The objective of this review was to ascertain the scope of the available literature on the effects of interrupting prolonged sitting time with frequent bouts of physical activity or standing on stroke and recurrent stroke risk factors. Databases Medline, Embase, AMED, CINAHL and Cochrane library were comprehensively searched from inception until 21st February 2018. Experimental trials which interrupted sitting time with frequent bouts of physical activity or standing in adults (≥ 18 years) were included. Comparison to a bout of prolonged sitting and a measure of at least one first or recurrent stroke risk factor was required to be included. Overall, 30 trials (35 articles) were identified to meet the inclusion criteria. Fifteen trials were completed in participants at an increased risk of having a first stroke and one trial in participants at risk of a recurrent stroke. Outcomes of hypertension and dysglycemia were found to be more favourable following predominately light- to moderate-intensity bouts of physical activity or standing compared to sitting in the majority of trials in participants at risk of having a first stroke. In the one trial of stroke survivors, only outcomes of hypertension were significantly improved. These findings are of significant importance taking into consideration hypertension is the leading risk factor for first and recurrent stroke. However, trials primarily focused on measuring outcomes of dysglycemia and without assessing a dose-response effect. Additional research is required on the dose-response effect of interrupting sitting with frequent bouts of physical activity or standing on first and recurrent stroke risk factors, in those high risk population groups.
Citation: Mackie P, Weerasekara I, Crowfoot G, Janssen H, Holliday E, Dunstan D, et al. (2019) What is the effect of interrupting prolonged sitting with frequent bouts of physical activity or standing on first or recurrent stroke risk factors? A scoping review. PLoS ONE 14(6): e0217981. https://doi.org/10.1371/journal.pone.0217981
Editor: Deirdre Dawson, University of Toronto, CANADA
Received: November 19, 2018; Accepted: May 22, 2019; Published: June 13, 2019
Copyright: © 2019 Mackie et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the manuscript and its Supporting Information files.
Funding: This paper presents independent research funded by the National Institute for Health Research (NIHR) under its Programme Grants for Applied Research Programme (Development and evaluation of strategies to reduce sedentary behaviour in patients after stroke and improve outcomes, Reference number RP-PG-0615-20019). The views expressed are those of the author(s) and not necessarily those of the NHS, the NIHR or the Department of Health. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Engaging in high levels of sitting is associated with detrimental risks of all-cause mortality, cardiovascular disease and diabetes [1–3]. Spending > 8 hours/day in sitting and engaging in < 2.5 metabolic equivalents (MET—defined by Jette et al.  as “the amount of oxygen consumed while sitting at rest and is equal to 3.5 ml O2/kg/min”) hours/week of physical activity accounts for a 59% increase in all-cause mortality relative to individuals who sit < 4 hours/day and engage in > 35.5 MET hours/week .
Stroke survivors, a population at high risk of having recurrent strokes, spend a large proportion of their day sitting [6, 7]. Pooled data from the National Health and Nutrition Survey (NHANES) found that American stroke survivors spend 8.5% (weighted prevalence) more time sitting than those from non-stroke populations . Stroke survivors spend on average 22% more time sitting than healthy age-matched controls . The high amount of time spent sitting likely augments the already compromised health and risk of stroke survivors.
Interventions that target specific modifiable risk factors associated with first and recurrent stroke risk could aid in improving the health of stroke survivors and reducing the risk of first and recurrent strokes. In a recent case-control study (n = 26,919) , 91% of the population attributable risk (PAR) for first stroke was associated with 10 modifiable factors (PAR: hypertension 48%, physical inactivity 36%, lipids 27%, poor diet 23%, waist to hip ratio 19%, psychosocial 17%, cardiac 9%, alcohol 6%, diabetes 4%). Risk of recurrent stroke was associated with six modifiable factors (hypertension, smoking, high cholesterol, glycated haemoglobin (HbA1c), low physical activity and weight management) . Interventions which incorporate physical activity have the potential to reduce these first and recurrent stroke risk factors [10, 11]. However, only 18% of stroke survivors meet the recommended guidelines for physical activity (150 minutes/week of moderate-intensity physical activity) . With such context, combined with the known susceptibility of stroke survivors to sit for large periods of the day, new paradigms such as breaking up prolonged sitting time may be a promising strategy to reduce the risk of recurrent strokes.
Experimental studies have shown that frequently breaking up sitting time with physical activity or standing bouts has beneficial effects on cardio-metabolic health in non-stroke populations [12–14]. Frequent bouts of light- or moderate-intensity walking, simple resistance activities or cycling, have been shown to attenuate the exaggerated postprandial glucose and insulin, and blood pressure response to prolonged sitting [14, 15], in those with type 2 diabetes [16, 17], postmenopausal women , overweight/obese [12, 15] and healthy . In the first ever study in-stroke survivors, 3-minute bouts of light-intensity exercises while standing (STAND-EX), performed every 30 minutes, resulted in significant reductions in systolic blood pressure (3.5 mmHg) when compared to 8 hours of prolonged sitting . However, in order to inform research development and subsequently promote effective clinical interventions, evidence is required regarding the effect of breaking up sitting time on first or recurrent stroke risk factors.
Reviews have previously investigated the benefits of interrupting sitting time with frequent bouts of physical activity or standing on markers associated with cardio-metabolic health, obesity and all-cause mortality [21–24]. However, they did not focus on outcome measures associated with first and recurrent stroke risk or identify population groups primarily targeted. Therefore, the aim of this study was to review the evidence for the effect of interrupting prolonged sitting with frequent bouts of physical activity or standing on first or recurrent stroke risk factors. Specifically, our research questions were:
- What are the characteristics of population groups assessed?
- What are the characteristics of the physical activity or standing bouts used (type, duration, frequency, intensity)?
- What first or recurrent stroke risk factors have been measured?
