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 Table of Contents  
STUDY PROTOCOL
Year : 2018  |  Volume : 3  |  Issue : 4  |  Page : 130-134

Effects of a heel raise program on central hemodynamics and cognitive performance in chronic stroke: Study protocol for a randomized, controlled, crossover trial


1 Department of Sport, Exercise and Health, University of Winchester, Winchester, UK
2 Faculty of Health Sciences, University of Southampton, Southampton, UK
3 Department of Exercise and Sport Science, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA

Date of Submission16-Jul-2018
Date of Decision04-Sep-2018
Date of Acceptance05-Sep-2018
Date of Web Publication3-Jan-2019

Correspondence Address:
Andrew Mitchelmore
Department of Sport, Exercise and Health, University of Winchester, Winchester
UK
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/2542-3975.248012

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  Abstract 


Background and objectives: As survival rates after incident stroke increase, the burden caused by secondary stroke and pressure placed on rehabilitation centers also rises. Lifestyle interventions have the potential to drive secondary-prevention treatments. Low-intensity interventions, such as heel raises, may offer a simple method of improving cardiovascular health and cognitive ability in chronic stroke. Here we present a protocol which attempts to determine whether a heel raise training program can improve markers of vascular health and cognitive function.
Design: A randomized, controlled, crossover trial.
Methods: Fifteen participants (> 3 months post-stroke diagnosis) will be randomly assigned to an intervention-first group (n = 8) or a control-first group (n = 7). In the intervention period, participants will complete 170 heel raises per day for 10 weeks. Heel raises will be completed in sets of ten, within a period of 170 minutes, from a seated position. In the control period, participants will go about their normal lives for 10 weeks. On completion of each program, participants will have a 4-week washout before commencing the alterative arm.
Outcome measures: The primary outcomes (pre- and post-measures of peripheral and central blood pressure and pulse wave velocity) will be recorded, as these variables are strongly linked to vascular health after stroke. Secondary outcomes (cognitive function and maximal voluntary contractions) will be assessed using the Stroop task and electromyography respectively. A mixed-model analysis of variance will identify whether a heel raise intervention has a significant effect on the proposed primary and secondary outcome variables.
Discussion: The potential improvements in vascular health may demonstrate that lower-limb heel raise exercise is a beneficial exercise stimulus for this population group.
Ethics and dissemination: The protocol received ethical approval from the University of Winchester Ethics Committee (approval No. BLS/17/11) on November 30, 2017 and will be conducted in accordance with the Declaration of Helsinki, formulated by the World Medical Association. Written informed consent will be obtained from all participants. Recruitment began in June 2018. Analysis of the primary and secondary outcome measures will be completed in January 2019, and the study will finish in February 2019.
Trial registration: The study was registered with ClinicalTrials.gov (NCT03423433) on February 6, 2018.

Keywords: central blood pressure; stroke; sedentary time; training program; pulse wave velocity; randomized controlled trial


How to cite this article:
Mitchelmore A, Lambrick D, Jobson S, Stoner L, Faulkner J. Effects of a heel raise program on central hemodynamics and cognitive performance in chronic stroke: Study protocol for a randomized, controlled, crossover trial. Clin Trials Degener Dis 2018;3:130-4

How to cite this URL:
Mitchelmore A, Lambrick D, Jobson S, Stoner L, Faulkner J. Effects of a heel raise program on central hemodynamics and cognitive performance in chronic stroke: Study protocol for a randomized, controlled, crossover trial. Clin Trials Degener Dis [serial online] 2018 [cited 2024 Mar 28];3:130-4. Available from: https://www.clinicaltdd.com/text.asp?2018/3/4/130/248012


  Introduction Top


Stroke has enormous physical and psychosocial impacts on individuals’ health-related quality of life. The risk of recurrent stroke is 26% within 5 years and 39% within 10 years of initial incidence of stroke.[1] With the burden of disease caused by stroke expected to double by 2030, there is now good evidence to support interventions in stroke rehabilitation.[2]

