Abstract
This study examined the association between smart device usage and the 1-year change in refractive error among a representative sample of Hong Kong children and adolescents aged 8–14 years. A total of 1597 participants (49.9% male, mean age 10.9, SD 2.0) who completed both baseline (2017–2018) and 1-year follow-up (2018–2019) eye examinations were included in the present study. The non-cycloplegic auto-refractive error was measured and the average spherical equivalent refraction (SER) was analyzed. The participants also self-reported their smart device usage at baseline. Multivariate regression adjusted for age, sex, baseline SER, parents’ short-sightedness, BMI, time spent on moderate-to-vigorous physical activity (MVPA), and caregiver-reported socio-economic status showed that, compared with the reference group (<2 h per day on both smartphone and tablet usages), those who spent ≥2 h per day using a smartphone and <2 h per day using a tablet had a significantly negative shift in refractive error (1-year change in SER −0.25 vs. −0.09 D, p = 0.01) for the right eye, while the level of significance was marginal (1-year change −0.28 vs. −0.15 D, p = 0.055) for the left eye. To conclude, our data suggested spending at most 2 h per day on both smartphones and tablets.
Keywords: handheld device, myopia, prospective, smartphone, tablet, teenage
1. Introduction
Uncorrected refractive error is the leading cause of visual impairment worldwide, according to reports by the World Health Organization [1]. Short-sightedness, also referred to as myopia, is the most common cause of uncorrected refractive error [2]. The progression of myopia has been a concerning topic from a public health perspective due to the increased risks it poses for numerous visually blinding conditions such as glaucoma and retinal detachment [3,4,5]. Myopia is becoming an epidemic worldwide, particularly in many East Asian countries where educational performance is strongly emphasized and outdoor activities are limited [6]. Hong Kong is no exception, and a recent study showed that more than a quarter of children aged 6–8 years were myopic [7,8]. A recent epidemiological study conducted in Japan has shown that the prevalence of myopia is estimated to be 76.5% and 94.9% for schoolchildren aged 6–11 and 12–14 years, respectively [9]. Myopia develops when there is a failure of emmetropization [10,11,12,13,14]. High demands in near work, close working distance, and lack of outdoor activities are known risk factors for myopia development and progression [15,16,17]. This vulnerability to environmental stress necessitates further attention in exploring the consequences of time spent on smart devices, such as smartphones and tablets, for school-aged children’s learning and overall developmental health. People who are myopic have impaired ability to see objects clear at distance, thereby potentially affecting their academic and job performance as well as career choices. Although clinical interventions that can effectively slow myopia progression, such as low dose atropine [18] and orthokeratology [19] are currently available, myopia progression intervention measures should also be implemented through early detection and early childhood education.
Current technological advances have made access to digital devices common among all population groups worldwide. The digitization trend has brought about new habits and demands in lifestyle ergonomics, introducing new public health burdens such as vision-related complications [20]. Schoolchildren are most vulnerable to visual influences, resulting in the onset of subjective symptoms such as visual fatigue, headaches, and blurry vision [21]. Nowadays, there is a surge in smartphone ownership, whereby it is very common to see children as young as two years old using smartphones as their new “electronic pacifier” [22]. The effect of time spent on smart devices among school-aged children has been explored in various studies, most reporting a need for interventional strategies to reduce their usage [23,24]. In Hong Kong, there is an increasing trend in which smart device usage affects sleep patterns among adolescents [25]. A number of studies also indicated that refractive error can be altered by sleep patterns [26,27]. A recent systemic review revealed that screen time was not associated with the prevalence and incidence of myopia [28], nor was it found to be associated with smartphone usage time in a cross-sectional study [29]. However, whether there is any long-term visual impact after smart device usage is yet to be determined [30,31].
Because of the popularity of smartphone use with school children and the introduction of electronically assisted teaching in schools, smart device usage is unavoidable, and appropriate guidelines ought to be developed. Therefore, it is important to explore its consequences for vision so that appropriate education can be provided to end-users to minimize this stress. In this study, we examined the association between smart device usage habits of primary and secondary school-aged children and their 1-year changes in refractive error.
2. Materials and Methods
2.1. Participants
Participants in this study were recruited in 11 primary schools and 4 secondary schools in Hong Kong. All students from participating schools studying P3–P5 (equivalent to Grades 3 to 5 in the US education system) and S1–S3 (equivalent to Grades 7 to 9 in the US education system) between ages 8 and 14 years were invited, and 1978 participants (response rate 60%) were recruited. They were invited to attend a health examination and completed a self-report questionnaire at baseline and 1-year follow-up. The primary parental caregivers of all participants were also invited to complete a self-report questionnaire at baseline and 1-year follow-up. Written consent was obtained from all participants at baseline. As all participants were under 18 years old, written parental consent was also obtained prior to their participation in this study. This study was approved by the Human Subjects Ethics Sub-committee of Hong Kong Polytechnic University (Reference number HSEARS20151121001). All study procedures followed the guidelines of the Declaration of Helsinki. The details of the study can be found in https://rfs1.fhb.gov.hk/app/fundedsearch/projectdetail.xhtml?id=1958.
