J Motor Control Learn

Image Credit:J Motor Control Learn

How Does Mirror Visual Feedback Therapy Effectively Reduce Behavioral Problems in Children with Unilateral Spastic Cerebral Palsy?

Author(s):
Pegah FarzamfarPegah Farzamfar1, Ali HeiraniAli HeiraniAli Heirani ORCID1,*, Mostafa SedighiMostafa Sedighi2
1Department of Motor Behavior and Corrective Exercises, Faculty of Sports Sciences, Razi University, Kermanshah, Iran
2Department of Pediatric Neurology, Kermanshah University of Medical Sciences, Kermanshah, Iran

Journal of Motor Control and Learning:Vol. 7, issue 3; e159725
Published online:Aug 31, 2025
Article type:Research Article
Received:Jan 22, 2025
Accepted:Aug 25, 2025
How to Cite:Farzamfar P, Heirani A, Sedighi M. How Does Mirror Visual Feedback Therapy Effectively Reduce Behavioral Problems in Children with Unilateral Spastic Cerebral Palsy?.J Motor Control Learn.2025;7(3):e159725.https://doi.org/10.5812/jmcl-159725.

Abstract

Background:

Unilateral spastic cerebral palsy (USCP), which is caused by an early brain injury, primarily affects one side of the body and is associated with sensory-motor deficits and spasticity. Cerebral palsy can also lead to cognitive, sensory, communicative, perceptual, and behavioral disorders, as well as seizures.

Objectives:

The present study investigated the effects of mirror visual feedback therapy (MVFT) on behavioral problems in children with USCP.

Methods:

Using a pretest-posttest experimental design, 14 children (aged 6 - 12 years) with hemiplegic CP were randomly assigned to either an experimental group (n = 7) that performed movements in front of a mirror or a control group (n = 7) that performed the same movements without a mirror. The Strengths and Difficulties Questionnaire (SDQ) was administered to assess behavioral problems at baseline and after 16 sessions of 30 minutes each. The experimental group performed finger, wrist, and elbow flexion/extension; forearm rotation; finger stretching; and making a fist with their unaffected hand in front of a mirror, while the control group performed identical exercises without a mirror. Data normality was confirmed using the Shapiro-Wilk test, and the data were analyzed using two-way repeated-measures ANOVA.

Results:

Posttest results showed a significant reduction in total difficulties (TD; P < 0.05) and a significant increase in prosocial behaviors (PB; P < 0.05) in the experimental group compared to the control group.

Conclusions:

The MVFT effectively reduced behavioral problems, suggesting that motor training in front of a mirror can be beneficial for children with USCP.

1. Background

Unilateral spastic cerebral palsy (USCP), resulting from early neurological lesions, is characterized by sensory-motor deficits and spasticity that predominantly affect one side of the body (1, 2). In addition to limitations in movement, cerebral palsy (CP) may also cause cognitive, sensory, communicative, seizure-related, perceptual and behavioral disorders (3, 4). Brain injuries do not cause specific behavioral patterns, but associated motor deficits can significantly influence a child’s behavior (5, 6). Children exhibiting disabilities of the central nervous system are at increased risk for encountering behavioral difficulties (6). Behavioral difficulties are defined as socially inappropriate actions that interfere with the conduct of daily life (7). Such behaviors may encompass challenges with peer interactions, attention deficits, hyperactivity, emotional disturbances, increased dependency, social withdrawal, obstinacy, and antisocial tendencies (5). These issues, reported in 26% to 40% of children with CP, significantly impact personal and social interactions (8). Few studies have explored behavioral issues in children with CP. Voyer et al. found that even those with high motor function (GMFCS levels I-II) can experience significant social impairments alongside motor challenges (9). Schuengel et al. also reported that perceived motor ability, physical appearance, and self-worth were positively related to aggression (10). Children with CP may struggle to maintain peer relationships and a sense of belonging because they leave the classroom for supportive services and feel anxious about fitting in at school. Dababneh (11) associated physical appearance concerns in children with CP with social and behavioral problems, citing reduced mirror neuron activity. Mirror neurons, primarily found in the ventral premotor cortex and parietal lobe, are widely distributed throughout the cerebral cortex, forming what is known as the mirror neuron system (MNS) (4). These neurons are localized in regions of the brain that are associated with advanced perceptual, motor and cognitive functions (12). Given the importance of these factors, the implementation of new therapies is crucial for children with CP (11). While approximately 182 therapeutic interventions are available, common motor-based approaches include constraint-induced movement therapy (CIMT), muscle strengthening programs, hippotherapy, and task-oriented training (4). Mirror visual feedback therapy (MVFT) is a modern, inexpensive, and effective option with no side effects, special equipment needs, or pain and can be easily performed without involving the affected limb (4, 13). It is believed to work by facilitating motor pathways, preventing learned disuse, and activating mirror neurons (14).

