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DOI: 10.1055/s-0043-1777132
Effect of Arm Ability Training on Functional Mobility and Dexterity in Hemiparetic Subjects
- Abstract
- Introduction
- Materials and Methodology
- Results
- Discussion
- Limitation and Suggestions
- Conclusion
- References
Abstract
Objective Hemiparesis occurs when a stroke causes paresis on the body, contralateral to the lesioned brain. In poststroke patients, upper limb impairments induce functional restrictions. Arm ability training is a unilateral treatment for mild arm paresis. We evaluated the effectiveness of arm ability training on functional mobility and dexterity in hemiparetic subjects
Materials and Methods Forty-two hemiparetic subjects were selected by convenient sampling technique. The subjects were given 40 minutes of arm ability training and 20 minutes of conventional physiotherapy daily, five sessions a week extending for 4 weeks. Functional mobility was assessed through wolf motor function test (WMFT) and dexterity by box and block test (BBT).
Results The pre- and post-test scores were evaluated by paired t-test using SPSS software after 4 weeks of training period subjects showed much improvement for the BBT (mean ± standard deviation [SD]: 20.31 ± 4.075 vs. 23.79 ± 4.291), functional ability of WMFT (mean ± SD: 45.38 ± 3.615 vs. 54.07 ± 3.790), time of WMFT (mean ± SD: 479.29 ± 117.79 vs. 434.4 ± 116.455), the strength of WMFT was (mean ± SD: 2.95 ± 0.731 vs. 3.9 ± 0.759), and grip strength of WMFT (mean ± SD: 2.9 ± 1.559 vs. 4.21 ± 1.539), all variables indicating statistical significance (p < 0.05).
Conclusion Arm ability training proved effective in improving functional mobility and dexterity in hemiparetic subjects.
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Keywords
hemiparesis - hand functions - arm ability training - wolf motor function and box and blockIntroduction
Stroke is a “rapidly acquired clinical symptom of focal (or global) impairment of brain function lasting longer than 24 hours or leading to death, with no evident cause other than vascular origin” (World Health Organization [WHO]).[1] Throughout the world, stroke is a major disease that leads to mortality.[2] The prevalence of this condition in a rural area is 84,262/100,000, whereas it is 334,424/100,000 in an urban area.[3] Approximately 85% of strokes are ischemic, and 17.8% of those over 45 years of age.[4] Pathological subtypes include ischemic and hemorrhagic stroke.[5] Ischemic strokes can be classified according to the cause, which includes large artery atherosclerosis and cardiac emboli.[6] Atherosclerosis is a primary cause of ischemic stroke.[7] Acute hemorrhagic strokes make up 5 to 21% of all acute strokes.[8] Hypertension is a common cause of hemorrhagic strokes.[9] Hemorrhagic strokes can also be caused by vascular abnormalities.[10]
Stroke symptoms include one-sided weakness, disturbed vision, changed speech, ataxia, and associated symptoms. This might vary according to the origin of the stroke.[11] Hemiparesis occurs when a stroke causes paresis on the body, contralateral to the lesioned brain.[12] Mild paretic patients will move the limb normally or almost normally; however, hemiplegic subjects cannot move at all.[13] The hemiparetic patients were aimed to restore enough sensorimotor control to the limb.[14]
Stroke reduces mobility and can cause serious long-term disability.[15] After a stroke, over 90% of survivors experience some form of disability, which leads to functional limits and low quality of life. It directly influences health systems, which results in substantial costs, and is also regarded as a global public health problem.[16] Approximately 80% of hemiparetic patients have upper limb involvement.[17]
Current treatment includes a variety of methods to improve functional ability in hemiparetic subjects, like Bobath therapy,[18] constraint-induced movement therapy (CIMT),[19] injections,[20] electrical stimulation,[21] mental imagery,[22] and mirror box therapy.[23] Common conventional therapeutic interventions are frequent change in position and exercise therapy technique, which relies on the therapist and the requirements.[24] Hemiparetic and hemiplegic patients have quite different motor control impairments.[25] Arm ability training (AAT) is a systematic, standardized repeating training structure with eight training activities.[26]
Platz and Lotze[27] concluded that AAT encourages dexterity improvement after a stroke and is clinically effective. Although this study was done with the stroke population, it did not address functional mobility; thus, the need arises to identify the effect of AAT on functional mobility and dexterity in hemiparetic subjects.
