Psychiatry Investig Search

CLOSE


Psychiatry Investig > Volume 23(1); 2026 > Article
Shin, Lee, Joo, Park, Shin, Lim, Park, and Kim: Digital Monitoring of Micro- and Macro-Movement Regularity in Psychiatric Inpatients With Depression

Abstract

Objective

Depression involves mood-related behavioral changes typically monitored through subjective reports, which are limited by recall bias and low temporal resolution. Digital mental health tools offer objective, continuous monitoring, but prior studies have focused on outpatients subject to environmental variability. In this preliminary feasibility study, we examined psychiatric inpatients in a controlled setting to assess associations between behavioral regularity and depression severity, highlighting the clinical potential of digital phenotyping.

Methods

Thirty-five adults from a closed psychiatric ward were recruited, and data from 10 inpatients with ≥7 days of valid monitoring were analyzed. Depression severity was assessed weekly using the Hamilton Depression Rating Scale (HAMD) and Dysfunctional Self-focus Attributes Scale, yielding 18 samples. Hourly accelerometer and location data from wearable devices and ward sensors were processed to generate digital phenotypes—interdaily stability (IS), intradaily variability (IV), ratio of IS to IV (ISV), entropy (EN), and normalized entropy (NE)—segmented into daytime and nighttime. Linear mixed models assessed group differences, and correlation and multiple regression examined associations with depression.

Results

Patients with asymptomatic/mild depression showed significantly higher IS_day and ISV_day, and lower EN_night, and NE_night (all p<0.05). These four features correlated with HAMD after false discovery rate (all p<0.05) correction. A regression model including IS_day and NE_night explained 60.6% of HAMD variance (p<0.05).

Conclusion

Digital monitoring provides an objective and continuous method to assess depression severity. By capturing macro- and micro-level movement regularity across day and night in an inpatient environment, this approach offers practical relevance for psychiatric care. However, results should be considered preliminary due to the limited sample size.

INTRODUCTION

Behavioral pattern changes are commonly observed in psychiatric patients and have become an area of research in psychiatric disorders, including major depressive disorder (MDD), bipolar disorder (BD), and schizophrenia [1-4]. In particular, depression is associated with mood changes that lead to corresponding behavioral alterations [5,6]. Traditional approaches in continuous monitoring and assessing depressive symptoms primarily rely on patient monitoring via staff patrols, Closed-Circuit Television (CCTV) surveillance, and subjective reports from patients and caregivers [7-9]. Such methods often face limitations owing to recall bias and difficulties in capturing real-time symptom changes, especially when a single provider oversees multiple patients [10-12]. Additionally, these conventional monitoring approaches may not detect or manage critical incidents such as violence, aggression, self-harm, and absconding if resources are insufficient [13,14]. The depression scales commonly used in traditional monitoring can be discontinuous, and their results may vary depending on who administers them, leading to inaccuracies such as over- or underestimation [15]. Consequently, digital mental health solutions that use digital phenotyping to continuously monitor a patient’s status and objectively capture depressive symptoms have gained traction as an alternative strategy, potentially mitigating these limitations and improving patients and healthcare staff [16].
Digital monitoring, often referred to as “remote sensing” or “digital phenotyping,” is an emerging field that provides new opportunities for improved management and treatment by enabling objective and continuous patient observation [17]. Previous studies in this area have identified actigraphy-based and location data as key approaches for assessing depression, deriving various phenotypes that serve as psychiatric monitoring tools. According to a meta-analysis, 29 studies collected data on sleep, 19 focused on physical activity, 13 examined circadian rhythms, and 11 investigated location patterns, with all these phenotypes showing significant associations with depression [18]. For example, time in bed and sleep fragmentation (indexed by the number of awakenings and wake after sleep onset) were strongly associated with high depression scores [19,20]. Common actigraphy-based mobility indicators include interdaily stability (IS), intradaily variability (IV), and relative amplitude, with findings indicating that individuals with MDD or BD often exhibit low IS, IV (suggesting more fragmented activity), and amplitude [21]. Meanwhile, location-based features—such as location variance (LV), entropy (EN), normalized entropy (NE), and homestay duration—have been associated with depression. Lower LV and EN (indicating reduced regularity in location patterns) and longer homestay duration are linked to more severe symptoms [22].
However, despite the extensive use of numerous phenotypes in various studies, methods of collecting, aggregating, and analyzing these data remain underdeveloped. A general lack of discussion exists regarding whether the devices used in these studies are valid or reliable for detecting the behaviors of interest. Although certain behaviors may seem relatively straightforward to infer from single sensors, such as Global Positioning System for location or accelerometry for physical activity, concerns about validity and reliability persist [23-25]. Moreover, because the association between each feature and depression tends to be diverse or somewhat opaque, ascertaining whether these features accurately capture depression and applying them effectively in clinical practice remains challenging [18].
Therefore, our analysis was based on the concept of “movement regularity” by integrating real-time data extracted from wrist-worn devices (accelerometer data, representing micro-level movements) and ward sensors (location data, representing macro-level movements). Activity level changes are a significant indicator included in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition criteria, and numerous studies have consistently demonstrated a robust link between such shifts in activity patterns and depressive symptoms [26]. By utilizing wearable and ward sensor data inputs from two distinct data sources, we aimed to provide a more comprehensive and objective interpretation of behavioral regularity.
Another limitation of current digital monitoring research is that most studies in this field are focused on outpatients, whose activities vary considerably owing to individual and environmental differences. However, this study targeted psychiatric inpatients with more severe symptoms in a controlled environment to address these constraints. By defining up to four specific locations where inpatients can move, we were able to monitor their movement precisely within a restricted setting. Additionally, because observations occurred continuously in a closed ward, we classified each measure into nocturnal and diurnal intervals on a 24-hour basis, allowing investigation on time-specific differences in behavioral regularity.
We hypothesized that digitally measured behavioral regularity could serve as a robust indicator of depression severity by adopting four non-parametric measures—IS, IV, EN, NE—along with the ratio of IS to IV (ISV) to examine behavioral patterns. We interpreted these digital phenotypes through micro-level movements (actigraphy data) and macro-level movements (location data), proposing a strong association with the severity of depressive symptoms. To our knowledge, no study has been conducted in a closed psychiatric ward that uses wearable devices and ward sensors to capture micro- and macro-level movements in inpatients, or has further subdivided these phenotypes into diurnal and nocturnal periods for analysis. Furthermore, by comparing these digital measures with self-and clinician-administered scales, this study demonstrates how digital mental health indicators can facilitate objective continuous monitoring of depression within psychiatric wards. We aimed to develop a more efficient framework for monitoring patients with depression, and we demonstrate that digital monitoring focused on behavioral regularity can serve as an effective tool for continuous functional monitoring in clinical settings.

