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Be Healthy, So Easy: FAMILY Education Project

10 de julio de 2018 actualizado por: 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.

Descripción general del estudio

Estado

Terminado

Condiciones

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Actual)

673

Fase

  • No aplica

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

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

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años a 100 años (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

Géneros elegibles para el estudio

Todos

Descripción

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 de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Prevención
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.
Comparador de placebos: 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.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in behavior on performing physical activity in relation to Zero-time Exercise, moderate and vigorous exercises
Periodo de tiempo: baseline, 3 months
Behaviors on performing physical activity will be assessed by outcome-based questionnaire
baseline, 3 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Change in behavior on performing physical activity in relation to Zero-time Exercise, moderate and vigorous exercises
Periodo de tiempo: 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
Periodo de tiempo: 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,
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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
Periodo de tiempo: 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)
Periodo de tiempo: 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,
Periodo de tiempo: 6 months
Family members' behavior on performing physical activity in relation to Zero-time Exercise will be assessed by outcome-based questionnaire
6 months

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

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

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio (Actual)

1 de julio de 2015

Finalización primaria (Actual)

1 de junio de 2017

Finalización del estudio (Actual)

1 de junio de 2017

Fechas de registro del estudio

Enviado por primera vez

5 de noviembre de 2015

Primero enviado que cumplió con los criterios de control de calidad

8 de noviembre de 2015

Publicado por primera vez (Estimar)

10 de noviembre de 2015

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

12 de julio de 2018

Última actualización enviada que cumplió con los criterios de control de calidad

10 de julio de 2018

Última verificación

1 de julio de 2018

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • UW 15-330

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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