Abstract
This study investigated the link between pre-stroke and acute-stage physical activity (PA) and sedentary behavior. Forty individuals with stroke (aged 73.6 ± 8.9 years) were enrolled. Post-stroke activity, including metabolic equivalents (METs), sedentary behavior, light PA, and moderate-to-vigorous PA (MVPA), was measured using a tri-axial accelerometer (ActiGraph wGT3X-BT) over 11 consecutive days starting from the 4th day post-stroke. Pre-stroke PA levels were assessed using the International Physical Activity Questionnaire (IPAQ). We measured skeletal muscle mass index (SMI) and phase angle using a bioelectrical impedance analyzer (Inbody S10) upon admission. Physical therapists assessed the Brunnstrom recovery stage (BRS) within 3 days post-stroke. Total daily activity averaged 1.05 ± 0.05 METs. Throughout the day, 91.2 ± 5.1, 7.6 ± 4.1, and 1.2 ± 1.3% was spent in sedentary behavior, light PA, and MVPA, respectively. Only pre-stroke PA was independently associated with METs (β = 0.66), sedentary behavior (β = −0.58), light PA (β = 0.50), and MVPA (β = 0.71) after adjusting for age, sex, stroke severity, and activities of daily living. This suggests that pre-stroke PA might play a crucial role in reducing sedentary behavior and promoting PA during the acute phase.
Introduction
Physical activity (PA) is a crucial, modifiable factor that influences not only long-term physical function1 but also life expectancy2 in survivors of stroke. During the acute phase, increasing PA through early mobilization during hospitalization can contribute to improved functional outcomes post-stroke3,4,5. A previous study using behavior mapping to monitor individuals with stroke every 10 min for 24 h, showed that they spent > 80% of their time either resting in bed or sitting out of bed in the stroke care unit6. A recent investigation into 24-h activity in the stroke care unit during the 1st week post-stroke employing accelerometers, demonstrated that the majority of the day (> 90%) was spent engaging in sedentary behavior (energy expenditure of ≤ 1.5 metabolic equivalents [METs])7.
To provide more effective rehabilitation for individuals with acute stroke, identifying the individual factors associated with PA during the acute phase is crucial. Although PA in stroke survivors living in the community is generally, lower than that in healthy older individuals8, a consensus exists that increasing PA after stroke offers health benefits and reduces stroke recurrence9,10. A recent review reported that PA was strongly associated with physical function in community-dwelling stroke survivors11. Therefore, hypothesizing that motor function with paralysis and muscle composition might affect PA during the acute post-stroke period. However, it remains unclear which individual patient factors are associated with PA in the acute phase, where medical issues often hinder PA and its compensation relies on medical staff.
High levels of pre-stroke PA are linked to a reduced stroke severity and improved of long-term functional outcomes12,13,14,15. Although stroke severity is a factor directly related to functional outcomes, higher pre-stroke PA is associated with better long-term outcomes, even when corrected for stroke severity at onset15. In other words, PA before stroke includes some factors that improve the outcomes in addition to reducing stroke severity. Higher PA in the acute phase after a stroke leads to enhanced functional outcomes3,4,5. If pre-stroke PA promotes post-stroke PA, the relationship between pre-stroke PA and long-term functional outcomes could be clarified more accurately. However, no study has examined the relationship between pre- and post-stroke PA during the acute phase.
This study aimed to investigate the relationships between post-stroke PA and sedentary behavior in the acute phase and patient characteristics such as pre-stroke PA, physical function at stroke onset, and musculoskeletal status on admission. We hypothesized that higher pre-stroke PA would be related to more time engaged in PA and less sedentary time in acute phase of stroke. Furthermore, we also anticipated that better physical function and musculoskeletal status would correlate with high-intensity PA.
Results
Participant characteristics
Among all patients hospitalized for stroke during the study period, 46 participants meeting the inclusion criteria were enrolled in this study. Six participants were excluded due to insufficient accelerometer measurement (< 7 days) resulting from early discharge or transfer to another convalescent rehabilitation hospital within the 1st week. Therefore, 40 participants were enrolled in the present study. Participants’ characteristics are shown in Table 1.
Characteristics of post-stroke activity
As an indicator of compliance with post-stroke activity measurements, participants averaged 10.0 ± 1.4 days with the accelerometer within the 11-day period, amounting to an average of 1269.5 ± 148.9 min/day out of the total 1440 min. These findings suggested a high compliance rate with the 24-h accelerometer measurements.
