The effect of impedance-controlled robotic gait training on walking ability and quality in individuals with chronic incomplete spinal cord injury: an explorative study
© Fleerkotte et al.; licensee BioMed Central Ltd. 2014
Received: 1 March 2013
Accepted: 14 February 2014
Published: 4 March 2014
There is increasing interest in the use of robotic gait-training devices in walking rehabilitation of incomplete spinal cord injured (iSCI) individuals. These devices provide promising opportunities to increase the intensity of training and reduce physical demands on therapists. Despite these potential benefits, robotic gait-training devices have not yet demonstrated clear advantages over conventional gait-training approaches, in terms of functional outcomes. This might be due to the reduced active participation and step-to-step variability in most robotic gait-training strategies, when compared to manually assisted therapy. Impedance-controlled devices can increase active participation and step-to-step variability. The aim of this study was to assess the effect of impedance-controlled robotic gait training on walking ability and quality in chronic iSCI individuals.
A group of 10 individuals with chronic iSCI participated in an explorative clinical trial. Participants trained three times a week for eight weeks using an impedance-controlled robotic gait trainer (LOPES: LOwer extremity Powered ExoSkeleton). Primary outcomes were the 10-meter walking test (10MWT), the Walking Index for Spinal Cord Injury (WISCI II), the six-meter walking test (6MWT), the Timed Up and Go test (TUG) and the Lower Extremity Motor Scores (LEMS). Secondary outcomes were spatiotemporal and kinematics measures. All participants were tested before, during, and after training and at 8 weeks follow-up.
Participants experienced significant improvements in walking speed (0.06 m/s, p = 0.008), distance (29 m, p = 0.005), TUG (3.4 s, p = 0.012), LEMS (3.4, p = 0.017) and WISCI after eight weeks of training with LOPES. At the eight-week follow-up, participants retained the improvements measured at the end of the training period. Significant improvements were also found in spatiotemporal measures and hip range of motion.
Robotic gait training using an impedance-controlled robot is feasible in gait rehabilitation of chronic iSCI individuals. It leads to improvements in walking ability, muscle strength, and quality of walking. Improvements observed at the end of the training period persisted at the eight-week follow-up. Slower walkers benefit the most from the training protocol and achieve the greatest relative improvement in speed and walking distance.
KeywordsSpinal cord injury Robotic gait rehabilitation Locomotor training Impedance control
Spinal cord injury (SCI) affects 10.4  to 83  per million individuals per year (in developed countries), leading to an estimated prevalence that ranges between 223 and 755 per million inhabitants . Learning to walk again is a major goal during SCI rehabilitation [4, 5]. Generally, more than 50 percent of patients have motor incomplete lesions (iSCI) , of which around 75 percent regain some ambulatory function . Still, many iSCI individuals experience limited hip flexion during swing phase and insufficient knee stability during the stance phase. Consequently, these individuals walk slower and often remain reliant on assistive devices. Over the last decades, many rehabilitation strategies have been explored to improve functional outcomes. Most are based on evidence suggesting that task-specific and intensive training, consisting of repetitive active movements and providing appropriate afferent feedback, engages spinal and supraspinal circuits, promoting neural plasticity (cortical reorganization) and increasing functional improvement [7–14].
Robotic gait-training devices have the potential to provide training sessions that support these key components. These devices reduce the labour-intensive demands on therapists and their discomfort, compared to manually assisted body-weight-supported treadmill training (BWSTT) . They also enable objective monitoring of a patient’s performance and progress and reduce the between-trainer variability in terms of the applied supportive forces . In the last decade, different robotic gait-training devices have been developed that are also used for other motor impairments, like stroke or multiple sclerosis. These robotic devices consist of a driven exoskeleton orthosis, like the Lokomat (Hocoma AG, Switzerland) or Auto/ReoAmbulator (HealthSouth/Motorika, USA) that drives the hip and knee joint, or driven footplates that facilitate a stepping motion like the Gait Trainer (Reha-Stim, Germany), G-EO (RehaTechnologies) or LokoHelp (LokoHelp Group, Germany).
Although these robotic gait-training devices have been on the market for more than a decade, research on their efficacy is still at an early and rather inconclusive state. On the one hand several studies showed improvements in walking ability between pre- and post-training in acute and chronic iSCI individuals who trained with the Lokomat [14, 17–20] or Gait Trainer [19, 21]. On the other hand, only very few randomized controlled trials (RCTs) [22–25] or other study designs [19, 26], were performed to investigate whether these improvements are superior to those obtained using conventional approaches. Results from these studies, however, show contradictory results. Recent reviews have also concluded that robotic gait-training devices have not yet demonstrated clear advantages over conventional gait-training approaches in terms of effectiveness of training [27–29].
The limited effectiveness of the first-generation robotic gait-training devices could be attributed to some inherent limitations of these devices, which were mainly position-controlled. This type of assistance may promote “slacking”, where the user starts to rely on the robot to perform the movement and reduces his muscular activity [30, 31]. In iSCI individuals, position-controlled robotic guidance, especially in individuals with some ability to walk, has been shown to actually reduce volitional activity (EMG and VO2) compared to therapist-assisted BWSTT [25, 32]. For motor learning in general, active subject participation is considered a very important factor [33, 34]. If, conversely, participants are encouraged to actively participate, they could be resisted by the position-controlled robot, causing abnormal alternations in muscle-activation patterns .
Another limiting factor of position-controlled robots is that they reduce movement variability to a minimum . Kinematic variability, and the possibility to make movement errors is necessary to (re)learn any new task [37, 38]. In this respect, traditional robotic gait-training devices only partly meet the requirement for task-specific, intensive, active, and variable training. In other words, they do not resemble the manual assistance provided by a therapist who is likely to be compliant, motivational, and intuitively adaptive to the needs of the individual and who inherently introduces a natural sense of variability.
This situation demonstrates the need to develop and improve control approaches that increase active participation and natural movement variability. This can be achieved by only providing assistance when needed, and not supporting the subject’s movements that are unimpaired. Technical implementation of this strategy often consists of controlling the interaction forces between the robot and the patient. Generally, these control strategies use a healthy control spatial path to define the desired motion, in combination with a “virtual wall”/force field that determines the amount of supportive force when the individual deviates from the template (impedance control). In some cases a “moving back wall” is introduced to assist the timing of the stepping pattern [39, 40].