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Materials and Methodology
Subjects
Ethical clearance was taken from the institutional ethical committee of Krupanidhi College of Physiotherapy (Ref. No: EC-MPT/21/PHY/015). All 42 hemiparetic subjects were described in the study, and informed consent was taken from them. The study design was made as a single group pre and post-test experimental study with a convenient sampling technique. The study was conducted at the outpatient department of Krupanidhi College of Physiotherapy, Hospitals in and around Bangalore, and home care centers. The duration of the study was from June 2021 to June 2022. Subjects who had the ischemic type of stroke with anterior cerebral artery involvement and who were in the subacute phase of stroke (3 weeks to 6 months' post-stroke) were included. Hemiparetic patients with Mini Mental State Evaluation scores more than 24 and muscle strength ⅗ for shoulder abduction and elbow flexion, according to Medical Research Council, were included. The subject should be able to move their fingers, and a precision grip should be preserved.[27] [28] The study includes both genders with an age limit of 45 to 70 years. Hemorrhagic stroke, deformities of the upper limb, epilepsy, fractures, sensory impairment, and visual & auditory deficits patients were excluded. Participants received 40 minutes of AAT and 20 minutes of conventional physical therapy. The treatment was given for five sessions in a week extending for 4 weeks. Measurements were taken before and after the treatment.
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Procedure
Arm Ability Training[28]
The participants were given AAT along with conventional therapy. Patients were given instructions regarding AAT, and a demonstration was done. AAT includes eight different extremity tasks: (a) Aiming—To touch a given aim with maximum speed; (b) Tapping is the alternative movement between the first, second, and third digits. (c) Cancellation: To cancel the circles of various sizes given on paper. (d) Turning: Turning of coins placed on a table surface. (e) Maze tracking: To track the maze printed on paper with a pencil. (f) Bolt and nut: to screw the nuts and bolts. (g) Placing small objects: placing small wooden blocks on top of each other. (h) Placing large objects: objects with different weights and volumes were moved side to side.
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Conventional Physiotherapy
Subjects were instructed to do the activities such as folding towels, removing bottle caps, turning keys, turning cards upside down, holding a pencil and drawing a line, and putting coins in the money box to increase functional mobility. Slow sustained stretching and strengthening exercises were also given for the paretic upper extremity.[29]
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Measurement Tools and Method
Wolf motor function test (WMFT)was taken to evaluate functional mobility.[30] The dexterity was measured using box and block test (BBT).[31]
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Statistical Analysis
Descriptive statistics were performed to calculate the demographic variables and outcome variables. A paired t-test was used to know the significant difference among the variables pre and post-test BBT and WMFT. The data were analyzed using SPSS version 29.0. The level of desired significance was kept at 5%. The samples that are collected from the subjects are normally distributed with 95% value.
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Results
The average age group of study subjects was 54.93 ± 7.819 years of 45 to 70 years. The average body mass index of the samples was 27.34 ± 2.424 kg/m2 of 23.2 to 32.6 kg/m2. The responses obtained were 28 (66.7%) and 14 (33.3%) from males and females respectively.
Paired t-test was used to analyze the pre- and post-treatment evaluation for BBT and WMFT. The results attained showed a significant improvement in all variables ([Table 1]); BBT pre-test mean ± standard deviation (SD; 20.31 ± 4.075) and post-test mean ± SD (23.79 ± 4.291), which indicate dexterity improvement. Functional ability of WMFT pre-test mean ± SD (45.38 ± 3.615) and post-test mean ± SD (54.07 ± 3.790) shows a significant improvement in functional ability. Time (seconds) of WMFT pre-test mean ± SD (479.29 ± 117.79) and post-test mean ± SD (434.4 ± 116.455) shows an improvement in time. Strength (lbs.) of WMFT pre-test mean ± SD (2.95 ± 0.731) and post-test mean ± SD (3.9 ± 0.759) shows an improvement in strength. Grip strength (kg) of WMFT pre-test mean ± SD (2.9 ± 1.559) and post-test mean ± SD (4.21 ± 1.539) shows an improvement in grip strength. There is a statistically significant difference for the variables BBT and WMFT (functional ability, time [seconds], strength [lbs.], and grip strength [kg]) and getting the p-value = 0.001 (<0.05) which indicates its highly significant.