The MVFT is thought to work through the MNS, where visuomotor neurons are activated during observation, imagination, or execution of motor tasks (15, 16). Observing an action increases excitability in visual and somatosensory areas, potentially reflecting increased attention to resolve perceptual incongruence (17). This process is linked to awareness of sensory feedback/agency control (insular cortex) and movement monitoring (DLPFC) (18, 19). Furthermore, increased activity in the posterior parietal and cingulate cortex suggests increased attentional demands. The posterior cingulate cortex (PCC) plays a role in cognitive control (12). Observation also increases excitability in the primary motor cortex (M1) and related muscle groups, aiding cortical reorganization crucial for hand recovery (20, 21). Children with USCP often develop "learned non-use" of the affected hand, leading to a preference for the unaffected side and further functional decline. The MVFT counteracts this by encouraging use of the impaired hand and reducing neglect. Applying MVFT to the less-affected hand has been shown to significantly improve gross motor performance in children with USCP (22). Although MVFT is known to improve motor function, its effects on behavioral issues common yet often overlooked in children with CP remain unclear. Addressing these behaviors is essential for enhancing therapeutic outcomes and family quality of life.

2. Objectives

The present study investigated the impact of MVFT on behavioral problems in children with USCP.

3. Methods

3.1. Subjects

A total of 14 patients with USCP participated in this between-group, randomized, counterbalanced, single-blind, and sham-controlled research. The sample size was calculated via G*Power software (version 3.1.9.2, Kiel, Germany) with the following parameters: Test family = F tests; statistical test = ANOVA: Repeated measures, between groups; error probability α = 0.05; statistical power (1-β) = 0.80; effect size = 1.14 (23). The software recommended at least 6 participants per group. Considering a 20% dropout rate, 7 participants were selected for each group, which were equally divided into mirror training and no-mirror training groups. In this research, the inclusion criteria for children with USCP (mean age 9 years) referred to the Kermanshah Medical Center were reviewed. The inclusion criteria required sufficient trunk control for independent sitting, along with adequate verbal and cognitive abilities (including concentration, working memory, and attention). Exclusion criteria consisted of pain or prior surgery in the affected hand, epilepsy, visual impairments, or cardiac issues. These strict criteria significantly reduced the number of eligible participants (22). Finally, 14 children were selected via convenience sampling and randomly divided into two groups, i.e., the MVFT or therapy group (7 children) and the control group or no mirror group (7 children).

3.2. Procedure

The study was conducted at Sepid Neurology Clinic in Kermanshah, Iran. Each participant underwent a total of 18 sessions. The first session served as an orientation, during which demographic and clinical data were collected using the Personal Information Questionnaire and the Strengths and Difficulties Questionnaire (SDQ). Participants were also familiarized with the motor assessment and intervention procedures. Written informed consent was obtained from the parents or legal guardians of all participants under the age of 16 prior to any formal evaluation. During the intervention, participants were instructed to focus for one to two minutes on the mirror image of their unaffected hand, aiming to visualize it as their affected limb behind the mirror. Treatment commenced once the participants perceived the mirror image as representing their affected limb.

The MVFT was administered over six weeks, with three 30-minute sessions per week. During the first two to three weeks, participants performed simple motor exercises — including finger, wrist, and elbow flexion/extension; forearm rotation; and finger stretching. They practiced unilateral, bilateral, affected-hand-guided, and therapist-guided movements (approximately 15 repetitions each). The movement that produced the strongest mirror illusion was selected for use in subsequent sessions. Training then progressed to more complex tasks, such as ball transfers, dumbbell wrist flexion/extension, forearm pronation/supination, palmar and finger ball presses, and ball grasping (Figure 1).

The flexion and extension movements of the unaffected hand
Figure 1.

The flexion and extension movements of the unaffected hand

During MVFT sessions, participants performed specific exercises with their unaffected hand. A key element of this therapy was the strategic placement of a mirror precisely in the sagittal plane between the two hands. This setup created a visual illusion intended to stimulate the brain: Participants could see the actual movement of their unaffected hand while simultaneously viewing its mirror reflection, which was carefully aligned with the hidden affected hand. This visual feedback was designed to create the powerful impression that the affected hand was moving symmetrically and smoothly. Consequently, participants were motivated to consciously attempt to mimic the observed movements with their affected hand, thereby promoting the feeling of coordinated bimanual motion. This process aims to facilitate neural plasticity and improve motor function in the affected limb by tricking the brain into perceiving improved movement in the impaired hand (22, 24-26).