This kind of control strategy can overcome the main criticisms against robot-aided gait training by making the robot’s behaviour more flexible and adaptive to the user’s needs. That is, the stiffness of the “virtual wall”/force field can be adapted to the capabilities, progress, and current participation of the user. This allows individuals to benefit from robot-aided treadmill training throughout the different stages of their recovery. At the initial stages of recovery, the robot can take charge (high impedance), whereas at the concluding stages of recovery, the user must contribute more to the prescribed motion (low impedance). To reduce the chance of the user becoming reliant on the support, some robotic gait-training devices use adaptive (“impedance shaping”) algorithms that reduce the stiffness of the virtual wall when kinematic errors are small [41, 42]. Flexibility between steps and the possibility of making small movement errors can be increased by lowering the impedance levels or by creating a “virtual tunnel”, “dead band,” or nonlinear force-field around the healthy control template [39, 40].
Lowering impedance levels might also increase motivation during training sessions. At lower impedance levels, the user has more control over his gait pattern, and additional effort/voluntary movement is reflected in the gait pattern. This way, individuals are aware of their increased activity, a sensation that can positively contribute to their active involvement. These types of controllers that 1) provide more freedom of movement, 2) only focus on the impaired aspects of gait, 3) promote active participation and 4) allow online modification of the amount of assistance (either manually or automatically), are referred to as “assist-as-needed” (AAN), “cooperative”, “adaptive”, or “interactive” controllers [39–47].
Despite the potential of AAN strategies, the superiority of this approach for iSCI individuals has not been demonstrated. In animal studies, Cai et al. and Ziegler et al. showed that AAN control algorithms allow more variation between steps and result in larger walking recovery than position-control algorithms [48–50]. Despite numerous experimental robotic gait-training devices that have been developed , very few of the new compliant-control strategies have been tested on iSCI individuals in multisession training protocols. In single-session experiments, Emken et al. showed that iSCI individuals trained with more variability when they used their “impedance-shaping algorithm” . Duschau-Wicke et al. evaluated their “patient-cooperative approach” in a single training session and showed that iSCI individuals trained with larger kinematic variability, and with larger muscle activity, compared to non-cooperative position-controlled training . Schück et al. evaluated this approach in a multisession training protocol. They used the Lokomat to train two iSCI (and two stroke) individuals for four weeks, with four training sessions of 45 minutes per week, However, they did not find a relevant increase in gait speed for iSCI individuals .
Most studies on robotic gait training only assess walking ability. They report functional outcome measures and clinical scales, like walking speed (10-Meter Walking Test), distance (Six-Minute Walking Test), or walking ability (WISCI II). Only a few studies assess the effect of robotic gait training on walking quality, in terms of spatiotemporal and kinematic measures [23, 25]. Assessment of walking quality can provide useful insights into whether gait training restores walking function by restoration of function (using more normal movement patterns) or by compensatory strategies.
The aim of this study was to evaluate the feasibility and effect of an eight-week, multi-session training protocol using an impedance-controlled gait trainer. The effect of training was assessed in terms of walking ability and walking quality. Individual assessments were used to determine which individuals were most likely to benefit from the training protocol. To evaluate if training effects were retained post-training, we performed follow-up testing eight weeks after completion of the training protocol.
Subjects with chronic, motor-incomplete SCI (iSCI) were recruited from Het Roessingh Centre for Rehabilitation in Enschede, The Netherlands. Inclusion criteria were iSCI sustained at least a half year prior to enrolment, age above 18 years, a stable medical condition, a physical condition that allows for three minutes of supported walking, the ability to bear their own body weight while standing, not currently enrolled in gait training therapy, and a stable dose of anti-spastic medicine during the study. Exclusion criteria were current orthopedic issues causing problems in walking or balance, the presence of other neurological disorders, a history of cardiac conditions that interfere with physical load, the absence of independent ambulation prior to SCI, chronic joint pain and inappropriate/ unsafe fit of the robotic trainer due to the participant’s body size (bodyweight > 100 kg) and/or joint contractures. All subjects provided written informed consent including permission for publication, prior to admittance to the study. The study protocol was approved by the local medical ethics committee, METC Twente (Enschede, The Netherlands).
The amount of robotic support was adjusted by changing the stiffness of the impedance controller. The impedance levels were set to a participant-specific percentage of the maximum stiffness that could be controlled by the LOPES (300 Nm/rad). In this study, the same percentage was used for hip and knee joints and for the left and right leg. To enable the participant to stay in control of his cadence, the reference walking pattern is not replayed as a function of time but is synchronized to the cadence of the participant .
Subjects participated in an eight-week training program. Participants trained three times per week, for a maximum of 60 minutes per session. The training period was divided in two four-week periods, with one week scheduled for clinical tests in between. During training sessions, rest intervals were introduced if required by the participant or suggested by the therapist. The first training session was used to 1) fit the LOPES to the subject, 2) let participants get used to walking in the device and 3) select their preferred walking speed.
To fit the LOPES to the subject, different anthropometric measurements were taken to adjust the exoskeleton segment lengths. Next, the subject was positioned into the LOPES and the trunk and lower extremities were secured. Three adjustable cuffs (one at the thigh, two at the shank) attached the lower extremities to the LOPES frame. Final adjustments were made to the cuffs to align the subject’s hip and knee joints with the axes of the exoskeleton joints. Bodyweight support was set at a minimal amount for each participant, preventing excessive knee flexion during stance phase or toe dragging during swing phase. Foot lifters were used in case of insufficient ankle dorsal flexion during swing phase.
Adjustments of training parameters were done by the physical therapist based on the quality of walking (adequate step height during swing phase and adequate knee stability during stance phase), current physical condition (observation of breathing rate and degree of transpiration), and motivation (as verbally indicated by the participant). All changes were made in agreement with the participant. All training parameters were stored for later analysis.
Primary outcome measures
To assess changes in muscle strength and walking ability, clinical tests were performed before (pre), during (mid), and after (post) eight weeks of training. To examine whether the training effects were retained, we also performed a follow-up eight weeks after the completion of the training protocol.
