Immediate Movement History Influences Reach-to-Grasp Action Selection in Children and Adults

The authors review studies of mentally simulated movements. In automatic or cyclical movements, actual and motor imagery (MI) durations are similar. When athletes simulate only dynamic phases of movement or perform MI just before competing, however, environmental and time constraints lead to an underestimation of actual duration. Conversely, complex attention-demanding movements take longer to image. Finally, participants can modify the speed of MI voluntarily when they receive specific instructions. To complete the available data, the authors compared imagined and actual durations in tennis and gymnastics. Results showed systematic and disproportionate overestimation of actual duration. The authors found a relationship between complex motor skills and MI duration. They discuss the factors leading to over- and underestimation and the hypotheses that could be tested.     

Effect of imagined movement speed on subsequent motor performance

Researchers realize that motor imagery (MI) duration is closely linked to actual motor action duration. In 2 experiments, the authors investigated the effect of changing MI speed on actual movement duration over a 3-week training period. Experiment 1 involved 2 series of body movements that 24 participants mentally performed faster or slower than their actual execution speeds. The fast MI group's actual times decreased on subsequent performance. Participants in Experiment 2 were 21 skilled athletes who increased (decreased) their well-rehearsed actual movement times after MI training at a slow (fast) speed. The effect was task-related, however: MI affected only self-initiated movement. The effect of MI on actual speed execution supports the ideomotor theory because anticipation of sensory consequences of actions is mentally represented.     

How does motor imagery speed affect motor performance times? Evaluating the effects of task specificity

The present experiment investigated whether motor imagery (MI) performed at a faster speed might influence the actual motor performance duration by comparing real‐time vs. fast MI of different finger movement sequences. Forty‐eight participants were either asked to do real‐time or fast MI practice of simple 8‐digit (unimanual), complex 8‐digit (bimanual), and long (16‐digit) finger movement sequences. The main findings revealed that both fast and real‐time MI resulted in actual speed gains in all experimental conditions, hence suggesting that performing fast MI did not systematically provide additional benefits as compared to real‐time MI. Interestingly, the results suggested that the speed at which movements were performed following an increase in MI speed was selectively influenced by the complexity of the task. MI training at higher speed seemed to be more effective in changing complex motor sequences compared with real‐time MI. Practical implications in motor learning and rehabilitation are also discussed. Copyright © 2010 John Wiley & Sons, Ltd.     

When music tempo affects the temporal congruence between physical practice and motor imagery

When people listen to music, they hear beat and a metrical structure in the rhythm; these perceived patterns enable coordination with the music. A clear correspondence between the tempo of actual movement (e.g., walking) and that of music has been demonstrated, but whether similar coordination occurs during motor imagery is unknown. Twenty participants walked naturally for 8 m, either physically or mentally, while listening to slow and fast music, or not listening to anything at all (control condition). Executed and imagined walking times were recorded to assess the temporal congruence between physical practice (PP) and motor imagery (MI). Results showed a difference when comparing slow and fast time conditions, but each of these durations did not differ from soundless condition times, hence showing that body movement may not necessarily change in order to synchronize with music. However, the main finding revealed that the ability to achieve temporal congruence between PP and MI times was altered when listening to either slow or fast music. These data suggest that when physical movement is modulated with respect to the musical tempo, the MI efficacy of the corresponding movement may be affected by the rhythm of the music. Practical applications in sport are discussed as athletes frequently listen to music before competing while they mentally practice their movements to be performed.     

Quantitative assessment of infant reaching movements

We have identified a fundamental property of human motor behavior as a tight coupling of the curvature-speed relationship in the reaching movements of 5- to 9-month-old infants. This relationship termed a movement unit, occurs regardless of the distance of duration of the reach and in spite of the developmental change that occurs in grasping during this period. Movement unit durations are tightly clustered around 200 ms regardless of overall duration or distance or the position of the unit in the reach. The curvature-speed coupling has been identified by others in adult reaching and handwriting. Models of biological motor control must account for this invariant relationship.     

Motor imagery may incorporate trial-to-trial error

The authors tested for 1/f noise in motor imagery (MI). Participants pointed and imagined pointing to a single target (Experiment 1), to targets of varied size (Experiment 2), and switched between pointing and grasping (Experiment 3). Experiment 1 showed comparable patterns of serial correlation in actual and imagined movement. Experiment 2 suggested increased correlation for MI and performance with increased task difficulty, perhaps reflecting adaptation to a more complex environment. Experiment 3 suggested a parallel decrease in correlation with task switching, perhaps reflecting discontinuity of mental set. Although present results do not conclusively reveal 1/f fluctuation, the emergent patterns suggest that MI could incorporate trial-to-trial error across a range of constraints.     

