Clinical application of computerized evaluation and re-education biofeedback prototype for sensorimotor control of the hand in stroke patients
© Hsu et al.; licensee BioMed Central Ltd. 2012
Received: 20 July 2011
Accepted: 20 April 2012
Published: 9 May 2012
Hemianaesthesia patients usually exhibit awkward and inefficient finger movements of the affected hands. Conventionally, most interventions emphasize the improvement of motor deficits, but rarely address sensory capability and sensorimotor control following stroke. Thus it is critical for stroke patients with sensory problems to incorporate appropriate strategies for dealing with sensory impairment, into traditional hand function rehabilitation programs. In this study, we used a custom-designed computerized evaluation and re-education biofeedback (CERB) prototype to analyze hand grasp performances, and monitor the training effects on hand coordination for stroke patients with sensory disturbance and without motor deficiency.
The CERB prototype was constructed to detect momentary pinch force modulation for 14 sub-acute and chronic stroke patients with sensory deficiency and 14 healthy controls. The other ten chronic stroke patients (ranges of stroke period: 6–60 months) were recruited to investigate the effects of 4-weeks computerized biofeedback treatments on the hand control ability. The biofeedback procedures provide visual and auditory cues to the participants when the interactive force of hand-to-object exceeded the target latitude in a pinch-up-holding task to trigger optimal motor strategy. Follow-up measurements were conducted one month after training. The hand sensibility, grip forces and results of hand functional tests were recorded and analyzed.
The affected hands of the 14 predominant sensory stroke patients exhibited statistically significant elevation in the magnitude of peak pinch force (p = 0.033) in pinching and lifting-up tasks, and poor results for hand function tests (p = 0.005) than sound hands did. In addition, the sound hands of patients were less efficient in force modulation (p = 0.009) than the hands of healthy subjects were. Training with the biofeedback system produced significant improvements in grip force modulation (p = 0.020) and better performances in the subtests of pin insertion (p = 0.019), and lifting of lightweight objects (p = 0.005).
The CERB prototype can provide momentary and interactive information for quantitative assessing and re-educating force modulation appropriately for stroke patients with sensory deficits. Furthermore, the patients could transfer the learned strategy to improve hand function.
Stroke-related impairment often restricts patients from properly participating in the activities of daily living, and impedes social interactions. The stroke is judged to be the sixth most common cause of reduced disability-adjusted life years, which provides a common metric for meaningful comparison of the burden of risk factors, disease, and injury . Motor deficits of the hands and upper extremities are important determinants, and strongly represent one’s ability to regain independence in daily and social living . Previous reports describe that approximately 60–70% of stroke patients exhibit mild to severe hand dysfunction [2–5]; and up to 20% of stroke survivors were dependent in their basic daily living activities . Such negative impacts on function are a strong motivation for researchers to investigate hand movement dynamics  and to develop effective therapeutic interventions for stroke patients .
Stroke patient hand dysfunction has been assessed by both quantitative and qualitative tests, such as the Brunnstrom recovery stages , maximum grip strength, the Fugl-Meyer assessment , and real-life Motor Activity Log questionnaires . However, use of these traditional and common evaluation methods does not assess the delicate controls of the hand, such as spatio-temporal coordination of multi-segmented movements and precise force modulation. Investigating hand-to-object interactions by analysis of sets of time-series data obtained from joints of the upper extremities can provide a thorough understanding of the hand coordination of stroke patients . During the past two decades, patient capacity for precision grip has become an indicator for investigating skilled movement control . When an object is lifted and moved around in space, the pinch force should be modulated simultaneously with movement-induced load fluctuations [14–16]. The task-related sensorimotor processing depends on a complicated integration of feed-forward and feedback control mechanisms. Due to the decline in sensorimotor function suffered by stroke patients, affected hands do not have the ability to produce finger forces appropriate to an object’s manipulation [17, 18]. A similar phenomenon was also observed in the sound hand of stroke patients . However, motor dysfunction is generally considered as the main cause of hand function deficit; by contrast, less emphasis has been directed to the effects of sensory disturbances on functional performances even though approximately 50–85% stroke survivors with dysfunction of different sensory modalities have been reported .
