- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02437149
Effectiveness of Distracted Driving Campaign
Effectiveness of Distracted Driving Campaign for Teenagers in the Emergency Department
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
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.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Florida
-
Miami, Florida, United States, 33155
- Nicklaus Children's Hospital f/k/a Miami Children's Hospital
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
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.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Prevention
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: None (Open Label)
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
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.
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Previous knowledge and attitudes towards distracted driving
Time Frame: 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
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Short Term Effectiveness of the Distracted Driving Campaign
Time Frame: 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
Time Frame: 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
|
Collaborators and Investigators
Investigators
- Principal Investigator: Michelle Blumstein, MD, Nicklaus Children's Hospital f/k/a Miami Children's Hospital
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Anticipated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- 20150548
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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