INTRODUCTION
Cerebral palsy (CP) is a group of persistent nonprogressive disorders associated with postural and motor impairments and movement disorders caused by damage to the immature developing brain.1 The type of movement disorder is determined by the neurological and topographic characteristics, generally classified into spastic (bilateral and unilateral), dyskinetic (dystonic and choreoathetotic), ataxic, and nonclassifiable. Spastic CP is the most common subtype and is characterized by an increased tone and pathological reflexes.2 More specifically, spasticity is a primary impairment, defined by Lance3 as a component of upper motor neuron syndrome, and is a motor disorder characterized by a velocity-dependent increase in the tonic stretch reflex (muscle tone), with exaggerated tendon jerks resulting from stretch reflex hyperexcitability. Spasticity causes pain, muscle stiffness, and a limited range of motion and leads to secondary musculoskeletal deformities (eg, joint contracture or subluxation), thereby limiting participants' postural control and compromising their mobility and activities of daily living.4
Although the relationship between spasticity , motor outcome, and functional improvements has not been established conclusively, spasticity has been reported to have a significant negative indirect effect on functional outcome through effects on gross motor function.5 Many intervention strategies to reduce spasticity currently used for children with CP include physical and occupational therapies, orthotic devices, oral pharmacological treatment, serial casting, electrical stimulation, botulinum toxin injection, neural block using phenol or alcohol, and surgical management, such as selective dorsal rhizotomy.6 , 7 However, the evidence, to date, of the long-term effects of nonsurgical treatment of spasticity reduction is scarce.8–10 For example, botulinum toxin are injectable agents frequently used in the focal treatment of spasticity .11 The long-term effect of botulinum toxin is an area of ongoing study, although recent evidence suggests its use is associated with skeletal muscle atrophy.11 , 12
Horseback riding elicits passive and active stretching in the rider and provides sensory stimulation through rhythmic, repetitive, and variable movements. Horseback riding exercises focus on progressively challenging the rider's ability to stretch and move, while maintaining balance and posture of all body parts through the slow, steady gait of a horse.13 These exercises facilitate righting and equilibrium reactions while on the horse.14 Two commonly used types of horseback riding interventions are hippotherapy and therapeutic horseback riding (THR). The former is applied by a licensed health care professional, physical or occupational therapist, or speech and language pathologist; horse movements are used to improve balance, posture control, and motor skills as a therapeutic intervention. THR is usually applied by a trained riding instructor (who is not a therapist) with therapy-trained horses; children are taught to control the horse using basic riding skills.15 Although there is a difference in definition between these therapies, both hippotherapy and THR focus on the continuous maintenance of balance and posture during therapy sessions.
Hippotherapy and THR have been successfully used as a treatment strategy in children with CP.16 , 17 When the horse walks, the multifaceted, swinging rhythm affects the patient's girdle twice as strongly as it does when the patient walks. The rhythmical sensory stimulation derived from the movement of the horse is similar to that caused by the movement of the human pelvis during walking.18 The rider can reproduce movement patterns similar to those of natural human activities. Thus, hippotherapy and THR improve balance and functional abilities and delay the progression of disorders, particularly in children with CP.18 , 19 According to the report by Debuse et al,20 many physical therapists who use hippotherapy have shared the opinion that no other intervention is as effective in reducing spasticity and regulating muscle tone as hippotherapy . According to neurophysiological standards, this reduction in spasticity may be attributed to the astride position inhibiting hip flexion, abduction, and external rotation, as well as to the imposition of rhythmic equine movements on a patient's pelvis and trunk.21 , 22
Although numerous studies have explored the use of hippotherapy or THR to treat spasticity in children with CP, whether there is a reduction in lower-limb muscle spasticity remains controversial.14 , 23 In addition, whether any initial effect is long-lasting remains unknown. Thus, we systematically reviewed studies on the use of hippotherapy or THR to reduce lower-limb spasticity in children with CP to identify the short-term effects. We compared the effects of single and multiple sessions to determine whether the effects are long-lasting.