Persons lacking sufficient ability for sensory modulation control generally use excessive force, or exercise clumsy manipulation when executing tasks [15, 16, 21–23]. Similar patterns occur for cerebral stroke patients with predominant sensory symptoms which indicate the patients with impaired sensibility still had sufficient hand motor functions, such as pinch and lift abilities [17, 18, 24], that is, improper programming of pinching behavior may lead to a clumsy hand in mild stroke patients. Thus, the purpose of sensory re-education is not only to provide opportunities to fulfill an individual’s sensory potential, but also to provide the chance to learn sensorimotor control strategies that are not emphasized in current clinical practices. Consequently, it is crucial for improving stroke patient quality of life to integrate suitable strategies for improving sensory function of the hand, and to promote useful sensorimotor operations into rehabilitation programs.
A better and more efficient motor response is learned using a well-integrated neurophysiological feedback system. However, most of the available biofeedback equipment and techniques currently available are used to retrain of movement and postural motor control [25, 26]. Only few feedback trainings methods in the literatures have been suggested focusing on the break-up synergistic patterns and facilitation on poorly recruited muscles of elbow, wrist and finger extensors [27, 28]. However, fine manipulative movements of thumb and fingers are difficult to regain, and it is challenging to monitor the outcomes via the feedback training. For those with hemiparesis post stroke, the ability to grasp may be an important indicator of the functional use of the upper extremities. A previous study found that biofeedback training provided significant restoration of grip force control in stroke patients ; training emphasis was placed on motor deficits and force production. Though awkward and inefficient finger movements of affected hands have been observed in hemianaesthesia patients [17, 18, 24], there was no literature mentioned on how to improve hand coordination caused by impaired sensibility. Therefore, we assumed that using of a system that can provide real-time and interactive information to patients with impaired sensation facilitates learning and execution at an appropriate functional level which offers a practical strategy for neuro-rehabilitation. According to the above-mentioned treatment framework, a control interface and software system, which linked up our previously designed pinch device [30, 31] to set up a computerized biofeedback system was created for functional sensibility intervention in this study. The first specific aim of our study was to assess the pathophysiology of the clumsy hand movements of stroke patients with predominant sensory deficiency. We analyzed the relationship between the ability to modulate in a functional task and the actual hand capacity of the patients. The second aim was to investigate whether the traditional rehabilitation program, combined with computerized biofeedback training could improve the pinch coordination of chronic stroke patients with sensory deficiency. Additionally, we analyzed whether or not the beneficial effects on fine motor coordination were sustained at a one-month follow-up assessment.
In the first part of the study, we recruited fourteen stroke patients (nine males and five females) with predominant sensory symptoms to assess the pathophysiology of clumsy performance by the hands following a predominant sensory-stroke in the period March 2009 to September 2009. The predominant sensory symptoms refer to the patients of this study who suffered from impaired sensibility but still had sufficient hand pinch and lift ability. The subjects were referred by the Department of Physical Medicine and Rehabilitation, National Cheng Kung University Hospital. They should met the following criteria: (1) unilateral cerebral infarction, (2) CT scan or MRI imaging excluding pathologies other than unilateral cerebral hemisphere injury which was diagnosis by a physiatrist of physical medicine and rehabilitation, (3) had the ability to pinch and lift a pinch apparatus with their thumb and index finger, (4) were right handed. Exclusion criteria were as follows: (1) patients had major cognitive-perception deficit, i.e., praxis, memory, alertness and intellect which were screened by Mini-mental state examination, Lowenstein occupational therapy cognitive assessment (2) patients who could not understand or follow instructions. The affected hands included six dominant hands and eight non-dominant hands. The age range was from 26 to 74 years, and the mean age was 57.86 ± 12.03 years. An equal number of healthy, age-and-gender matched control participants, who were without evidence of any neurological deficit or orthopedic abnormality, were also recruited into this part. The second part of this study analyzed the effects of computerized biofeedback training for patients who should meet the criteria of the first part of the study. In addition, the probability for spontaneously regaining hand dexterity of the stroke patients should not be expected after 6 months of stroke onset . To understand how the learned strategy through the prototype impacts on movement control of the affected hands, the essential requirement should be greater than 6 months post stroke onset. Ten subjects (seven males and three females) who fitted the requirements were recruited; the mean age was 57.1 ± 15.1 (age range: 26 to 74 years) years old. The mean time from stroke onset to our first evaluation was 18.8 ± 18.4 (duration range: 6–60) months. All participants were informed of the purpose of this study and signed consent forms approved by the Hospital’s Institutional Review Board.
