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International Journal of Sports Physical Therapy logoLink to International Journal of Sports Physical Therapy
. 2021 Apr 1;16(2):552–564. doi: 10.26603/001c.21251

Visual Perturbation to Enhance Return to Sport Rehabilitation after Anterior Cruciate Ligament Injury: A Clinical Commentary

Timothy R Wohl 2, Cody R Criss 1, Dustin R Grooms 3,
PMCID: PMC8016421  PMID: 33842051

Abstract

Anterior cruciate ligament (ACL) tears are common traumatic knee injuries causing joint instability, quadriceps muscle weakness and impaired motor coordination. The neuromuscular consequences of injury are not limited to the joint and surrounding musculature, but may modulate central nervous system reorganization. Neuroimaging data suggest patients with ACL injuries may require greater levels of visual-motor and neurocognitive processing activity to sustain lower limb control relative to healthy matched counterparts. Therapy currently fails to adequately address these nuanced consequences of ACL injury, which likely contributes to impaired neuromuscular control when visually or cognitively challenged and high rates of re-injury. This gap in rehabilitation may be filled by visual perturbation training, which may reweight sensory neural processing toward proprioception and reduce the dependency on vision to perform lower extremity motor tasks and/or increase visuomotor processing efficiency. This clinical commentary details a novel approach to supplement the current standard of care for ACL injury by incorporating stroboscopic glasses with key motor learning principles customized to target visual and cognitive dependence for motor control after ACL injury.

Level of Evidence

5

Keywords: anterior cruciate ligament, acl, rehabilitation, stroboscopic glasses

Introduction

Anterior cruciate ligament (ACL) tears are common orthopedic injuries,1 involving an extensive plan of care and physical therapy following surgical reconstruction.2 Despite receiving comprehensive approaches to restore knee function, quadriceps strength,3,4 and joint stability,5–7 re-injury rates remain high, especially among young female athletes.4,8–17 This increased risk of re-injury may stem from nuanced neuromuscular consequences of ACL injury that therapy may not adequately address.

While ACL tears are peripheral joint injuries, the combination of effusion, pain, mechanical instability and deafferentation secondary to loss of joint mechanoreceptors may modulate central nervous system (CNS) reorganization.18,19 The CNS reorganization manifests as proprioceptive deficits and impaired motor coordination secondary to increased attentional, cognitive20–23 and visual relative to proprioceptive processing demands for motor control.20–35 A potential avenue to augment ACL rehabilitation is to facilitate sensory reweighting (nervous system adjustment of relative sensory input/processing for motor control) by shifting the post-injury reliance on vision for motor control to remaining proprioceptive inputs (e.g., the joint capsule, other ligaments, muscle spindles). Specifically, the use of visual perturbation training, which aims to reduce visual input availability during standard rehabilitative exercises, may reduce the dependency on vision and reweight neural processing toward proprioception and/or increase visuomotor processing efficiency.36 Additionally, the application of key motor learning principles may support visual perturbation training, such as 1) an external visual focus of attention or cueing to help ensure visuospatial demands during training and 2) implicit learning to reduce the cognitive requirements for motor control and promote movement automaticity.37–40 The following commentary details an example of a sensory reweighting protocol that combines the use of stroboscopic glasses and key motor learning principles.

Behavioral Support for Increased Visual Reliance & Neurocognitive Motor Planning following ACL Injury

Increased Visual Reliance

A series of investigations in ACL deficient (ACL-D) and reconstructed (ACL-R) patients provide support for increased visual reliance for motor control.26–35 During postural control tasks, patients with ACL injuries and uninjured controls performed similarly when vision was unobstructed.31,32 However, when vision was perturbed, patients with ACL injuries performed significantly worse (e.g., increased postural sway, failure in task completion).28,30,33–35 While a recent meta-analysis indicated patients with ACL-R are not as dependent on vision for postural control as patients with ACL-D,41 the mixed finding may be secondary to not challenging knee control during single-leg stance (by allowing a straight leg position), static postural control not being sufficiently challenging in those with reconstruction or complete vision obstruction not perturbating visuospatial processing sufficiently to elicit a deficit. This is exemplified by patients with ACL-R being more affected by visual perturbation (i.e., stroboscopic glasses) during drop landing and the transition from double to single leg stance with eyes closed and when challenged with visuocognitive tasks relative to matched controls.27,34,42

An increased weighting towards visual input and processing for postural and lower extremity motor control following ACL injury may emerge from a sensory reweighting phenomenon that is driven, in part, by insult to the underlying joint tissue and ligament mechanoreceptors.25 These mechanoreceptors, including Ruffini and Pacinian corpuscles, provide information about joint position, motion and acceleration, and their loss compromises proprioception and functional stability.43–46 Consequently, the CNS may employ functional strategies, such as sensory reweighting to more reliable stimuli (e.g., vision, vestibular), or increase cognitive and attentional processes to maintain adequate motor control.36,47–51 The Bayesian optimal integration model details how weighting sensory stimuli by reliability reduces the uncertainty of perception, thereby optimizing performance.52–54 Further, physical therapy following ACL injury may also increase visual attention to the knee, as clinicians primarily utilize visually-dominated exercises and provide feedback with an internal focus of attention (i.e., emphasizing movement kinematics or muscle activation, rather than movement actions) to the injured joint.37,55–59 However, weighting vision to guide lower limb movement may be maladaptive for athletes returning to a competitive sport environment, where the high demand to integrate dynamic visual information may limit the CNS’s capacity to allocate neural resources to guide movement. Therefore, patients with ACL injuries may benefit from therapeutic interventions that encourage sensory reweighting from vision towards proprioception for motor control.

Increased Neurocognitive Motor Planning

Excessive knee valgus has been identified as a major risk factor for primary and secondary ACL injury, with high sensitivity (78%) and specificity (73%).60 Herman and Barth identified a significant relationship between baseline neurocognition and knee valgus motion, where those with lower visual-memory and neurocognitive ability demonstrate increased knee valgus motion during a drop-landing task involving an unanticipated rebound immediately after landing.61 These studies suggest an athlete’s baseline neurocognitive function may contribute to his or her risk of injury.60,61 A common therapeutic modality used to target neurocognitive function is dual-tasking, which involves the completion of two or more tasks simultaneously (e.g., balancing on one leg while counting down from 1,000 by 7).62 For example, patients with ACL injuries exhibit higher dual task-related costs during postural stability, gait and balance tasks.23,63–66 Taken together, following ACL injury, patients may experience a reduced capability to simultaneously engage in cognitive processing and motor performance. Neural mechanisms for this deficit may be secondary to the disruption of typical ACL afferent information utilized by the primary motor cortex, which may result in increased frontal activity (e.g., presupplementary motor area, supplementary motor area) to compensate.21,67,68 Thus, the cognitive demands of sport may exceed the patient’s capability to optimally attend to external visual stimuli (e.g., opponents, balls) and maintain low injury-risk biomechanics.

Neuroimaging Investigations following ACL Injury

ACL Injury Associated Visuomotor & Visuospatial Brain Activation

Cross-sectional studies using functional magnetic resonance imaging (fMRI) have assessed neural activation differences for knee motor control in patients with ACL-D and ACL-R compared to uninjured, matched controls.20,21,69,70 In patients with ACL-D ~two years post-injury, fMRI identified increased activation in the posterior inferior temporal gyrus during a unilateral knee flexion/extension task.69 The posterior inferior temporal gyrus has been implicated in the recognition of biological movements, such as gait-like motion, rather than random motion.71 For patients with ACL-R ~3 years post-surgery, fMRI further identified increased neural activity within the lingual gyrus for both knee and combined hip-knee coordinated movements.70,72 The lingual gyrus is involved in the cross-modal integration of congruent visual and tactile stimuli in a spatially-specific manner.73,74 Increased neural activity requirements for the posterior inferior temporal gyrus and lingual gyrus corroborate the behavioral investigations, indicating an increased reliance or shift in visual information processing during motor control following ACL injury.

