- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02616237
A Facebook-based Weight Loss Programme for Obese Adults in Hong Kong
Effects of a Facebook-based Weight Loss Programme for Obese Adults in Hong Kong
Descripción general del estudio
Descripción detallada
Obese individuals often are at higher risk for developing non-communicable diseases such as diabetes and cardiovascular disease. The regular physical activity, healthy diet and social support have been shown to be beneficial for weight loss.
This is a two-arm parallel design randomized controlled trial for 6 months. Participants who completed the baseline assessment will be randomly allocated, after stratified by gender, to either a control group or Facebook-based intervention group. The control group will receive information on healthy eating, physical activity, obesity and cancer via three government printed health pamphlets. In addition to the government health pamphlets, the intervention group will receive a programme delivered through Facebook.
The interventions include participation in a private research group on Facebook for health education, self monitoring and social support. Participants will receive 12 weekly lessons related to nutrition, physical activity, Chinese food therapy, acupressure, weight loss. A registered nutritionist and a registered Chinese medicine practitioner will join the Facebook group as health partners. Both of them are also registered nurses.
Data collection will be carried out at baseline, 3 months and 6 months. Each time, both groups will complete online questionnaires and attend in-person anthropometric measurements
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Hong Kong, Hong Kong
- The Hong Kong Polytechnic University
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- university full-time employees;
- age 18 to 60 years,
- BMI of 25 to 40 kg/m2,
- have access to Internet and Facebook;
- able to communicate in both English and Chinese at F.5 secondary school level or above.
- agree to communicate with Internet, email, Facebook group and respect privacy.
Exclusion Criteria:
- Smoker;
- an unstable medical or mental status;
- history of myocardial infarction or stroke, or cancer in the past 5 years;
- orthopedic or joint problems that would prohibit exercise;
- in treatment for alcohol or drug dependency;
- an eating disorder;
- pregnant, breastfeeding, or planning on becoming pregnant within the next 6 months;
- use of medication that might affect body weight;
- a recent weight loss of more than 4.5 kg in the previous 6 months;
- currently participating in a weight loss program;
- organic obesity;
- unable to attend assessments or increase physical activity.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Tratamiento
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Intervention Group
Lifestyle Intervention: The interventions include participation in a private research group on Facebook for health education, self monitoring and social support. Participants will receive 12 weekly lessons related to nutrition, physical activity, Chinese food therapy, acupressure, weight loss. A registered nutritionist and a registered Chinese medicine practitioner will join the Facebook group as health partners. Both of them are also registered nurses. Besides the Facebook contents, the participants will also receive government printed health information on healthy eating, physical activity, obesity and cancers. |
East-meets-West Lifestyle Intervention elements include nutrition and exercise from the Western perspective, food therapy and acupressure from the Traditional Chinese Medicine perspective, self-monitoring, and motivational videos of successful stories from working colleagues.
The group participants in the Facebook are encouraged to post their health behaviors and questions, self-monitor, pledge for weight loss, seek social support and interact with health partners and other participants.
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Sin intervención: Control Group
The participants randomized into the Control Group will only receive government printed health information on healthy eating, physical activity, obesity and cancers.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Changes in body weight
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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Weights will be taken in light clothes without shoes using a digital scale
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Measures are done in three time points: baseline, 3 months and 6 months
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Changes in Body Mass Index
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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Height will be taken at baseline using a wall-mounted stadiometer.
BMI will be calculated as weight (kg)/height (m2)
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Measures are done in three time points: baseline, 3 months and 6 months
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Changes in waist circumference
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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Waist circumference will be measured by using an inelastic tape measure
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Measures are done in three time points: baseline, 3 months and 6 months
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
---|---|---|
Changes in Stages of Change
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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A 5-item questionnaire will be used to categorize participants into stages of change (pre-contemplation, contemplation, preparation, action, maintenance)
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Measures are done in three time points: baseline, 3 months and 6 months
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Changes in weight self-efficacy
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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Self-efficacy for weight loss will be assessed by using a 20-item Weight Efficacy Lifestyle Questionnaire (WEL).
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Measures are done in three time points: baseline, 3 months and 6 months
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Changes in physical activity self-efficacy
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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A questionnaire of perceived confidence to engage in physical activity under a variety of circumstances on a 5-point Likert scale will be used.
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Measures are done in three time points: baseline, 3 months and 6 months
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Changes in weight decisional balance
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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A 20-item questionnaire of perceived pros and cons of weight loss on a 5-point Likert scale.
The balance of the two scores >0 indicate more advantages than disadvantages to weight loss
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Measures are done in three time points: baseline, 3 months and 6 months
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Changes in social support
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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A questionnaire will be used to measure the perceived support and sabotage from friends and family for healthy eating and physical activity
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Measures are done in three time points: baseline, 3 months and 6 months
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Changes in dietary intake of fruits and vegetables
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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A questionnaire will be used to assess self-reported intake of fruits and vegetables in terms of portion size and frequency
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Measures are done in three time points: baseline, 3 months and 6 months
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Changes in physical activity
Periodo de tiempo: Measures are done in three time points: baseline, 3 months and 6 months
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The International Physical Activity Questionnaire will be used to assess the changes in physical activity
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Measures are done in three time points: baseline, 3 months and 6 months
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: WanChaw SHAE, The Hong Kong Polytechnic University
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- 20131213002
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
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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