Computerized Evaluation and Re-education Biofeedback (CERB) prototype
The computer interface consisted of a manual setting panel and real-time feedback display panel. Before the execution of the biofeedback intervention, the therapist should set up the target force range using the manual setting system. The target force range was selected to be in a range within the pinch apparatus loads up to 94% of the peak pinch force by the affected hand obtained during the initial evaluation. The 94% of peak pinch force value, was determined according to result of the average non-dominant hand producing 6% excessive force than the dominant hand to complete pinch-lifting task obtained in our previous study . Based on the motor re-learning theory, motor planning of the affected hand would be more accurately programmed to optimize force during lifting through practice; therefore, we decided that this 6% difference could be possibly improved upon by the CERB prototype. Patients next performed new PUHA test trials in the training session. The detected force in the new test was compared with the target force level by a feedback loop. Once the force output fell outside the target range, visual and auditory cues were activated to inform the subject. Each participant received five repeated PUHA training runs in each treatment session. The exerted force and the force ratio between pinch force and load force were recorded, and displayed on the monitor in real time. The CERB protocol required 10–15 minutes per session, 3 times a week for 4 weeks.
Traditional sensory test
Traditional sensory evaluations including static and moving two-point discrimination (2PD) tests and the Semmes-Weinstein (SW) monofilament test were used to measure sensibility of the thumb pulp. The 2 PD test is a meaningful method of assessing tactile gnosis, while the SW monofilament test is used to measure the cutaneous pressure threshold. To understand the ability of sensing joints movement of patients, the proprioception test was set patient’s sound arm into a specific position then patient is asked to place their sound arm into the same position.
Hand function test
In the study, we used two timed measure of hand function tests. The Purdue pegboard test was used to test the gross movement of arm, and fine fingertip dexterity . Subjects were asked to pick and place as many pins as possible into the holes in thirty seconds. To understand the ability of adapting the manipulative forces in executing functional task, subtests 6 and 7 (lifting an empty tin can and a full tin can weighing 1 lb, respectively) of the Jebsen-Taylor Hand Function Test were used as force –matching tasks to assess how peripheral sensory information contributed to hand function . Each of the tests is the widely used as an outcome measure for hand functions.
All subjects received their initial evaluations by recording basic personal information, the force parameters obtained from a PUHA test, results of the Purdue pegboard test, the Jebsen-Taylor hand function test, and traditional sensibility tests. Participants in the intervention group received a 25-minute traditional rehabilitation program (including task-based trainings by functional activities, inhibition techniques for normalizing the abnormal tone and training with daily living skills), in addition to the ten-minutes biofeedback training over 12 successive sessions, which were conducted three times per week and supervised by an occupational therapist. After undergoing this 4-week program, tests carried out in the initial evaluations were repeated for comparison purposes. Follow-up measurements were conducted one-month post-training.
We analyzed precision pinch ability of stroke patients with predominant sensory deficits for improvement of hand function resulting from the computerized biofeedback training. The precision grip parameters were the peak pinch force (FPpeak), and the FPpeak and FLmax force ratio achieved during the PUHA test.
The Wilcoxon signed ranks test was used to test the differences in pinch force adjustment parameters obtained in the PUHA task and hand function tests, for the stroke patients’ normal and affected hands. The Wilcoxon signed ranks test was also used to analyze the differences in the magnitude of force ratio between the sound hand of stroke patients and the matched-hand of healthy control subjects. The Pearson correlation test was used to determine the correlation between tactile sensibility and pinch force adjustment in the PUHA task, and the hand function test in stroke patients. To understand the training effect of CERB prototype, the Friedman’s test was used to analyze the responsibility of pinch force modulation and results of hand function test for the stroke patients before, after and 1-month’s follow-up completing computerized biofeedback training.
