Trial Outcomes & Findings for Evaluating the Impact of JJVC Senofilcon A - Based Contact Lens With New UV-blocker on Day and Night Driving Performance (NCT NCT03330275)

NCT ID: NCT03330275

Last Updated: 2018-08-07

Results Overview

Overall driving performance score is a composite score calculated as the mean of the Z-scores of the following six driving measures: average sign recognition distance (in meters), percentage of correctly identified sign (\~42 signs), percentage of hazard avoidance/detection (9 hazards), average pedestrian recognition distance (in meters), lane keeping (percentage of time inside the lane) and the inverse of driving lap time (in seconds).). Equal weighting was assigned to each measure. The individual Z scores were transformed (inverted) such that positive Z scores relate to better performance than the mean. Z scores follow a standard normal distribution (ranging from minus infinity to positive infinity). Overall Z score for night time driving was reported for each study lens.

Recruitment status

COMPLETED

Study phase

PHASE2

Target enrollment

24 participants

Primary outcome timeframe

15 Minutes Post Lens Fitting

Results posted on

2018-08-07

Participant Flow

A total of 24 subjects were enrolled into this study. All enrolled subjects met all eligibility criteria and were dispensed a study lens. Of the dispensed subjects, all 24 completed the study.

A 2X2 William's crossover design was utilized for visit 1. A 3X3 William's Crossover design was utilized for visits 2, 3 and 4.

Participant milestones

Participant milestones
Measure
Test/Control1
Subjects that were randomized to receive the Test lens during period 1 of visit 1 and the Control 1 lens during period 2 of visit 1.
Control1/Test
Subjects that were randomized to receive the Control 1 lens during period 1 of visit 1 and the Test lens during period 2 of visit 1.
Test/Control2
Subjects that were randomized to receive the Test lens during period 1 of visit 1 and the Control 2 lens during period 2 of visit 1.
Control2/Test
Subjects that were randomized to receive the Control 2 lens during period 1 of visit 1 and the Test lens during period 2 of visit 1.
Test/Control1/Control2
Subjects that were randomized to receive the Test lens during period 1, the Control 1 lens during period 2 and the Control 2 lens during period 3. This applies to visits 2, 3 and 4.
Test/Control2/Control1
Subjects that were randomized to receive the Test lens during period 1, the Control 2 lens during period 2 and the Control 1 lens during period 3. This applies to visits 2, 3 and 4.
Control1/Control2/Test
Subjects that were randomized to receive the Control 1 lens during period 1, the Control 2 lens during period 2 and the Test lens during period 3. This applies to visits 2, 3 and 4.
Control1/Test/Control2
Subjects that were randomized to receive the Control 1 lens during period 1, the Test lens during period 2 and the Control 2 lens during period 3. This applies to visits 2, 3 and 4.
Control2/Control1/Test
Subjects that were randomized to receive the Control 2 lens during period 1, the Control 1 lens during period 2 and the Test lens during period 3. This applies to visits 2, 3 and 4.
Control2/Test/Control1
Subjects that were randomized to receive the Control 2 lens during period 1, the Test lens during period 2 and the Control 1 lens during period 3. This applies to visits 2, 3 and 4.
Visit 1 - Period 1
STARTED
6
6
6
6
0
0
0
0
0
0
Visit 1 - Period 1
COMPLETED
6
6
6
6
0
0
0
0
0
0
Visit 1 - Period 1
NOT COMPLETED
0
0
0
0
0
0
0
0
0
0
Visit 1 - Period 2
STARTED
6
6
6
6
0
0
0
0
0
0
Visit 1 - Period 2
COMPLETED
6
6
6
6
0
0
0
0
0
0
Visit 1 - Period 2
NOT COMPLETED
0
0
0
0
0
0
0
0
0
0
Visits 2, 3 and 4 - Period 1
STARTED
0
0
0
0
4
4
4
4
4
4
Visits 2, 3 and 4 - Period 1
COMPLETED
0
0
0
0
4
4
4
4
4
4
Visits 2, 3 and 4 - Period 1
NOT COMPLETED
0
0
0
0
0
0
0
0
0
0
Visits 2, 3 and 4 - Period 2
STARTED
0
0
0
0
4
4
4
4
4
4
Visits 2, 3 and 4 - Period 2
COMPLETED
0
0
0
0
4
4
4
4
4
4
Visits 2, 3 and 4 - Period 2
NOT COMPLETED
0
0
0
0
0
0
0
0
0
0
Visits 2, 3 and 4 - Period 3
STARTED
0
0
0
0
4
4
4
4
4
4
Visits 2, 3 and 4 - Period 3
COMPLETED
0
0
0
0
4
4
4
4
4
4
Visits 2, 3 and 4 - Period 3
NOT COMPLETED
0
0
0
0
0
0
0
0
0
0