2.2. Data Collection
2.2.1. Self-Administered Questionnaire
Time spent on smartphones and tablets per day was self-reported, and participants reported the time spent on school days and holidays separately. The daily time spent was calculated as the weighted sum of the time spent on school days and holidays. Time spent on moderate-to-vigorous physical activity (MVPA) was measured using the Global Physical Activity Questionnaire (GPAQ) [32].
2.2.2. Health Examination
Non-cycloplegic refraction was measured by an open-field autorefractor (Grand Seiko WAM-5500). Each eye was measured three times and the average spherical and cylindrical powers were analyzed. SER was computed as the sum of sphere power and half of the cylinder power. Axial length was measured with a Carl Zeiss IOL Master 500 Optical Biometer, with each eye measured five times and averaged.
2.2.3. BMI
The height (to the nearest 0.1 cm) and weight (to the nearest 0.1 kg) of the participants were measured by trained research assistants using a SECA 213 portable stadiometer and Tanita BMI body fat analyzer BC-541N. BMI was computed as weight (kg)/(height [m])2.
2.2.4. Caregiver Questionnaire
The primary parental caregiver of each participant (decided among the caregivers) was invited to complete a self-administered questionnaire that collected basic demographic and socio-economic characteristics of the participants (type of accommodation, primary caregiver’s level of education, and monthly household income).
2.3. Data Analysis
The sample was weighted according to the 2016 Population By-census to increase its representativeness. Since the 1-year change in the spherical equivalent refraction (SER) of right eyes and left eyes showed only moderate correlation (rho = 0.53), we used multivariate regressions to examine the association between smart device usage and SER instead of analyzing the SER of one eye (mostly the right eye in the literature). Pillai’s trace test was used to examine the overall significance of smart device usage and SER. The SER of right and left eyes were the dependent variables, and numerous possible confounders including age, sex, baseline SER, parents’ short-sightedness, BMI, time spent on MVPA, and caregiver-reported socio-economic status were controlled. The working distance of using smartphones and tablets was not controlled due to its low correlation with SER (right eye: −0.04, left eye: −0.06). Missing data in the confounders were imputed using multiple imputations. The fully conditional specification method was used to impute the missing data, and the average results performed with 10 imputed datasets were reported. All data analysis was performed using SPSS 25.0. (IBM Corp., Armonk, NY, USA) p-values of <0.05 were considered significant.
3. Results
Table 1 shows the participants’ characteristics. The sample was gender-balanced and the mean age was 10.87 years (SD 2.00). Approximately half of the participants spent more than 4 h per day on smartphones, and approximately 40% spent at least 1 h per day on tablets. The average SERs at baseline were −1.69 D (right eye) and −1.64 D (left eye). At the 1-year follow-up, they progressed to −1.90 D and −1.84 D, respectively.
Table 1.
Variable | Mean | SD |
---|---|---|
Age (years) | 10.87 | 2.00 |
Spherical equivalent refraction (D) | ||
Right eye, baseline | −1.69 | 2.14 |
Right eye, 1-year follow-up | −1.90 | 2.20 |
Right eye, change | −0.21 | 1.01 |
Left eye, baseline | −1.64 | 2.12 |
Left eye, 1-year follow-up | −1.84 | 2.18 |
Left eye, change | −0.20 | 1.00 |
BMI (kg/m2) | 18.55 | 3.56 |
MVPA (h/wk) | 11.62 | 14.53 |
Variable | Frequency | Percentage |
Gender | ||
Male | 797 | 49.9 |
Female | 800 | 50.1 |
Smartphone usage (h/day) | ||
0–1 | 295 | 18.5 |
1–2 | 184 | 11.5 |
2–3 | 145 | 9.1 |
3–4 | 167 | 10.5 |
4+ | 806 | 50.5 |
Tablet usage (h/day) | ||
0–1 | 990 | 62.0 |
1–2 | 188 | 11.8 |
2–3 | 116 | 7.3 |
3–4 | 73 | 4.6 |
4+ | 230 | 14.4 |
Parents’ short-sightedness | ||
Both | 298 | 19.0 |
Only father | 302 | 19.2 |
Only mother | 234 | 14.9 |
Neither | 530 | 33.7 |
Do not know | 208 | 13.2 |
Type of accommodations | ||
Public housing | 1021 | 67.6 |
Home-ownership scheme | 193 | 12.8 |
Private housing | 296 | 19.6 |
Primary caregiver’s level of education | ||
No formal education | 17 | 1.1 |
Primary | 182 | 12.3 |
Secondary | 1127 | 76.0 |
Tertiary or above | 157 | 10.6 |
Monthly household income | ||
0–9999 | 219 | 14.9 |
10,000–19,999 | 589 | 40.1 |
20,000–29,999 | 343 | 23.3 |
30,000–39,999 | 163 | 11.1 |
40,000–49,999 | 76 | 5.2 |
50,000+ | 79 | 5.4 |
BMI: Body Mass Index, MVPA: moderate-to-vigorous physical activity.
