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Vol. 18. Issue 3.
(July - September 2025)
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3632
Vol. 18. Issue 3.
(July - September 2025)
Review
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Evidence on the parameters of oculomotor skills and normative values: A systematic review

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3632
Mario Cantó-Cerdána,b,
Corresponding author
mario.canto@vissum.com

Corresponding author at: Avda de Denia s/n, Vissum Alicante 03016 Alicante, Spain.
, Carlos Javier Hernández-Rodríguezc,d, Antonio Martínez-Abada,b
a Department of Optometry. Vissum (Miranza Group), Alicante, Spain
b Grupo de Investigación en Optometría (GIOptom), University of Alicante, Alicante, Spain
c Department of Optometry, OKYO Ophthalmics, Alicante, Spain
d Department of Ophthalmology, Quirónsalud Medical Center, Elche
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Table 1. Characteristics of the 42 studies included in the review.
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Table 2. Most commonly measured aspects of oculomotor parameters in the articles reviewed.
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Table 3. Quality rating of the 42 included studies in the systematic review (QUADAS-2 results) (☺: low risk; ☹: high risk; ?: unclear risk.)
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Abstract
Purpose

To evaluate the current evidence on oculomotor measurement parameters and their normative values through a systematic review.

Methods

A search of primary studies was conducted using a search equation with free language. Original articles analyzing normal oculomotor function parameters in healthy populations of any age, studies that included a clearly differentiated healthy control group, and articles using any oculomotor measurement test were included. The QUADAS-2 tool was used to assess the risk of bias, applicability, and quality of the studies. The review was conducted independently by the authors and then pooled to determine the final inclusion.

Results

A total of 915 articles were identified, of which 750 were excluded after the first review of the title and abstract. In the second step, 133 out of 165 investigations were discarded. Ultimately, 32 articles from the initial search were included, along with 10 additional articles identified through a manual search. The findings revealed variations in how oculomotor skills are measured, including differences in stimuli, measurement distances, and parameters assessed. A high risk of bias was observed (≥50% in the areas of “flow and timing”, “reference standard” and “patient selection”) along with poor applicability (≥50% in all aspects).

Conclusions

There is no clear evidence on normative values for oculomotor skills, nor is there a consensus on the measurement methods, stimulus used, or working distance. Furthermore, there is no agreement on which aspects of oculomotor skills should be assessed. To enhance reliability and applicability, measurement criteria should be standardized, and normative values should be established.

Keywords:
Oculomotor skills
Oculomotor function
Systematic review
Gaze processing
Saccadic
Smooth pursuits
Fixation
Nnormative values
Full Text
Introduction

Oculomotor function refers to an individual’s innate ability to execute eye movements in a seamless, coordinated, and fluid manner, ensuring the maintenance of a clear, fused, and stable image on the central region of the retina. When an object is in motion, it is crucial to sustain this visual stability as the object moves. To achieve accurate oculomotor performance, three fundamental skills must be assessed: tracking movements, saccadic movements, and fixation movements. These skills should be well developed monocularly and must also be coordinated to ensure efficient oculomotor function.1

Oculomotor skills are currently being studied across various disciplines within the health sciences.2 Most research is focused on the neurological field, including schizophrenia,3 cognitive impairment,4 depression,5 biomarkers of neurodegenerative diseases,6 neurodevelopmental disorders,7 and even post-COVID conditions.8 Additionally, oculomotor skills play a crucial role in non-health-related fields, such as marketing9 or enabling individuals with amyotrophic lateral sclerosis to communicate using eye-tracking technology.10

In the field of optometry, oculomotor studies have grown over the past decade, largely due to advancements in eye-tracking technologies.11 Research has focused on various areas, including visual dysfunctions, strabismus, amblyopia, nystagmus, and visual impairment. Additionally, oculomotor studies have extended to vision-related fields such as refractive surgery, sports vision or driving vision.2,11,12

However, despite this exponential growth, concerns remain regarding the diagnostic methodology for oculomotor abnormalities. No clear range of normal values has been established for the parameters used to assess ocular motility, and no gold standard or reference test has been defined.13 Classical tests, such as the Developmental Eye Movement Test (DEM),14 the Northeastern State University College of Optometry (NSUCO) Oculomotor Test,15 and the King-Devick Test (K-D)16 have been used for many years. However, these tests have the disadvantage of being subjective for both the examiner and the patient. With the advent of new eye-tracking technologies, equipment has been developed to measure oculomotor parameters objectively. However, these systems vary in the parameters they assess, the psychophysics of measurement, the stimulus used, and the measurement distance.11-13

Research has been conducted to establish normative ranges for different subjective tests,14-16 as well as for some of the new technologies.17-20 However, there is still no scientific consensus regarding the psychophysics of measurement, the range of values, or the parameters to be assessed. This lack of standardization highlights the need for a unified approach to these aspects.