- What are the effects of frequent bouts of physical activity or standing on first or recurrent stroke risk factors?
The methodological framework by Arksey and O’Malley  and further recommendations from Levac et al.  were utilised in this scoping review. The stages underpinning the review were: (I) identifying the research question, (II) identifying relevant studies, (III) study selection, (IV) charting the data, and (V) collating, summarising, and reporting the results. The quality of studies was not assessed in this review as per recommendations by Arksey and O’Malley .
Identification of the research question
The four stage PICO format (Population, Intervention, Comparison, and Outcome) was used to design and define the research question. The section below clarifies each aspect of the research question.
Trials had to be conducted in adult (aged ≥ 18 years) males and females. Adults included stroke and non-stroke population groups.
Intervention and comparison.
The intervention(s) in each trial had to involve frequent (≥ 2) bouts of physical activity or standing, and include a comparison of uninterrupted, prolonged sitting. Interventions had to be supervised to ensure protocol adherence. Supervision was defined as whereby participants were observed, monitored or supervised throughout conditions, or where interventions were conducted within a research facility (e.g. laboratory setting). There were no restrictions placed on the type (e.g. walking, standing, cycling), duration, frequency or intensity of physical activity bouts.
Trials were required to include a measure of at least one risk factor associated with first or recurrent stroke risk. First and recurrent stroke risk factors identified from the INTERSTROKE case control trial , the Global Burden of Disease Study (2013)  and the Stenting and Aggressive Medical Management for Preventing Recurrent Stroke in Intracranial Stenosis  are reported in Table 1.
Identifying relevant studies for selection
The search strategy developed was guided by a Hunter New England Health librarian and revised by the research team. It was developed in Medline (Ovid) and adapted to other relevant databases including Embase (Ovid), Allied and Complementary Medicine (AMED; Ovid), Cumulative Index to Nursing and Allied Health Literature (CINAHL; EBSCOhost) and the Cochran library (Wiley). Databases were searched comprehensively from the date of inception to 14th July 2017. A final search was completed on the 21st February 2018.
Relevant trial registries were also searched for unpublished trials and to assist in identifying the trials which had been published across several articles.
Search terms included Medical Subject Headings (MeSH) and keywords related to, but not limited to, “sedentary behaviour” (e.g. sitting, sedentary lifestyle, uninterrupted) and “interventions” (e.g. bouts, walking, standing). The full Medline search strategy is included in S1 Appendix. Restrictions on searches were limited to English language and humans. The PRISMA checklist made relevant to this scoping review is included in S2 Appendix.
To be included, studies had to meet the following criteria: (I) include a supervised intervention of interrupting sitting time with frequent bouts of physical activity or standing (experimental studies), (II) involve human adult participants (age ≥ 18 years), (III) be written in English, and (IV) include at least one outcome measure related to a first or recurrent stroke risk factor. Exclusion criteria included: (I) non-experimental (e.g. observational, case-control, cross-sectional, longitudinal) studies investigating associations of sedentary behaviour and activity bouts (without implementation of an intervention). Relevant reviews (systematic and met-analysis) identified were excluded, but reference lists were hand-searched to identify additional eligible articles.
Title and abstract (PM and GC), and full text screening (PM and IW) were completed separately, with each article independently screened by the principal investigator (PM) and other members of the research team (IW and GC). Discrepancies during screening and reviewing were resolved by a third member of the research team (CE).
Charting the data for extraction
Data extraction was independently completed by two reviewers (PM and IW). The data extraction spreadsheet was designed to capture all relevant details required to answer the research questions and included: author, year published, sample size, population characteristics (e.g. age, comorbidities, anthropometrics), outcome measures associated with first and recurrent stroke risk factors (see Table 1), assessment times of outcomes (e.g. frequency of measures and on which assessment day), study length (e.g. number of days), physical activity bout type (e.g. walking, standing), frequency (how often bouts were completed), duration and intensity, and study setting (e.g. laboratory, workplace). The spreadsheet was refined via an iterative process in collaboration with the two reviewers.
A total of 29 trials (33 articles) were identified in our search as meeting all inclusion criteria (Fig 1). One (two articles [20, 30]) additional trial was included on the 13th June 2018. Therefore, a total of 30 trials (35 articles) were included in this review, of which 53% were not registered with a trial registry.
All trials used a randomised crossover design, expect for one which used a balanced crossover design . In 20 trials, interventions occurred in a laboratory or research facility where participants were supervised during each condition [12, 14, 16, 18, 20, 30, 32–50]. One trial was completed under supervised conditions in an office setting  and nine trials were conducted in a laboratory or research facility [19, 31, 52–58] where participants where not reported to be observed during conditions.
Characteristics of population groups
Participants of included studies were categorised into five distinct groups: (I) healthy adults, (II) overweight/obese adults, (III) individuals with type 2 diabetes, (IV) postmenopausal women, and (V) people with stroke.
Of the 30 trials included, 14 trials [19, 31, 32, 39–41, 43, 47, 48, 51–53, 56, 57] specifically recruited healthy adults. The characteristics of the included participants is summarised in Table 2. Notably, eight trials [19, 31, 32, 39, 43, 47, 53, 57] included adults of normal weight (Body mass index: BMI < 25 kg.m-2) and three trials [41, 48, 51] included overweight participants (BMI ≥ 25 kg.m-2 and < 29.9 kg.m-2). The age groups ranged from 21 years to 52 ± 5 years, with the primary focus (79%) being in young adults aged ≥ 18 years and ≤ 35 years (11 trials [19, 31, 32, 40, 41, 43, 47, 52, 53, 56, 57]).