Abbreviations: BBT, box and block test; SD, standard deviation; WMFT, wolf motor function test.
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Discussion
After a stroke, the paretic hand is a typical motor disability in which dexterity becomes impaired, which may restrict activities of daily living performance and social engagement and lower the quality of life for stroke patients.[32] The primary factor in determining how well the affected arm functions is the return of use to a paretic hand. Therefore, enhancing hand functions to encourage functional recovery is one of stroke rehabilitation's main objectives.[33] The AAT is a complicated motor training program specifically created for hemiparetic subjects.[34] The study objective was to know the effectiveness of AAT on functional mobility in hemiparetic patients. The efficacy of this study revealed improvement in upper limb functional mobility, time, grip strength, strength, and dexterity in hemiparetic patients.
In a study by Jose et al,[35] similar results were found showing good improvement in the upper limb functional skills in Parkinson's subjects. Similarly, Ladda et al[36] demonstrated an increase in the grip force in a study of 15 participants (t = −3.02, p = 0.01). Improvements were also observed in performance level over time in fine movements measured with Nine Hole Peg Test (NHPT; left: p = 0.01 and right: p = 0.05). There was a good improvement in hand performance over time (left: 34.1 ± 1.2 and right: 23.8 ± 1.0). Similar findings were also noticed in a study by Horn et al,[37] where all 12 patients had shown improvement in performing the task. The duration of AAT tasks decreased by 27.7% (t =17.61, p = 0.001). The NHPT duration declined by 25.2% (t =3.28, p = 0.007). BBT (number of block) increased by 20.9% (t =8.74, p = 0.001). This study is also supportive from the study results by Lotze et al,[38] where the arm's ability showed (27.79 ± 4.70) improvement within 2 weeks, which is a significant improvement in time (t = 20.07; p = 0.001). While the unaffected side's performance on the Test Evaluation es Membres Suprieurs de Personnes Agres (TEMPA) tasks did not change with time, the impacted side did (p = 0.001). AAT and TEMPA improvement in the paretic arm was positively correlated (r = 0.59; p = 0.028). Platz et al[28] found that the AAT decreased the focal impairment in hemiplegic and traumatic brain injury subjects with upper extremity paralysis. The patients showed the improvement by reducing the time required to complete the TEMPA tasks. The effects were unaffected significantly by knowing the outcome. At the 1-year follow-up, a functional advantage was seen as patients' TEMPA task summary time scores improved by 51.3 seconds (p = 0.0012) over pretest scores.
AAT facilitates motor learning in terms of maintenance and generalization of training effects.[34] Its design encourages intrinsic motivation, places premium neuroplasticity, and significantly improves a range of sensorimotor hand and arm abilities with lasting consequences, and also the functional reorganization of the brain with activation of premotor cortex among hemiparetic subjects underlies training-induced recovery of arm functions and similarly training-induced plasticity.[26] Additionally, two fundamental treatment philosophies shape conventional physiotherapeutic methods; the first is that the adult central nervous system may adapt or reorganize itself in some ways to restore impaired cognitive and motor functions, and the second is that, at any point following the onset of a stroke, ongoing improvement requires progressive skillful motor practice. Therefore, the repetition of certain tasks and exercises, local facilitation approaches, and motor relearning procedures can all be credited with the results.[39] With the above-discussed mechanism, it is proved that AAT and conventional physical therapy can result in greater functional mobility and dexterity in hemi-paretic patients.
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Limitation and Suggestions
The study was conducted only on a single group. It can be done with CIMT for comparison. The study findings cannot be generalized to all stroke patients. A study can be done with chronic stroke patients and large sample size to determine the effectiveness. The study lacks follow-up; the long-term effect of the intervention can be checked.
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Conclusion
Hemiparesis can result in functional restriction due to upper extremity weakness. It was proposed that AAT is a useful intervention for enhancing hemiparetic individuals' upper extremity function. The results demonstrate that adding AAT to the rehabilitation routine significantly improved stroke patients' upper extremity function, strength, grip strength, and dexterity. The proposed AAT can be used as adjunct training to be included with the conventional program to improve the patient's functional ability in hemiparesis.
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Conflict of Interest
None declared.
