Comparison of the Freiburg Visual Acuity Test (FrACT) With the EDTRS- and Landoltring Charts (FEL)

Schiefer Ulrich

Status: Completed

Conditions: Ophthalmologically Normal Subjects

Treatments: Device: Methodology of visual acuity assessment

Study type: Observational

Funder types: Other

Identifiers

NCT02198534

F-2014-049

Details and patient eligibility

About

A) For the investigation of Visual acuity, inter-test agreement and the test-retest reliability were used three different visual acuity tests: ETDRS charts, Landoltring chart and Freiburg Visual Acuity Test (FrACt). The examinees passed each visual acuity test twice but the sequence of the visual acuity tests were randomize and so different for each examinee. The examinees were 24 adult Aalen university students (except students of ophthalmic optics in terms 2 - 7) with a minimal distant visual acuity without or with correction of 0.2. Another inclusion criteria was a maximum myopia of sph -2,00 dpt, a maximum hyperopia of sph +5,50 dpt and a maximum astigmatism of cyl 2,50 dpt. The Landolt C was projected in eight-orientations. For the FrACT Test we used two different devices for response input: a modified keypad with Landoltring symbols (FrACTk) and a haptic Landolt device with an adjustable Landoltring (FrACTh). The primary objective was the comparison between FrACTk and FrACTh. The secondary Objective contains the comparison between all visual acuity tests.

B) Background: Landolt Cs and letters are commonly used optotypes. In the explorative study we compare four different ways of applying them: The Freiburg visual acuity test (FrACT) using a keypad and a haptic Landolt device, a Landolt C chart in accordance to ISO 8596 and DIN 58220 with eight-orientated Landolt C and ETDRS charts. The aims of the survey were to determine examinee´s/examiner´s subjective ratings using Visual analogue scales (VAS), the inter-test agreement between the tests and test-retest reliability of the tests, concerning the test duration.

Subjects and Methods: Twenty-four adult examinees with a visual acuity of ≥ 0,2 were included in the explorative study. The visual acuity of one eye was measured monocularly, randomized with regard to the leading/non-leading eye. The subjects passed every visual acuity test twice in a randomized sequence of the visual acuity tests, which is maintained by a pre-specified randomization list, making use of forced choice.

Full description

1. FrACT (internet version 3.8.1) 1.1 haptic Landolt Ring device (FrACTh) 1.2 modified keypad with Landolt Ring symbols (FrACTk)

2. ETDRS Visual Acuity Tester (Steinbeis Transferzentrum Biomedizinische Optik, Tübingen/Germany)

3. Landoltring chart (Visus GmbH, Stuttgart/Germany)

4. VISUCAT monitor with single optotype display(numbers; Argus Individuell Optic GmbG, Putzbrunn/Germany)

5. Room illuminance level 250 lx, assessed with digital luxmeter (Peak Tech 5025, Peak Tech Prüf - und Messtechnik GmbH, Ahrensburg/Germany)

6. Laptopdisplay (TravelMate, Acer, 8372 Taipeh/China):

   luminance level 151 cd/m2 , surround luminance level 75 cd/m2 , assessed with luminance meter (IS-110 Laptop Minolta, Tokyo/Japan)

7. ETDRS Visual Acuity Tester:

   luminance level: 237 cd/m², surround luminance level 85 cd/m²

8. Landoltring Chart:

   luminance level: 236 cd/m², surround luminance level 84 cd/m²

9. VISUCAT:

   luminance level: 380 cd/m², surround luminance level 70 cd/m²

10. Stopwatch (Apple iPhone 4S, Cupertino CA/USA)

11. Laser Rangefinder (GLM 80 Professional, Bosch GmbH, Stuttgart/Germany)

Enrollment: 25 patients

Sex: All

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• age ≥ 18 years
• Minimum distant visual acuity (without/with correction) 0.2 (Visucat, single letter optotypes [numbers], initial session). As long as minimum distant visual acuity limits are exceeded, test runs without optical corrections are preferred in order to enhance the spectrum/variety of tested visual acuity values
• Ametropia:

maximum myopia sph -2.00 dpt maximum hyperopia sph +5.50 dpt maximum astigmatism cyl 2.5 dpt

• informed consent

Exclusion criteria

• Epilepsy / psychiatric disorders
• Drugs affect the reaction time and / or determining the visual acuity, or the refractive power of the eye
• Ophthalmic Education
• Amblyopia
• strabismus
• Glaucoma IOP> 22 mmHg
• Nystagmus
• Diabetic retinopathy (blood sugar-related retinal disease)
• Very dry eyes (sicca symptoms)
• eye surgery back are less than 3 months
• Infectious diseases (conjunctivitis, corneal inflammation, choroidal inflammation)
• miosis drugs
• Pronounced eye injuries
• Other eye disorders that affect the image quality
• Macular diseases
• albinism

Trial design

25 participants in 1 patient group

ophthalomogically normal subjects

Treatment:

Device: Methodology of visual acuity assessment