Reasons for withdrawal

Withdrawal data not reported

Baseline Characteristics

Evaluating the Impact of JJVC Senofilcon A - Based Contact Lens With New UV-blocker on Day and Night Driving Performance

Baseline characteristics by cohort

Baseline characteristics by cohort
Measure
Dispensed Subjects
n=24 Participants
All subjects that were dispensed at least one study lens.
Age, Continuous
29.8 Years
STANDARD_DEVIATION 7.71 • n=39 Participants
Sex: Female, Male
Female
14 Participants
n=39 Participants
Sex: Female, Male
Male
10 Participants
n=39 Participants
Race/Ethnicity, Customized
Asian
9 Participants
n=39 Participants
Race/Ethnicity, Customized
White
13 Participants
n=39 Participants
Race/Ethnicity, Customized
Other
2 Participants
n=39 Participants
Region of Enrollment
Australia
24 Participants
n=39 Participants

PRIMARY outcome

Timeframe: 15 Minutes Post Lens Fitting

Population: All subjects that completed the study without a major protocol violation.

Overall driving performance score is a composite score calculated as the mean of the Z-scores of the following six driving measures: average sign recognition distance (in meters), percentage of correctly identified sign (\~42 signs), percentage of hazard avoidance/detection (9 hazards), average pedestrian recognition distance (in meters), lane keeping (percentage of time inside the lane) and the inverse of driving lap time (in seconds).). Equal weighting was assigned to each measure. The individual Z scores were transformed (inverted) such that positive Z scores relate to better performance than the mean. Z scores follow a standard normal distribution (ranging from minus infinity to positive infinity). Overall Z score for night time driving was reported for each study lens.

Outcome measures

Outcome measures
Measure
Test
n=24 Participants
Subjects that wore the Test lens during any of the three study periods at either visit 3 or visit 4.
Control 1
n=24 Participants
Subjects that wore the Control 1 lens during any of the three study periods at either visit 3 or visit 4.
Control 2
n=24 Participants
Subjects that wore the Control 2 lens during any of the three study periods at either visit 3 or visit 4.
Overall Nighttime Driving Score
-0.308 Z-Score
Standard Deviation 0.4718
-0.375 Z-Score
Standard Deviation 0.4361
-0.430 Z-Score
Standard Deviation 0.4761

SECONDARY outcome

Timeframe: 15 Minutes Post Lens Fitting

Population: All subjects that completed the study without a major protocol deviation.

Binocular visual acuity was assessed under Low luminance (\~1 lux) high contrast (90%) conditions at a distance of 4 meters. The ETDRS logMAR chart were used, which is scored on a letter by letter basis (-0.02 log units per letter correctly identified). A number of different EDTRS charts was used to reduce potential learning effects. The average LogMAR acuity for each lens was reported.

Outcome measures

Outcome measures
Measure
Test
n=24 Participants
Subjects that wore the Test lens during any of the three study periods at either visit 3 or visit 4.
Control 1
n=24 Participants
Subjects that wore the Control 1 lens during any of the three study periods at either visit 3 or visit 4.
Control 2
n=24 Participants
Subjects that wore the Control 2 lens during any of the three study periods at either visit 3 or visit 4.
Binocular Visual Acuity
0.251 logMAR
Standard Deviation 0.0722
0.273 logMAR
Standard Deviation 0.0705
0.298 logMAR
Standard Deviation 0.0739

SECONDARY outcome

Timeframe: 15 Minutes Post Lens Fitting

Population: All subjects that completed the study without a major protocol deviation.

Binocular contrast sensitivity was assessed under low luminance conditions. Five Landolt C targets in random orientation were presented for each of the four contrast levels 95%, 80%, 63% and 50%. Participants were asked to correctly identify the orientation of the Landolt C. The percentage of subjects that were able to correct identify the orientation of all 5 Landolt's C was reported for each lens type.

Outcome measures

Outcome measures
Measure
Test
n=24 Participants
Subjects that wore the Test lens during any of the three study periods at either visit 3 or visit 4.
Control 1
n=24 Participants
Subjects that wore the Control 1 lens during any of the three study periods at either visit 3 or visit 4.
Control 2
n=24 Participants
Subjects that wore the Control 2 lens during any of the three study periods at either visit 3 or visit 4.
Binocular Contrast Threshold Without Glare
95% Contrast
100 Percentage of Participants
100 Percentage of Participants
100 Percentage of Participants
Binocular Contrast Threshold Without Glare
80% Contrast
100 Percentage of Participants
95.8 Percentage of Participants
95.8 Percentage of Participants
Binocular Contrast Threshold Without Glare
63% Contrast
91.7 Percentage of Participants
91.7 Percentage of Participants
87.5 Percentage of Participants
Binocular Contrast Threshold Without Glare
50%
87.5 Percentage of Participants
75.0 Percentage of Participants
58.3 Percentage of Participants

SECONDARY outcome

Timeframe: 15 Minutes Post Lens Fitting

Population: All subjects that completed the study without a major protocol deviation.