ACL Injury Associated Neurocognitive Motor Planning Brain Activation

Other regions with increased neural activity include the presupplementary motor area in patients with ACL-D ~two years after injury as well as the frontal gyri, inferior frontal pole, paracingulate gyrus and anterior cingulate gyrus for patients with ACL-R ~five years post-surgery.22,69 While both injured populations performed identical tasks, differences in neural activation patterns are likely attributed to demographic (high vs. low functioning patients, activity level), surgical, time from injury, and rehabilitation protocol differences. Increased activation of the presupplementary motor area in patients with ACL-D may reflect increased cortical activity for planning simple movements.69 Increased activation across the frontal lobe in regions responsible for motor control further supports the hypothesis that patients with ACL injuries utilize increased cognitive resources for motor control by engaging in less efficient neural activation strategies.22 Neural efficiency refers to the reduced neural activity requirements of experts to perform a learned skill or task relative to novices, suggesting relative magnitude of neural activity scales with expertise and the ability to handle more complex coordination or environmental perturbations.75–78

The lack of neural efficiency and associated frontal region activity is corroborated with electroencephalography (EEG), indicating increased frontal theta power during force control and joint position tasks in patients with ACL-R ~one year post-surgery compared to uninjured controls.20,21 Frontal Theta power is an indicator of focused attention and task complexity,20 which may indicate that simple knee force control and joint position tasks are more complex and require greater attention for patients with ACL-R. Additionally, EEG has revealed that patients with ACL-D require more cognition/attention resources relative to healthy controls during walking, running and landing tasks as evidenced by significant increases in delta, theta, alpha, and beta band power, as well as asymmetry of the beta band power across the frontal and parietal lobes during jogging and landing.79 Increased activation across the frontal lobe, presupplementary motor area, increased frontal theta power during joint position sense and force matching tasks and increased cognition/attention during walking, jogging and landing support the behavioral data indicating increased neurocognitive motor planning neural activity following ACL injury. Taken together, patients with ACL injuries may experience a loss of neural efficiency to engage in motor control, thereby contributing to both 1) impaired motor performance during dual-tasking or unanticipated movements and 2) an increased risk of secondary injury when attempting to rapidly increase motor complexity and environmental stimuli during early return to sport.23,63–66,80–82

Sensory Reweighting Therapy

Visual Perturbation Training

Functional navigation and interaction with the environment rely heavily upon continual integration of visual information.71,83,84 Visual information processing is further recruited for motor control following ACL injury, potentially due to sensory reweighting from the deafferentation of joint mechanoreceptors and/or the use of visually-dominated exercises and internal feedback to the injured joint during physical therapy.36,37,55–59 While patients may be able to compensate with increased visual processing for simple exercises, an inundation of dynamic visual information on the sporting field may overwhelm neural processing resources and the visually biased movement compensation strategy may become a re-injury risk liability. ACL rehabilitation efforts may consider incorporating complex sensory challenges, like visual perturbation, in order to simulate the dynamic sport environment that athletes will face once they leave the clinic.20,21,29,85–87

Stroboscopic glasses (SG) provide a novel approach to train visuomotor function by perturbating and reducing visual feedback.36 Typically, visual perturbation training has been limited to eyes open and eyes closed conditions with no progression between, but SG provides the ability to incrementally perturb visual information by increasing the duration of the opaque state (range: 25 to 900 msec) relative to the constant duration of the transparent state (100 msec).88 Originally designed to be a mobile sports training tool, SG has allowed researchers to investigate the effects of perturbed vision in context-specific environments.89 Early research with SG explored behavioral performance on motion coherence, divided attention, multiple-object tracking,90 short-term visual memory,91 and anticipation,92 as well as performance on sports-specific tasks from single-leg squatting,93 ice hockey,94 tennis,95 and badminton.96 These authors concluded visual perturbation training improves sport-specific behavioral performance and aspects of neurocognition including visual memory, anticipatory timing of moving visual stimuli, and central visual field motion sensitivity and transient attention ability.

SG simulates the dynamic visuomotor and cognitive/attentional demands of athletic activity while remaining in a controlled clinical environment.92,94,97,98 As patients with ACL injuries exhibit degraded motor control during drop-jump landing, cutting, and postural control under impaired visual conditions relative to normal vision,27,28,30,33–35,99,100 SG may facilitate increased proprioceptive integration in response to perturbed visuospatial information.36,89 ACL rehabilitation efforts that incorporate SG may be able to alter sensory weighting by decreasing the amount of visual information available to the athlete, thereby requiring the athlete to upregulate their use of remaining proprioceptive or vestibular inputs to guide movement. Utilizing SG in ACL rehabilitation may also enhance visuomotor processing efficiency in a compensatory manner to handle the increased reliance on vision to maintain low injury-risk biomechanics.48

Motor Learning Principles

A key limitation of ACL rehabilitation is the inability to facilitate the acquisition of injury-resistant motor patterns that persist beyond the clinic.101 This limitation likely contributes to high rates of secondary injury and long-term pathologic sequalae, such as aberrant joint loading and early-onset osteoarthritis.102 The incorporation of motor learning principles may facilitate the acquisition of lasting, injury-resistant movement patterns that persist beyond the clinic and into the field,103 since these principles can facilitate neuroplasticity in cortical regions dedicated to movement.104,105 Specifically, the use of an external focus of attention and implicit learning may serve an adjunctive role to sensory reweighting therapy. An external visual focus of attention can ensure visuospatial demands during training and implicit learning can reduce the cognitive demands for motor control to potentially enhance training.37–40

i. Modified External Focus of Attention for Visuospatial Attention

While the classic definition of external focus (EF) feedback is purely an attentional manipulation, this clinical commentary modified the traditional EF framework to push attentional focus toward the external visuospatial environment. ACL therapy that employs a visual EF can simulate real-world training scenarios that better prepare athletes for return to activity when visual attention is focused on the environment and not the body. Training with EF prioritizes the movement goal or the movement’s effect on the environment, rather than an internal focus (IF) on the movement or body segment itself.106 For example, a therapist who directs patients to balance a light-weight bar horizontally with their outstretched arm while performing a single-leg balance task employs visual EF.37,107 In contrast, a therapist who directs patients to actively attend to their ankle, knee and hip alignment while balancing employs IF, which is the predominant strategy in ACL therapy. An IF approach to therapy may hinder the translational benefits of rehabilitation, as humans typically navigate the world with a visual EF on the environment (e.g., running to a ball) – not on their moving joints or mechanics.108

The Constrained Action Hypothesis posits conscious (cortical) awareness of movement constrains the automatic, subcortical processes that would otherwise facilitate movement.109 By training with EF, one may relieve the attentional demands on the cortex by shifting motor control to subcortical regions and enhance motor learning and performance relative to training with IF.102,110–113 Behaviorally, training with EF improves agility performance,57 increases jump height,114 and promotes safer landing patterns during a single-leg hop for distance task in patients with ACL-R compared to performance with IF.115 Additionally, engaging in EF increases time to failure, reduces ratings of perceived exertion,116,117 and increases movement efficiency potentially by reducing unnecessary muscle contributions by modulating the inhibitory mechanisms within the primary motor cortex.117,118

ii. Implicit Learning

Developmentally, humans learn to move through observation and implicit trial-and-error (e.g., learning to ride a bike, walk, throw).119 Implicit feedback facilitates motor learning without explicit, declarative instructions or cuing,37 thereby increasing neural efficiency by reducing the attentional demands to engage in complex movement. While explicit cuing engages cognitive processes (frontoparietal regions), implicit cuing facilitates more direct sensorimotor activity.120 Further, training with implicit cuing has recently been associated with motor cortex reorganization, potentially supporting more efficient premotor or cortical interneuron processes.121 While few studies have examined the behavioral impacts of implicit cues for sports medicine, Popovic et al. demonstrated improved landing biomechanics with implicit feedback relative to explicit/no feedback.40 Thus, instructional language informed by implicit learning may augment visual perturbation training by modulating sensorimotor neural activity and potentially increasing neural efficiency by reducing the cognitive load of learning injury-resistant movement strategies. The newly freed cortical resources may enable athletes to more readily attend to visual distractors during high-level sport (e.g., the ball, opponents) while maintaining neuromuscular control.37,122

For example, consider the scenario where a therapist trains an athlete with an ACL injury to land correctly after a drop vertical jump. A therapist may opt to follow an explicit learning model and inform the athlete of all the biomechanical variables he or she is evaluating (e.g., trunk flexion, knee flexion, knee valgus, foot rotation, etc.). This type of learning requires the athlete to attend to multiple aspects of his or her landing mechanics, thereby occupying a substantial amount of his or her cognitive resources. However, a therapist who opts-in to implicit learning may instead provide metaphorical instructional language (e.g., “land like a feather”) and simple “yes/no” or “good/bad” feedback to train the athlete to land. This trial-and-error method may augment visual perturbation training by alleviating the burden of attending to biomechanical variables, thereby freeing the athlete’s cognitive resources to attend to external visual stimuli without compromising their neuromuscular control.

Clinical Application

Future studies are needed to explore the therapeutic efficacy of combining SG and motor learning principles (i.e., EF, implicit learning) with traditional therapeutic exercises during ACL rehabilitation. A barrier to such studies is a lack of clearly defined and easily replicable exercises that combine these novel modalities. This clinical commentary details ways therapists and researchers can supplement the current standard of care by adding SG and motor learning principles to agility, balance and plyometric exercises in novel ways. Provided are example exercises with specific instructional language and visual targets (Table 1). Further clinical examples of EF and implicit learning can be found in the work of Gokeler et al.37 An error scoring system with detailed criteria to assess behavioral performance while wearing SG is provided as well (Table 2).

Table 1: Instrumentation and Instruction to Facilitate Perception-Action that Employs Visual External Focus and Implicit Learning Principles.

Exercise Visual Cues Implicit Cues
T-test Tap the cones "Run as fast as a cheetah"
Agility Ladder Drills The confines of the ladder "The floor is as hot as lava"
Single-leg Deadlifts Place an object by the cone(s) "Flow like water"
Single-leg Stance (on foam) Hold the bar horizontally "Be steady as a rock"
Vertical Jumps Hit the overhead target "Explode like a volcano"
Squat Jumps Land facing the cones "Jump like a kangaroo"

Table 2: Error Scoring System Used to Assess Behavioral Performance.