The average total activity amounted to 1.05 ± 0.05 METs/day. The mean percentage and variability of each activity intensity per day is shown in Fig. 1. Sedentary behavior was significantly longer during the first 5 days compared with the subsequent 5 days (91.5 ± 5.7% vs. 90.6 ± 4.9%, p = 0.01); on weekends compared with weekdays (91.8 ± 5.1% vs. 91.0 ± 5.1%, p < 0.01); and during the night compared with the morning, afternoon, and evening (93.3 ± 3.5% vs. 89.6 ± 8.0%, 89.7 ± 6.4%, and 90.5 ± 6.8%, p < 0.01, p < 0.01, and p < 0.01). Light PA was significantly lower on weekends compared with weekdays (7.2 ± 4.0% vs. 7.8 ± 4.2%, p < 0.01); and in the night compared with the morning, afternoon, and evening (6.4 ± 3.3% vs. 8.4 ± 6.3%, 8.4 ± 4.8%, and 8.4 ± 5.6%, p = 0.01, p < 0.01, and p < 0.01). Moderate-to-vigorous PA (MVPA) was significantly lower on the first 5 days compared with the subsequent 5 days (0.9 ± 1.3% vs. 1.7 ± 1.7%, p < 0.01); on weekends compared with weekdays (1.0 ± 1.3% vs. 1.3 ± 1.3%, p = 0.02); and during the night compared with the morning, afternoon, and evening (0.4 ± 0.4% vs. 2.0 ± 2.1%, 1.9 ± 2.0%, and 1.0 ± 1.5%, p < 0.01, p < 0.01, and p < 0.01).

Sedentary behavior and physical activity. (A) Average percentage of sedentary behavior and physical activity for 11 days. Comparisons include: (B) between the first 5 days (4th to 8th day from stroke onset) and the subsequent 5 days (10th to 14th day); (C) between weekdays and weekends; (D) between morning (7:00–12:00), afternoon (12:00–17:00), evening (17:00–22:00), and night (22:00–7:00). *Denotes a significant difference between day 4–8 and day 10–14 or between weekdays and weekends (p < 0.05). The letters “a”, “b”, and “c” represent significant difference from morning, afternoon, and evening, respectively (p < 0.05). PA: Physical activity, MVPA: Moderate to vigorous physical activity.
Multiple regression analysis for sedentary behavior and PA
Table 2 presents the results of the multiple linear regression analysis. Pre-stroke PA assessed by the International Physical Activity Questionnaire (IPAQ), skeletal muscle mass index (SMI), and Brunnstrom recovery stage (BRS) independently correlated with METs/day (model 1). After adjusting for age, sex, the National Institutes of Health Stroke Scale (NIHSS), and the Functional Independence Measure (FIM) motor score, a higher pre-stroke PA time per week was associated with the daily average of METs after the stroke (model 2). Only pre-stroke PA was independently associated with sedentary behavior and light PA (model 1). Pre-stroke PA and BRS were independently associated with MVPA (model 1). After adjustment, higher pre-stroke PA was associated with shorter sedentary behavior, longer light PA, and greater MVPA time (model 2). Scatterplots illustrating the relationship between pre- and post-stroke PA are displayed in Fig. 2.

The relationships of physical activity between before and after stroke. The scatterplots illustrate the correlations between METs-min/week calculated from IPAQ and (A) total activity (METs/day); (B) % in sedentary; (C) % in light PA; (D) % in MVPA. METs: Metabolic equivalents, IPAQ: International Physical Activity Questionnaire, PA: Physical activity, MVPA: Moderate to vigorous physical activity.
Discussion
In our study, we used a tri-axial accelerometer to measure total activity (METs), sedentary behavior, light PA, and MVPA in individuals with acute stroke. Consistent with our hypothesis, a higher level of pre-stroke PA was associated with spending longer time in post-stroke PA and shorter time in sedentary behavior. The expected relationship between physical function, musculoskeletal status, and high-intensity PA was supported by the significant correlation between BRS or SMI and METs or MVPA. However, these relationships lost significance after adjusting for moderator variables.
The most noteworthy finding of our study was the extensive association between pre-stroke PA and post-stroke activity. To the best of our knowledge, this report is the first to established that PA before stroke is related to sedentary behavior and PA in the acute post-stroke period. Low PA before stroke may pose a risk for prolonged sedentary behavior and reduced PA during the acute phase, potentially influencing long-term outcomes as shown in a previous study15.
Our results showed that individuals with acute stroke spent > 90% of their time in sedentary behavior, approximately 8% in light PA, and approximately 1% in MVPA. This result was comparable with previous studies that reported sedentary behavior and PA in the acute stroke phase7,16. Another study demonstrated that PA in individuals with ischemic stroke was 71% lower than that in individuals with transient ischemic attack as a control group17. In this previous study17, it was unclear why PA was lower in individuals with stroke than in those with transient ischemic attacks, despite involving the same hospitalization conditions. Therefore, investigating the characteristics of PA in individuals with stroke, including time of day utilized and diurnal variations, is crucial. Additionally, we identified that sedentary behavior was more prolonged in the early post-onset period, on weekends, and during the evening. These results suggest that, aside from environmental factors, such as caregiver availability and rehabilitation resources may contribute to lower PA in patients with stroke. Therefore, interventions targeting individuals with extended sedentary behavior due to these environmental factors should be considered.