Ten trials (12 articles [12, 14, 15, 33, 35, 37, 38, 42, 49, 50, 54, 55]) specifically recruited overweight/obese adults (Table 3). Seven trials (9 articles [12, 15, 33, 35, 37, 38, 42, 50, 55]) included obese adults (BMI of ≥ 30 kg.m-2 and < 34.9 kg.m-2) and three trials [14, 49, 54] included overweight adults. The age ranges of participants in these trials varied and included young adults (four trials [14, 33, 54, 55]), middle aged adults (> 35 and < 65 years) (five trials, [12, 15, 35, 37, 42, 49, 50]) and older adults (≥ 65 years) (one trial ).
Only two trials (four articles) recruited individuals with type 2 diabetes [16, 44–46] (Table 2), where one included overweight adults with type 2 diabetes  and the other included obese adults with type 2 diabetes [16, 44, 45]. All trials were completed in middle age adults with a range of 62 ± 6 years to 64 ± 1 years.
Three trials [18, 34, 58] recruited postmenopausal women (aged > 65 years) (Table 2) who were normal weight  or overweight [18, 34]. Only one trial presented data for stroke survivors who were 0.25 to 10 years post-stroke, older adults (68 ± 2 years) and overweight [20, 30].
Characteristics of the physical activity bouts
The type, duration, frequency and intensity of activity bouts varied across trials, as did the length of the intervention periods (see Table 2). Assessments were completed either on a single day or over multiple days.
Stroke and recurrent stroke risk factors measured
Ten trials included measures of hypertension [14–16, 20, 30, 33, 34, 41, 42, 50, 52], 26 included measures of dysglycemia [12, 18–20, 30, 32–35, 37–41, 43–51, 53–58], one included measures of anthropometric risk factors , and four trials included measures of hypercholesterolemia [31, 32, 41, 43]. No trials presented behavioural, psychosocial or cardiac risk factors (Table 3).
Effects of physical activity bouts on stroke or recurrent stroke risk factors
Outcomes associated with hypertension (mean arterial pressure , systolic blood pressure and diastolic blood pressure ) were examined in two trials involving healthy adults. Regular short bouts of standing, walking or calisthenics did not significantly change mean arterial pressure, systolic blood pressure or diastolic blood pressure when compared to uninterrupted sitting.
Nine trials measured dysglycemia over a single day [19, 32, 39–41, 43, 48, 51, 53]. Three trials found no significant effects of physical activity bouts on postprandial glucose compared to uninterrupted sitting [32, 40, 53]. The remaining five trials [19, 39, 41, 48, 51] observed significant reductions in postprandial glucose with varying physical activity bout types (walking and standing), durations (1 minute 40 seconds to 5 minutes) and frequencies (every 20 to 30 minutes). Another trial, taking place over 27 hours, found sitting interrupted by regular standing bouts reduced postprandial glucose on the day of and the morning after the intervention .
Three trials measured dysglycemia over multiple days (two [47, 57] to four  days) using measures of fasting and/or postprandial plasma glucose. Fasting glucose was measured in all three trials and showed no significant between condition differences for physical activity bouts compared to prolonged sitting. With regards to postprandial glucose, one trial found no significant between condition differences , while two trials found significant reductions in postprandial glucose following a single bout of walking (30 minute)  and running (60 minute)  (completed the day before glucose assessments). Kim et al.  also found a significant reduction in postprandial glucose the day after intermittent bouts of walking.
Four trials measured outcomes associated with hypercholesterolemia and found no significant between condition differences in total cholesterol, low density lipoprotein (LDL) cholesterol  and high density lipoprotein (HDL) cholesterol [32, 41, 43], expect for one trial which found a reduction in HDL cholesterol . Engeroff et al.  found frequent bouts of cycling (6 minutes every 40 minutes) had a negative impact on HDL cholesterol.
A total of five trials [14, 15, 33, 42, 50] measured outcomes associated with hypertension in overweight/obese participants. Systolic blood pressure was measured in all five trials, while diastolic blood pressure was measured in four trials [14, 15, 42, 50] and mean arterial pressure in three trials [15, 33, 42]. In two of the five trials, systolic blood pressure did not significantly differ between conditions [42, 50]. The remaining three trials found significant reductions in systolic blood pressure following frequent bouts (2 to 30 minutes every 20 to 60 minutes) of physical activity (light to moderate intensity walking, standing and cycling) [14, 15] and a single bout of moderate-intensity walking (30 minutes) . Diastolic blood pressure did not significantly reduce in one trial , but was reduced in the remaining three trials following different types (walking, cycling and standing), durations (2 minutes to 30 minutes), frequencies (every 20 to 60 minutes) and intensities (light to moderate) of physical activity bouts [14, 15, 42]. In two trials, mean arterial pressure was significantly reduced following frequent standing bouts (30 minutes every 30 minutes)  and a single bout of moderate-intensity walking (30 minutes) . One trial found no significant condition differences compared to sitting for mean arterial pressure .
Dysglycemia over a single day (postprandial glucose) was measured in six trials [12, 33, 37, 38, 50, 54, 55]. Three trials found no significant reductions in postprandial glucose following activity bouts compared to prolonged sitting [50, 54, 55]. However, the trial by Homlstrup et al.  found a significant increase in postprandial glucose iAUC following a single bout of walking compared to uninterrupted sitting. The remaining three trials [12, 33, 37, 38] found significant between condition improvements in postprandial glucose with varying physical activity bout types (arm ergometry, walking, standing), durations (2 to 30 minutes), frequencies (20 to 60 minutes) and intensities (light, moderate and vigorous).
Dysglycemia (fasting and postprandial glucose) was also measured over multiple (three to five) days. Two trials found regular bouts of standing (30 minutes every 30 minutes)  and light-intensity walking (2 minutes every 20 minutes)  significantly reduced postprandial glucose compared to prolonged sitting. No significant differences were found for fasting glucose responses in both trials.
The only trial to assess anthropometric risk factors  found no significant effect of conditions on weight loss over a five day period.
Type 2 diabetes participants.