METHODS

Study samples

We recruited 35 adult participants (aged 19-80 years) who were admitted to the closed psychiatric ward at Asan Medical Center, a university-affiliated hospital. All patients provided written informed consent to participate in wearable device monitoring. Of the 35 participants enrolled, 25 were excluded: 12 withdrew from the study due to personal choice, symptom exacerbation, inter-hospital transfer, or sensor malfunction; and 13 were excluded for having fewer than 7 days of valid data. The final analysis included 10 inpatients with at least 7 days of valid data. Most participants contributed data over 2 or more weeks, while 3 contributed only 1 week. In total, 18 weekly samples were analyzed, with a median participation duration of 17 days. Inclusion criteria allowed for a range of psychiatric diagnoses, including schizophrenia spectrum disorders, BD, and adjustment disorder. The study was approved by the Institutional Review Board of Asan Medical Center (IRB No. 2022-1130), and written informed consent was obtained from all participants.

Assessment

Participants completed demographic and depression assessments, including the Hamilton Depression Rating Scale (HAMD) and Dysfunctional Self-focus Attributes Scale (DSAS). The HAMD, administered by trained clinicians, is widely used to assess the severity of depressive symptoms [18]. However, the DSAS is a self-reported measure designed to assess attentional bias [27], and it correlates with depression and its cognitive symptom of rumination [28]. Both scales were administered weekly to determine whether digital phenotypes better explained clinician-rated assessments or self-reported measures of depression severity. Before the study began, the average scores for the HAMD and DSAS were approximately 14.3 (standard deviation [SD]=6.28) and 46.5 (SD=11.2), respectively, indicating mild depression according to HAMD classification criteria [29].

Digital monitoring

Participants wore a Patron URBAN HR Smart Band (600S; Patron) on the left wrist, except when self-harm scars were present, in which case it was worn on the right. Researchers checked device usage and verified data daily through an inhouse server to ensure proper wear and signal integrity. The collected biological signals were stored and managed on this server, and digital features were extracted from preprocessed actigraphy and location data.
In the closed psychiatric ward, patient location was continuously tracked via wireless receivers installed on ward ceilings, which identified location based on the detecting receiver. To enhance motion detection, additional modalities such as wireless fidelity and radio frequency devices and thermal imaging cameras were used in isolation rooms. All devices were non-invasive, battery-operated (3.7 V), and clinically validated for safety, with no reported adverse events.
Smart bands transmitted anonymized data—including device ID, pseudonymized patient ID, room information, and biometric signals—via bluetooth low energy (BLE) to the hospital’s monitoring server, excluding any hospital-registered identifiers. Vital signs were monitored continuously, and if abnormal values unrelated to clinical changes were detected, environmental influences were documented by the research team.

Data preprocessing

The goal of data preprocessing was to enable reliable feature extraction from accelerometer and location data. Accelerometer signals underwent basic preprocessing, including noise reduction and signal quality checks. To address device-induced spike noise, we replaced affected segments with the median of the initial 50 observations. Raw data were then converted to acceleration units (m/s²) using sensor sensitivity and the analog-to-digital converter (ADC) range, as shown below:
Accelerationm/s2=raw data×Sensor measurement rangeADC resolution×9.81.
The sensor range was set to 4 g and the ADC resolution to 16 bits. Due to variable raw data sampling rates (2-10 Hz), signals were resampled to a uniform 30 Hz via linear interpolation.
Processed signals were used to compute the sum of vector magnitude (SVM), minimizing rotational artifacts and capturing overall acceleration across x, y, and z axes [30]:
SVM=x2+y2+z2

Location data handling

For each hour, we identified visited locations and computed the time proportion spent at each. Coordinates were mapped to BLE scanner positions using the Haversine formula. Location shifts ≤5 seconds were treated as noise and excluded, while missing data were interpolated at 1-second intervals using forward fill. A 1-hour window was applied to determine each patient’s dominant location. For analysis, ward locations were grouped into five categories despite the blueprint showing more detailed zoning: patient room: the patient’s private space; group therapy room: a designated area where patients participate in therapy sessions; dining area: a designated space for meals; lounge: a communal and activity space where patients can freely engage in activities and spend time at their own will; and other areas (others): hallways, restrooms, and other uncategorized locations.

Accelerometer preprocessing

For the accelerometer data, activity levels measured using SVM from ward sensors were quantified using non-parametric indicators. This approach allowed for the analysis of activity pattern regularity through phenotypes, providing a detailed understanding of the stability of movement patterns.
Figure 1 presents a time-series analysis of individual patients’ daily activity patterns using SVM. We computed the average activity for each period over the 6 days preceding the day before the depression scale assessment. This approach laid the groundwork for its application in digital phenotyping. The timing and magnitude of activity peaks varied among patients, with fluctuations persisting at the individual level.

Digital features

Accelerometer and location data were collected on a time-series hourly basis for each patient, using data spanning six days. To analyze the relationship between these digital phenotypes and depression scores (i.e., IS, IV, ISV, EN, and NE; see Table 1 for definitions), we designated the assessment date of the weekly depression scales (HAMD, DSAS) as “Dd.” We averaged data over the 6 days immediately preceding Dd (i.e., Dd-6 through Dd-1), excluding both Dd and the prior assessment day (Dd-7).
For a more detailed analysis, the data for each phenotype were segmented into daytime (09:00-16:59) and nighttime (22:00-05:59) periods. Subsequently, we examined the association between these averaged digital phenotypes and the HAMD and DSAS scores recorded on Dd. These diurnal windows and the six-day averaging were applied identically to both actigraphy-derived (micro-movement) and ward-sensor-derived (macro-movement) features, and hours outside these windows (17:00-21:59 and 06:00-08:59) were excluded from diurnal (daytime) and nocturnal (nighttime) analyses by design.

Number of clusters

The number of clusters represents the count of distinct locations within the closed ward where a patient was present during a given hour. It is determined based on the proportion (pi) of time spent in each location (patient room, group therapy room, dining area, and lounge), considering only locations where pi is greater than zero (pi>0).

