http://wso.sagepub.com/content/early/2016/10/27/1747493016676616.abstract
- Heidi Janssen1,2,3,4⇑
- David W Dunstan5
- Julie Bernhardt6,7
- Frederick R Walker2,4,8
- Amanda Patterson3
- Robin Callister2,4,8,9
- Ashlee Dunn9
- Neil J Spratt2,4,8,10
- Coralie English2,3,4
- 1Hunter Stroke Service, Hunter New England Local Health District, Newcastle NSW, Australia
- 2Centre for Research Excellence in Stroke Rehabilitation and Recovery, Hunter Medical Research Institute, Newcastle NSW, Australia
- 3School of Health Sciences, Faculty of Health, University of Newcastle, Newcastle NSW, Australia
- 4Priority Research Centre for Stroke and Brain Injury, University of Newcastle, Newcastle NSW, Australia
- 5Baker IDI Heart and Diabetes Institute, Melbourne VIC, Australia
- 6Centre for Research Excellence in Stroke Rehabilitation and Recovery, Florey Institute of Neuroscience and Mental Health, Heidelberg VIC, Australia
- 7University of Melbourne, Parkville VIC, Australia
- 8School of Biomedical Science and Pharmacy, Faculty of Health, University of Newcastle, Newcastle NSW, Australia
- 9Priority Research Centre for Physical Activity and Nutrition, University of Newcastle, Newcastle NSW, Australia
- 10Department of Neurology, John Hunter Hospital, Hunter New England Local Health District, Newcastle NSW, Australia
- Heidi Janssen, Hunter Medical Research Institute, Stroke Recovery Group, Level 3 East, Kookaburra Crt, New Lambton Heights, NSW 2305, Australia. Email: heidi.janssen@hnehealth.nsw.gov.au
Abstract
Rationale Prolonged sitting is associated with an increased risk of cardiovascular and all-cause mortality and morbidity. The metabolic
and cardiovascular effects of breaking up sitting time in people with stroke are unknown.
Aims and hypotheses To
determine the (i) metabolic and cardiovascular effects and (ii) safety
and feasibility of an experimental protocol to
break up uninterrupted sitting in people with
stroke. We hypothesize that activity breaks will attenuate the effects
of uninterrupted
sitting on glucose and insulin metabolism, blood
pressure, lipid profiles, and plasma fibrinogen and that it will be
both
safe and feasible.
Sample size estimate
Based on previous estimates of population variability (SD 1% glucose and
30% insulin), 19 paired observations (i.e. participants)
will achieve a power of 0.9 to detect a
difference of 0.8% in glucose and 24% in insulin area under the curve
(two-tailed
testing, α = 0.05).
Methods and design
People with stroke will complete three experimental conditions one week
apart in randomized order: (a) uninterrupted sitting,
(b) prolonged sitting with intermittent walking,
and (c) prolonged sitting with intermittent standing exercises. Serial
blood
samples will be collected and blood pressure
measured at 30 min intervals for 8 h.
Study outcomes Primary outcome will be postprandial glucose and insulin responses. Secondary outcomes will include fibrinogen concentrations,
blood pressure, and adverse events and protocol feasibility.
Discussion This is the
first important step in determining the cardiovascular effects of
breaking up sitting time after stroke. Findings
will guide future studies testing behavioral
strategies to reduce sitting time for the purpose of lowering recurrent
stroke
risk.
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