To minimize the influence of daily variations in bodily function, all training sessions were conducted at the same time of day for each participant, controlling for potential circadian effects. The control group performed identical motor tasks using their unaffected hand, but without the use of a mirror. The two groups attended sessions on separate days to prevent awareness of the alternative intervention, and parents were not informed of the specific exercise details to reduce the risk of bias.

3.3. Measurement of Behavioral Problems

The SDQ, a screening tool for behavioral problems in children and adolescents aged 4 to 16 years, was used to assess participants before and after the intervention. Designed by Robert Goodman in England in 1997, the SDQ has parent, teacher, and self-report versions (the latter for ages 11 - 16). The questionnaire consists of 25 items divided into five scales, each containing five items: Emotional symptoms, conduct problems, hyperactivity/inattention, peer relationship problems, and prosocial behavior. The parent-report version was used in this study. Respondents rated each item as "not true" (scoring 0), "somewhat true" (scoring 1), or "certainly true" (scoring 2). Scale scores are calculated by summing the scores of the five items within each scale, resulting in a range of 0 to 10 for each subscale. The internal consistency (Cronbach’s alpha) for the parent SDQ in this study was α = 0.7 (27, 28).

3.4. Data Analysis

Data are presented as mean ± standard deviation (M ± SD). The normality of the data was confirmed using the Shapiro-Wilk test. A two-way repeated-measures ANOVA (2 groups × 2 time points) was employed to analyze the SDQ scores. In the case of a significant group × time interaction, Bonferroni post hoc tests were used for pairwise comparisons.

For the ANOVA, effect sizes were reported as partial eta-squared (ηp2) and interpreted as follows: Small (0.01 - 0.059), medium (0.06 - 0.139), or large (≥ 0.14). For pairwise comparisons, effect sizes were calculated using Cohen’s d and classified as small (0.20 - 0.49), medium (0.50 - 0.79), or large (≥ 0.80). The percentage change (Δ%) from pretest to posttest was also calculated for each condition.

All statistical analyses were performed using SPSS version 27 (SPSS Inc., Chicago, IL, USA), with the significance level set at P < 0.05. Figures were prepared using Microsoft Excel.

4. Results

The M ± SDs of the participants’ scores by group and measurement time period are presented in Table 1.

Table 1.Mean and Standard Deviation at the Two Time Points of the Pretest and Posttest in the Two Groups a
SubscalesGroups
ExperimentalControl
PretestPosttestPretestPosttest
Emotional symptoms4.71 ± 0.953.14 ± 1.064.57 ± 0.784.57 ± 0.78
Conduct problems2.42 ± 0.972.14 ± 0.692.57 ± 0.972.42 ± 0.97
Hyperactivity problems4.14 ± 1.342.42 ± 0.974.00 ± 1.293.85 ±1.34
Peer problems3.42 ± 0.781.71 ± 0.483.28 ± 0.753.14 ± 0.89
TD 14.71 ± 2.629.28 ± 2.2114.42 ± 2.1414.00 ± 2.23
BP4.00 ± 0.815.85 ± 1.214.14 ± 0.694.28 ± 0.48

Abbreviations: TD, total difficulties; PB, prosocial behaviors.

a Values are expressed as M ± SD.

The results of the mixed analysis of variance revealed that for the total difficulties (TD) variable, the interaction effects of group × time [F(1.12) = 54.04, P < 0.001] and time [F(1.12) = 74.16, P < 0.001] were statistically significant, whereas the main effect of group [F(1.12) = 3.465, P > 0.001] was not statistically significant. The simple effects of group and time were analyzed separately because of the significance of the interaction effect. The results revealed that in the pretest phase, there was no significant difference in the average TD between the two intervention groups (P > 0.05). Compared with the control group, the experimental group presented a significant reduction in TD (P < 0.001, dav = 2.12, Δ = -40.5%) at the posttest. Pairwise comparisons revealed that TD improved significantly from pretest to postintervention (P < 0.001, dav = 2.24, Δ = -36.91%) in the experimental group.