EN

EN is a metric used to assess the regularity of patients’ time distribution across different location clusters. This measure is based on information theory [31] and is calculated as follows:
EN=i=1Npilogpi.
Let i=1,2,…,N represent the number of clusters, where N is at least 1 and at most 4, corresponding to the total number of location clusters. The variable pi denotes the percentage of time a participant spent in location cluster i within a given hour.
A high EN value indicates that the patient distributed their time uniformly across all location clusters, suggesting regular and stable movement throughout the ward. Conversely, a low EN value suggests an uneven distribution of time, meaning that the patient either spent significantly more time in a specific location or exhibited a highly biased movement pattern.

NE

NE is calculated by dividing EN by its maximum value, which is the logarithm of the total number of clusters. Unlike EN, NE is independent of the number of clusters and more directly reflects the distribution of time across different locations. The value ranges between 0 and 1 [32]:
• A value of 0 indicates that the patient spent all their time in a single location.
• A value of 1 indicates that the patient evenly distributed their time across all clusters.
NE=ENlog(N)

IS

IS quantifies the stability of daily activity levels, assessing how consistent an individual’s activity is across different days [33,34]. A low IS indicates a significant day-to-day irregularity in activity patterns. It is calculated by normalizing actigraphy samples at 24-hour values using the following formula:
IS=h=1pxhx¯2Ni=1Nxix¯2p.
N is the total count of data points collected hourly (in this case maximum of six days); p corresponds to the daily data count, reaching up to 24 per day; xh shows values of each hour from the mean 24-hour profile; xi represents each given hour of raw data; and x - is the mean of all data points.

IV

IV measures the fragmentation of activity patterns within a 24-hour period [33,34]. A high IV value indicates a great alternation between active-rest states, reflecting more fragmented activity rhythms, such as daytime napping or nighttime arousals. It is calculated using the following formula:
IV=i=2Nxixi12Ni=1Nxix¯2(N1).
N is the total count of data points collected hourly (in this case, a maximum of six days), xi represents each given hour of raw data, and x¯ is the mean of all data points.

ISV

ISV represents the balance between the stability of daily activity levels and the fragmentation of activity patterns within a 24-hour period. It provides a unified measure of circadian rhythm integrity, where higher values suggest more structured and stable daily activity, with fewer abrupt transitions between active and inactive states. This may indicate better circadian regulation and healthier behavioral patterns, while lower values indicate more disrupted and fragmented activity, suggesting irregular daily routines and frequent shifts between movement and rest periods. This could be associated with mental health conditions, fatigue, or sleep disturbances.
ISV=ISIV.

Statistical analyses

All statistical analyses were conducted using the R software (version 4.4.1; R Development Core Team).

Daily activity patterns using accelerometer data

We quantified daily activity levels for each patient by calculating the mean SVM value for each day. These daily averages were visualized in a time-series graph to assess the variability in daily physical activity for each individual.

Group differences

Using the HAMD with a cutoff score of 13 [29], we categorized the dataset into two groups: asymptomatic/mild depression (HAMD ≤13, n=11 samples) and moderate/severe depression (HAMD >13, n=7 samples). A linear mixed-effects model (LMM) was applied to compare digital phenotypes reflecting movement regularity (i.e., IS, IV, ISV, EN, and NE) between the two groups. Statistical significance was defined as p<0.05. Because weekly group assignments were based on repeated samples from the same participants, formal comparisons of demographic characteristics between the two groups were not conducted.

Relationship between digital phenotypes and depression

We used Pearson correlation to assess associations between digital phenotypes of movement regularity and depression severity, measured by HAMD and DSAS. To adjust for multiple comparisons, false discovery rate (FDR) correction was applied. Statistically significant correlations (FDR p<0.05) were visualized with scatter plots and regression lines. To quantify uncertainty, 95% confidence intervals for correlation coefficients were calculated using Fisher’s Z transformation (Supplementary Table 1). Additional analyses examined interrelationships among digital features.
Multiple linear regression analyses were conducted with HAMD and DSAS as dependent variables, using digital phenotypes that showed significant Pearson correlations as predictors. Age and length of stay were included as covariates in exploratory regression models. Model assumptions (normality, linearity, independence, multicollinearity, and homoscedasticity) were thoroughly evaluated. Only random intercepts were included in the LMMs, as the small sample size precluded the use of random slopes. Model fit indices (AIC and BIC) and 95% confidence intervals for regression coefficients are reported in Supplementary Table 2.

RESULTS

Demographic and clinical characteristics of the study population

The analysis included 10 participants, consisting of six females and four males, aged 21-60 years, with a mean age of 28.5 years (SD=11.83). Their heights ranged from 159-176 cm, averaging 167.1 cm (SD=6.47), while their weights ranged from 46-93 kg, averaging 70.22 kg (SD=17.91). The dataset, structured in a patient-week format, totaled 18 entries owing to varying amounts of weekly data collected from each patient. Regarding depression assessments, HAMD scores ranged from 0-19, averaging 11.18 (SD=6.22), while DSAS scores ranged from 25-66, averaging 45.33 (SD=9.94). Additional features are listed in Table 2.

Group differences in diurnal micro-movements and nocturnal macro-movements

A LMM was employed to examine differences in digital behavioral features between two patient groups classified by depression severity: asymptomatic/mild depression (HAMD ≤13, n=11) and moderate/severe depression (HAMD >13, n=7). Each model included the digital feature as the dependent variable, depression severity group as a fixed effect, and a random intercept for each participant to account for within-subject variability.
Figure 2 illustrates the group comparisons of statistically significant digital features, showing that IS_day (β=-0.1413, p=0.014) and ISV_day (β=-0.1592, p=0.014) were lower in the moderate/severe depression group than in the asymptomatic/mild depression group, while IV_day (estimate=0.3152, p=0.045), EN_night (β=0.0329, p=0.025), and NE_night (β=0.0491, p=0.018) were higher in the moderate/severe depression group than in the asymptomatic/mild depression group. Table 3 provides a detailed summary of the LMM results, presenting specific statistical values for each digital phenotype.