Time spent on smartphones at baseline was negatively and significantly associated with the SER of both eyes at baseline and 1-year follow-up (Table 2, both ps < 0.001). Time spent on tablets was insignificantly associated with baseline SER but significantly associated with SER at 1-year follow-up (both ps < 0.05), with participants who spent 2–3 h per day on tablets having had the most negative SER (−2.30 D for the right eye and −2.21 D for the left eye), that is, having the most negative refractive error. Time spent on both smartphones and tablets at baseline was insignificantly associated with changes in the SER of both eyes.
Table 2.
Smartphone | Usage (h/day) | Baseline | 1-Year Follow-Up | Change |
---|---|---|---|---|
Right eye | ||||
0–1 | −1.21 (2.10) | −1.38 (2.06) | −0.17 (1.17) | |
1–2 | −1.55 (2.00) | −1.73 (1.94) | −0.17 (1.07) | |
2–3 | −1.75 (2.29) | −2.05 (2.41) | −0.30 (0.70) | |
3–4 | −1.78 (2.27) | −1.97 (2.46) | −0.19 (0.98) | |
4+ | −1.87 (2.10) | −2.09 (2.18) | −0.22 (0.98) | |
p-value | <0.001 | <0.001 | 0.72 | |
Left eye | ||||
0–1 | −1.16 (2.06) | −1.38 (2.04) | −0.22 (1.20) | |
1–2 | −1.56 (1.97) | −1.75 (2.03) | −0.19 (1.04) | |
2–3 | −1.76 (2.24) | −2.02 (2.36) | −0.26 (0.70) | |
3–4 | −1.63 (2.28) | −1.88 (2.28) | −0.25 (0.84) | |
4+ | −1.81 (2.10) | −1.99 (2.19) | −0.18 (0.99) | |
p-value | <0.001 | 0.001 | 0.84 | |
Tablet | Usage (h/day) | Baseline | 1-Year Follow-Up | Change |
Right eye | ||||
0–1 | −1.72 (2.18) | −1.96 (2.27) | −0.24 (1.01) | |
1–2 | −1.53 (2.00) | −1.62 (1.88) | −0.09 (1.14) | |
2–3 | −2.06 (2.39) | −2.30 (2.48) | −0.24 (0.90) | |
3–4 | −1.33 (2.06) | −1.58 (1.95) | −0.25 (0.87) | |
4+ | −1.62 (1.93) | −1.78 (1.99) | −0.16 (0.96) | |
p-value | 0.13 | 0.04 | 0.37 | |
Left eye | ||||
0–1 | −1.70 (2.18) | −1.92 (2.26) | −0.23 (1.05) | |
1–2 | −1.42 (1.98) | −1.53 (1.88) | −0.11 (0.95) | |
2–3 | −1.93 (2.26) | −2.21 (2.38) | −0.27 (0.81) | |
3–4 | −1.28 (2.00) | −1.48 (1.87) | −0.20 (1.05) | |
4+ | −1.51 (1.94) | −1.66 (1.98) | −0.15 (0.92) | |
p-value | 0.10 | 0.02 | 0.48 |
Unadjusted and adjusted analyses of the association between smart device usage and changes in SER showed similar results (Table 3 and Table 4). p-values from Pillai’s trace were insignificant. When the time spent on smartphones was 2–3, 3–4, and 4+ hours per day, the adjusted means of the 1-year change in SER ranged from −0.20 to −0.26 D and were all significantly different from zero. When the time spent on tablets was 0–1, 2–3, and 3–4 h per day, the adjusted means of the 1-year change in SER ranged from −0.18 to −0.23 D, and were all significantly different from zero.
Table 3.
Model 1 | Model 2 | Model 3 | ||||
---|---|---|---|---|---|---|
Usage (h/day) | Mean (95% CI) | p-Value (Comparison with 0–1) | Mean (95% CI) | p-Value (Comparison with 0–1) | Mean (95% CI) | p-Value (Comparison with 0–1) |
Right eye | ||||||
0–1 | −0.12 (−0.24, −0.01) | Ref | −0.11 (−0.24, 0.003) | Ref | −0.11 (−0.26, 0.04) | Ref |
1–2 | −0.13 (−0.27, 0.02) | 0.97 | −0.14 (−0.29, 0.01) | 0.79 | −0.11 (−0.28, 0.07) | 0.83 |
2–3 | −0.28 (−0.44, −0.13) | 0.10 | −0.29 (−0.46, −0.13) | 0.12 | −0.25 (−0.44, −0.06) | 0.09 |
3–4 | −0.18 (−0.33, −0.04) | 0.53 | −0.21 (−0.36, −0.06) | 0.71 | −0.20 (−0.38, −0.01) | 0.30 |
4+ | −0.25 (−0.32, −0.18) | 0.08 | −0.27 (−0.34, −0.19) | 0.07 | −0.23 (−0.37, −0.10) | 0.04 |
Left eye | ||||||
0–1 | −0.60 (−0.28, −0.04) | Ref | −0.14 (−0.26, −0.02) | Ref | −0.16 (−0.31, −0.01) | Ref |
1–2 | −0.16 (−0.30, −0.01) | 0.97 | −0.15 (−0.30, −0.01) | 0.90 | −0.17 (−0.34, 0.01) | 0.93 |
2–3 | −0.26 (−0.41, −0.10) | 0.33 | −0.26 (−0.42, −0.10) | 0.12 | −0.26 (−0.45, −0.07) | 0.27 |
3–4 | −0.19 (−0.34, −0.05) | 0.74 | −0.23 (−0.38, −0.08) | 0.71 | −0.25 (−0.43, −0.07) | 0.38 |
4+ | −0.22 (−0.29, −0.15) | 0.42 | −0.23 (−0.30, −0.15) | 0.07 | −0.24 (−0.37, −0.11) | 0.28 |
Pillai’s trace p-value | 0.68 | 0.59 | 0.59 |
Model 1 adjusted for age, sex, and baseline SER; Model 2 adjusted for age, sex, baseline SER, parents’ short-sightedness, BMI, and time spent on moderate-to-vigorous physical activity; Model 3 adjusted for age, sex, baseline SER, parents’ short-sightedness, BMI, time spent on moderate-to-vigorous physical activity, and caregiver-reported socio-economic status.
