- Study protocol
- Open Access
Effectiveness of a structured circuit class therapy model in stroke rehabilitation: a protocol for a randomised controlled trial
BMC Neurology volume 15, Article number: 88 (2015)
Currently, the key advocacy in neuroscientific studies for stroke rehabilitation is that therapy should be directed towards task specificity performed with multiple repetitions. Circuit Class Therapy (CCT) is well suited to accomplish multiple task-specific activities. However, while repetitive task practice is achievable with circuit class therapy, in stroke survivors repetitive activities may be affected by poor neurologic inputs to motor units, resulting in decreases in discharging rates which consequently may reduce the efficiency of muscular contraction. To accomplish multiple repetitions, stroke survivors may require augmented duration of practice. To date, no study has examined the effect of augmented duration of CCT in stroke rehabilitation, and specifically what duration of CCT is more effective in influencing functional capacity among stroke survivors.
Using a randomised controlled trial with blinded outcome assessment, this study is aimed at determining the effectiveness of structured augmented CCT in stroke rehabilitation. Sixty-eight stroke survivors (to be recruited from a tertiary health institution in Kano, Northwest, Nigeria) will be randomised into one of four groups: three intervention groups of differing CCT durations namely: 60 min, 90 min, and 120minuntes respectively, and a control group. Participants will take part in an 8-week structured intensive CCT intervention. Participants will be assessed at baseline, post-intervention, and six-month follow-up for the effectiveness of the varied durations of therapy, using standardised tools. Based on the WHO-ICF model, the outcomes are body structure/function, activity limitation, and participation restriction measures.
It is expected that the outcome of this study will clarify whether increasing CCT duration leads to better recovery of motor function in stroke survivors.
Pan African Clinical Trial Registry (PACTR): PACTR201311000701191
Stroke is a growing global health-care crisis, with grave and disabling consequences . In most countries, stroke is the second or third most common cause of death, and one of the main causes of acquired adult disability [1, 2]. Motor impairments (of upper and lower extremities) are the major recognisable impairments caused by stroke, which are associated with limitations or decline in independent mobility [3–6].
Substantial evidence suggests that task-specific training can assist functional recovery in stroke rehabilitation, with the goal of achieving true recovery of function based on motor learning principles, including purposefulness, multiple repetitions, and intensified activity [7, 8]. Circuit Class Therapy (CCT) is a form of Task Specific Training (TST) that involves the practice of structuring tasks in a circuit or series of workstations. It satisfies the three key characteristics of an effective and efficient skill training programme  including: (i) using different workstations that allow people to practice intensively in a meaningful and progressive way to suit their respective needs; (ii) efficient utilisation of therapists’/trainees’ time; and (iii) it encompasses group dynamics such as peer support and social support [9, 11]. Several research trials have shown that CCT is effective in improving balance, transfers, gait, gait-related activities (such as climbing stairs) and upper limb functions in stroke survivors [12, 13], especially when applied within the first six months after stroke [12, 14–16] and even later [10, 13, 17–20].
The goal of CCT in stroke rehabilitation is to institute an enduring motor learning in order to optimise motor and functional recovery necessary for the achievement of community reintegration of stroke survivors. To accomplish sustained motor learning, rehabilitation must be geared towards a relatively permanent behavioural change, which is currently believed to manifest as a result of neuroplastic change in the brain itself . Compelling evidence from neuroscientific studies suggest that neuroplastic changes in the cerebral cortex and in other parts of the central nervous system (CNS) are the physiological mechanism for effective motor skill retraining following stroke [22–26]. These studies identified TST and intensity of multiple repetitions as critical nexuses to enhancing neural reorganisation and “rewiring” in the CNS. By implication the damaged brain will therefore benefit from repeated sensorimotor inputs (efferent-afferent feedback loops) in order to remodel effectively for the attainment of motor/functional recovery in stroke survivors. This signifies the need for rehabilitation professionals to focus on meaningful, repetitive, and intensive specific tasks during a rehabilitation session .