In the only trial investigating outcome measures related to hypertension in participants with type 2 diabetes , bouts of light-intensity walking and simple resistance activities (3 minutes every 30 minutes) significantly lowered systolic blood pressure and diastolic blood pressure response in comparison to prolonged sitting.
Postprandial glucose was the only marker associated with dsyglycemia to be measured in this population, and was investigated in two trials [44–46]. One trial found that interrupting prolonged sitting with frequent bouts of activities of daily living (15 minutes completed after meal) and a 45 minute single bout of cycling, lowered postprandial glucose response compared to sitting . The other trial by Dempsey et al. [44, 45] found a significant reduction in postprandial glucose following 3 minutes of walking and simple resistance activities every 20 minutes, when compared to uninterrupted sitting.
One trial found no significant difference between conditions for systolic and diastolic blood pressure in postmenopausal women .
Postprandial glucose was measured in a total of three trials [18, 34, 58]. Two trials found no significant effect of physical activity bouts compared to prolonged sitting on postprandial glucose over one day [34, 58]. One trial, completed over two days, found postprandial glucose to be significantly reduced on both days following 5 minutes of standing and walking every 30 minutes completed on Day 1 .
The only trial in stroke saw a significant reduction in systolic blood pressure following 3 minutes of standing activity, every 30 minutes, in comparison to uninterrupted sitting .
Frequent activity bouts (standing or walking) did not significantly alter postprandial glucose compared to uninterrupted sitting .
This review has synthesised available evidence regarding the effect of interrupting prolonged sitting with frequent bouts of physical activity or standing on risk factors for first or recurrent stroke. A total of 15 trials recruited participants at risk of first stroke (overweight/obese, type 2 diabetes, postmenopausal women/older adults) and one trial in participants at risk of recurrent stroke (one trial; stroke survivors). Four key first or recurrent stroke risk factors (hypertension, hypercholesterolaemia, dysglycemia and weight loss) were measured. In populations identified at high risk of first or recurrent stroke, interrupting prolonged sitting with frequent bouts of physical activity or standing tended to show beneficial effects on outcomes associated with hypertension and dysglycemia, but not on hypercholesterolaemia and weight loss.
With regard to the relevance to stroke risk, a large proportion of trials were conducted in participants characterised as being at risk of first stroke. In the majority of these trials, participants were characterised as overweight (13 trials) or obese (4 trials). This is highly relevant given that an elevated BMI is recognised as a prominent risk factor for stroke . The incidence of a first stroke is also greater with advancing age [59, 60] and in individuals with type 2 diabetes . However, only four trials included participants characterised as older adults (3 trials in postmenopausal women and one trial in overweight/obese older adults) and only two trials included participants with type 2 diabetes, representing a limited number of trials in these high risk population groups. Furthermore, no trials focused on older adults in the healthy population group. Overall, the characteristics of participants in the 17 trials considered at risk of stroke were representative of the participant characteristics in the trial by English et al. [20, 30].
Outcomes associated with hypertension
Hypertension is the foremost risk factor associated with first and recurrent stroke, with elevated systolic blood pressure recognised as the primary measure of hypertension [8, 9, 27]. Interrupting prolonged sitting with frequent bouts of physical activity improved systolic blood pressure in the majority of participants at risk of a stroke (overweight/obese or those who have type 2 diabetes), following predominately short bouts of light- to moderate-intensity physical activity (walking, cycling, standing and simple body weight exercises) [14–16, 33]. More importantly, in the one trial completed in stroke survivors, systolic blood pressure was significantly reduced in response to frequent bouts of light-intensity exercise while standing . The light- to moderate-intensity of physical activity bouts prescribed are comparable to the recommendations from the American Heart Association and American Stroke Association for promoting physical activity after stroke . Additional measures of hypertension, such as diastolic blood pressure and mean arterial pressure [28, 29], were also positively influenced following frequent bouts of physical activity [14–16, 33, 42]. The overall improvements in blood pressure response in these high risk populations are encouraging, even allowing for the small number of trials measuring hypertension outcomes. Dempsey et al.  confirms the potential benefits of interrupting prolonged sitting in controlling blood pressure in population groups at risk. To build on the promising findings in this review, further work is needed to develop and test clinically meaningful interventions of frequent bouts of physical activity or standing to reduce outcomes of hypertension in populations at greater risk of first and recurrent stroke. The assessment of ambulatory blood pressure in future work would also add to the clinical importance of results.
Outcomes of dysglycemia
Outcomes of dysglycemia are similarly important risk factors related to first and recurrent stroke [8, 9]. Two recent reviews investigating risk factors for first stroke assessed dysglycemia by measuring either fasting plasma glucose or HbA1c [8, 27]. With a focus on fasting plasma glucose, frequent bouts of physical activity appeared to be ineffective at reducing fasting plasma glucose in participants at risk of stroke (overweight/obese) [35, 49]. This response is consistent with previous literature investigating the short-term effect of exercise on fasting glucose control [63, 64]. However, fasting plasma glucose does not provide an indication of the fluctuations in glucose concentrations over a day. Instead, postprandial glucose is used as an indicator for glycaemic control in the hours after a meal and is an associated risk factor for first and recurrent stroke risk [8, 29, 65]. Frequent bouts of physical activity or standing led to significant reductions in postprandial glucose response in the majority of trials involving overweight/obese participants and in those with type 2 diabetes [12, 33, 35, 37, 38, 44–46, 49]. In trials of postmenopausal women, only one of three trials found a significant improvement in postprandial glucose following frequent bouts of standing and walking . The improvement found in the trial by Henson et al.  could be due to participants being dysglycemic. Likewise, in the community dwelling stroke survivors in the study by English et al. , postprandial glucose was not affected by frequent bouts of physical activity. Nevertheless, future trials are needed to further understand the effects of frequent bouts of physical activity on the postprandial glucose response in stroke survivors. Additional trials investigating fasting plasma glucose are further required in populations at risk of first and recurrent stroke.