Although total activity (METs/day) and MVPA correlated with the motor function of the affected lower limb (BRS), sedentary behavior and light PA were not associated with BRS. This indicates that high physical motor functioning is necessary for engaging in higher-intensity PA beyond walking, but it is not a prerequisite for reducing sedentary behavior. Light activities, such as self-care tasks (eating, dressing, transferring, and toileting), fall within the 1.5–2.5 METs range18. Hence, even if performing high-intensity PAs such as walking or carrying loads is challenging, increasing the frequency and time spent on these self-care activities can reduce sitting time. Exercise has been known to mitigate fatigue and depression19,20, and pre-stroke PA habits can provide protection against depression21. Thus, PA seems to be influenced by both physical function and psychological states, including motivation, fatigue, and depression. Consequently, stable psychological conditions due to pre-stroke PA habits may encourage an increase in light PA, while simultaneously associating pre-stroke PA with sedentary behavior.
Adequate compliance with an accelerometer measure was obtained with a wearing period of 10.0 ± 1.4 days for 11 days and a wearing time of 1269.5 ± 148.9 min for 1440 min. Both the wearing period and time in our study were longer than those in previous studies of the acute stroke phase7,16,17. This strength of our study would increase the validity of our results, as activity can vary over different times and days. However, limitations exist in the present study. Wearing the accelerometer on the lower back or thigh is recommended to accurately reflect body movement22. In this study, it was placed on the ankle of the non-paretic lower extremity for wearing compliance and to prevent skin damage. Furthermore, the type of movement causing a measured intensity of activity was unknown because we had no records of behavior for PA measurement in this study. Therefore, one must consider the validity of the results concerning the specific movements involved, and exercising caution when comparing these results with those from previous studies is crucial. Furthermore, we included only those who understood and consented to the study immediately after the onset of stroke. Therefore, selection bias would exist because those who were relatively well-functioning in the overall population of individuals with stroke were recruited. However, the possibility of recall bias or the underestimation of IPAQ cannot be ruled out. Although the association between PA before and after stroke was found in controlling for potentially confounding variables, an outlier may have influenced the results as Fig. 2 shows. Moreover, the number of cases that could be recruited is small, and care must be taken in interpreting the statistical results. In the future, investigating interventions aimed at increasing PA in severe cases may be crucial. Finally, other factors11, such as depression, fatigue, self-efficacy, and quality of life, related to post-stroke PA were not included in this study. Furthermore, we excluded patients with unstable medical conditions including those at high risk of stroke recurrence, therefore, almost all participants were allowed to leave the bed freely, without any bed rest restrictions instructed by their doctors. However, we had not considered the possibility of recurrence and the risk of falls although these factors could have influenced reduced PA because participants were unable to increase their PA owing to these medical conditions.
The results of our study revealed that individuals with acute stroke devote > 90% of their time to sedentary behavior (with an energy expenditure of ≤ 1.5 METs) and allocate less time to engaging in PA. Moreover, pre-stroke PA was strongly associated with post-stroke activity (METs, sedentary behavior, light PA, and MVPA). This implies that low pre-stroke PA may pose a risk for reduced PA during the acute phase of stroke.
Methods
Study design and participants
A single center observational study was conducted. Inclusion criteria: Patients hospitalized in Kyoto University Hospital; aged 20–90 years old; diagnosed with stroke (cerebral infarction or hemorrhage) by board-certified neurologists or neurosurgeons at Kyoto University Hospital from January 2021 to June 2022, and who provided consent within 3 days of stroke onset. Patients who could not agree with the study concept, follow instructions, or sign the consent form due to a significant decline in consciousness level, cognitive or motor functioning, as well as those who had experienced limitations of physical movement before admission, were unable to participate owing to their medical conditions including those at high risk of stroke recurrence, or were discharged or transferred to another hospital without 7 days of accelerometer measurement, were excluded. All participants were fully informed of the procedures and purpose of the study, which conformed to the tenets of the Declaration of Helsinki. Written informed consent was obtained from all participants. This study was approved by the ethics committee of Kyoto University Graduate School and the Faculty of Medicine (R2748).
PA
Pre-stroke PA was investigated using the IPAQ Short Form, which was validated in the investigation of PA23. The duration of time per day and frequency per week were investigated for each of the four intensity levels: (1) vigorous-intensity activities such as carrying heavy loads and jogging, (2) moderate intensity activities such as carrying light loads, (3) walking, and (4) sitting for the usual 7-day recall. The total value of each activity intensity multiplied by the time in a week (METs-min/week) was calculated from the results obtained according to the IPAQ guidelines24.