Blood pressure post-stroke

Peripheral blood pressures are positively and continuously related to stroke incident, however central blood pressures may be more indicative of the pathophysiology associated with central organ damage.[3],[4] These measures are particularly pertinent as around 30% of peripherally normotensive males and 10% of peripherally normotensive females may have central pressures in common with those in stage I peripheral hypertension.[5] Although traditionally contraindicated due to the invasive nature of the procedure, recent technological advances in oscillometric devices allow central blood pressure to be estimated using brachial arm cuffs through pulse wave analysis (PWA).[6] Peripheral and central blood pressures are both risk factors of cardiovascular disease, including stroke.[5],[7] Behaviourably modifiable risk factors can be targeted through lifestyle changes. One aspect of lifestyle which is relatively easy to target post-stroke is the application of interventions that may decrease sedentary time.

Sedentary behaviour post-stroke

Physical disability and the loss of physical function following a stroke frequently leads to increased levels of sedentary time.[8] Stroke survivors typically spend 11 hours per day in a seated position (75% of waking hours), of which many of these hours are accumulated during prolonged periods of sitting.[9] Extended bouts of seated time may be particularly bad for health,[10] leading to decreased levels of physical activity and subsequent cardiovascular deconditioning. As sedentary behaviour has also been linked with mild cognitive impairment,[11] interventions to counter sedentary behaviours should be put in place. If not, the physiological and cognitive improvements that may be observed during in-patient stays may be lost in the months and years that follow hospital discharge.[12]

Strategies for breaking up sedentary behaviour post-stroke

This study hypothesizes that the engagement of patients in movement patterns such as heel raises may reduce the physical and cognitive damage caused by extended sedentary time. Although low-intensity movements may not increase aerobic fitness, they have the potential to reduce prolonged inactivity and, by extension, reduce the risk of future vascular events. Heel raises have been demonstrated to elicit physiological changes over the course of a prescribed program in elderly populations. Daily bouts of 100 heel raises over 40 days,[13] 6 weeks,[14] and 2 months[15] have been reported to show significant improvement in plantarflexor strength, balance, gait speed, improvements in ankle movement and decreases in postural fluctuation. The effect of resistance-free heel raises on physiological measures such as peripheral and central blood pressure and central systolic loading has not, to our knowledge, been investigated, despite each of these measures being indicative of cerebrovascular risk both before and after stroke.

Objectives

This study will investigate whether a daily, 10-week, heel raise intervention affects the peripheral and central hemodynamics, and cognitive performance of chronic stroke survivors. The study hypothesizes that a daily 10-week heel raise protocol will cause a significant decrease in peripheral and central blood pressure, measures of systolic loading and a significant increase in cognitive performance in individuals living with stroke.


  Methods/Design Top


Study design

This is a randomized, controlled, crossover trial. The study team will recruit stroke survivors from local, community-based stroke support groups through declarations of interest and without financial incentives. The path that participants will take is outlined in [Figure 1]. Participants will then be randomized into an intervention-first (heel raise) group or a control-first group. All participants have previously been diagnosed with stroke by a stroke consultant from a UK National Health Service Foundation Trust and have received standard inpatient and outpatient care (physiotherapy, occupational therapy etc.) in accordance with the National Institute for Health and Care Excellence (NICE) guidelines.[2]
Figure 1: Study enrolment flow chart.
Note: TBC: To be confirmed.


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Eligibility criteria

Inclusion criteria

The inclusion criteria are as follows:

  • Over the age of 50 years
  • Diagnosed with stroke by a stroke consultant from a UK National Health Service Foundation Trust 3 months to 5 years before the start of the study
  • Patients who are cognitively aware and able to provide informed consent
  • Patients who are currently medically stable
  • Patients who are able to complete the full range of motion in plantarflexion when seated (heel raise)


Exclusion criteria

The exclusion criteria are as follows:

  • Unresolved deep vein thrombosis
  • Dementia or an inability to provide informed consent
  • Type I or II diabetes or unstable glycaemic control


Randomization

A web-based randomization program will assign participants to either the intervention-first or control-first groups.

  1. Intervention-first group: daily, 10-week, home-based, heel raise program.
  2. Control-first group: 10-week usual care; no home-based, heel raise program.