Rapid visual feedback processing in single-aiming movements

A major line of behavioral support for motor-program theory derives from evidence indicating that feedback does not influence the execution and control of limited duration movements. Since feedback cannot be utilized, the motor-program is assumed to act as the controlling agent. in a classic study, Keele and Posner observed that visual feedback had no effect on the accuracy of 190-msec single-aiming movements. Therefore visual feedback processing time is greater than 190 msec, and, more importantly, limited duration movements are governed by motor programs. In the present paper, we observed that visual feedback can affect the spatial accuracy of movement with durations much less than 190 msec. We hypothesize that visual feedback can aid motor control via processes not associated with intermittent error corrections.     

The emergence of motor imagery in children

A total of 80 children (40 5-year-olds and 40 7-year-olds) took part in an experiment to evaluate their capacity to mentally evoke a motor image of their own displacement. Using a chronometry paradigm, movement duration was compared in a task where children were asked to move in order to take a puppet back to its home (actual) and to think about themselves executing the same action (virtual). Movement durations for actual and virtual displacements were obtained in two conditions, where either no information was provided about the weight of the puppet to be displaced (standard situation) or the puppet was described as being heavy (informed situation). A significant correlation between actual and virtual walking durations was observed for 7-year-olds in the informed condition. This result provides evidence for a motor imagery process emerging in 7-year-olds when children are required to think about themselves in action.     

Motor imagery effectiveness for mirror reversed movements

Physical practice is known to enhance motor adaptation skills, which refer to the individual ability to compensate for environmental changes. So far, it is still unknown whether a similar effect can be observed following motor imagery (MI). Thirty-nine participants were tested during a joystick tracking task under both normal and mirror conditions (i.e., the inductive direction of the joystick was reversed), before and after a physical practice or MI training phase. Eye movements and electromyographic activity were recorded during MI. Motor performance was also evaluated after a 6 h interval during daytime. As compared to the control group, the results revealed that both MI and physical practice improved motor performance in the mirror condition, during the post-training test. Furthermore, the time to complete the task was further reduced after 6 hours, both in the normal and mirror conditions. These results demonstrate the effectiveness of MI for learning mirror-reversed movements, and for the consolidation process that follows motor adaptation.     

Timing and the Control of Rhythmic Upper-Limb Movements

Accurate timing of limb displacement is crucial for effective motor control. The authors examined the effects of movement velocity, duration, direction, added mass, and auditory cueing on timing, spatial, and trajectory variability of single- and multijoint rhythmic movements. During single-joint movements, increased velocity decreased timing and spatial variability, whereas increased movement duration increased timing variability but decreased spatial variability. For multijoint movements, regardless of condition, increasing velocity decreased joint timing, spatial, and trajectory variability, but all hand variabilities were unaffected by velocity, duration, load, or direction. Timing, spatial, and trajectory variability was greater at the shoulder compared with the elbow and minimal at the hand, supporting the notion that reaching movements are planned in hand space as opposed to joint space.     

Exploring biases in self-reported exercising behavior heuristics based on recency, frequency, and preference

This study investigated biases in the recall of frequency and duration of physical exercise. Following an initial computer-administered self-report interview, 77 subjects maintained diaries for four weeks, in which they recorded the day, time, duration, and type of each exercising bout. Then the interview was administered again, and subjects recalled they exercised more often and for shorter durations than they recorded in their diaries. While social desirability may explain the overestimation of the number of days exercised, the underestimation of exercise duration poses a puzzle. The heuristic of frequency, recency, or prototype could not account for this underestimation. Alternative explanations are explored. Self-reported estimates of exercising duration and frequency should not be taken at face-value until the processes and heuristics used to record and recall exercising behaviors are better understood.     

Imagery ability classification: Commentary on «Kinaesthetic imagery ability moderates the effect of an AO+MI intervention on golf putt performance: A pilot study» by McNeill et al. (2020)

McNeill et al. (2020) recently published a study that first aimed to assess the effect of a combination of motor imagery (MI) and action observation (AO) on golf putt performance and then to determine if the evolution of this performance could be moderated by participants’ kinesthetic imagery ability. To assess golfers’ MI ability, the authors used the third version of the Movement Imagery Questionnaire. Participants notably self-estimated their kinesthetic MI ability by using a Likert-type scale, with scores ranging from 1 “very difficult to feel” to 7 “very easy to feel”. Athletes were categorized as either “poor” or “good” kinesthetic imagers, with mean scores of 4.93 and 6.63, respectively, in the intervention groups. Although a similar categorization procedure had previously been used in the literature for “good imagers”, the mean scores for “poor” imagers were much higher than those noted in previous studies evaluating the effect of MI ability on motor accuracy. Moreover, the low number of participants in the intervention group (n = 22) meant that participants were considered “poor” imagers even though their mean scores corresponded to “quite easy to feel” kinesthetic images of movements. This could notably explain the lack of differences between “poor” and “good” imagers in terms of putting performance in the intervention group. Despite these methodological limitations, the results of McNeill et al.‘s study show promising evidence for the efficacy of an AO plus MI intervention in relation to putting performance and should lead to further investigations. We suggest that research in the area of motor imagery ability include larger samples to explore, in individuals with very low imagery ability scores, the effects of the combination of AO and MI on motor performance.     