Stroke survivors demonstrate poor activity tolerance  and performance . These may suggest the need for longer duration to tolerate and perform repetitive activities. The need to augment the duration of therapy in CCT for stroke survivors can be considered based on pathophysiologic and clinical domains. Pathophysiologically, the sequelae of an upper motor neuron lesion result in hemiparesis/hemiplegia, marred balance and coordination and decreased proprioceptive feedback . These put together will negatively affect daily activities and exercise performance, leading to activity intolerance, increased energy cost of activity, and a decline in overall performance after stroke . Cumulatively, these factors result in longer reaction time and longer time to accomplish tasks, thus suggesting the need to give adequate time for the performance of multiple repetitive tasks in stroke survivors, well beyond age and gender-matched individuals without history of stroke. Four systematic reviews and one Cochrane review have shown that augmentation of exercise therapy and/or time of exercise therapy results in significant small to moderate gains in ADL, walking ability and walking speed [31–34].
Clinically, in CCT, participants are exposed to multiple progressively structured tasks to be accomplished within a session, and considering the pathophysiological challenge of stroke survivors, they may need more time to perform multiple repetitions to enable neuroplastic changes. Rose et al.  have proposed that planning the contents of a session in advance with predetermined progression of tasks may allow more time for in-session practice.
In summary, pathophysiological and clinical factors may in isolation or collectively support the need to examine the effect of augmented therapy time in CCT. However, while there is a need to investigate the effect of augmenting the duration of therapy, it is equally imperative to determine how acceptable these CCT durations are among stroke survivors.
The objective of this study is to investigate the relative effectiveness of augmented durations of CCT on the functional capacity of stroke survivors. Additionally, the study will investigate the effectiveness of augmented duration of CCT on upper and lower extremity functions (with respect to body structure/function, activity limitation and participation restriction) post-stroke and the acceptability of the various CCT durations among stroke survivors. For these to be achieved outcomes of interest will be assessed based on the World Health Organisation International Classification of Function, Disability and Health model (WHO-ICF) .
This study is a randomised controlled trial of the effectiveness of augmented durations of a structured CCT model in the rehabilitation of stroke survivors. All participants will be recruited from Aminu Kano Teaching Hospital (AKTH) in Kano State, Northwest of Nigeria. The hospital (AKTH) is a tertiary health institution, situated in Kano, the most populous state in Nigeria, with over 9 million inhabitants . It is a 500-bed-capacity hospital that receives patients from within Kano and the neighbouring states of Jigawa, Katsina, Kaduna, Bauchi and Zamfara states. The patronage list comprises primarily the indigenous Hausa Fulani tribe, although Nigerians of other tribes such as the Ibo and Yoruba ethnic groups also constitute a sizeable number of the clientele.
Participants will include all stroke survivors in AKTH referred for physiotherapy by consulting physicians. However, only participants who meet the inclusion criteria will be considered for randomisation into the study groups (involving intervention and control groups). Participants will be considered eligible if: stroke is ascertained to be due to cerebrovascular accident; leading to unilateral motor deficits ; they provide a written informed consent; they are adult stroke survivors of ≥18 years of age; onset of stroke is ≥30 days; they possess sufficient cognition to participate (having a score of ≥24 points on mini-mental state examination); they are willing to participate in an 8-week intensive CCT programme; have the ability to walk for 10 m unsupported (walking aid is allowed); and have a minimum active wrist extension (2/5 on manual muscle testing). Participants will be considered ineligible if they present with precluding medical comorbidity to exercise, and history of any major surgical procedure significant enough to interfere with performance (general or orthopaedic) in an exercise therapy intervention.
Stroke survivors who meet the eligibility criteria will be randomised into one of four arms of the study, including three intervention categories (60 min CCT, 90 min CCT and 120 min CCT) and one control (60 min standard physiotherapy).