Exercise Error Count
T-test
  1. Miss a cone

  2. Cut to the wrong direction

Agility Ladder Drills
  1. Hit the ladder

  2. Incorrect foot placement

Single-leg Deadlifts
  1. Opposite foot touches ground

  2. Either hand touches ground

  3. Object placed in wrong location

Single-leg Stance (on foam)
  1. Opposite foot touches ground

  2. Either hand touches ground

Vertical Jumps
  1. Miss the target

  2. Land on wrong foot

Squat Jumps
  1. Land facing wrong orientation

Agility Drills

(1) The T-test requires the athlete to run 10 m to tap a cone, cut to the right or left for 5 m to tap another cone, cut to the opposite direction for 10 m to tap the third cone, return to the center by cutting 5 m to tap the first cone and then run 10 m back to the start position - thereby running in a "T" formation (Figure 1A). A modification that increases the difficulty of this task and simulates the cognitive demands of sport is to have the clinician call out “Left” or “Right” to indicate which direction the athlete should cut prior to reaching the first cone, thereby creating an unanticipated cutting task which has been previously associated with increased injury-risk biomechanics compared to anticipated trials.123 (2) Agility ladder drills require athletes to match specified foot-placement patterns within the context of an agility ladder (Figure 1B).

Figure 1: Exercise examples with clinical applications: (A) T-test, (B) Agility ladder drills, (C) Single-leg deadlifts, (D) Single-leg stance (on foam), (E) Vertical jumps, and (F) Squat jumps.

Figure 1:

Balance

(1) Single-leg deadlifts may be modified by requiring athletes to gently place a small object on the ground next to a cone target (Figure 1C). To increase the difficulty, multiple cones can be placed at different angles within the athlete’s field-of-view, set at distances equal to his or her max volitional reaching distance while standing on one leg. For example, if the clinician chooses to use three targets, then he or she may call out “Left,” “Center,” or “Right” to vary the task order and difficulty. (2) Single-leg stance on a foam surface may be modified by having the participant hold a light-weight bar with an outstretched arm and focus on keeping it steadily horizontal (Figure 1D).

Plyometrics

(1) The VERTEC is a therapeutic tool that assesses maximum vertical jump height by requiring athletes to jump and hit an overhead target (Figure 1E). While using the VERTEC to have athletes hit a mark equal to 80% of their maximal jump height, clinicians may call out “Left” or “Right” during the initial flight phase of the jump to signal to the athlete to unilaterally land on his or her left or right leg.124,125 The use of spontaneous cuing creates an unanticipated landing task, which has been previously associated with increased injury-risk biomechanics compared to anticipated landing.126 (2) Jump squats may be modified by placing four cones around the participant at 0, 90, 180 and 270 degree positions (Figure 1F). After numbering each cone one through four, the clinician may then rapidly call out cues to the athlete to specify which cone they should face after each jump squat. To increase the difficulty of this cognitive challenge, the clinician can introduce more cones or increase the rapidity of cuing.

SG Level

Clinicians should first verify their athlete can perform all exercises successfully before incorporating SG. Then clinicians may expose their athlete to SG by beginning at the easiest difficulty level (highest frequency of fluctuation between transparent and opaque states). As their athlete improves performance behaviorally, clinicians may increase SG difficulty to increase the visual-cognitive demand.

In addition to the provided Error Scoring System (Table 2), clinicians may use the NASA Task Load Index questionnaire or Borg’s Rating of Perceived Exertion scale to optimize the SG difficulty level during training.127–129 These tools allow clinicians to assess an athlete’s perceived level of difficulty performing exercises with SG. For example, if clinicians want to simulate “hard/difficult” sports scenarios with SG, but their athlete rates his or her experience as “moderate,” clinicians may increase the visual perturbation by raising the SG difficulty level.

Alternatively, clinicians may opt to only incorporate SG into exercises that are below their athlete’s current physical capability initially. For example, if an athlete only recently performed a single-leg hop successfully, their clinician may choose to perturbate a single-leg balance exercise by adding SG. After successful completion of the single-leg balance exercise with SG, the clinician may then choose to advance the athlete’s training by incorporating SG into the harder single-leg hop task. This style of initially incorporating perturbations into exercises that are below a patient’s current physical capability is common in rehabilitation.

Conclusion

A novel approach to ACL rehabilitation that incorporates sensory reweighting therapy may shift neural processing toward proprioception and reduce the dependency on vision for motor control and/or increase visuomotor efficiency. ACL rehabilitation efforts that incorporate visual-perturbation training supplemented by motor learning principles (visual EF and implicit learning) may fill this gap. Future studies are needed to evaluate the therapeutic efficacy of sensory reweighting therapy in ACL rehabilitation.

Conflicts of Interest

The authors report no conflicts of interest.