Walking speed was measured using the 10-Meter Walk Test (10MWT). Participants were instructed to walk in a straight line at their own comfortable speed. Distance/endurance was tested with the Six-Minute Walk Test (6MWT), where participants ambulated for six minutes at their self-selected speed. The Timed Up and Go (TUG) test assessed the combination of balance during walking, gait speed, and sit-to-stand transitions. In this composite test, the patient must get up from a chair, walk 3 meters, return, and sit down again. For these three tests, participants were permitted to use braces and walking devices. The Walking Index for Spinal Cord Injury II (WISCI-II) was used to quantify the amount of assistance required during over-ground ambulation and to assess the use of assistive devices and/or orthoses. Category 0 indicates the participant could not walk or stand and category 20 indicates the participant could walk at least 10 m without assistance or use of assistive devices. All of these measures were taken according to van Hedel et al. . Muscle strength was determined by the Lower Extremity Motor Scores (LEMS), utilized by the American Spinal Injury Association (ASIA). The strength of five key muscles are graded from 0 to 5 (0 indicates absence of muscle contraction and 5 is a normative active movement with full range of motion against full resistance). The cumulative score for lower extremities is between 0 and 50 . All measures were recorded by an experienced physical therapist, not involved in the training.
Secondary outcome measures
To assess changes in gait quality, kinematic data and spatiotemporal measures were taken pre- and post-training. Gait kinematics were recorded using an optical tracking system, consisting of six infrared cameras (Vicon PlugIn Gait Model, VICON, Oxford Metrics, Oxford, UK) and reflective markers. Participants walked at their preferred speed across a 7-meter walkway approximately 10 times and were allowed to rest between rounds. Kinematic data from right and left limbs of each participant were extracted and averaged over at least 10 steps, using custom-written software (MATLAB, Mathworks Inc., Natick, MA, USA). The use of assistive walking devices and orthotic devices for safe over-ground walking was allowed (and kept constant during the pre- and post-measurements).
A total of nine parameters were extracted from the kinematic data: walking speed, cycle time, step symmetry index, step length, step width, relative stance phase duration, maximum knee flexion during the swing phase, range of motion (ROM) of the knee during the stance phase (initial- and mid-stance) and hip ROM. These parameters were used for comparison between pre- and post-training.
SLs represents the step length of the stronger leg and SLw the step length of the weaker leg. Here, a symmetry index of zero indicates perfect symmetry between the two legs. Similarly to Nooijen et al. , the stronger leg was defined as the leg that, on average, made the largest steps during the pre-test. In all participants, the weak leg during the pre- and post-training remained the same.
The step length, relative stance phase duration, maximum knee flexion during the swing phase, ROM of the knee during the stance phase and the hip ROM were also separately calculated for the weaker and stronger leg.
Measurements of walking ability were assessed pre-, mid-, and post-training and at follow-up. Because of the lack of normally distributed data (determined by Shapiro-Wilk test) and the relatively small number of participants, nonparametric statistical tests were used to detect changes throughout the training period. Statistical analysis was done on the absolute values for all measurements. To assess the effect of the training protocol on functional outcome (10MWT, 6MWT, WISCI II, TUG and LEMS), the Friedman analysis of variance by ranks was used, with P < 0.05. Post-hoc comparisons were performed using the Wilcoxon signed-rank test and a Bonferroni correction to account for multiple comparisons (P < 0.017). To assess retention of the functional level at follow-up, a Wilcoxon signed-rank test was performed to detect changes between post-training and follow-up with significance P < 0.05. Spearman correlation coefficients were calculated to identify possible correlations between the initial performance on the walking ability tests and the absolute change in these measures (P < 0.05). Measurements of walking quality (kinematic and spatiotemporal measures) were only assessed pre- and post-training. Changes in walking quality between pre- and post-training were determined with the Wilcoxon signed-rank test (P < 0.05). All statistical tests were performed with SPSS Statistics (IBM Corp., Armonk, NY, USA).
Descriptive information of participants
Motor level of injury*
Post- injury time (months)
46,75 ± 41.03
Primary outcome measures
Statistical results primary outcome measures
Improvement in % of subjects (pre-post)
Main effect of timep
Walking speed (m/s)
χ2(2) = 8.7 0.013*
Walking distance (m)
χ2(2) = 12.8 0.002*
χ2(2) = 10.8 0.005*
χ2(2) = 6.5 0.039*
χ2(2) = 6.9 0.032*
All participants retained the functional level reached at completion of their training. No significant differences were found between follow-up and post-training in any of the primary outcome measures (Table 2).
Relationship between initial impairment levels and absolute increase
There were no significant correlations between the initial performance on walking ability tests and the absolute increase in test performance. Still, for walking speed and distance, for example, assuming an equal increase in absolute performance suggests that slower ambulators experience the greatest relative improvement. Indeed, the relative improvement in 10 MWT (ρ = -0.68, p = 0.04) and 6 MWT (ρ = -0.79, p = 0.01) showed a significant negative correlation with the initial score on these tests. The initial score on the TUG, WISI-II and LEMS did not prove to be an indicator of the relative increase in the corresponding score.
Secondary outcome measures
Statistical results secondary outcome measures
Increase in % of subjects (pre-post)
Walking speed (m/s)
Cycle time (s)
Step symmetry index (%)
Step width (m)
Step length (m)
Strong and weak
Rel. stance phase duration (%)
Strong and weak
Maximum knee flexion (swing) (deg)
Strong and weak
Knee ROM (initial and mid stance) (deg)
Strong and weak
Hip ROM (deg)
Strong and weak
Participant 7 was excluded for analysis of kinematic and spatiotemporal data because of the use of orthotic devices, limiting accurate 3D kinematic data collection.
The aim of the present study was to examine the effects of an eight-week training program on the walking ability and quality in iSCI individuals, using an impedance-control strategy. In this study, we used a prototype of the LOPES gait trainer. The training protocol was tolerated well by all 10 participants and was performed without difficulties for eight weeks. Participants improved significantly on functional outcomes, muscle strength, kinematics, and spatiotemporal measures after eight weeks of LOPES training. Subsequent follow-up evaluations revealed that participants retained their training-induced functional improvements. The main improvement in kinematics occurred at the hip. The range of motion of the hip joint increased, whereas the different measures for the knee joint were unaffected by the training protocol. Participants with the most limited initial walking function showed the largest relative improvements.
Our main findings were a significant functional improvement and an increased muscle strength. Comparing our results with those of others is hampered because of differences in robotic devices, protocols, patient characteristics, outcome measures and the number of individuals. Furthermore, most robotic gait-training devices are rapidly evolving with increasing functionalities, making robotic gait-training strategies hard to categorize.
