Abstract
Purpose
NOMOPHOBIA (NO MObile PHone PhoBIA) or problematic smartphone use is a psychological disorder in which people are afraid of being cut off from their mobile phones. Currently, there has been no direct assessment of mobile phone screen size in the home setting and its effect on nomophobia and related symptoms, such as insomnia. Thus, we investigated the association between nomophobia, insomnia, and mobile phone screen size in a young adult population in Bahrain.
Patients and Methods
Using a descriptive, cross-sectional design, we surveyed participants aged 18 to 35 between August and September 2020 using an online questionnaire. Participants completed demographic questions and questions about personal mobile phones, the Nomophobia Questionnaire (NMP-Q), and the Insomnia Severity Index (ISI). The mobile phone screen size was determined using an open-source online database. Crude and adjusted regression analyses were fitted to examine the associations between the study variables.
Results
A total of 549 individuals, 54% females, were included in the final analyses. One hundred and fourteen participants (21%) had severe nomophobia, and 81 (14%) had clinical insomnia. A strong positive pair-wise linear association was observed between NMP-Q and ISI β 0.15, P = 0.001. Age, sex, BMI, and mobile phone screen size showed no association with the NMP-Q.
Conclusion
Nomophobia is very prevalent in young adult men and women, and it is closely associated with insomnia, regardless of mobile phone screen size, suggesting that mobile phone screen size should not be used as a proxy for hazardous usage.
Keywords: blue light, insomnia, ISI, no mobile phone phobia, problematic smartphone use, sleep problems
Introduction
Smart mobile phones are increasingly being incorporated into daily life. The many perks they provide, such as personal diary, instant messaging and e-mail exchanges, music and video play, games, camera, and calculator, have transformed it from a status symbol to a necessity.1 Along with these benefits come problems such as nomophobia, particularly among young people and those individuals whose daily activities have been rendered dependent on smartphone use.2 Some examples of daily activities include work or studying, online shopping, making payments, entry passes, travel e-tickets, QR codes access, and many more.
The term nomophobia (no mobile phone phobia) describes an emerging digital and virtual societal disorder emanating from pathological anxiety of being without a mobile device.3–5 Nomophobia has been defined as a mental health condition resulting in illogical fear of being detached from or not being able to use a mobile phone due, for example, to the lack of signal or internet connectivity or drained battery.6 Four dimensions describe nomophobia: fear of not being able to interact with others promptly, concern about losing connection, concern with difficulty getting information quickly, and discomfort not having a mobile device with self.7 The heightened level of nervousness, fear, or anxiety crystallizes with the inability to communicate instantly.8,9
The condition has been linked to various mental health problems and poor functioning.10,11 Nomophobia is associated with sleep problems (primarily insomnia),6,12 depressive symptoms,10,13 anger problems,14 stress disorders,5 anxiety,5,10,13 hyperactivity and oppositional problems,5,15 poor self-esteem,16 poor quality of life,13,17 and poor academic performance.18–20
To date, the disorder has been studied primarily in students,13,21–27 especially those studying health sciences as undergraduates, mainly nursing,28,29 in which self-esteem, extraversion, conscientiousness, and emotional instability appeared to be associated with the disorder.30
A recent meta-analysis of twenty studies involving 12,462 participants documented that the prevalence of severe nomophobia is approximately 21% [95% CI 16%; 28%], suggesting that the societal burden of the condition is significant.11
Although nomophobia research is still in its early phases, available evidence suggests that neither age nor sex is a significant moderator of nomophobia.11 A recent study also concluded that nomophobia is also present equally at the different educational stages.22 Consequently, the presence of a person having nomophobia cannot be assumed based on age, sex, or education.11,22