Additionally, the results of the mixed analysis of variance revealed that for the prosocial behaviors (PB) variable, the interaction effects of group × time [F(1.12) = 33.23, P < 0.001] and time [F(1.12) = 45.23, P < 0.001] were statistically significant, whereas the main effect of group [F(1.12) = 3.465, P > 0.001] was not statistically significant. The simple effects of group and time were analyzed separately because of the significance of the interaction effect. The results revealed that in the pretest phase, there was no significant difference in the average PB between the two intervention groups (P > 0.05). The PB was also significantly greater in the experimental group than in the control group (P = 0.008, dav = 1.86, Δ = 0.31%) at the posttest. Pairwise comparisons revealed that PB improved significantly from pretest to postintervention (P < 0.001, dav = 1.01, Δ = +46.25%) in the experimental group (Figure 2).

Comparison of improvements in behavioral problems between the two groups (*significant difference with the pretest and #significant difference with the control group)
Figure 2.

Comparison of improvements in behavioral problems between the two groups (*significant difference with the pretest and #significant difference with the control group)

5. Discussion

This study is the first to examine the effect of MVFT on behavioral problems in children with USCP. The results demonstrated that MVFT significantly reduces behavioral problems and increases PB. These findings are consistent with Whittingham et al. (29), who reported that stepping stones triple P (SSTP) reduces behavioral problems in children with CP, with additional benefits from acceptance and commitment therapy (ACT). While behavioral interventions directly improve conduct, persistent motor impairments may contribute to problem recurrence, as supported by Dababneh (11), who linked social-behavioral difficulties in CP to concerns about physical appearance and reduced mirror neuron activity. In contrast, the current study applied MVFT to address motor dysfunction directly.

Supporting this approach, Farzamfar et al. (22) showed that MVFT enhances motor performance in hemiplegia. Proposed mechanisms include reduced visual attention to the affected limb (30), enhanced visual feedback, and MNS activation (31). These processes may facilitate corticospinal tract activation and rebalance interhemispheric inhibition, thereby improving motor function (20). Observing the unaffected hand’s mirror image generates motor imagery of the affected hand, activating the MNS. Buccino et al. (32) further indicated that MNS engagement stimulates the M1 cortex and reactivates motor regions related to observed actions, ultimately improving motor skills (6, 33, 34).

Sankar and Gordon et al. (35, 36) used the "Constraint Induced Movement Therapy (CIMT)" strategy to improve the affected hand of hemiplegic children. This involves physical constraint of the unaffected hand to increase the use of the affected hand, which is associated with pain in the affected limb. Yamaguchi et al. reported that while pain intensity appears to be associated with behavioral and emotional problems in children, pain anxiety may still be more strongly associated (7). The experience of pain appears to disrupt activities associated with the default mode network (DMN) and with cognitive performance (37). As a result, in the present research, focusing on exercise in the mirror by a healthy hand reduced pain anxiety in the patient and thus improved behavioral problems. Early rehabilitation on the affected side and the use of a healthy limb with the aim of stimulating the affected side stimulate the residual involved tissue to compensate for functional deficits and provide a better position for tissue reconstruction and improvement of motor and behavioral problems (38).

Additionally, mirror neurons support emotion, social interaction, and empathy (39). The MNS is essential for social communication, empathy, imitation, and action understanding, illustrating how motor function influences behavior (40). This system is part of a broader network affecting behavior, especially emotional behavior. The cerebral cortex consists of specialized regions interconnected by complex axonal pathways (41). The DMN includes subsystems linked by hubs (42), such as the PCC, insular cortex, precuneus, and parietal and prefrontal cortices (41). These regions are highly interconnected (43), with the PCC acting as an information hub involved in cognitive control (12). The PCC subregions interact with executive, attentional, motor, language, and DMNs (44). Thus, MVFT improves motor function and reduces behavioral problems (11, 45). Cummins et al. (46) found that poor motor performance reduces a child’s self-esteem, increasing peer problems, potentially due to negative peer attitudes toward children with USCP (8, 47). Improved motor function and physical appearance may help reduce these peer issues.

Schuengel et al. and Sigurdardottir highlighted that motor impairments restrict activities in young children, leading to frustration, social isolation, and maladaptive behaviors. Improving motor function in children with USCP reduces behavioral problems (10, 48), likely by decreasing frustration, promoting social inclusion, and reducing maladaptive behaviors. While MVFT shows promise in enhancing motor skills and reducing behavioral issues, it remains unclear whether these behavioral benefits stem directly from motor improvement or from a more direct neuromodulatory effect on behavior-related neural pathways. Future studies should incorporate brain imaging to precisely identify the brain regions modulated by MVFT and clarify whether it acts primarily on motor networks or directly influences behavioral and emotional circuits.