Table 4.
Model 1 | Model 2 | Model 3 | ||||
---|---|---|---|---|---|---|
Usage (h/day) | Mean (95% CI) | p-Value (Comparison with 0–1) | Mean (95% CI) | p-Value (Comparison with 0–1) | Mean (95% CI) | p-Value (Comparison with 0–1) |
Right eye | ||||||
0–1 | −0.24 (−0.30, −0.18) | Ref | −0.25 (−0.32, −0.19) | Ref | −0.22 (−0.34, −0.09) | Ref |
1–2 | −0.09 (−0.23, 0.05) | 0.053 | −0.09 (−0.23, 0.05) | 0.04 | −0.07 (−0.24, 0.10) | 0.04 |
2–3 | −0.25 (−0.42, −0.07) | 0.94 | −0.28 (−0.46, −0.10) | 0.80 | −0.22 (−0.42, −0.02) | 0.80 |
3–4 | −0.21 (−0.44, 0.01) | 0.84 | −0.22 (−0.44, 0.01) | 0.76 | −0.18 (−0.43, 0.06) | 0.74 |
4+ | −0.16 (−0.28, −0.03) | 0.26 | −0.17 (−0.30, −0.04) | 0.27 | −0.14 (−0.31, 0.03) | 0.28 |
Left eye | ||||||
0–1 | −0.24 (−0.30, −0.18) | Ref | −0.24 (−0.30, −0.18) | Ref | −0.23 (−0.36, −0.10) | Ref |
1–2 | −0.08 (−0.22, 0.06) | 0.08 | −0.07 (−0.22, 0.07) | 0.03 | −0.10 (−0.27, 0.07) | 0.04 |
2–3 | −0.26 (−0.43, −0.08) | 0.09 | −0.28 (−0.46, −0.10) | 0.71 | −0.26 (−0.46, −0.05) | 0.80 |
3–4 | −0.18 (−0.40, 0.04) | 0.12 | −0.16 (−0.39, 0.06) | 0.52 | −0.18 (−0.42, 0.06) | 0.49 |
4+ | −0.13 (−0.25, −0.03) | 0.07 | −0.14 (−0.27, −0.01) | 0.16 | −0.15 (−0.32, 0.02) | 0.14 |
Pillai’s trace p-value | 0.59 | 0.52 | 0.52 |
Model 1 adjusted for age, sex, and baseline SER; Model 2 adjusted for age, sex, baseline SER, parents’ short-sightedness, BMI, and time spent on moderate-to-vigorous physical activity; Model 3 adjusted for age, sex, baseline SER, parents’ short-sightedness, BMI, time spent on moderate-to-vigorous physical activity, and caregiver-reported socio-economic status.
From the above results, 2 h per day of smart device usage appeared to be a cutoff for SER change, and this cutoff was thus used in the following analysis. Table 5 shows the interactive association of smartphone and tablet usage on the 1-year change in SER. The high smartphone usage (≥2 h per day) and low tablet usage (<2 h per day) subgroup was the group with the highest negative refractive error at both baseline and 1-year follow-up (both ps < 0.001). Multivariate regression was performed to examine the interactive effect of smartphone and tablet usage on the 1-year change in SER while controlling for potential confounders (Table 6). For right eyes, compared with the reference group (those with <2 h per day on both smartphone and tablet usages), individuals spending ≥2 h per day on smartphone usage and <2 h per day on tablet usage had a significantly larger decrease in SER (1-year change −0.09 vs. −0.25 D, p = 0.01), while the level of significance was marginal (1-year change −0.15 vs. −0.28 D, p = 0.055) for the left eye. The other two subgroups had insignificant differences in SER compared with those of the reference group.
Table 5.