Correlation of digital phenotypes with depression severity

To investigate the relationship between digital behavioral features and depression severity, Pearson correlation analysis was conducted between HAMD scores and 10 digital activity markers. FDR correction was applied to control for multiple comparisons.
Figure 3 illustrates scatter plots with correlation coefficients (r), unadjusted p-values, and FDR-adjusted p-values for each feature. The analysis identified significant negative correlations for IS_day (r=-0.57, p=0.014, FDR p=0.034) and ISV_day (r=-0.65, p=0.004, FDR p=0.028) and positive correlations for EN_night (r=0.68, p=0.009, FDR p=0.028) and NE_night (r=0.61, p=0.007, FDR p=0.028), indicating that higher depression severity was linked to greater instability in daytime activity and increased randomness in nighttime activity. IV_day showed a moderate correlation with HAMD (r=0.47, p=0.047), and although its FDR-adjusted p-value (FDR p=0.093) was slightly above the significance threshold, it still suggests a potential association with depression severity. No significant correlations were found for IV_day, EN_day, IS_night, IV_night, or ISV_night after FDR correction. Additionally, Pearson correlation analysis between DSAS and digital behavioral features did not reveal any statistically significant associations.
We conducted exploratory multiple linear regression analyses to examine associations between digital phenotypes derived from actigraphy and ward-location data and depression severity (HAMD, DSAS). Eleven regression models were constructed, each incorporating an actigraphy-derived variable and a location variable. The results of these models are summarized in Table 4. Among the 11 models, the most explanatory model was NE_night+IS_day, with an adjusted R2 of 0.606, indicating that this combination accounted for approximately 60.6% of the variance in HAMD scores. A comparable model as regards explanatory power was EN_night+IS_day, with an adjusted R2 of 0.602. Across all models, EN_night and NE_night were consistently identified as significant independent variables (p<0.05), indicating a strong association between nighttime activity patterns and depression severity. In contrast, IS_day and ISV_day were significant in some models, suggesting that the stability and variability of daytime mobility contribute to depression severity to a low extent. Moreover, the low explanatory power (adjusted R2 values, 0.159-0.282) and the lack of significant predictors suggest that DSAS may not have a strong association with digital activity patterns in this sample.
A correlation analysis across digital behavioral features revealed several significant relationships. As expected, ISV_day and IS_day (r=0.82, p<0.001); ISV_night and IS_day (r=0.52, p<0.05); ISV_night and IV_night (r=-0.77, p<0.001); ISV_day and IV_day (r=-0.81, p<0.001); ISV_night and IV_night (r=-0.77, p<0.001); and NE_day and EN_day (r=0.99, p<0.001) were strongly correlated, which is unsurprising given that ISV represents the ratio of IS and IV, and NE_night is a normalized version of EN_night. A significant correlation was also found between IS_night and IV_day (r=-0.52, p<0.05) and IV_night and IS_day (r=-0.55, p<0.05). Figure 4 presents the Pearson correlation matrix, illustrating these relationships among digital phenotypes.