Sensory status of recruited subjects
Proprioception of shoulder and elbow
Proprioception of hand
*Classification of 2PD sensibility
**Scale of interpretation of SW test
Loss of protective sensation
Diminished light touch
Diminished light touch
Diminished light touch
Loss of protective sensation
Diminished light touch
Loss of protective sensation
Diminished protective sensation
Loss of protective sensation
Diminished light touch
Diminished light touch
Diminished light touch
Diminished protective sensation
Diminished light touch
The difference of force parameters and hand function between the affected and sound hand of stroke patients (n = 14)
Affected hand Mean (SD)
Sound hand Mean (SD)
Force ratio: FPPeak/FLmax
Peak Pinch force: FPpeak (N)
Jebsen-Taylor lifting light object (secs)
Jebsen-Taylor lifting heavy object (secs)
Correlation between force parameters, hand function tests and pressure threshold test in a lifting performance
Force ratio (Max)
Pinch force (Max)
Time (lifting light objects)
Time (lifting heavy objects)
S-W (pressure threshold test)
Training effects of computerized force re-education on finger dexterity
Pre-training Mean (SD)
Post-training Mean (SD)
Follow-up Mean (SD)
Inserting pins (Numbers)
Time of lifting light objects (seconds)
Time of lifting heavy objects (seconds)
Sensory-related deficits are mentioned less often than motor impairment is, when discussing the rehabilitation outcome of stroke patients. However, some researchers have proposed that insufficient sensory information contributes to impaired hand function [15, 37]. In this study, 100% of the patients with impaired-to-loss pressure threshold could not response to stimulation accurately and immediately; eight (57%) of them with impaired pressure threshold also exhibited diminished discriminative sensation, that is, the patients could not recognize objects which they were holding; and six (42.8%) of them with impaired-to-loss proprioception of the shoulder and elbow were unable to sense movement of joints when moving properly. Though the motor function was unaffected of the recruited patients, the impaired sensory function resulted in inefficient force interaction between fingers and object so much as overall hand functions of the patients (Table 2). The force parameters acquired during the pinch task indicate that the subject’s sound hands perform with greater force-control precision in functional tasks, and produce better results in the hand function test than the affected hands do, and previous studies produced similar results [2, 17, 18]. In recent years, there was a growing literature exploring how the sensory disturbance leaded to motor symptoms and clumsy hand function [34, 38]. Insufficient sensory signals from mechanoreceptors of digits making the patient unable to judge the characters of the object timely, such as: shape, texture and weight ; therefore, elevation of pinch force is a compensatory strategy used by patients with impaired sensibility to prevent an object from slipping during execution of a functional task . Results of a recent longitudinal study revealed that a strong relationship between finger force control ability and moving 2PD tests and SW monofilament test (correlation coefficient was 0.810 and 0.852 respectively) for the peripheral nerve injury patients . Similar finding was obtained in this study, we observed a statistically significant moderate and quantitative correlation between the ability to exercise force control, and tactile threshold and a similar correlation occurred between hand function and tactile threshold. In particular, a significantly high correlation between tactile sensibility and the time required to lift light objects demonstrated that subjects needed considerable time to adapt exertion force to lifting a lightweight object, when they were unable to acquire sufficient sensory information about the objects’ physical characteristics.
The finger-force modulation PUHA task results for sound hand of the subjects with sensory pre-dominant stroke also showed greater inefficiency than results for healthy control subjects did. A few researchers reported similar findings, using different experimental models [18, 19]. Motor deficits are often evident on the side of the body that is contralateral to the side with brain damage following stroke, and the inter-limb coupling mechanism might contribute to the subtle impairment seen on the sound side [42, 43]. Stroke patients receiving traditional assessments for evaluation of stroke patient hand function demands concentration while performing the motor tasks, and unfortunately such assessments cannot always detect the true abilities of the sound hand . While the coupling of pinch force modulation, with changes in loading is an automated response, it is not subject to the examinee’s conscious control . Therefore, reduced motor control efficiency is a potential indicator of sound hand function, because of reduced sensorimotor control, though in the present study, motor control efficiency was unaffected by attention or cognitive deficits. That is to say, detection of the hand-to-object force interaction could be a valid and reliable tool for testing the sound hand function of stroke patients, and could be an indicator of the ability to participate in daily living activities.