References

  1. Incidence of anterior cruciate ligament tears and reconstruction: A 21-year population-based study. Sanders Thomas L., Maradit Kremers Hilal, Bryan Andrew J., Larson Dirk R., Dahm Diane L., Levy Bruce A., Stuart Michael J., Krych Aaron J. Jun;2016 The American Journal of Sports Medicine. 44(6):1502–1507. doi: 10.1177/0363546516629944. PMID: 26920430. [DOI] [PubMed] [Google Scholar]
  2. Beliefs and attitudes of members of the American Academy of Orthopaedic Surgeons regarding the treatment of anterior cruciate ligament injury. Marx Robert G., Jones Edward C., Angel Michael, Wickiewicz Thomas L., Warren Russell F. Sep;2003 Arthroscopy: The Journal of Arthroscopic & Related Surgery: Official Publication of the Arthroscopy Association of North America and the International Arthroscopy Association. 19(7):762–770. doi: 10.1016/s0749-8063(03)00398-0. PMID: 12966385. [DOI] [PubMed] [Google Scholar]
  3. ACL Rehabilitation progression: Where are we now? Cavanaugh John T., Powers Matthew. Aug 8;2017 Current Reviews in Musculoskeletal Medicine. 10(3):289–296. doi: 10.1007/s12178-017-9426-3. PMID: 28791612 PMCID: PMC5577427. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Anterior cruciate ligament reconstruction rehabilitation: MOON guidelines. Wright Rick W., Haas Amanda K., Anderson Joy, Calabrese Gary, Cavanaugh John, Hewett Timothy E., Lorring Dawn, McKenzie Christopher, Preston Emily, Williams Glenn, MOON Group May;2015 Sports Health. 7(3):239–243. doi: 10.1177/1941738113517855. PMID: 26131301 PMCID: PMC4482298. [DOI] [PMC free article] [PubMed] [Google Scholar]
  5. Evidence-based clinical practice update: practice guidelines for anterior cruciate ligament rehabilitation based on a systematic review and multidisciplinary consensus. Melick Nicky van, Cingel Robert E. H. van, Brooijmans Frans, Neeter Camille, Tienen Tony, Hullegie Wim, Sanden Maria W. G. Nijhuis-van. Dec 1;2016 British Journal of Sports Medicine. 50(24):1506–1515. doi: 10.1136/bjsports-2015-095898. PMID: 27539507. [DOI] [PubMed] [Google Scholar]
  6. Rehabilitation practice patterns following anterior cruciate ligament reconstruction: A survey of physical therapists. Greenberg Elliot M., Greenberg Eric T., Albaugh Jeffrey, Storey Eileen, Ganley Theodore J. May 22;2018 Journal of Orthopaedic & Sports Physical Therapy. 48(10):801–811. doi: 10.2519/jospt.2018.8264. [DOI] [PubMed] [Google Scholar]
  7. The challenge of return to sports for patients post-ACL reconstruction. Simoneau Guy G., Wilk Kevin E. Apr;2012 The Journal of Orthopaedic and Sports Physical Therapy. 42(4):300–301. doi: 10.2519/jospt.2012.0106. PMID: 22570882. [DOI] [PubMed] [Google Scholar]
  8. Fifteen-year outcome of endoscopic anterior cruciate ligament reconstruction with patellar tendon autograft for "isolated" anterior cruciate ligament tear. Hui Catherine, Salmon Lucy J., Kok Alison, Maeno Shinichi, Linklater James, Pinczewski Leo A. Jan;2011 The American Journal of Sports Medicine. 39(1):89–98. doi: 10.1177/0363546510379975. PMID: 20962336. [DOI] [PubMed] [Google Scholar]
  9. Biomechanical measures during landing and postural stability predict second anterior cruciate ligament injury after anterior cruciate ligament reconstruction and return to sport. Paterno Mark V., Schmitt Laura C., Ford Kevin R., Rauh Mitchell J., Myer Gregory D., Huang Bin, Hewett Timothy E. Oct;2010 The American Journal of Sports Medicine. 38(10):1968–1978. doi: 10.1177/0363546510376053. PMID: 20702858 PMCID: PMC4920967. [DOI] [PMC free article] [PubMed] [Google Scholar]
  10. Incidence of contralateral and ipsilateral anterior cruciate ligament (ACL) injury after primary ACL reconstruction and return to sport. Paterno Mark V., Rauh Mitchell J., Schmitt Laura C., Ford Kevin R., Hewett Timothy E. Mar;2012 Clinical Journal of Sport Medicine: Official Journal of the Canadian Academy of Sport Medicine. 22(2):116–121. doi: 10.1097/JSM.0b013e318246ef9e. PMID: 22343967 PMCID: PMC4168893. [DOI] [PMC free article] [PubMed] [Google Scholar]
  11. Incidence and risk factors for graft rupture and contralateral rupture after anterior cruciate ligament reconstruction. Salmon Lucy, Russell Vivianne, Musgrove Tim, Pinczewski Leo, Refshauge Kathryn. Aug 1;2005 Arthroscopy. 21(8):948–957. doi: 10.1016/j.arthro.2005.04.110. [DOI] [PubMed] [Google Scholar]
  12. Incidence of subsequent injury to either knee within 5 years after anterior cruciate ligament reconstruction with patellar tendon autograft. Shelbourne K. Donald, Gray Tinker, Haro Marc. Feb;2009 The American Journal of Sports Medicine. 37(2):246–251. doi: 10.1177/0363546508325665. PMID: 19109531. [DOI] [PubMed] [Google Scholar]
  13. Incidence of injury in texas girls' high school basketball. Gomez E., DeLee J. C., Farney W. C. Oct;1996 The American Journal of Sports Medicine. 24(5):684–687. doi: 10.1177/036354659602400521. PMID: 8883693. [DOI] [PubMed] [Google Scholar]
  14. Epidemiology of anterior cruciate ligament reconstruction: trends, readmissions, and subsequent knee surgery. Lyman Stephen, Koulouvaris Panagiotis, Sherman Seth, Do Huong, Mandl Lisa A., Marx Robert G. Oct;2009 The Journal of Bone and Joint Surgery. American Volume. 91(10):2321–2328. doi: 10.2106/JBJS.H.00539. PMID: 19797565. [DOI] [PubMed] [Google Scholar]
  15. The incidence of injury in Texas high school basketball. A prospective study among male and female athletes. Messina D. F., Farney W. C., DeLee J. C. Jun;1999 The American Journal of Sports Medicine. 27(3):294–299. doi: 10.1177/03635465990270030401. PMID: 10352762. [DOI] [PubMed] [Google Scholar]
  16. A 10-year comparison of anterior cruciate ligament reconstructions with hamstring tendon and patellar tendon autograft: a controlled, prospective trial. Pinczewski Leo A., Lyman Jeffrey, Salmon Lucy J., Russell Vivianne J., Roe Justin, Linklater James. Apr;2007 The American Journal of Sports Medicine. 35(4):564–574. doi: 10.1177/0363546506296042. PMID: 17261567. [DOI] [PubMed] [Google Scholar]
  17. Subsequent injury patterns in girls' high school sports. Rauh Mitchell J, Macera Caroline A, Ji Ming, Wiksten Denise L. 2007Journal of Athletic Training. 42(4):486–494. PMID: 18176621 PMCID: PMC2140074. [PMC free article] [PubMed] [Google Scholar]
  18. Consequences of a ligament injury on neuromuscular function and relevance to rehabilitation - using the anterior cruciate ligament-injured knee as model. Ageberg Eva. Jun;2002 Journal of Electromyography and Kinesiology: Official Journal of the International Society of Electrophysiological Kinesiology. 12(3):205–212. doi: 10.1016/s1050-6411(02)00022-6. PMID: 12086815. [DOI] [PubMed] [Google Scholar]
  19. Neuromuscular consequences of anterior cruciate ligament injury. Ingersoll Christopher D., Grindstaff Terry L., Pietrosimone Brian G., Hart Joseph M. Jul;2008 Clinics in Sports Medicine. 27(3):383–404, vii. doi: 10.1016/j.csm.2008.03.004. PMID: 18503874. [DOI] [PubMed] [Google Scholar]
  20. Changed cortical activity after anterior cruciate ligament reconstruction in a joint position paradigm: an EEG study. Baumeister J., Reinecke K., Weiss M. Aug;2008 Scandinavian Journal of Medicine & Science in Sports. 18(4):473–484. doi: 10.1111/j.1600-0838.2007.00702.x. PMID: 18067525. [DOI] [PubMed] [Google Scholar]
  21. Altered electrocortical brain activity after ACL reconstruction during force control. Baumeister Jochen, Reinecke Kirsten, Schubert Michael, Weiss Michael. Sep;2011 Journal of Orthopaedic Research: Official Publication of the Orthopaedic Research Society. 29(9):1383–1389. doi: 10.1002/jor.21380. PMID: 21437965. [DOI] [PubMed] [Google Scholar]
  22. Quadriceps muscle function following anterior cruciate ligament reconstruction: systemic differences in neural and morphological characteristics. Lepley Adam S., Grooms Dustin R., Burland Julie P., Davi Steven M., Kinsella-Shaw Jeffrey M., Lepley Lindsey K. May;2019 Experimental Brain Research. 237(5):1267–1278. doi: 10.1007/s00221-019-05499-x. PMID: 30852644. [DOI] [PubMed] [Google Scholar]
  23. Attentional demands of postural control during single leg stance in patients with anterior cruciate ligament reconstruction. Negahban Hossein, Ahmadi Payam, Salehi Reza, Mehravar Mohammad, Goharpey Shahin. Nov 27;2013 Neuroscience Letters. 556:118–123. doi: 10.1016/j.neulet.2013.10.022. PMID: 24157849. [DOI] [PubMed] [Google Scholar]
  24. The anterior cruciate ligament deficiency as a model of brain plasticity. Kapreli Eleni, Athanasopoulos Spyridon. 2006Medical Hypotheses. 67(3):645–650. doi: 10.1016/j.mehy.2006.01.063. PMID: 16698187. [DOI] [PubMed] [Google Scholar]