DISCUSSION

In this preliminary feasibility study using exploratory models, digital markers of movement regularity were associated with clinician-rated depression. We investigated how behavioral regularity, as measured by digital phenotypes, reflects depression severity in psychiatric inpatients. We found that the diurnal micro-movements obtained from actigraphy-based data and the nocturnal macro-movements obtained from location data effectively explained disturbances in depression, suggesting their potential as digital correlates. Moreover, these digital indicators showed more pronounced differences in patients with moderate/severe depression, indicating that they may be particularly meaningful in an inpatient population with more severe depressive symptoms, rather than in outpatient settings. Consequently, assessing behavioral patterns through digital monitoring not only addresses the limitations of traditional monitoring but offers a more continuous and objective method to closely observe patients, supporting its role as a valuable explanatory measure for depression.
We collected data from 10 inpatients in a psychiatric ward, totaling 18 sets of samples. These participants presented with various psychiatric conditions, including schizophrenia, psychosis, brief psychotic disorder, bipolar I disorder, bipolar II disorder, and adjustment disorder. Focusing on inpatients with more severe symptoms allowed for a very in-depth investigation of their clinical status within a controlled environment, minimizing the influence of individual lifestyles and diverse external settings. Moreover, by encompassing patients with a range of diagnoses, this study captured processes that extend beyond a single diagnostic label, leveraging the strengths of transdiagnostic methodologies. Given that depressive symptoms and behavioral irregularities are frequently observed across multiple psychiatric disorders [35-37], our broad approach enhances the scope of mental health research.
While actigraphy and location data are considered the gold standard for assessing movement in digital health [18,38,39], our approach emphasized the regularity in each dataset by integrating both data types. This multimodal strategy addressed limitations inherent to studies that focused on a single source [40]. Beyond reliance on a single wearable device, we incorporated wireless ward sensors, thereby mitigating issues such as false alarms and discrepancies in wrist-actigraphy measurements. This approach facilitated more effective long-term monitoring [23,41,42]. Moreover, the digital indicators demonstrated stronger correlations with the HAMD. These findings illustrate the interoperability between device-derived data and data from clinical evaluation, highlighting the potential of digital devices to mitigate biases such as the overestimation and underestimation commonly associated with self-reported measures [12,43-45]. Since traditional monitoring methods rely on staff patrols and CCTV [9], remote sensing can offer a valuable alternative for managing patients and alleviating the constraints of conventional surveillance. Finally, by utilizing two distinct data sources, we could evaluate both macro- and micro-level movements. The ward sensors that collect location data via wireless sensors provided insight into patients’ macro-level movements (how they physically walk to specified ward locations), while wrist-worn accelerometers captured micro-level activity patterns. This two-tiered approach provided a comprehensive interpretation of movement behavior, which offered insights from a broad and granular perspective, further enhancing our understanding of depressive symptoms.
We focused on movement regularity for two primary reasons. First, as shown in Figure 1, no significant consistent movement patterns emerged, and individual data fluctuated continuously, indicating a lack of daily activity regularity. The six-day data extraction period varied among participants, resulting in differences in the number of weekend days included. Moreover, simply averaging activity levels over 6 days can be directly influenced by reduced activity due to medication, and baseline activity levels may vary substantially among patients. Hence, raw averages of SVM values can fail to accurately reflect each patient’s condition. To address these challenges, we adopted the IS and IV concepts to quantify the regularity and fragmentation of activity levels, rather than relying solely on raw averages.
For location data, unlike previous studies, we conducted our research in a closed psychiatric ward where movement was highly restricted, limited to four predefined clusters. To track behavioral changes within these clusters, we applied the EN concept, allowing an assessment of patients’ movement regularity beyond mere location proportions. Through these indicators of behavioral patterns, we aimed to determine how stable and regular activity levels influence depression severity. Additionally, because daytime and nighttime activity patterns significantly differed, leading to compensatory effects in overall measures, we divided the analysis into diurnal and nocturnal phases for a more nuanced evaluation.
We identified five key variables that effectively capture behavioral regularity and its relationship to depression severity: IS_day, ISV_day, IV_day, EN_night, and NE_night. ISV is of particular interest, as it represents the ratio between IS and IV, underscoring the significance of both stability and fragmentation in movement regularity. Through LMM analysis, we observed significant differences in these variables between the asymptomatic/mild depression group (HAMD ≤13) and the moderate/severe depression group (HAMD >13). Notably, all five variables showed consistent differences between these groups, suggesting that individuals with greater depression severity exhibit more fragmented, irregular daytime activity rhythms and increased randomness in nighttime activity. Therefore, movement regularity across temporal scales (day and night) showed a stronger association with individuals experiencing more severe depression. Furthermore, Pearson correlation analysis indicated that these five variables align with previous research linking them to depression severity [22]. The classification into daytime and nighttime showed that more severe depression correlates with greater daytime behavioral instability and heightened nighttime activity; however, DSAS scores did not significantly relate to these digital markers.
Additionally, our correlation analysis revealed that the digital phenotypes representing micro-movements are interrelated, indicating that regularity and fragmentation are intertwined elements of movement behavior. The correlation coefficients between IV_night and IS_day, as well as IV_day and IS_night, were particularly noteworthy. One tentative interpretation is that relatively stable sleep patterns may be accompanied by larger daytime activity fluctuations, whereas irregular nighttime behavior may co-occur with differences in the perceived structure of daytime patterns. However, this remains speculative, necessitating further research to clarify the precise relationship between IV and IS.
In multiple regression, a model incorporating EN_night and IS_day accounted for 63% of the variance in HAMD scores (in-sample explanatory capacity). These results suggest that nighttime activity variability and daytime mobility stability can serve as vital digital markers for assessing depression severity in inpatient psychiatric settings. When comparing our regression findings with self-reported measures, we found that digital phenotypes correlated more strongly with clinician-administered assessments than with self-report scales, suggesting that digital monitoring may provide a more objective evaluation of the depressive states of patients. This may in turn help compensate for the discontinuity inherent in clinician-associated assessments and serve as a valuable adjunct tool in clinical practice.
This study has some limitations. First, the small sample size (10 patients, 18 samples) substantially limits statistical power and reduces the stability of correlation and regression estimates. Consequently, these findings should be regarded as preliminary and exploratory, intended primarily for hypothesis generation rather than confirmatory inference. To illustrate uncertainty, 95% confidence intervals for key associations and regression coefficients are reported in Supplementary Tables 1 and 2. The limited sample also restricted the inclusion of potential confounders, such as diagnosis and medication use, and precluded a meaningful post hoc power calculation given the complexity of the mixed-effects modeling approach. These constraints underscore the need for larger, more homogeneous cohorts and longitudinal designs to confirm these findings and improve generalizability.
Second, the SVM values obtained from accelerometer data were averaged hourly for each patient and used to calculate IS and IV. As these hourly averages occasionally contained missing data, errors arose in calculating IS and IV, particularly when large gaps existed between measurements. Such gaps complicate the accurate depiction of movement regularity (including stability or variability) by obscuring potential fluctuations in the data.
Third, we defined four clusters and categorized all other locations as “others.” However, this classification caused several challenges. When “others” reached 100%, it was treated as missing data, since EN was calculated solely from the four predefined clusters. This approach made it difficult to accurately capture behavioral regularity. For instance, a patient who consistently visits non-clustered spaces, such as the bathroom or hallway, should theoretically display high EN, yet those locations were labeled as “others,” resulting in EN exclusions or a zero value for missing data. Furthermore, if a patient occasionally removed their watch while sleeping outside the designated patient room, thereby generating hours of “others” at 100%, those hours also became missing from EN calculations.
Nevertheless, defining “others” yielded practical benefits in resolving technical issues. Occasionally, sensor signals showed overlapping location errors within the same room, depending on the bed position, or recorded multiple areas simultaneously during nighttime when patients were expected to remain in their rooms, likely owing to technical or data transmission errors. As interpreting movement regularity under these conditions proved difficult, we excluded “others” from the predefined clusters and refrained from attaching specific meanings to each cluster. The calculation of EN as a digital phenotype remained unaffected because the majority of signals overlapping with the patient room were registered as “others.” When computing EN, we recalculated the percentage of time spent in each cluster (excluding “others”) and derived an adjusted EN value, thus addressing data overlap.
Although continuous monitoring of depressive symptoms through digital tools offers a longitudinal approach that captures evolving data over time and accommodates temporal relationships, it remains insufficient for definitively establishing causality or encompassing all facets of depression. Moreover, the best way to process raw digital data into a valid, explanatory phenotype remains unclear. Whether the current indicators, particularly those derived from an average of six days, truly reflect real-time movement patterns is also open to question. While correlations between digital phenotypes and depression severity have been identified, future studies should refine these indicators and employ more rigorous designs to discern causal relationships. Consequently, further research is warranted to validate continuous digital monitoring as a practical tool, particularly in larger, more homogeneous samples and longitudinal frameworks, to generalize its use in populations with depression.
Despite these limitations, the present findings provide a concrete foundation for translating digital phenotyping into real-world psychiatric care. Circadian rhythm has long been recognized as a central mechanism in mood regulation, with interventions such as light therapy and structured daily routines demonstrating therapeutic efficacy [46,47]. In this context, our digital indices of daytime macro-movement and nighttime micro-movement regularity may serve as behavioral proxies of circadian stability. Leveraging these features for clinical use could open pathways to rhythm-based interventions that are tailored to individual patterns.
Building upon these implications, our dual-level approach—capturing both macro- and micro-level regularity—offers a unique contribution to the field of digital psychiatry. In practical terms, these metrics could be incorporated into real-time monitoring platforms for psychiatric inpatients. For example, nursing staff could receive automated alerts when a patient exhibits a sudden drop in daytime regularity (e.g., IS_day) or an unexpected increase in nighttime EN (e.g., EN_night). Such threshold-based alert systems may facilitate earlier detection of clinical deterioration, reduce monitoring burden, and enable more consistent, personalized care. While specific cutoff values and predictive thresholds remain to be validated in larger studies, the implementation of such tools holds promise for enhancing inpatient psychiatric care through data-driven, individualized decision support.
Despite promising findings, challenges remain in translating digital phenotyping into psychiatric practice. In particular, future research should validate the reliability and clinical utility of behavioral regularity derived from macro- and micro-level movement data. This study underscores the clinical potential of digital phenotyping in psychiatry by integrating macro- and micro-level behavioral regularity. Together, these results underscore the clinical potential of dual-level digital monitoring and suggest a path toward future diagnostic precision and individualized psychiatric intervention.