Acknowledgment
The authors extend their heartfelt gratitude to the Management of Krupanidhi College of Physiotherapy and Krupanidhi Research and Incubation Center (KRIC) for laying down immense guidance and support throughout.
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References
- 1 Aho K, Harmsen P, Hatano S, Marquardsen J, Smirnov VE, Strasser T. Cerebrovascular disease in the community: results of a WHO collaborative study. Bull World Health Organ 1980; 58 (01) 113-130
- 2 Avan A, Digaleh H, Di Napoli M. et al. Socioeconomic status and stroke incidence, prevalence, mortality, and worldwide burden: an ecological analysis from the Global Burden of Disease Study 2017. BMC Med 2019; 17 (01) 191
- 3 Venketasubramanian N, Yoon BW, Pandian J, Navarro JC. Stroke epidemiology in south, east, and south-east Asia: a review. J Stroke 2017; 19 (03) 286-294
- 4 Guzik A, Bushnell C. Stroke epidemiology and risk factor management. Continuum (Minneap Minn) 2017; 23 (1, Cerebrovascular Disease): 15-39
- 5 Johnson CO, Nguyen M, Roth GA. et al; GBD 2016 Stroke Collaborators. Global, regional, and national burden of stroke, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol 2019; 18 (05) 439-458
- 6 Yamada Y, Kato K, Oguri M. et al. Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population. J Med Genet 2008; 45 (04) 216-221
- 7 Raghavan P. Upper limb motor impairment after stroke. Phys Med Rehabil Clin N Am 2015; 26 (04) 599-610
- 8 Knight-Greenfield A, Nario JJQ, Gupta A. Causes of acute stroke: a patterned approach. Radiol Clin North Am 2019; 57 (06) 1093-1108
- 9 Hakimi R, Garg A. Imaging of hemorrhagic stroke. Continuum (Minneap Minn) 2016; 22 (5, Neuroimaging): 1424-1450
- 10 Heit JJ, Iv M, Wintermark M. Imaging of intracranial hemorrhage. J Stroke 2017; 19 (01) 11-27
- 11 Hankey GJ, Blacker DJ. Is it a stroke?. BMJ 2015; 350: 1-6
- 12 Bindawas SM, Mawajdeh HM, Vennu VS, Alhaidary HM. Functional recovery differences after stroke rehabilitation in patients with uni- or bilateral hemiparesis. Neurosciences (Riyadh) 2017; 22 (03) 186-191
- 13 Lang CE, Bland MD, Bailey RR, Schaefer SY, Birkenmeier RL. Assessment of upper extremity impairment, function, and activity after stroke: foundations for clinical decision making. J Hand Ther 2013; 26 (02) 104-114 , quiz 115
- 14 Lang CE, Wagner JM, Edwards DF, Dromerick AW. Upper extremity use in people with hemiparesis in the first few weeks after stroke. J Neurol Phys Ther 2007; 31 (02) 56-63
- 15 Benjamin EJ, Muntner P, Alonso A. et al; American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart disease and stroke statistics—2019 update: a report from the American Heart Association. Circulation 2019; 139 (10) e56-e528
- 16 Ramos-Lima MJM, Brasileiro IC, Lima TL, Braga-Neto P. Quality of life after stroke: impact of clinical and sociodemographic factors. Clinics (São Paulo) 2018; 73: e418
- 17 Pulman J, Buckley E. Assessing the efficacy of different upper limb hemiparesis interventions on improving health-related quality of life in stroke patients: a systematic review. Top Stroke Rehabil 2013; 20 (02) 171-188
- 18 Díaz-Arribas MJ, Martín-Casas P, Cano-de-la-Cuerda R, Plaza-Manzano G. Effectiveness of the Bobath concept in the treatment of stroke: a systematic review. Disabil Rehabil 2020; 42 (12) 1636-1649
- 19 Kwakkel G, Veerbeek JM, van Wegen EE, Wolf SL. Constraint-induced movement therapy after stroke. Lancet Neurol 2015; 14 (02) 224-234
- 20 Bethoux F. Spasticity management after stroke. Phys Med Rehabil Clin N Am 2015; 26 (04) 625-639
- 21 Eraifej J, Clark W, France B, Desando S, Moore D. Effectiveness of upper limb functional electrical stimulation after stroke for the improvement of activities of daily living and motor function: a systematic review and meta-analysis. Syst Rev 2017; 6 (01) 40
