Video Feedback Intervention for Cognitively Impaired Older Drivers
NCT ID: NCT02600026
Last Updated: 2018-05-15
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
UNKNOWN
PHASE1/PHASE2
60 participants
INTERVENTIONAL
2015-11-30
2019-06-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Video Intervention to Enhance the Safety Of Cognitively Impaired Older Drivers
NCT02593552
Driving Rehabilitation and Innovation for Evaluating Risk in Post-Intensive Care Unit Survivors
NCT05999903
Enhancing Emotion Regulation During Driving in OEF/OIF Veterans
NCT01336764
Evaluation of the Veterans' In-home Program
NCT01831830
Smart Phone Application for Postconcussion Symptom Reduction
NCT02501642
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
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.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
RANDOMIZED
PARALLEL
PREVENTION
NONE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Video Camera: Intervention
DriveCam video event recorder with feedback
DriveCam
Video event monitoring device
Feedback
Video feedback intervention
Video Camera: Monitoring
DriveCam video event recorder with no feedback
DriveCam
Video event monitoring device
Interventions
Learn about the drugs, procedures, or behavioral strategies being tested and how they are applied within this trial.
DriveCam
Video event monitoring device
Feedback
Video feedback intervention
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* 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
* 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.
50 Years
90 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Alzheimer's Association
OTHER
Rhode Island Hospital
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Brian Ott
Brian R. Ott, MD
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Brian Ott, MD
Role: PRINCIPAL_INVESTIGATOR
Rhode Island Hospital
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Rhode Island Hospital
Providence, Rhode Island, United States
Countries
Review the countries where the study has at least one active or historical site.
Central Contacts
Reach out to these primary contacts for questions about participation or study logistics.
Facility Contacts
Find local site contact details for specific facilities participating in the trial.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
799824-2
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.