Sample size and power calculation
Using power calculations to detect a between-group difference of 42.5 m (0.43 effect size) for a 4-group repeated measure MANOVA in walking distance with 90 % power at α = 0.05, a total sample size of 56 was generated, using an estimated standard deviation (SD) for the calculation as adopted from a meta-analysis . The 42.3 m was proposed as the minimum clinically important difference in walking distance, based on previous studies of implicit measurement error following repeated measurement of speed. The generated total sample size of 56, by implication, will give 14 participants as samples for each group. To incorporate drop-out to follow-up, we hope to recruit a total of 68 participants (17 participants per group). The power calculation was conducted using G*Power version 3.0.10.
Randomisation and blinding
Randomisation will be conducted using a computer-generated random allocation sequence schedule held by a third party, who will randomly allocate recruited participants into the study group (Fig. 1. outline of the study flow diagram based on CONSORT ). To eliminate bias, the assessment of outcome will be performed by (experienced/trained) blinded assessors, who will be blinded to the nature/type of intervention as well as the intervention groups of the participants. Participants will also be instructed not to disclose their individual intervention groups to the assessors.
This study has been approved by both the Senate Research Grants and Study Leave Committee University of the Western Cape (South Africa) (ethics number 13/9/33) and the Human Research Ethics Committee of Aminu Kano Teaching Hospital (Nigeria) (NHREC/21/082008/AKTH/EC/1232).
Assessment of participants will be conducted at three stages (baseline, post-intervention, and at 6-months follow-up). To ensure a comprehensive assessment, we chose a battery of measures covering the WHO-ICF model . We selected certain tools to cover the three key domains proposed by the ICF: body structures and function, activity and participation. At baseline, participants will be assessed for socio-demographic characteristics which will include personal demographic information and stroke-specific information. The personal demographic information will include age, sex, height, weight, marital status (pre- and post-stroke), educational qualification, employment (pre- and post-stroke), and tribe. The stroke-specific information will include time since stroke, type of stroke, hemispheric side of lesion, and use of cane. This will be followed by ICF-based assessments, all at baseline. The outcome measures to be employed for these assessments and their function/application are presented in Table 1.
All baseline measures will be repeated immediately post-intervention and 6 months follow-up, excluding descriptive personal and stroke data. Also at this time, the intervention acceptability measure will also be applied.
Participant adherence will be duly monitored and recorded for each session in terms of attendance (number of sessions) and amount of practice (within sessions – time spent and repetitions where relevant). Fidelity of the intervention will be monitored by the primary investigator performing video recordings of randomly chosen sessions in each arm. Co-investigators will review these videos for compliance with the established practice protocols. Safety issues and adverse events will be recorded by treating staff in each group and monitored by the co-investigators. Previous trials using CCT have found no increase in adverse events as compared to usual care .
The intervention groups are the three intensities (durations) of CCT namely 60 min, 90 min, and 120 min, tagged groups A, B and C respectively. All participants will be assessed at baseline (prior to the intervention), post-intervention and at six-month follow-up. A total of 10 workstations will be made available in the circuit, arranged to progress in complexity. These stations will be made up of task-specific activities for the upper and lower extremity, structured alternately across the circuit (i.e., after every lower extremity workstation an upper extremity workstation follows), ensuring a 1:1 ratio of upper to lower extremity activities. This is to allow for adequate concentration, specificity of activity choice, and distribution of equal activity duration for both upper and lower extremities. A minute change period (not within specified duration of intervention) will be allowed for crossing from one workstation to the next.
The intervention is an 8-week, 3-times weekly training programme, giving a total of 24 sessions. Activities will be individualised allowing each participant to perform at a level based on his/her ability, and progress steadily within the allotted time for each group.
The upper extremity task-orientated CCT activities will include activities to improve fine motor skills, grasp and reach, sensory function, and proximal control. Similarly, tasks for the lower extremity will be targeted to balance, strength, cardiovascular endurance, and retraining of gait mobility. All CCT sessions will be conducted by three trained physiotherapists, with each treatment session structured at a 3:1 ratio of patients to therapists. Table 2 (below) presents the CCT task-specific activities to be implemented in this study.
