- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01733537
Improving Motorcycle Taxi Driver Visibility in Tanzania
Improving Motorcycle Taxi Driver Visibility in Tanzania-A Cluster Randomized Controlled Trial
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
Road traffic injuries are the 4th leading cause of death among individuals in the economically productive age group (age 15 to 59) in low and middle income countries. The Africa region currently has some of the world's highest traffic injury rates, with vulnerable road users, including motorcycle riders, bearing a disproportionate share of the injury burden.
Motorcycles are a rapidly growing form of transport in Africa, both for personal and commercial transportation. Conspicuity measures-factors that increase a motorcycle rider's visibility-for the prevention of motorcycle crash have been previously studied and found to be associated with a decreased risk of crash.
Motorcycle taxi drivers are a particularly high risk population for motorcycle crash as they operate a motorcycle for several hours a day. Reflective, fluorescent safety vests are a common article worn by motorcycle drivers in some locations; however, penetration of such clothing in Moshi is currently low. This study aims to increase use of reflective vests among commercial motorcycle drivers. We will test whether provision of a free reflective, fluorescent vest increases use of reflective, fluorescent clothing compared to education about wearing reflective, fluorescent clothing alone.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
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Kilimanjaro Region, Tanzania
- Kilimanjaro region, Tanzania
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- motorcycle riders who identify themselves as motorcycle taxi drivers
- individuals must work at least 2 days a week as a motorcycle taxi driver
- have a telephone number for ride solicitation
- have a license plate that is able to be recorded
- are at least 18 years old
- are willing to have us contact them in the future for repeat surveys
Exclusion Criteria:
- motorcycle riders who do not meet the above criteria
- motorcycle riders who do not consent to participate
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: Vest and Education
Motorcycle Taxi Drivers provided with a reflective, fluorescent vest and basic education about recommended measures to increase their visibility
|
Motorcycle taxi drivers in the intervention arm will receive a free reflective, fluorescent vest
Both arms will receive brief, basic education about recommended measures to increase their visibility
|
|
Other: Education Alone
Motorcycle Taxi Drivers provided with basic education about recommended measures to increase their visibility
|
Both arms will receive brief, basic education about recommended measures to increase their visibility
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Use of reflective or fluorescent clothing
Time Frame: 3-5 months
|
The use of reflective or fluorescent clothing will be compared between the intervention and control groups over the observation period
|
3-5 months
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Wearing White Helmet
Time Frame: 3-5 months
|
The use of white helmets will be compared between the intervention and control groups over the observation period
|
3-5 months
|
|
Daytime Running Headlights
Time Frame: 3-5 months
|
The use of daytime running headlights will be compared between the intervention and control groups over the observation period
|
3-5 months
|
Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Nathan M Thielman, MD, MPH, Duke University
- Study Director: Steven A Sumner, MD, Duke University
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Estimate)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Other Study ID Numbers
- Pro00034415
- 1R25TW009337-01 (U.S. NIH Grant/Contract)
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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