Overview of studies using robotic gait training in patients with spinal cord injury
Participants time since onset device
Training parameters (average number of sessions)
10 MWT Speed (m/s) (pre – post)
6 MWT Distance (mtr) (pre – post)
TUG (sec) (pre – post)
WISCI II (pre – post)
LEMS (pre – post)
Wirz et al., 2005 
N = 20 (4) Chronic Average: 70.8 months Lokomat
8 weeks; 45 min; 3-5 ×/wk; (26 sessions)
0.38 – 0.49*
121 – 165*
61 – 36*
No significant. increase
32 – 35* (N=10)
Field-Fote et al, 2011 
N = 14 Chronic ≥ 12 month N = 14 Lokomat
12 weeks; 45 min; 5 ×/wk; (49 sessions)
0.17 – 0.18
50.4 – 53.7
Left leg 12.7 – 13.9 Right leg 12.9 – 14.1*
Alcobendas-Maestro et al. 2012 
N = 37 (23) Sub-acute Average: 4 months Lokomat
8 weeks; 30 min; 5 ×/wk; (40 sessions)
0.3 – 0.4
4 – 16
33 – 40
Benito-Penalva et al. 2012 
N = 105 Sub-acute <6 month N = 81 6-12 month N = 8 >12 month N = 16 Lokomat (N = 39), GT (N = 66)
8 weeks; 45 min; 5 ×/wk; (40 sessions)
0.08 – 0.26*
Van Nunen et al. 2013 
N = 18 (9) Sub-acute and chronic <12 month N = 7 >12 month N = 11 Median: 28.8 months
12 weeks; 60 min; 2 ×/wk; (24 sessions) (20-45 min)
No significant. Increase (N = 6)
No significant. increase
Fleerkotte et al.
N = 10 Chronic Average: 45.3 months
8 weeks; 60 min; 3 ×/wk; (20 sessions) (19 min)
0.61 – 0.67*
184.4 – 212.9*
24.4 – 20.2*
13.5 – 14.4
34.4 – 37.8*
From the studies including chronic iSCI individuals, Nunen et al.  reported similar improvements in walking speed. Wirz et al. , who also included only chronic iSCI survivors, observed larger improvements in walking speeds. Possible explanations for their higher gains are a greater number of training sessions (26 vs. 20), longer session durations (45 vs. 19 min), and lower initial walking speeds (0.38 vs. 0.61 m/s). A lower initial walking speed possibly allows more room for improvement. Although not discussed by Nunen et al., their results indicate that participants with initial walking speeds around 0.4 m/s show the largest improvements in walking speeds. Therefore, it seems reasonable to assume that the greater effect sizes found by Wirz et al., can be explained by the initial functional level of their participants . Field-Fote et al. , who trained chronic iSCI individuals with very low initial walking speeds, did not find any significant effects of robotic gait training on walking speed. Apparently, iSCI individuals must have a certain level of initial walking speed/function to benefit from robotic gait training.
Although the Friedman analysis showed a significant training effect on the WISCI II score, there was no significant improvement in WISCI II scores between pre-and post-training. This is in line with other studies, taking into account the types of participants. It is known that the WISCI II is more sensitive in monitoring recovery of walking capacity in iSCI subjects during the acute stage of recovery rather than the chronic stage . Similar to Wirz et al. , Nunen et al.  and others [14, 17, 21], we did not find effect in the WISCI II score in chronic individuals, whereas Alcobendas et al.  and Benito-Penalva et al.  reported significant increases in acute patients. Improvement in LEMS scores are similar to the results found in other studies among chronic iSCI individuals .
Follow-up measurements revealed that participants in our study retained the level of functional improvement measured at the end of the training period. Studies on robotic gait training in iSCI individuals rarely include a follow-up. Field–Fote et al. did perform a follow-up among 10 individuals whose improvements exceeded 0.05 m/s to assess their retention of relearned gait abilities . They concluded that walking speeds declined between the conclusion of the training and follow-up, but remained above pre-training levels. However, their follow-up group included only two chronic iSCI participants who received robotic gait training, hampering a fair comparison.
It is important to note the timing of follow-up, which was, on average 20.3 months in their study and only eight weeks in ours. Although Field-Fote et al. did not find a correlation between time since the conclusion of training and the decline in walking speed, it seems likely that participants lose some of their relearned walking abilities over time, especially if they do not exploit their relearned walking abilities in daily life [60, 61].
Spatiotemporal and kinematic measures
To our knowledge, this is the first study reporting significant changes in spatiotemporal and kinematic measures associated with increased walking ability due to robotic gait training. We found significant changes in most spatiotemporal and kinematic measures after robotic gait training. Previous studies showed small increases in cadence, step and stride length, and step-length symmetry  or sagittal plane excursions , but these were not significant. In this study, most of these measures were significantly higher after training. It is important to note that Nooijen et al.  and Hornby et al.  used the LOKOMAT without the option to decrease guidance forces, as this option was unavailable on the device at the time of their study. Although both studies encouraged participants to "walk with the machine", they both state that constant guidance may minimize the voluntary effort during training and subsequently limit improvements in gait function.
In this study, improvements in spatiotemporal and kinematic measures were greater in the weaker leg. The larger improvements in step length and hip ROM in the weaker leg resulted in significant increases in symmetry between the two legs. This may indicate that gait training restores walking function by restoration of function using more normal movement patterns, rather than compensation.
Improvements in walking speed were caused by improvements in step length as well as cadence. The increased walking speed might explain some of the observed changes in other spatiotemporal measures. Here, the increase in walking speed probably explains the decrease in stance phase duration  and the decrease in step width . Whether the increased hip flexion is enabled by an increased hip flexion strength (mean increase in LEMS score of 3,4), or is simply a consequence of the increased walking speed  cannot be answered.
Most current rehabilitation strategies focus on recovery through intense practice of a specific task. In BWSTT training, intensity depends on a combination of duration (time or number of steps), speed, training frequency, and the amount of BWS. In this study training intensity was maximized by increasing training speed and duration, and lowering the BWS levels when possible. With the development of robotic gait trainers that can potentially support the whole movement, the amount of robotic support is also an important parameter that affects training intensity. Often the precise setting of these parameters is based on a therapist’s clinical judgment and not on experimental evidence . For some parameters, the effects on training outcome are known, but for many they are not. Furthermore, the interaction among the different parameters is not being investigated. For example, reducing the amount of BWS and training at higher treadmill speeds increases efferent input. This is known to affect the neural control of stepping and is suggested to promote functional recovery [11, 65]. Still, the interactive effect of BWS and walking speed in individuals following SCI is unknown. Also the tradeoff between training duration and frequency remains unknown.