Supplementary Materials

The Supplement is available with this article at https://doi.org/10.30773/pi.2025.0130.
Supplementary Table 1.
Correlations between digital movement variables and HAMD scores with 95% CIs and FDR-adjusted pvalues
pi-2025-0130-Supplementary-Table-1.pdf
Supplementary Table 2.
Multiple regression models predicting HAMD scores based on movement regularity metrics, including 95% CIs, AIC, and BIC
pi-2025-0130-Supplementary-Table-2.pdf

Notes

Availability of Data and Material

The datasets generated or analyzed during the study are not publicly available due to ethical, legal, and privacy restrictions.

Conflicts of Interest

JungSun Lee, a contributing editor of the Psychiatry Investigation, was not involved in the editorial evaluation or decision to publish this article. All remaining authors have declared no conflicts of interest.

Author Contributions

Conceptualization: Jaewook Shin, JungSun Lee, Sung Woo Joo. Data curation: Jaewook Shin, JungSun Lee, Hyeon Gyu Park, Hamin Lim, Hangsik Shin. Formal analysis: Jaewook Shin, JungSun Lee. Supervision: JungSun Lee. Writing—original draft: Jaewook Shin. Writing—review & editing: Jaewook Shin, JungSun Lee, Sun Min Kim, Hyeon Gyu Park, Ji Hyu Park, Sung Woo Joo.

Funding Statement

This work was supported by the Korea Health Technology R&D Project through the Korea Health Industry Development Institute (KHIDI), funded by the Ministry of Health and Welfare, Republic of Korea (Grant No. HI22C1668, awarded to JL).

Acknowledgments

None

Figure 1.
Time-series trends of daily activity using sum of vector magnitude (SVM). The graph illustrates the daily mean SVM derived from hourly actigraphy measurements for individual patients throughout their hospitalization period. The x-axis represents the absolute number of days since admission, while the y-axis denotes the daily mean SVM, reflecting overall activity levels.
pi-2025-0130f1.jpg
Figure 2.
Group comparisons of significant digital behavioral features based on depression severity using a linear mixed-effects model. Comparison of digital phenotypes between two groups classified by depression severity: asymptomatic/mild depression (HAMD ≤13; red) and moderate/severe depression (HAMD >13; blue). Boxes extend between 25th and 75th percentiles, and solid lines inside the boxes are medians. *shows significant differences at p<0.05. IS, interdaily stability; IV, intradaily variability; ISV, ratio of IS to IV; EN, entropy; NE, normalized entropy; HAMD, Hamilton Depression Rating Scale.
pi-2025-0130f2.jpg
Figure 3.
Scatterplots of digital phenotypes correlated with depression severity using the HAMD. Scatter plots for digital phenotypes versus HAMD scores. The coefficient of correlation between each feature and HAMD scores, along with its corresponding p-value and FDR-adjusted p-value, is displayed at the top of each plot. A blue trend line represents the linear regression fit, illustrating the direction and strength of the relationship. A gray-shaded area around the trend line indicates the confidence interval, reflecting the uncertainty of the estimated regression line. The trend line and confidence interval are shown only for significant variables. HAMD, Hamilton Depression Rating Scale; FDR, false discovery rate; IS, interdaily stability; IV, intradaily variability; ISV, ratio of IS to IV; EN, entropy; NE, normalized entropy.
pi-2025-0130f3.jpg
Figure 4.
Pearson correlation matrix of digital features: coefficients of correlation between digital features. *p<0.05; ***p<0.001. IS, interdaily stability; IV, intradaily variability; ISV, ratio of IS to IV; EN, entropy; NE, normalized entropy.
pi-2025-0130f4.jpg
Table 1.
Abbreviations and definitions of digital phenotypes
Abbreviation Term Definition
IS Interdaily stability Quantifies the stability of daily activity levels by comparing the consistency of 24-hour activity patterns across days. A higher IS indicates a more regular and stable daily routine.
IV Intradaily variability Measures the fragmentation of activity within a 24-hour period. A higher IV reflects frequent transitions between active and resting states, indicating more erratic rhythms.
ISV Ratio of IS to IV Ratio between IS and IV. A higher ISV suggests better circadian regularity, with more stable and less fragmented activity patterns.
EN Entropy Captures the randomness in time spent across predefined ward locations (excluding “others”). Higher EN implies more spatially distributed and diverse movement.
NE Normalized entropy EN normalized by the maximum possible entropy given the number of locations. It ranges from 0 to 1, where 1 indicates uniform time distribution across visited locations.
Table 2.
Demographic and clinical characteristics of the study population
Variable Value
Demographics
 Number of participants 10
 Age (yr) 28.5±11.83
 Male 4 (40.0)
Clinical characteristics
 Length of stay (day) 18 (7-28.5)
 Observation period (day) 6 (3-15)
Primary psychiatric diagnosis
 Schizophrenia spectrum disorder
  Psychosis 2 (20.0)
  Brief psychosis 1 (10.0)
  Schizophrenia 1 (10.0)
 Bipolar and related disorder
  Bipolar I disorder 4 (40.0)
  Bipolar II disorder 1 (10.0)
 Neurosis
  Adjustment disorder 1 (10.0)
Depression scales
 HAMD 11.18±6.22
 DSAS 45.33±9.94

Values are presented as number only, mean±standard deviation, or median (interquartile range). HAMD, Hamilton Depression Rating Scale; DSAS, Dysfunctional Self-focus Attributes Scale.