Smartphone Usage (h/day) | Tablet Usage (h/day) | Baseline | 1-Year Follow-Up | Change | |
---|---|---|---|---|---|
Right eye | |||||
<2 | <2 | −1.29 (2.02) | −1.46 (1.98) | −0.17 (1.18) | |
≥2 | <2 | −1.88 (2.19) | −2.12 (2.30) | −0.24 (0.96) | |
<2 | ≥2 | −1.54 (2.22) | −1.72 (2.16) | −0.18 (0.90) | |
≥2 | ≥2 | −1.73 (2.07) | −1.94 (2.14) | −0.20 (0.93) | |
p-value | <0.001 | <0.001 | 0.68 | ||
Left eye | |||||
<2 | <2 | −1.27 (2.02) | −1.47 (2.04) | −0.20 (1.20) | |
≥2 | <2 | −1.84 (2.18) | −2.05 (2.27) | −0.21 (0.94) | |
<2 | ≥2 | −1.48 (2.08) | −1.74 (2.05) | −0.27 (0.89) | |
≥2 | ≥2 | −1.62 (2.04) | −1.79 (2.10) | −0.17 (0.92) | |
p-value | <0.001 | <0.001 | 0.86 |
Table 6.
Smartphone Usage (h/day) | Tablet Usage (h/day) | Model 1 | Model 2 | Model 3 | ||||
---|---|---|---|---|---|---|---|---|
Mean (95% CI) | p-Value (Comparison with <2 Hours per Day on Both Smartphone and Tablet Usages) | Mean (95% CI) | p-Value (Comparison with 0–1) | Mean (95% CI) | p-Value (Comparison with <2 Hours per Day on Both Smartphone and Tablet Usages) | |||
Right eye | ||||||||
<2 | <2 | −0.10 (−0.21, −0.01) | Ref | −0.12 (−0.22, −0.01) | Ref | −0.09 (−0.24, 0.05) | Ref | |
≥2 | <2 | −0.27 (−0.34, −0.20) | 0.02 | −0.28 (−0.35, −0.21) | 0.02 | −0.25 (−0.38, −0.13) | 0.01 | |
<2 | ≥2 | −0.15 (−0.35, 0.05) | 0.73 | −0.16 (−0.36, 0.05) | 0.73 | −0.13 (−0.36, 0.09) | 0.71 | |
≥2 | ≥2 | −0.21 (−0.32, −0.11) | 0.18 | −0.22 (−0.33, −0.11) | 0.17 | −0.20 (−0.34, −0.05) | 0.17 | |
Left eye | ||||||||
<2 | <2 | −0.13 (−0.23, −0.03) | Ref | −0.13 (−0.23, −0.02) | Ref | −0.15 (−0.29, −0.003) | Ref | |
≥2 | <2 | −0.25 (−0.32, −0.18) | 0.07 | −0.26 (−0.33, −0.18) | 0.051 | −0.28 (−0.40, −0.15) | 0.055 | |
<2 | ≥2 | −0.22 (−0.42, −0.01) | 0.11 | −0.21 (−0.42, −0.01) | 0.45 | −0.22 (−0.44, 0.0005) | 0.52 | |
≥2 | ≥2 | −0.17 (−0.27, −0.06) | 0.08 | −0.17 (−0.28, −0.06) | 0.57 | −0.18 (−0.33, −0.04) | 0.64 | |
Pillai’s trace p-value | 0.27 | 0.002 | 0.25 |
Model 1 adjusted for age, sex, and baseline SER; Model 2 adjusted for age, sex, baseline SER, parents’ short-sightedness, BMI, and time spent on moderate-to-vigorous physical activity; Model 3 adjusted for age, sex, baseline SER, parents’ short-sightedness, BMI, time spent on moderate-to-vigorous physical activity, and caregiver-reported socio-economic status.
4. Discussion
In this study, we found that smartphone use in young children was associated with a negative shift in refractive error. Children who spent more time (≥2 h per day) on smartphones, but less time (<2 h per day) on tablets showed greater negative shift in refractive error than those who spent more time on both devices. These results suggested that prolonged smartphone usage may present a higher risk of myopia progression than tablet usage. The study results suggested that children and adolescents should spend at most 2 h per day on both smartphones and tablets to reduce myopia progression. It is believed that tablet usage has less impact on SER because of the difference in posture when one uses tablets and smartphones. Studies have shown that people tend to place tablets further away than smartphones during use [33], the convergence demand during tablet use is less than that of smartphone use [34], and this prolonged accommodative convergence may contribute to myopia progression [35].
This study explored a dilemma in the current education system. While smart devices have been widely used to augment learning through online teaching, whether they pose long-term visual repercussions such as myopia progression in school children is yet to be confirmed. Given this uncertainty regarding the prevalence of myopia, when increased smart device usage is necessary, a monitoring model should be applied until further evidence clearly indicates the long-term effects of electronic screen time on children’s myopia development. Our results showed that school-children who spent more time on smart devices had a higher magnitude of myopia, at both the baseline and 1-year follow-up measurements. This finding is consistent with a recent cross-sectional study conducted in urban areas of Tianjin [36]. On the other hand, the myopia progression, as determined by SER changes over a 1-year period, did not differ significantly among groups with different smartphone/tablet usage. Nonetheless, we observed that school-aged children who reported using smart devices for two hours or more per day tended to have a greater increase in myopia change within a 1-year follow-up period. This discrepancy could be caused by the limited duration of the study, as the annual changes in refractive error in Hong Kong schoolchildren are estimated to be 0.5D [37], rendering the detection of subtle differences challenging. In addition, the negative correlation between smartphone/tablet usage and SER at the baseline visit may suggest a potential causal relationship, as a child might have already been using smartphones/tablets for years before the baseline measurement in this study. Although myopia progression was evident in all groups at the 1-year follow-up, its progression parallels in significance to the duration of usage. Further studies with more frequent measurements are required to confirm this finding by monitoring screen time and changes in SER for a longer period.
