- Open Access
Effects of underestimating the kinematics of trunk rotation on simultaneous reaching movements: predictions of a biomechanical model
© Simoneau et al.; licensee BioMed Central Ltd. 2013
Received: 4 June 2012
Accepted: 6 June 2013
Published: 12 June 2013
Rotation of the torso while reaching produces torques (e.g., Coriolis torque) that deviate the arm from its planned trajectory. To ensure an accurate reaching movement, the brain may take these perturbing torques into account during movement planning or, alternatively, it may correct hand trajectory during movement execution. Irrespective of the process selected, it is expected that an underestimation of trunk rotation would likely induce inaccurate shoulder and elbow torques, resulting in hand deviation. Nonetheless, it is still undetermined to what extent a small error in the perception of trunk rotations, translating into an inappropriate selection of motor commands, would affect reaching accuracy.
To investigate, we adapted a biomechanical model (J Neurophysiol 89: 276-289, 2003) to predict the consequences of underestimating trunk rotations on right hand reaching movements performed during either clockwise or counter clockwise torso rotations.
The results revealed that regardless of the degree to which the torso rotation was underestimated, the amplitude of hand deviation was much larger for counter clockwise rotations than for clockwise rotations. This was attributed to the fact that the Coriolis and centripetal joint torques were acting in the same direction during counter clockwise rotation yet in opposite directions during clockwise rotations, effectively cancelling each other out.
These findings suggest that in order to anticipate and compensate for the interaction torques generated during torso rotation while reaching, the brain must have an accurate prediction of torso rotation kinematics. The present study proposes that when designing upper limb prostheses controllers, adding a sensor to monitor trunk kinematics may improve prostheses control and performance.
Arm movements are among the most frequent and important actions in the human voluntary motor repertoire. These complex movements enable us to feed and look after ourselves as well as others, build safe shelter and perform other life-sustaining activities. Reaching is a complex motor action as shoulder and elbow joint torques arise not only from muscles acting at both joints, but also from interactions due to the movement of other limbs. For instance, extending the elbow while flexing the shoulder generates an interaction torque at the shoulder joint. These torques depend, in a nonlinear fashion, on the motion of adjacent joints. Both behavioral and simulation studies indicate that a failure of the motor commands to account for the interaction torques results in severe disturbances of the movement trajectory[1–3]. Understanding the biomechanical and sensorimotor control processes involved in reaching may help clinicians identify the location of deficits occurring in individuals with neurological disorders.
Arm movements often occur simultaneously with trunk rotations, such as when approaching an object out of reach on our side. Moving the trunk can also be used as a strategy to move the arm in space when arm movements are impaired as a result of brain damage. Importantly, trunk rotation during reaching produces Coriolis torques that push the arm perpendicularly to the hand-velocity vector and in the opposite direction of the rotation. Without taking into account these torques, it would be impossible for the brain to command smooth and accurate arm movements. These movements may include those that accompany our own displacements or more specifically, those that we admire in sports and dance. The inertial Coriolis force is dependent on the cross product of the linear velocity of the arm and the angular velocity of torso rotation. Several studies have shown that when body rotations cannot be detected accurately, as during sustained passive body rotation at a constant velocity, the trajectories and endpoints of reaching movements are first deviated in the direction of the Coriolis force applied on the arm[6–9]. After a few movements produced under such conditions, the hand trajectory straightens, thereby increasing endpoint accuracy e.g.,. It is believed that this improvement is a result of motor adaptations to Coriolis perturbations. Furthermore, Pigeon et al. showed that when we reach for an object while simultaneously rotating the torso, despite the potential for trunk motion to perturb arm movement, the reach is still accurate. This observation holds true even in the absence of visual feedback from the hand. The authors demonstrated that, under these circumstances, one does not minimize the Coriolis torques incumbent on trunk rotation by sequencing the arm and trunk motions into a turn followed by a reach. Rather, when reaching for an eccentric object, we generally move both the arm and trunk simultaneously. In building an inverse dynamic model of unrestrained reaching movements, Bortolami and colleagues[10, 11] showed that the Coriolis torques at the shoulder joint could be nearly six times larger with torso rotation compared to without. One way to maintain movement accuracy while simultaneously reaching and rotating the trunk would be to correct the deviations of hand trajectory that result from the additional Coriolis torques evoked from the rotation. However, experimental studies have suggested that the brain predicts the consequences of Coriolis torques either prior to or during trunk rotations[5, 12]. In either case, a reliable estimate of head-trunk kinematics appears to be necessary in order to assess the mechanical consequences for the reaching arm.
