Video Feedback Intervention for Cognitively Impaired Older Drivers

Sponsor
Rhode Island Hospital (Other)
Overall Status
Unknown status
CT.gov ID
NCT02600026
Collaborator
Alzheimer's Association (Other)
60
1
2
43
1.4

Study Details

Study Description

Brief Summary

This study will use an in-car monitoring system supplemented with video feedback to reduce the number of unsafe driving behaviors. If successful, this technology will provide a means to enhance public safety on the roads that could be adopted immediately in this at-risk group of drivers. The intervention will also maximize the time for independent driving, improving the overall quality of life of these individuals.

Condition or Disease Intervention/Treatment Phase
  • Device: DriveCam
  • Behavioral: Feedback
Phase 1/Phase 2

Detailed Description

The goals of this clinical trial are to 1) document real-time impaired driving behaviors, and 2) reduce their occurrence, to improve the safety of cognitively impaired elders who continue to drive. This will be accomplished by placing small digital video event recording devices in the vehicles of 60 older cognitively impaired drivers. A 3-month baseline will establish the frequency of unsafe driving events, followed by a 3-month video feedback intervention during which the driver and family member will review the video recorded errors on a weekly basis. Active treatment will be compared to video monitoring with no feedback. A 6-month post-intervention phase will establish sustainability of the treatment.

The results of this clinical trial will confirm the potential to improve driving safety among older drivers with cognitive impairment using a behavior modification approach aimed directly at the problem behaviors observed in their natural driving environment. Knowledge gained about the magnitude and duration of the treatment effect and the potential of using an internet based feedback program will provide the impetus to optimize and ultimately implement the intervention to improve the safety of older drivers with mild cognitive impairment and early AD.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
60 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Prevention
Official Title:
Video Feedback Intervention for Cognitively Impaired Older Drivers
Study Start Date :
Nov 1, 2015
Anticipated Primary Completion Date :
Jun 1, 2019
Anticipated Study Completion Date :
Jun 1, 2019

Arms and Interventions

Arm Intervention/Treatment
Experimental: Video Camera: Intervention

DriveCam video event recorder with feedback

Device: DriveCam
Video event monitoring device

Behavioral: Feedback
Video feedback intervention

Placebo Comparator: Video Camera: Monitoring

DriveCam video event recorder with no feedback

Device: DriveCam
Video event monitoring device

Outcome Measures

Primary Outcome Measures

  1. Number of unsafe driving events [9 months]

    Unsafe events rated as > 5 points using a modification of standard scale developed by Drivecam monitoring video service. This includes incidents, near-crashes, and crashes, sub classified as being triggered by hard turns, severe braking, and/or impact, adjusted for miles driven.

Secondary Outcome Measures

  1. Severity score of unsafe driving events [9 months]

    Measured by sum of all demerit points for events rated >5 adjusted for miles driven, during intervention and 6-month follow-up. The severity rating score derived and reported by DriveCam experts has been previously used in a longitudinal study of ambulance drivers demonstrating reduction in not only events, but also severity scores for events, as well as our own feasibility study. This measure will provide additional evidence supporting improvement in safe driving for our intervention trial. To demonstrate safe driving as an outcome, one would like to show not only a reduction in frequency of events, but also a reduction in the severity of those driving errors.

  2. Time to driving cessation [1-2 years]

    Time to driving cessation (e.g., due to road-test failure, at-fault motor vehicle accident, cognitive decline progression) measured over one to two years from baseline. Information on time to driving cessation, i.e., "driving retirement," will be obtained from annual telephone follow-up calls to the driving participant and family member up to the end of the 3-year study period.

Eligibility Criteria

Criteria

Ages Eligible for Study:
50 Years to 90 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • age 50-90

  • will be categorized as CDR= 0.5, or 1

  • English speaking

  • currently driving adults

  • have a valid driving license

  • have at least 10 years of driving experience

  • have a MMSE < 28

  • have an adult family member or other caregiver, age >21, to participate in video feedback

Exclusion Criteria:
  • ophthalmologic, physical, or neurologic disorders other than dementia that impair their driving abilities

  • visual acuity worse than 20/40 in best eye using distance vision measured by wall chart

  • homonymous hemianopia or bitemporal hemianopia

  • musculoskeletal disorders causing major physical handicaps

  • history of alcohol or substance abuse by DSM V criteria within the past year

  • sedating medications that impair level of consciousness or attention

  • language impairment that would interfere with the ability to participate in the educational intervention

  • previous road test evaluation or opinion of caregiver or health professional that participant is unsafe to drive.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Rhode Island Hospital Providence Rhode Island United States 02903

Sponsors and Collaborators

  • Rhode Island Hospital
  • Alzheimer's Association

Investigators

  • Principal Investigator: Brian Ott, MD, Rhode Island Hospital

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Brian Ott, Brian R. Ott, MD, Rhode Island Hospital
ClinicalTrials.gov Identifier:
NCT02600026
Other Study ID Numbers:
  • 799824-2
First Posted:
Nov 9, 2015
Last Update Posted:
May 15, 2018
Last Verified:
May 1, 2018

Study Results

No Results Posted as of May 15, 2018