With the rapidly expanding use of visual display technology in mobile phones and other modern household devices, concern has developed regarding the potential hazards emanating from their use. It is not easily discernible whether nomophobia originates from problematic smartphone use or pre-existing anxiety.5 Other potential risk factors associated with the current culture of mobile phone use, including the characteristic features of the phones themselves, have not yet been researched. For example, it is known that mobile phone screen light spectrum includes blue to green light and can inhibit melatonin activity, resulting in reduced drowsiness, trouble inducing sleep, and non-restorative sleep.31 These fears have probably been exacerbated by the increases in the brightness and sizes of screens employed in these devices, the number of screens in the environment, and increased exposure to short-wavelength visible light (ie, blue to green) emission from such screens in daily domestic use.32
Wibirama and Nugroho investigated the effect of screen size on immersion in video gamers33 and showed that mobile devices with larger screen sizes gave a more significant immersion experience than mobile phone devices with small screen sizes. Furthermore, it has been suggested that a larger screen size may attract more viewer attention and hence and may deliver more light.34
The COVID-19 pandemic increased the use of electronic devices, primarily smartphones, as a means of mitigating the negative effects of social isolation, and connecting with the world, all while protecting the need for social distancing.35–37 Thus, the number of studies reporting the harmful effects of excessive mobile devices on mental and physical health is steadily increasing.11,37
To date, there has been no direct assessment of mobile phone screen size in the home setting and its effect on nomophobia. We hypothesized that the nomophobia score is higher in people using larger mobile phone screens and that insomnia scores are higher in people using larger mobile phone screens. Therefore, this study was designed to assess the association between nomophobia, insomnia, and mobile phone screen size in young adults.
Materials and Methods
Study Design and Setting
The information for this study in Bahrain was gathered using a descriptive, cross-sectional research methodology. Data were collected between August – September 2020 using self-administered, structured questionnaires distributed via instant message groups and social media ads. Participants were urged to forward the survey link to friends and family who might meet the eligibility requirements. Using social media channels to recruit the specified sample allowed access to a larger demographic and geographic catchment with less effort and at a lower cost than traditional face-to-face recruitment.38 To improve the standard of research design and documentation, the recommendations for Strengthening the Reporting of Observational Studies of Epidemiology (STROBE)39 were implemented in this study. The Checklist for Reporting Results of Internet E-Surveys was used to create the electronic survey.40 The use of “mandatory” fields was used in our survey for all variables to eliminate missing data.
Participants and Sample Size
A convenience non-probability sample of individuals between the ages of 18 and 35 defined as ‘young adults’,41 of both sexes, who owned at least one mobile device and was willing to participate in the study was included. Participants with a formal diagnosis of any mental illness were excluded using a brief screening, direct questioning skip logic algorithm. In addition, self-reports of receiving a physician’s diagnosis or regular treatment for cardiovascular disease, chronic respiratory problems, diabetes mellitus, gastroesophageal reflux disease, neurological disorders, renal disease, and thyroid disease were excluded.
We estimated a minimum needed sample size of 384 participants to have 95% confidence that the real value would be within 5% α (type I error) level and 20% β (type II error) level of the observations made.42
The following formula for the sample size n, was used: n N*X/(X + N – 1), where
X Zα/22*p*(1-p)/MOE2. Zα/2 is the critical value of the Normal distribution at α/2 (eg, for a confidence level of 95%, α is 0.05, and the critical value is 1.96), MOE is the margin of error, p is the sample proportion, and N is the population size.42
Ethical Considerations
All processes were carried out under the Helsinki Declaration of 1964 and its modifications. The Bahraini Ministry of Health’s Secondary Healthcare Research Ethics Committee (REC) evaluated and authorized this study (SHCRC/EF/14/10/2020). Written informed consent was sought and obtained from all participants before data collection.
Data Sources and Measurement
A structured survey was used to collect the data. The survey comprised demographic questions and questions about personal mobile phones, the Nomophobia Questionnaire (NMP-Q), and the Insomnia Severity Index (ISI).