  25. Neuromuscular deficits after peripheral joint injury: a neurophysiological hypothesis. Ward Sarah, Pearce Alan J., Pietrosimone Brian, Bennell Kim, Clark Ross, Bryant Adam L. Mar;2015 Muscle & Nerve. 51(3):327–332. doi: 10.1002/mus.24463. PMID: 25255714. [DOI] [PubMed] [Google Scholar]
  26. Knee kinematics following acl reconstruction in females; the effect of vision on performance during a cutting task. Bjornaraa Jaynie, Di Fabio Richard P. Dec;2011 International Journal of Sports Physical Therapy. 6(4):271–284. PMID: 22163089 PMCID: PMC3233270. [PMC free article] [PubMed] [Google Scholar]
  27. Visual-motor control of drop landing after anterior cruciate ligament reconstruction. Grooms Dustin R., Chaudhari Ajit, Page Stephen J., Nichols-Larsen Deborah S., Onate James A. May;2018 Journal of Athletic Training. 53(5):486–496. doi: 10.4085/1062-6050-178-16. PMID: 29749751 PMCID: PMC6107770. [DOI] [PMC free article] [PubMed] [Google Scholar]
  28. Change in posture control after recent knee anterior cruciate ligament reconstruction? Dauty Marc, Collon Sylvie, Dubois Charles. May;2010 Clinical Physiology and Functional Imaging. 30(3):187–191. doi: 10.1111/j.1475-097X.2010.00926.x. PMID: 20345971. [DOI] [PubMed] [Google Scholar]
  29. Function after anterior cruciate ligament injuries. Influence of visual control and proprioception. Fridén T., Roberts D., Movin T., Wredmark T. Dec;1998 Acta Orthopaedica Scandinavica. 69(6):590–594. doi: 10.3109/17453679808999261. PMID: 9930103. [DOI] [PubMed] [Google Scholar]
  30. Visual utilization during postural control in anterior cruciate ligament- deficient and -reconstructed patients: Systematic reviews and meta-analyses. Wikstrom Erik A., Song Kyeongtak, Pietrosimone Brian G., Blackburn J. Troy, Padua Darin A. 2017Archives of Physical Medicine and Rehabilitation. 98(10):2052–2065. doi: 10.1016/j.apmr.2017.04.010. PMID: 28483655. [DOI] [PubMed] [Google Scholar]
  31. An Investigation of postural control in postoperative anterior cruciate ligament reconstruction patients. Hoffman Mark, Schrader John, Koceja David. 1999Journal of Athletic Training. 34(2):130–136. PMID: 16558555 PMCID: PMC1322901. [PMC free article] [PubMed] [Google Scholar]
  32. Strength, functional outcome, and postural stability after anterior cruciate ligament reconstruction. Mattacola Carl G., Perrin David H., Gansneder Bruce M., Gieck Joe H., Saliba Ethan N., McCue Frank C. 2002Journal of Athletic Training. 37(3):262–268. PMID: 12937583 PMCID: PMC164354. [PMC free article] [PubMed] [Google Scholar]
  33. Postural sway and balance testing: a comparison of normal and anterior cruciate ligament deficient knees. O'Connell M, George K, Stock D. Oct 1;1998 Gait & Posture. 8(2):136–142. doi: 10.1016/s0966-6362(98)00023-x. PMID: 10200404. [DOI] [PubMed] [Google Scholar]
  34. Postural stability deficits during the transition from double-leg stance to single-leg stance in anterior cruciate ligament reconstructed subjects. Dingenen Bart, Janssens Luc, Claes Steven, Bellemans Johan, Staes Filip F. Jun;2015 Human Movement Science. 41:46–58. doi: 10.1016/j.humov.2015.02.001. PMID: 25744596. [DOI] [PubMed] [Google Scholar]
  35. Effect of vision on postural sway in anterior cruciate ligament injured knees. Okuda Kazuhiro, Abe Nobuhiro, Katayama Yoshimi, Senda Masuo, Kuroda Takayuki, Inoue Hajime. May;2005 Journal of Orthopaedic Science: Official Journal of the Japanese Orthopaedic Association. 10(3):277–283. doi: 10.1007/s00776-005-0893-9. PMID: 15928890. [DOI] [PubMed] [Google Scholar]
  36. Neuroplasticity following anterior cruciate ligament injury: a framework for visual-motor training approaches in rehabilitation. Grooms Dustin, Appelbaum Gregory, Onate James. May;2015 The Journal of Orthopaedic and Sports Physical Therapy. 45(5):381–393. doi: 10.2519/jospt.2015.5549. PMID: 25579692. [DOI] [PubMed] [Google Scholar]
  37. Principles of motor learning to support neuroplasticity after ACL injury: Implications for optimizing performance and reducing risk of second ACL injury. Gokeler Alli, Neuhaus Dorothee, Benjaminse Anne, Grooms Dustin R., Baumeister Jochen. Jun;2019 Sports Medicine (Auckland, N.Z.) 49(6):853–865. doi: 10.1007/s40279-019-01058-0. PMID: 30719683. [DOI] [PMC free article] [PubMed] [Google Scholar]
  38. Primary motor and premotor cortex in implicit sequence learning--evidence for competition between implicit and explicit human motor memory systems. Kantak Shailesh S., Mummidisetty Chaithanya K., Stinear James W. Sep;2012 The European Journal of Neuroscience. 36(5):2710–2715. doi: 10.1111/j.1460-9568.2012.08175.x. PMID: 22758604. [DOI] [PubMed] [Google Scholar]
  39. The role of vision and movement automization on the focus of attention effect. Porter Jared, Makaruk Hubert, Starzak Marcin. Dec 1;2016 Journal of Motor Learning and Development. 4:152–168. doi: 10.1123/jmld.2015-0020. [DOI] [Google Scholar]
  40. Implicit video feedback produces positive changes in landing mechanics. Popovic Tijana, Caswell Shane V., Benjaminse Anne, Siragy Tarique, Ambegaonkar Jatin, Cortes Nelson. May 2;2018 [2019-12-17];Journal of Experimental Orthopaedics. 5 doi: 10.1186/s40634-018-0129-5. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5931948/ PMID: 29721781 PMCID: PMC5931948. [DOI] [PMC free article] [PubMed] [Google Scholar]
  41. ACL reconstructed individuals do not demonstrate deficits in postural control as measured by single-leg balance. Bodkin Stephan G., Slater Lindsay V., Norte Grant E., Goetschius John, Hart Joseph M. 2018Gait & Posture. 66:296–299. doi: 10.1016/j.gaitpost.2018.06.120. PMID: 29958793. [DOI] [PubMed] [Google Scholar]
  42. Postural stability during visual-based cognitive and motor dual-tasks after ACLR. Miko Sarah C., Simon Janet E., Monfort Scott M., Yom Jae P., Ulloa Sergio, Grooms Dustin R. Jul 28;2020 [2020-8-7];Journal of Science and Medicine in Sport. doi: 10.1016/j.jsams.2020.07.008. http://www.sciencedirect.com/science/article/pii/S1440244020306915 [DOI] [PubMed]
  43. Nerve supply of the human knee and its functional importance. Kennedy J. C., Alexander I. J., Hayes K. C. Dec;1982 The American Journal of Sports Medicine. 10(6):329–335. doi: 10.1177/036354658201000601. PMID: 6897495. [DOI] [PubMed] [Google Scholar]
  44. Neural anatomy of the human anterior cruciate ligament. Schutte M. J., Dabezies E. J., Zimny M. L., Happel L. T. Feb;1987 The Journal of Bone and Joint Surgery. American Volume. 69(2):243–247. PMID: 3805085. [PubMed] [Google Scholar]
  45. Mechanoreceptors in the human anterior cruciate ligament. Zimny M. L., Schutte M., Dabezies E. Feb;1986 The Anatomical Record. 214(2):204–209. doi: 10.1002/ar.1092140216. PMID: 3954077. [DOI] [PubMed] [Google Scholar]
  46. Proprioception in anterior cruciate ligament deficient knees and its relevance in anterior cruciate ligament reconstruction. Dhillon Mandeep S, Bali Kamal, Prabhakar Sharad. 2011Indian Journal of Orthopaedics. 45(4):294–300. doi: 10.4103/0019-5413.80320. PMID: 21772620 PMCID: PMC3134012. [DOI] [PMC free article] [PubMed] [Google Scholar]
  47. Sensory reweighting dynamics in human postural control. Assländer Lorenz, Peterka Robert J. May;2014 Journal of Neurophysiology. 111(9):1852–1864. doi: 10.1152/jn.00669.2013. PMID: 24501263 PMCID: PMC4044370. [DOI] [PMC free article] [PubMed] [Google Scholar]
  48. Balancing sensory inputs: Sensory reweighting of ankle proprioception and vision during a bipedal posture task. Kabbaligere Rakshatha, Lee Beom-Chan, Layne Charles S. 2017Gait & Posture. 52:244–250. doi: 10.1016/j.gaitpost.2016.12.009. PMID: 27978501. [DOI] [PubMed] [Google Scholar]
  49. Multisensory integration during motor planning. Sober Samuel J., Sabes Philip N. Aug 6;2003 The Journal of Neuroscience: The Official Journal of the Society for Neuroscience. 23(18):6982–6992. doi: 10.1523/JNEUROSCI.23-18-06982.2003. PMID: 12904459. [DOI] [PMC free article] [PubMed] [Google Scholar]
  50. Proprioceptive and behavior impairments in individuals with anterior cruciate ligament reconstructed knees. Bonfim Thátia R., Jansen Paccola Cleber Antonio, Barela José A. Aug;2003 Archives of Physical Medicine and Rehabilitation. 84(8):1217–1223. doi: 10.1016/s0003-9993(03)00147-3. PMID: 12917863. [DOI] [PubMed] [Google Scholar]
  51. Proprioceptive sensitivity and performance in anterior cruciate ligament-deficient knee joints. Fischer-Rasmussen T., Jensen P. E. Apr;2000 Scandinavian Journal of Medicine & Science in Sports. 10(2):85–89. doi: 10.1034/j.1600-0838.2000.010002085.x. PMID: 10755278. [DOI] [PubMed] [Google Scholar]