Therefore, the aim of this study is to evaluate the current evidence on oculomotor measurement parameters and their normative values through a systematic review.

Methods

The study has been registered in the PROSPERO database. A comprehensive search was conducted using a search strategy (Supplementary Material) in three databases: PubMed, Web of Science, and Scopus. The search included all age groups and imposed no time restrictions to ensure that no relevant articles were overlooked. After the initial search, a refined selection of articles was made based on the following criteria:

Inclusion criteria

  • Original descriptive articles analyzing normal oculomotor parameters (pursuit, saccadic movements, fixation, saccadic velocity, and reading saccades) in a healthy population of any age.

  • Originals comparative articles analyzing oculomotor parameters, whose design includes a well-defined control group not accomplishing inclusion criteria.

  • Articles utilizing a subjective test currently used in the clinical practice such as NSUCO, DEM, ADEM, or K-D.

  • Articles utilizing an objective test currently used in the clinical practice such as eye-tracker, or video-oculography.

Exclusion criteria

  • Case series, clinical case reports, and animal studies.

  • Studies involving populations with neurological, developmental, or ocular pathologies that lack a well-defined control group or include fewer than 20 subjects.

  • Methods employing complex stimuli different to standard geometrical shapes (dot, cross, square or similar) or related to language (numbers, letters), as faces or pictures, that aim to assess cognitive skills or related with attention.

  • Methods providing non quantitative results such as graphs or interpretations.

  • Samples where visual evaluations were performed diagnosing binocular anomalies, such as amblyopia and strabismus in its subjects.

The article selection process followed a sequential approach. First, titles and abstracts were reviewed to exclude irrelevant studies, and duplicates were removed. Second, full-text articles were examined, and only those that met the predefined inclusion criteria and addressed the research question were selected. Third, a manual search considering studies known by articles and reviewing references of included articles was conducted to identify additional references that might not have appeared in the initial search. Articles with control groups that did not clearly report results were excluded.

Finally, to assess the risk of bias, applicability, and quality of the studies, the QUADAS-2 tool was used. This tool is divided into domains that evaluate key aspects of each article, such as participant selection, index test, reference test, and the flow and timing of the study. Following the guidelines of the evaluation tool, the risk of bias was classified into three evidence level groups: studies with a low risk of bias, studies with an unclear risk of bias, and studies with a high risk of bias.

The article selection and the quality analysis using the QUADAS-2 procedure were performed blindly and independently by three investigators to ensure accurate classification of the included studies. In cases of discrepancies, a consensus was reached between the authors, with all three authors discussing and agreeing.21

The initial literature search was conducted in February 2024, and the databases were reviewed again in September 2024 using the same methodology.

Results

The study selection process for this systematic review is illustrated in a flowchart in Fig. 1. Initially, 915 documents were retrieved during the search. After reviewing titles and abstracts and removing duplicates, 165 articles were selected for full-text evaluation. Of these, 133 were excluded for not meeting the inclusion criteria. Ultimately, 32 articles were included. Additionally, a manual search identified 10 more articles, bringing the total to 42 articles that were analyzed in this review.

Fig. 1.

Flow chart of eligible papers used in the meta-analysis (PRISMA statement). PRISMA, preferred reporting items for systematic reviews.

Study characteristics

Table 1 presents the characteristics of the 42 included studies, which span from 1980 to 2023. The studies included sample sizes ranging from 20 to 2075 subjects. Of these, 26 studies (61.9%) were descriptive cross-sectional, 15 studies (35.7%) were comparative cross-sectional, and 1 study (2.4%) was pseudo-experimental.

Table 1.

Characteristics of the 42 studies included in the review.