This study had several limitations. Some patients had difficulty focusing on the healthy limb’s image, which may have affected the results. Future studies should use more engaging exercises and shorter sessions with frequent breaks to address this. Another limitation was patient distraction with the mirror image and difficulty locating the affected hand behind it, which reduced treatment efficacy. Using a mirror box to conceal the affected hand is recommended for future research. Furthermore, the study focused on children aged 6 - 12, a critical period for prefrontal cortex development. Age-related physiological changes, such as decreased synaptic plasticity, can reduce the brain’s capacity for plasticity, as shown by PAS protocols. Since the intensity of PAS-induced plasticity is greater in younger individuals (49, 50), understanding the effect of age on MVFT outcomes is crucial. Future research should therefore include older age groups and utilize the self-report version of the SDQ to identify potential age-related differences in response.

The MVFT may reduce behavioral challenges in children with USCP. Motor training using a mirror shows promise as a valuable therapeutic intervention for improving behavioral outcomes in this population.

Footnotes

References

  • 1.
    Ortega-Martinez A, Palomo-Carrion R, Varela-Ferro C, Bagur-Calafat MC. Feasibility of a Home-Based Mirror Therapy Program in Children with Unilateral Spastic Cerebral Palsy. Healthcare (Basel). 2023;11(12). [PubMed ID: 37372915]. [PubMed Central ID: PMC10298458]. https://doi.org/10.3390/healthcare11121797.
  • 2.
    Patel DR, Neelakantan M, Pandher K, Merrick J. Cerebral palsy in children: a clinical overview. Transl Pediatr. 2020;9(Suppl 1):S125-35. [PubMed ID: 32206590]. [PubMed Central ID: PMC7082248]. https://doi.org/10.21037/tp.2020.01.01.
  • 3.
    Kara OK, Yardimci BN, Sahin S, Orhan C, Livanelioglu A, Soylu AR. Combined Effects of Mirror Therapy and Exercises on the Upper Extremities in Children with Unilateral Cerebral Palsy: A Randomized Controlled Trial. Dev Neurorehabil. 2020;23(4):253-64. [PubMed ID: 31514564]. https://doi.org/10.1080/17518423.2019.1662853.
  • 4.
    Alipour J, Askary R, Ahmadzadeh M. Mirror Therapy in Children with Cerebral Palsy: A Narrative Review. Journal of Clinical Physiotherapy Research. 2023;8(4):e96.
  • 5.
    Freitas PM, Haase VG. Behavioral Disorders in Unilateral and Bilateral Cerebral Palsy: A Comparative Study. International Journal of Psychiatry Research. 2024;7(6). https://doi.org/10.33425/2641-4317.1208.
  • 6.
    Brossard-Racine M, Hall N, Majnemer A, Shevell MI, Law M, Poulin C, et al. Behavioural problems in school age children with cerebral palsy. Eur J Paediatr Neurol. 2012;16(1):35-41. [PubMed ID: 22036311]. https://doi.org/10.1016/j.ejpn.2011.10.001.
  • 7.
    Yamaguchi R, Nicholson Perry K, Hines M. Pain, pain anxiety and emotional and behavioural problems in children with cerebral palsy. Disabil Rehabil. 2014;36(2):125-30. [PubMed ID: 23596998]. https://doi.org/10.3109/09638288.2013.782356.
  • 8.
    Parkes J, White-Koning M, Dickinson HO, Thyen U, Arnaud C, Beckung E, et al. Psychological problems in children with cerebral palsy: a cross-sectional European study. J Child Psychol Psychiatry. 2008;49(4):405-13. [PubMed ID: 18081767]. https://doi.org/10.1111/j.1469-7610.2007.01845.x.
  • 9.
    Voyer AP, Nadeau L, Tessier R. Social dominance in children with cerebral palsy during a problem-solving task with peers. Disabil Rehabil. 2018;40(19):2288-92. [PubMed ID: 28585442]. https://doi.org/10.1080/09638288.2017.1334237.
  • 10.
    Schuengel C, Voorman J, Stolk J, Dallmeijer A, Vermeer A, Becher J. Self-worth, perceived competence, and behaviour problems in children with cerebral palsy. Disabil Rehabil. 2006;28(20):1251-8. [PubMed ID: 17083170]. https://doi.org/10.1080/09638280600554652.