The vestibular system provides feedback regarding the linear and angular motion of the head over a wide range of velocities and frequencies relative to the outside world. The integration of this information with proprioceptive input from the neck muscles provides the brain with information on trunk motion[14, 15]. There is evidence that the brain may use information regarding trunk movements to predict the perturbing effects of torso rotation on reaching movements[16, 17]. However, there are several instances where vestibular perception of body rotation is impaired. For instance, perception of motion may deteriorate with age, various diseases (e.g., midline cerebellar lesions, vestibular neuronitis, idiopathic scoliosis) and body rotation at a constant velocity[6–8]. In such situations, where the detection of trunk kinematics is compromised, reaching movements should be less accurate. However, it is unknown to what extent reaching accuracy deteriorates as a result of errors in the perception of trunk rotation. On the other hand, because the direction of shoulder and elbow torques depends upon the direction of torso rotation, it is possible that the relationship between underestimating torso rotation and reaching error is different for clockwise and counter clockwise rotations. To our knowledge, there is no straightforward procedure to investigate these issues in human or animal subjects. One major difficulty involves assessing the subject’s’ perception of their rotation while they are simultaneously engaged in a reaching task. Reaching errors may also result from errors in movement planning or in controlling arm movements without visual feedback[22–24].Therefore, the trajectory deviations produced by humans during torso rotation would not provide a direct estimate of the effects of miscalculating trunk rotations on reaching movements. In this context, the use of a biomechanical model emerges as an effective means to determine the consequences of underestimating torso rotation on simultaneous reaching movements. Here, we adapted the biomechanical model of right hand reaching movements proposed by Pigeon et al. to address the following questions: i) to what extend is the brain required to alter reaching motor commands to ensure accurate hand trajectory despite torso rotation?, ii) what is the effect of underestimating torso rotation on right hand reaching accuracy? and, iii) does underestimating counter- versus clockwise rotations have the same influence on reaching accuracy?
where L1 and L2 are the length (m) of the upper and lower arm segments, respectively, and x and y are the coordinates of the hand position in a shoulder-centered system.
Matrix H and are described in detail by Pigeon et al., 2003. The anthropometric data were related to the height (1.78 m) and mass (80 kg) of the model according to the literature. Segment length (L), expressed as a percentage of body height, was drawn from. Segment mass (m), moment of inertia (I) and distance to the centre of mass from the proximal joint (r) were computed from Dempster’s table.
Then, from the elbow and shoulder joint angular kinematics, hand trajectories were determined using forward kinematics.
Torso rotation while reaching for an object creates additional torques (e.g., Coriolis) on the arm that must be accounted for by motor commands in order to ensure accurate movement. As the magnitudes of these torques depend on trunk angular kinematics, misperception of trunk rotation may therefore alter reaching accuracy. The feedforward 2-D biomechanical model presented herein aimed to assess the consequences of underestimating torso rotation on reaching accuracy and to determine whether these consequences depend on the direction of torso rotation.
The outcomes of the current model support the model proposed by Bortolami et al.. Their model showed that for counter clockwise rotations, in comparison to reaching in the absence of torso rotation, the amplitudes of the net shoulder and elbow torques are scaled up to ensure accurate final hand position despite body rotations. However, this model was not developed to determine the consequences of the direction and the misperception of torso rotations on reaching accuracy. The novel observation provided by the present model is that the accuracy of reaching movements performed during trunk rotation decreases with increasing underestimations of trunk rotation. As well, this model shows that the amplitude of the final hand error is larger for counter clockwise rotations than for clockwise rotations. Indeed, regardless of the magnitude of the underestimation for clockwise rotation, the Coriolis and centripetal torques partly cancel out, thereby reducing the detrimental effect of errors in perceiving trunk rotation on right hand trajectory. As these torques acted in the same direction for counter clockwise trunk rotations, the resulting net sum of residual torques at the shoulder and elbow joints were considerable. In this case, movement accuracy was largely affected by rotational underestimations. If the simulated reaching movement had been performed with the left hand, the underestimation of clockwise rotation would have induced a larger final hand error as the Coriolis and Centripetal torque errors would not, in this case, cancel each other out. In contrast, a smaller final hand error would be observed for left hand reaching during counter clockwise rotation.