Control group (standard physiotherapy)
The standard physiotherapy group, like the intervention groups, will involve the same number of sessions (24), duration (60 min) and frequency per week (3) of therapy. Standard physiotherapy will comprise one-to-one therapist/patient sessions engaging in impairment-centred mobilisation techniques, standing balance (using varying methods) and functional activities for both upper and lower extremities. All the activities for the control group will be implemented by regular therapists (who are similar in qualification/experience to therapist implementing the CCT programme) in the Physiotherapy Department of AKTH.
Data will be recorded in Microsoft Excel before being exported to Statistical Package for Social Science (SPSS). Both descriptive and inferential statistics will be used to examine the outcomes of the study.
Descriptive statistics of frequencies, percentages, mean, and standard deviation will all be used to describe baseline assessments and demographic characteristics of participants. Where appropriate, they will also be used at post-intervention and follow-up to describe relevant findings.
Between-groups relative mean differences of the dependent variables, (spasticity, muscle strength, functional independence, ADL, functional capacity, gait speed, upper extremity function and impairment) will be determined using the general linear model repeated measures, MANCOVA models (for each study domain, adjusted central on baseline as covariates). If the MANCOVA is found to be significant (Roy’s largest root), univariate between-groups results will be reported and pair-wise post hoc analysis will be performed using least significant difference.
A multiple regression analysis will be performed to investigate the relation between improvement at different time periods of CCT and performance in each of the specific dependent variables, to detect which of the durations most effectively predicts improvement in such a variable.
Augmenting exercise therapy time to improve recovery outcomes has been supported by some research findings [31–34]. However, the amount of augmented time is not known, using CCT as a delivery model. In this era of evidence-based practice, there is an urgent need to support all facets of implementing CCT with cogent evidence prior to adoption. The need to augment the duration of therapy in stroke survivors might not be challenged, but exactly what duration (intensity) is suitable, in terms of acceptability and therapeutic benefit to the stroke survivor, needs to be supported empirically.
Reporting the outcome of this study using the ICF model will provide an opportunity to identify which of the domains – body structure/function, activity or participation – will be more responsive to change following intervention, and to which specific duration of intervention.
It is envisaged that engaging in task-specific upper limb practice and task-specific practice involving the lower limb will add credence to this study in explaining which section of these body parts will be functionally better responsive to a particular augmented duration of CCT.
The fact that this study is taking place in a minimally resourced country, will further support the cost benefit of CCT in any setting, and will globalise the empirical findings for CCT.
Finally, if the outcomes of this study support a specific duration of CCT, it will serve as a guide for clinical recommendations in CCT implementation.
Circuit class therapy
Task specific training
Central nervous system
Pan African clinical trial registry
World Health Organization
International classification of function
Aminu Kano teaching hospital
Activities of daily living
Statistical package for social sciences
Modified Tardieu Scale
Manual muscle testing
Modified rankin scale
Modified Barthel Index
Six-minute walk test
10 Meter walk test
Action research arm test
Motor activity log
Stroke specific quality of life questionnaire
Warlow CP, van Gijn J, Dennis MS, Wardlaw JM, Bamford JM, Hankley GJ, et al. Stroke: practical management. 3rd ed. Oxford: Blackwell Publishing; 2008.
Bonita R, Mendis S, Truelsen T, Bogousslavsky J, Toole J, Yatsu F. The global stroke initiative. Lancet Neurol. 2004;3:391–3.
Kelly-Hayes M, Beiser A, Kase CS, Scaramucci A, D’Agostino RB, Wolf PA. The influence of gender and age on disability following ischemic stroke: the Framingham study. J Stroke Cerebrovasc Dis. 2003;12:119–26.