METHODS
We used the Preferred Reporting Items for Systematic Review and Meta-Analyses (PRISMA) checklist.24
Search Strategy
PubMed, EMBASE, the Cochrane Library, and Google Scholar databases were searched from their inception to April 2020 for interventional studies that used hippotherapy or THR to reduce muscle spasticity in children with CP. First, we searched PubMed using the following terms: (“pediatrics” OR “child” OR “children” OR “adolescent”) AND (“cerebral palsy ”) AND (“hippotherapy ” OR “horseback riding” OR “riding therapy” OR “therapeutic horseback riding ”) AND (“spasticity ” OR “Ashworth scale” OR “muscle tone”). Other databases were similarly searched. We checked all reference lists for potentially relevant articles.14 , 25 In additional, although reviews, correspondence, and editorials were excluded, their reference lists were reviewed to identify eligible studies.
Study Selection
Two investigators independently screened all titles and abstracts. Studies comparing spasticity before and after hippotherapy or THR in children with CP were included; reports describing interventions other than physical therapy were excluded. In addition, all included articles used the Ashworth scale (AS) or modified Ashworth scale (MAS) in pre- and posttreatment evaluations. Specifically, the inclusion criteria were as follows: a quantitative study design, investigation of the effects of hippotherapy or THR, evaluation using the AS or MAS, and inclusion of children with CP. Initially, the search was limited to studies published in English; thereafter, studies written in other languages that were mentioned in the studies of the initial search were considered. We included randomized controlled trials (RCTs), non-RCTs, repeated-measures design trials, and case series.
Data Extraction
We recorded the authors, publication year, study design, number of participants enrolled, number of hippotherapy or THR sessions, and results (post- vs pretreatment AS or MAS lower-extremity scores). Data on horse gait (trot, walk-trot) and the specific lower-extremity muscles tested for spasticity were not analyzed.
Although all studies used AS or MAS scores, some differences in methodology were apparent. Three studies26–28 converted 1+ to 1.5 and used a scale ranging from 0 to 4; another study23 converted 1+ to 2 and used a scale ranging from 0 to 5. Furthermore, one study25 used a scale ranging from 1 to 6, in reverse order. Another study29 scaled the AS scores per se from 0 to 4. In addition, one study30 scored flaccidity as 0, normality as 2, and mild, severe, and very severe resistance to movement of more than half the range as 4, 6, and 7, respectively. Since the tools for measuring spasticity differed across studies, the standardized mean difference (SMD) was used to normalize the data. Two studies28 , 29 expressed outcomes in medians and ranges, which were converted to means and standard deviations using the method described by Hozo et al.31 Furthermore, one study23 measured 2 hip adductors and 2 studies28 , 30 divided participants into 2 groups and measured the MAS scores separately; for these studies, we derived the mean MAS value after combining the groups/hips. For one study27 that only presented results graphically, numerical values were derived using a tool in Adobe Acrobat XI (Adobe Systems Inc, San Jose, California).
Assessment of Study Quality
The PEDro scale was used to assess the quality of evidence in each study.32 The PEDro scale uses 11 items to assess the methodological quality of a study based on important criteria, such as concealed allocation, blinding, intention-to-treat analyses, and adequate follow-up. However, in calculating the method score, 1 item (eligibility criteria) was not used; therefore, the reported score has a range of 0 to 10. A higher PEDro scale score indicates a lower risk of bias. Two reviewers independently conducted the evaluations. Cohen's kappa value, a tool used to check the consistency between reviewers, was calculated; values of 0.01 to 0.20 indicate no to slight agreement; 0.21 to 0.40, fair agreement; 0.41 to 0.60, moderate agreement; 0.61 to 0.80, substantial agreement; and 0.81 to 1.00, almost perfect agreement.33 Disagreements regarding study quality were resolved by consensus with a third reviewer.
Statistical Analysis
Three studies23 , 29 , 30 compared hippotherapy or THR + long-term conventional rehabilitation with conventional rehabilitation therapy alone; therefore, we analyzed the additive effect of hippotherapy or THR. None of these studies found that conventional rehabilitation alone was effective. Thus, we used preintervention scores as control values and compared them with postintervention scores.