Blinding

Outcomes assessors and data analysts will be blinded to group allocation (intervention-first and control-first) and will not be aware of the randomization procedure. It is not possible to blind participants to group allocation. The fidelity of blinding will be checked at each assessment.

Baseline measures and participant schedule

Participants will be fasted (> 12 hours), refrain from caffeine consumption for more than 12 hours, and will not undertake structured moderate to strenuous physical activity in the 24 hours prior to the initial baseline assessment. Pertinent outcome measures assessed in the baseline visit are presented in [Table 1]. During this session, and following 20 minutes of supine rest, PWA and pulse wave velocity (PWV) will be recorded on both the affected and unaffected sides using the SphygmoCor XCEL (Sydney, Australia). Both PWA and PWV are markers of cardiovascular health that have been linked to incident and recurrent stroke risk,[16],[17] whilst a supine posture is the most reliable posture when using the SphygmoCor XCEL in an older (> 50 years) population.[18] Participants will also perform three maximal voluntary contractions of the medial gastrocnemius through a heel raise against maximum resistance, during which, skeletal muscle activity will be recorded using electromyography (Delsys Trigno, USA). Five Stroop tasks will be completed to provide baseline data of cognitive performance and to ensure no learning effect takes place in the 10-week follow-up sessions. After each 10-week period, a session identical to the baseline visits will be completed. [Table 2] describes the schedule of enrolment and participation for control and intervention time-frames.
Table 1: Primary and secondary outcome measures

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Table 2: Enrolment and participation schedule

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Intervention

Following randomization, participants who are firstly assigned to the intervention group will complete 170 heel raises per day, for 10 weeks, with ten heel raises performed every 10 minutes for 2 hours and 50 minutes of seated time per day. This number is in accordance with a study investigating the acute effects of heel raises in stroke which is currently under review. Bouts of 100 heel raises have been demonstrated to be viable in elderly, non-clinical population.[13],[14] Participants will record their daily adherence to the heel raise intervention. In the control group, participants will go about their normal lives (usual care) for ten weeks before attending the follow-up session. On completion of the follow-up assessment, and following a 2-week washout period, participants will complete the alternative testing group.

Sample size

A minimum sample size of 15 was calculated using G*Power 3.1 software (University of Dusseldorf, Germany) based on alpha being set at 0.05, power at 0.80, a medium F effect size of 0.5, and when accounting for a 10% dropout rate.[19] Participants will be recruited and randomly assigned to intervention-first or control-first groups.

Ethical approval and consent

The protocol has received approval from the University of Winchester Ethics Committee (BLS/17/11) on November 30, 2017 (Additional file 1 [Additional file 1]) and has been registered with ClinicalTrials.gov (NCT03423433). Participants will provide written informed consent (Additional file 2 [Additional file 2]) before taking part in the study and will maintain the right to withdraw at any time. The protocol adheres to the recommendations provided by the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) 2013[20] (Additional file 3 [Additional file 3]). An independent data monitoring committee has been established and will meet every 6 months following commencement of the trial. This study will be conducted in accordance with the Declaration of Helsinki, formulated by the World Medical Association.

Data analysis

A mixed model analysis of variance with between- (Condition; heel raise intervention, control) and within- (Time; baseline, follow-up) subjects factors will be used to identify whether a heel raise program has a significant effect on all primary and secondary outcome measures. Statistical significance will be set at P < 0.05. All analyses will be conducted using SPSS (v.24.0, SPSS, Chicago, IL, USA).


  Discussion Top


With an ever-increasing population of individuals with stroke-related disability, it is of great importance to discover and implement appropriate lifestyle interventions to reduce this burden. One of the key lifestyle choices which raises recurrent stroke risk is elevated levels of sedentary time and physical inactivity. Stroke survivors tend to live extremely sedentary lifestyles due to physical impairments or a lack of confidence, and a large proportion of this sedentary time takes place in prolonged bouts.[9],[21] These extended periods, of predominantly sitting time, are particularly damaging to the health of an individual. As a result, this predisposition to inactivity causes these survivors to be at an even greater risk of recurrent stroke events, placing ever greater stress on acute-treatment services which are already accommodating increased numbers of total stroke.