In the second part of the study, all the computerized force re-education subjects were in the chronic phase (post-event duration was greater than 6 months). Though a lot of literatures proved that the probability of regaining upper extremity function should not be expected at 3–6 months after stroke onset [3, 32]; nevertheless, we found that administering the computerized biofeedback intervention could improve pinch force modulation for stroke patients with sensory deficiencies. One previous study proposed a novel tracking system for the assessment and training of grip force control in a patient with traumatic brain injury; the authors found the patient gained improvements in grip force control after training with the tracking system . However, the patient’s sensory condition and hand manipulation ability had not been quantitatively analyzed in their series of investigations. In our study, subjects exhibited a noticeable training effect, not only on the pinch force modulation, but also in hand coordination, and still showed these gains one month after completing the computerized biofeedback and re-education program. Thus, the sensorimotor retraining program was successful in improving the subjects’ functional performances. The improvements seen in the hand function test following completion of the training program meant that patients had learned to modify their pinch strategy to meet the demands of the task, and so facilitate movement control of their hand. This study’s results support the hypothesis that a learned strategy for control of pinch force can promote hand coordination of stroke patients in functional tests. The biofeedback re-education program was suited for providing threshold adjustments, monitoring, and real-time feedback to aid the restoration of deficient sensorimotor controls. The CERB prototype could be used as an enrichment of existing sensorimotor therapy, to enhance the function of an affected hand, especially in the Purdue pegboard pin insertion test, and the Jebson Taylor lightweight object lifting task subtests. The experimental evidence indicates that meaningful sensorimotor retraining should commence following a stroke to improve functional use of the affected hand, and our novel bio-interface feedback system is an effective therapy device for such hand function retraining.
This report introduced a system that can provide real-time and interactive information for quantitative assessing and re-educating the delicate hand function for stroke patients with sensory deficits. Though the numbers of recruited subjects were relatively small, we demonstrated that there exists a direct correlation between the measured application force and actual hand function. In addition, the obtained results of the study showed strong evidence that the benefit of using CERB prototype in stroke rehabilitation is not only improving the ability to modulate force appropriately and the learned strategy also could be transferred to improve hand functions. Furthermore, the effectiveness of treatment could be maintained for one month after completing the treatment. Thus, we conclude that the proposed conjunct system in this study are suited for evaluating and restoring sensorimotor function for patients with impaired sensibility even for chronic stage patients. In future work, we intend to investigate long-term effects of biofeedback training on hand function for patients with sensorimotor dysfunction.
This work was supported by National Science Council grant NSC94-2314-B-006-104, TAIWAN.
- Murray CJ, Lopez AD: Global mortality, disability, and the contribution of risk factors: Global Burden of Disease Study. Lancet. 1997, 349: 1436-1442. 10.1016/S0140-6736(96)07495-8.View ArticlePubMedGoogle Scholar
- Hunter SM, Crome P: Hand function and stroke. Rev Clin Gerontol. 2002, 12: 68-81.View ArticleGoogle Scholar
- Nakayama H, Jorgensen HS, Raaschou HO, Olsen TS: Recovery of upper extremity function in stroke patients: the Copenhagen Stroke Study. Arch Phys Med Rehabil. 1994, 75: 394-398. 10.1016/0003-9993(94)90161-9.View ArticlePubMedGoogle Scholar
- Wade DT, Langton-Hewer R, Wood VA, Skilbeck CE, Ismail HM: The hemiplegic arm after stroke: measurement and recovery. J Neurol Neurosurg Psychiatry. 1983, 46: 521-524. 10.1136/jnnp.46.6.521.PubMed CentralView ArticlePubMedGoogle Scholar
