- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02359981
MyBehavior: Persuasion by Adapting to User Behavior and User Preference
Descripción general del estudio
Estado
Condiciones
Intervención / Tratamiento
Descripción detallada
A dramatic rise in self-tracking applications for smartphones has occurred recently. Rich user interfaces make manual logging of users' behavior easier and more pleasant; sensors make tracking effortless. To date, however, feedback technologies have been limited to providing counts or attractive visualization of tracked data. Human experts (health coaches) have needed to interpret the data and tailor make customized recommendations. No automated recommendation systems like Pandora, Netflix or personalized search for the web have been available to translate self-tracked data into actionable suggestions that promote healthier lifestyle without needing to involve a human interventionist.
MyBehavior aims to fill this gap. It takes a deeper look into physical activity and dietary intake data and reveal patterns of both healthy and unhealthy behavior that could be leveraged for personalized feedback. Based on common patterns from a user's life, suggestions are created that ask users to continue, change or avoid existing behaviors to achieve certain fitness goals. Such an approach is different from existing literature in two important aspects: (1) suggestions are contextualized to a user's life and are built on existing user behaviors. As a result, users can act on these suggestions easily, with minimal effort and interruption to daily routines; (2) unique suggestions are created for each individual. This personalized approach differs from traditional one-size-fits-all or targeted intervention models where identical suggestions are applied for groups of similar people or the entire population.
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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New York
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Ithaca, New York, Estados Unidos, 14850
- Cornell 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:
- In relatively healthy condition. Also, users must be interested in health and fitness.
Exclusion Criteria:
- Individuals with physical disability and dietary problems are excluded.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Prevención
- Asignación: Aleatorizado
- Modelo Intervencionista: Asignación paralela
- Enmascaramiento: Único
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Comparador activo: Generic suggestions
Control group participants received suggestions generated by the a nutritionist and exercise trainer.
These suggestions didn't relate to user's life or their past behavior.
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A nutritionist and an exercise trainer jointly created 45 food and exercise suggestions based on guidelines posted by the NIH.
These suggestions ask users to walk for 30 minutes or eat healthier foods.
These suggestions however doesn't personalize to users daily behavior into account.
An Android Smartphone with operating system version higher than 2.2
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Experimental: MyBehavior
Experiment group participants received personalized suggestions from MyBehavior that relates their life and past behavior.
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An Android Smartphone with operating system version higher than 2.2
The intervention automatically provides personalized suggestions based on users behavior and user context.
Suggestions relates to users life and how often they have done them in the past.
Since the suggestions relate to users' lives, they are easy to follow.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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User intentions to follow automated suggestions and behavior change
Periodo de tiempo: 3 weeks
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The primary outcome is to measure efficacy of MyBehavior suggestions. Efficacy will be measured in two dimensions (1) whether users intend to follow the automated suggestions from MyBehavior (2) effectiveness of automated suggestions in actual behavior change. User intentions towards following MyBehavior suggestions are measured using a 5 point likert scale. The investigators will ask users to rate whether they can follow the suggestions on an average day within a scale of 1-5 (1- I can't follow the suggestion, 5 - I can easily follow the suggestion). On the other hand, behavior change is measured from food (calories in per meal consumed) and activity (walking, running or exercise durations per day etc.) log collected using their smartphone. Regarding physical activity, how much physical activity users are performing will be compared across experiment conditions. Similarly, calorie consumption change in food will be used to compare dietary behavior change. |
3 weeks
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Usability improvements of automated suggestions
Periodo de tiempo: 3 weeks
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MyBehavior is the first system to provide health suggestions for food and activity automatically.
Thus there are scopes of usability improvement on how to effectively present the automatically generated information to the user.
Qualitative interviews at the end of study will be conducted to gather user experience of using MyBehavior.
This interviews will help to build a better and more usable version of MyBehavior for future larger scale deployments.
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3 weeks
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Colaboradores e Investigadores
Patrocinador
Investigadores
- Investigador principal: Mashfiqui Rabbi, BS, Cornell University
Publicaciones y enlaces útiles
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (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
- 1302003617
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. .