For robotic gait training, the optimal amount of support also remains unclear, although reducing the amount of support according to the AAN principle seems most suitable. Here, one might follow the concepts provided in the “Challenge-Point Framework” . This framework states that, for each skill level, there exists an optimal level of task difficulty. When skill levels increase, further learning will be best facilitated by increasing task difficulty. In this study, task difficulty was increased by lowering impedance levels.
To gain a better understanding of the combined effect of training duration, speed, frequency, the amount of BWS and robotic support levels, these intensity parameters should be carefully reported in future studies . For example, average walking speed and BWS levels in the robotic device are rarely reported in robotic gait-training studies. Additionally, often only the total session duration is reported, which does not represent the actual training time (excluding setup time and rest periods). With the increasing interest in robotic gait-training devices that have (adaptive) impedance levels, it is also advised to report impedance levels of the robot.
Among the different robotic gait-training studies, there is a great diversity in training frequency, ranging between three to five sessions per week, and duration, ranging from 30-45 minutes per session (Table 4). These parameters are often based on financial and practical reasons . In this study, training frequency fell within this range but the mean training duration (19 minutes) was considerably lower. The relatively low training duration is thought to be the result of the use of the impedance control. By lowering the impedance levels when possible, the active contribution required from participants was relatively high. As a result, some participants, especially the slowest walkers, could not train for the same duration as seen in other position-controlled gait-training studies. Still, we showed that similar gains in walking ability can be accomplished with less training time. Actually, the biggest gains in walking ability were observed in slow walkers with the lowest training duration, suggesting that active participation is equally important as training duration.
In this study, 90 percent of participants increased their walking speed on the 10MWT, 100 percent increased their distance on the 6MWT and 100 percent reduced their time on the TUG. Although this resulted in an average significant change of 0.6 m/s, 29 m and 3.4 s (Figure 5), it should be noted that there was considerable variation among subjects. Whether these improvements represent a detectable (and clinically relevant) change is debatable. The minimally detectable change (MDC), which defines the minimal amount of change required to distinguish (with 95 percent confidence) a “true” performance change from a change due to variability in performance or measurement error, is reported to be around 0.13 m/s, 45.8 m, and 10.8 s . Criteria for what clinicians define as “clinically relevant” or “meaningful” can be even higher. Although MDC criteria for detecting “true” improvements are conservative, according to them, only one participant showed a “true” improvement on the 10MWT, 6MWT and TUG tests. Still, small gains in functional improvement that can lead to reduced reliance on assistive devices could be of great personal relevance to these individuals .
Limitations and future perspectives
The major limitation of this study is the lack of a control group. The rationale for not including a control group was that at this stage a pilot study was set up to assess the possible effect of impedance-controlled robotic gait training, how well it can be applied, the utility of the outcome measures chosen and the variability in patient responses . It was not intended to afford a basis on which to claim that this kind of training can produce greater functional improvements than those achieved through manually assisted gait training or other forms of conventional therapy. It only shows that chronic iSCI individuals still have the capacity to improve their walking function when provided with an intensive robotic gait-training program.
Patients and therapists will probably benefit the most from robotic gait-training devices during acute stages of recovery . Still, in this study, all participants were chronic individuals. We included chronic individuals (>12 months) because they typically have reached a stable level of recovery . The average time since onset was 46 months, suggesting that observed improvements can be attributed to the intervention rather than spontaneous recovery. That the participants reached a stable level of recovery was also confirmed by a lack of correlation between the time since onset of the injury and the relative (or absolute) increases in walking speed. Thus, to investigate the true potential of impedance-controlled gait training, acute and sub-acute individuals should also be included in future studies. However, these trials will require larger patient numbers to reach significance due to the potential for underlying spontaneous recovery .
Apart from time since injury [19, 20, 58, 69, 70], previous studies also showed that ASIA levels [6, 19, 69, 71], LEMS scores [25, 71, 72] (for recent injuries, for chronic results vary [18, 20, 22]), sensation [71, 73], and age [6, 71] are distinguishing factors for the degree of ambulatory capacity after gait rehabilitation. Several studies purely focus on increased walking speed, which is considered to be closely related to functional ambulation . Patients who start rehabilitation programs early after injury, have higher ASIA/LEMS/sensory scores, or are younger generally show greater improvements. Factors like ethology, levels of injury, or sex seem to be less predictive [19, 71]. Because of the relatively small number of participants in this study, we did not perform an analysis to relate clinical improvement to patient characteristics. Future studies should carefully document these characteristics, or stratify study participants, to determine which iSCI sub-population responds better to robotic gait training. These predictors might be different for robotic gait training where age or sensation, for instance, do not seem to have a clear effect on functional outcomes [19, 70].
This first explorative study using an impedance-controlled robotic gait trainer shows significant improvements in functional and qualitative walking parameters after an eight-week training program in chronic iSCI individuals. We were able to provide task-specific and intensive training sessions, even for severely affected individuals, with a minimal workload on the therapist. Compared to position-controlled robotic gait-training strategies, the training duration was relatively short, whereas improvements in functional outcomes were similar. Additionally, improvements observed at the end of the training period persisted at the eight-week follow-up. The most impaired ambulators, based on their initial walking speed, benefitted most from the training protocol in relative improvements in walking speed and walking distance.
This study was supported by a grant from the Dutch Ministry of Economic affairs and Province of Overijssel, the Netherlands (grant: PID082004). We would like to thank Martijn Postma, Bram van Gemeren, and Leontien Zonnevijlle, from Het Roessingh, Centre for Rehabilitation, for their assistance during the experiments and their experience in treadmill training.
