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Biomedical subjects

Romeo Chua

Publications and source records attributed to Romeo Chua.

At least 19 recordsLinked to original sources
PubMed2007

Startle produces early response latencies that are distinct from stimulus intensity effects.

Recent experiments pairing a startling stimulus with a simple reaction time (RT) task have shown that when participants are startled, a prepared movement was initiated earlier in comparison to voluntary initiation. It has been argued that the startle acts to trigger the response involuntarily. However, an alternative explanation is that the decrease in RT may be due to stimulus intensity effects, not involuntary triggering. Thus the aim of the current investigation was to determine if RT simply declined in a linear fashion with increasing stimulus intensity, or if there was a point at which RT dramatically decreased. In the present experiment participants completed 50 active wrist extension trials to a target in response to an auditory stimulus of varying stimulus intensity (83-123 dB). The presented data show that RTs associated with a startle response are separate from stimulus intensity facilitated responses. Furthermore, this startle facilitation is more highly associated with sternocleidomastoid electromyographic (EMG) activity, rather than the EMG from the widely used startle response indicator muscle orbicularis oculi.

Acoustic Stimulation↗
PubMed2006

Use of visual information in the correction of interceptive actions.

Use of visual information in interceptive actions requiring large-scale changes to movement timing was investigated. The task consisted of intercepting a moving target on a monitor screen through an angular arm movement. In half of the trials, the initial target velocity of 8 cm/s was unexpectedly decreased to 4 cm/s or increased to 12 cm/s, leaving 800 ms to target arrival after velocity change. Visual information about target displacement was manipulated by interpolating full vision with occlusion of the last 200, 400, or 600 ms before the due time of interception. The results revealed that reduction of visual exposure of target displacement affected movement variability, but not arm velocity or directional trend of temporal errors. This finding supports the concept that motor control in interception is based on an internal representation of target displacement, formed during the initial portion of visual exposure following velocity change, which is updated by further visual information of target displacement.

Adult↗
PubMed2006

Updating of an internal model without proprioception: a deafferentation study.

This study sought to determine whether intact proprioception is required to adapt to a novel kinematic environment. We compared adaptation with a rotated visual feedback between a deafferented patient and healthy participants. They performed reaching movements towards visible targets while vision of the cursor was rotated by 30 degrees with respect to hand position. The patient adapted at the same rate and to the same extent as the controls when exposed to the rotated visual feedback. She also presented large aftereffects following removal of the perturbation. This suggests that proprioception is not an absolute requirement to update a kinematic internal model. Adaptation was likely mediated by a comparison between the sensory consequences of a movement as predicted by a forward model and the visual feedback from that movement.

Adaptation, Physiological↗
PubMed2006

Sensorimotor adaptation in response to proprioceptive bias.

Studies investigating visuo-motor adaptation typically introduce sensory conflicts by manipulating visual information (prisms, cursor gains). The purpose of the present study was to determine whether similar adaptation would be observed when a conflict is created through distortion of the proprioceptive sense, rather than through visual distortion. We used a coordinated movement task that required participants to release thumb and index finger at a specific elbow angle during passive elbow extension. Participants could not see their arm, but were shown a cursor representing the forearm on a video screen. In the proprioceptive group, a sensory conflict was introduced by vibrating the biceps brachii muscle, introducing a discrepancy of approximately 7.5 degrees between the proprioceptively perceived and visually perceived elbow angle. In the visual group, a conflict of similar magnitude was obtained by introducing a gain of 7.5 degrees to the cursor with respect to forearm position. Adaptation was assessed by the presence of plastic changes in release elbow angles following a period of exposure to the sensory conflict (i.e., aftereffects). Both groups showed high accuracy during exposure despite the sensory conflicts. More importantly, the visual group presented large and persistent aftereffects, while the proprioceptive group presented none. We suggest that the proprioceptive group's lack of adaptation was due to the artificial muscle spindle activity resulting from vibration, which prevented visual and proprioceptive signals to be merged into a common frame of reference.

Adaptation, Physiological↗
PubMed2006

On-line control of pointing is modified by unseen visual shapes.