Outcomes of anthropometric measures
The risk of first and recurrent stroke is also elevated in individuals with a high BMI [9, 27]. Only one trial involving overweight/obese participants investigated the effects of frequent bouts of standing on anthropometric risk factors (weight management) , with no beneficial improvements found. The absence of a response could be in part due to the short duration of the trial (5 days), in conjunction with an insufficient increase in energy expenditure to produce a sufficient energy deficit for weight loss . Trials of greater duration and intensity would be required to explore the effects of frequent bouts of physical activity upon weight management.
Outcomes of hypercholesterolaemia
Hypercholesterolaemia accounts for a small proportion of the stroke risk (5%) as estimated in the global burden of disease trial . With regards to recurrent stroke risk, LDL and HDL cholesterol are important risk factors, with LDL cholesterol recognised as a more prominent risk factor . However, outcomes of hypercholesterolaemia were only measured in the healthy population (four trials) [31, 32, 41, 43]. Although no significant beneficial effects of frequent bouts of physical activity or standing were found, the trial by Engeroff et al.  found significant trial x time interactions. The pre- to post-intervention changes in total cholesterol were significantly different between frequent bouts of physical activity (negative change) and a single bout of physical activity (positive change), but not uninterrupted sitting (positive change). HDL cholesterol during the frequent bouts of physical activity differed significantly (negative change) compared to a single bout of physical activity (positive change) and uninterrupted sitting (positive change). Reduced HDL cholesterol concentrations are linked to an increased risk of having a stroke [8, 67], although conversely, O’Donnell et al.  found a direct relationship between elevated HDL cholesterol and risk of an intracerebral haemorrhagic stroke. However, the trial by Engeroff et al.  was conducted in young, normal weight adults who are at a reduced risk of having a stroke. Given the importance of hypercholesterolaemia on stroke risk, more trials are required in populations at high risk of stroke to identify the effects of frequent bouts of physical activity on outcomes of hypercholesterolaemia.
Strengths of this review are that it focused on outcome measures associated with first and recurrent stroke risk. Our definition of supervised interventions may be considered a limitation of this review. A small proportion of trials did not use the terms ‘supervised’, ‘monitored’ or ‘observed’ and simply stated that trials were completed in a laboratory or research facility. However, protocol adherence was monitored in the majority of trials with activity monitors, giving an indication that bouts of physical activity were adhered to in the trials. Additionally, this review was designed to provide a broad overview of experimental trials on breaking up prolonged sitting time with frequent bouts of physical activity or standing and therefore did not report on the magnitude of effect of interventions. While we are confident that we identified all relevant literature at the time of searching, this is a rapidly expanding field and further papers may have been published since.
In conclusion, there is consistent evidence from a number of trials that breaking up prolonged sitting with frequent bouts of physical activity or standing has positive effects on some stroke risk factors (hypertension and dysglycemia) in population groups at risk of a stroke. In the only study of people with stroke, positive effects were seen for hypertension only. Given hypertension is the leading risk factor for stroke, this review provides a solid rationale for further work to determine the optimal frequency, intensity and duration of physical activity bouts to reduce blood pressure, and if effects are maintained.
- 1. Petersen CB, Bauman A, Grønbæk M, Helge JW, Thygesen LC, Tolstrup JS. Total sitting time and risk of myocardial infarction, coronary heart disease and all-cause mortality in a prospective cohort of Danish adults. International Journal of Behavioral Nutrition and Physical Activity. 2014;11(1):13. pmid:24498933
- 2. Katzmarzyk PT, Church TS, Craig CL, Bouchard C. Sitting time and mortality from all causes, cardiovascular disease, and cancer. Medicine & Science in Sports & Exercise. 2009;41(5):998–1005.
- 3. Wilmot E, Edwardson C, Achana F, Davies M, Gorely T, Gray L, et al. Sedentary time in adults and the association with diabetes, cardiovascular disease and death: systematic review and meta-analysis. Diabetologia. 2012;55:2895–905. pmid:22890825
- 4. Jette M, Sidney K, Blümchen G. Metabolic equivalents (METS) in exercise testing, exercise prescription, and evaluation of functional capacity. Clinical cardiology. 1990;13(8):555–65. pmid:2204507
- 5. Ekelund U, Steene-Johannessen J, Brown WJ, Fagerland MW, Owen N, Powell KE, et al. Does physical activity attenuate, or even eliminate, the detrimental association of sitting time with mortality? A harmonised meta-analysis of data from more than 1 million men and women. The Lancet. 2016.
- 6. English C, Healy GN, Coates A, Lewis L, Olds T, Bernhardt J. Sitting and activity time in people with stroke. Phys Ther. 2016;96(2):193. pmid:26112254
- 7. Butler EN, Evenson KR. Prevalence of physical activity and sedentary behavior among stroke survivors in the United States. Top Stroke Rehabil. 2014;21(3):246–55. http://dx.doi.org/10.1310/tscir2101-246 pmid:24985392.
- 8. O'Donnell MJ, Chin SL, Rangarajan S, Xavier D, Liu L, Zhang H, et al. Global and regional effects of potentially modifiable risk factors associated with acute stroke in 32 countries (INTERSTROKE): a case-control study. The Lancet. 2016;388(10046):761–75. http://dx.doi.org/10.1016/S0140-6736(16)30506-2
- 9. Turan TN, Nizam A, Lynn MJ, Egan BM, Le N-A, Lopes-Virella MF, et al. Relationship between risk factor control and vascular events in the SAMMPRIS trial. Neurology. 2017;88(4):379–85. pmid:28003500.
- 10. Lee CD, Folsom AR, Blair SN. Physical Activity and Stroke Risk. Stroke. 2003;34(10):2475–81. pmid:14500932
- 11. Flemming KD, Brown RD Jr, editors. Secondary prevention strategies in ischemic stroke: identification and optimal management of modifiable risk factors. Mayo Clinic Proceedings; 2004: Elsevier.