  • 11.
    Dababneh KA. The socio-emotional behavioural problems of children with cerebral palsy according to their parents' perspectives. International Journal of Adolescence and Youth. 2013;18(2):85-104. https://doi.org/10.1080/02673843.2012.655443.
  • 12.
    Deconinck FJ, Smorenburg AR, Benham A, Ledebt A, Feltham MG, Savelsbergh GJ. Reflections on mirror therapy: a systematic review of the effect of mirror visual feedback on the brain. Neurorehabil Neural Repair. 2015;29(4):349-61. [PubMed ID: 25160567]. https://doi.org/10.1177/1545968314546134.
  • 13.
    Michielsen ME, Selles RW, van der Geest JN, Eckhardt M, Yavuzer G, Stam HJ, et al. Motor recovery and cortical reorganization after mirror therapy in chronic stroke patients: a phase II randomized controlled trial. Neurorehabil Neural Repair. 2011;25(3):223-33. [PubMed ID: 21051765]. https://doi.org/10.1177/1545968310385127.
  • 14.
    Xing T, Liu X, Liu R, Shan S, Wang G. Mirror therapy: a potential rehabilitation treatment. TMR Non-Drug Therapy. 2019;2(4). https://doi.org/10.53388/tmrnd201902019.
  • 15.
    Matthys K, Smits M, Van der Geest JN, Van der Lugt A, Seurinck R, Stam HJ, et al. Mirror-induced visual illusion of hand movements: a functional magnetic resonance imaging study. Arch Phys Med Rehabil. 2009;90(4):675-81. [PubMed ID: 19345786]. https://doi.org/10.1016/j.apmr.2008.09.571.
  • 16.
    Ramachandran VS, Altschuler EL. The use of visual feedback, in particular mirror visual feedback, in restoring brain function. Brain. 2009;132(Pt 7):1693-710. [PubMed ID: 19506071]. https://doi.org/10.1093/brain/awp135.
  • 17.
    Wasaka T, Kakigi R. The effect of unpredicted visual feedback on activation in the secondary somatosensory cortex during movement execution. BMC Neurosci. 2012;13:138. [PubMed ID: 23126264]. [PubMed Central ID: PMC3508609]. https://doi.org/10.1186/1471-2202-13-138.
  • 18.
    Farrer C, Frith CD. Experiencing oneself vs another person as being the cause of an action: the neural correlates of the experience of agency. Neuroimage. 2002;15(3):596-603. [PubMed ID: 11848702]. https://doi.org/10.1006/nimg.2001.1009.
  • 19.
    Mima T, Nagamine T, Nakamura K, Shibasaki H. Attention modulates both primary and second somatosensory cortical activities in humans: a magnetoencephalographic study. J Neurophysiol. 1998;80(4):2215-21. [PubMed ID: 9772274]. https://doi.org/10.1152/jn.1998.80.4.2215.
  • 20.
    Cheng CH, Lin SH, Wu CY, Liao YH, Chang KC, Hsieh YW. Mirror Illusion Modulates M1 Activities and Functional Connectivity Patterns of Perceptual-Attention Circuits During Bimanual Movements: A Magnetoencephalography Study. Front Neurosci. 2019;13:1363. [PubMed ID: 32009873]. [PubMed Central ID: PMC6972502]. https://doi.org/10.3389/fnins.2019.01363.
  • 21.
    Chen CY, Rich TL, Cassidy JM, Gillick BT. Corticospinal Excitability in Children with Congenital Hemiparesis. Brain Sci. 2016;6(4). [PubMed ID: 27775599]. [PubMed Central ID: PMC5187563]. https://doi.org/10.3390/brainsci6040049.
  • 22.
    Farzamfar P, Heirani A, Sedighi M. The Effect of Motor Training in Mirror Therapy on Gross Motor Skills of the Affected Hand in Children With Hemiplegia. Iranian Rehabilitation Journal. 2017;15(3):243-8. https://doi.org/10.29252/nrip.irj.15.3.243.
  • 23.
    Palomo-Carrion R, Zuil-Escobar JC, Cabrera-Guerra M, Barreda-Martinez P, Martinez-Cepa CB. Mirror Therapy and Action Observation Therapy to Increase the Affected Upper Limb Functionality in Children with Hemiplegia: A Randomized Controlled Trial Protocol. Int J Environ Res Public Health. 2021;18(3). [PubMed ID: 33504040]. [PubMed Central ID: PMC7908253]. https://doi.org/10.3390/ijerph18031051.
  • 24.