- van Asbeck FW, Post MW: An epidemiological description of spinal cord injuries in The Netherlands in 1994. Spinal Cord. 2000, 38 (7): 420-424.View ArticlePubMedGoogle Scholar
- Warren S, Moore M, Johnson MS: Traumatic head and spinal cord injuries in Alaska (1991-1993). Alaska Med. 1995, 37 (1): 11-19.PubMedGoogle Scholar
- Wyndaele M, Wyndaele JJ: Incidence, prevalence and epidemiology of spinal cord injury: what learns a worldwide literature survey?. Spinal cord. 2006, 44 (9): 523-529.View ArticlePubMedGoogle Scholar
- Anderson KD: Targeting recovery: priorities of the spinal cord-injured population. J Neurotrauma. 2004, 21 (10): 1371-1383.View ArticlePubMedGoogle Scholar
- Ditunno PL, Patrick M, Stineman M, Ditunno JF: Who wants to walk? Preferences for recovery after SCI: a longitudinal and cross-sectional study. Spinal Cord. 2008, 47 (3): 500-506.View ArticleGoogle Scholar
- Burns SP, Golding DG, Rolle WA, Graziani V, Ditunno JF: Recovery of ambulation in motor-incomplete tetraplegia. Arch Phys Med Rehabil. 1997, 78 (11): 1169-1172.View ArticlePubMedGoogle Scholar
- Behrman AL, Bowden MG, Nair PM: Neuroplasticity after spinal cord injury and training: An emerging paradigm shift in rehabilitation and walking recovery. Phys Ther. 2006, 86 (10): 1406-1425.View ArticlePubMedGoogle Scholar
- Harness ET, Yozbatiran N, Cramer SC: Effects of intense exercise in chronic spinal cord injury. Spinal Cord. 2008, 46 (11): 733-737.View ArticlePubMedGoogle Scholar
- van Hedel HJA, Dietz V: Rehabilitation of locomotion after spinal cord injury. RestorNeurol Neurosci. 2010, 28 (1): 123-134.Google Scholar
- Hubli M, Dietz V: The physiological basis of neurorehabilitation - locomotor training after spinal cord injury. J Neuroeng Rehabil. 2013, 10 (1): 5-View ArticlePubMedPubMed CentralGoogle Scholar
- Dietz V, Muller R, Colombo G: Locomotor activity in spinal man: significance of afferent input from joint and load receptors. Brain. 2002, 125: 2626-2634.View ArticlePubMedGoogle Scholar
- Edgerton VR, Leon RD, Harkema SJ, Hodgson JA, London N, Reinkensmeyer DJ, Roy RR, Talmadge RJ, Tillakaratne NJ, Timoszyk W, Tobin A: Retraining the injured spinal cord. J Physiol. 2001, 533: 15-22.View ArticlePubMedPubMed CentralGoogle Scholar
- Barbeau H, Nadeau S, Garneau C: Physical determinants, emerging concepts, and training approaches in gait of individuals with spinal cord injury. J Neurotrauma. 2006, 23 (3): 571-585.View ArticlePubMedGoogle Scholar
- Winchester P, McColl R, Querry R, Foreman N, Mosby J, Tansey K, Williamson J: Changes in supraspinal activation patterns following robotic locomotor therapy in motor-incomplete spinal cord injury. Neurorehabil Neural Repair. 2005, 19 (4): 313-324.View ArticlePubMedGoogle Scholar
- Freivogel S, Schmalohr D, Mehrholz J: Improved walking ability and reduced therapeutic stress with an electromechanical gait device. J Rehabil Med. 2009, 41 (9): 734-739.View ArticlePubMedGoogle Scholar
- Galvez JA, Budovitch A, Harkema SJ, Reinkensmeyer DJ: Trainer variability during step training after spinal cord injury: implications for robotic gait-training device design. J Rehabil Res Dev. 2011, 48 (2): 147-160.View ArticlePubMedGoogle Scholar
- Hornby TG, Zemon DH, Campbell D: Robotic-assisted, body-weight-supported treadmill training in individuals following motor incomplete spinal cord injury. Physical therapy. 2005, 85 (1): 52-66.PubMedGoogle Scholar
- Wirz M, Zemon DH, Rupp R, Scheel A, Colombo G, Dietz V, Hornby TG: Effectiveness of automated locomotor training in patients with chronic incomplete spinal cord injury: A multicenter trial. Arch Phys Med Rehabil. 2005, 86 (4): 672-680.View ArticlePubMedGoogle Scholar
- Benito-Penalva J, Edwards DJ, Opisso E, Cortes M, Lopez-Blazquez M, Murillo N, Costa U, Tormos JM, Vidal-Samsó J, Valls-Solé J, Medina J: Gait training in human spinal cord injury using electromechanical systems: Effect of device type and patient characteristics. Arch Phys Med Rehabil. 2012, 93 (3): 404-412.View ArticlePubMedGoogle Scholar
- van Nunen M: Recovery of walking ability using a robotic device. 2013, Universiteit van Amsterdam: PhD thesisGoogle Scholar
- Hesse S, Werner C, Bardeleben A: Electromechanical gait training with functional electrical stimulation: Case studies in spinal cord injury. Spinal Cord. 2004, 42 (6): 346-352.View ArticlePubMedGoogle Scholar
- Field-Fote EC, Roach KE: Influence of a locomotor training approach on walking speed and distance in people with chronic spinal cord injury: A randomized clinical trial. Physical therapy. 2011, 91 (1): 48-60.View ArticlePubMedPubMed CentralGoogle Scholar
- Nooijen CF, Ter Hoeve N, Field-Fote EC: Gait quality is improved by locomotor training in individuals with SCI regardless of training approach. J Neuroeng Rehabi. 2009, 6 (6): 36-View ArticleGoogle Scholar
- Alcobendas-Maestro M, Esclarín-Ruz A, Casado-López RM, Muñoz-González A, Pérez-Mateos G, González-Valdizán E, Martín JLR: Lokomat robotic-assisted versus over-ground training within 3 to 6 months of incomplete spinal cord lesion: Randomized controlled trial. Neurorehabil Neural Repair. 2012, 26 (9): 1058-1063.View ArticlePubMedGoogle Scholar
- Hornby TG, Campbell DD, Zemon DH, Kahn JH: Clinical and quantitative evaluation of robotic-assisted treadmill walking to retrain ambulation after spinal cord injury. Top Spinal Cord Inj Rehabil. 2005, 11: 1-17.View ArticleGoogle Scholar
- Schwartz I, Sajina A, Neeb M, Fisher I, Katz-Luerer M, Meiner Z: Locomotor training using a robotic device in patients with subacute spinal cord injury. Spinal Cord. 2011, 49 (10): 1062-1067.View ArticlePubMedGoogle Scholar