  52. Bayesian integration of visual and auditory signals for spatial localization. Battaglia Peter W., Jacobs Robert A., Aslin Richard N. Jul 1;2003 JOSA A. 20(7):1391–1397. doi: 10.1364/JOSAA.20.001391. [DOI] [PubMed] [Google Scholar]
  53. Humans integrate visual and haptic information in a statistically optimal fashion. Ernst Marc O., Banks Martin S. Jan;2002 Nature. 415(6870):429. doi: 10.1038/415429a. [DOI] [PubMed] [Google Scholar]
  54. The Bayesian brain: the role of uncertainty in neural coding and computation. Knill David C., Pouget Alexandre. Dec 1;2004 Trends in Neurosciences. 27(12):712–719. doi: 10.1016/j.tins.2004.10.007. [DOI] [PubMed] [Google Scholar]
  55. Internal and external focus of attention during gait re-education: an observational study of physical therapist practice in stroke rehabilitation. Johnson Louise, Burridge Jane H., Demain Sara H. Jul;2013 Physical Therapy. 93(7):957–966. doi: 10.2522/ptj.20120300. PMID: 23559523. [DOI] [PubMed] [Google Scholar]
  56. Coaching cues in amateur boxing: an analysis of ringside feedback provided between rounds of competition. Halperin Israel, Chapman Dale W., Martin David T., Abbiss Chris R., Wulf Gabriele. 2016 [2020-3-6];25:44–50. [Google Scholar]
  57. Directing attention externally enhances agility performance: a qualitative and quantitative analysis of the efficacy of using verbal instructions to focus attention. Porter Jared M., Nolan Russell P., Ostrowski Erik J., Wulf Gabriele. 2010Frontiers in Psychology. 1:216. doi: 10.3389/fpsyg.2010.00216. PMID: 21833271 PMCID: PMC3153821. [DOI] [PMC free article] [PubMed] [Google Scholar]
  58. Use of information feedback and attentional focus of feedback in treating the person with a hemiplegic arm. Durham Katherine, Van Vliet Paulette M., Badger Frances, Sackley Catherine. Jun;2009 Physiotherapy Research International: The Journal for Researchers and Clinicians in Physical Therapy. 14(2):77–90. doi: 10.1002/pri.431. PMID: 19107706. [DOI] [PubMed] [Google Scholar]
  59. The impact of attentional focus on the treatment of musculoskeletal and movement disorders. Hunt Christopher, Paez Arsenio, Folmar Eric. Nov;2017 International Journal of Sports Physical Therapy. 12(6):901–907. PMID: 29158952 PMCID: PMC5675366. [PMC free article] [PubMed] [Google Scholar]
  60. Biomechanical measures of neuromuscular control and valgus loading of the knee predict anterior cruciate ligament injury risk in female athletes: a prospective study. Hewett Timothy E., Myer Gregory D., Ford Kevin R., Heidt Robert S., Colosimo Angelo J., McLean Scott G., Bogert Antonie J., Paterno Mark V., Succop Paul. Apr;2005 The American Journal of Sports Medicine. 33(4):492–501. doi: 10.1177/0363546504269591. PMID: 15722287. [DOI] [PubMed] [Google Scholar]
  61. Drop-jump landing varies with baseline neurocognition: Implications for anterior cruciate ligament injury risk and prevention. Herman Daniel C., Barth Jeffrey T. Sep;2016 The American Journal of Sports Medicine. 44(9):2347–2353. doi: 10.1177/0363546516657338. PMID: 27474381 PMCID: PMC6039105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  62. The effects of cognitive loading on motor behavior in injured individuals: a systematic review. Burcal Christopher J., Needle Alan R., Custer Lisa, Rosen Adam B. Aug;2019 Sports Medicine (Auckland, N.Z.) 49(8):1233–1253. doi: 10.1007/s40279-019-01116-7. PMID: 31066022. [DOI] [PubMed] [Google Scholar]
  63. Dual-tasking effects on dynamic postural stability in athletes with and without anterior cruciate ligament reconstruction. Mohammadi-Rad Shahrzad, Salavati Mahyar, Ebrahimi-Takamjani Ismail, Akhbari Behnam, Sherafat Shiva, Negahban Hossein, Lali Pezhman, Mazaheri Masood. Dec;2016 Journal of Sport Rehabilitation. 25(4):324–329. doi: 10.1123/jsr.2015-0012. PMID: 27632858. [DOI] [PubMed] [Google Scholar]
  64. Gait speed is more challenging than cognitive load on the stride-to-stride variability in individuals with anterior cruciate ligament deficiency. Nazary-Moghadam Salman, Salavati Mahyar, Esteki Ali, Akhbari Behnam, Keyhani Sohrab, Zeinalzadeh Afsaneh. Jan;2019 The Knee. 26(1):88–96. doi: 10.1016/j.knee.2018.11.009. PMID: 30473374. [DOI] [PubMed] [Google Scholar]
  65. Effect of dual task on gait asymmetry in patients after anterior cruciate ligament reconstruction. Shi Huijuan, Huang Hongshi, Yu Yuanyuan, Liang Zixuan, Zhang Si, Yu Bing, Liu Hui, Ao Yingfang. Aug 13;2018 [2019-11-20];Scientific Reports. 8 doi: 10.1038/s41598-018-30459-w. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6089886/ PMID: 30104568 PMCID: PMC6089886. [DOI] [PMC free article] [PubMed] [Google Scholar]
  66. Reliability of dynamic balance simultaneously with cognitive performance in patients with ACL deficiency and after ACL reconstructions and in healthy controls. Akhbari Behnam, Salavati Mahyar, Ahadi Jalal, Ferdowsi Forough, Sarmadi Alireza, Keyhani Sohrab, Mohammadi Farshid. Nov;2015 Knee surgery, sports traumatology, arthroscopy: official journal of the ESSKA. 23(11):3178–3185. doi: 10.1007/s00167-014-3116-0. PMID: 24917539. [DOI] [PubMed] [Google Scholar]
  67. Primary motor cortex organization is altered in persistent patellofemoral pain. Te Maxine, Baptista Abrahão F., Chipchase Lucy S., Schabrun Siobhan M. Nov 1;2017 Pain Medicine (Malden, Mass.) 18(11):2224–2234. doi: 10.1093/pm/pnx036. PMID: 28340134. [DOI] [PubMed] [Google Scholar]
  68. Organisation of the motor cortex differs between people with and without knee osteoarthritis. Shanahan Camille J., Hodges Paul W., Wrigley Tim V., Bennell Kim L., Farrell Michael J. Jun 18;2015 Arthritis Research & Therapy. 17:164. doi: 10.1186/s13075-015-0676-4. PMID: 26080802 PMCID: PMC4494800. [DOI] [PMC free article] [PubMed] [Google Scholar]
  69. Anterior cruciate ligament deficiency causes brain plasticity: a functional MRI study. Kapreli Eleni, Athanasopoulos Spyros, Gliatis John, Papathanasiou Matilda, Peeters Ronald, Strimpakos Nikolaos, Van Hecke Paul, Gouliamos Athanasios, Sunaert Stefan. Dec;2009 The American Journal of Sports Medicine. 37(12):2419–2426. doi: 10.1177/0363546509343201. PMID: 19940314. [DOI] [PubMed] [Google Scholar]
  70. Neuroplasticity associated with anterior cruciate ligament reconstruction. Grooms Dustin R., Page Stephen J., Nichols-Larsen Deborah S., Chaudhari Ajit M.W., White Susan E., Onate James A. Nov 5;2016 Journal of Orthopaedic & Sports Physical Therapy. 47(3):180–189. doi: 10.2519/jospt.2017.7003. [DOI] [PubMed] [Google Scholar]
  71. Specificity of regions processing biological motion. Peuskens H., Vanrie J., Verfaillie K., Orban G. A. May;2005 The European Journal of Neuroscience. 21(10):2864–2875. doi: 10.1111/j.1460-9568.2005.04106.x. PMID: 15926934. [DOI] [PubMed] [Google Scholar]
  72. Neural activity for hip-knee control in those with anterior cruciate ligament reconstruction: A task-based functional connectivity analysis. Criss Cody R., Onate James A., Grooms Dustin R. May 5;2020 Neuroscience Letters. 730:134985. doi: 10.1016/j.neulet.2020.134985. PMID: 32380143. [DOI] [PubMed] [Google Scholar]
  73. Modulation of human visual cortex by crossmodal spatial attention. Macaluso E., Frith C. D., Driver J. Aug 18;2000 Science (New York, N.Y.) 289(5482):1206–1208. doi: 10.1126/science.289.5482.1206. PMID: 10947990. [DOI] [PubMed] [Google Scholar]
  74. Spatial attention and crossmodal interactions between vision and touch. Macaluso E., Driver J. 2001Neuropsychologia. 39(12):1304–1316. doi: 10.1016/s0028-3932(01)00119-1. PMID: 11566313. [DOI] [PubMed] [Google Scholar]
  75. Neural correlates of cognitive efficiency. Rypma Bart, Berger Jeffrey S., Prabhakaran Vivek, Bly Benjamin Martin, Kimberg Daniel Y., Biswal Bharat B., D'Esposito Mark. Nov 15;2006 NeuroImage. 33(3):969–979. doi: 10.1016/j.neuroimage.2006.05.065. PMID: 17010646. [DOI] [PubMed] [Google Scholar]
  76. Neural efficiency in expert cognitive-motor performers during affective challenge. Costanzo Michelle E., VanMeter John W., Janelle Christopher M., Braun Allen, Miller Matthew W., Oldham Jessica, Russell Bartlett A. H., Hatfield Bradley D. Dec;2016 Journal of Motor Behavior. 48(6):573–588. doi: 10.1080/00222895.2016.1161591. PMID: 27715496. [DOI] [PubMed] [Google Scholar]
