- Open Access
Effects of a robot-assisted training of grasp and pronation/supination in chronic stroke: a pilot study
© Lambercy et al; licensee BioMed Central Ltd. 2011
Received: 14 February 2011
Accepted: 16 November 2011
Published: 16 November 2011
Rehabilitation of hand function is challenging, and only few studies have investigated robot-assisted rehabilitation focusing on distal joints of the upper limb. This paper investigates the feasibility of using the HapticKnob, a table-top end-effector device, for robot-assisted rehabilitation of grasping and forearm pronation/supination, two important functions for activities of daily living involving the hand, and which are often impaired in chronic stroke patients. It evaluates the effectiveness of this device for improving hand function and the transfer of improvement to arm function.
A single group of fifteen chronic stroke patients with impaired arm and hand functions (Fugl-Meyer motor assessment scale (FM) 10-45/66) participated in a 6-week 3-hours/week rehabilitation program with the HapticKnob. Outcome measures consisted primarily of the FM and Motricity Index (MI) and their respective subsections related to distal and proximal arm function, and were assessed at the beginning, end of treatment and in a 6-weeks follow-up.
Thirteen subjects successfully completed robot-assisted therapy, with significantly improved hand and arm motor functions, demonstrated by an average 3.00 points increase on the FM and 4.55 on the MI at the completion of the therapy (4.85 FM and 6.84 MI six weeks post-therapy). Improvements were observed both in distal and proximal components of the clinical scales at the completion of the study (2.00 FM wrist/hand, 2.55 FM shoulder/elbow, 2.23 MI hand and 4.23 MI shoulder/elbow). In addition, improvements in hand function were observed, as measured by the Motor Assessment Scale, grip force, and a decrease in arm muscle spasticity. These results were confirmed by motion data collected by the robot.
The results of this study show the feasibility of this robot-assisted therapy with patients presenting a large range of impairment levels. A significant homogeneous improvement in both hand and arm function was observed, which was maintained 6 weeks after end of the therapy.
Stroke is one of the leading causes of adult disability. While there is strong evidence that physiotherapy promotes recovery, conventional therapy remains suboptimal due to limited financial and human resources, and there are many open questions, e.g. when therapy should be started, how to optimally engage the patient, what is the best dosage, etc. [1–3]. Furthermore, exercise therapy of the upper limb has been shown to be only of limited impact on arm function in stroke patients .
Robot-assisted rehabilitation can address these shortcomings and complement traditional rehabilitation strategies. Robots designed to accurately control interaction forces and progressively adapt assistance/resistance to the patients' abilities can record the patient's motion and interaction forces to objectively and precisely quantify motor performance, monitor progress, and automatically adapt therapy to the patient's state.
Studies with robots such as the MIT-Manus, the ARM Guide or the MIME have demonstrated improved proximal arm function after stroke [5–8], although these improvements did not transfer to the distal arm function which is necessary for most Activities of Daily Living (ADL) [9–11]. Robot-assisted training which specifically targets the hand might be required to achieve significant improvements in hand function. Furthermore, several studies indicate a generalization effect of distal arm training, e.g. hand and wrist, on proximal arm function, i.e. elbow and shoulder, which may lead to improved control of the entire arm [10, 12, 13].
We therefore focused on robot-assisted rehabilitation of the hand, adopting a functional approach based on the combined training of grasping and forearm pronation/supination, two critical functions for manipulation. This paper presents the results of a pilot study using the HapticKnob, a portable end-effector based robotic device to train hand opening/closing and forearm rotation. In contrast to robotic devices based on exoskeletons attached to the arm , the HapticKnob applies minimal constraints to the different joints of the upper arm, thus corresponding to situations encountered during ADL. The forearm rests on an adjustable padded support, while the shoulder and upper arm are not restrained.
The objectives of this pilot study were to determine the feasibility of training chronic stroke patients with the HapticKnob, and to reduce motor impairment of the upper limb in a safe and acceptable manner. Although a few studies have investigated post-stroke rehabilitation of the hand [12, 13], ours is the first to use robot-assisted training that combines grasp and forearm pronation/supination to perform functional tasks. With this pilot study, we tested the hypothesis that training the hand using this functional approach improves function of the entire arm.
