Is Locomotor Distance Estimation Guided by Visual Imagery?

1989 ◽  
Vol 69 (3-2) ◽  
pp. 1267-1272 ◽  
Author(s):  
John T. Corlett ◽  
John Anton ◽  
Steve Kozub ◽  
Michel Tardif

70 subjects were tested for their visual subscale scores on the Movement Imagery Questionnaire and also for their ability to walk, without vision, to a previously viewed target location 9 m away. Imagery ability was hypothesized to correlate with accuracy of “blind” target-directed walking which the literature suggests, without empirical support, is imagery-dependent. No support for this hypothesis was found. Low, medium, and high imagers showed no differences in ability to reproduce target distance accurately or consistently by walking the estimated distance without further visual updating. The results call into question whether task performance is imagery-based or whether subjects use alternative strategies to approach the target.

1989 ◽  
Vol 69 (3_suppl) ◽  
pp. 1267-1272 ◽  
Author(s):  
John T. Corlett ◽  
John Anton ◽  
Steve Kozub ◽  
Michel Tardif

70 subjects were tested for their visual subscale scores on the Movement Imagery Questionnaire and also for their ability to walk, without vision, to a previously viewed target location 9 m away. Imagery ability was hypothesized to correlate with accuracy of “blind” target-directed walking which the literature suggests, without empirical support, is imagery-dependent. No support for this hypothesis was found. Low, medium, and high imagers showed no differences in ability to reproduce target distance accurately or consistently by walking the estimated distance without further visual updating. The results call into question whether task performance is imagery-based or whether subjects use alternative strategies to approach the target.


2008 ◽  
Vol 30 (2) ◽  
pp. 200-221 ◽  
Author(s):  
Ross Roberts ◽  
Nichola Callow ◽  
Lew Hardy ◽  
David Markland ◽  
Joy Bringer

The purpose of this research was to amend the Vividness of Movement Imagery Questionnaire (VMIQ; Isaac, Marks, & Russell, 1986) in line with contemporary imagery modality and perspective conceptualizations, and to test the validity of the amended questionnaire (i.e., the VMIQ-2). Study 1 had 351 athletes complete the 3-factor (internal visual imagery, external visual imagery, and kinesthetic imagery) 24-item VMIQ-2. Following single-factor confirmatory factor analyses and item deletion, a 12-item version was subject to correlated traits / correlated uniqueness (CTCU) analysis. An acceptable fit was revealed. Study 2 used a different sample of 355 athletes. The CTCU analysis confirmed the factorial validity of the 12-item VMIQ-2. In Study 3, the concurrent and construct validity of the VMIQ-2 was supported. Taken together, the results of the 3 studies provide preliminary support for the revised VMIQ-2 as a psychometrically valid questionnaire.


2019 ◽  
Vol 19 (2) ◽  
pp. 124-134
Author(s):  
Pedro Alexandre Duarte Mendes ◽  
Daniel Almeida Marinho ◽  
Diogo Monteiro ◽  
Luís Cid ◽  
Rui Paulo ◽  
...  

The ability to generate and control mental images is present in all of us, but it differs from person to person. Therefore, it is important to understand that imagery ability can be changed through training and experimentation, it is not a fixed ability (Cumming & Williams, 2012). The aim of this study is to compare imagery ability in elite, sub-elite and non-elite athletes in a sport which involves closed and continuous motor skills, such as swimming. 79 swimmers (male N = 37; female N = 42) at an average age of 17 took part in this study. In order to assess imagery ability, the Movement Imagery Questionnaire 3 was used, Portuguese version (Mendes et al., 2016). After analysis of the results, these show that in each and every imagery modality, the scores in the three groups differ significantly. In kinesthetic and external visual imagery the elite and sub-elite groups’ scores, although not statistically different from each other, are significantly higher than those of the non-elite group. In internal visual imagery, the differences between all the compared pairs of groups are statistically significant. The elite group got the highest scores, followed by the sub-elite group average scores and finally the non-elite group average scores. According to these results, the conclusion is that athletes with better performance show greater imagery ability and that apparently the external visual imagery proved to be the best intervention method among swimming athletes.