- 22 Ietswaart M, Johnston M, Dijkerman HC. et al. Mental practice with motor imagery in stroke recovery: randomized controlled trial of efficacy. Brain 2011; 134 (Pt 5): 1373-1386
- 23 Pérez-Cruzado D, Merchán-Baeza JA, González-Sánchez M, Cuesta-Vargas AI. Systematic review of mirror therapy compared with conventional rehabilitation in upper extremity function in stroke survivors. Aust Occup Ther J 2017; 64 (02) 91-112
- 24 Rahayu UB, Wibowo S, Setyopranoto I, Hibatullah Romli M. Effectiveness of physiotherapy interventions in brain plasticity, balance and functional ability in acute stroke survivors: a randomized controlled trial. Neuro Rehabil 2020; 31: 1-8
- 25 Nakayama H, Jørgensen HS, Raaschou HO, Olsen TS. Recovery of upper extremity function in stroke patients: the Copenhagen Stroke Study. Arch Phys Med Rehabil 1994; 75 (04) 394-398
- 26 Platz T, van Kaick S, Mehrholz J, Leidner O, Eickhof C, Pohl M. Best conventional therapy versus modular impairment-oriented training for arm paresis after stroke: a single-blind, multicenter randomized controlled trial. Neurorehabil Neural Repair 2009; 23 (07) 706-716
- 27 Platz T, Lotze M. Arm Ability Training (AAT) promotes dexterity recovery after a stroke—a review of its design, clinical effectiveness, and the neurobiology of the actions. Front Neurol 2018; 9: 1082
- 28 Platz T, Winter T, Müller N, Pinkowski C, Eickhof C, Mauritz KH. Arm ability training for stroke and traumatic brain injury patients with mild arm paresis: a single-blind, randomized, controlled trial. Arch Phys Med Rehabil 2001; 82 (07) 961-968
- 29 Kisner C, Colby LA, Borstad J. Therapeutic Exercise: Foundations and Techniques. 7th ed.. Philadelphia: FA Davis; 2018: 534-584
- 30 Edwards DF, Lang CE, Wagner JM, Birkenmeier R, Dromerick AW. An evaluation of the Wolf Motor Function Test in motor trials early after stroke. Arch Phys Med Rehabil 2012; 93 (04) 660-668
- 31 Lin KC, Chuang LL, Wu CY, Hsieh YW, Chang WY. Responsiveness and validity of three dexterous function measures in stroke rehabilitation. J Rehabil Res Dev 2010; 47 (06) 563-571
- 32 Lin KC, Chen YA, Chen CL, Wu CY, Chang YF. The effects of bilateral arm training on motor control and functional performance in chronic stroke: a randomized controlled study. Neurorehabil Neural Repair 2010; 24 (01) 42-51
- 33 Jung-Hee K, Byoung-hee L. The effect of mirror therapy on functional recovery of upper extremity after stroke: a randomized pilot study. J Exp Stroke Transl Med 2017; •••: 1-7
- 34 Platz T, Roschka S, Doppl K. et al. Prolonged motor skill learning–a combined behavioural training and θ burst TMS study. Restor Neurol Neurosci 2012; 30 (03) 213-224
- 35 Jose F, Meena SK, Jain N. Effectiveness of combined use of arm ability training with arm weight support to improve upper extremity functional skills and ADL skills in Parkinsonism patients. EPRA Int J Multidisciplinary Res 2021; 7 (07) 283-289 (IJMR)
- 36 Ladda AM, Pfannmoeller JP, Kalisch T. et al. Effects of combining 2 weeks of passive sensory stimulation with active hand motor training in healthy adults. PLoS One 2014; 9 (01) e84402
- 37 Horn U, Roschka S, Eyme K, Walz AD, Platz T, Lotze M. Increased ventral premotor cortex recruitment after arm training in an fMRI study with subacute stroke patients. Behav Brain Res 2016; 308: 152-159
- 38 Lotze M, Roschka S, Domin M, Platz T. Predicting training gain for a 3 week period of arm ability training in the sub-acute stage after stroke. Front Neurol 2018; 9 (854) 854
- 39 Dobkin BH, Dorsch A. New evidence for therapies in stroke rehabilitation. Curr Atheroscler Rep 2013; 15 (06) 331