Simple exercises, such as heel raises, may have the potential to decrease sedentary time after stroke, improve cardiovascular health and improve cognition. Heel raises have previously been demonstrated to improve muscle strength, gait speed and balance,[13],[14],[15] but the effect on central and peripheral hemodynamic variables are yet to be investigated. Furthermore, interventions such as heel raises may lead individuals to feel more confident in their ability to perform physical tasks, and may attenuate impaired cognition as a result of sedentary behaviours. The consideration of a robust methodological design, such as the implementation of a randomized controlled crossover trial, is a particular strength to this study. Data from this study may demonstrate whether a heel raise program of this nature is physically demanding enough to elicit physiological changes over a 10-week period in a chronic stroke population

To better contextualize any future findings, protocol limitations should be addressed. It should be noted that the wide recruitment window (3 months to 5 years post-stroke diagnosis) could influence any potential effects from the prescribed heel raise intervention. A further limitation is that the engagement in the actual 10 week heel raise protocol is self-reported. Although participants will be asked to record their participation, the actual adherence to the program is purely based on participant feedback.

The conclusions of this study may provide a statistical rationale for the implementation of simple lower limb exercises in chronic stroke and a demonstration of the specific physiological pathways (i.e., arterial compliance, cognitive function) which may be improved using these low-intensity heel raise motions.


  Trial Status Top


The trial status of this study is currently recruiting. It is anticipated that data analysis will be completed in January 2019 with study completion achieved by February 2019. Findings will be published thereafter.

Additional files

Additional file 1: Ethical approval documentation.

Additional file 2: Model consent form.

Additional file 3: SPIRIT checklist.

Author contributions

All authors contributed towards concept, design, literature search, and critically revising the manuscript for important intellectual content. All authors gave final approval for publication.

Conflicts of interest

The authors declare that they have no conflicts of interest.

Financial support

None.

Institutional review board statement

This study protocol was approved by the University of Winchester Ethics Committee (approval No. BLS/17/11) on November 30, 2017 and will be performed in accordance with the Declaration of Helsinki.

Declaration of patient consent

The authors certify that they will obtain all appropriate patient consent forms. In the form the patients will give their consent for their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity.

Reporting statement

This study follows the Standard Protocol Items: Recommendations for Interventional Trials (SPIRIT) guidance for protocol reporting.

Biostatistics statement

The statistical analysis was decided by the research authors as all individuals on this manuscript have extensive experience in managing and analyzing studies such as the one presented here.

Copyright license agreement

The Copyright License Agreement has been signed by all authors before publication.

Data sharing statement

Anonymized individual data will be available immediately after study publication upon request from those who wish to access the data for 5 years. If anonymized data is provided, it should be done so after proposals to [email protected]. Raw data (including personal information and participant codes) will be stored in a locked cabinet at the University of Winchester for this time period before being destroyed. Personal results will also be available to participants upon request. If requested, study protocols and outputs of statistical analysis will be available.

Plagiarism check

Checked twice by iThenticate.

Peer review

Externally peer reviewed.

 
  References Top

1.
Mohan KM, Wolfe CD, Rudd AG, Heuschmann PU, Kolominsky-Rabas PL, Grieve AP. Risk and cumulative risk of stroke recurrence: a systematic review and meta-analysis. Stroke. 2011;42:1489-1494.  Back to cited text no. 1
    
2.
NICE clinical guideline 68. Stroke and transient ischaemic attack in over 16s: diagnosis and initial management. 2017. https://www.nice.org.uk/guidance/CG68. Accessed June 15 2018.  Back to cited text no. 2
    
3.
Chalmers J, Chapman N. Progress in reducing the burden of stroke. Clin Exp Pharmacol Physiol. 2001;28:1091-1095.  Back to cited text no. 3
    
4.
Chatterjee P, Roberts ET, Boden-Albala B. Socioeconomic and patient factors associated with pre-stroke treatment of hypertension. International Stroke Conference Oral Abstracts. 2015;46:A211.  Back to cited text no. 4
    