Consistent with previous findings, this study factored in potentially extraneous factors that could lead to an increase in myopia, including the parental history of myopia [8,38]. Our sampling included the core public schools representing the typical Hong Kong education experience, which further highlights the need for myopia progression monitoring. One limitation of our study was that cycloplegic agents were not used due to ethical issues, as the data were collected on normal school days and cycloplegic agent installation would interrupt the subjects’ daily school activities. Lack of cycloplegic agents may potentially affect the results of the autorefraction, as the subjects may have a tendency to accommodate, resulting in a more negative SER [39]. However, our data showed that SERs were strongly correlated with the axial length measurements (baseline r = 0.74, p < 0.001), and hence, we expected that the measured SER should also be strongly correlated with the actual SER. Other limitations include a more objective measure of screen time (e.g., screen time app) usage that tracks students’ usage over the year, which may be required to provide more accurate results on the usage of devices rather than questionnaire-based data. With that, screen time usage over the entire experimental period can be monitored more precisely. Finally, the moderately-correlated 1-year change in SER of right and left eyes might be contributed by the position of the smart device during use, but we did not collect data on the hand they commonly used for holding the smart devices so our hypothesis could not be tested.
5. Conclusions
In summary, based on the 1-year data, we suggest that additional consideration may be needed when introducing new forms of learning using smart devices. Our data indicated the prevalence of their habitual use and the potentially detrimental consequences for eye health. Our results will allow public health practitioners to steer strategic evaluations of the need for potential intervention strategies for children regarding screen-time control. Future research should also be directed towards exploring school health service models on how we could enhance the delivery of eye screening and/or examination to students, as well as educate them about the potential impact of screen time on eye health.
Acknowledgments
We like to express gratitude to all members of the vision screening team (School of Optometry, Hong Kong Polytechnic University) who provided support and expertise in testing the subjects throughout this study.
Author Contributions
C.-w.D., L.Y.L.C., and P.H.L. drafted the manuscript. P.H.L. designed the study, helped supervise the data collection, and conducted the data analysis. C.-w.D., A.C.Y.T., T.C., B.C.L.S., W.C.T., W.Y.Y., G.C.H.C., and G.P.Y.S. helped supervise the data collection. A.C.Y.T., B.C.L.S., and R.L.T.L. helped the school recruitment. All authors critically reviewed the manuscript and agree to be accountable for all aspects of the work in ensuring that questions related to the accuracy or integrity of any part of the work are appropriately investigated and resolved. All authors have read and agreed to the published version of the manuscript.
Funding
The Food and Health Bureau of the Hong Kong Special Administrative Region, China, provided financial support in the form of a grant from the Health and Medical Research Fund (Ref 13144041). The equipment/resources were donated by a COVD Research Grant, Vision of Love Fund, and The Hong Kong Jockey Club Charities Trust Fund. The sponsors had no role in designing or conducting this research.
Conflicts of Interest
The authors declare no conflict of interest.
Footnotes
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.
References
- 1.Bourne R.R.A., Flaxman S.R., Braithwaite T., Cicinelli M.V., Das A., Jonas J.B., Keeffe J., Kempen J.H., Leasher J., Limburg H., et al. Vision Loss Expert Group Magnitude, temporal trends, and projections of the global prevalence of blindness and distance and near vision impairment: A systematic review and meta-analysis. Lancet Glob. Health. 2017;5:e888–e897. doi: 10.1016/S2214-109X(17)30293-0. [DOI] [PubMed] [Google Scholar]
- 2.Morgan I.G., Matsui-Ohno K., Saw S.M. Myopia. Lancet. 2012;379:1739–1748. doi: 10.1016/S0140-6736(12)60272-4. [DOI] [PubMed] [Google Scholar]