2012 ◽  
Vol 34 (5) ◽  
pp. 621-646 ◽  
Author(s):  
Sarah E. Williams ◽  
Jennifer Cumming ◽  
Nikos Ntoumanis ◽  
Sanna M. Nordin-Bates ◽  
Richard Ramsey ◽  
...  

This research validated and extended the Movement Imagery Questionnaire-Revised (MIQ-R; Hall & Martin, 1997). Study 1 (N = 400) examined the MIQ-R’s factor structure via multitrait-multimethod confirmatory factor analysis. The questionnaire was then modified in Study 2 (N = 370) to separately assess the ease of imaging external visual imagery and internal visual imagery, as well as kinesthetic imagery (termed the Movement Imagery Questionnaire-3; MIQ-3). Both Studies 1 and 2 found that a correlated-traits correlated-uniqueness model provided the best fit to the data, while displaying gender invariance and no significant differences in latent mean scores across gender. Study 3 (N = 97) demonstrated the MIQ-3’s predictive validity revealing the relationships between imagery ability and observational learning use. Findings highlight the method effects that occur by assessing each type of imagery ability using the same four movements and demonstrate that better imagers report greater use of observational learning.


Motricidade ◽  
2018 ◽  
Vol 13 (4) ◽  
pp. 46
Author(s):  
André Amorim ◽  
Bruno Travassos ◽  
Pedro Mendes

The aim of this study was to analyse and compare movement visualization ability in federate and non-federate Boccia athletes, and among federate Boccia medical sport groups. Forty-two Boccia athletes (Federate N = 24; Non-federate N = 18) at an average age of 35.8 (SD = 11.19) participated in this study. The Portuguese version of Movement Imagery Questionnaire - 3 (MIQ-3), was used for this study. The participants were evaluated on the internal and external visual imagery. Statistics was carried out following the method of interference based on the magnitude of the effects. Results showed a great effect of expertise in imagery ability. The comparison between federate and non-federate Boccia athletes showed a great effect in the Internal Visual subscale and a moderate effect in the External Visual subscale. It was also observed differences between athletes from different medical-sports groups, revealing that the requirements of the sport linked to their action abilities provides them with different Imagery abilities. These results clearly influence the prescription of imagery training programs for different groups taking into account different medical-practice groups.


Author(s):  
John K. Parker ◽  
Geoff P. Lovell ◽  
Martin I. Jones

Abstract Objectives The use of imagery to improve golf performance is well established and recognised as a key psychological technique in developing and maintaining excellence. However, the relationship between a golfer’s imagery ability and their imagery use is still poorly understood. The current study examined differences in participants vividness of movement imagery and imagery use and the extent their vividness of movement imagery predicted functions of imagery use. Methods One hundred and one male skilled golfers (Mage=27.80, SD=11.03) with CONGU recognised handicaps ranging from plus 4 to 5 (Mhandicap=1.32, SD=2.74) completed both the Vividness of Movement Imagery Questionnaire-2 (Roberts, R., Callow, N., Hardy, L., Markland, D., & Bringer, J. (2008). Movement imagery ability: Development and assessment of a revised version of the vividness of movement imagery questionnaire. Journal of Sport & Exercise Psychology, 30(2), 200–221) and Sports Imagery Questionnaire (Hall, C. R., Mack, D. E., Paivio, A., & Hauesenblas, H. A. (1998). Imagery use by athletes: Development of the sport imagery questionnaire. International Journal of Sport Psychology, 29, 73–89). Results The results demonstrated no significant differences between Internal and External visual imagery, however, Kinaesthetic imagery scores were significantly higher than External visual imagery scores. Significant differences in imagery use were recorded with participants reporting higher Cognitive specific imagery use scores compared to other functions of imagery use. Regression analyses indicted that golf handicap accounted for 12% in the variance of Cognitive specific imagery use with an additional 12% accounted for by Internal visual imagery and 7% Kinaesthetic imagery. For Cognitive general imagery use golf handicap accounted for 4% of the variance with Internal visual imagery adding a further 5% to the model. Conclusions Our findings highlight that vividness of movement imagery; specifically, Internal and Kinaesthetic imagery ability are significant predictors of skilled golfers Cognitive specific and Cognitive general imagery use.