Year  Author  Characteristics of the control group (n, ranged age)  Study design  Oculomotor skills  Measurments system  Stimulus  Optometric examination  Work Distance (cm) 
1980  Schalen22  20, age 22-70  Cross-sectional, descriptive  SAC, SP  Electro-oculography  Light Spot in computer  No  160 cm 
1983  Lieberman16  1202 normal subjects, age 6-14  Cross-sectional, descriptive  SAC  K-D  Numbers on test card  No  40 cm 
1984  Bergenius23  60, age 11-70  Cross-sectional, descriptive  SAC, SP  Electro-oculography  Light Spot in computer  No  70 cm 
1990  Garzia14  534 normal subjects aged 6-13  Cross-sectional, descriptive  SAC  DEM  Numbers on test card  No  33 cm 
1992  Maples15  1714 normal subjects aged 5-14  Cross-sectional, descriptive  SAC, SP  NSUCO  Sphere  No  Not described 
1992  Versino24  76 normal subjects aged 12-77  Cross-sectional, descriptive  SAC  Electro-oculography  Light Spot  No  Not described 
1993  Ross25  53 normal subjects aged 7-15  Cross-sectional, descriptive  SAC, SP  Eyetracker  Small target in computer  No  43 cm 
1993  Wilson20  122 normal subjects aged 16-72  Cross-sectional, descriptive  SAC  Electro-Oculography  LED 690nm  No  67 cm 
1997  Litman26  24 normal subjects  Cross-sectional, comparative  SAC, SP  Eyetracker  Bright Square  No  43 cm 
1997  Ross27  25 normal subjects  Cross-sectional, comparative  SAC, SP  Eyetracker  White disc in screen  No  120 cm 
1999  Campana28  65 normal subjects  Cross-sectional, comparative  SAC  Eyetracker  Light Spot  No  90 cm 
2003Jimenez291056 normal subjects aged 6-12Cross-sectional, descriptiveSACDEM and Scheiman & Wick  Numbers on test card and fixing pointYes40 cm // 33 cm DEM
procedure 
2006  Rutsche18  358 normal subjects aged 0-6  Cross-sectional, descriptive  SAC, SP  Pupil reflex  Color lights  Yes  40 cm 
2007  Aring30  135 normal subjects aged 4-15  Cross-sectional, descriptive  FIX  Infrared light  Dot  Yes  53 cm 
2010van Tritch3128 normal subjects aged 15-35Cross-sectional, comparativeSAC, SPDouble magnetic  Red light laser spotNoNot described
induction method 
2011  Goepel32  31 normal subjects age 7-12  Cross-sectional, descriptive  SAC  Eyetracker  Cartoons in computer  No  51,8 cm 
2011  Kattoulas33  2075 normal subjects aged 18-25  Cross-sectional, descriptive  SAC, SP, FIX  Eyetracker  Cross  No  Not described 
2011  Webber34  59 normal subjects aged 9-10  Cross-sectional, descriptive  SAC  Eyetracker and DEM  Numbers on test card  Yes  Not described 
2012  Shi35  20 normal subjects aged 6-12  Cross-sectional, comparative  FIX  Eyetracker  Light spot  Yes  200 cm 
2012  Boot36  213 normal subjects aged 0-12  Cross-sectional, descriptive  FIX  Eyetracker  White Dots  No  60 cm 
2015  Seferlis37  250 normal subjects aged 18-70  Cross-sectional, descriptive  SAC, SP, FIX  Video-oculography  Light spot  Yes  170 cm 
2015  Doettl38  62 normal subjects: 4-44  Cross-sectional, comparative  SAC, SP  Videonystagmography  Snellen chart  Yes  127 cm 
2016  Zalla39  20 normal subjects  Cross-sectional, comparative  SAC  Eyetracker  Grid of 13 points  No  60 cm 
2016  Yang40  50 normal subjects aged 20-69  Cross-sectional, descriptive  SAC, SP  Video-oculography  Point  No  100 cm 
2017  Choi41  63 normal subjects: aged 19-80  Cross-sectional, comparative  SAC, FIX  Eyetracker  Text  No  85 cm 
2017  Ferreira42  31 normal subjects aged 18-45  Cross-sectional, comparative  SAC  Eyetracker  Cross  No  70 cm 
2017  Vinyuela-Navarro43  120 normal subjects aged 4-11  Cross-sectional, descriptive  SAC, FIX  Eyetracker  Animal Cartoon  Yes  65 cm 
2018  Rizzo44  42 normal subjects aged 19-52  Cross-sectional, comparative  SAC  Eyetracker and K-D  Numbers on test card  No  Not described 
2018  Wetzel45  75 normal subjects aged 21-53  Cross-sectional, comparative  SAC  Eyetracker  Nine separated points  No  75 cm 
2019  Hoffmann46  40 normal subjects  Cross-sectional, comparative  SAC  Eyetracker  Circle  No  Not described 
2019  Chehrehnegar47  59 normal subjects  Cross-sectional, comparative  SAC  Eyetracker  Cross (Simon task)  No  60 cm 
2019  Vinyuela-Navarro48  169 normal subjects aged 4-11  Cross-sectional, descriptive  SAC, SP  Eyetracker  Animal Cartoon  Yes  65 cm 
2019  Wetzel49  75 normal subjects aged 18-65  Cross-sectional, comparative  SAC, SP  Eyetracker  Nine separated points  No  75 cm 
2020  Wertli50  25 normal subjects aged 10-11  Cross-sectional, descriptive  SAC, FIX  Eyetracker  Text  Yes  Between 50 to 80 cm 
2020  Sinno19  120 normal subjects aged 5-17  Cross-sectional, descriptive  SAC, SP  Videonystagmography  White Square  No  120 cm 
2021  Hindmarsh51  196 subjects aged 7.3-8.9  Cross-sectional, descriptive  SAC, SP, FIX  Eyetracker and DEM  Numbers on test card  Yes  60 cm 
2021  Kullmann52  466 normal subjects aged 18-45  Cross-sectional, descriptive  SAC, SP  Eyetracker  Dot  No  Not described 
2021  Amato53  54 normal subjects aged 18-28  Pseudoexperimental  SAC  Eyetracker  Videogame  No  Not described 
2022  D’Addio54  34 normal subjects  Cross-sectional, comparative  FIX  Eyetracker  White disc in screen  No  65 cm 
2022  Eichler55  52 normal subjects aged 9-34  Cross-sectional, descriptive  SAC  Eyetracker  OMAT  Yes  25 cm 
2023  Orduna-Hospital56  52 normal subjects aged 18-30  Cross-sectional, descriptive  SAC, FIX  Eyetracker and DEM  Numbers on test card  Yes  60 cm 
2023  Wertli57  118 normal subjects aged 7-12  Cross-sectional, descriptive  SAC, FIX  Eyetracker  Text  Yes  Between 50 to 80 cm 
  SAC: saccadicSP: smooth pursuitsFIX: fixationDEM: developmental eye movementOMAT: OculoMotor Assessment Tool Test 