Motor imagery vividness and symptom severity in Parkinson's disease

Motor imagery (MI), the mental simulation of movement in the absence of overt motor output, has demonstrated potential as a technique to support rehabilitation of movement in neurological conditions such as Parkinson's disease (PD). Existing evidence suggests that MI is largely preserved in PD, but previous studies have typically examined global measures of MI and have not considered the potential impact of individual differences in symptom presentation on MI. The present study investigated the influence of severity of overall motor symptoms, bradykinesia and tremor on MI vividness scores in 44 individuals with mild to moderate idiopathic PD. Linear mixed effects modelling revealed that imagery modality and the severity of left side bradykinesia significantly influenced MI vividness ratings. Consistent with previous findings, participants rated visual motor imagery (VMI) to be more vivid than kinesthetic motor imagery (KMI). Greater severity of left side bradykinesia (but not right side bradykinesia) predicted increased vividness of KMI, while tremor severity and overall motor symptom severity did not predict vividness of MI. The specificity of the effect of bradykinesia to the left side may reflect greater premorbid vividness for the dominant (right) side or increased attention to more effortful movements on the left side of the body resulting in more vivid motor imagery.     

Relations between emotion,memory encoding,and time perception

This study examined duration judgments for taboo and neutral words in prospective and retrospective timing tasks. In the prospective task, participants attended to time from the beginning and generated shorter duration estimates for taboo than neutral words and for words that they subsequently recalled in a surprise free recall task. These findings suggested that memory encoding took priority over estimating durations, directing attention away from time and causing better recall but shorter perceived durations for taboo than neutral words. However, in the retrospective task, participants only judged durations in a surprise test at the end, and their duration estimates were longer for taboo than neutral words. Present findings therefore suggest that the same emotion-linked memory encoding processes can cause underestimation of durations in prospective tasks but overestimation in retrospective tasks, as if emotion enhances recall of ongoing events but causes overestimation of the durations of those events in retrospect.     

The "short-long" reaction time effect in duration programming

The programming processes concerned with response duration were studied in a precueing and in a priming reaction time (RT) paradigm. Participants had to produce a motor response of a specified duration as soon as possible after a response signal (RS) preceded by a warning signal (WS), which could deliver information on 2 response parameters (duration and effector). In Experiment I (precueing; N = 12), 3 effectors (the right hand, the left hand, or the knees) and 3 durations (.7, 2.5, or 5.5 s) were contrasted. Two responses differing in their biomechanical features were required in 2 blocks of trials: Subjects had to accurately time the duration of either a sustained button press or an interval between 2 brief presses. The RT patterns revealed a short-long effect: Shorter RTs were produced before the short duration than before the longer, provided that the duration was not precued. This short-long effect occurred whatever type of response and effector were involved. Two conclusions were reached. First, response duration was included in the motor program elaborated before execution, whatever the biomechanical features of the response; and, second, the program for the short duration was activated on all trials and was used as a basis for programming longer durations when needed. These conclusions were tested in Experiment 2 (priming; N = 12), in which a small proportion of invalid trials concerning duration was provided. Thus, the duration required by the RS differed from that primed by the WS. Two durations (.7 or 2.5 s) and 2 effectors (the index or the middle finger) were involved. In the invalid trials, the responses of short and long durations did not yield any RT differences, thus confirming the particular status of the short duration. This suggests that deprogramming operations (which lengthen the RT) are needed after a RS to produce short response durations but not after a RS to produce long response durations in the invalid trials.     