AS and MAS scores were statistically analyzed. We used effect sizes as standard measures of the interventional effects on the outcome variable. Heterogeneity was calculated using the I 2 test, which identifies the percentage of variation across studies attributable to heterogeneity rather than chance. The score ranges from 0 (no heterogeneity) to 100 (maximum heterogeneity). Although both random- and fixed-effects models were used, we used the latter to check for publication bias and outcomes because significant heterogeneity (I 2 > 50) was evident. The model assumed that the true treatment effects among individual studies may not be identical and that such effects were normally distributed. The intervention period was 5 to 18 weeks in 5 studies, and 2 studies included only single sessions. Thus, we evaluated single- and multiple-session studies (the latter extending over at least 4 weeks) separately.
Given the small number of included studies, we evaluated publication bias using a funnel plot. Funnel plots were plotted with standard error and odds ratio (effect size), under the assumption that the sample error decreases and precision decreases as the number of samples in the study increases. Accordingly, publication bias was verified by checking whether there was left-right asymmetry in the plot and quantitatively evaluated using the Begg and Egger tests.
The Rmeta package in R was used for data management, statistical analyses, and graphic visualization (http://www.r-project.org ). All results are presented with 95% confidence intervals (CIs) and 2-tailed P values.
RESULTS
Search Results
A flow diagram of the study selection is given in Figure 1 . Of the 73 articles initially identified, 7 fulfilled all inclusion criteria (1 RCT, 2 non-RCTs, 2 repeated-measures design trials, and 2 case series). The full texts were reviewed by 2 authors. The extracted data are summarized in Table 1 .
Fig. 1.: Flowchart of study selection. AS indicates Ashworth scale; MAS, modified Ashworth scale.
TABLE 1 -
Summary of Reports on
Hippotherapy and
Therapeutic Horseback Riding and AS or MAS Scores
Study
Country
Study Design
Sampling (Group: Number, Age, CP, or HC)
Intervention Description
Numbers of Interventions
Sample Size
AS or MAS Scores (Pre-Tx)
AS or MAS SDs (Pre-Tx)
AS or MAS Scores (Post-Tx)
AS or MAS SDs (Post-Tx)
PEDro Scale (/10)
Alemdaroğlu et al29
Turkey
Non-RCT
IG: 9; 7.5 ± 1.7 y; CP CG: 7; 7.5 ± 1.7 y; CP
IG: 5-wk THR with Con. Tx CG: Con. Tx
10
9
2
0.57
1.25
0.32
5
Cherng et al30
Taiwan
RMD
IG: 14; [3 y 1 mo-11 y 5 mo]; CP Divided as IGA : 9, IGB : 5 after randomization
Two THR groups with different program components with 1-wk washout period IGA (9): 16-wk THR + Con. Tx, followed by 16-wk Con. Tx only IGB (5): 16-wk Con. Tx only, followed by 16-wk THR + Con. Tx
32
14
4.62
1.08
3.86
1.26
5
Lee et al26
Korea
Case series
IG: 9; 9.00 ± 2.2 y; CP
IG: 8-wk HT
16
9
1.88
0.48
1.22
0.36
4
Lucena-Antón et al23
Spain
RCT
IG: 22; 9.5 y; CP CG: 22; 8.25 y; CP
IG: 12-wk HT with Con. Tx CG: 12-wk Con. Tx
12
22
2.51
1.21
2.2
1.16
7
Baik et al25
Korea
Non-RCT
IG: 8; 12.12 ± 3.60 y; CP CG: 8; 8.12 ± 2.58 y; CP
IG: 12-wk THR CG: not described
24
8
3.75a
1.03
4.75a
0.7
5
Antunes et al28
Brazil
RMD
IG: 10; between 5 and 15 y; CP Divided as IGA : 5, IGB : 5 after randomization
Two HT groups with different orders of program (walk and walk-trot) with 1-wk washout period IGA (5): walk, followed by walk-trot IGB (5): walk-trot, followed by walk
1
20
2.13
0.44
1.36
0.59
6
Yokoyama et al27
Japan
Case series
IG: 22; 7.7 ± 2.2 y; CP
IG: 1 session of HT
1
22
2.26
1.11
0.79
0.75
4
Abbreviations: AS, Ashworth scale; CG, control group; Con. Tx, conventional treatment; CP, cerebral palsy ; HC, healthy controls; HT, hippotherapy ; IG, intervention group; MAS, modified Ashworth scale; RCT, randomized controlled trial; RMD, repeated-measures design; SD, standard deviation; THR, therapeutic horseback riding ; Tx, treatment.
a MAS grade was recorded in reverse order.