Demographic characteristics and stroke subtypes (N = 15)
initial Fugl-Meyer score
left basal ganglia
right basal ganglia
left basal ganglia
right temporal, basal ganglia, corona radiata, thalamus
right frontal-temporal, insula
right temporal, basal ganglia
right basal ganglia
left basal ganglia
right frontal lobe
right corona radiata, basal ganglia
right basal ganglia, corona radiata, external capsule frontal-parietal, thalamus
right parietal lobe
right basal ganglia
left basal ganglia
right basal ganglia
55.5 ± 14.6
597.5 ± 294.1
32.4 ± 10.5
Two simple task-oriented exercises corresponding to typical ADL were implemented on the HapticKnob. One first objective is to reduce hand impairment, i.e. spasticity and limited active finger range-of-motion (ROM), by providing passive assistance similar to stretching  for hand opening movements that often are too difficult for perform. Active force production is promoted to increase muscle strength, improve control of the impaired limb and facilitate acquisition and retention of skills.
(i) opening/closing exercise, training extension then flexion of the fingers to simulate grasping of an object. In a first phase of the exercise, the robot opened the fingers to an extended position adapted to the subject's range of motion (ROM), which was selected between 10 and 15 cm from the tip of the thumb to the tip of the opposing fingers for the subjects of this study. At the end of the opening phase, the robot maintained the position for three seconds during which subjects were asked to relax and apply minimal grasping force. An audio signal indicated the beginning of the closing phase, which required the subject to actively flex the fingers against a resistive load between 0 to 30N generated by the robot, according to the difficulty level of the exercise. To train grasping force control, subjects were asked to smoothly close the hand by following a reference position profile (RPP) displayed on the monitor (Figure 1B), which corresponded to a fifth order polynomial defining a minimal jerk movement between the open and closed positions, as natural movements tend to follow .
(ii) pronation/supination exercise, training forearm rotation and coordination between grasping and turning required to manipulate knobs . In this exercise, subjects were asked to supinate or pronate the forearm towards a specific target orientation, while the linear DOF of the HapticKnob remained in the closed position. This task required the subjects to produce accurate rotation movements, reach a [-1°, 1°] position window around the target in a minimal time, and remain there for 2 seconds (without exiting). This window was adapted to the human discrimination threshold in orientation, which is between 0.4-1° . In this study, the amplitude of forearm rotation was selected between 25° and 45°, corresponding to the subjects' ROM. In addition, a resistive torque load adapted to the subject's impairment level and comprised between 0 and 1Nm was applied by the robot during the exercise in order to require the subject to hold the knob firmly during the movement.
During training, interactive and intuitive visual feedback was provided to the subject to promote concentration and motivation. A picture that was stretched in the open/close exercise and rotated in the pronation/supination exercise (Figure 1B), in function of the movement performed with the subject was displayed on the monitor, while the target position to reach was represented by a white frame. In addition, exercises were presented as games with a score calculated based on the timing and precision of the task. This score was provided as feedback to the subject, and used to adjust the level of difficulty of the task . During each trial, position and force signals were sampled at a frequency of 100Hz and stored for post-processing.
Robot-assisted therapy consisted of 18 one-hour sessions of training with the HapticKnob over a period of 6 weeks. Prior to the first therapy session, a preliminary test session was performed to ensure that subjects were able to interact with the robot and understood the exercises. All sessions were supervised by an occupational therapist. Before starting the exercises, 10 minutes were devoted to stretching to reduce muscle tone and to comfortably position the subject. Each exercise consisted of 5 sets of 10 trials, lasting about 25 minutes. There was a short rest period between each set to prevent muscle fatigue and a 5-minute break between the two exercises to stretch and relax arm muscles (Figure 1C).
During therapy sessions, subjects sat in an upright position, placed the forearm on the padded support and grasped the HapticKnob with the hand. The arm support and the height of the table on which the robot was placed were adjusted to offer the subject a comfortable position, with the arm resting on the support during the experiment, the shoulder abducted at 40° and the elbow flexed at 90°. No support was provided at the level of the proximal arm, so that subjects could position and move their upper arm freely. Possible compensatory trunk movement or abnormal wrist hyper-flexion were monitored and manually prevented by the occupational therapist supervising the therapy. If the subject had difficulty holding the knob, Velcro® bands were used to prevent fingers and thumb from slipping off the knob.