- 12. Dunstan DW, Kingwell BA, Larsen R, Healy GN, Cerin E, Hamilton MT, et al. Breaking up prolonged sitting reduces postprandial glucose and insulin responses. Diabetes Care. 2012;35(5):976–83. Epub 2012/03/01. pmid:22374636; PubMed Central PMCID: PMC3329818.
- 13. Dempsey PC, Sacre JW, Larsen RN, Straznicky NE, Sethi P, Cohen ND, et al. Interrupting prolonged sitting with brief bouts of light walking or simple resistance activities reduces resting blood pressure and plasma noradrenaline in type 2 diabetes. J Hypertens. 2016;34(12):2376–82. pmid:27512975
- 14. Zeigler ZS, Mullane SL, Crespo NC, Buman MP, Gaesser GA. Effects of Standing and Light-Intensity Activity on Ambulatory Blood Pressure. Medicine and science in sports and exercise. 2016;48(2):175–81. pmid:26285021
- 15. Larsen R, Kingwell B, Sethi P, Cerin E, Owen N, Dunstan D. Breaking up prolonged sitting reduces resting blood pressure in overweight/obese adults. Nutrition, Metabolism and Cardiovascular Diseases. 2014;24(9):976–82. pmid:24875670
- 16. Dempsey PC, Sacre JW, Larsen RN, Straznicky NE, Sethi P, Cohen ND, et al. Interrupting prolonged sitting with brief bouts of light walking or simple resistance activities reduces resting blood pressure and plasma noradrenaline in type 2 diabetes. Journal of Hypertension. 2016;34(12):2376–82. http://dx.doi.org/10.1097/HJH.0000000000001101 pmid:27512975.
- 17. Dempsey P, Sacre J, Straznicky N, Lambert G, Cohen N, Owen N, et al. Interrupting prolonged sitting reduces resting blood pressure and plasma norepinephrine in adults with type 2 diabetes2015; 132(no pagination). Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/055/CN-01199055/frame.html.
- 18. Henson J, Davies M, Bodicoat D, Edwardson C, Gill J, Stensel D, et al. Breaking Up Prolonged Sitting With Standing or Walking Attenuates the Postprandial Metabolic Response in Postmenopausal Women: A Randomized Acute Study2016; 39(1):[130–8 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/184/CN-01141184/frame.html pmid:26628415
- 19. Peddie M, Bone J, Rehrer N, Skeaff C, Gray A, Perry T. Breaking prolonged sitting reduces postprandial glycemia in healthy, normal-weight adults: a randomized crossover trial2013; 98(2):[358–66 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/331/CN-00963331/frame.html.
- 20. English C, Janssen H, Crowfoot G, Bourne J, Callister R, Dunn A, et al. Frequent, short bouts of light-intensity exercises while standing decreases systolic blood pressure: Breaking Up Sitting Time after Stroke (BUST-Stroke) trial. International journal of stroke. 2018.
- 21. Chastin SFM, De Craemer M, De Cocker K, Powell L, Van Cauwenberg J, Dall P, et al. How does light-intensity physical activity associate with adult cardiometabolic health and mortality? Systematic review with meta-analysis of experimental and observational studies. British Journal of Sports Medicine. 2018. pmid:29695511
- 22. Keadle SK, Conroy DE, Buman MP, Dunstan DW, Matthews CE. Targeting Reductions in Sitting Time to Increase Physical Activity and Improve Health. Medicine and science in sports and exercise. 2017;49(8):1572–82. pmid:28272267.
- 23. Chastin SF, Egerton T, Leask C, Stamatakis E. Meta‐analysis of the relationship between breaks in sedentary behavior and cardiometabolic health. Obesity. 2015;23(9):1800–10. pmid:26308477
- 24. Benatti FB, Ried-Larsen M. The effects of breaking up prolonged sitting time: a review of experimental studies. Medicine & Science in Sports & Exercise. 2015;47(10):2053–61.
- 25. Arksey H, O'Malley L. Scoping studies: towards a methodological framework. International journal of social research methodology. 2005;8(1):19–32.
- 26. Levac D, Colquhoun H, O'Brien KK. Scoping studies: advancing the methodology. Implementation Science. 2010;5(1):69.
- 27. Feigin VL, Roth GA, Naghavi M, Parmar P, Krishnamurthi R, Chugh S, et al. Global burden of stroke and risk factors in 188 countries, during 1990–2013: a systematic analysis for the Global Burden of Disease Study 2013. The Lancet Neurology. 2016;15(9):913–24. pmid:27291521
- 28. Glasser SP, Halberg DL, Sands CD, Mosher A, Muntner PM, Howard G. Is Pulse Pressure an Independent Risk Factor for Incident Stroke, REasons for Geographic And Racial Differences in Stroke. American Journal of Hypertension. 2015;28(8):987–94. PubMed PMID: PMC4542637. pmid:25588699
- 29. MEMBERS WG, Benjamin EJ, Blaha MJ, Chiuve SE, Cushman M, Das SR, et al. Heart disease and stroke statistics—2017 update: a report from the American Heart Association. Circulation. 2017;135(10):e146. pmid:28122885
- 30. English C, Janssen H, Crowfoot G, Callister R, Dunn A, Mackie P, et al. Breaking up sitting time after stroke (BUST-stroke). International journal of stroke. 2018:1747493018801222.
- 31. Engeroff T, Fuzeki E, Vogt L, Banzer W. Breaking up sedentary time, physical activity and lipoprotein metabolism. Journal of Science and Medicine in Sport. 2017;20(7):678–83. http://dx.doi.org/10.1016/j.jsams.2016.11.018 pmid:28139402.