- Stroke Rehabilitation: The Recovery of Motor Control. Edited by: Duncan PW, Badke MB. 1988, Year Book Medical Publishers, Chicago, IllGoogle Scholar
- Rosamond W, Flegal K, Furie K, Go A, Greenlund K, Haase N, Hailpern SM, Ho M, Howard V, Kissela B, et al: Heart disease and stroke statistics–2008 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. Circulation. 2008, 117: e25-e146.View ArticlePubMedGoogle Scholar
- Trombly CA: Deficits of reaching in subjects with left hemiparesis: a pilot study. Am J Occup Ther. 1992, 46: 887-897. 10.5014/ajot.46.10.887.View ArticlePubMedGoogle Scholar
- Johansson BB: Current trends in stroke rehabilitation. A review with focus on brain plasticity. Acta Neurol Scand. 2011, 123: 147-159.View ArticlePubMedGoogle Scholar
- Brunnstrom S: Motor testing procedures in hemiplegia: based on sequential recovery stages. Phys Ther. 1966, 46: 357-375.PubMedGoogle Scholar
- Fugl-Meyer AR, Jaasko L, Leyman I, Olsson S, Steglind S: The post-stroke hemiplegic patient. 1. a method for evaluation of physical performance. Scand J Rehabil Med. 1975, 7: 13-31.PubMedGoogle Scholar
- Uswatte G, Taub E, Morris D, Light K, Thompson PA: The Motor Activity Log-28: assessing daily use of the hemiparetic arm after stroke. Neurology. 2006, 67: 1189-1194. 10.1212/01.wnl.0000238164.90657.c2.View ArticlePubMedGoogle Scholar
- Nowak DA: The impact of stroke on the performance of grasping: usefulness of kinetic and kinematic motion analysis. Neurosci Biobehav Rev. 2008, 32: 1439-1450. 10.1016/j.neubiorev.2008.05.021.View ArticlePubMedGoogle Scholar
- Witney AG, Wing A, Thonnard JL, Smith AM: The cutaneous contribution to adaptive precision grip. Trends Neurosci. 2004, 27: 637-643. 10.1016/j.tins.2004.08.006.View ArticlePubMedGoogle Scholar
- Johansson RS, Hager C, Riso R: Somatosensory control of precision grip during unpredictable pulling loads. II. Changes in load force rate. Exp Brain Res. 1992, 89: 192-203. 10.1007/BF00229016.View ArticlePubMedGoogle Scholar
- Johansson RS, Westling G: Roles of glabrous skin receptors and sensorimotor memory in automatic control of precision grip when lifting rougher or more slippery objects. Exp Brain Res. 1984, 56: 550-564.View ArticlePubMedGoogle Scholar
- Westling G, Johansson RS: Factors influencing the force control during precision grip. Exp Brain Res. 1984, 53: 277-284.View ArticlePubMedGoogle Scholar
- Hermsdorfer J, Hagl E, Nowak DA, Marquardt C: Grip force control during object manipulation in cerebral stroke. Clin Neurophysiol. 2003, 114: 915-929. 10.1016/S1388-2457(03)00042-7.View ArticlePubMedGoogle Scholar
- Nowak DA, Grefkes C, Dafotakis M, Kust J, Karbe H, Fink GR: Dexterity is impaired at both hands following unilateral subcortical middle cerebral artery stroke. Eur J Neurosci. 2007, 25: 3173-3184. 10.1111/j.1460-9568.2007.05551.x.View ArticlePubMedGoogle Scholar
- Quaney BM, Perera S, Maletsky R, Luchies CW, Nudo RJ: Impaired grip force modulation in the ipsilesional hand after unilateral middle cerebral artery stroke. Neurorehabil Neural Repair. 2005, 19: 338-349. 10.1177/1545968305282269.View ArticlePubMedGoogle Scholar
- Kim JS, Choi-Kwon S: Discriminative sensory dysfunction after unilateral stroke. Stroke. 1996, 27: 677-682. 10.1161/01.STR.27.4.677.View ArticlePubMedGoogle Scholar
- Augurelle AS, Smith AM, Lejeune T, Thonnard JL: Importance of cutaneous feedback in maintaining a secure grip during manipulation of hand-held objects. J Neurophysiol. 2003, 89: 665-671.View ArticlePubMedGoogle Scholar
- Johansson RS, Riso R, Hager C, Backstrom L: Somatosensory control of precision grip during unpredictable pulling loads. I. Changes in load force amplitude. Exp Brain Res. 1992, 89: 181-191. 10.1007/BF00229015.View ArticlePubMedGoogle Scholar
- Moberg E: Objective methods for determining the functional value of sensibility in the hand. J Bone Joint Surg Br. 1958, 40-B: 454-476.PubMedGoogle Scholar
- Jeannerod M, Michel F, Prablanc C: The control of hand movements in a case of hemianaesthesia following a parietal lesion. Brain. 1984, 107 (Pt 3): 899-920.View ArticlePubMedGoogle Scholar
- Wolf SL: Electromyographic biofeedback applications to stroke patients. Crit Rev Phys Ther. 1983, 63: 1448-1459.Google Scholar