Author(s):  
Peter Khooshabeh ◽  
Mary Hegarty ◽  
Thomas F. Shipley

Two experiments tested the hypothesis that imagery ability and figural complexity interact to affect the choice of mental rotation strategies. Participants performed the Shepard and Metzler (1971) mental rotation task. On half of the trials, the 3-D figures were manipulated to create “fragmented” figures, with some cubes missing. Good imagers were less accurate and had longer response times on fragmented figures than on complete figures. Poor imagers performed similarly on fragmented and complete figures. These results suggest that good imagers use holistic mental rotation strategies by default, but switch to alternative strategies depending on task demands, whereas poor imagers are less flexible and use piecemeal strategies regardless of the task demands.


Author(s):  
Jessica Schnabel

Mind wandering, or “daydreaming,” is a shift in the contents of a thought away from a task and/or event in the external environment, to self-generated thoughts and feelings. This research seeks to test the reliability of eye tracking as an objective of measure mind wandering using the Wandering Eye Paradigm, as well as examine the relationships between mind wandering and individual characteristics. Fifty participants will be recruited for two appointments a day apart, on each day on each day completing two eye tracking sessions following a moving target. In this task, participants will be instructed to press the space bar if they feel they are mind wandering, and then answer three questions about their episode content. Questionnaires measuring mind wandering, procrastination, mindfulness, creativity and personality (in particular conscientiousness) will be completed between eye tracking sessions. By comparing the eye tracking data in the period prior to the spacebar press we can determine quantifiable indicators of the onset and duration of mind wandering episodes by analyzing gaze location in relation to the target location. It has been hypothesized that severity of task performance failures (losing track of the target) should correlate with the “depth” of the mind wandering episode content. Additionally, we expect the frequency of mind wandering episodes to correlate with individual characteristics, and that these measures will be consistent across trials. This research would provide a novel objective way to identify and measure mind wandering, and would help further advance the understanding of its behavioral and subjective dimensions.


1998 ◽  
Vol 80 (5) ◽  
pp. 2405-2416 ◽  
Author(s):  
Josh Wallman ◽  
Albert F. Fuchs

Wallman, Josh and Albert F. Fuchs. Saccadic gain modification: visual error drives motor adaptation. J. Neurophysiol. 80: 2405–2416, 1998. The brain maintains the accuracy of saccadic eye movements by adjusting saccadic amplitude relative to the target distance (i.e., saccade gain) on the basis of the performance of recent saccades. If an experimenter surreptitiously moves the target backward during each saccade, thereby causing the eyes to land beyond their targets, saccades undergo a gradual gain reduction. The error signal driving this conventional saccadic gain adaptation could be either visual (the postsaccadic distance of the target from the fovea) or motoric (the direction and size of the corrective saccade that brings the eye onto the back-stepped target). Similarly, the adaptation itself might be a motor adjustment (change in the size of saccade for a given perceived target distance) or a visual remapping (change in the perceived target distance). We studied these possibilities in experiments both with rhesus macaques and with humans. To test whether the error signal is motoric, we used a paradigm devised by Heiner Deubel. The Deubel paradigm differed from the conventional adaptation paradigm in that the backward step that occurred during the saccade was brief, and the target then returned to its original displaced location. This ploy replaced most of the usual backward corrective saccades with forward ones. Nevertheless, saccadic gain gradually decreased over hundreds of trials. Therefore, we conclude that the direction of saccadic gain adaptation is not determined by the direction of corrective saccades. To test whether gain adaptation is a manifestation of a static visual remapping, we decreased the gain of 10° horizontal saccades by conventional adaptation and then tested the gain to targets appearing at retinal locations unused during adaptation. To make the target appear in such “virgin territory,” we had it jump first vertically and then 10° horizontally; both jumps were completed and the target spot extinguished before saccades were made sequentially to the remembered target locations. Conventional adaptation decreased the gain of the second, horizontal saccade even though the target was in a nonadapted retinal location. In contrast, the horizontal component of oblique saccades made directly to the same virgin location showed much less gain decrease, suggesting that the adaptation is specific to saccade direction rather than to target location. Thus visual remapping cannot account for the entire reduction of saccadic gain. We conclude that saccadic gain adaptation involves an error signal that is primarily visual, not motor, but that the adaptation itself is primarily motor, not visual.


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