- 32. Altenburg T, Rotteveel J, Dunstan D, Salmon J, Chinapaw M. The effect of interrupting prolonged sitting time with short, hourly, moderate-intensity cycling bouts on cardiometabolic risk factors in healthy, young adults2013; 115(12):[1751–6 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/597/CN-01014597/frame.html.
- 33. Bhammar DM, Sawyer BJ, Tucker WJ, Gaesser GA. Breaks in Sitting Time: Effects on Continuously Monitored Glucose and Blood Pressure. Medicine & Science in Sports & Exercise. 2017;49(10):2119–30. https://dx.doi.org/10.1249/MSS.0000000000001315 pmid:28514264.
- 34. Kerr J, Crist K, Vital DG, Dillon L, Aden SA, Trivedi M, et al. Acute glucoregulatory and vascular outcomes of three strategies for interrupting prolonged sitting time in postmenopausal women: A pilot, laboratory-based, randomized, controlled, 4-condition, 4-period crossover trial. PLoS ONE [Electronic Resource]. 2017;12 (11) (no pagination)(e0188544). http://dx.doi.org/10.1371/journal.pone.0188544 pmid:619472868.
- 35. Larsen R, Kingwell B, Robinson C, Hammond L, Cerin E, Shaw J, et al. Breaking up of prolonged sitting over three days sustains, but does not enhance, lowering of postprandial plasma glucose and insulin in overweight and obese adults2015; 129(2):[117–27 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/328/CN-01110328/frame.html pmid:25731923
- 36. Larsen R, Kingwell B, Sethi P, Cerin E, Owen N, Dunstan D. Breaking up prolonged sitting reduces resting blood pressure in overweight/obese adults2014; 24(9):[976–82 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/621/CN-01051621/frame.html.
- 37. Latouche C, Jowett J, Carey A, Bertovic D, Owen N, Dunstan D, et al. Effects of breaking up prolonged sitting on skeletal muscle gene expression2013; 114(4):[453–60 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/386/CN-00872386/frame.html.
- 38. McCarthy M, Edwardson CL, Davies MJ, Henson J, Rowlands A, King JA, et al. Breaking up sedentary time with seated upper body activity can regulate metabolic health in obese high-risk adults: A randomized crossover trial. Diabetes, Obesity and Metabolism. 2017;19(12):1732–9. http://dx.doi.org/10.1111/dom.13016 pmid:28544202.
- 39. McCarthy M, Edwardson CL, Davies MJ, Henson J, Bodicoat DH, Khunti K, et al. Fitness Moderates Glycemic Responses to Sitting and Light Activity Breaks. Medicine & Science in Sports & Exercise. 2017;49(11):2216–22. https://dx.doi.org/10.1249/MSS.0000000000001338 pmid:28594657.
- 40. Bailey D, Broom D, Chrismas B, Taylor L, Flynn E, Hough J. Breaking up prolonged sitting time with walking does not affect appetite or gut hormone concentrations but does induce an energy deficit and suppresses postprandial glycaemia in sedentary adults2016; 41(3):[324–31 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/527/CN-01373527/frame.html.
- 41. Bailey D, Locke C. Breaking up prolonged sitting with light-intensity walking improves postprandial glycemia, but breaking up sitting with standing does not2015; 18(3):[294–8 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/633/CN-01077633/frame.html pmid:24704421
- 42. Barone Gibbs B, Kowalsky RJ, Perdomo SJ, Taormina JM, Balzer JR, Jakicic JM. Effect of alternating standing and sitting on blood pressure and pulse wave velocity during a simulated workday in adults with overweight/obesity. Journal of Hypertension. 2017;35(12):2411–8. http://dx.doi.org/10.1097/HJH.0000000000001463 pmid:28704258.
- 43. Benatti FB, Larsen SA, Kofoed K, Nielsen ST, Harder-Lauridsen NM, Lyngbaek MP, et al. Intermittent Standing but not a Moderate Exercise Bout Reduces Postprandial Glycemia. Medicine & Science in Sports & Exercise. 2017;49(11):2305–14. https://dx.doi.org/10.1249/MSS.0000000000001354 pmid:28640061.
- 44. Dempsey P, Larsen R, Sethi P, Sacre J, Straznicky N, Cohen N, et al. Benefits for Type 2 Diabetes of Interrupting Prolonged Sitting With Brief Bouts of Light Walking or Simple Resistance Activities2016; 39(6):[964–72 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/241/CN-01158241/frame.html pmid:27208318
- 45. Dempsey P, Blankenship J, Larsen R, Sacre J, Sethi P, Straznicky N, et al. Interrupting prolonged sitting in type 2 diabetes: nocturnal persistence of improved glycaemic control2017; 60(3):[499–507 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/951/CN-01329951/frame.html.
- 46. Dijk J, Venema M, Mechelen W, Stehouwer C, Hartgens F, Loon L. Effect of moderate-intensity exercise versus activities of daily living on 24-hour blood glucose homeostasis in male patients with type 2 diabetes2013; 36(11):[3448–53 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/400/CN-00979400/frame.html.
- 47. Homer AR, Fenemor SP, Perry TL, Rehrer NJ, Cameron CM, Skeaff CM, et al. Regular activity breaks combined with physical activity improve postprandial plasma triglyceride, nonesterified fatty acid, and insulin responses in healthy, normal weight adults: A randomized crossover trial. Journal of Clinical Lipidology. 2017. http://dx.doi.org/10.1016/j.jacl.2017.06.007 pmid:617072082.
- 48. Pulsford R, Blackwell J, Hillsdon M, Kos K. Intermittent walking, but not standing, improves postprandial insulin and glucose relative to sustained sitting: a randomised cross-over study in inactive middle-aged men2017; 20(3):[278–83 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/197/CN-01337197/frame.html pmid:27633397
- 49. Thorp A, Kingwell B, Sethi P, Hammond L, Owen N, Dunstan D. Alternating bouts of sitting and standing attenuate postprandial glucose responses2014; 46(11):[2053–61 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/776/CN-01117776/frame.html.