Motor imagery combined with action observation training optimized for individual motor skills further improves motor skills close to a plateau

The acquisition of high-level motor skills beyond a “plateau” is important in sports training and rehabilitation. We aimed to investigate whether motor skills close to a plateau state can be improved further by performing motor imagery (MI) training while observing movements with difficulty levels optimized for individual motor skills. The subjects were divided randomly into four groups (n = 10 per group): the control group and three groups of MI combined with action observation (MI + AO) training with varying difficulty levels. The task was to rotate the two cork balls 20 times counterclockwise using the left hand. The subjects performed 30 and 10 successful trials of this task before and after MI + AO training, respectively. In the three training groups, MI training was performed while observing videos showing ball rotation movements adjusted to the same level, a moderately higher level, or a remarkably higher level of difficulty than that achieved by the individual subjects. The improvement rate of the ball rotation time after MI + AO training was significantly higher in the moderate-difficulty than in the control group and remarkably higher level of difficulty group. The other two MI + AO training groups did not differ significantly compared with the control group. The vividness of the MI during MI + AO training was significantly greater in the moderate-difficulty vs. the remarkably-high-difficulty group. These results suggest that performing MI training while observing movement at a level that is moderately higher than an individual's ability can promote improvements in motor skills (close to a plateau state) in rehabilitation and sports training. The vividness of MI may be an important index for determining the difficulty level of the movement to be observed during MI + AO training.     

Adaptive motor behavior of cerebellar patients during exposure to unfamiliar external forces

The authors investigated adaptation of goal-directed forearm movements to an unknown external viscous force assisting forearm flexion in 6 patients with cerebellar dysfunction and in 6 control participants. Motor performance was generally degraded in cerebellar patients and was markedly reduced under the force condition in both groups. However, patients and controls were able to adapt to the novel force within 8 trials. Only the healthy controls were able to improve motor performance when readapting to a null-force condition. The results indicate that cerebellar patients' motor control system has imprecise estimations of actual limb dynamics at its disposal. Force adaptation may have been preserved because single-joint movements were performed, whereas the negative viscous force alone and no interaction forces had to be compensated.     

Daytime naps improve motor imagery learning

Sleep is known to contribute to motor memory consolidation. Recent studies have provided evidence that a night of sleep plays a similar functional role following motor imagery (MI), while the simple passage of time does not result in performance gains. Here, we examined the benefits of a daytime nap on motor memory consolidation after MI practice. Participants were trained by MI on an explicitly known sequence of finger movements at 11:00. Half of the participants were then subjected (at 14:00) to either a short nap (10 min of stage 2 sleep) or a long nap (60–90 min, including slow wave sleep and rapid eye movement sleep). We also collected data from both quiet and active rest control groups. All participants remained in the lab until being retested at 16:00. The data revealed that a daytime nap after imagery practice improved motor performance and, therefore, facilitated motor memory consolidation, as compared with spending a similar time interval in the wake state. Interestingly, the results revealed that both short and long naps resulted in similar delayed performance gains. The data might also suggest that the presence of slow wave and rapid eye movement sleep does not provide additional benefits for the sleep-dependent motor skill consolidation following MI practice.     

Effects of utterance length on lip kinematics in aphasia

Most existing models of language production and speech motor control do not explicitly address how language requirements affect speech motor functions, as these domains are usually treated as separate and independent from one another. This investigation compared lip movements during bilabial closure between five individuals with mild aphasia and five age and gender-matched control speakers when the linguistic characteristics of the stimuli were varied by increasing the number of syllables. Upper and lower lip movement data were collected for mono-, bi- and tri-syllabic nonword sequences using an AG 100 EMMA system. Each task was performed under both normal and fast rate conditions. Single articulator kinematic parameters (peak velocity, amplitude, duration, and cyclic spatio-temporal index) were measured to characterize lip movements. Results revealed that compared to control speakers, individuals with aphasia showed significantly longer movement duration and lower movement stability for longer items (bi- and tri-syllables). Moreover, utterance length affected the lip kinematics, in that the monosyllables had smaller peak velocities, smaller amplitudes and shorter durations compared to bi- and trisyllables, and movement stability was lowest for the trisyllables. In addition, the rate-induced changes (smaller amplitude and shorter duration with increased rate) were most prominent for the short items (i.e., monosyllables). These findings provide further support for the notion that linguistic changes have an impact on the characteristics of speech movements, and that individuals with aphasia are more affected by such changes than control speakers.     

Are Fast Complex Movements Unimaginable? Pupillometric Studies of Motor Imagery in Expert Piano Playing

Motor imagery (MI; mental simulation of actions) shares certain mental representations and processes with executed movement (ME). This neurocognitive overlap between MI and ME may explain why the systematic use of MI improves skilled performance in numerous domains. Unfortunately, the attentional mechanisms underlying MI remain unresolved. Therefore, the present studies investigated the role of attentional effort (as measured by pupil dilation) in MI. We evaluated the effects of movement complexity and speed on expert pianists' pupil dilation as they physically executed and used MI to perform easy/complex and slow/fast music phrases. Results revealed that easy movements required similar levels of attentional effort during MI and ME. However, during complex movements performed at a fast speed, the correspondence between execution and imagery of movement was disrupted.