- 3.Qiu M., Wang S.Y., Singh K., Lin S.C. Association between myopia and glaucoma in the United States population. Investig. Ophthalmol. Vis. Sci. 2013;54:830–835. doi: 10.1167/iovs.12-11158. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.The Eye Disease Case-Control Study Group Risk factors for idiopathic rhegmatogenous retinal detachment. Am. J. Epidemiol. 1993;137:749–757. doi: 10.1093/oxfordjournals.aje.a116735. [DOI] [PubMed] [Google Scholar]
- 5.Younan C., Mitchell P., Cumming R.G., Rochtchina E., Wang J.J. Myopia and incident cataract and cataract surgery: The blue mountains eye study. Investig. Ophthalmol. Vis. Sci. 2002;43:3625–3632. [PubMed] [Google Scholar]
- 6.Dolgin E. The myopia boom. Nature. 2015;519:276–278. doi: 10.1038/519276a. [DOI] [PubMed] [Google Scholar]
- 7.Yam J.C., Tang S.M., Kam K.W., Chen L.J., Yu M., Law A.K., Yip B.H., Wang Y.M., Cheung C.Y.L., Ng D.S.C., et al. High prevalence of myopia in children and their parents in Hong Kong Chinese Population: The Hong Kong Children Eye Study. Acta Ophthalmol. 2020 doi: 10.1111/aos.14350. article in press. [DOI] [PubMed] [Google Scholar]
- 8.Lam C.S.Y., Lam C.H., Cheng S.C.K., Chan L.Y.L. Prevalence of myopia among Hong Kong Chinese schoolchildren: Changes over two decades. Ophthalmic Physiol. Opt. 2012;32:17–24. doi: 10.1111/j.1475-1313.2011.00886.x. [DOI] [PubMed] [Google Scholar]
- 9.Yotsukura E., Torii H., Inokuchi M., Tokumura M., Uchino M., Nakamura K., Hyodo M., Mori K., Jiang X., Ikeda S.I., et al. Current prevalence of myopia and association of myopia with environmental factors among schoolchildren in Japan. JAMA Ophthalmol. 2019;137:1233–1239. doi: 10.1001/jamaophthalmol.2019.3103. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Ip J.M., Rose K.A., Morgan I.G., Burlutsky G., Mitchell P. Myopia and the urban environment: Findings in a sample of 12-year-old Australian school children. Investig. Ophthalmol. Vis. Sci. 2008;49:3858–3863. doi: 10.1167/iovs.07-1451. [DOI] [PubMed] [Google Scholar]
- 11.Choi K.Y., Yu W.Y., Lam C.H.I., Li Z.C., Chin M.P., Lakshmanan Y., Wong F.S.Y., Do C.W., Lee P.H., Chan H.H.L. Childhood exposure to constricted living space: A possible environmental threat for myopia development. Ophthalmic. Physiol. Opt. 2017;37:568–575. doi: 10.1111/opo.12397. [DOI] [PubMed] [Google Scholar]
- 12.French A.N., Morgan I.G., Mitchell P., Rose K.A. Risk factors for incident myopia in Australian schoolchildren: The Sydney adolescent vascular and eye study. Ophthalmology. 2013;120:2100–2108. doi: 10.1016/j.ophtha.2013.02.035. [DOI] [PubMed] [Google Scholar]
- 13.Guggenheim J.A., Kirov G., Hodson S.A. The heritability of high myopia: A reanalysis of Goldschmidt’s data. J. Med. Genet. 2000;37:227–231. doi: 10.1136/jmg.37.3.227. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 14.Wojciechowski R. Nature and nurture: The complex genetics of myopia and refractive error. Clin. Genet. 2011;79:301–320. doi: 10.1111/j.1399-0004.2010.01592.x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Huang H.-M., Chang D.S.-T., Wu P.-C. The association between near work activities and myopia in children—A systematic review and meta-analysis. PLoS ONE. 2015;10:e0140419. doi: 10.1371/journal.pone.0140419. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 16.Ip J.M., Saw S.M., Rose K.A., Morgan I., Kifley A., Wang J.J., Mitchell P. Role of near work in myopia: Findings in a sample of Australian school children. Investig. Ophthalmol. Vis. Sci. 2008;49:2903–2910. doi: 10.1167/iovs.07-0804. [DOI] [PubMed] [Google Scholar]
- 17.Rose K.A., Morgan I., Ip J.M., Kifley A., Huynh S., Smith W., Mitchell P. Outdoor activity reduces the prevalence of myopia in children. Ophthalmology. 2008;115:1279–1285. doi: 10.1016/j.ophtha.2007.12.019. [DOI] [PubMed] [Google Scholar]
- 18.Fu A., Stapleton F., Wei L., Wang W., Zhao B., Watt K., Ji N., Lyu Y. Effect of low-dose atropine on myopia progression, pupil diameter and accommodative amplitude: Low-dose atropine and myopia progression. Br. J. Ophthalmol. 2020 doi: 10.1136/bjophthalmol-2019-315440. article in press. [DOI] [PubMed] [Google Scholar]
- 19.Cho P., Tan Q. Myopia and orthokeratology for myopia control. Clin. Exp. Ophthalmol. 2019;102:364–377. doi: 10.1111/cxo.12839. [DOI] [PubMed] [Google Scholar]
- 20.Optometry Times How Digital Devices Are Affecting Vision. [(accessed on 12 May 2020)]; Available online: https://www.optometrytimes.com/modern-medicine-cases/how-digital-devices-are-affecting-vision.