Regarding oculomotor skills, 38 out of the 42 studies (90.5%) addressed saccadic movements, 17 studies (40.5%) focused on smooth pursuits movements, and 12 studies (28.6%) investigated fixation movements. In terms of technology and measurement systems, a significant amount of variability was found, with classical tests such as the DEM test, NSUCO test, and electro-oculography in studies performed more than 30 years ago, alongside newer technologies, like eye trackers, video-oculography, and video-nystagmography in recent evidence. The stimuli used also varied widely, including letters, texts, reading tests, numbers, and monochromatic, colored, or illuminated figures. It difficulted the stratified analysis by type test. Similar limitation was found for age because 21 of 42 studies (50.0%) was performed exclusively in children but ones in babies and others in adolescents, 16 of 42 (38.1%) were performed exclusively in adults, and 5 of 42 (11.9%) was performed combining both populations. Notably, only 14 of the 42 studies (33.3%) conducted an optometric examination prior to the oculomotor assessment. Finally, regarding the working distance for measuring oculomotor values, variability was observed, ranging from 25 cm to 200 cm. It is important to note that 9 studies (21.4%) did not specify the working distance, and 2 studies (4.8%) provided a range but did not specify an exact value.

Oculomotor skills aspects

Table 2 presents the aspects of oculomotor skills measured for each parameter (saccadic, smooth pursuit, and fixation movements), extracted from the studies included in this systematic review. It is evident that there is considerable diversity in the parameters analyzed for each test. Additionally, it can be observed that most of these parameters are not analyzed in more than 20% of the articles. Differences between subjective and objective assessment methods can also be observed in Table 2. The description of the parameters included was the following:

  • Number of saccades: Total count of discrete eye movements made from one fixation point to another during a task.

  • Latency of saccades: Interval between the onset of a target stimulus and the beginning of the corresponding saccadic eye movement.

  • Velocity of saccades: Rate of change in eye position over time during a saccade.

  • Amplitude of saccades: Difference in eye position between the starting point and ending point of a saccadic eye movement.

  • Smooth pursuit gain: Ratio of eye velocity to target velocity during smooth pursuit tracking.

  • Fixation time: Length of a continuous period during which the gaze is held within a small spatial area without significant movement.

Table 2.

Most commonly measured aspects of oculomotor parameters in the articles reviewed.