    Garry MI, Loftus A, Summers JJ. Mirror, mirror on the wall: viewing a mirror reflection of unilateral hand movements facilitates ipsilateral M1 excitability. Exp Brain Res. 2005;163(1):118-22. [PubMed ID: 15754176]. https://doi.org/10.1007/s00221-005-2226-9.
  • 25.
    Smorenburg AR, Ledebt A, Deconinck FJ, Savelsbergh GJ. Matching accuracy in hemiparetic cerebral palsy during unimanual and bimanual movements with (mirror) visual feedback. Res Dev Disabil. 2012;33(6):2088-98. [PubMed ID: 22771984]. https://doi.org/10.1016/j.ridd.2012.06.004.
  • 26.
    Toh SFM, Fong KN. Systematic Review on the Effectiveness of Mirror Therapy in Training Upper Limb Hemiparesis after Stroke. Hong Kong Journal of Occupational Therapy. 2012;22(2):84-95. https://doi.org/10.1016/j.hkjot.2012.12.009.
  • 27.
    Giannakopoulos G, Dimitrakaki C, Papadopoulou K, Tzavara C, Kolaitis G, Ravens-Sieberer U, et al. Reliability and validity of the Strengths and Difficulties Questionnaire in Greek adolescents and their parents. Health. 2013;5(11):1774-83. https://doi.org/10.4236/health.2013.511239.
  • 28.
    Mieloo C, Raat H, van Oort F, Bevaart F, Vogel I, Donker M, et al. Validity and reliability of the strengths and difficulties questionnaire in 5-6 year olds: differences by gender or by parental education? PLoS One. 2012;7(5). e36805. [PubMed ID: 22629332]. [PubMed Central ID: PMC3356337]. https://doi.org/10.1371/journal.pone.0036805.
  • 29.
    Whittingham K, Sanders M, McKinlay L, Boyd RN. Interventions to reduce behavioral problems in children with cerebral palsy: an RCT. Pediatrics. 2014;133(5):e1249-57. [PubMed ID: 24709926]. https://doi.org/10.1542/peds.2013-3620.
  • 30.
    Moseley LG, Wiech K. The effect of tactile discrimination training is enhanced when patients watch the reflected image of their unaffected limb during training. Pain. 2009;144(3):314-9. [PubMed ID: 19501965]. https://doi.org/10.1016/j.pain.2009.04.030.
  • 31.
    Park EJ, Baek SH, Park S. Systematic review of the effects of mirror therapy in children with cerebral palsy. J Phys Ther Sci. 2016;28(11):3227-31. [PubMed ID: 27942154]. [PubMed Central ID: PMC5140834]. https://doi.org/10.1589/jpts.28.3227.
  • 32.
    Buccino G, Binkofski F, Riggio L. The mirror neuron system and action recognition. Brain Lang. 2004;89(2):370-6. [PubMed ID: 15068920]. https://doi.org/10.1016/S0093-934X(03)00356-0.
  • 33.
    Lingam R, Jongmans MJ, Ellis M, Hunt LP, Golding J, Emond A. Mental health difficulties in children with developmental coordination disorder. Pediatrics. 2012;129(4):e882-91. [PubMed ID: 22451706]. https://doi.org/10.1542/peds.2011-1556.
  • 34.
    Cairney J, Veldhuizen S, Szatmari P. Motor coordination and emotional-behavioral problems in children. Curr Opin Psychiatry. 2010;23(4):324-9. [PubMed ID: 20520549]. https://doi.org/10.1097/YCO.0b013e32833aa0aa.
  • 35.
    Gordon AM, Charles J, Wolf SL. Methods of constraint-induced movement therapy for children with hemiplegic cerebral palsy: development of a child-friendly intervention for improving upper-extremity function. Arch Phys Med Rehabil. 2005;86(4):837-44. [PubMed ID: 15827942]. https://doi.org/10.1016/j.apmr.2004.10.008.
  • 36.
    DeLuca SC, Case-Smith J, Stevenson R, Ramey SL. Constraint-induced movement therapy (CIMT) for young children with cerebral palsy: effects of therapeutic dosage. J Pediatr Rehabil Med. 2012;5(2):133-42. [PubMed ID: 22699104]. https://doi.org/10.3233/PRM-2012-0206.
  • 37.
    Tajik-Parvinchi D, Davis A, Roth S, Rosenbaum P, Hopmans SN, Dudin A, et al. Functional connectivity and quality of life in young adults with cerebral palsy: a feasibility study. BMC Neurol. 2020;20(1):388. [PubMed ID: 33096988]. [PubMed Central ID: PMC7583292]. https://doi.org/10.1186/s12883-020-01950-7.
  • 38.