- Wolf SL, Binder-MacLeod SA: Electromyographic biofeedback applications to the hemiplegic patient. Changes in lower extremity neuromuscular and functional status. Phys Ther. 1983, 63: 1404-1413.PubMedGoogle Scholar
- Wolf SL, Binder-MacLeod SA: Electromyographic biofeedback applications to the hemiplegic patient. Changes in upper extremity neuromuscular and functional status. Phys Ther. 1983, 63: 1393-1403.PubMedGoogle Scholar
- Honer J, Mohr T, Roth R: Electromyographic biofeedback to dissociate an upper extremity synergy pattern: a case report. Phys Ther. 1982, 62: 299-303.PubMedGoogle Scholar
- Kurillo G, Gregoric M, Goljar N, Bajd T: Grip force tracking system for assessment and rehabilitation of hand function. Technol Health Care. 2005, 13: 137-149.PubMedGoogle Scholar
- Chiu HY, Hsu HY, Kuo LC, Chang JH, Su FC: Functional sensibility assessment. Part I: develop a reliable apparatus to assess momentary pinch force control. J Orthop Res. 2009, 27: 1116-1121. 10.1002/jor.20859.View ArticlePubMedGoogle Scholar
- Hsu HY, Kuo LC, Chiu HY, Jou IM, Su FC: Functional sensibility assessment. Part II: Effects of sensory improvement on precise pinch force modulation after transverse carpal tunnel release. J Orthop Res. 2009, 27: 1534-1539. 10.1002/jor.20903.View ArticlePubMedGoogle Scholar
- Kollen B, Kwakkel G, Lindeman E: Functional recovery after stroke: a review of current developments in stroke rehabilitation research. Rev Recent Clin Trials. 2006, 1: 75-80. 10.2174/157488706775246111.View ArticlePubMedGoogle Scholar
- Yancosek KE, Howell D: A narrative review of dexterity assessments. J Hand Ther. 2009, 22: 258-269. 10.1016/j.jht.2008.11.004. quiz 270View ArticlePubMedGoogle Scholar
- Gao KL, Ng SS, Kwok JW, Chow RT, Tsang WW: Eye-hand coordination and its relationship with sensori-motor impairments in stroke survivors. J Rehabil Med. 2010, 42: 368-373.View ArticlePubMedGoogle Scholar
- Carmeli E, Patish H, Coleman R: The aging hand. J Gerontol A Biol Sci Med Sci. 2003, 58: 146-152. 10.1093/gerona/58.2.M146.View ArticlePubMedGoogle Scholar
- Tamburin S, Cacciatori C, Marani S, Zanette G: Pain and motor function in carpal tunnel syndrome: a clinical, neurophysiological and psychophysical study. J Neurol. 2008, 255: 1636-1643. 10.1007/s00415-008-0895-6.View ArticlePubMedGoogle Scholar
- Johansson RS, Lemon RN, Westling G: Time-varying enhancement of human cortical excitability mediated by cutaneous inputs during precision grip. J Physiol. 1994, 481 (Pt 3): 761-775.PubMed CentralView ArticlePubMedGoogle Scholar
- Schenker M, Burstedt MK, Wiberg M, Johansson RS: Precision grip function after hand replantation and digital nerve injury. J Plast Reconstr Aesthet Surg. 2006, 59: 706-716. 10.1016/j.bjps.2005.12.004.View ArticlePubMedGoogle Scholar
- Shieh SJ, Hsu HY, Kuo LC, Su FC, Chiu HY: Correlation of digital sensibility and precision of pinch force modulation in patients with nerve repair. J Orthop Res. 2011, 29: 1210-1215. 10.1002/jor.21365.View ArticlePubMedGoogle Scholar
- Brodal A: Neurological anatomy in relation to clinical medicine. 1981, Oxford University, New York, 3Google Scholar
- Glees P, Cole J: Ipsilateral representation in the cerebral cortex; its significance in relation to motor function. Lancet. 1952, 1: 1191-1192.View ArticlePubMedGoogle Scholar
- Sunderland A, Bowers MP, Sluman SM, Wilcock DJ, Ardron ME: Impaired dexterity of the ipsilateral hand after stroke and the relationship to cognitive deficit. Stroke. 1999, 30: 949-955. 10.1161/01.STR.30.5.949.View ArticlePubMedGoogle Scholar
- Hermsdörfer J, Nowak DA, Lee A, Rost K, Timmann D, Mühlau M, Boecker H: The representation of predictive force control and internal forward models: evidence from lesion studies and brain imaging. Cogn Process. 2005, 6: 48-58. 10.1007/s10339-004-0042-y.View ArticleGoogle Scholar
- Zachary RB, Holmes W: Primary suture of nerves. Surg Gynecol Obstet. 1946, 82: 632-651.PubMedGoogle Scholar
- Bell-Krotoski JA, Buford WL: The force/time relationship of clinically used sensory testing instruments. J Hand Ther. 1997, 10: 297-309. 10.1016/S0894-1130(97)80045-2.View ArticlePubMedGoogle Scholar
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