Table 3.
Classification of participants with asymptomatic/mild and moderate/severe depressive symptoms and comparison of digital phenotypes
Group
Statistic
HAMD ≤13 (N=11) HAMD >13 (N=7) Estimate (β) Standard error p
Actigraphy-based
 IS_day 0.518±0.076 0.384±0.141 -0.1413 0.0508 0.014
 IS_night 0.441±0.183 0.444±0.066 0.0021 0.0728 0.978
 IV_day 1.410±0.305 1.720±0.289 0.3152 0.1445 0.045
 IV_night 1.290±0.416 1.250±0.523 -0.0387 0.2233 0.865
 ISV_day 0.390±0.127 0.231±0.106 -0.1592 0.0578 0.014
 ISV_night 0.380±0.177 0.413±0.184 0.0345 0.0833 0.684
Location-based
 EN_day 0.304±0.061 0.300±0.140 0.0240 0.0373 0.531
 EN_night 0.025±0.026 0.066±0.028 0.0329 0.0133 0.025
 NE_day 0.375±0.068 0.372±0.165 0.0204 0.0450 0.658
 NE_night 0.034±0.036 0.094±0.040 0.0491 0.0186 0.018

IS, interdaily stability; IV, intradaily variability; ISV, ratio of IS to IV; EN, entropy; NE, normalized entropy; HAMD, Hamilton Depression Rating Scale.

Table 4.
Linear regression model associating severity of depression using Hamilton Depression Rating Scale scores
Regression model Statistic
β1 β2 p Adjusted R²
EN_night+IS_day 102.609 -26.483 0.002 0.602
EN_night+ISV_day 81.270 -21.026 0.006 0.536
EN_night+IV_day 79.158 4.237 0.048 0.344
EN_night 93.135 0.031 0.344
NE_night+IS_day 72.764 -26.257 0.002 0.606
NE_night+ISV_day 58.393 -20.989 0.006 0.543
NE_night+IV_day 57.014 4.209 0.045 0.352
NE_night 66.730 0.028 0.351
IS_day -23.875 0.037 0.325
ISV_day -23.618 0.021 0.379
IV_day 6.824 0.088 0.227

IS, interdaily stability; IV, intradaily variability; ISV, ratio of IS to IV; EN, entropy; NE, normalized entropy.