Goulding R, Thompson D, Beech C. Caring for patients with hemiplegia in an arm following stroke. Br J Nurs. 2004;13(9):534–9.
Danielsson A, Willen C, Sunnerhagen KS. Physical activity, ambulation, and motor impairment late after stroke. Stroke Res Treat. 2012;2012:818513. doi:10.1155/2012/818513. 5 pages.
Dobkin BH. Strategies for stroke rehabilitation. Lancet Neurol. 2004;3:528–36.
Krakauer JW, Mazzoni P, Ghazizadeh A, Ravindran R, Shadmehr R. Generalisation of motor learning depends on the history of prior action. PLoS Biol. 2006;4:e316.
Kleim JA, Jones TA. Principles of experience-dependent neural plasticity: implications for rehabilitation after brain damage. J Speech Lang Hear Res. 2008;51(1):S225–39.
Wevers L, van de Port I, Vermue M, Mead G, Kwakkel G. Effects of task-oriented circuit class training on walking competency after stroke. A systematic review. Stroke. 2009;40:2450–9.
Dean CM, Richards CL, Malouin F. Task-related circuit training improves performance of locomotor tasks in chronic stroke: a randomised, controlled pilot trial. Arch Phys Med Rehabil. 2000;81:409–17.
Blennerhassett J, Dite W. Additional task-related practice improves mobility and upper limb function early after stroke: a randomised controlled trial. Aust J Physiother. 2004;50:219–24.
English C, Hillier SL. Circuit class therapy for improving mobility after stroke. Cochrane Database Syst Rev. 2010;7:CD007513.
Robinson K, Mahon J, Yeoman L, Janssen J. A case series to review the effectiveness of an upper limb circuit training group on the performance of the upper limb in stroke patients. N Z J Physiother. 2011;39(2):69–74.
English CK, Hillier SL, Stiller KR, Warden-Flood A. Circuit class therapy versus individual physiotherapy sessions during inpatient stroke rehabilitation: a controlled trial. Arch Phys Med Rehabil. 2007;88:955–63.
Outermans JC, Van Peppen RP, Wittink H, Takken T, Kwakkel G. Effects of a high-intensity task-oriented training on gait performance early after stroke: a pilot study. Clin Rehabil. 2010;24:979–87.
van de Port IGL, Wevers LEG, Lindeman E, Kwakkel G. Effects of circuit training as alternative to usual physiotherapy after stroke: randomised controlled trial. BMJ. 2012;344:e2672.
Salbach NM, Mayo NE, Wood-Dauphinee S, Hanley JA, Richards CL, Cote R. A task-orientated intervention enhances walking distance and speed in the first year post stroke: a randomised controlled trial. Clin Rehabil. 2004;18:509–19.
Pang MY, Eng JJ, Dawson AS, McKay HA, Harris JE. A community-based fitness and mobility exercise program for older adults with chronic stroke: a randomised, controlled trial. J Am Geriatr Soc. 2005;53:1667–74.
Marigold D, Eng J, Dawson A, Inglis J, Harris J, Gylfadóttir S. Exercise leads to faster postural reflexes, improved balance and mobility, and fewer falls in older persons with chronic stroke. J Am Geriatr Soc. 2005;53:426–3.
Mudge S, Barber PA, Stott NS. Circuit-based rehabilitation improves gait endurance but not usual walking activity in chronic stroke: a randomised controlled trial. Arch Phys Med Rehabil. 2009;90:1989–96.
Arya KN, Pandian S, Verma R, Garg RK. Movement therapy induced neural reorganisation and motor recovery in stroke: A review. J Body Mov Ther. 2011;15:528–37.
Chan DYL, Chan CCH, Au DKS. Motor relearning programme for stroke patients: a randomised controlled trial. Clin Rehabil. 2006;20(3):191–200.
Gauthier LV, Taub E, Perkins C, Ortmann M, Mark VW, Uswatte G. Remodeling the brain: plastic structural brain changes produced by different motor therapies after stroke. Stroke. 2008;39:1520–5.