- Tefertiller C, Pharo B, Evans N, Winchester P: Efficacy of rehabilitation robotics for walking training in neurological disorders: a review. J Rehabil Res Dev. 2011, 48 (4): 387-View ArticlePubMedGoogle Scholar
- Mehrholz J, Kugler J, Pohl M: Locomotor training for walking after spinal cord injury. Spine. 2008, 33 (21): E768-E777.View ArticlePubMedGoogle Scholar
- Swinnen E, Duerinck S, Baeyens J-P, Meeusen R, Kerckhofs E: Effectiveness of robot-assisted gait training in persons with spinal cord injury: A systematic review. J Rehabil Med. 2010, 42 (6): 520-526.View ArticlePubMedGoogle Scholar
- Reinkensmeyer DJ, Akoner OM, Ferris DP, Gordon KE: Slacking by the human motor system: Computational models and implications for robotic orthoses. 2005, Minnesota, USA: Proceedings IEEE Conf. Medicine and Biology SocietyGoogle Scholar
- Emken JL, Benitez R, Sideris A, Bobrow JE, Reinkensmeyer DJ: Motor adaptation as a greedy optimization of error and effort. J Neurophys. 2007, 97 (6): 3997-4006.View ArticleGoogle Scholar
- Israel JF, Campbell DD, Kahn JH, Hornby TG: Metabolic costs and muscle activity patterns during robotic- and therapist-assisted treadmill walking in individuals with incomplete spinal cord injury. Physical therapy. 2006, 86 (11): 1466-1478.View ArticlePubMedGoogle Scholar
- Lotze M, Braun C, Birbaumer N, Anders S, Cohen LG: Motor learning elicited by voluntary drive. Brain. 2003, 126: 866-872.View ArticlePubMedGoogle Scholar
- Kaelin-Lang A, Luft AR, Sawaki L, Burstein AH, Sohn YH, Cohen LG: Modulation of human corticomotor excitability by somatosensory input. J Neurophys. 2002, 540: 623-633.Google Scholar
- Hidler JM, Wall AE: Alterations in muscle activation patterns during robotic-assisted walking. Clin Biomech. 2005, 20 (2): 184-193.View ArticleGoogle Scholar
- Hidler JM, Wisman W, Neckel N: Kinematic trajectories while walking within the Lokomat robotic. Clin Biomech. 2008, 23 (10): 1251-1259.View ArticleGoogle Scholar
- Emken JL, Reinkensmeyer DJ: Robot-enhanced motor learning: Accelerating internal model formation during locomotion by transient dynamic amplification. IEEE Trans Neural Syst Rehabil Eng. 2005, 13 (1): 33-View ArticlePubMedGoogle Scholar
- Scheidt RA, Dingwell JB, Mussa-Ivaldi FA: Learning to move amid uncertainty. J Neurophys. 2001, 86 (2): 971-985.Google Scholar
- Banala SK, Kim SH, Agrawal SK, Scholz JP: Robot assisted gait training with active Leg exoskeleton (ALEX). IEEE Trans Neural Syst Rehabil Eng. 2009, 17: 2-8.View ArticlePubMedGoogle Scholar
- Duschau-Wicke A, Caprez A, Riener R: Patient-cooperative control increases active participation of individuals with SCI during robot-aided gait training. J Neuroeng Rehabil. 2010, 7: 43-View ArticlePubMedPubMed CentralGoogle Scholar
- Emken JL, Harkema SJ, Beres-Jones JA, Ferreira CK, Reinkensmeyer DJ: Feasibility of manual teach-and-replay and continuous impedance shaping for robotic locomotor training following spinal cord injury. IEEE Trans Biomed Eng. 2008, 55: 322-334.View ArticlePubMedGoogle Scholar
- Koopman B, van Asseldonk EH, van der Kooij H: Selective control of gait subtasks in robotic gait training: Foot clearance support in stroke survivors with a powered exoskeleton. J Neuroeng Rehabil. 2013, 10: 3-View ArticlePubMedPubMed CentralGoogle Scholar
- Aoyagi D, Ichinose WE, Harkema SJ, Reinkensmeyer DJ, Bobrow JE: A robot and control algorithm that can synchronously assist in naturalistic motion during body-weight-supported gait training following neurologic injury. IEEE Trans Neural Syst Rehabil Eng. 2007, 15 (3): 387-400.View ArticlePubMedGoogle Scholar
- Emken JL, Bobrow JE, Reinkensmeyer DJ: Robotic movement training as an optimization problem: Designing a controller that assists only as needed. 2005, Chigao, USA: Proceedings IEEE International Conference on Rehabilitation Robotics: 28 June -1July 2005Google Scholar
- Riener R, Lunenburger L, Jezernik S, Anderschitz M, Colombo G, Dietz V: Patient-cooperative strategies for robot-aided treadmill training: first experimental results. IEEE Trans Neural Syst Rehabil Eng. 2005, 13 (3): 380-394.View ArticlePubMedGoogle Scholar
- Duschau-Wicke A, Von Zitzewitz J, Caprez A, Lunenburger L, Riener R: Path control: A method for patient-cooperative robot-aided gait rehabilitation. IEEE Trans Neural Rehabil Syst Eng. 2010, 18: 38-48.View ArticleGoogle Scholar
- Jezernik S, Colombo G, Morani M: Automatic Gait-pattern adaptation algorithms for rehabilitation with a 4-DOF robotic orthosis. IEEE Trans Robotics Auto. 2004, 20 (3): 574-2004.View ArticleGoogle Scholar
- Cai LL, Fong AJ, Otoshi CK, Liang YQ, Cham JG, Zhong V, Roy RR, Edgerton VR, Burdick JW: Effects of consistency vs. Variability in robotically controlled training of stepping in adult spinal mice. 2005, Chicago, IL, USA: Proceedings. IEEE 9th Int. Conf. Rehabilitation. Robotics: 28 June - 1 July 2005View ArticleGoogle Scholar
- Cai LL, Fong AJ, Otoshi CK, Liang YQ, Burdick JW, Roy RR, Edgerton VR: Implications of assist-as-needed robotic step training after a complete spinal cord injury on intrinsic strategies of motor learning. J Neurosci. 2006, 26 (41): 10564-10568.View ArticlePubMedGoogle Scholar
- Ziegler MD, Zhong H, Roy RR, Edgerton VR: Why variability facilitates spinal learning. J Neurosci. 2010, 30 (32): 10720-10726.View ArticlePubMedPubMed CentralGoogle Scholar
- Sale P, Franceschini M, Waldner A, Hesse S: Use of the robot-assisted gait therapy in rehabilitation of patients with stroke and spinal cord injury. Eur J Phys Rehabil Med. 2012, 48: 111-121.PubMedGoogle Scholar