25
Quality Evaluation
The kappa index between assessors was 96.7% for the quality assessment of the included studies, indicating almost perfect agreement. According to the PEDro scale, the methodological quality of the included studies ranged from 4 to 7 (Table 2 ). As hippotherapy was directly administered to participants, concealment and blinding were evaluated as “no” in all studies. Based on the PEDro scale, 2 studies had a score of 6 to 7, which was evaluated as good, with a low risk of bias. The remaining 5 studies were evaluated as having a fair or moderate risk of bias.34
TABLE 2 -
Methodological Quality Assessment for Reports With the PEDro Scale
a
Study
A
B
C
D
E
F
G
H
I
J
K
Score
Alemdaroğlu et al29
Yes
No
No
Yes
No
No
No
Yes
Yes
Yes
Yes
5/11
Cherng et al30
Yes
No
No
Yes
No
No
Yes
No
Yes
Yes
Yes
5/11
Lee et al26
Yes
No
No
No
No
No
No
Yes
Yes
Yes
Yes
4/11
Lucena-Antón et al23
Yes
Yes
No
Yes
No
No
Yes
Yes
Yes
Yes
Yes
7/11
Baik et al25
Yes
No
No
Yes
No
No
No
Yes
Yes
Yes
Yes
5/11
Antunes et al28
Yes
Yes
No
Yes
No
No
No
Yes
Yes
Yes
Yes
6/11
Yokoyama et al27
Yes
No
No
No
No
No
No
Yes
Yes
Yes
Yes
4/11
a A: eligibility criteria were specified; B: subjects were randomly allocated to groups; C: allocation was concealed; D: the groups were similar at baseline regarding the most important outcome indicators; E: there was blinding of all subjects; F: there was blinding of all therapists; G: there was blinding of all assessors; H: measures of at least one key outcome were obtained from more than 85% of the subjects initially allocated to groups; I: all subjects for whom outcome measures were available received the treatment or, where this was not the case, data for at least one key outcome was analyzed by “intention to treat”; J: the results of between-group statistical comparisons were reported for at least one key outcome; K: the study provided both point measures and measures of variability for at least one key outcome.
Outcomes
Figure 2 graphs a forest plot summarizing the meta-analysis. Heterogeneity was evident (I 2 = 52.1%, P = .051) in terms of the clinical improvements reported after hippotherapy or THR. Using AS or MAS scores, the SMD in the fixed-effects model was −1.021 (95% CI, −1.318 to −0.724; z = −6.74; P < .001), while the SMD in the random-effects model was −1.083 (95% CI, −1.528 to −0.639; z = −4.78; P < .001); the random-effects model was preferred because of the high levels of heterogeneity. Through this meta-analysis, we determined that there was a statistically significant improvement with hippotherapy for lower-limb muscle spasticity in the short term in children with CP. When single and multiple treatments were compared, the fixed- and random-effects statistics were Q = 5.57 (P = .018) and Q = 2.95 (P = .086), respectively. There was a trend of small reduction in spasticity in multiple treatments. This trend was the same in both models, but the results differed because the probabilities varied. In the random-effects model adopted because of heterogeneity, this difference between single and multiple treatments was not significant.
Fig. 2.: Forest plot of the effects of hippotherapy and therapeutic horseback riding on lower-limb muscle spasticity . TX indicates treatment; SD, standard deviation; SMD, standardized mean difference; CI, confidence interval.
The results of the funnel plot analysis are given in Figure 3 . Our funnel plot appeared to be asymmetrical, suggesting a publication bias. However, neither the Begg test (P = .652) nor the Egger test (P = .288) indicated a significant publication bias.
Fig. 3.: Funnel plot of the pooled estimate of the random-effects model. Diagonal lines demarcate the area where 95% of points lie when a publication bias is absent.
DISCUSSION
Hippotherapy has been used for the treatment of spasticity in children with CP, but the evidence remains unclear. The present meta-analysis comprised 7 studies that reported on the effectiveness of hippotherapy or THR in reducing lower-limb muscle spasticity in children with CP. This is the first meta-analysis to confirm that hippotherapy or THR can reduce lower-limb muscle spasticity for the short term in children with CP. There was no significant difference between single and multiple sessions.