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Article published online:
01 December 2023
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References
- 1 Aho K, Harmsen P, Hatano S, Marquardsen J, Smirnov VE, Strasser T. Cerebrovascular disease in the community: results of a WHO collaborative study. Bull World Health Organ 1980; 58 (01) 113-130
- 2 Avan A, Digaleh H, Di Napoli M. et al. Socioeconomic status and stroke incidence, prevalence, mortality, and worldwide burden: an ecological analysis from the Global Burden of Disease Study 2017. BMC Med 2019; 17 (01) 191
- 3 Venketasubramanian N, Yoon BW, Pandian J, Navarro JC. Stroke epidemiology in south, east, and south-east Asia: a review. J Stroke 2017; 19 (03) 286-294
- 4 Guzik A, Bushnell C. Stroke epidemiology and risk factor management. Continuum (Minneap Minn) 2017; 23 (1, Cerebrovascular Disease): 15-39
- 5 Johnson CO, Nguyen M, Roth GA. et al; GBD 2016 Stroke Collaborators. Global, regional, and national burden of stroke, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016. Lancet Neurol 2019; 18 (05) 439-458
- 6 Yamada Y, Kato K, Oguri M. et al. Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population. J Med Genet 2008; 45 (04) 216-221
- 7 Raghavan P. Upper limb motor impairment after stroke. Phys Med Rehabil Clin N Am 2015; 26 (04) 599-610
- 8 Knight-Greenfield A, Nario JJQ, Gupta A. Causes of acute stroke: a patterned approach. Radiol Clin North Am 2019; 57 (06) 1093-1108
- 9 Hakimi R, Garg A. Imaging of hemorrhagic stroke. Continuum (Minneap Minn) 2016; 22 (5, Neuroimaging): 1424-1450
- 10 Heit JJ, Iv M, Wintermark M. Imaging of intracranial hemorrhage. J Stroke 2017; 19 (01) 11-27
- 11 Hankey GJ, Blacker DJ. Is it a stroke?. BMJ 2015; 350: 1-6
- 12 Bindawas SM, Mawajdeh HM, Vennu VS, Alhaidary HM. Functional recovery differences after stroke rehabilitation in patients with uni- or bilateral hemiparesis. Neurosciences (Riyadh) 2017; 22 (03) 186-191
- 13 Lang CE, Bland MD, Bailey RR, Schaefer SY, Birkenmeier RL. Assessment of upper extremity impairment, function, and activity after stroke: foundations for clinical decision making. J Hand Ther 2013; 26 (02) 104-114 , quiz 115
- 14 Lang CE, Wagner JM, Edwards DF, Dromerick AW. Upper extremity use in people with hemiparesis in the first few weeks after stroke. J Neurol Phys Ther 2007; 31 (02) 56-63
- 15 Benjamin EJ, Muntner P, Alonso A. et al; American Heart Association Council on Epidemiology and Prevention Statistics Committee and Stroke Statistics Subcommittee. Heart disease and stroke statistics—2019 update: a report from the American Heart Association. Circulation 2019; 139 (10) e56-e528
- 16 Ramos-Lima MJM, Brasileiro IC, Lima TL, Braga-Neto P. Quality of life after stroke: impact of clinical and sociodemographic factors. Clinics (São Paulo) 2018; 73: e418
- 17 Pulman J, Buckley E. Assessing the efficacy of different upper limb hemiparesis interventions on improving health-related quality of life in stroke patients: a systematic review. Top Stroke Rehabil 2013; 20 (02) 171-188
- 18 Díaz-Arribas MJ, Martín-Casas P, Cano-de-la-Cuerda R, Plaza-Manzano G. Effectiveness of the Bobath concept in the treatment of stroke: a systematic review. Disabil Rehabil 2020; 42 (12) 1636-1649
- 19 Kwakkel G, Veerbeek JM, van Wegen EE, Wolf SL. Constraint-induced movement therapy after stroke. Lancet Neurol 2015; 14 (02) 224-234
- 20 Bethoux F. Spasticity management after stroke. Phys Med Rehabil Clin N Am 2015; 26 (04) 625-639
- 21 Eraifej J, Clark W, France B, Desando S, Moore D. Effectiveness of upper limb functional electrical stimulation after stroke for the improvement of activities of daily living and motor function: a systematic review and meta-analysis. Syst Rev 2017; 6 (01) 40