Robotic outcome measures
Kinematic data collected by the HapticKnob can be used to evaluate motor performance in the functional tasks trained with the device. To evaluate hand motor control during the opening/closing exercise, the mean absolute error εp between the RPP and the position waveform during closing. Motion smoothness was estimated from the number of zero crossings of the acceleration n0 (indicating putative velocity submotions ), normalized by the duration of the closing movement. In the pronation/supination exercise, coordination between grasping and fine forearm orientation was assessed by the time tr required to reach the target window, and the time ta to adjust the angular position once the target is reached for the first time . Robotic data were processed using Matlab R2010a (The MathWorks, Inc.).
Clinical outcome measures
Subjects were assessed at three times during the study: prior to the beginning of the therapy (week 0), at its completion (week 6), and 6 weeks post-therapy (week 12). Between week 6 and week 12, patients did not receive any further rehabilitation therapy focusing on upper extremity motor function. All assessments were done by an occupational therapist not involved in the HapticKnob training. The primary objective of the proposed training being to decrease impairment and upper limb improve motor function, the Fugl-Meyer motor assessment for the upper extremity (FM, range (0-66) ) and the Motricity Index (MI) for motor function of the upper limb were selected as primary outcome measures. FM scores were subdivided into wrist-hand scores (0-24), and shoulder-elbow scores including coordination (0-42). MI scores were converted from raw scores to subscores with a total of 100 points . Similarly to FM scores, MI scores were subdivided into hand scores (0-33) and shoulder-elbow scores (0-66).
Secondary outcomes were selected to investigate independent neurophysiological changes not covered by the primary outcome measures, and included the Motor Assessment Scale (MS, range (0-18)) to assess everyday motor function involving the arm and hand , the Modified Ashworth Scale as a measure of spasticity in shoulder abductors, elbow, wrist, finger and thumb flexors (modified MAS, range (0-5) ), the Functional Test of Hemiparetic Upper Extremity (FTHUE, range (0-7) ), the Nine Hole Peg Test (NHPT) , and grip force measurement using a Jamar Grip Dynamometer. Pain was assessed using a Visual Analog Scale (VAS range (0-10)) and the subject provided a score of satisfaction with the therapy (1 = 'poor', 2 = 'satisfactory', 3 = 'good' or 4 = 'excellent').
Data were analyzed using SPSS v18 statistical analysis package (IBM). Due to the small sample size, non-parametric tests were used to investigate differences in means. Statistical difference was first investigated for each clinical measure using a two-tailed Friedman test. Bonferroni correction was used to compensate for the two primary outcome measures of upper limb motor function, so that all tests were applied using a 0.025 significance level. Post-hoc analysis for possible differences between baseline discharge and follow-up was then performed using Wilcoxon signed rank tests (0.05 significance level). For the secondary outcome measures, no Bonferroni correction was used to correct for the multiple assessments, as these are assumed to be independent. For the robotic measures, Wilcoxon tests with a 0.05 significance level were used to investigate differences in means between results of the first and last training sessions.
All of the 15 post-stroke subjects completed the pilot study, consisting of 18 hours of HapticKnob training over 6 weeks. However, subject A12 had to stop therapy for a week due to an unrelated fall at home. Further, A11 had severe concentration problems and suffered from depression Therefore, data from these two subjects were excluded from the analysis.
Primary outcome measures at week 0, week 6 and week 12 for the 13 subjects that were retained for data analysis (mean ± std), and p-values of the statistical analysis (Friedman tests with 0.025 significance level and post-hoc Wilcoxon tests with 0.05 significance level).
Primary outcome measures
Wilcoxon test 0-6
Wilcoxon test 0-12
Fugl-Meyer total (normal = 66)
32.15 ± 11.31
35.15 ± 12.05
37.00 ± 11.21
Subportion wrist/hand (normal = 24)
8.23 ± 4.38
9.15 ± 4.74
10.23 ± 5.40
Subportion shoulder/elbow (normal = 42)
23.92 ± 8.54
26.00 ± 8.81
26.77 ± 7.56
Motricity Index (normal = 100)
50.62 ± 15.41
55.16 ± 17.99
57.46 ± 16.26
Subportion hand/fingers (normal = 33)
12.46 ± 16.25
13.54 ± 10.84
14.69 ± 11.33
Subportion shoulder/elbow (normal = 66)
37.15 ± 9.94
40.62 ± 11.74
41.38 ± 11.16
Secondary outcome measures at week 0, week 6 and week 12 for the 13 subjects that were retained for data analysis (mean ± std), and p-values of the statistical analysis (Friedman tests with 0.05 significance level and post-hoc Wilcoxon tests with 0.05 significance level).
