The University of Hong Kong
In recent years, Hong Kong has been undergoing rapid changes with macro social and economic trends. The increasingly complex and diverse family structure contribute to concerns regarding the well-being of families in Hong Kong, including their health, happiness and harmony (FAMILY 3Hs). Family life and health education should be strengthened to meet the increasing needs of promoting healthy active lifestyle among Hong Kong families. In this connection, the FAMILY Project initiates the Fitter Families Project (FFP) with a focus on "FAMILY Holistic Health", will be conducted in order to increase the awareness of the importance of FAMILY 3Hs. FFP is a community-based research project with 3 main components - train-the-trainers programs, community-based family interventions and public education events. It is expected that trainees from the train-the-trainers programs will acquire adequate skills to organize community-based health education programs effectively. Participants of the community-based family interventions will gain knowledge on family holistic health and live a healthy active lifestyle. Attendees of the public education events will become more aware of the importance of FAMILY 3Hs.

Aperçu de l'étude

Description détaillée

In 2011, United Nations (UN) addressed the prevention and control of four non-communicable diseases (NCDs: cancer, cardiovascular disease, chronic respiratory disease, and diabetes mellitus) worldwide. The UN, in its Political Declaration, recognized the critical importance of reducing the exposure to the common modifiable risk factors for NCDs, namely, tobacco use, unhealthy diet, physical inactivity, and the harmful use of alcohol. In Hong Kong, NCDs are responsible for more than 85% of all deaths and most of these are preventable. FAMILY Project Cohort Study (2014) also found that 88.6% of Hong Kong people had inadequate vegetable and fruit intake, 70.6% had inadequate physical exercise, 26.4% were overweight and 5.4% were obese. Hong Kong, being the most westernized and developed city of China, can take a leading role in promoting and implementing the UN Political Declaration.

Families worldwide have been undergoing rapid changes with macro, social and economic trends. Demographic shifts, economic upheavals, changing societal norms and values, immigration across national borders and migration within nations are creating new and altered structures, processes and relationships within families. The increasingly complex and diverse family structure contributes to concerns regarding the well-being of families in Hong Kong, including their health, happiness and harmony (FAMILY 3Hs). Family life and health education should be strengthened to meet the increasing needs of promoting healthy lifestyle among Hong Kong families. The results from the baseline findings of FAMILY Project Cohort Study (2014) revealed that only 27.9% of the participants considered themselves to be 'happy', while 15.6% of the participants were classified as 'unhappy'. Nearly one-third (30.7%) of the participants reported having experienced at least one stressful life event in the previous year due to heavier workload (10.8%), serious health problems of a family member (6.8%), worsening financial situation (6.2%), health problems of oneself (5.1%), or death of a family member (4.7%). Furthermore, more than half of the participants (52.5%) reported having some source of dyadic conflicts with family members. In response to these changes in the contexts and nature of the family, the Fitter Families Project (FFP) with a focus on "FAMILY Holistic Health", will be conducted in order to increase the awareness of the importance of FAMILY 3Hs.

There are several definitions of family health. On the functional level, the terms family health, family functioning, and healthy family are often used interchangeably. Family health has been described as complex system, interactions, relationships and processes with the potential to enhance both well-being and the entire household's health, and routines in the family may affect family health. Despite the different perspectives in the definitions, family health should be holistically defined, encompass both wellness and illness variables and focus on the interactive, developmental, functional, psychosocial, and health processes of family experience. Therefore, family health may be described as a dynamic process that maintains or changes the relative state of well-being, including elements of family systems, such as biological, psychological, spiritual, and sociocultural aspects. Hence, the FFP focuses on "FAMILY Holistic Health" which is to emphasize a more comprehensive and wide reaching aim and includes physical, mental and social health and well-being.

Over the past six years, the FAMILY project has been working on community-based projects to promote FAMILY 3Hs. Since 2010, the Christian Family Service Centre (CFSC) in collaboration with the School of Public Health of the University of the Hong Kong (HKU) implemented a community-based Learning Families Project (LFP) to promote family health, happiness and harmony (3Hs). As a component of the FAMILY Project, the LFP had built up an effective practice model through collaboration among various project partners and showed good evidence of effectiveness in developing a learning culture in the families, enhancing family communication time and quality, increasing neighborhood cohesion and resilience and promoting FAMILY 3Hs. Therefore, the FFP is developed based on the strong foundation of the LFP in the previous years. In view of the health challenges locally and globally, the new phase of FAMILY project will put more emphasis on health in the upcoming three years. Following the theme on FAMILY 3Hs, the FFP focuses on family holistic health with emphasis on the interaction and integration of both physical and psychosocial health.

In Hong Kong, most 'health projects' only focus on individual's physical health and usually separate physical from mental or psychosocial health. This new project focuses not only on individuals' health but on the whole family and holistic health. The investigators strive to help family members influence each other to have better holistic health. The focus on family is a new and unique concept which is an innovative, long-term and highly sustainable approach at the community level. With the involvement of family members, Hong Kong families can develop and change their lifestyles which impact on families' health. The investigators will use a family-focused approach and adopt a holistic perspective to design a sustainable family holistic health intervention model in the community to meet the global health challenges identified by UN.

The innovative family holistic health intervention model will emphasize on the interaction and integration of physical health and psychosocial health, using physical exercise as the platform to promote fitter families, which will ultimately enhance the FAMILY 3Hs. Thus, the ultimate objective of this community-based project is "FAMILY holistic health" for FAMILY 3Hs.