The 7 included studies had significant levels of heterogeneous characteristics in the participants and study methodologies, limiting the interpretation of the results. Six of the 7 studies (the exception was Cherng et al30 ) reported that hippotherapy or THR helped reduce lower-limb muscle spasticity . Cherng et al30 reported no improvement in hip adductor muscle tone after THR. Three studies25 , 29 , 30 used THR, while the other 4 used hippotherapy . Four studies23 , 25 , 29 , 30 had a control group, while the remaining 3 studies only evaluated an intervention group, without a comparison group. Three of the 4 studies with a control group23 , 25 , 29 evaluated children with CP under similar conditions to those of the comparison group; the exception was Antunes et al,28 who used children who were developing typically as controls but did not evaluate spasticity before and after the therapy sessions. Both Antunes et al28 and Cherng et al30 used a repeated-measures design to overcome their small sample size. Three studies23 , 29 , 30 compared conventional therapy in combination with hippotherapy or THR with conventional therapy alone. In these studies, the group with conventional therapy alone did not show a reduction in lower-extremity spasticity . To assess the cumulative effect of hippotherapy or THR, we compared pre- and post-therapy sessions in children with CP in a meta-analysis.
In addition, the 7 included studies measured spasticity in various muscles and used various analytical methods. Alemdaroğlu et al,29 Cherng et al,30 Lucena-Antón et al,23 and Antunes et al28 used hip adductors; Lee et al26 used knee flexors; and Yokoyama et al27 used the gastrocnemius muscle. To evaluate spasticity , Alemdaroğlu et al29 used the AS score, while the other studies used the MAS score. Furthermore, the score was interpreted differently across studies; thus, the SMD was applied to normalize the data. In addition, we evaluated the potential publication bias of the studies and overrepresentation of benefits by reporting only positive results. The slight asymmetry observed in the funnel plot can be considered as indicating a publication bias, but further analysis by the Begg and Egger tests failed to reveal a significant publication bias in this study.
Hippotherapy or THR can be described as a treatment approach using motor learning and sensory integration.35 At first, children with CP suffer many errors, with inconsistent attention, during hippotherapy or THR; later, unnecessary movement disappears and adaptation occurs.36 Repetitive and rhythmical movements aim to aid in learning how to provide compensatory movement by allowing the child to anticipate movements.35 Several previous studies compared the effects of short-term and long-term treatments with hippotherapy or THR in children with CP through various outcome measures such as muscle asymmetry or Gross Motor Function Measure (GMFM) scores. McGibbon et al37 reported that adductor muscle asymmetry scores were better after 12 weeks of hippotherapy than after a single session. Using the GMFM score to assess function, Žalienė et al38 found that long-term intervention (1-5 years) improved function but no short-term (10 sessions over 5 weeks) effects were identified. Žalienė et al38 explained that long-term treatment may be more effective because repetition of pelvic movements gradually restructures the child's central nervous system to increase functional activities.
However, in terms of spasticity , only short-term effects were demonstrated in our study. Evidence of a superior effect with long-term intervention compared with short-term intervention was not demonstrated. Lucena-Antón et al23 hypothesized that the improvement in muscle recruitment pattern through hippotherapy could reduce abnormal neurological spasticity -related activity. Through hippotherapy and THR, sensory stimulation is given to the entire hip and trunk muscle, similar to gait in children with CP, and through this, the change in muscle recruitment pattern is expressed as muscle activation. However, muscle activation may decrease over time. Ribeiro et al36 performed electromyography of the rectus femoris muscle after 1, 10, 20, and 25 hippotherapy sessions; improvements were evident from sessions 1 to 10 but declined thereafter in both children with CP and healthy children. Ribeiro et al36 interpreted these results as indicating that less muscle activation occurred after long-term hippotherapy due to a gradual increase in motor learning. Considering the opinion of Ribeiro et al and the intuition of Lucena-Antón et al, it may be concluded that in the initial session of hippotherapy , muscle activation occurred and spasticity reduced; however, as time passed, muscle activation occurred less and the effect on spasticity reduction decreased.