    Total  Subjective test  Objective test
Skills  Aspects     
SaccadesNumber of Saccades  13  31.0    2.4    12  28.6 
Amplitude of Saccades  11  26.2    0.0    11  26.2 
Velocity of Saccades  21.4    0.0    21.4 
Latency of Saccades  13  31.0    0.0    13  31.0 
          00.0  1126.2
Smooth Pursuits  Pursuit Gain  11  26.2     
           
Fixation  Fixation Time  10  23.8    2.4    21.4 

For saccadic movements, the most frequently analyzed parameters are the number of saccades (31.0%), latency (31.0%), velocity (21.4%) and amplitude (26.2%). In pursuits movements, the most commonly measured aspect is pursuit gain (26.2%). Lastly, for fixation movements, the most frequently measured parameter is fixation time (23.8%). Most aspects of oculomotor function have been evaluated through objective methods of measurement. In addition, authors did not find reported data on Bivariate Contour Ellipse Area (BCEA), a standard metric of fixation stability.

Other aspects were also measured by the authors of the included articles, such as Peak Velocity in saccadic movements, velocity in smooth pursuits and number of fixations in fixation movements. However, these aspects were measured less frequently, in fewer than 20% of the articles.

Assessment of quality and bias of included studies

Table 3 and Fig. 2 present the analysis of the 42 included studies using the QUADAS-2 tool, which evaluates the risk of bias and applicability. In general, it can be observed that there is a high risk of bias (≥50% in the aspects of “flow and timing”, “reference standard” and “patient selection,” as well as poor applicability (≥50%), across all aspects.

Table 3.

Quality rating of the 42 included studies in the systematic review (QUADAS-2 results) (☺: low risk; ☹: high risk; ?: unclear risk.)

Study  Risk of biasApplicability concerns
  Patient selection  Index test  Reference standard  Flow and timing  Patient selection  Index test  Reference standard 
1980 Schalen22  ☹  ☹  ☺  ☹  ☹  ☺ 
1983 Lieberman16  ☺  ☹  ☹  ☹  ☺  ☺ 
1984 Berginus23  ☺  ☺  ☹  ☹  ☺ 
1990 Garzia14  ☹  ☺  ☺  ☹  ☹  ☺ 
1992 Maples15  ☹  ☹  ☺  ☹  ☹  ☺ 
1992 Versino24  ☹  ☺  ☹  ☹  ☹  ☺ 
1993 Ross25  ☹  ☺  ☹  ☹  ☺  ☺ 
1993 Wilson20  ☹  ☹  ☹  ☹  ☹  ☺ 
1997 Litman26  ☹  ☹  ☹  ☹  ☹ 
1997 Ross27  ☹  ☹  ☹  ☹  ☺  ☹ 
1999 Campana28  ☹  ☺  ☹  ☹  ☹  ☹  ☹ 
2003 Jimenez29  ☺  ☺  ☹  ☺  ☺  ☺ 
2006 Rütsche18  ☺  ☺  ☹  ☹  ☺  ☹  ☹ 
2007 Aring30  ☺  ☺  ☹  ☹  ☺  ☺  ☺ 
2010 van Tritch31  ☹  ☹  ☹  ☹  ☹  ☹  ☹ 
2011 Goepel32  ☹  ☹  ☹  ☹  ☹  ☹ 
2011 Kattoulas33  ☺  ☹  ☹  ☺  ☺ 
2011 Webber34  ☺  ☺  ☺  ☹  ☺  ☺  ☺ 
2012 Shi35  ☺  ☹  ☺  ☹ 
2012 Boot36  ☺  ☺  ☹  ☹  ☺  ☹ 
2015 Seferlis37  ☺  ☺  ☹  ☹  ☺  ☺  ☺ 
2015 Doettl38  ☺  ☺  ☹  ☹  ☹ 
2016 Zalla39  ☹  ☺  ☹  ☹  ☹  ☹ 
2016 Yang40  ☹  ☺  ☹  ☹  ☹  ☺ 
2017 Choi41  ☹  ☹  ☹  ☹  ☹  ☹  ☹ 
2017 Ferreira42  ☹  ☹  ☹  ☹  ☹  ☹  ☹ 
2017 Vinyuela-Navarro43  ☺  ☺  ☹  ☹  ☺  ☹ 
2018 Rizzo44  ☺  ☹  ☹  ☹  ☹ 
2018 Wetzel45  ☹  ☺  ☹  ☹  ☹  ☹  ☹ 
2019 Hoffman46  ☹  ☺  ☹  ☹  ☹  ☹  ☹ 
2019 Chehrehnegar47  ☹  ☺  ☹  ☹  ☹  ☹  ☹ 
2019 Vinyuela-Navarro48  ☺  ☺  ☹  ☹  ☺  ☺ 
2019 Wetzel49  ☹  ☺  ☹  ☹  ☹  ☹ 
2020 Wertli50  ☺  ☺  ☹  ☹  ☺ 
2020 Sinno19  ☺  ☺  ☹  ☹  ☺  ☺  ☺ 
2021 Hindmarsh51  ☺  ☺  ☺  ☹  ☺  ☺ 
2021 Kullman52  ☺  ☺  ☹  ☹  ☺  ☺ 
2021 Amato53  ☹  ☹  ☹  ☹  ☹  ☹  ☹ 
2022 D’Addio54  ☹  ☹  ☹  ☹  ☹  ☹  ☹ 
2022 Eichler55  ☺  ☺  ☹  ☹  ☺  ☺  ☺ 
2023 Orduna-Hospital56  ☺  ☺  ☺  ☹  ☺  ☺ 
2023 Wertli57  ☺  ☺  ☹  ☹  ☺ 
Fig. 2.