Sociodemographic and Anthropometric Measures
The demographic questions included age, sex, self-reported body weight, self-reported body height, and the screening questions about physical and mental health. The BMI is expressed in kilograms per square meter (kg/m2), with a body mass in kilograms and height in meters, and was determined based on a person’s weight and height by dividing the body mass by the square of the body height. BMI was categories as underweight ≤18.5 kg/m2; normal weight 18.5–24.9 kg/m2; overweight 25–29.9 kg/m2; and obese ≥30 kg/m2.
Participants were also asked to identify their primary mobile phone device manufacturer and model number. We identified the viewport, resolution, pixel density, and mobile phone screen size from a database of mobile devices.43
Nomophobia and Insomnia Measures
The NMP-Q7 was used to assess the severity of nomophobia, defined as participants’ phobia/anxiety of being without a smartphone or handheld mobile device. The NMP-Q contains 20 questions, each of which is rated on a 7-point Likert-like scale ranging from 1 (“strongly disagree”) to 7 (“strongly agree”).7 The overall scoring is divided into four categories: <20 No Nomophobia; 21–59 Mild Nomophobia; 60–99 Moderate Nomophobia; and 100–140 Severe Nomophobia. The Arabic validated version of the NMP-Q was used in this study, and it has outstanding psychometric characteristics, with a Cronbach’s alpha coefficient of 0.90.44
The ISI45 was used to assess the severity of diurnal and nocturnal insomnia symptoms. The ISI comprises seven questions that measure various facets of insomnia: difficulty falling or staying asleep, early awakenings, satisfaction with sleep efficiency, interfering with functioning, and anxiety associated with disturbed sleep. Each item is rated for the prior two weeks on a five-point Likert scale (0=no problem, 4=severe problem). Total scores of 0–7 represent no clinically relevant insomnia, 8–14 represent subthreshold insomnia, 15–21 represent clinical insomnia (moderate severity), and 22–28 represent clinical insomnia (severe). The ISI has excellent psychometric properties and has been validated in Arabic.46 ISI has a sensitivity of 86% and a specificity of 88%, respectively.45 In clinical groups, an ISI score of 15 or higher is considered insomnia.45
Statistical Analysis
Descriptive statistics were used to identify and report the demographic characteristics of the subjects, personal mobile phone parameters, NMP-Q, and ISI scores. The arithmetic mean and standard deviation were reported for continuous variables, and for categorical variables, the frequency count and percentages were used.
The independent samples t-test was used to examine the difference between men and women regarding average mobile phone screen size, NMP-Q, and ISI scores. When applicable, Cohen’s d was also reported as effect size and defined as a difference in means proportional to the pooled variation. Chi-square statistic (χ2) was used to examine the differences between men and women regarding their mobile phone screen size preference.
To test if there are any statistically significant variations between the means (of age, BMI, NMP-Q, and ISI), a one-way analysis of variance (ANOVA) was employed using the groupings of mobile phone screen sizes.
Pearson’s product-moment correlation coefficient was used to measure the degree to which two variables (NMP-Q and ISI) correlate linearly and are presented as r. Regression analysis was used to estimate the association NMP-Q, ISI, and selected characteristics of the study participants. Univariate linear regression analysis was used to estimate the association between NMP-Q and ISI. Univariate logistic regression analysis was used to investigate the association between the dependent variables NMP-Q or ISI and age, male sex, BMI, and mobile phone screen size as independent variables. Logistic regression analysis was also used in a multivariate analysis to estimate the association between NMP-Q or ISI and mobile phone screen size after correcting for age, sex, and ISI to estimate NMP-Q or NMP-Q for estimating ISI.
Statistical significance was described as a p-value of less than 0.05. The R statistical computing 4.1.047 packages were used to analyze the data.
Results
A total of 549 individuals (54% females) were included in the final analyses. The mean age of the study participants was 27.33 ± 4.83 years. The mean BMI was 25.56 ± 5.69 kg/m2. About one-quarter (23%) of the participants were obese. The mean NMP-Q was 77.05 ± 17.80, the mean ISI was 8.24 ± 4.21, and the mean mobile phone screen size was 5.50 ± 0.50 inches. Approximately 80% of the participants had a mild or moderate level of nomophobia. Insomnia was much less common, with 14% of participants meeting the ISI of > 15 criteria for clinical insomnia. A total of 114 (21%) participants had a severe level of nomophobia, and 81 (14%) had clinical insomnia. The most common mobile phone screen size was 5.8 inch with approximately one-third of the sample owning a device of such size. Table 1 shows the descriptive statistics of the participants in the study.