Secondary outcome measures
Wilcoxon test 0-6
Wilcoxon test 0-12
Motor Assessment Scale (normal = 18)
4.08 ± 3.30
5.08 ± 3.30
5.23 ± 3.63
Modified Ashworth Scale (normal = 0)
8.31 ± 3.12
7.38 ± 2.43
7.08 ± 3.15
Functional Test of Hemiparetic Upper Extremity (normal = 7)
2.92 ± 0.64
3.08 ± 0.64
3.08 ± 0.64
Nine Hole Peg Test *
Grip force (impaired hand/unimpaired hand) [%] †
21.92 ± 15.26
24.60 ± 12.94
22.02 ± 9.11
Pain (Visual Analog Scale)
0.46 ± 1.39
0.00 ± 0.00
0.00 ± 0.00
3.08 ± 0.76
In addition, there was a 12.3% gain in grip strength ratio (grip strength of impaired hand over unimpaired hand) at week 6, though this change was not significant. There was no significant gain in upper arm function as measured by the FTHUE, which could be explained by the low sensitivity of this categorical scale, and the fact that the tasks comprising the FTHUE required a higher level of hand function than that reached by most subjects. Similarly, only one patient was able to perform the NHPT, compromising the use of this assessment in the present study.
Minimal pain experienced by two subjects at the beginning of the study progressively disappeared during the robot-assisted therapy. Therapy with the HapticKnob was well accepted by stroke patients, and 10 out of 13 (76.9%) subjects rated their satisfaction post-training as good or excellent.
Robotic outcome measures at week 0 and week 6 for the 13 subjects that were retained for data analysis (mean ± std), and p-values of the statistical analysis (Wilcoxon tests with 0.05 significance level).
week 0 (session 1)
week 6 (session 18)
3.03 ± 2.45
1.52 ± 1.21
6.06 ± 0.52
5.75 ± 0.47
7.40 ± 3.63
4.67 ± 3.24
7.44 ± 3.23
5.24 ± 3.32
Fifteen chronic stroke subjects with slight to severe arm and hand impairment (mean admission FM of 32.15) performed a robot-assisted rehabilitation therapy program with the HapticKnob involving hand opening/closing and forearm pronation/supination. Upper limb motor impairment decreased during the treatment period, as revealed by significant increases in the FM and MI scores, indicating a noticeable improvement of arm and hand function, together with increased upper extremity strength. In the literature, a 3-point improvement on the FM scale is often considered as a minimum impairment change necessary to achieve significant functional gains . Results of the clinical assessments, which were also confirmed by analysis of the robot motion data , suggest that intensive use of the forearm and hand in a repetitive robot-assisted training program can improve motor function in chronic stroke subjects even long after completion of conventional therapy (mean 597.5 days post-stroke). Improvement in the robotic parameters suggests that patients could learn to perform the tasks and progressively improve their performance, indicating better hand control and coordination between hand and forearm during the functional tasks proposed during training with the HapticKnob. Nevertheless, it is not possible verify whether the improvements observed in the motion data during the training translate to significant gains in functional activities in daily life.
Improvements in arm and hand function were maintained 6 weeks after the completion of the therapy, suggesting a stable improvement of the motor condition. In fact, the primary outcome measures increased further during the 6 weeks after the therapy. The reduction in arm and hand spasticity (although not statistically significant when individual arm components were analyzed) could have facilitated increased use of the impaired hand to perform daily tasks, as could the reduction in pain levels in the two subjects who initially presented with minimal pain. Robot-assisted training may have helped pass a threshold of spontaneous arm use where ADL tasks involving arm and hand are performed at home, thus leading to additional improvement in upper limb motor function and decreasing learned non-use of the affected limb . Subjects reported improvement in ADL at home at the end of the therapy. However, improvements in ADL tasks were not confirmed by corresponding clinical outcome measures, which is also observed in most robot-assisted studies . Changes in fine hand function could not be captured by the NHPT as most patients were unable to complete this dexterity test. A different test such as the Box and Block test  should be considered as outcome measure of hand function in future studies.