Harvey RL. Improving Post stroke Recovery: Neuroplasticity and Task-Oriented Training. Curr Treat Options Cardiovasc Med. 2009;11:251–9.
Jones TA, Allred RP, Adkins DL, Hsu JE, O’Bryant A, Maldonado MA. Remodeling the brain with behavioral experience after stroke. Stroke. 2009;40(3 Suppl):S136–8.
Daly JJ, Ruff RL. Construction of efficacious gait and upper limb functional interventions based on brain plasticity evidence and model-based measures for stroke patients. Scientific World Journal. 2007;20(7):2031–45.
Roth EJ, Harvey RL. Rehabilitation of stroke syndromes. In: Braddom RL, editor. Physical Medicine and Rehabilitation. 2nd ed. Philadelphia, Pa: WB Saunders; 2000. p. 1117–63.
Gordon NF, Gulanick M, Costa F, Fletcher G, Franklin BA, Roth EJ, et al. Physical activity and exercise recommendations for stroke survivors: an American Heart Association scientific statement from the Council on Clinical Cardiology, Subcommittee on Exercise, Cardiac Rehabilitation, and Prevention; the Council on Cardiovascular Nursing; the Council on Nutrition, Physical Activity, and Metabolism; and the Stroke Council. Stroke. 2004;35:1230–40.
MacKay-Lyons MJ, Howlett J. Exercise capacity and cardiovascular adaptations to aerobic training early after stroke. Top Stroke Rehabil. 2005;12(1):31–44.
Billinger SA, Coughenour E, MacKay-Lyons MJ, Ivey FM. Reduced cardiorespiratory fitness after stroke: biological consequences and exercise-induced adaptations. Stroke Res Treat. 2012;2012:959120. doi:10.1155/2012/959120. 11 pages.
Kwakkel G, van Peppen R, Wagenaar RC, Wood DS, Richards C, Ashburn A, et al. Effects of augmented exercise therapy time after stroke: a meta-analysis. Stroke. 2004;35:2529–39.
French B, Thomas LH, Leathley MJ, Sutton CJ, McAdam J, Forster A, et al. Repetitive task training for improving functional ability after stroke. Cochrane Database Syst Rev. 2007;4:CD006073.
Langhorne P, Coupar F, Pollock A. Motor recovery after stroke: a systematic review. Lancet Neurol. 2009;8:741–54.
Veerbeek JM, Kwakkel G, van Wegen EE, Ket JC, Heymans MW. Early prediction of outcome of activities of daily living after stroke: a systematic review. Stroke. 2011;42:1482–8.
Rose D, Paris T, Crews E, Wu SS, Sun A, Behrman AL, et al. Feasibility and effectiveness of circuit training in acute stroke rehabilitation. Neurorehabil Neural Repair. 2011;25(2):140–8.
World Health Organisation. International Classification of Impairments, Disabilities and Health. Geneva: WHO; 2001.
Population council. Report of Nigeria's National Population Commission on the 2006 census source. Popul Dev Rev 2007; 33(1):206–210.
Schulz KF, Altman DG, Moher D. CONSORT 2010 statement: updated guidelines for reporting parallel group randomised trials. BMJ. 2010;340:698–702.
Patrick E, Ada L. The Tardieu Scale differentiates contracture from spasticity whereas the Ashworts Scale is confounded by it. Clin Rehabil. 2006;20(2):173–81.
Paulis WD, Horemans HLD, Brouwer BS, Stam HJ. Excellent test–retest and inter-rater reliability for Tardieu Scale measurements with inertial sensors in elbow flexors of stroke patients. Gait Posture. 2011;33:185–9.
James MA. Use of the medical research council muscle strength grading system in the upper extremity. J Hand Surg. 2007;32(2):154–6.
Youdas JW, Madson TJ, Hollman JH. Usefulness of the Trendelenburg test for identification of patients with hip joint osteoarthritis. Physiother Theory Pract. 2010;26(3):184–94.