Table 1.
Age, y | 27.33 ± 4.83 |
Body weight, kg | 69.22 ± 14.92 |
Body height, cm | 164.86 ± 8.30 |
BMI, kg/m2 | 25.56 ± 5.69 |
NMP-Q | 77.06 ± 17.80 |
ISI | 8.24 ± 4.21 |
MP screen size, INCH | 5.50 ± 0.50 |
MP pixel density, PPI | 480.01 ± 90.05 |
Active MP data plan | |
-Yes | 549 (100%) |
Sex | |
-Male | 253 (46%) |
-Female | 296 (54%) |
BMI Categories | |
-Underweight | 42 (8%) |
-Normal weight | 215 (39%) |
-Overweight | 168 (31%) |
-Obese | 124 (23%) |
NMP-Q Categories | |
-No nomophobia | None (0%) |
-Mild nomophobia | 35 (6%) |
-Moderate nomophobia | 400 (73%) |
-Severe nomophobia | 114 (21%) |
ISI Categories | |
-No clinically significant insomnia | 346 (63%) |
-Subthreshold insomnia | 122 (22%) |
-Clinical insomnia (moderate severity) | 73 (13%) |
-Clinical insomnia (severe) | 8 (1%) |
MP screen size categories, inch | |
−4.7 inch | 83 (15%) |
−5.1 inch | 92 (17%) |
−5.2 inch | 41 (7%) |
−5.5 inch | 93 (17%) |
−5.8 inch | 150 (27%) |
−6.1 inch | 12 (2%) |
−6.2 inch | 38 (7%) |
−6.3 inch | 28 (5%) |
−6.5 inch | 12 (2%) |
Notes: Values are expressed as mean ± standard deviation for continuous data or frequency count (percentage) for categorical data. BMI body mass index, underweight ≤18.5 kg/m2; normal weight 18.5–24.9 kg/m2; overweight 25–29.9 kg/m2; and obese ≥30 kg/m2. NMP-Q Nomophobia Questionnaire, ≤20 no nomophobia, 21–59 mild nomophobia, 60–99 moderate nomophobia, and 100–140 severe nomophobia. ISI Insomnia Severity Index, ≤7 represents no clinically relevant insomnia, 8–14 represents subthreshold insomnia, 15–21 represents clinical insomnia (moderate), and 22–28 represents clinical insomnia (severe).
Abbreviations: MP, mobile phone; PPI, pixels per inch.
Table 2 shows detailed differences in the study parameters by sex. Independent samples t-tests showed that: women had a statistically significant higher ISI score than men P =0.036, Cohen’s d 0.20. However, men and women had similar NMP-Q scores and mean mobile phone screen size. The mean mobile phone screen for men and women were 5.50 ± 0.51 and 5.49 ± 0.49, respectively, P = 0.73, Cohen’s d - 0.03. For the NMP-Q men and women scored 76.03 ± 17.00 and 77.94 ± 18.44, respectively, P = 0.21, Cohen’s d 0.11. BMI was significantly higher in men compared to women, 27.59 ± 6.48 and 23.83 ± 4.20, respectively, P = 0.001, Cohen’s d - 0.70.
Table 2.