  77. Is there a "neural efficiency" in athletes? a high-resolution eeg study. Del Percio Claudio, Rossini Paolo M., Marzano Nicola, Iacoboni Marco, Infarinato Francesco, Aschieri Pierluigi, Lino Andrea, Fiore Antonio, Toran Giancarlo, Babiloni Claudio, Eusebi Fabrizio. Oct 1;2008 NeuroImage. 42(4):1544–1553. doi: 10.1016/j.neuroimage.2008.05.061. PMID: 18602484. [DOI] [PubMed] [Google Scholar]
  78. "neural efficiency" of athletes' brain for upright standing: a high-resolution eeg study. Del Percio Claudio, Babiloni Claudio, Marzano Nicola, Iacoboni Marco, Infarinato Francesco, Vecchio Fabrizio, Lizio Roberta, Aschieri Pierluigi, Fiore Antonio, Toràn Giancarlo, Gallamini Michele, Baratto Marta, Eusebi Fabrizio. May 29;2009 Brain Research Bulletin. 79(3-4):193–200. doi: 10.1016/j.brainresbull.2009.02.001. PMID: 19429191. [DOI] [PubMed] [Google Scholar]
  79. The characteristics of EEG power spectra changes after ACL rupture. Miao Xin, Huang Hongshi, Hu Xiaoqing, Li Dai, Yu Yuanyuan, Ao Yingfang. 2017PloS One. 12(2):e0170455. doi: 10.1371/journal.pone.0170455. PMID: 28182627 PMCID: PMC5300146. [DOI] [PMC free article] [PubMed] [Google Scholar]
  80. Should return to sport be delayed until two years after anterior cruciate ligament reconstruction? Biological and functional considerations. Nagelli Christopher V., Hewett Timothy E. Feb;2017 Sports medicine (Auckland, N.Z.) 47(2):221–232. doi: 10.1007/s40279-016-0584-z. PMID: 27402457 PMCID: PMC5226931. [DOI] [PMC free article] [PubMed] [Google Scholar]
  81. Lower limb kinetic asymmetries in professional soccer players with and without anterior cruciate ligament reconstruction: Nine months is not enough time to restore "functional" symmetry or return to performance. Read Paul J., Michael Auliffe Sean, Wilson Mathew G., Graham-Smith Philip. May;2020 The American Journal of Sports Medicine. 48(6):1365–1373. doi: 10.1177/0363546520912218. PMID: 32293904. [DOI] [PubMed] [Google Scholar]
  82. Young athletes who return to sport before 9 months after anterior cruciate ligament reconstruction have a rate of new injury 7 times that of those who delay return. Beischer Susanne, Gustavsson Linnéa, Senorski Eric Hamrin, Karlsson Jón, Thomeé Christoffer, Samuelsson Kristian, Thomeé Roland. Feb;2020 The Journal of Orthopaedic and Sports Physical Therapy. 50(2):83–90. doi: 10.2519/jospt.2020.9071. PMID: 32005095. [DOI] [PubMed] [Google Scholar]
  83. Optic flow is used to control human walking. Warren W. H., Kay B. A., Zosh W. D., Duchon A. P., Sahuc S. Feb;2001 Nature Neuroscience. 4(2):213–216. doi: 10.1038/84054. PMID: 11175884. [DOI] [PubMed] [Google Scholar]
  84. The effects of delayed and displaced visual feedback on motor control. Smith William M., Bowen Kevin F. Jun 1;1980 Journal of Motor Behavior. 12(2):91–101. doi: 10.1080/00222895.1980.10735209. PMID: 15215054. [DOI] [PubMed] [Google Scholar]
  85. ACL injury prevention, more effective with a different way of motor learning? Benjaminse Anne, Otten Egbert. Apr;2011 Knee surgery, sports traumatology, arthroscopy: official journal of the ESSKA. 19(4):622–627. doi: 10.1007/s00167-010-1313-z. PMID: 21079917 PMCID: PMC3062033. [DOI] [PMC free article] [PubMed] [Google Scholar]
  86. Normalized motor function but impaired sensory function after unilateral non-reconstructed ACL injury: patients compared with uninjured controls. Ageberg Eva, Fridén Thomas. May;2008 Knee surgery, sports traumatology, arthroscopy: official journal of the ESSKA. 16(5):449–456. doi: 10.1007/s00167-008-0499-9. PMID: 18305924. [DOI] [PubMed] [Google Scholar]
  87. Variability of practice and contextual interference in motor skill learning. Hall K. G., Magill R. A. Dec;1995 Journal of Motor Behavior. 27(4):299–309. doi: 10.1080/00222895.1995.9941719. PMID: 12529226. [DOI] [PubMed] [Google Scholar]
  88. Stroboscopic vision to induce sensory reweighting during postural control. Kim Kyung-Min, Kim Joo-Sung, Grooms Dustin R. 2017Journal of Sport Rehabilitation. 26(5) doi: 10.1123/jsr.2017-0035. PMID: 28605310. [DOI] [PubMed] [Google Scholar]
  89. An early review of stroboscopic visual training: insights, challenges and accomplishments to guide future studies. Wilkins Luke, Appelbaum Lawrence. Mar 1;2019 International Review of Sport and Exercise Psychology. :1–16. doi: 10.1080/1750984X.2019.1582081. [DOI]
  90. Improved visual cognition through stroboscopic training. Appelbaum L. Gregory, Schroeder Julia E., Cain Matthew S., Mitroff Stephen R. 2011Frontiers in Psychology. 2:276. doi: 10.3389/fpsyg.2011.00276. PMID: 22059078 PMCID: PMC3203550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  91. Stroboscopic visual training improves information encoding in short-term memory. Appelbaum L. Gregory, Cain Matthew S., Schroeder Julia E., Darling Elise F., Mitroff Stephen R. Nov;2012 Attention, Perception & Psychophysics. 74(8):1681–1691. doi: 10.3758/s13414-012-0344-6. PMID: 22810559. [DOI] [PubMed] [Google Scholar]
  92. Stroboscopic training enhances anticipatory timing. Smith Trevor Q., Mitroff Stephen R. Oct 15;2012 International Journal of Exercise Science. 5(4):344–353. doi: 10.70252/OTSW1297. PMID: 27182391 PMCID: PMC4738880. [DOI] [PMC free article] [PubMed] [Google Scholar]
  93. The effect of visual perturbation upon femoral acceleration during the single and bilateral squat. Dale R. Barry, Gollapalli Ravi P., Price Taylor, Megahee Katie, Duncan Morgan, Tolstick Nick, Ford Luke. Sep;2017 Physical Therapy in Sport: Official Journal of the Association of Chartered Physiotherapists in Sports Medicine. 27:24–28. doi: 10.1016/j.ptsp.2017.06.003. PMID: 28806721. [DOI] [PubMed] [Google Scholar]
  94. Enhancing ice hockey skills through stroboscopic visual training: a pilot study. Mitroff Stephen, Friesen Peter, Bennett Doug, Yoo Herb, W. Reichow Alan. Nov 1;2013 Athletic Training & Sports Health Care. 5:261–264. doi: 10.3928/19425864-20131030-02. [DOI] [Google Scholar]
  95. Effects of Stroboscopic visual training on visual attention, motion perception, and catching performance. Wilkins Luke, Gray Rob. Aug;2015 Perceptual and Motor Skills. 121(1):57–79. doi: 10.2466/22.25.PMS.121c11x0. PMID: 26126135. [DOI] [PubMed] [Google Scholar]
  96. The effect of 4-Week stroboscopic training on visual function and sport-specific visuomotor performance in top-level badminton players. Hülsdünker Thorben, Rentz Clara, Ruhnow Diemo, Käsbauer Hannes, Strüder Heiko K., Mierau Andreas. Mar 1;2019 International Journal of Sports Physiology and Performance. 14(3):343–350. doi: 10.1123/ijspp.2018-0302. PMID: 30160560. [DOI] [PubMed] [Google Scholar]
  97. Stroboscopic vision when interacting with multiple moving objects: Perturbation is not the same as elimination. Bennett Simon J., Hayes Spencer J., Uji Makoto. 2018Frontiers in Psychology. 9:1290. doi: 10.3389/fpsyg.2018.01290. PMID: 30090080 PMCID: PMC6068388. [DOI] [PMC free article] [PubMed] [Google Scholar]
  98. Neuromuscular training to target deficits associated with second anterior cruciate ligament injury. Di Stasi Stephanie, Myer Gregory D., Hewett Timothy E. Nov;2013 The Journal of Orthopaedic and Sports Physical Therapy. 43(11):777–792, A1. doi: 10.2519/jospt.2013.4693. PMID: 24175599 PMCID: PMC4163697. [DOI] [PMC free article] [PubMed] [Google Scholar]
  99. Effect of gender and defensive opponent on the biomechanics of sidestep cutting. McLean Scott G., Lipfert Susanne W., Bogert Antonie J. Jun;2004 Medicine and Science in Sports and Exercise. 36(6):1008–1016. doi: 10.1249/01.mss.0000128180.51443.83. PMID: 15179171. [DOI] [PubMed] [Google Scholar]
  100. Analysis of EMG patterns of control subjects and subjects with ACL deficiency during an unanticipated walking cut task. Houck Jeff R., Wilding Gregory E., Gupta Resmi, De Haven Kenneth E., Maloney Mike. Apr;2007 Gait & Posture. 25(4):628–638. doi: 10.1016/j.gaitpost.2006.07.001. PMID: 16916604. [DOI] [PubMed] [Google Scholar]
  101. Augmented feedback supports skill transfer and reduces high-risk injury landing mechanics: a double-blind, randomized controlled laboratory study. Myer Gregory D., Stroube Benjamin W., DiCesare Christopher A., Brent Jensen L., Ford Kevin R., Heidt Robert S., Hewett Timothy E. Mar;2013 The American Journal of Sports Medicine. 41(3):669–677. doi: 10.1177/0363546512472977. PMID: 23371471 PMCID: PMC4166501. [DOI] [PMC free article] [PubMed] [Google Scholar]
  102. Feedback techniques to target functional deficits following anterior cruciate ligament reconstruction: Implications for motor control and reduction of second injury risk. Gokeler Alli, Benjaminse Anne, Hewett Timothy E., Paterno Mark V., Ford Kevin R., Otten Egbert, Myer Gregory D. Nov;2013 Sports medicine (Auckland, N.Z.) 43(11):1065–1074. doi: 10.1007/s40279-013-0095-0. PMID: 24062274 PMCID: PMC4166506. [DOI] [PMC free article] [PubMed] [Google Scholar]