Participants were instructed to report the identity of a percentage of the standard road signs (typically about 42 signs dependent on the route travelled) containing about 65 items of information as they drove around the circuit. The percentage of correctly identified signs was reported for each study lens.

Outcome measures

Outcome measures
Measure
Test
n=24 Participants
Subjects that wore the Test lens during any of the three study periods at either visit 3 or visit 4.
Control 1
n=24 Participants
Subjects that wore the Control 1 lens during any of the three study periods at either visit 3 or visit 4.
Control 2
n=24 Participants
Subjects that wore the Control 2 lens during any of the three study periods at either visit 3 or visit 4.
Percentage of Road Signs Correctly Identified During Night Driving
72.7 Percentage of participants
73.3 Percentage of participants
73.3 Percentage of participants

SECONDARY outcome

Timeframe: 15 Minutes Post Lens Fitting

Population: All subjects that completed the study without a major protocol deviation.

Measure Description The distance (measured in meters) to recognize a pre-determined road sign was recorded for each subject and lens type at either visit 3 or visit 4, using the in-vehicle measurement system while the participant was driving. The in-vehicle measurement system consisted of a subject pressing a button once the subject was able to recognize the road sign. The average distance in meters was reported for each lens type. Larger distance indicate that a subject was able to identify the pre-determined road sign sooner.

Outcome measures

Outcome measures
Measure
Test
n=24 Participants
Subjects that wore the Test lens during any of the three study periods at either visit 3 or visit 4.
Control 1
n=24 Participants
Subjects that wore the Control 1 lens during any of the three study periods at either visit 3 or visit 4.
Control 2
n=24 Participants
Subjects that wore the Control 2 lens during any of the three study periods at either visit 3 or visit 4.
Average Distance to Correctly Identify Road Signs During Night Driving
110.3 Meters
Standard Deviation 23.45
101.5 Meters
Standard Deviation 25.53
95.0 Meters
Standard Deviation 22.83

SECONDARY outcome

Timeframe: 15 Minutes Post Lens Fitting

Population: All subjects that completed the study without a major protocol deviation.

Participants were required to report and avoid hitting any of nine large, low contrast grey foam "hazards" (220 cm x 80 cm x 15 cm) positioned orthogonally in the driving lane along the roadway, the locations of which will be randomized between study lenses. The percentage of Hazards avoided for each study lens was reported.

Outcome measures

Outcome measures
Measure
Test
n=24 Participants
Subjects that wore the Test lens during any of the three study periods at either visit 3 or visit 4.
Control 1
n=24 Participants
Subjects that wore the Control 1 lens during any of the three study periods at either visit 3 or visit 4.
Control 2
n=24 Participants
Subjects that wore the Control 2 lens during any of the three study periods at either visit 3 or visit 4.
Percentage of Hazards Avoided During Night Driving
95.4 Percentage of Participants
95.4 Percentage of Participants
93.1 Percentage of Participants

SECONDARY outcome

Timeframe: 15 Minutes Post Lens Fitting

Population: All subjects that completed the study without a major protocol deviation.

The in-vehicle measurement system was utilized to determine the distance at which the participant (as a driver) first recognizes the presence of two pedestrians positioned at the side of the road. An experimenter acted as the pedestrian and "walked in-place" at the end of a 400 m straight section of roadway which starts and finishes at approximately the same elevation, but features a dip halfway along its length. The pedestrian was not surrounded by any visual clutter or lighting. To reduce expectancy effects, a series of four flashing LEDs and four retro-reflective bollards was positioned around the circuit to increase the instances of flashing lights and retro-reflective material being presented to the driver. The average distance to recognize a pedestrian for each lens type was reported.

Outcome measures

Outcome measures
Measure
Test
n=24 Participants
Subjects that wore the Test lens during any of the three study periods at either visit 3 or visit 4.
Control 1
n=24 Participants
Subjects that wore the Control 1 lens during any of the three study periods at either visit 3 or visit 4.
Control 2
n=24 Participants
Subjects that wore the Control 2 lens during any of the three study periods at either visit 3 or visit 4.
Average Pedestrian Recognition Distance
208.3 Meters
Standard Deviation 60.46
201.1 Meters
Standard Deviation 62.92
195.5 Meters
Standard Deviation 60.70

Adverse Events

Control 1

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Control 2

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Test

Serious events: 0 serious events
Other events: 0 other events
Deaths: 0 deaths

Serious adverse events

Adverse event data not reported

Other adverse events

Adverse event data not reported

Additional Information

John Buch- SENIOR PRINCIPAL RESEARCH OPTOMETRIST

Johnson & Johnson Vision Care, Inc.

Phone: 904 443-1707

Results disclosure agreements

  • Principal investigator is a sponsor employee
  • Publication restrictions are in place

Restriction type: GT60