Parameter | Male n 253 | Female n 296 | P-value |
---|---|---|---|
NMP-Q | 76.03 ± 17.00 | 77.94 ± 18.44 | 0.21 |
ISI | 7.83 ± 3.85 | 8.58 ± 4.48 | 0.036 |
MP screen size, inch | 5.50 ± 0.51 | 5.49 ± 0.49 | 0.73 |
BMI, kg/m2 | 27.59 ± 6.48 | 23.83 ± 4.20 | 0.001 |
NMP-Q categories | |||
-No nomophobia | None (0%) | None (0%) | 0.49 |
-Mild nomophobia | 16 (6%) | 19 (6%) | |
-Moderate nomophobia | 190 (75%) | 210 (71%) | |
-Severe nomophobia | 47 (19%) | 67 (23%) | |
ISI categories | |||
-No clinically significant insomnia | 175 (69%) | 171 (58%) | 0.042 |
-Subthreshold insomnia | 48 (19%) | 74 (25%) | |
-Clinical insomnia (moderate severity) | 28 (11%) | 45 (15%) | |
-Clinical insomnia (severe) | 2 (1%) | 6 (2%) | |
MP screen size categories, inch | |||
−4.7 inch | 43 (17%) | 40 (14%) | 0.80 |
−5.1 inch | 35 (14%) | 57 (19%) | |
−5.2 inch | 18 (7%) | 23 (8%) | |
−5.5 inch | 42 (17% | 51 (17%) | |
−5.8 inch | 71 (28%) | 79 (27%) | |
−6.1 inch | 6 (2%) | 6 (2%) | |
−6.2 inch | 17 (7%) | 21 (7%) | |
−6.3 inch | 15 (6%) | 13 (4%) | |
−6.5 inch | 6 (2%) | 6 (2%) |
Notes: Values are expressed as mean ± standard deviation for continuous data or frequency count (percentage) for categorical data. NMP-Q Nomophobia Questionnaire, ≤20 no nomophobia, 21–59 mild nomophobia, 60–99 moderate nomophobia, and 100–140 severe nomophobia. ISI Insomnia Severity Index, ≤ 7 represents no clinically relevant insomnia, 8–14 represents subthreshold insomnia, 15–21 represents clinical insomnia (moderate), and 22–28 represents clinical insomnia (severe). MP mobile phone. PPI pixels per inch. Independent samples t-test for continuous data, and Chi-square statistic for categorical data. P-value was significant < 0.05.
One-way ANOVA revealed no statistically significant difference in the means of age, BMI, NMP-Q, ISI by mobile phone screen size. Figure 1 shows the mean NMP-Q score by mobile phone screen size and Figure 2 shows the mean ISI score by mobile phone screen size.
A strong positive correlation was obtained between NMP-Q and ISI r = 0.63, P = 0.001. The results of examining the association between the NMP-Q and the ISI and selected features of the study participants are shown in Table 3. A strong positive pair-wise linear association was observed between NMP-Q and ISI, β = 0.15, P = 0.001. Age, sex, BMI, and mobile phone screen size showed no association with the NMP-Q.
Table 3.
Correlation Analysis | |||
---|---|---|---|
r | P-value | ||
NMP-Q (Continuous) | ISI (Continuous) | 0.63 | 0.001 |
Regression analysis | |||
Model 1 | |||
Independent Variable | Dependent Variable | Estimate β (95% CI) | P-value |
NMP-Q (Continuous) | ISI (Continuous) | 0.15 (0.13–0.17) | 0 0.001 |
Model 2 | |||
Age | ISI | 1.00 (0.96–1.06) | 0.85 |
NMP-Q | 1.02 (0.95–1.10) | 0.53 | |
Sex (Male) | ISI | 0.65 (0.40–1.05) | 0.08 |
NMP-Q | 1.02 (0.51–2.02) | 0.96 | |
BMI | ISI | 0.98 (0.94–1.03) | 0.46 |
NMP-Q | 1.00 (0.94–1.06) | 0.92 | |
MP screen size | ISI | 0.80 (0.50–1.28) | 0.35 |
NMP-Q | 1.32 (0.66–2.61) | 0.43 | |
Model 3 | |||
MP screen size | NMP-Q | 1.36 (0.69–2.68) | 0.38 |
MP screen size | ISI | 0.54 (0.25–1.16) | 0.12 |
Notes: Correlation analysis is measure of linear association is denoted by the letter r, which is the Pearson product-moment coefficient. Regression analysis, reported estimates are β coefficient for linear regression analysis and odds ratio for logistic regression analysis. Model 1 is univariate linear regression analysis. Model 2 is univariate logistic regression analysis. Model 3 multivariate logistic regression analysis correcting for age, sex and ISI for estimating NMP-Q or NMP-Q for estimating ISI. For models 2 and 3: ISI was categorized as insomnia ISI ≥ 15 or healthy ISI < 15. NMP-Q was categorized as moderate to severe nomophobia NMP-Q ≥ 60 or mild nomophobia < 60. MPSS mobile phone. P-value was significant < 0.05.
