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Effectiveness of Distracted Driving Campaign

Effectiveness of Distracted Driving Campaign for Teenagers in the Emergency Department

The study will measure the effectiveness of a distracted driving campaign in the emergency department in teenagers, 15 to 18 years old, to determine if it changes their attitudes towards texting while driving. It will also assess previous knowledge and behaviors in this age group, regarding distracted driving and what educational tool (power point vs. videos vs. brochure) has the most impact changing the attitudes towards texting and driving.

Descripción general del estudio

Estado

Desconocido

Condiciones

Descripción detallada

Distracted driving is defined by the National Highway Safety Administration (NHTSA) as any activity that could withdraw a person's attention away from the primary task of driving. It includes, talking or texting on a cell phone, grooming, eating or drinking, changing radio stations, or talking to passengers. Of all these activities text messaging is by far the most alarming distraction because it requires visual, manual, and cognitive attention from the driver.

The NHTSA Research Note on distracted driving found that in 2011, 10% percent of fatal crashes were reported as distraction-affected crashes. This research also showed that teens between 15 to 19 years old are currently the largest group with distracted driving affected crashes, with 21% percent of them getting distracted while using their cell phones.

During the last few years, multiple public awareness campaigns have been launched in attempt to reduce this problem. These massive campaigns have included television, radio and internet campaigns, posters, billboards and brochures among others. Nevertheless, there are no studies assessing the success of these methods.

The research project will use visual and verbal educational tools to engage this population in order to maximize the learning process. The project will include brochures, video presentations and power point presentations. The investigators intend to test a potentially new and effective way to teach our teenagers about the dangers of distracted driving. The project primary goal is to assess if a distracting driving campaign in the emergency department is effective in changing the attitudes towards texting while driving. The investigator also intends to assess the current knowledge about distracted driving and to determine which tool (visual vs. verbal) is most effective to deliver this message.

Tipo de estudio

Intervencionista

Inscripción (Anticipado)

273

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

    • Florida
      • Miami, Florida, Estados Unidos, 33155
        • Nicklaus Children's Hospital f/k/a Miami Children's Hospital

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

15 años a 18 años (Niño, Adulto)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Todos

Descripción

Inclusion Criteria:

  • Adolescents between the ages of 15 to 18 years

Exclusion Criteria:

  • Adolescents refusing to participate in the Distracted Driving Campaign.
  • Adolescents visiting the emergency department with a chief complaint related to mental illness, suicide ideation or attempt, or any complaint limiting the ability to complete the questionnaire.
  • Adolescents with diagnosis of developmental delay that could affect his or her ability to complete the questionnaire.
  • Adolescents that do not speak English (the videos about real people who have had accidents while texting and driving found at http://www.distraction.gov/faces/index.html are available only in English.

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: Video and Brochure
Real stories video presentation and a brochure with information about distracted driving will be given to the participant.
Real stories video presentation about distracted driving. Produced by the National Highway Traffic Safety Administration.
Brochure with the National Highway Traffic Safety Administration information about distracting driving.
Experimental: Power Point and Brochure
Brief power point presentation and a brochure with information about distracted driving will be given to the participant.
Brochure with the National Highway Traffic Safety Administration information about distracting driving.
Brief power point presentation with information about distracted driving. Produced by the National Highway Traffic Safety Administration.
Experimental: Brochure Only
Only a brochure with information about distracting driving will be given to the participant.
Brochure with the National Highway Traffic Safety Administration information about distracting driving.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Previous knowledge and attitudes towards distracted driving
Periodo de tiempo: 6 months
A "Pre Campaign Survey" will be given to every participant before the intervention. The survey is a validated questionnaire that assess previous knowledge and attitudes towards distracted driving and demographic variables.
6 months

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Short Term Effectiveness of the Distracted Driving Campaign
Periodo de tiempo: 6 months
A validated post campaign survey will be given, to each participant, immediately after the intervention. The "Post Campaign Survey 1" will assess the short term effectiveness of the campaign.
6 months
Long Term Effectiveness of the Distracted Driving Campaign
Periodo de tiempo: 6 months
A "Post Campaign Survey 2" will be obtain by phone call, at least one month after the intervention is done, to assess long term effectiveness of the campaign.
6 months

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Michelle Blumstein, MD, Nicklaus Children's Hospital f/k/a Miami Children's Hospital

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

1 de junio de 2015

Finalización primaria (Actual)

1 de diciembre de 2016

Finalización del estudio (Anticipado)

1 de junio de 2017

Fechas de registro del estudio

Enviado por primera vez

23 de abril de 2015

Primero enviado que cumplió con los criterios de control de calidad

4 de mayo de 2015

Publicado por primera vez (Estimar)

7 de mayo de 2015

Actualizaciones de registros de estudio

Última actualización publicada (Actual)

5 de mayo de 2017

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

4 de mayo de 2017

Última verificación

1 de mayo de 2017

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • 20150548

Plan de datos de participantes individuales (IPD)

¿Planea compartir datos de participantes individuales (IPD)?

Indeciso

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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