  103. Motor learning and performance: A problem-based learning approach. Pringle RK. Jun 1;2000 Journal of manipulative and physiological therapeutics. 23:300–1. doi: 10.1016/S0161-4754(00)90186-6. [DOI] [PubMed] [Google Scholar]
  104. Functional reorganisation of the corticomotor projection to the hand in skilled racquet players. Pearce A. J., Thickbroom G. W., Byrnes M. L., Mastaglia F. L. Jan 1;2000 Experimental Brain Research. 130(2):238–243. doi: 10.1007/s002219900236. [DOI] [PubMed] [Google Scholar]
  105. Corticospinal adaptations and strength maintenance in the immobilized arm following 3 weeks unilateral strength training. Pearce A. J., Hendy A., Bowen W. A., Kidgell D. J. Dec;2013 Scandinavian Journal of Medicine & Science in Sports. 23(6):740–748. doi: 10.1111/j.1600-0838.2012.01453.x. PMID: 22429184. [DOI] [PubMed] [Google Scholar]
  106. How changing the focus of attention affects performance, kinematics, and electromyography in dart throwing. Lohse Keith R., Sherwood David E., Healy Alice F. Aug;2010 Human Movement Science. 29(4):542–555. doi: 10.1016/j.humov.2010.05.001. PMID: 20541275. [DOI] [PubMed] [Google Scholar]
  107. A novel approach to enhance ACL injury prevention programs. Gokeler Alli, Seil Romain, Kerkhoffs Gino, Verhagen Evert. Jun 18;2018 Journal of Experimental Orthopaedics. 5(1):22. doi: 10.1186/s40634-018-0137-5. PMID: 29916182 PMCID: PMC6005994. [DOI] [PMC free article] [PubMed] [Google Scholar]
  108. Gaze and the control of foot placement when walking in natural terrain. Matthis Jonathan Samir, Yates Jacob L., Hayhoe Mary M. Apr 23;2018 Current Biology. 28(8):1224–1233.e5. doi: 10.1016/j.cub.2018.03.008. [DOI] [PMC free article] [PubMed] [Google Scholar]
  109. Increasing the distance of an external focus of attention enhances learning. McNevin Nancy H., Shea Charles H., Wulf Gabriele. Feb;2003 Psychological Research. 67(1):22–29. doi: 10.1007/s00426-002-0093-6. PMID: 12589447. [DOI] [PubMed] [Google Scholar]
  110. Neuroanatomical correlates of motor acquisition and motor transfer. Seidler R. D., Noll D. C. Apr;2008 Journal of Neurophysiology. 99(4):1836–1845. doi: 10.1152/jn.01187.2007. PMID: 18272874. [DOI] [PubMed] [Google Scholar]
  111. Mechanisms underlying ACL injury-prevention training: The brain-behavior relationship. Powers Christopher M., Fisher Beth. 2010Journal of Athletic Training. 45(5):513–515. doi: 10.4085/1062-6050-45.5.513. PMID: 20831400 PMCID: PMC2938326. [DOI] [PMC free article] [PubMed] [Google Scholar]
  112. Attentional focus and motor learning: a review of 15 years. Wulf Gabriele. Sep 1;2013 International Review of Sport and Exercise Psychology. 6(1):77–104. doi: 10.1080/1750984X.2012.723728. [DOI] [Google Scholar]
  113. Novel methods of instruction in ACL injury prevention programs, a systematic review. Benjaminse Anne, Welling Wouter, Otten Bert, Gokeler Alli. May;2015 Physical Therapy in Sport: Official Journal of the Association of Chartered Physiotherapists in Sports Medicine. 16(2):176–186. doi: 10.1016/j.ptsp.2014.06.003. PMID: 25042094. [DOI] [PubMed] [Google Scholar]
  114. Increased jump height and reduced EMG activity with an external focus. Wulf Gabriele, Dufek Janet S., Lozano Leonardo, Pettigrew Christina. Jun;2010 Human Movement Science. 29(3):440–448. doi: 10.1016/j.humov.2009.11.008. PMID: 20409600. [DOI] [PubMed] [Google Scholar]
  115. The effects of attentional focus on jump performance and knee joint kinematics in patients after ACL reconstruction. Gokeler Alli, Benjaminse Anne, Welling Wouter, Alferink Malou, Eppinga Peter, Otten Bert. May;2015 Physical Therapy in Sport: Official Journal of the Association of Chartered Physiotherapists in Sports Medicine. 16(2):114–120. doi: 10.1016/j.ptsp.2014.06.002. PMID: 25443228. [DOI] [PubMed] [Google Scholar]
  116. Defining the focus of attention: Effects of attention on perceived exertion and fatigue. Lohse Keith R., Sherwood David E. Nov 14;2011 [2019-12-17];Frontiers in Psychology. 2 doi: 10.3389/fpsyg.2011.00332. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214735/ PMID: 22102843 PMCID: PMC3214735. [DOI] [PMC free article] [PubMed] [Google Scholar]
  117. Adopting an external focus of attention alters intracortical inhibition within the primary motor cortex. Kuhn Y.-A., Keller M., Ruffieux J., Taube W. 2017Acta Physiologica (Oxford, England) 220(2):289–299. doi: 10.1111/apha.12807. PMID: 27653020 PMCID: PMC5484339. [DOI] [PMC free article] [PubMed] [Google Scholar]
  118. Surround inhibition can instantly be modulated by changing the attentional focus. Kuhn Yves-Alain, Keller Martin, Lauber Benedikt, Taube Wolfgang. Jan 18;2018 [2019-12-17];Scientific Reports. 8 doi: 10.1038/s41598-017-19077-0. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5773585/ PMID: 29348536 PMCID: PMC5773585. [DOI] [PMC free article] [PubMed] [Google Scholar]
  119. Gluck Mark A., Mercardo Eduardo, Myers Catherine E. Learning and memory: from brain to behavior; New York City, New York. New York City, New York: Worth Publishers; [2019-12-21]. [Google Scholar]
  120. Dynamic cortical involvement in implicit and explicit motor sequence learning. A PET study. Honda M., Deiber M. P., Ibáñez V., Pascual-Leone A., Zhuang P., Hallett M. Nov;1998 Brain: A Journal of Neurology. 121 ( Pt 11):2159–2173. doi: 10.1093/brain/121.11.2159. PMID: 9827775. [DOI] [PubMed] [Google Scholar]
  121. Different effects of implicit and explicit motor sequence learning on latency of motor evoked potential evoked by transcranial magnetic stimulation on the primary motor cortex. Hirano Masato, Kubota Shinji, Koizume Yoshiki, Tanaka Shinya, Funase Kozo. Jan 4;2017 [2019-12-17];Frontiers in Human Neuroscience. 10 doi: 10.3389/fnhum.2016.00671. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5209357/ PMID: 28101014 PMCID: PMC5209357. [DOI] [PMC free article] [PubMed] [Google Scholar]
  122. Implicit motor learning and complex decision making in time-constrained environments. Masters R. S. W., Poolton J. M., Maxwell J. P., Raab M. Jan;2008 Journal of Motor Behavior. 40(1):71–79. doi: 10.3200/JMBR.40.1.71-80. PMID: 18316298. [DOI] [PubMed] [Google Scholar]
  123. Anticipatory effects on lower extremity neuromechanics during a cutting task. Meinerz Carolyn M., Malloy Philip, Geiser Christopher F., Kipp Kristof. Sep;2015 Journal of Athletic Training. 50(9):905–913. doi: 10.4085/1062-6050-50.8.02. PMID: 26285089 PMCID: PMC4639880. [DOI] [PMC free article] [PubMed] [Google Scholar]
  124. Unanticipated jump-landing after anterior cruciate ligament reconstruction: Does unanticipated jump-landing testing deliver additional return to sport information to traditional jump performance tests? Niemeyer Philipp, Niederer Daniel, Giesche Florian, Janko Maren, Frank Johannes, Vogt Lutz, Banzer Winfried. Dec;2019 Clinical Biomechanics (Bristol, Avon) 70:72–79. doi: 10.1016/j.clinbiomech.2019.08.003. PMID: 31408765. [DOI] [PubMed] [Google Scholar]
  125. Unanticipated jump-landing quality in patients with anterior cruciate ligament reconstruction: How long after the surgery and return to sport does the re-injury risk factor persist? Niederer Daniel, Giesche Florian, Janko Maren, Niemeyer Philipp, Wilke Jan, Engeroff Tobias, Stein Thomas, Frank Johannes, Banzer Winfried, Vogt Lutz. Feb 1;2020 Clinical Biomechanics. 72:195–201. doi: 10.1016/j.clinbiomech.2019.12.021. [DOI] [PubMed] [Google Scholar]
  126. Changes in lower-limb biomechanics, soft tissue vibrations, and muscle activation during unanticipated bipedal landings. Zhang Shen, Fu Weijie, Liu Yu. Jun;2019 Journal of Human Kinetics. 67:25–35. doi: 10.2478/hukin-2019-0003. PMID: 31523304 PMCID: PMC6714375. [DOI] [PMC free article] [PubMed] [Google Scholar]
  127. Hart Sandra G., Staveland Lowell E. Development of NASA-TLX (Task Load Index): Results of empirical and theoretical research; Human mental workload; Oxford, England. Oxford, England: North-Holland; pp. 139–183. DOI: 10.1016/S0166-4115(08)62386-9. [Google Scholar]
  128. Perceived exertion as an indicator of somatic stress. Borg G. 1970Scandinavian Journal of Rehabilitation Medicine. 2(2):92–98. PMID: 5523831. [PubMed] [Google Scholar]
  129. Psychophysical bases of perceived exertion. Borg G. A. 1982Medicine and Science in Sports and Exercise. 14(5):377–381. PMID: 7154893. [PubMed] [Google Scholar]

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