Discussion
Our results showed that nomophobia is a modern-day virtual and digital society condition and refers to a pathological dread of being without mobile phone technology. The condition is highly prevalent among young adult men and women, strongly associated with clinically significant insomnia but unassociated with personal mobile phone screen size or obesity. However, many aspects of nomophobia’s epidemiology, risk factors, psychological and behavioral characteristics are unclear. Therefore, research is strongly encouraged to better understand this condition.
Nomophobia symptoms are highly associated with insomnia symptoms in our study sample of young adults. This is in line with other research studies that have found a significant association between nomophobia and sleep difficulties.18,20,48–54 Several potential explanations have been put forward for the detrimental impact of smartphone use on sleep. First, continued smartphone usage, particularly before bedtime, lowers the amount of time spent sleeping, resulting in inadequate sleep.54 Second, some smartphone users prefer to spend their evenings browsing mobile websites. Users may experience anxiety and excitement as a result of inappropriate material on these websites, which might make it difficult to fall asleep due to emotional arousal.55 Third, two studies reporting morphological evidence from structural and functional magnetic resonance imaging that measured brain activity by detecting changes associated with blood flow showed changes in gray matter quantity and white matter integrity in young adults with nomophobia.56,57 Fourth, exposure to light and radiation from smartphone displays before bedtime may affect the start timing and secretion of melatonin, resulting in sleep-wake rhythm problems.58,59 A recent systematic review pointed that melatonin is suppressed by a two-hour exposure to blue light (460 nm) in the evening, with the shortest wavelengths having the most effect (424 nm, violet).60 Luckily, the melatonin levels rebounded quickly after the exposure ended, within 15 minutes, indicating a short-term or simultaneous effect of light exposure on melatonin production. Although melatonin production and suppression decrease with age, the light-induced circadian phase progression does not. The circadian phase of melatonin levels is influenced by light exposure in the evening, night, and morning. Furthermore, even the longest wavelengths (631 nm, red) and intermittent light exposure can adversely affect normal melatonin rhythmicity.60 Some solutions are now in the experimental phase; for example, a recent randomized clinical trial showed that wearing amber glasses lenses instead of clear lenses to block blue light for two hours before bedtime for a total period of one week resulted in better sleep and significantly reduced insomnia scores.31 From a biophysics perspective, the accessed content can modify the amount of blue light by modifying the average relative illuminance (ARI) in percent; for example, accessing a spreadsheet would allow ARI 90% compared to a movie which allows ARI 20%.61 Thus, counseling individuals with insomnia on the timing, duration, and content of access to a smartphone, computer, and other device screens is a possibly effective intervention strategy.