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McEniery CM, Cockcroft JR, Roman MJ, Franklin SS, Wilkinson IB. Central blood pressure: current evidence and clinical importance. Eur Heart J. 2014;35:1719-1725.  Back to cited text no. 5
    
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Agabiti-Rosei E, Mancia G, O’Rourke MF, et al. Central blood pressure measurements and antihypertensive therapy. Hypertension. 2007;50:154-160.  Back to cited text no. 6
    
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SPS3 Study Group. Blood-pressure targets in patients with recent lacunar stroke: the SPS3 randomised trial. Lancet. 2013;382:507-515.  Back to cited text no. 7
    
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Saunders DH, van Wijck F, Townley B, Skelton DA, Fitzimons C, Mead G. The BASES expert statement on fitness, physical activity and exercise after stroke. Sport Exerc Sci. 2016;49:22-23.  Back to cited text no. 8
    
9.
English C, Healy GN, Coates A, Lewis LK, Olds T, Bernhardt J. Sitting time and physical activity after stroke: physical ability is only part of the story. Top Stroke Rehabil. 2016;23:36-42.  Back to cited text no. 9
    
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Diaz KM, Howard VJ, Hutto B, et al. Patterns of sedentary behavior and mortality in U.S. middle-aged and older adults: a national cohort study. Ann Intern Med. 2017;167:465-475.  Back to cited text no. 10
    
11.
Falck RS, Davis JC, Liu-Ambrose T. What is the association between sedentary behaviour and cognitive function? A systematic review. Br J Sports Med. 2017;51:800-811.  Back to cited text no. 11
    
12.
Ezeugwu VE, Garga N, Manns PJ. Reducing sedentary behaviour after stroke: perspectives of ambulatory individuals with stroke. Disabil Rehabil. 2017;39:2551-2558.  Back to cited text no. 12
    
13.
Fujiwara K, Toyama H, Asai H, Maeda K, Yaguchi C. Regular heel-raise training focused on the soleus for the elderly: evaluation of muscle thickness by ultrasound. J Physiol Anthropol. 2010;29:23-28.  Back to cited text no. 13
    
14.
Lee SM, Cynn HS, Yoon TL, Lee JH. Effects of different heel-raise-lower exercise interventions on the strength of plantarflexion, balance, and gait parameters in stroke survivors. Physiother Theory Pract. 2017;33:706-715.  Back to cited text no. 14
    
15.
Fujiwara K, Toyama H, Asai H, et al. Effects of regular heel-raise training aimed at the soleus muscle on dynamic balance associated with arm movement in elderly women. J Strength Cond Res. 2011;25:2605-2615.  Back to cited text no. 15
    
16.
Gasecki D, Rojek A, Kwarciany M, et al. Pulse wave velocity is associated with early clinical outcome after ischemic stroke. Atherosclerosis. 2012;225:348-352.  Back to cited text no. 16
    
17.
Higgins P, Walters MR, Murray HM, et al. Allopurinol reduces brachial and central blood pressure, and carotid intima-media thickness progression after ischaemic stroke and transient ischaemic attack: a randomised controlled trial. Heart. 2014;100:1085-1092.  Back to cited text no. 17
    
18.
Mitchelmore A, Stoner L, Lambrick D, Jobson S, Faulkner J. Reliability of oscillometric central blood pressure and central systolic loading in individuals over 50 years: Effects of posture and fasting. Atherosclerosis. 2018;269: 79-85.  Back to cited text no. 18
    
19.
Faul F, Erdfelder E, Buchner A, Lang AG. Statistical power analyses using G*Power 3.1: Tests for correlation and regression analyses. Behav Res Methods. 2009;41:1149-1160.  Back to cited text no. 19
    
20.
Chan AW, Tetzlaff JM, Altman DG, et al. SPIRIT 2013 Statement: defining standard protocol items for clinical trials. Ann Intern Med. 2013;158:200.  Back to cited text no. 20
    
21.
English C, Manns PJ, Tucak C, Bernhardt J. Physical activity and sedentary behaviors in people with stroke living in the community: a systematic review. Phys Ther. 2014;94:185-196.  Back to cited text no. 21
    


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