REFERENCES

1. Collier S, Monette P, Hobbs K, Tabasky E, Forester BP, Vahia IV. Mapping movement: applying motion measurement technologies to the psychiatric care of older adults. Curr Psychiatry Rep 2018;20:64
crossref pmid pdf
2. Depp CA, Bashem J, Moore RC, Holden JL, Mikhael T, Swendsen J, et al. GPS mobility as a digital biomarker of negative symptoms in schizophrenia: a case control study. NPJ Digit Med 2019;2:108
crossref pmid pmc pdf
3. Difrancesco S, Penninx BWJH, Riese H, Giltay EJ, Lamers F. The role of depressive symptoms and symptom dimensions in actigraphy-assessed sleep, circadian rhythm, and physical activity. Psychol Med 2022;52:2760-2766.
crossref pmid pmc
4. Merikangas KR, Swendsen J, Hickie IB, Cui L, Shou H, Merikangas AK, et al. Real-time mobile monitoring of the dynamic associations among motor activity, energy, mood, and sleep in adults with bipolar disorder. JAMA Psychiatry 2019;76:190-198.
crossref pmid pmc
5. Schelde JT. Major depression: behavioral markers of depression and recovery. J Nerv Ment Dis 1998;186:133-140.
crossref pmid
6. Zhu X, Haegele JA, Healy S. Movement and mental health: behavioral correlates of anxiety and depression among children of 6-17 years old in the U.S. Ment Health Phys Act 2019;16:60-65.
crossref
7. Kim J. The research gap in evaluating community-based mental health interventions in Korea: a comparative analysis with the United Kingdom. Asian J Psychiatr 2025;103:104348
crossref pmid
8. Lee MS, Hoe M, Hwang TY, Lee YM. Service priority and standard performance of community mental health centers in South Korea: a delphi approach. Psychiatry Investig 2009;6:59-65.
crossref pmid pmc
9. Ray R, Perkins E, Meijer B. The evolution of practice changes in the use of special observations. Arch Psychiatr Nurs 2011;25:90-100.
crossref pmid
10. Pavlova B, Uher R. Assessment of psychopathology: is asking questions good enough? JAMA Psychiatry 2020;77:557-558.
crossref pmid
11. Hong M, Kang RR, Yang JH, Rhee SJ, Lee H, Kim YG, et al. Comprehensive symptom prediction in inpatients with acute psychiatric disorders using wearable-based deep learning models: development and validation study. J Med Internet Res 2024;26:e65994
crossref pmid pmc
12. Solhan MB, Trull TJ, Jahng S, Wood PK. Clinical assessment of affective instability: comparing EMA indices, questionnaire reports, and retrospective recall. Psychol Assess 2009;21:425-436.
crossref pmid pmc
13. Iozzino L, Ferrari C, Large M, Nielssen O, de Girolamo G. Prevalence and risk factors of violence by psychiatric acute inpatients: a systematic review and meta-analysis. PLoS One 2015;10:e0128536
crossref pmid pmc
14. Olofsson B, Jacobsson L. A plea for respect: involuntarily hospitalized psychiatric patients’ narratives about being subjected to coercion. J Psychiatr Ment Health Nurs 2001;8:357-366.
crossref pmid pdf
15. Bech P. Rating scales in depression: limitations and pitfalls. Dialogues Clin Neurosci 2006;8:207-215.
crossref pmid pmc
16. Needham I, Abderhalden C, Halfens RJ, Fischer JE, Dassen T. Non-somatic effects of patient aggression on nurses: a systematic review. J Adv Nurs 2005;49:283-296.
crossref pmid
17. Appelboom G, Camacho E, Abraham ME, Bruce SS, Dumont EL, Zacharia BE, et al. Smart wearable body sensors for patient self-assessment and monitoring. Arch Public Health 2014;72:28
crossref pmid pmc pdf
18. De Angel V, Lewis S, White K, Oetzmann C, Leightley D, Oprea E, et al. Digital health tools for the passive monitoring of depression: a systematic review of methods. NPJ Digit Med 2022;5:3
pmid pmc
19. Yan B, Zhao B, Jin X, Xi W, Yang J, Yang L, et al. Sleep efficiency may predict depression in a large population-based study. Front Psychiatry 2022;13:838907
crossref pmid pmc
20. Moshe I, Terhorst Y, Opoku Asare K, Sander LB, Ferreira D, Baumeister H, et al. Predicting symptoms of depression and anxiety using smartphone and wearable data. Front Psychiatry 2021;12:625247
crossref pmid pmc
21. Ho FY, Poon CY, Wong VW, Chan KW, Law KW, Yeung WF, et al. Actigraphic monitoring of sleep and circadian rest-activity rhythm in individuals with major depressive disorder or depressive symptoms: a meta-analysis. J Affect Disord 2024;361:224-244.
crossref pmid
22. Saeb S, Zhang M, Karr CJ, Schueller SM, Corden ME, Kording KP, et al. Mobile phone sensor correlates of depressive symptom severity in daily-life behavior: an exploratory study. J Med Internet Res 2015;17:e175
crossref pmid pmc
23. Hickey BA, Chalmers T, Newton P, Lin CT, Sibbritt D, McLachlan CS, et al. Smart devices and wearable technologies to detect and monitor mental health conditions and stress: a systematic review. Sensors (Basel) 2021;21:3461
crossref pmid pmc
24. Canali S, Schiaffonati V, Aliverti A. Challenges and recommendations for wearable devices in digital health: data quality, interoperability, health equity, fairness. PLOS Digit Health 2022;1:e0000104
crossref pmid pmc
25. Stuart T, Hanna J, Gutruf P. Wearable devices for continuous monitoring of biosignals: challenges and opportunities. APL Bioeng 2022;6:021502
crossref pmid pmc pdf
26. Difrancesco S, Lamers F, Riese H, Merikangas KR, Beekman ATF, van Hemert AM, et al. Sleep, circadian rhythm, and physical activity patterns in depressive and anxiety disorders: a 2-week ambulatory assessment study. Depress Anxiety 2019;36:975-986.
crossref pmid pmc pdf
27. Kim H, Lee HJ. [Development and validation of dysfunctional self-focus attributes scale]. Kor J Clin Psychol 2012;31:487-505. Korean.
crossref
28. Kaiser RH, Snyder HR, Goer F, Clegg R, Ironside M, Pizzagalli DA. Attention bias in rumination and depression: cognitive mechanisms and brain networks. Clin Psychol Sci 2018;6:765-782.
crossref pmid pmc pdf
29. Hamilton M. Development of a rating scale for primary depressive illness. Br J Soc Clin Psychol 1967;6:278-296.
crossref pmid
30. Lee PMY, Huang B, Liao G, Chan CK, Tai LB, Tsang CYJ, et al. Changes in physical activity and rest-activity circadian rhythm among Hong Kong community aged population before and during COVID-19. BMC Public Health 2021;21:836
crossref pmid pmc pdf
31. Shannon CE. The mathematical theory of communication. 1963. MD Comput 1997;14:306-317.
pmid
32. Saeb S, Lattie EG, Schueller SM, Kording KP, Mohr DC. The relationship between mobile phone location sensor data and depressive symptom severity. PeerJ 2016;4:e2537
crossref pmid pmc pdf
33. Makarem N, German CA, Zhang Z, Diaz KM, Palta P, Duncan DT, et al. Rest-activity rhythms are associated with prevalent cardiovascular disease, hypertension, obesity, and central adiposity in a nationally representative sample of US adults. J Am Heart Assoc 2024;13:e032073
crossref pmid
34. Rykov Y, Thach TQ, Bojic I, Christopoulos G, Car J. Digital biomarkers for depression screening with wearable devices: cross-sectional study with machine learning modeling. JMIR Mhealth Uhealth 2021;9:e24872
crossref pmid pmc
35. Buckley PF, Miller BJ, Lehrer DS, Castle DJ. Psychiatric comorbidities and schizophrenia. Schizophr Bull 2009;35:383-402.
crossref pmid pmc
36. Noyes R Jr. Comorbidity in generalized anxiety disorder. Psychiatr Clin North Am 2001;24:41-55.
crossref pmid
37. Xu YM, Li F, Liu XB, Zhong BL. Depressive symptoms in Chinese male inpatients with schizophrenia: prevalence and clinical correlates. Psychiatry Res 2018;264:380-384.
crossref pmid
38. Niemeijer K, Mestdagh M, Kuppens P. Tracking subjective sleep quality and mood with mobile sensing: multiverse study. J Med Internet Res 2022;24:e25643
crossref pmid pmc
39. Breasail MÓ, Biswas B, Smith MD, Mazhar MKA, Tenison E, Cullen A, et al. Wearable GPS and accelerometer technologies for monitoring mobility and physical activity in neurodegenerative disorders: a systematic review. Sensors (Basel) 2021;21:8261
crossref pmid pmc
40. Kang SJ, Leroux A, Guo W, Dey D, Strippoli MF, Di J, et al. Integrative modeling of accelerometry-derived sleep, physical activity, and circadian rhythm domains with current or remitted major depression. JAMA Psychiatry 2024;81:911-918.
crossref pmid pmc
41. Brennan G, Flood C, Bowers L. Constraints and blocks to change and improvement on acute psychiatric wards--lessons from the City Nurses project. J Psychiatr Ment Health Nurs 2006;13:475-482.
crossref pmid
42. Clifton L, Clifton DA, Pimentel MA, Watkinson PJ, Tarassenko L. Predictive monitoring of mobile patients by combining clinical observations with data from wearable sensors. IEEE J Biomed Health Inform 2014;18:722-730.
crossref pmid
43. Gurrin C, Smeaton AF, Doherty AR. Lifelogging: personal big data. Foundations and Trends® in Information Retrieval 2014;8:1-125.
crossref pdf
44. Hsin H, Fromer M, Peterson B, Walter C, Fleck M, Campbell A, et al. Transforming psychiatry into data-driven medicine with digital measurement tools. NPJ Digit Med 2018;1:37
crossref pmid pmc pdf
45. Oudin A, Maatoug R, Bourla A, Ferreri F, Bonnot O, Millet B, et al. Digital phenotyping: data-driven psychiatry to redefine mental health. J Med Internet Res 2023;25:e44502
crossref pmid pmc
46. McClung CA. Circadian rhythms and mood regulation: insights from pre-clinical models. Eur Neuropsychopharmacol 2011;21 Suppl 4:S683-S693.
crossref pmid pmc
47. Blume C, Garbazza C, Spitschan M. Effects of light on human circadian rhythms, sleep and mood. Somnologie (Berl) 2019;23:147-156.
crossref pmid pmc pdf


ABOUT
AUTHOR INFORMATION
ARTICLE CATEGORY

Browse all articles >

BROWSE ARTICLES
Editorial Office
#522, G-five Central Plaza, 27 Seochojungang-ro 24-gil, Seocho-gu, Seoul 06601, Korea
Tel: +82-2-537-6171  Fax: +82-2-537-6174    E-mail: psychiatryinvest@gmail.com                

Copyright © 2026 by Korean Neuropsychiatric Association.

Developed in M2PI

Close layer
prev next