Post-stroke activity was measured using a tri-axial accelerometer (ActiGraph wGT3X-BT, ActiGraph LLC, Pensacola, FL, USA) placed on the ankle of the non-paralyzed side. The accelerometer was worn daily for 24 h, except during bathing or examinations from the day of consent to discharge from the hospital. The data for 11 consecutive days (from the 4th day following stroke onset) were used in the analysis to align the measurement period for each participant. The analysis of the accelerometer was conducted using specialized software (ActiLife Version 6.13.4; ActiGraph LLC, Pensacola, FL, USA). The total activity (METs) and the total time of each activity intensity (sedentary behavior, light PA, MVPA) were calculated from the acceleration data using the aforementioned software. The cut-off points for activity intensity were based on the validity study25: sedentary behavior, ≤ 99 counts per min; light PA, 100–1951 counts per min; MVPA, ≥ 1952 counts per min.
Outcome measures
NIHSS score (a 15-item impairment scale, with a score range of 0–42, encompassing no neurological deficit to very severe neurological deficits)26, BRS (a measure of motor function recovery assessing spasticity and involuntary muscle movement, ranging from stage I–VI)27, and the FIM motor score28 were measured by the doctor or physical therapist as an index of disease severity and affected lower limb motor function. NIHSS was evaluated by the doctor right after admission or immediately following thrombectomy or recombinant tissue plasminogen activator therapy. BRS of the paralyzed lower extremity and the FIM motor score was evaluated by a physical therapist within 3 days after stroke onset. SMI and phase angle were measured by using a bioelectrical impedance analyzer (InBody S10; InBody Co., Ltd., Seoul, Korea) on the same day as the BRS and FIM measurements. After resting, the participants were measured for body composition in the supine position. Please refer to previous literature for detailed measurement procedures29. SMI and phase angle were used to evaluate body composition in terms of both muscle quantity and quality30,31. SMI was calculated by dividing appendicular skeletal muscle mass by height squared. The phase angle at 50 kHz was calculated using the following equation: phase angle (°) = arctan (reactance/resistance) × (180/π).
Statistical analysis
Statistical analyses were performed using SPSS version 28.0 (IBM, Armonk, NY, USA). The percentage of sedentary behavior, light PA, and MVPA for 11 days were calculated. We compared each activity during the first 5 days and the last 5 days, both on weekdays and weekends, as well as different time segments: morning (7:00–12:00), afternoon (12:00–17:00), evening (17:00–22:00), and night (22:00–7:00). We employed a paired t-test with Shaffer correction for this analysis. In the analysis of the initial and subsequent halves of the measurement, the analysis interval was divided into two equal parts: the first 5 days (4th–8th) and the subsequent 5 days (10th–14th day). Therefore, data for PA on the 9th day were not included in this analysis.
Multiple linear regression analysis was performed to determine predictors for each activity (METs, sedentary behavior, light PA, MVPA). Pre-stroke PA (IPAQ), SMI, phase angle, and BRS were set as an independent variable (model 1). Subsequently, age, sex, NIHSS, and FIM motor score were set as moderator variable (model 2). A p-value of < 0.05 was considered statistically significant.
Data availability
The datasets used and/or analyzed during the current study are available from the corresponding author on reasonable request.
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Acknowledgements
We are extremely grateful to participants in the present study and collaborated nursing staff in the hospital. This work was supported by JSPS KAKENHI Grant Number JP22K21239.
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Contributions
Conception and design: H.T., G.K., Masashi.T., and N.I. Acquisition of data: H.T., G.K., and Mayu.T. Analysis and interpretation of data: H.T., G.K., Mayu.T., M.N., Masashi.T., and N.I. Drafting the article: H.T., G.K., M.N., Masashi.T., T.K., and T.M. Critically revising the article: R.I., Susumu.M., R.T., Shuichi.M., and N.I. Reviewed submitted version of manuscript: all authors. Statistical analysis: H.T., Masashi.T. Administrative/technical/material support: R.I., Shuichi.M. Study supervision: Susumu.M., R.T., Shuichi.M., and N.I.
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Tanaka, H., Kitamura, G., Tamura, M. et al. Pre-stroke physical activity is associated with post-stroke physical activity and sedentary behavior in the acute phase.
Sci Rep 13, 21298 (2023). https://doi.org/10.1038/s41598-023-48232-z
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Received: 08 November 2022
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Accepted: 23 November 2023
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Published: 02 December 2023
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DOI: https://doi.org/10.1038/s41598-023-48232-z
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