- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02764983
Occupational Therapy Driving Intervention for Returning Combat Veterans.
Efficacy of a Driving Program on Safe Community Mobility for Combat Veterans
Study Overview
Status
Intervention / Treatment
- Behavioral: Driving Behavior Interview
- Behavioral: Fitness-to-Drive Screening Measure
- Other: Clinical Driving Assessment
- Behavioral: Propensity for Angry Driving Scale
- Behavioral: Community Integration Questionnaire
- Behavioral: Satisfaction with Life Questionnaire
- Procedure: Driving simulator evaluation
- Other: Focus Group Discussion Interview Guide
Detailed Description
This research study is being done to determine if Occupational Therapy Driving Intervention (OT-DI) can improve the safe driving performance (less errors) over the short term (immediately following intervention) and intermediate term (3 months).
Baseline testing-Pre-test 1-- will include clinical battery of tests and a simulated driving test, a Brief Driving Questionnaire, Community Integration Questionnaire, and a Satisfaction with Life Questionnaire. Caregivers/ family members will rate the participants' driving behaviors using a Fitness-to-Drive Screening Measure( FTDS). After baseline testing the 60 participants (and 60 associated caregivers) will be randomly assigned to a balanced intervention group (15 participants with Traumatic Brain Injury (TBI)/ Post Traumatic Stress Disorder (PTSD) and 15 participants with orthopedic conditions and caregivers) and a control group (15 with TBI/PTSD and 15 with orthopedic conditions and caregivers).
The intervention group receives Occupational Therapy Driving Intervention (OT-DI), consisting of three x 1 hour sessions will include: Session 1: Driving evaluator reviews explicit driving errors with participants; Session 2: Driving evaluator provide tailored strategies to mitigate errors; Session 3: Participants drive simulator with targeted feedback from driving evaluator.
The control group will receive, from a driving safety professional, three x 1 hour general safety sessions (Session 1: General traffic safety discussion; Session 2: Rules of the road and knowledge of the road discussion; Session 3: drive the simulator without any feedback from traffic safety professional). Immediately after session 3, Post-test 1 will occur using the same standardized protocol outlined for baseline testing. Post-test 2 will consist of testing with the same standardized protocol as administered during baseline testing. Caregivers/ family members will rate the participant driving behaviors using the FTDS. In addition, the investigators will obtain driving data from the Department of Motor Vehicles which will include: citations, violations, driving mishaps, and crashes that have occurred for each participant.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
-
-
Florida
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Gainesville, Florida, United States, 32610
- University of Florida
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Gainesville, Florida, United States, 32608
- Malcom Randall VA Medical Center
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- A combat veteran with polytrauma (mild traumatic brain injury/with an accompanying post traumatic stress disorder (PTSD), traumatic limb amputation/ fractures), who drove prior to the injury/condition;
- have a valid driver's license or are eligible for a driver's license;
- are community dwelling;
- may experience self, physician or other clinical staff identified issues with driving behaviors;
- have a history of citations, violations or other driving mishaps in real world driving;
- have potential for following driving safety recommendations (Mini Mental State Examination, (MMSE 24/30);
- have potential for following community integration strategies (MMSE 24/30);
- are able to participate in driving evaluation battery.
Exclusion Criteria:
- A combat veteran diagnosed with a severe psychiatric (psychoses) or physical conditions (missing both arms and/or legs) that will limit ability to drive;
- have multiple psychotropic medications that may impact mental or physical (due to side-effects) functioning as per the consulting physician;
- have severe, irremediable medical conditions (severe TBI) as per the consulting physician;
- pregnant females (as determined by a urine test) or those planning pregnancy;
- VA Employees; and
- veterans who have received rehabilitation services for TBI/PTSD and who show, as per the screening of the driving rehabilitation specialist, a poor prognosis for improvement based on a driving intervention.
Inclusion Criteria for Caregivers:
- ability to complete a driving questionnaire pre and post intervention.
Exclusion Criteria for Caregivers:
- the presence of a cognitive or physical impairment that would hinder participants ability to complete the questionnaires or make an active contribution.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: Control Group
Participants in this group will have the following performed: Institute of Mobility Activity and Participation (I-MAP's) clinical battery of tests and a simulated driving test, a Brief Driving Behavior Interview, Propensity for Angry Driving Scale, Clinical Driving Assessment, Community Integration Questionnaire, and a Satisfaction with Life Questionnaire.