All 15 chronic stroke subjects were capable of training with the proposed protocol in a safe manner, without experiencing any complication related to the use of the robot, and with significant improvement of motor function in their hand and arm. These results demonstrate the feasibility of using the HapticKnob as a rehabilitation tool for chronic stroke patients with a large range of sensorimotor deficits. These results are consistent with results obtained in other robot-assisted studies on upper limb rehabilitation of chronic stroke patients, where improvements of 3.0 to 7.6 points in the FM were found [7, 10, 11, 13, 14, 30]. However, there is a lack of comparison groups for hand rehabilitation, and the variation in improvement between these studies can be attributed to the differences in experimental protocols, such as intensity and duration of therapy, as well as to initial motor impairment of the stroke subjects involved in the study. In contrast to the devices used in previous studies, the HapticKnob is a compact system that could easily be transported and placed in hospitals and homes. It requires only minimal function to place the hand on the robot and thereby makes it accessible to a wide range of subjects, right or left handed, and with various levels of physical impairment, e.g., an initial FM score lower than 15, as demonstrated by this study.
It is likely that the severity of motor impairment is a key factor in rehabilitation outcomes and in the choice of a rehabilitation protocol. Severely impaired subjects may require longer or more intensive therapy to first strengthen the muscles, decrease spasticity and reduce other impairments that limit their performance so as to focus on the restoration of neuromotor pathways without introducing additional complex tasks . In our study, a larger increase in functional assessment scores during therapy was observed in subjects initially with moderate impairment (FM > 35), suggesting that subjects already having some motor function of the arm and hand benefit more from the functional hand therapy with the HapticKnob. Nevertheless, this difference between moderately and more severely impaired patients was not statistically significant.
In previous studies, improvement in elbow and shoulder function after training involving these proximal segments did not seem to transfer to the wrist or hand [9–11]. In contrast, the results obtained with the HapticKnob indicate that training involving only distal segments of the arm could lead to improvements in both the proximal and distal subsections of the primary outcome measures. Improvement was significant in the hand/wrist subsection of the FM, but not in the shoulder/elbow section after Bonferroni correction. On the other hand, a significant increase was observed in the shoulder/elbow component of the MI, but not in the hand component of MI. Explanations for these seemingly conflicting results include the fact that the distal component of the MI assesses thumb/finger function rather than wrist/hand function and the limited number of subjects included in the study. Nevertheless, a clear positive trend can be observed in all subsections of the two scales, which is confirmed by the secondary outcome measures, with improvement in both arm and hand functional tasks as measured by the MS, and reduced spasticity in all of the arm segments, with the greatest reduction for shoulder abductors and elbow flexors.
These findings support the hypothesis that exercising distal joints of the arm may benefit the proximal joints [10, 13, 32, 33]. As the arm was not fixed but only supported, this effect may be due to a recruitment of all arm segments in a task-oriented way to promote restoration of motor function of the entire arm. In fact, the pronation/supination exercise trains coordination between fingers, wrist and forearm, as subjects are required to firmly grasp the handle and then rotate it and also requires stabilization of the upper arm. Also, distal training requires activation of nerves and muscles that control each segment of the upper limb, and will thus result in proximal as well as distal muscle activity. This is partly because some muscles like the biceps are multi-functional, e.g. supinating the forearm and flexing the elbow and shoulder whereas others are needed to stabilize the more proximal joints even when the forearm is supported. Alternatively, patients may have developed compensatory strategies to achieve forearm pronation/supination with their shoulder, which could account for part of the increase of MI and FM scores. This effect may be monitored in future studies. Finally, these results should be interpreted with caution, as no control group receiving dose-matched conventional or robotic training focusing on the proximal arm segment was included in the study design. Further limitations of the current study include single baseline measure, and absence of a long-term follow-up, which will be considered in future clinical studies.
The results of this pilot study suggest that upper limb robot-assisted rehabilitation, which currently focuses primarily on training elbow and shoulder movement, would advantageously include training of the hand and fingers, which can be provided using compact desktop robots such as the HapticKnob. Whole-arm training, which is a commonly used approach in robot-assisted neurorehabilitation, may not be required, as distal training in a functional way could benefit the whole arm.
This project was funded in part by a grant from NUS (R265-000-168-112), the FP7 HUMOUR project and the NCCR Neural Plasticity and Repair, Swiss National Science Foundation.