In practice, the investigators will use innovative integrated public health theories and minimal methods to plan brief, simple and cost-effective interventions targeted at families, with collaboration with experienced NGO partners and community stakeholders. Hence, a larger number of people will be able to benefit from the program, leading to greater sustainability and wider dissemination as the administration of project will be easier and the costs will be lower. The "FAMILY Holistic Health" community-based project aims at promoting a higher level of physical exercise for people of all ages which will enhance family interaction, pleasure and well-being. The project can help families to build positive attitudes with stronger motivation for family members to improve their holistic health by encouraging each other to have healthy active lifestyle and enjoy the processes with quick and measurable benefits.

The evaluations conducted will be vigorous and evidence generating with quantitative and qualitative methods and follow-ups to assess behavioral changes and improvements in the key components of family well-being. The data will be provided to the participants for developing their own health action plan. In order to assess the effectiveness of the interventions on improving individual and family well-being and for future program development, the data will also be used for program evaluation. Thus, this proposal is to seek approval from IRB to collect data from the participants, to use the data for in depth analyses, and to write up scientific papers based on the findings.

Type d'étude

Interventionnel

Inscription (Réel)

953

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
        • Christian Family Service Center

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

12 ans et plus (Enfant, Adulte, Adulte plus âgé)

Accepte les volontaires sains

Oui

Sexes éligibles pour l'étude

Tout

La description

Inclusion Criteria:

  • Cantonese speaking, Intact verbal and hearing abilities for interpersonal communication, Reading and writing abilities for questionnaire completion, aged 12 or above

Exclusion Criteria:

  • Participants who fail to meet the inclusion criteria

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: Talk and leaders
This group will comprise of health talk and regular contact with community leaders.
Health talk on zero-time exercise.
Regular contact with community leaders to remind them do zero-time exercise.
Expérimental: Talk, leaders and equipment
This group will comprise of health talk and regular contact with community leaders. Moreover, a home-based equipment (handgrip) will be delivered to them
Health talk on zero-time exercise.
Regular contact with community leaders to remind them do zero-time exercise.
This is a home-based equipment
Comparateur actif: Talk
This group will comprise of a health talk only.
Health talk on zero-time exercise.

Que mesure l'étude ?

Principaux critères de jugement

Mesure des résultats
Description de la mesure
Délai
Changes in family harmony from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Family harmony will be assessed by a 0-10 score at 3 time points
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in family happiness from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Family happiness will be assessed by a 0-10 score at 3 time points
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in family health from baseline to 3 months after intervention
Délai: Baseline, at 1 month follow-up, and at 3 months after intervention
Family health will be assessed by a 0-10 score at 3 time points
Baseline, at 1 month follow-up, and at 3 months after intervention

Mesures de résultats secondaires

Mesure des résultats
Description de la mesure
Délai
Changes in knowledge on zero-time exercise from baseline to 3 months after intervention
Délai: Baseline, immediately after intervention, at 1 month after intervention, and at 3 months after intervention
Questionnaire will be used to investigate the changes in participants' knowledge on zero-time exercise.
Baseline, immediately after intervention, at 1 month after intervention, and at 3 months after intervention
Changes in attitude towards performing zero-time exercise from baseline to 3 months after intervention
Délai: Baseline, immediately after intervention, at 1 month after intervention, and at 3 months after intervention
Questionnaire will be used to investigate the changes in participants' attitude towards performing zero-time exercise.
Baseline, immediately after intervention, at 1 month after intervention, and at 3 months after intervention
Changes in intention at performing zero-time exercise from baseline to 3 months after intervention
Délai: Baseline, immediately after intervention, at 1 month after intervention, and at 3 months after intervention
Questionnaire will be used to investigate the changes in participants' intention at performing zero-time exercise.
Baseline, immediately after intervention, at 1 month after intervention, and at 3 months after intervention
Changes in the frequency and amount on performing exercise from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Questionnaire will be used to investigate the changes in participants' frequency and amount on performing moderate exercise (e.g. cycling or quick walking), vigorous exercise (e.g. swimming or jogging), zero-time exercise and walking.
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in neighborhood cohesion from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Questionnaire will be used to investigate the changes in participants' neighborhood cohesion by a 5-items scale.
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in utilization of community resources from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Questionnaire will be used to investigate the changes in participants' utilization of community resources to perform exercise.
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in grip strength (kg) from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Grip strength will be assessed by a hand grip strength measurement instrument.
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in chair stand (times) from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Chair stand will be assessed by a test counting times of chair stand in 30 seconds.
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in single leg stand (s) from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Single leg stand will be assessed by a test measuring the longest duration of single leg stand in 120 seconds.
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in seat and reach (cm) from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Seat and reach will be assessed by a ruler.
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in body fat (%) from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in body fat will be assessed by a standard body fat measuring scale.
Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in body weight (kg) from baseline to 3 months after intervention
Délai: Baseline, at 1 month after intervention, and at 3 months after intervention
Changes in body weight will be assessed by a standard body fat measuring scale.
Baseline, at 1 month after intervention, and at 3 months after intervention
Satisfaction towards the program
Délai: Immediately after intervention
Questionnaire will be used to investigate the participants' satisfaction towards the program immediately after intervention.
Immediately after intervention

Collaborateurs et enquêteurs

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

Les enquêteurs

  • Chercheur principal: Chen Shen, PhD, 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 septembre 2015

Achèvement primaire (Réel)

1 décembre 2016

Achèvement de l'étude (Réel)

1 juin 2017

Dates d'inscription aux études

Première soumission

10 mars 2016

Première soumission répondant aux critères de contrôle qualité

20 mars 2016

Première publication (Estimation)

24 mars 2016

Mises à jour des dossiers d'étude

Dernière mise à jour publiée (Réel)

5 juillet 2017

Dernière mise à jour soumise répondant aux critères de contrôle qualité

2 juillet 2017

Dernière vérification

1 juillet 2017

Plus d'information

Termes liés à cette étude

Autres numéros d'identification d'étude

  • UW15-401

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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