This meta-analysis has several limitations. In the included studies, the participant group was specified as children with CP; however, the participant group was heterogeneous in severity and type. In addition, it is difficult to generalize the findings because the sample size was small in each of the included studies. Second, although the AS or MAS score is often used to evaluate spasticity , it does not accurately assess the condition. Bohannon and Smith39 evaluated the MAS in measuring elbow flexor spasticity ; the interrater reliability was 86.7%, and the correlation was significant (P < .001). However, Scholtes et al40 recommended the use of the Tardieu scale rather than the MAS. Second, most of the included studies used additional conventional physical therapy, rendering it difficult to analyze the effects of hippotherapy or THR alone. Furthermore, physical therapy programs were often insufficiently described and occupational therapies were not described at all. We did not consider possible confounding effects of occupational therapy or conventional treatment. Third, in some studies, median values were presented; these were converted into means and standard deviations to increase the effect size, possibly introducing errors.
Despite these limitations, we found that hippotherapy and THR reduced spasticity in the short term but had no cumulative effects on muscle spasticity in children with CP. Both therapies seem to be auxiliary methods that temporarily alleviate side effects. However, further studies are needed to ascertain whether spasticity changes over time when measured using the MAS and Tardieu scales and when hippotherapy and THR protocols are standardized.
CONCLUSION
This meta-analysis included 7 studies and analyzed the effect of hippotherapy or THR on lower-limb muscle spasticity in children with CP. The results suggest that clinicians can use hippotherapy or THR to reduce spasticity in the short term in children with CP. There was no superior effect of multiple treatments over that of a single session, which may be related to a lack of muscle activation after motor learning and adaptation.
REFERENCES
1. Rosenbaum P, Paneth N, Leviton A, et al. A report: the definition and classification of
cerebral palsy April 2006. Dev Med Child Neurol Suppl. 2007;109:8–14.
2. Surveillance of
Cerebral Palsy in Europe. Surveillance of
cerebral palsy in Europe: a collaboration of
cerebral palsy surveys and registers. Surveillance of
Cerebral Palsy in Europe (SCPE). Dev Med Child Neurol. 2000;42(12):816–824.
3. Lance JW. Pathophysiology of
spasticity and clinical experience with baclofen. In: Lance JW, Feldman RG, Young RR, Koella WP, eds.
Spasticity : Disordered Motor Control. Chicago, IL: Year Book Medical Publishers; 1980:185–204.
4. Bhimani R, Anderson L. Clinical understanding of
spasticity : implications for practice. Rehabil Res Pract. 2014;2014:279175.
5. Kim WH, Park EY. Causal relation between
spasticity , strength, gross motor function, and functional outcome in children with
cerebral palsy : a path analysis. Dev Med Child Neurol. 2011;53(1):68–73.
6. Flett PJ. Rehabilitation of
spasticity and related problems in childhood
cerebral palsy . J Pediatr Child Health. 2003;39(1):6–14.
7. Butler C, Darrah J. Effects of neurodevelopmental treatment (NDT) for
cerebral palsy : an AACPDM evidence report. Dev Med Child Neurol. 2001;43(11):778–790.
8. Ward AB. Long-term modification of
spasticity . J Rehabil Med Suppl. 2003;(41)(suppl):60–65.
9. Kim H, Park J, Nam K. Effect of extracorporeal shockwave therapy on muscle
spasticity in participants with
cerebral palsy : meta-analysis and systematic review. Eur J Phys Rehabil Med. 2019;55(6):761–771.
10. Damiano DL. Rehabilitative therapies in
cerebral palsy : the good, the not as good, and the possible. J Child Neurol. 2009;24(9):1200–1204.
11. Nahm NJ, Graham HK, Gormley ME Jr, Georgiadis AG. Management of hypertonia in
cerebral palsy . Curr Opin Pediatr. 2018;30(1):57–64.
12. Mathevon L, Michel F, Decavel P, Fernandez B, Parratte B, Calmels P. Muscle structure and stiffness assessment after botulinum toxin type A injection. A systematic review. Ann Phys Rehabil Med. 2015;58(6):343–350.
13. Sterba JA. Does horseback riding therapy or therapist-directed
hippotherapy rehabilitate children with
cerebral palsy ? Dev Med Child Neurol. 2007;49(1):68–73.