    Risedal A, Zeng J, Johansson BB. Early training may exacerbate brain damage after focal brain ischemia in the rat. J Cereb Blood Flow Metab. 1999;19(9):997-1003. [PubMed ID: 10478651]. https://doi.org/10.1097/00004647-199909000-00007.
  • 39.
    Gallese V. Embodied simulation: from mirror neuron systems to interpersonal relations. Empathy and Fairness: Novartis Foundation Symposium 278. Wiley Online Library; 2006. p. 3-19.
  • 40.
    Oberman LM, Pineda JA, Ramachandran VS. The human mirror neuron system: a link between action observation and social skills. Soc Cogn Affect Neurosci. 2007;2(1):62-6. [PubMed ID: 18985120]. [PubMed Central ID: PMC2555434]. https://doi.org/10.1093/scan/nsl022.
  • 41.
    Hagmann P, Cammoun L, Gigandet X, Meuli R, Honey CJ, Wedeen VJ, et al. Mapping the structural core of human cerebral cortex. PLoS Biol. 2008;6(7). e159. [PubMed ID: 18597554]. [PubMed Central ID: PMC2443193]. https://doi.org/10.1371/journal.pbio.0060159.
  • 42.
    Buckner RL, Andrews-Hanna JR, Schacter DL. The brain's default network: anatomy, function, and relevance to disease. Ann N Y Acad Sci. 2008;1124:1-38. [PubMed ID: 18400922]. https://doi.org/10.1196/annals.1440.011.
  • 43.
    Parvizi J, Van Hoesen GW, Buckwalter J, Damasio A. Neural connections of the posteromedial cortex in the macaque. Proc Natl Acad Sci U S A. 2006;103(5):1563-8. [PubMed ID: 16432221]. [PubMed Central ID: PMC1345704]. https://doi.org/10.1073/pnas.0507729103.
  • 44.
    Leech R, Braga R, Sharp DJ. Echoes of the brain within the posterior cingulate cortex. J Neurosci. 2012;32(1):215-22. [PubMed ID: 22219283]. [PubMed Central ID: PMC6621313]. https://doi.org/10.1523/JNEUROSCI.3689-11.2012.
  • 45.
    Peters LH, Maathuis CG, Hadders-Algra M. Children with behavioral problems and motor problems have a worse neurological condition than children with behavioral problems only. Early Hum Dev. 2014;90(12):803-7. [PubMed ID: 25463824]. https://doi.org/10.1016/j.earlhumdev.2014.09.001.
  • 46.
    Cummins A, Piek JP, Dyck MJ. Motor coordination, empathy, and social behaviour in school-aged children. Developmental Medicine & Child Neurology. 2005;47(7):437-42. https://doi.org/10.1017/s001216220500085x.
  • 47.
    Yude C, Goodman R, McConachie H. Peer problems of children with hemiplegia in mainstream primary schools. J Child Psychol Psychiatry. 1998;39(4):533-41. [PubMed ID: 9599781].
  • 48.
    Sigurdardottir S, Indredavik MS, Eiriksdottir A, Einarsdottir K, Gudmundsson HS, Vik T. Behavioural and emotional symptoms of preschool children with cerebral palsy: a population-based study. Dev Med Child Neurol. 2010;52(11):1056-61. [PubMed ID: 20497458]. https://doi.org/10.1111/j.1469-8749.2010.03698.x.
  • 49.
    Ridding MC, Ziemann U. Determinants of the induction of cortical plasticity by non-invasive brain stimulation in healthy subjects. J Physiol. 2010;588(Pt 13):2291-304. [PubMed ID: 20478978]. [PubMed Central ID: PMC2915507]. https://doi.org/10.1113/jphysiol.2010.190314.
  • 50.
    Ghasemian-Shirvan E, Farnad L, Mosayebi-Samani M, Verstraelen S, Meesen RLJ, Kuo MF, et al. Age-related differences of motor cortex plasticity in adults: A transcranial direct current stimulation study. Brain Stimul. 2020;13(6):1588-99. [PubMed ID: 32949779]. https://doi.org/10.1016/j.brs.2020.09.004.

Crossmark
Crossmark
Checking
Share on
Cited by
Metrics

Purchasing Reprints

  • Copyright Clearance Center (CCC) handles bulk orders for article reprints for Brieflands. To place an order for reprints, please click here (   https://www.copyright.com/landing/reprintsinquiryform/ ). Clicking this link will bring you to a CCC request form where you can provide the details of your order. Once complete, please click the ‘Submit Request’ button and CCC’s Reprints Services team will generate a quote for your review.
Search Relations

Author(s):

Related Articles