The international commission on non-ionizing radiation protection (ICNIRP) is an independent organization that publishes various scientific information and science-based advice on non-ionizing radiation protection. The ICNIRP recommends limiting exposure time and, in certain circumstances, source size to minimize the harmful health effects from visible radiation on the eye and skin.62 In healthy young adults, exposure to blue light increases the activity of the prefrontal cortex (PFC), particularly the dorsolateral PFC (DLPFC) and ventrolateral PFC (VLPFC), which improves working memory and alertness while interfering with sleep.63 Blue light influences stress levels and may produce long-term insomnia symptoms by affecting certain glucocorticoid hormones, such as cortisol, and the sympathetic nervous system markers, such as α-amylase.64
Our findings rejected our hypothesis, suggesting that the smartphone screen size was not an effect modifier of either nomophobia or insomnia. The explanations for the lack of association between screen size and insomnia are unclear. One possibility is that the viewing distance with larger screens may be more than that for smaller screens.34,65 While a television screen size is larger than a tablet screen, the distance one watches is generally much far from the larger screen. Thus, although a larger screen may emit more blue light, the viewing distance may counterbalance its impact. Moreover, a study that monitored eye movements to assess the total duration of eye fixation on the screen from participants playing video games demonstrated that the larger the screen size, the less the duration of fixation. Thus, the less duration of fixation may translate to less exposure to blue light. Therefore, further research in this area is needed in both laboratory and home environments to evaluate smartphone-generated light effects on the human circadian system.
Worldwide cohort research is looking into the long-term consequences of using mobile phones and other wireless technology for one’s health; the COSMOS Study (Cohort Study of Mobile Phone Use and Health) concluded that insomnia in the highest users of mobile phones [62]. Besides blue light, mobile phones emit radiofrequency electromagnetic fields (RF EMF). The Australian radiation protection and nuclear safety agency recommend three changes to reduce mobile phone’s RF EME exposure.66 First, increasing the distance between the mobile phone and your body. Second, reducing the time of exposure to mobile phones. Third, reducing the power by using the phone in an area with good reception and thus transmitting at considerably lower levels than in a reception-challenged location.66 While these suggestions were mainly targeted to reduce the RF EMF, we argue they may work on blue light too. Smartphone use may affect insomnia through multiple mechanisms, eg, blue light and RF EMF; thus, proper randomized controlled trials are needed to confirm this.
Our results suggest that nomophobia is not associated with age, sex, or BMI. According to a recent systematic review, nomophobia is more common in women, which reported that in 24 studies, women have nomophobia more than men, while eight studies found the reverse.10 Detailed inspection reveals that most of the studies finding women to have a higher prevalence of nomophobia were conducted in India and Turkey, compared with other Asian, European, and American countries. Thus, cultural diversity may explain this sex difference. Regarding age, most of the existing studies have a limited age range, which may affect subsequent interpretation. A recent systematic review showed that younger people are more susceptible to nomophobia.10 Our interpretation of the existing literature is that these findings are not mutually contradictory within age or sex but rather simply indicate that age and sex may be related to nomophobia in particular ways, impacted by cultural, economic, and logistical differences.
The major limitations of the study are: only young adults were sampled; convenience sampling was employed, and the self-reporting nature of the data collection process may all limit the generalizability of findings. We encourage future studies to employ objective measures approaches using, for example, commercial wearable devices (eg, smart bands, sleep trackers) to objectively monitor sleep and applications to monitor the frequency and duration of screen exposure throughout the day. Biophysics approaches can then estimate the daily dose of blue light for controlled analysis. In addition, future research might consider controlling for the use of prescription and blue light blocking eyewear.
Another delimitation of our work is the possible confounding effect of the COVID-19 pandemic on mobile phone use and/or sleep changes. It is also possible for methods of variance to overestimate the association between studied variables (nomophobia and insomnia). To illustrate, findings from a recent systematic review and meta-analysis showed that sleep problems are prevalent during the COVID-19 pandemic, affecting approximately 40% of the general population.67 Similarly, 50% of adults increased their screen time on at least two different devices during the pandemic to stay informed of important issues (eg, governmental directives).68
We recommend that future studies examine potentially problematic online activities (gambling, online gaming, pornography viewing, etc.) and their possible impact on problematic smartphone use.
Conclusion
Nomophobia is a modern-day virtual and digital society condition characterized by a pathological fear of being without mobile technology. The disorder is highly prevalent in young adult men and women, and it is closely associated with insomnia, regardless of the size of the mobile phone screen, indicating that the size of the mobile phone screen should not be used as a proxy for hazardous usage.
Disclosure
The authors report no conflicts of interest in this work.
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