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Comparison of Four Methods for Entering the Gap Position of Landolt Cs

Comparison of Four Methods for Entering the Gap Position of Landolt Cs With Respect to Validity, Retest Reliability, Examination Duration and Test Subject Satisfaction

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04299659
Acronym
LC_Entry
Enrollment
24
Registered
2020-03-09
Start date
2022-07-22
Completion date
2023-06-30
Last updated
2023-07-20

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Quality Control, Validation Study

Keywords

psychophysics, visual acuity, response, response entry, validity, retest reliability, reproducibility, evaluation, optotype, Landolt C

Brief summary

The aim of this study is to investigate and compare the validity of four different input methods for Landolt Cs, i.e. the proportion of correct gap positions in relation to the total number of performances. The four input methods are a numeric keypad, an eight-positions rocker switch, a remote control and voice feedback.

Detailed description

The measurement of visual acuity is the most frequent and one of the most important ophthalmological functional investigations. Therefore, it is particularly important to find a measuring procedure with as little input errors as possible. The 8-position Landolt C (LC) is the internationally accepted, well-standardised optotype for the determination of visual acuity. Usually, the subjects informs the examiner verbally about the perceived position of each LC. According to the current literature, about 20 to 30 % of the population suffers from a right/left weakness. Furthermore, language barriers are an additional considerable hurdle. Therefore, it is important to find an input method for the LC gap positions with minimal entry mistakes. In oder to avoid the thresholding procedure and its inherent difficulties, highly supra-threshold (10 times above the previously determined individual central visual acuity threshold) 8-position LCs are presented. The study compares four input methods for entering of the Landolt C gap positions: a modified numeric keypad, an 8-position rocker switch, a modified TV remote control and voice/verbal feedback. Each subject will perform all four input methods, with 2 test runs of 16 Landolt C presentations, each. A forced-choice method will be applied, i.e. the test is not continued until the test person has responded ot each single presentation. Regardless of whether the entry was correct or incorrect, the next Landolt C is displayed. The optotypes are presented using modified version of the Freiburg Visual Acuity and Contrast Test (FrACT), which allows to present the 8-position Landolt Cs in a standardized way on a video display unit (VDU). The sequence of the input methods is randomized. This study is carried out in a within-subject design, i.e. all test persons go through all test conditions and serve as their own controls.

Interventions

DIAGNOSTIC_TESTLandolt C entry method

Four different methods for entering the Landolt C gap position are compared

Sponsors

Aalen University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to 80 Years
Healthy volunteers
Yes

Inclusion criteria

* Age: ≥ 18 years * Informed consent * (Distance) visual acuity with best correction: ≥ 0.8 * (Distant) ametropia: ≤+8.0 Diopters (spherical equivalent) * Anisometropia ≤ 3 dpt * Astigmatism ≤ 2.5 dpt

Exclusion criteria

* Prolonged reaction time caused by drugs (medications)/ drugs/alcohol * Movement disorders (of hands) such as Parkinson's disease * Indication of amblyopia (strabismus surgery, occlusion therapy etc.) * Eye movement disorders/double vision * Defective stereo vision (according to LANG \[I\] stereo test) * Presence of a relative afferent pupil defect (swinging flashlight test) * Any hint of visual pathway lesion or other chronic or progressive eye disease

Design outcomes

Primary

MeasureTime frameDescription
validityThrough study completion, an average of 3 monthsProportion of correct gap position entries in relation to the total number of LC presentations by the four different entry methods

Secondary

MeasureTime frameDescription
retest reliabilityThrough study completion, an average of 3 monthsComparison of the correct gap position entry between first and second test run by the four different entry methods
Examination durationThrough study completion, an average of 3 monthsComparison of the examination duration of the the four different entry methods and by the first and second run
Subjects´ satisfactionThrough study completion, an average of 3 monthsSubjects´ evaluation (using a questionnaire) for the four different entry methods

Countries

Germany

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026