- 22 Ietswaart M, Johnston M, Dijkerman HC. et al. Mental practice with motor imagery in stroke recovery: randomized controlled trial of efficacy. Brain 2011; 134 (Pt 5): 1373-1386
- 23 Pérez-Cruzado D, Merchán-Baeza JA, González-Sánchez M, Cuesta-Vargas AI. Systematic review of mirror therapy compared with conventional rehabilitation in upper extremity function in stroke survivors. Aust Occup Ther J 2017; 64 (02) 91-112
- 24 Rahayu UB, Wibowo S, Setyopranoto I, Hibatullah Romli M. Effectiveness of physiotherapy interventions in brain plasticity, balance and functional ability in acute stroke survivors: a randomized controlled trial. Neuro Rehabil 2020; 31: 1-8
- 25 Nakayama H, Jørgensen HS, Raaschou HO, Olsen TS. Recovery of upper extremity function in stroke patients: the Copenhagen Stroke Study. Arch Phys Med Rehabil 1994; 75 (04) 394-398
- 26 Platz T, van Kaick S, Mehrholz J, Leidner O, Eickhof C, Pohl M. Best conventional therapy versus modular impairment-oriented training for arm paresis after stroke: a single-blind, multicenter randomized controlled trial. Neurorehabil Neural Repair 2009; 23 (07) 706-716
- 27 Platz T, Lotze M. Arm Ability Training (AAT) promotes dexterity recovery after a stroke—a review of its design, clinical effectiveness, and the neurobiology of the actions. Front Neurol 2018; 9: 1082
- 28 Platz T, Winter T, Müller N, Pinkowski C, Eickhof C, Mauritz KH. Arm ability training for stroke and traumatic brain injury patients with mild arm paresis: a single-blind, randomized, controlled trial. Arch Phys Med Rehabil 2001; 82 (07) 961-968
- 29 Kisner C, Colby LA, Borstad J. Therapeutic Exercise: Foundations and Techniques. 7th ed.. Philadelphia: FA Davis; 2018: 534-584
- 30 Edwards DF, Lang CE, Wagner JM, Birkenmeier R, Dromerick AW. An evaluation of the Wolf Motor Function Test in motor trials early after stroke. Arch Phys Med Rehabil 2012; 93 (04) 660-668
- 31 Lin KC, Chuang LL, Wu CY, Hsieh YW, Chang WY. Responsiveness and validity of three dexterous function measures in stroke rehabilitation. J Rehabil Res Dev 2010; 47 (06) 563-571
- 32 Lin KC, Chen YA, Chen CL, Wu CY, Chang YF. The effects of bilateral arm training on motor control and functional performance in chronic stroke: a randomized controlled study. Neurorehabil Neural Repair 2010; 24 (01) 42-51
- 33 Jung-Hee K, Byoung-hee L. The effect of mirror therapy on functional recovery of upper extremity after stroke: a randomized pilot study. J Exp Stroke Transl Med 2017; •••: 1-7
- 34 Platz T, Roschka S, Doppl K. et al. Prolonged motor skill learning–a combined behavioural training and θ burst TMS study. Restor Neurol Neurosci 2012; 30 (03) 213-224
- 35 Jose F, Meena SK, Jain N. Effectiveness of combined use of arm ability training with arm weight support to improve upper extremity functional skills and ADL skills in Parkinsonism patients. EPRA Int J Multidisciplinary Res 2021; 7 (07) 283-289 (IJMR)
- 36 Ladda AM, Pfannmoeller JP, Kalisch T. et al. Effects of combining 2 weeks of passive sensory stimulation with active hand motor training in healthy adults. PLoS One 2014; 9 (01) e84402
- 37 Horn U, Roschka S, Eyme K, Walz AD, Platz T, Lotze M. Increased ventral premotor cortex recruitment after arm training in an fMRI study with subacute stroke patients. Behav Brain Res 2016; 308: 152-159
- 38 Lotze M, Roschka S, Domin M, Platz T. Predicting training gain for a 3 week period of arm ability training in the sub-acute stage after stroke. Front Neurol 2018; 9 (854) 854
- 39 Dobkin BH, Dorsch A. New evidence for therapies in stroke rehabilitation. Curr Atheroscler Rep 2013; 15 (06) 331