QUADAS-2 domain for articles included in the systematic review.

Discussion

Oculomotor function has gained increasing relevance in recent years. In fact, more than half of the studies analyzed in this review (22 out of 42; 52.4%) have been conducted in the last decade.19,37-57

Firstly, the technology used to measure oculomotor function has advanced considerably. Early studies relied on electrooculography and subjective assessments, whereas more recent research utilizes eye-tracking systems and video-nystagmography (Table 1). This shift suggests a notable improvement in the quantitative analysis of ocular motor skills. Secondly, it is now demonstrated that oculomotor disturbances may be present in some systemic conditions, such as neurological diseases3-6,53 or development disorders.7 Despite current devices seeming to measure oculomotor function in a better way, it is not completely demonstrated because there is a great methodological variability between studies in terms of the type of stimulus, the complexity of the task, the working distance, and even the analyzed parameters. Such variability precludes direct comparison of measurements across different systems and constrains the ability to perform agreement analyses between devices. Consequently, there are very few studies comparing subjective methods (DEM, K-D, NSUCO) with objective methods based on eyetrackers,34,44,51 and even fewer comparing several objective methods with one another. Not only are comparisons between devices not adequately developed in scientific literature, but also the validation with a single device is also insufficient because typically only one measurement is taken for each subject, preventing the development of repeatability analysis. In fact, only the DEM14 and NSUCO15 techniques have been thoroughly validated by measuring twice for each subject and calculating intrasession repeatability. The impossibility of generalizing the results is also supported by the study design and population. Oculomotor function is highly age-dependent,14,15,18,19,33,37,58 and there are multiple studies involving adults, children or both. In contrast, almost half of the studies analyzed in this paper (15 of 42 studies; 35.7%)26-28,31,35,38,39,41,42,44-47,49,54 are cross-sectional with comparative design incorporating a control group whose ocular movements are compared to those obtained by a specific group with a particular condition or disorder. This involves selecting the control group based on the study group’s characteristics, inducing a patient selection bias that prevents the results from being generalized to the broader population. Another finding observed in this systematic review, potentially affecting the inference process, is the lack of an optometric evaluation in the majority of studies (28 of 38 studies; 66.6%).14-16,19,20,22-28,31-33,36,39-42,44-47,49,52-54 Among 14 articles that conducted previous eye tests,18,29,30,34,35,37,38,43,48,50,51,55-57 three studies performed a comprehensive optometric examination evaluating accommodation, vergences, and stereopsis.43,48,56 Eight articles conducted some accommodative and binocular tests, but these were insufficient for the purposes of this study, tests,18,29,30,34,50,51,55,57 and the other three articles only included VA measures.35,37,38 It represents a very remarkable limitation of the current evidence because an evaluation of refraction, accommodation and vergences would be elementary in this topic as indicated Cacho-Martínez et al.59 Moreover, difficulty in focusing or maintaining single vision is related to the efficiency of fixations and saccades. Therefore, a prior optometric examination is important to detect binocular or accommodative dysfunctions that may affect oculomotor performance.60