Noreau L, Vachon J. Comparison of three methods to assess muscular strength in individuals with spinal cord injury. Spinal Cord. 1998;36(10):716–23.
Quinn TJ, Dawson J, Walters MR, Lees KR. Reliability of the Modified Rankin Scale: A Systematic Review. Stroke. 2009;40:3393–5.
Tilley BC, Marler J, Geller NL, Lu M, Legler J, Brott T, et al. Use of a global test for multiple outcomes in stroke trials with application to the national institute of neurological disorders and stroke t-PA stroke trial. Stroke. 1996;27:2136–42.
Shah S, Vanclay F, Cooper B. Improving the sensitivity of the Barthel Index for stroke rehabilitation. J Clin Epidemiol. 1989;42(8):703–9.
Anderson K, Aito S, Biering-Søresen F, Charlifue S, Curt A, Ditunno J, et al. Functional Recovery Measures for Spinal Cord Injury: An Evidence-Based Review for Clinical Practice and Research. J Spinal Cord Med. 2008;31:133–44.
Fulk GD, Echternach JL, Nof L, O’Sullivan S. Clinometric properties of the six-minute walk test in individuals undergoing rehabilitation poststroke. Physiother Theory Pract. 2008;24:195–204.
Fulk GD, Echternach JL. Test-retest reliability and minimal detectable change of gait speed in individuals undergoing rehabilitation after stroke. J Neurol Phys Ther. 2008;32(1):8–13.
Nijland R, van Wegen E, Verbunt J, van Wijk R, van Kordelaar J, Kwakkel G. A comparison of two validated tests for upper limb function after stroke: The wolf motor function test and the action research arm test. J Rehabil Med. 2010;42:694–6.
Plats T, Eickhof C, Nuyens G, Vuadens P. Clinical scales for the assessment of spasticity, associated phenomena, and function: a systematic review of the literature. Disabil Rehabil. 2005;27:7–18.
Uswatte G, Taub E, Morris D, Light K, Thompson P. The Motor Activity Log-28: assessing daily use of the hemiparetic arm after stroke. Neurology. 2006;67:1189–94.
Lin K, Fu T, Wu C, Hsieh C. Assessing the stroke-specific quality of life for outcome measurement in stroke rehabilitation: minimal detectable change and clinically important difference. Health Qual Life Outcomes. 2011;9:5.
Teixeira-Salmela LF, Gomes-Neto M, Magalhaes LC, Lima RCM, Faria CDCM. Content comparisons of stroke-specific quality of life based upon the international classification of functioning, disability, and health. Qual Life Res. 2009;18:765–73.
Hunsley J. Development of the treatment acceptability questionnaire. J Psychopathol Behav. 1992;14(1):55–64.
English C, Hillier S. Circuit class therapy intervention manual version 1.0. University of South Australia: International Centre for Allied Health Evidence; 2012.
There is no special funding for this study. However, the authors would like to acknowledge Ms. H. Ellen for editorial assistance.
The authors declare that they have no competing interests.
IUL, AR and SH conceived the idea for the study and developed the title. IUL, AR and SH contributed to the research design. IUL, AR, SH and TKH were principally responsible for the drafting of the manuscript. All authors contributed in deciding the choice of intervention and outcome measures of the study. AR, SH and TKH assisted in editing the final submitted manuscript. All authors have read and approved the manuscript.
Susan L. Hillier, Talhatu K. Hamzat, and Anthea Rhoda contributed equally to this work.
About this article
Cite this article
Lawal, I.U., Hillier, S.L., Hamzat, T.K. et al. Effectiveness of a structured circuit class therapy model in stroke rehabilitation: a protocol for a randomised controlled trial. BMC Neurol 15, 88 (2015). https://doi.org/10.1186/s12883-015-0348-7
- ICF model
- Circuit class therapy
- Exercise intensity