- 21.Scheiman M.M., Rouse M.W. Optometric Management of Learning-Related Vision Problems. 2nd ed. Mosby-Elsevier; St. Louis, MO, USA: 2006. [Google Scholar]
- 22.Hong Kong Special Administrative Region Department of Health Family Health Service . Survey on Television Viewing and Use of Electronic Screen Products among Pre-School Children. Hong Kong SAR Government; Hong Kong, China: 2017. [Google Scholar]
- 23.Saxena R., Vashist P., Tandon R., Pandey R.M., Bhardawaj A., Gupta V., Menon V. Incidence and progression of myopia and associated factors in urban school children in Delhi: The North India Myopia Study (NIM Study) PLoS ONE. 2017;12:e0189774. doi: 10.1371/journal.pone.0189774. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Guan H., Yu N.N., Wang H., Boswell M., Shi Y., Rozelle S., Congdon N. Impact of various types of near work and time spent outdoors at different times of day on visual acuity and refractive error among Chinese school-going children. PLoS ONE. 2019;14:e0215827. doi: 10.1371/journal.pone.0215827. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Mak Y.W., Wu C.S.T., Hui D.W.S., Lam S.P., Tse H.Y., Yu W.Y., Wong H.T. Association between Screen Viewing Duration and Sleep Duration, Sleep Quality, and Excessive Daytime Sleepiness among Adolescents in Hong Kong. Int. J. Environ. Res. Public Health. 2014;11:11201–11219. doi: 10.3390/ijerph111111201. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Jee D., Morgan I.G., Kim E.C. Inverse relationship between sleep duration and myopia. Acta Ophthalmol. 2016;94:e204–e210. doi: 10.1111/aos.12776. [DOI] [PubMed] [Google Scholar]
- 27.Xu X., Wang D., Xiao G., Yu K., Gong Y. Sleep less, myopia more. Theory Clin. Pract. Pediatr. 2017;1:1–17. doi: 10.25082/TCPP.2017.01.004. [DOI] [Google Scholar]
- 28.Lanca C., Saw S.M. The association between digital screen time and myopia: A systematic review. Ophthalmic Physiol. Opt. 2020;40:216–229. doi: 10.1111/opo.12657. [DOI] [PubMed] [Google Scholar]
- 29.McCrann S., Loughman J., Butler J.S., Paudel N., Flitcroft D.I. Smartphone use as a possible risk factor for myopia. Clin. Exp. Ophthalmol. 2020 doi: 10.1111/cxo.13092. article in press. [DOI] [PubMed] [Google Scholar]
- 30.Huang L., Kawasaki H., Liu Y., Wang Z. The prevalence of myopia and the factors associated with it among university students in Nanjing: A cross-sectional study. Medicine. 2019;98:e14777. doi: 10.1097/MD.0000000000014777. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Long J., Cheung R., Duong S., Paynter R., Asper L. Viewing distance and eyestrain symptoms with prolonged viewing of smartphones. Clin. Exp. Optom. 2017;100:133–137. doi: 10.1111/cxo.12453. [DOI] [PubMed] [Google Scholar]
- 32.Bull F.C., Maslin T.S., Armstrong T. Global physical activity questionnaire (GPAQ): Nine country reliability and validity study. J. Phys. Act. Health. 2009;6:790–804. doi: 10.1123/jpah.6.6.790. [DOI] [PubMed] [Google Scholar]
- 33.Maniwa H., Kotani K., Suzuki S., Asao T. Changes in posture of the upper extremity through the use of various sizes of tablets and characters. In: Yamamoto S., editor. Proceedings of the Human-Computer Interaction: Users and Contexts of Use: 15th International Conference, HCI International 2013; Las Vegas, NV, USA. 21–26 July 2013; Las Negas, NV, USA: Springer; 2013. pp. 89–96. [Google Scholar]
- 34.Miranda A.M., Nunes-Pereira E.J., Baskaran K., Macedo A.F. Eye movements, convergence distance and pupil-size when reading from smartphone, computer, print and tablet. Scand. J. Optom. Vis. Sci. 2018;11:1–5. doi: 10.5384/sjovs.vol11i1p1-5. [DOI] [Google Scholar]
- 35.Bayramlar H., Çekiç O., Hepşen İ.F. Does convergence, not accommodation, cause axial-length elongation at near? Ophthalmic Res. 1999;31:304–308. doi: 10.1159/000055551. [DOI] [PubMed] [Google Scholar]
- 36.Tatar A., Kayiran S.M., Saltukoglu G., Ozkut E.Ş.Z., Emeksiz M. Analysis of the Center for Epidemiologic Studies Depression Scale (CES-D) in Children and Adolescents from the Perspective of the Item Response Theory. Klin. Psikofarmakol. Bülteni-Bull. Clin. Psychopharmacol. 2016;23:242–253. doi: 10.5455/bcp.20130324030600. [DOI] [Google Scholar]
- 37.Lam C.S.Y., Tang W.C., Tse D.Y., Lee R.P.K., Chun R.K.M., Hasegawa K., Qi H., Hatanaka T., To C.H. Defocus Incorporated Multiple Segments (DIMS) spectacle lenses slow myopia progression: A 2-year randomised clinical trial. Br. J. Ophthalmol. 2020;104:363–368. doi: 10.1136/bjophthalmol-2018-313739. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 38.Ma Y., Zou H., Lin S., Xu X., Zhao R., Lu L., Zhao H., Li Q., Wang L., Zhu J., et al. Cohort study with 4-year follow-up of myopia and refractive parameters in primary schoolchildren in Baoshan District, Shanghai. Clin. Exp. Ophthalmol. 2018;46:861–872. doi: 10.1111/ceo.13195. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 39.Fotedar R., Rochtchina E., Morgan I., Wang J.J., Mitchell P., Rose K.A. Necessity of cycloplegia for assessing refractive error in 12-year-old children: A population-based study. Am. J. Ophthalmol. 2007;144:307–309. doi: 10.1016/j.ajo.2007.03.041. [DOI] [PubMed] [Google Scholar]