Shapes that are rendered invisible through backward masking are still able to influence motor responses: this is called masked priming. Yet it is unknown whether this influence is on the control of ongoing action, or whether it merely influences the initiation of an already-programmed action. We modified a masked priming procedure (Schmidt, 2002) such that the critical prime-mask sequence was displayed during the execution of an already-initiated goal-directed pointing movement. Psychophysical tests of prime visibility indicated that the identity of the prime shapes were not accessible to participants for conscious report. Yet detailed kinematic analysis of the finger in motion revealed that masked primes had an influence on the pointing trajectories within 277ms of their appearance, 56ms earlier than the trajectory deviations observed in response to the visible masks. These results indicate that subliminal shapes can indeed influence the control of ongoing motor activity.

Adult↗
PubMed2006

Inferring online and offline processing of visual feedback in target-directed movements from kinematic data.

Vision plays an important role in the planning and execution of target-directed aiming movements. In this review, we highlight the limitations that exist in detecting visual regulation of limb trajectories from traditional kinematic analyses such as the identification of discontinuities in velocity and acceleration. Alternative kinematic analyses that involve examining variability in limb trajectories to infer visual control processes are evaluated. The basic assumption underlying these methods is that noise exists in the neuromotor system that subsequently leads to variability in motor output. This leads to systematic relations in limb trajectory variability at different stages of the movement that are altered when trajectories are modified during movement execution. Hence, by examining the variability in limb trajectories and correlations of kinematic variables throughout movement for vision and no vision conditions, the contribution of visual feedback in the planning and control of movement can be determined.

Animals↗
PubMed2006

Temporal uncertainty does not affect response latencies of movements produced during startle reactions.

Previous research has shown that a startle 'go' stimulus, presented at a constant latency with respect to a warning stimulus, is capable of eliciting an intended voluntary movement in a simple reaction time (RT) task at very short latencies without involvement of the cerebral cortex (Carlsen et al. in Exp Brain Res 152:510-518, 2003; J Motor Behav 36:253-264, 2004a; Exp Brain Res 159:301-309 2004b; Valls-Solé et al. in J Physiol 516:931-938, 1999). The purpose of the present experiment was to determine the effect of temporal uncertainty on response latency during an RT task that comprised a startle stimulus. Participants were required to perform an active 20 degrees wrist extension movement in response to an auditory tone that was presented 2,500 to 5,500 ms after a warning stimulus, in 1,000 ms increments. On certain trials the control auditory stimulus (80 dB) was unexpectedly replaced by the startle stimulus (124 dB). When participants were startled the intended voluntary movement was initiated at approximately 70 ms, regardless of foreperiod duration. The magnitude and invariance of response latencies to the startle stimulus suggest that the intended movement had indeed been prepared prior to the arrival of the imperative go stimulus, within 2.5 s of the warning stimulus. Furthermore, there was no evidence that the prepared movement decayed over a period of at least 3 s.

Acoustic Stimulation↗
PubMed2006

Compatibility effects in stopping and response initiation in a continuous tracking task.

Two experiments explored stopping performance using a new stimulus-response compatibility effect spanning action initiation and stopping. Participants tracked a sometimes-moving, sometimes-stationary target by controlling the speed of a response marker via a force sensor. In the compatible condition, participants pressed the sensor in response to the target moving and stopped pressing in response to the target stopping. In the incompatible condition, participants stopped pressing in response to the target moving and initiated pressing in response to the target stopping. Response initiation and stopping were found to be faster under compatible than under incompatible conditions, regardless of whether compatible and incompatible trials were blocked or mixed. These findings indicate that stopping, like response initiation, is influenced by stimulus-response properties such as compatibility. This in turn suggests that stopping is governed by constraints similar to those of other behaviours.

Adolescent↗
PubMed2006

Gross motor skill acquisition in adolescents with Down syndrome.