- Barreca S, Wolf S, Fasoli S, Bohannon R: Treatment Interventions for the paretic upper limb of stroke survivors: acritical review. Neurorehabil Neural Repair 2003, 17: 220-226. 10.1177/0888439003259415View ArticlePubMedGoogle Scholar
- van Der Lee J, Snels I, Beckerman H, Lankhorst G, Wagenaar R, Bouter L: Exercise therapy for arm function in stroke patients: a systematic review of randomized controlled trials. Clin Rehabil 2001, 15: 20-31. 10.1191/026921501677557755View ArticlePubMedGoogle Scholar
- Winstein C, Wing A, Withall J: Motor control and learning principles for rehabilitation of upper limb movements after brain injury. In Handbook of Neuropsychology. Volume 9. 2nd edition. Edited by: Grafman J. Elsevier Health Sciences; 2003:77-137.Google Scholar
- Teasell RW, Foley NC, Bhogal SK, Speechley MR: An evidence-based review of stroke rehabilitation. Top Stroke Rehabil 2003, 10: 39-58.Google Scholar
- Hogan N, Krebs HI, Sharon A, Charnnarong J: Interactive robotic therapist. US patent 5466213; 1995.Google Scholar
- Reinkensmeyer DJ, Emken JL, Cramer SC: Robotics, motor learning, and neurologic recovery. Annu Rev Biomed Eng 2004, 6: 497-525. 10.1146/annurev.bioeng.6.040803.140223View ArticlePubMedGoogle Scholar
- Lum PS, Burgar CG, Shor PC, Majmundar M, Van der Loos M: Robot-assisted movement training compared with conventional therapy techniques for the rehabilitation of upper-limb motor function after stroke. Arch Phys Med Rehabil 2002, 83: 952-959. 10.1053/apmr.2001.33101View ArticlePubMedGoogle Scholar
- Kwakkel G, Kollen BJ, Krebs HI: Effects of robot-assisted therapy on upper limb recovery after stroke: a systematic review. Neurorehab Neural Repair 2008, 22: 111-121.View ArticleGoogle Scholar
- Volpe BT, Krebs HI, Hogan N, Edelstein OL, Diels C, Aisen M: A novel approach to stroke rehabilitation: robot-aided sensorimotor stimulation. Neurology 2000, 54: 1938-1944.View ArticlePubMedGoogle Scholar
- Krebs HI, Volpe BT, Williams D, Celestino J, Charles SK, Lynch D, Hogan N: Robot-aided neurorehabilitation: A robot for wrist rehabilitation. IEEE T Neur Sys Reh 2007, 15: 327-335.View ArticleGoogle Scholar
- Volpe BT, Lynch D, Rykman-Berland A, Ferraro M, Galgano M, Hogan N, Krebs HI: Intensive sensorimotor arm training mediated by therapist or robot improves hemiparesis in patients with chronic stroke. Neurorehab Neural Repair 2008, 22: 305-310. 10.1177/1545968307311102View ArticleGoogle Scholar
- Hesse S, Werner C, Pohl M, Rueckriem S, Mehrholz J, Lingnau ML: Computerized arm training improves the motor control of the severely affected arm after stroke - A single-blinded randomized trial in two centers. Stroke 2005, 36: 1960-1966. 10.1161/01.STR.0000177865.37334.ceView ArticlePubMedGoogle Scholar
- Takahashi CD, Der-Yeghiaian L, Le V, Motiwala RR, Cramer SC: Robot-based hand motor therapy after stroke. Brain 2008, 131: 425-437. 10.1093/brain/awm311View ArticlePubMedGoogle Scholar
- Nef T, Mihelj M, Kiefer G, Perndl C, Mueller R, Riener R: ARMin - Exoskeleton for arm therapy in stroke patients. 2007 IEEE 10th International Conference on Rehabilitation Robotics, Vols 1 and 2 2007, 68-74.View ArticleGoogle Scholar
- Lambercy O, Dovat L, Gassert R, Burdet E, Teo CL, Milner T: A haptic knob for rehabilitation of hand function. IEEE T Neur Sys Reh 2007, 15: 356-366.View ArticleGoogle Scholar
- Krylow AM, Rymer WZ: Role of intrinsic muscle properties in producing smooth movements. IEEE Trans Biomed Eng 1997, 44: 165-176. 10.1109/10.552246View ArticlePubMedGoogle Scholar
- Vasquez P, Cano M, Acuna C: Discrimination of line orientation in humans and monkeys. J Neurophysiol 2000, 83: 2639-2648.Google Scholar
