Reducing Distracted Driving With the Flip of a Switch

April 18, 2022 updated by: M. Kit Delgado, MD, University of Pennsylvania
We propose to test a potential intervention to reduce distracted driving among high school students that could be used as part of future research trials and school campaigns. This intervention is designed to encourage use of a setting that silences incoming calls and messages while the person is driving.

Study Overview

Status

Withdrawn

Conditions

Detailed Description

The purpose of this study is to test an intervention to reduce distracted driving among high school students. We're interested in learning the use of Do Not Disturb While Driving (DNDWD) by high school students. Participants will be recruited to participate into a 4-week study. Those that consent will download a driving app that will monitor their phone use while driving. Halfway through the monitoring period, we will ask participants to turn on DNDWD. Participants will also have the opportunity to enroll into an auto-reply message contest for best message. Once the 4- week monitoring period is complete participants will complete and exit survey

Study Type

Interventional

Phase

  • Not Applicable

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

16 years to 19 years (Child, Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

All

Description

Inclusion Criteria:

  1. High School student with school assigned email address
  2. Has a cell phone with ability to download Way to Drive app
  3. Has a driver's license and typically drives every week

Exclusion Criteria:

  1. Unable to read or understand English
  2. Under 18 years old and no parental consent

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Prevention
  • Allocation: N/A
  • Interventional Model: Single Group Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Experimental: Monitoring phase
Participants will be monitored for 4 weeks. Halfway through the monitoring period, participants will be asked to turn on DNDWD.
Participants will be asked to turn on Do Not Disturb While Driving on their smartphones.

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in self-reported DNDWD
Time Frame: For the duration of the study; 4 weeks
Change is reported use. Dichotomy of use or non-use pre and post intervention
For the duration of the study; 4 weeks

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Seconds of active (handheld) phone use per hour of driving
Time Frame: For the duration of the study; 4 weeks
This is a composite outcome that measures the proportion of total trip time in which the driver is engaged in handheld phone call use or non-call handheld use (e.g. texting, swiping, and typing), as measured by the Way to Drive app. Several studies (e.g. Klauer, NEJM, 2014) have demonstrated the association between handheld phone use (e.g., reaching for phone, typing, swiping, dialing) and increased crash risk. This outcome is also known as the active phone use percentage. Passive phone use (e.g. phone is streaming GPS navigation directions or music without any typing, swiping, and handheld holding of the phone) is not included in this outcome. Trips are only counted if the app predicts the user was a driver for the trip based on the phone sensor data and the user does not correct the app; or, if the user corrects the app and indicates they were driving.
For the duration of the study; 4 weeks
Seconds of active (handheld) call use per hour of driving.
Time Frame: For the duration of the study; 4 weeks
We will analyze the components of the secondary outcome separately.
For the duration of the study; 4 weeks
Seconds of active (handheld) non-call use per hour of driving
Time Frame: For the duration of the study; 4 weeks
We will analyze the components of the secondary outcome separately.
For the duration of the study; 4 weeks
Seconds of passive (hands-free) call use per hour of driving
Time Frame: For the duration of the study; 4 weeks
Use of DNDWD should also cut down on hands-free driving distraction.
For the duration of the study; 4 weeks
Seconds of passive (hands-free) non-call use per hour of driving.
Time Frame: For the duration of the study; 4 weeks
Use of DNDWD should also cut down on hands-free driving distraction.
For the duration of the study; 4 weeks
Seconds of speeding per hour of driving
Time Frame: For the duration of the study; 4 weeks
. Speeding events, defined as >10 mph above the posted speed limit, are detected by the app.
For the duration of the study; 4 weeks
Hard braking events per 100 miles.
Time Frame: For the duration of the study; 4 weeks
Hard braking events are detected by the app.
For the duration of the study; 4 weeks
Fast acceleration events per 100 miles.
Time Frame: For the duration of the study; 4 weeks

Fast acceleration events are detected by the app.

Acceptability of interventions will be measured using a mixed-methods approach:

For the duration of the study; 4 weeks
Net promoter score
Time Frame: For the duration of the study; 4 weeks
In the exit survey, participants will be asked "How likely is it that you would recommend this program to a friend or colleague?" on a 0 to 10 scale.
For the duration of the study; 4 weeks
Responses to open-ended questions in exit survey
Time Frame: For the duration of the study; 4 weeks
Participants will be asked the following two open-ended questions: 1) "Please tell us what you liked about participating in this study;" 2) "Please tell us what you didn't like about participating in this study and how we should improve the experience in the future." These qualitative responses will be coded for content related to intervention acceptability and emerging themes will be identified.
For the duration of the study; 4 weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

March 31, 2022

Primary Completion (Actual)

March 31, 2022

Study Completion (Actual)

March 31, 2022

Study Registration Dates

First Submitted

March 17, 2022

First Submitted That Met QC Criteria

March 17, 2022

First Posted (Actual)

March 28, 2022

Study Record Updates

Last Update Posted (Actual)

April 25, 2022

Last Update Submitted That Met QC Criteria

April 18, 2022

Last Verified

April 1, 2022

More Information

Terms related to this study

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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