- 50. Wennberg P, Boraxbekk CJ, Wheeler M, Howard B, Dempsey PC, Lambert G, et al. Acute effects of breaking up prolonged sitting on fatigue and cognition: a pilot study. BMJ Open. 2016;6(2):e009630. https://dx.doi.org/10.1136/bmjopen-2015-009630 pmid:26920441.
- 51. Brocklebank LA, Andrews RC, Page A, Falconer CL, Leary S, Cooper A. The Acute Effects of Breaking Up Seated Office Work With Standing or Light-Intensity Walking on Interstitial Glucose Concentration: A Randomized Crossover Trial. Journal of Physical Activity & Health. 2017;14(8):617–25. https://dx.doi.org/10.1123/jpah.2016-0366 pmid:28422556.
- 52. Carter SE, Gladwell VF. Effect of breaking up sedentary time with callisthenics on endothelial function. Journal of Sports Sciences. 2017;35(15):1508–14. pmid:27559678. Language: English. Entry Date: 20170511. Revision Date: 20170513. Publication Type: Article. Journal Subset: Allied Health.
- 53. Hansen R, Andersen J, Vinther A, Pielmeier U, Larsen R. Breaking up Prolonged Sitting does not Alter Postprandial Glycemia in Young, Normal-Weight Men and Women2016; 37(14):[1097–102 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/474/CN-01342474/frame.html pmid:27716865
- 54. Hawari NSA, Al-Shayji I, Wilson J, Gill JMR. Frequency of Breaks in Sedentary Time and Postprandial Metabolic Responses. Medicine & Science in Sports & Exercise. 2016;48(12):2495–502. pmid:119486704. Language: English. Entry Date: 20170103. Revision Date: 20170103. Publication Type: Article. Journal Subset: Allied Health.
- 55. Holmstrup M, Fairchild T, Keslacy S, Weinstock R, Kanaley J. Multiple short bouts of exercise over 12-h period reduce glucose excursions more than an energy-matched single bout of exercise. Metabolism. 2014;63(4):510–9. https://dx.doi.org/10.1016/j.metabol.2013.12.006 pmid:24439242.
- 56. Il-Young K, Sanghee P, Trombold JR, Coyle EF. Effects of Moderate- and Intermittent Low-Intensity Exercise on Postprandial Lipemia. Medicine & Science in Sports & Exercise. 2014;46(10):1882–90. pmid:107828583. Language: English. Entry Date: 20140929. Revision Date: 20150712. Publication Type: Journal Article.
- 57. Miyashita M, Park J, Takahashi M, Suzuki K, Stensel D, Nakamura Y. Postprandial lipaemia: effects of sitting, standing and walking in healthy normolipidaemic humans2013; 34(1):[21–7 pp.]. Available from: http://onlinelibrary.wiley.com/o/cochrane/clcentral/articles/354/CN-00920354/frame.html.
- 58. Miyashita M, Edamoto K, Kidokoro T, Yanaoka T, Kashiwabara K, Takahashi M, et al. Interrupting Sitting Time with Regular Walks Attenuates Postprandial Triglycerides. Int J Sports Med. 2016;37(2):97–103. https://dx.doi.org/10.1055/s-0035-1559791 pmid:26509374.
- 59. Kissela BM, Khoury JC, Alwell K, Moomaw CJ, Woo D, Adeoye O, et al. Age at stroke: temporal trends in stroke incidence in a large, biracial population. Neurology. 2012;79(17):1781–7. pmid:23054237
- 60. Feigin VL, Forouzanfar MH, Krishnamurthi R, Mensah GA, Connor M, Bennett DA, et al. Global and regional burden of stroke during 1990–2010: findings from the Global Burden of Disease Study 2010. The Lancet. 2014;383(9913):245–55.
- 61. Billinger SA, Arena R, Bernhardt J, Eng JJ, Franklin BA, Johnson CM, et al. Physical activity and exercise recommendations for stroke survivors: a statement for healthcare professionals from the American Heart Association/American Stroke Association. Stroke. 2014;45(8):2532–53. pmid:24846875
- 62. Dempsey PC, Larsen RN, Dunstan DW, Owen N, Kingwell BA. Sitting Less and Moving More: Implications for Hypertension. Hypertension (Dallas, Tex: 1979). 2018;72(5):1037–46. Epub 2018/10/26. pmid:30354827.
- 63. Thomas DE, Elliott EJ, Naughton GA. Exercise for type 2 diabetes mellitus. The Cochrane database of systematic reviews. 2006;(3):Cd002968. Epub 2006/07/21. pmid:16855995.
- 64. MacLeod SF, Terada T, Chahal BS, Boule NG. Exercise lowers postprandial glucose but not fasting glucose in type 2 diabetes: a meta-analysis of studies using continuous glucose monitoring. Diabetes/metabolism research and reviews. 2013;29(8):593–603. Epub 2013/09/17. pmid:24038928.
- 65. Imano H, Iso H, Kitamura A, Yamagishi K, Hayama-Terada M, Muraki I, et al. Nonfasting Glucose and Incident Stroke and Its Types― The Circulatory Risk in Communities Study (CIRCS) ―. Circulation Journal. 2018;advpub. pmid:29445058
- 66. Mabire L. Physical activity guidelines for weight loss: global and national perspectives. British Journal of Sports Medicine. 2016;50(20):1235–6. pmid:27084883
- 67. Reina SA, Llabre MM, Allison MA, Wilkins JT, Mendez AJ, Arnan MK, et al. HDL cholesterol and stroke risk: the Multi-Ethnic Study of Atherosclerosis. Atherosclerosis. 2015;243(1):314–9. pmid:26425994