- Lambercy O, Dovat L, Yun H, Wee SK, Kuah C, Chua K, Gassert R, Milner TE, Teo CL, Burdet E: Exercises for rehabilitation and assessment of hand motor function with the Haptic Knob. 2009 3rd i-CREATe Conference 2009, 74-78.Google Scholar
- Burdet E, Milner TE: Quantization of human motions and learning of accurate movements. Biol Cybern 1998, 78: 307-318. 10.1007/s004220050435View ArticlePubMedGoogle Scholar
- Lambercy O, Dovat L, Yun H, Wee SK, Kuah C, Chua K, Gassert R, Milner T, Teo CL, Burdet E: Robotic Assessment of Hand Function with the HapticKnob. Proc 4th International Convention for Rehabilitation Engineering & Assistive Technology (i-CREATe) 2010.Google Scholar
- Fugl-Meyer AR, Jaasko L, Leyman I, Olsson S, Steglind S: The post-stroke hemiplegic patient: A method for evaluation of physical performance. Scand J Rehabil Med 1975, 7: 13-31.PubMedGoogle Scholar
- Collin C, Wade D: Assessing motor impairment after stroke: a pilot reliability study. J Neurol Neurosurg Psychiatry 1990, 53: 576-579. 10.1136/jnnp.53.7.576PubMed CentralView ArticlePubMedGoogle Scholar
- Carr JH, Shepherd RB, Nordholm L, Lynne D: Investigation of a new motor assessment scale for stroke patients. Phys Ther 1985, 65: 175-180.PubMedGoogle Scholar
- Bohannon RW, Smith MB: Interrater reliability of a modified Ashworth scale of muscle spasticity. Phys Ther 1987, 67: 206-207.PubMedGoogle Scholar
- Wilson DJ, Baker LL, Craddock JA: Functional test for the hemiparetic upper extremity. Am J Occup Ther 1984, 38: 159-164.View ArticlePubMedGoogle Scholar
- Grice KO, Vogel KA, Le V, Mitchell A, Muniz S, Vollmer MA: Adult norms for a commercially available nine hole peg test for finger dexterity. American Journal of Occupational Therapy 2003, 57: 570-573. 10.5014/ajot.57.5.570View ArticleGoogle Scholar
- Schweighofer N, Han CE, Wolf SL, Arbib MA, Winstein CJ: A Functional Threshold for Long-Term Use of Hand and Arm Function Can Be Determined: Predictions From a Computational Model and Supporting Data From the Extremity Constraint-Induced Therapy Evaluation (EXCITE) Trial. Physical Therapy 2009, 89: 1327-1336. 10.2522/ptj.20080402PubMed CentralView ArticlePubMedGoogle Scholar
- Mehrholz J, Platz T, Kugler J, Pohl M: Electromechanical and robot-assisted arm training for improving arm function and activities of daily living after stroke. Cochrane Database Syst Rev 2008, CD006876.Google Scholar
- Mathiowetz V, Volland G, Kashman N, Weber K: Adult norms for the Box and Block Test of manual dexterity. Am J Occup Ther 1985, 39: 386-391.View ArticlePubMedGoogle Scholar
- Fasoli SE, Krebs HI, Stein J, Frontera WR, Hughes R, Hogan N: Robotic therapy for chronic motor impairments after stroke: Follow-up results. Arch Phys Med Rehab 2004, 85: 1106-1111. 10.1016/j.apmr.2003.11.028View ArticleGoogle Scholar
- Fasoli SE, Krebs HI, Hughes R, Stein J, Hogan N: Functionally-based rehabilitation: Benefit or buzzword? 2005 IEEE 9th International Conference on Rehabilitation Robotics 2005, 223-226.Google Scholar
- Butefisch C, Hummelsheim H, Denzler P, Mauritz KH: Repetitive training of isolated movements improves the outcome of motor rehabilitation of the centrally paretic hand. J Neurol Sci 1995, 130: 59-68. 10.1016/0022-510X(95)00003-KView ArticlePubMedGoogle Scholar
- Carey JR, Kimberley TJ, Lewis SM, Auerbach EJ, Dorsey L, Rundquist P, Ugurbil K: Analysis of fMRI and finger tracking training in subjects with chronic stroke. Brain 2002, 125: 773-788. 10.1093/brain/awf091View ArticlePubMedGoogle Scholar
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