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Completed

NCT Number: NCT02903147

The Efficacy of a Functional Meta-Cognitive Intervention to Improve Human Factors of Professional Drivers

The objective of the study is to examine the effectiveness of a functional-meta-cognitive intervention program to reduce driving risk factors amongst professional bus drivers.

Completed

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Key information

Age range

21 year and older

Sex eligibility

Male

Study type

Interventional

Phase

Not applicable

About this study

In Israel, the percentage of professional drivers involved in lethal car accidents is high in relation to their number on the roads. Every car accident involving a bus driver could potentially put at risk the lives of tens of passengers, and cause damages both direct and indirect at high costs. Due to the high risk of the bus drivers and their passengers, it is highly important to identify and improve the driving characteristics which are necessary for safer driving of said drivers. Many studies have assessed and identified the risk factors of safe driving, but there is relatively little research-based evidence concerning the ability to improve the driving skills of drivers in general and in particular of bus drivers, which are considered a high risk group.

According to the National Road Safety Authority, 88% of road accidents are caused by driver errors. Therefore, the real challenge is to provide a better understanding in the role of human factors in causing road accidents to try and develop a variety of effective interventions to reduce these risk factors. This understanding can contribute both to a better assessment of professional drivers' driving fitness and to intervene accordingly. In this study, we have focused on main aspects that exist in relevant literature and are human risk factors: Cognitive-perceptual, ergonomic and personality risk factors, and checked the connection between these risk factors and actual monitored driving scores as recorder by an In-Vehicle Data Recorder (IVDR). In addition, we examined the effectiveness of a functional-meta-cognitive intervention program designed to increase drivers' awareness to their way of driving. The research model is based on previous driving models and the guiding occupational therapy practice framework model in Israel, while adjusting the model to the professional driving in public transportation line of work and its particular risk factors.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Male gender.
  • Having a valid bus driver's license.
  • Working for a specific large bus company in the center of Israel.

Exclusion criteria

  • Drivers who had less than 50 hours of IVDR data were excluded.

Treatment and study plan

Functional Meta-Cognitive Intervention

Behavioral

Functional-Meta-Cognitive Intervention Program was focused on raising awareness to safe driving risk factors identified at pre-screening, with reference to the difficulties that the driver raises and providing coping strategies. The intervention has been customized for each driver and included three sessions of two hours.

The employer's training

Behavioral

Primary outcomes

  1. Change in In Vehicle Data Recorder (IVDR) risk score

    Time frame: Change from baseline IVDR risk score at 1 year

    Assessing the degree of change in the rate of IVDR events before and after intervention.

Secondary outcomes

  1. Change in car accident rate

    Time frame: Change from ratings of questionnaire pre intervention to ratings at an average of 1 year post intervention.

    Assessing the change in the rate of accidents per year before and after the intervention in the intervention group.

  2. Change in subjective ratings of driving performance questionnaire.

    Time frame: Change from ratings of questionnaire at baseline pre intervention to reratings at an average of 1 year post intervention..

    Assessing the change in the subjective ratings of the level of performance and of satisfaction with performance before and after the intervention in the intervention group.

Sponsors and collaborators

Lead sponsor

Tel Aviv University

Other

Registry information

Important dates

Study start
2010
Primary completion
2015
Study completion
2015
First posted
Sep 16, 2016
Registry last updated
Sep 16, 2016

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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