Our feedforward model simulated error (i.e., underestimation of torso acceleration) occurring during the planning stage of reaching. Therefore, it excluded any online correction of hand deviation based on arm proprioception or vestibular and visual information (i.e., feedback control). According to current motor control models, for self-generated torso and reaching movements, the brain may use motor commands in conjunction with internal models of both the arm and trunk to anticipate the resultant perturbing torques and thereby adjust the arm motor commands in a feedforward manner e.g.,. For example, while reaching in the absence of trunk movement, muscle activity in the shoulder and elbow joints varies in a predictive manner to compensate for interaction torques arising from multi-joint dynamics[3, 30–32]. Therefore, to reach accurately while the torso is rotating, the brain likely uses internal models to predict and offset the kinematic consequences of intersegmental dynamics[5, 16, 17]. Sensory information is crucial to develop, maintain and update such internal models e.g.,[33, 34]. Consequently, accurate internal models of the trunk and arm are essential to perform accurate reaching movements during voluntary head and torso rotations. Based on this proposition and our model, hand movement inaccuracies observed in patients with vestibular defects most likely result from an underestimation of the mechanical consequences of trunk movements on their arm[35–37]. In addition, patients with moderate and severe impairments in a paretic arm will move their trunk to reach an object even if it is not necessary. Therefore, it is possible that any reaching inaccuracy they experience may, in part, be due to an imprecise internal model of trunk motion. Consequently, training programs aiming to improve reaching movements in these populations should involve exercises implying arm movements towards various target locations during trunk rotations. Furthermore, the present results suggest that when designing upper limb prostheses controllers, adding a sensor that monitors trunk kinematics could improve prostheses control and performance as torso motions would be taken into account by the controller.
Our feedforward model did not attempt to evaluate the use of sensory cues related to trunk kinematics to correct hand trajectory during the movement (i.e., online correction based on error-feedback signals). It is likely that these cues (e.g. vestibular), in conjunction with the monitoring of the motor commands, offer enough information to control self-induced interaction torques as they arise during torso rotation. Nonetheless, well-learned movements such as manual reaching do not heavily rely on continuous feedback control. For example, adaptation studies have revealed that a sudden change in the inertial configuration of the arm during reaching induces initial errors in reaching that can be well predicted by an open-looped forward model. On the other hand, the lack of experimental data to validate the outcomes of the biomechanical model could be seen as another limitation of the present study. The acquisition of such data would require us to determine the perception of torso rotation, either in healthy individuals or subjects with neurological pathologies. While this can be performed relatively easily after the rotations[39–41], assessing real-time errors in the perception of torso rotation kinematics proves to be much more challenging, especially when subjects are involved in a concomitant reaching task. Finally, to further explore the effect of torso rotation misperception on reaching accuracy, it would be informative to assess the effect of arm movements in different directions relative to the body and to gravity.
The present study demonstrates that even small errors in perceiving or predicting the kinematics of counter clockwise torso rotation may impair the accuracy of reaching movements. However, errors in estimating clockwise rotation appear less detrimental to movement accuracy as in this instance, the shoulder and elbow joint torques work to effectively reduce hand deviation. Finally, according to the outcomes of the feed forward model, healthy individuals likely possess accurate internal models of their arm and torso kinematics so that they normally show small errors when reaching for a target while simultaneously rotating their trunk[5, 42].
1As vestibular receptors respond to head acceleration, the perception of body motion is impaired when the body rotates at constant velocity. The large reaching errors that have been reported during such rotations[6–9] suggest that proprioceptive and cutaneous inputs provide little information about body rotations.
This research was supported by a Natural Sciences and Engineering Research Council of Canada Discovery Grant to MS.
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