It is reported that oculomotor function is impaired in individuals with amblyopia61 and strabismus,62 affecting both the dominant and amblyopic eye.63 Additionally, monocular and binocular oculomotor skills differ.64 In cases of convergence insufficiency, alterations in reading saccades are also observed.65 Difficulties in near vision due to accommodative issues and/or uncorrected refractive errors may also contribute to oculomotor dysfunction, as suggested by Liu et al.60 Therefore, a comprehensive visual examination that includes binocular, accommodative, and sensory assessments is necessary to rule out the presence of amblyopia, strabismus, non-strabismic binocular dysfunctions, and oculomotor dysfunctions. Such an approach would reduce the number of visual variables that interfere with measurement and facilitate the establishment of normative oculomotor parameters. It is also essential to measure monocular and binocular visual acuity at both distance and near. Furthermore, it should be noted that the presence of strabismus can result in a number of abnormalities across numerous brain areas involved in visual functions and eye movements.66,67 Indeed, not all eye tracker software is designed for the precise measurement of strabismus. Some software merely detects the initial position of the eyes during calibration, without the capability to distinguish whether the eyes are aligned or if strabismus is present. Considering that oculomotor function is altered when patients do not use the best optical correction or have other visual anomalies,68 the low rate of studies including an optometric evaluation in their sample represents an important limitation.59 Other potential biases and applicability concerns have been analyzed in this paper using the QUADAS-2 tool (Table 3, Fig. 2).

Regarding the methods used to measure oculomotor function in the articles included in this systematic review, Table 1 highlights the presence of various stimuli, measurement distances, technologies, and types of visual tasks. Starting with the stimuli employed, a wide range of tests was used, including classic tests such as DEM, NSUCO, K-D, or reading a text, as well as the use of computers to project points, shapes, letters, or cartoons, and even a video game or the OculoMotor Assessment Tool (OMAT). This variety of stimuli, differing in shape, size, color, and cognitive processing difficulty, represents a limitation when attempting to compare them. In fact, the cognitive processes required to follow a moving point differ significantly from those involved in reading text, numbers, or shapes, and are distinct from observing drawings or playing a video game.12 Therefore, this variability constitutes a critical factor when measuring oculomotor function. Moreover, certain eye movements require specific techniques and stimuli for proper assessment, such as fixation, which is commonly evaluated in clinical practice using the BCEA through microperimetry. However, this parameter was not reported in the included studies, possibly because fixation is assessed alongside other eye movements, such as saccades. Further research is needed to specifically analyze oculomotor movements in isolation.

During the measurement process, attention loss due to the appearance of another stimulus or, in the case of computers or screens, the presence of additional objects can influence the results. Similarly, the working distance is another limitation. As shown in Table 1, five studies (11.9%) performed measurements at a near distance (≤ 40 cm),14,16,18,29,55 21 studies (50.0%) at an intermediate distance (between 40 and 100 cm),20,23,25,26,28,30,32,36,39,41-43,45,47-51,54,56,57 seven studies (16.7%) at a medium-far distance (≥ 100 cm),19,22,27,35,37,38,40 and nine studies (21.4%) did not specify the working distance.15,24,31,33,34,44,46,52,53 Although no gold standard exists for the working distance, it can affect the accuracy of eye movement recordings. While it is true that the eye's angular orientation relative to the stimulus is key—and at different distances but the same angular orientation, the eyes should theoretically behave similarly in their movement—factors such as peripheral vision capacity or the limitation of specific ocular muscles may affect the measurement. At greater distances, these factors could introduce errors. These errors are due to the interaction between the accommodative and vergence system,69,70 and it has been shown in scientific literature that variation in working distance produces variation in the accommodative and vergence system.71

Regarding the technology used, there has been significant progress from the early methods, such as electrooculography (an invasive technique), to the development of video nystagmography, video oculography, and the most widely used technology: eye trackers. The use of eye trackers in studies has grown exponentially, particularly in the optometric field, enabling more precise and objective measurements of oculomotor function. However, it is essential to consider that each technology differs in its stimuli, working distances, and limitations, complicating comparisons between studies due to the lack of a gold standard for measurement.

Other factors that may influence results include the ergonomics of the measurement systems. Modern systems, such as eye trackers or video-oculographs, exhibit considerable variability, including trial frames with side-mounted cameras, helmets, virtual reality glasses, and bars placed on computer screens. Additionally, some devices are not commercially available but are laboratory prototypes or optical bench setups. Establishing unified ergonomic criteria would be beneficial.

During the evaluation of oculomotor function, it is essential to consider the subject's age. Scientific literature has demonstrated that oculomotor function varies with age, and studies that propose normative values present results based on age.16,19,20,48,50-52,55-57 Research suggests that oculomotor performance improves during the early years of life (approximately from 4 to 15 years)72-74 and subsequently declines.58,74,75 Another critical aspect to consider is the subject's cognitive level. Neurodevelopmental disorders,76,77 neurological diseases,78,79 or, as mentioned earlier, age—particularly in early childhood and older adulthood—can significantly influence the measurements.