The purpose of this study was to assess whether verbal-motor performances deficits exhibited by individuals with Down syndrome limited their ability to acquire gross motor skills when given visual and verbal instruction together and then transferred to either a visual or verbal instructional mode to reproduce the movement. Nine individuals with Down syndrome (6 males, 3 females) performed 3 gross motor skills. Both visual and verbal instructional guidance was given to the participants over a 4-day period. Twenty-four hours later, the participants were video recorded as they produced the movements (used as baseline measures). On Day 6, they were randomly assigned into verbal and visual groups and required to reproduce the skills while the experimenter provided either visual demonstration or verbal instructions depending on the group. Based on skill performance scores, participants in the verbal-motor performance group demonstrated a lower level of proficiency and an increased number of performance errors when compared to participants in the visual-motor performance group. Moreover, while the visual group demonstrated an increase in performance levels compared to baseline measures, the opposite effect was seen for the verbal group.

Activities of Daily Living↗
PubMed2006

Anchoring strategies for learning a bimanual coordination pattern.

Anchoring has been defined as synchronizing a point in a movement cycle with an external stimulus (W. D. Byblow, R. G. Carson, & D. Goodman, 1994). Previously, investigators have examined anchoring during in-phase and antiphase movements. The present authors examined anchoring during acquisition of a novel bimanual coordination pattern. Participants performed a 90 degrees pattern at 1 Hz, with a 2- or 4-Hz metronome. No group differences were found in pattern performance; however, the 4-Hz group developed more consistent anchoring relative to the metronome. Mechanical anchor-point variability differed by hand, position (midpoint vs. endpoint), and direction (flexion vs. extension) but not by metronome frequency. Those results support and extend previous findings but leave unanswered questions regarding the benefits and effectiveness of anchoring during a 90 degrees pattern.

Hand↗
PubMed2006

Decay in visuomotor representations during manual aiming.

The time course of the decay of spatial representations used for planning and controlling manual aiming has not been established. The authors' purpose in the present investigation was to generate a psychometric function for memory-guided reaching movements. Eight university-aged students performed a reciprocal tapping task for 10 s. Participants could see the targets for 5 s; then, vision of the targets was occluded. The present findings provide mixed support for 2 prominent theories concerning memory representations. Variability increased concurrently with the removal of vision of the targets, supporting the real-time hypothesis. However, a brief plateau in the curve was apparent for approximately 2 s after vision was removed, consistent with the use of a highly accurate representation for action.

Hand↗
PubMed2006

Determinants of offline processing of visual information for the control of reaching movements.

The authors investigated the use of visual feedback as a form of knowledge of results (KR) for the control of rapid (200-250 ms) reaching movements in 40 participants. They compared endpoint accuracy and intraindividual variability of a full-vision group (FV) with those of no-vision groups provided with KR regarding (a) the endpoint in numerical form, (b) the endpoint in visual form, or (c) the endpoint and the trajectory in visual form (DEL). The FV group was more accurate and less variable than were the no-vision groups, and the analysis of limb trajectory variability indicated that their superior performance resulted primarily from better movement planning rather than from online visual processes. The FV group outperformed the DEL group even though both groups were obtaining the same amount of spatial visual information from every movement. That finding suggests that the effectiveness with which visual feedback is processed offline is not a simple function of the amount of visual information available, but depends on how that information is presented.

Adult↗
PubMed2006

Reprogramming of interceptive actions: time course of temporal corrections for unexpected target velocity change.

The authors investigated the time course of reprogramming of the temporal dimension of motor acts in a task requiring interception of a moving target. The target moved at a constant velocity on a monitor screen; in part of the trials, target velocity was unexpectedly increased or decreased. Those modifications were produced at different moments during target displacement, leaving periods of time from 100 to 800 ms for movement timing correction. The authors assessed the effects of probability of target velocity change (25% vs. 50%), uncertainty about direction of velocity change (unidirectional vs. bidirectional), and direction of velocity change (increase vs. decrease). Analysis of 24 participants' arm acceleration showed that fast adjustments took place between 100 and 200 ms after target velocity change similarly for all uncertainty conditions. Analysis of temporal error indicated that the combination of high probability of target velocity change and certainty on direction of target velocity change led to the most successful movement timing reprogramming. For the other experimental conditions, temporal accuracy was still poor when a period of 800 ms was available for correction. Movement reprogramming was a continuous process that was more efficient for target velocity increase than for target velocity decrease.