Driving safety professional, three x 1 hour sessions to discuss traffic safety, rules of the road, defensive driving, driving under influence, driver attitudes and safety.
Additionally, the study will obtain real world driving data from the Department of Motor Vehicles (public records) which will include citations, violations, and recorded collisions/ crashes.
|
This will be completed thrice, at baseline, post-test1 and at post-test2
This will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
Clinical Driving Assessment includes Optec vision screening, Useful Field of View, Range of Motion, Strength.
This will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
This questionnaire will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
Other Names:
This questionnaire will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
This questionnaire will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
The driving simulator evaluation uses a driving simulator with simulated drives engineered to address Veteran driving concerns such as reactions to other drivers and road conditions (e.g., debris).
The simulator is used at baseline and post-tests 1 and 2. The intervention sessions (X3) also occur using simulator.
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EXPERIMENTAL: Experimental Group
Participants in this group will have the following performed: Institute of Mobility Activity and Participation (I-MAP's) clinical battery of tests and a simulated driving test, a Brief Driving Behavior Interview, Propensity for Angry Driving Scale, Clinical Driving Assessment, Community Integration Questionnaire, and a Satisfaction with Life Questionnaire.
Occupational Therapy Driving Intervention (OT-DI) consisting of three x 1 hour sessions to review explicit driving errors, strategies to mitigate errors, and driving simulator with feedback.
The study will also obtain real world driving data from the Department of Motor Vehicles (public records) which includes citations, violations, and recorded collisions/crashes.
|
This will be completed thrice, at baseline, post-test1 and at post-test2
This will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
Clinical Driving Assessment includes Optec vision screening, Useful Field of View, Range of Motion, Strength.
This will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
This questionnaire will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
Other Names:
This questionnaire will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
This questionnaire will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
The driving simulator evaluation uses a driving simulator with simulated drives engineered to address Veteran driving concerns such as reactions to other drivers and road conditions (e.g., debris).
The simulator is used at baseline and post-tests 1 and 2. The intervention sessions (X3) also occur using simulator.
|
ACTIVE_COMPARATOR: Caregiver Control Group
Participants in this group will perform the following: Fitness-to-Drive Screening Measure(FTDS) will be filled out at baseline and again at the end of the study.
|
This will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
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ACTIVE_COMPARATOR: Caregiver Experimental Group
Participants in this group will perform the following: Fitness-to-Drive Screening Measure(FTDS) will be filled out at baseline and again at the end of the study.
|
This will be completed thrice, at baseline, post-test1 and at post-test2 (3 months after post test1)
|
OTHER: Focus Group Discussion Interview Guide
This group will comprise of a subset of the control and experimental groups.
A focus group with 8 participants (4 with Traumatic Brain Injury/Post Traumatic Stress Disorder and 4 with orthopedic conditions).
The focus group will meet once for a discussion which will be guided with a semi-structured interview that will explore the driving behavior prior to war, during war and post-deployment.
Responses will be outlined in an intervention matrix.
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Focus group discussion will occur once using the interview guide
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Driving errors changes between the groups at baseline, months 2 and 3
Time Frame: Changes in baseline months 2 and 3
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Determine if the Occupational Therapy Driving Intervention (OT-DI) reduces driving errors in the intervention group.
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Changes in baseline months 2 and 3
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Perceptions of Combat Veterans regarding driving performance
Time Frame: Occurs approximately 2 months after baseline (75 minutes)
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Semi-structured interview questions will be used to guide the focus group discussions.
The results will be outlined in an intervention matrix which will be used to address specific driving errors and the behavior underlying those errors in the intervention process.
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Occurs approximately 2 months after baseline (75 minutes)
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Change in driving records from baseline and at 11months
Time Frame: From baseline (approximately 11months)
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Driving records from the Department of Motor Vehicle will be collected to determine if driving errors have reduced.
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From baseline (approximately 11months)
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Collaborators and Investigators
Sponsor
Collaborators
Investigators
- Principal Investigator: Sandra Winter, PhD, University of Florida
Publications and helpful links
Study record dates
Study Major Dates
Study Start (ACTUAL)
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 (ACTUAL)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- 652-2011
- IRB201702264 (OTHER: University of Florida)
- JW140063 (OTHER_GRANT: Department of Defense)
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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