- Schück A, Labruyère R, Vallery H, Riener R, Duschau-Wicke A: Feasibility and effects of patient-cooperative robot-aided gait training applied in a 4-week pilot trial. J Neuroeng Rehabil. 2012, 9: 31-View ArticlePubMedPubMed CentralGoogle Scholar
- Veneman JF, Kruidhof R, Hekman EEG, Ekkelenkamp R, Van Asseldonk EHF, Van der Kooij H: Design and evaluation of the LOPES exoskeleton robot for interactive gait rehabilitation. IEEE Trans Neural Syst Rehabil Eng. 2007, 15 (3): 379-386.View ArticlePubMedGoogle Scholar
- Koopman B, Van Asseldonk EHF, Van der Kooij H: Speed-dependent reference joint trajectory generation for robotic gait support. J Biomech. 2014, in press. [http://dx.doi.org/10.1016/j.jbiomech.2014.01.037]Google Scholar
- Van Hedel HJA, Wirz M, Dietz V: Assessing walking ability in subjects with spinal cord injury: validity and reliability of 3 walking tests. Arch Phys Med Rehab. 2005, 86 (2): 190-196.View ArticleGoogle Scholar
- Maynard FM, Bracken MB, Creasey G, Ditunno JF, Donovan WH, Ducker TB, Garber SL, Marino RJ, Stover SL, Tator CH, Waters RL, Wilberger JE: International standards for neurological and functional classification of spinal cord injury. Spinal Cord. 1997, 35: 266-274.View ArticlePubMedGoogle Scholar
- Dean JC, Alexander NB, Kuo AD: The effect of lateral stabilization on walking in young and old adults. IEEE Trans Biomed Eng. 2007, 54 (11): 1919-1926.View ArticlePubMedGoogle Scholar
- Fawcett JW, Curt A, Steeves JD, Coleman WP, Tuszynski MH, Lammertse D, Bartlett PF, Blight AR, Dietz V, Ditunno J, Dobkin BH, Havton LA, Ellaway PH, Fehlings MG, Privat A, Grossman R, Guest JD, Kleitman N, Nakamura M, Gaviria M, Short D: Guidelines for the conduct of clinical trials for spinal cord injury as developed by the ICCP panel: spontaneous recovery after spinal cord injury and statistical power needed for therapeutic clinical trials. Spinal Cord. 2007, 45 (3): 190-205.View ArticlePubMedGoogle Scholar
- Jackson AB, Carnel CT, Ditunno JF, Read MS, Boninger ML, Schmeler MR, Williams SR, Donovan WH: Outcome measures for gait and ambulation in the spinal cord injury population. J Spinal Cord Med. 2008, 31 (5): 487-499.PubMedPubMed CentralGoogle Scholar
- Wirz M, Colombo G, Dietz V: Long term effects of locomotor training in spinal humans. J Neurol Neurosurg Psych. 2001, 71: 93-96.View ArticleGoogle Scholar
- Hicks AL, Adams MM, Martin Ginis K, Giangregorio L, Latimer A, Phillips SM, McCartney N: Long-term body-weight-supported treadmill training and subsequent follow-up in persons with chronic SCI: effects on functional walking ability and measures of subjective well-being. Spinal Cord. 2005, 43 (5): 291-298.View ArticlePubMedGoogle Scholar
- Stoquart G, Detrembleur C, Lejeune T: Effect of speed on kinematic, kinetic, electromyographic and energetic reference values during treadmill walking. Neurophys Clin. 2008, 38 (2): 105-116.View ArticleGoogle Scholar
- Helbostad JL, Moe-Nilssen R: The effect of gait speed on lateral balance control during walking in healthy elderly. Gait Posture. 2003, 18 (2): 27-36.View ArticlePubMedGoogle Scholar
- Lelas JL, Merriman GJ, Riley PO, Kerrigan DC: Predicting peak kinematic and kinetic parameters from gait speed. Gait Posture. 2003, 17 (2): 106-112.View ArticlePubMedGoogle Scholar
- Harkema SJ, Hurley SL, Patel UK, Requejo PS, Dobkin BH, Edgerton VR: Human lumbosacral spinal cord interprets loading during stepping. J Neurophys. 1997, 77 (2): 797-811.Google Scholar
- Guadagnoli MA, Lee T: Challenge point: A framework for conceptualizing the effects of various practice conditions in motor learning. J Motor Behavior. 2004, 36 (2): 212-224.View ArticleGoogle Scholar
- Dobkin BH: Progressive staging of pilot studies to improve phase III trials for motor interventions. Neurorehabil Neural Repair. 2009, 23 (3): 197-206.View ArticlePubMedPubMed CentralGoogle Scholar
- Perera S, Mody SH, Woodman RC, Studenski SA: Meaningful change and responsiveness in common physical performance measures in older adults. J Am Ger Soc. 2006, 54 (4): 743-749.View ArticleGoogle Scholar
- Harkema SJ, Schmidt-Read M, Lorenz DJ, Edgerton VR, Behrman AL: Balance and ambulation improvements in individuals with chronic incomplete spinal cord injury using locomotor training-based rehabilitation. Arch Phys Med Rehabil. 2012, 93 (9): 1508-1517.View ArticlePubMedGoogle Scholar
- Winchester P, Smith P, Foreman N, Mosby JM, Pacheco J, Querry R, Tansey K: A prediction model for determining over ground walking speed after locomotor training in persons with motor incomplete spinal cord injury. J Spinal Cord Med. 2009, 32: 63-71.PubMedPubMed CentralGoogle Scholar
- Van Middendorp JJ, Hosman AJF, Donders ART, Pouw MH, Ditunno JF, Curt A, Geurts ACH, Van de Meent H: A clinical prediction rule for ambulation outcomes after traumatic spinal cord injury: a longitudinal cohort study. Lancet. 2011, 377: 1004-1010.View ArticlePubMedGoogle Scholar
- Ditunno JF, Barbeau H, Dobkin BH, Elashoff R, Harkema S, Marino RJ, Hauck WW, Apple D, Basso DM, Behrman A, Deforge D, Fugate L, Saulino M, Scott M, Chung J: Validity of the walking scale for spinal cord injury and other domains of function in a multicenter clinical trial. Neurorehabil Neural Repair. 2007, 21 (6): 539-550.View ArticlePubMedPubMed CentralGoogle Scholar
- Oleson CV, Burns AS, Ditunno JF, Geisler FH, Coleman WP: Prognostic value of pinprick preservation in motor complete, sensory incomplete spinal cord injury. Arch Phys Med Rehabil. 2005, 86 (5): 988-992.View ArticlePubMedGoogle Scholar
- Van Hedel HJA: Gait speed in relation to categories of functional ambulation after spinal cord injury. Neurorehabil Neural Repair. 2009, 23 (4): 343-350.View ArticlePubMedGoogle Scholar
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