Adult↗
PubMed2005

No automatic pilot for visually guided aiming based on colour.

It has been claimed that visually guided limb movements are automatically corrected in response to a change in target location but not when the same change in target is cued through a colour switch (Pisella et al. 2000). These findings were based solely on limb endpoint data. Here we examine the kinematic trajectory of the hand during the entire movement. Participants pointed rapidly to a target object that could change position either by changing spatial location, or by switching colour with a second object. Participants performed in two instructional conditions: a "go" condition to index intentional movements and a "stop" condition in which failures to stop pointing indexed automatic limb guidance. Kinematic analysis indicated efficient intentional pointing in both location and colour change conditions. However, only targets that changed spatial location elicited involuntary limb modifications and these occurred within 150 ms of the change. This conclusion held even after baseline differences in the efficiency of processing colour-defined targets were taken into account, thereby strengthening the claim of a strongly automatic pilot for visually guided limb movements.

Adolescent↗
PubMed2005

Is proprioception calibrated during visually guided movements?

In the present study, a visuomotor adaptation paradigm was used to determine whether proprioception is calibrated during visually guided movements. A full vision group (FV) was given vision of a cursor representing hand position and was asked to aim towards visible targets. A no vision group (NV) performed the same task without vision of the cursor and was given knowledge of results (KR) after movement completion. A directional bias was introduced between the location of the cursor and the location of the hand in an adaptation phase, which resulted in a deviation to the right of the intended target. Of interest was whether participants would still show rightward deviations in a post-test series of trials in which vision was removed (aftereffects). The NV group presented strong aftereffects. However, the FV group only showed modest aftereffects early in the post-test, which rapidly decayed over the course of the post-test. Further analyses showed that the presence of those early aftereffects was due to an offline influence of vision on movement planning.

Adult↗
PubMed2005

Does Joe influence Fred's action? Inhibition of return across different nervous systems.

Inhibition of return (IOR) refers to the slowing of responses to a target that appears in the same location as a previous event. Many researchers have speculated that IOR arises from inhibitory neural processes that have developed through evolution to facilitate efficient search patterns by biasing the action and/or attention of an individual towards novel locations. Throughout evolution, however, humans conducted searches as individuals as well as members of a group. In this context, we sought to determine if IOR could also be observed in the behavior of one individual after the observation of another's behavior. Consistent with our reasoning, there was no difference in the magnitude of the IOR effect found when participants followed their own response or the response of their partner. These results are discussed in the context of action-based attention and possible underlying neural mechanisms.

Adolescent↗
PubMed2005

Identifying visual-vestibular contributions during target-directed locomotion.

The purpose of this experiment was to examine the potential interaction between visual and vestibular inputs as participants walked towards 1 of 3 targets located on a barrier 5m away. Visual and vestibular inputs were perturbed with displacing prisms and galvanic vestibular stimulation (GVS), respectively. For each target there were three vision conditions (no prisms, prisms left, and prisms right), and three GVS conditions (no GVS, anode left, and anode right). Participants were instructed to start with eyes closed, and to open the eyes at heel contact of the first step. GVS and target illumination were triggered by the first heel contact. This ensured that the upcoming visual condition and target were unknown and that both sensory perturbations occurred simultaneously. Lateral displacement was determined every 40 cm. Irrespective of target or direction, GVS or prism perturbation alone resulted in similar lateral deviations. When combined, the GVS and prism perturbations that had similar singular effects led to significantly larger deviations in the direction of the perturbations. The deviations were approximately equal to the sum of the single deviations indicating that the combined effects were additive. Conflicting GVS and prism perturbations led to significantly smaller deviations that were close to zero, indicating that opposite perturbations cancelled each other. These results show that when both visual and vestibular information remain important during task performance, the nervous system integrates the inputs equally.

Adult↗