Furthermore, maintaining the subject's attention is crucial. Oculomotor measurements typically last between 30 seconds and 5 minutes, and any loss of attention during the evaluation can lead to inconsistent or unreliable results. Similarly, fatigue and exhaustion during the test — especially in lengthy, tedious evaluations involving complex stimuli or requiring high cognitive demand — can introduce biases into the measurements.80 A clear parallel can be observed in visual field testing, where efforts have been made for years to shorten the test duration to mitigate these biases.

All these factors — age, cognitive level, attention, fatigue, and exhaustion — must be carefully considered when establishing a gold standard for oculomotor function measurement. Unified criteria should be defined to ensure consistency and reliability in the evaluation process.

Following the identification of methodological considerations frequently neglected in the literature and warranting careful attention, it is equally imperative to undertake a critical appraisal of the overall quality and methodological rigor of the included studies. In this systematic review, this analysis was conducted using the QUADAS-2 tool (Table 3, Figure 2), which demonstrated a high incidence of studies with significant risks of bias and important limitations regarding applicability concerns. In particular, the most common risk of bias is related to reference standards, as only 4 out of 42 studies (9.5%)29,34,51,56 compare the test under study with a gold standard technique or at least other independent method capable of measuring similar parameters of oculomotor function. This lack of comparison prevents validation of the measurements due to the impossibility of performing an agreement analysis. Similarly, flow and timing are also highly affected by a high risk of bias in almost all studies, with only 3 out of 42 studies (7.1%)14,15,22 being free of this type of bias. The bias was generally caused by the predominance of single measurements per device, which prevents repeatability analysis. This finding further contributes to the generation of non-validated measurements that cannot be used as normative values.

Patient selection is another significant source of bias present in most studies, as many included subjects with highly specific characteristics – for example, only highly educated individuals41 or only students53 – limiting extrapolation to the general population. Additionally, the selection of normal subjects was often influenced by the demographics and characteristics of other study groups involved in comparative studies. Therefore, recruitment in these comparative studies is not randomized. Furthermore, comparative studies often attempt to match ages between groups, leading to significant heterogeneity among control groups depending on the nature of the study.

On the other hand, it is important to highlight the higher-quality results regarding measurement methodology or index test in the current review, as 30 out of 42 studies (71.4%) provide a complete description of the procedure.14,16,18,19,23-25,28,30,33-40,43-52,55-57 However, despite an accurate description of the measurement process, technology, and tasks, in some cases, the methodology remains difficult to replicate, affecting its applicability. This limitation is primary due to the use of outdated technology,22-24 implementation of subjective tests,15 non-standardized texts that introduce cognitive and educational dependencies,41,57 and highly complex tests that are difficult to replicate, such as the Convirt Test53 or OMAT Test.55

Applicability concerns are further compounded by unclear or questionable inclusion criteria for subjects, as well as the lack of proper characterization of measurements, leading to data that do not contribute to establishing normative values.

Regarding the limitations of the present study, the scarcity of specific articles evaluating normative values must be noted, as most studies focus on comparative or interventional approaches rather than the characterization of oculomotor function. Additionally, intrinsic limitations of the current tools used to assess study quality may lead to incomplete considerations or misinterpretations, even though QUADAS-2 remains the most appropriate tool for the objectives of this investigation. Because of these limitations a unique standardization of oculomotor measurements is currently not possible. Future studies should be conducted to propose a preliminary oculomotor protocol by an expert committee which should be validated in different sample characteristics.

On the other hand, key strengths of this study include its innovative and applicable focus, emphasizing the need to establish normative values. Moreover, the development and analysis of the procedure were conducted independently by three investigators, with a final consensus to enhance the evaluation of the current evidence.

Conclusion

Based on these findings, this systematic review concludes that there is no clear evidence on normative values for oculomotor skills, nor is there a consensus on the measurement methods, stimuli used, or working distances. Furthermore, there is no agreement on which specific aspects of oculomotor skills should be assessed, and due to the quality evaluation of these studies, the risk of bias remains predominantly high.

Additionally, it is concerning that the vast majority of studies do not include a comprehensive optometric assessment – incorporating refractive, accommodative, and binocular tests – which may introduce bias in the results. To enhance reliability and applicability, measurement criteria should be standardized, and normative values should be established.

Disclosure

The authors report no conflict of interests and have no proprietary interest in any of the materials mentioned in this article.

Funding information

No funding

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