14. Rigby BR, Grandjean PW. The efficacy of equine-assisted activities and therapies on improving physical function. J Altern Complement Med. 2016;22(1):9–24.
15. Snider L, Korner-Bitensky N, Kammann C, Warner S, Saleh M. Horseback riding as therapy for children with
cerebral palsy : is there evidence of its effectiveness? Phys Occup Ther Pediatr. 2007;27(2):5–23.
16. Zadnikar M, Kastrin A. Effects of
hippotherapy and
therapeutic horseback riding on postural control or balance in children with
cerebral palsy : a meta-analysis. Dev Med Child Neurol. 2011;53(8):684–691.
17. Whalen CN, Case-Smith J. Therapeutic effects of horseback riding therapy on gross motor function in children with
cerebral palsy : a systematic review. Phys Occup Ther Pediatr. 2012;32(3):229–242.
18. Koca TT, Ataseven H. What is
hippotherapy ? The indications and effectiveness of
hippotherapy . North Clin Istanb. 2015;2(3):247–252.
19. Meregillano G.
Hippotherapy . Phys Med Rehabil Clin N Am. 2004;15(4):843–854, vii.
20. Debuse D, Chandler C, Gibb C. An exploration of German and British physical therapists' views on the effects of
hippotherapy and their measurement. Physiother Theory Pract. 2005;21(4):219–242.
21. Lechner HE, Kakebeeke TH, Hegemann D, Baumberger M. The effect of
hippotherapy on
spasticity and on mental well-being of persons with spinal cord injury. Arch Phys Med Rehabil. 2007;88(10):1241–1248.
22. Künzle U. [
Hippotherapy Based on the Functional Theory of Movement Klein-Vogelbach:
Hippotherapy -K® Theory, Practical Application, Proof of Effectiveness]. Berlin, Germany: Springer-Verlag; 2013.
23. Lucena-Antón D, Rosety-Rodríguez I, Moral-Munoz JA. Effects of a
hippotherapy intervention on muscle
spasticity in children with
cerebral palsy : a randomized controlled trial. Complement Ther Clin Pract. 2018;31:188–192.
24. Moher D, Liberati A, Tetzlaff J, Altman DG. PRISMA Group. Preferred reporting items for systematic reviews and meta-analyses: the PRISMA statement. Int J Surg. 2010;8(5):336–341.
25. Baik K, Byeun J-K, Baek J-K. The effects of horseback riding participation on the muscle tone and range of motion for children with spastic
cerebral palsy . J Exerc Rehabil. 2014;10(5):265–270.
26. Lee I-S, Kim J-S, So-Young. The effect of
hippotherapy on
spasticity and muscular activity in children with
cerebral palsy . J Korean Soc Occup Ther. 2011;19:117–124.
27. Yokoyama M, Kaname T, Tabata M, et al.
Hippotherapy to improve hypertonia caused by an autonomic imbalance in children with spastic
cerebral palsy . Kitasato Med J. 2013;43:67–73.
28. Antunes FN, do Pinho AS, Kleiner AFR, et al. Different horse's paces during
hippotherapy on spatio-temporal parameters of gait in children with bilateral spastic
cerebral palsy : a feasibility study. Res Dev Disabil. 2016;59:65–72.
29. Alemdaroğlu E, Yanıkoğlu İ, Öken Ö, et al. Horseback riding therapy in addition to conventional rehabilitation program decreases
spasticity in children with
cerebral palsy : a small sample study. Complement Ther Clin Pract. 2016;23:26–29.
30. Cherng R-J, Liao H-F, Leung HW, Hwang A-W. The effectiveness of
therapeutic horseback riding in children with spastic
cerebral palsy . Adapt Phys Activ Q. 2004;21:103–121.
31. Hozo SP, Djulbegovic B, Hozo I. Estimating the mean and variance from the median, range, and the size of a sample. BMC Med Res Methodol. 2005;5:13.
32. Moseley AM, Herbert RD, Sherrington C, Maher CG. Evidence for physical therapy practice: a survey of the Physiotherapy Evidence Database (PEDro). Aust J Physiother. 2002;48(1):43–49.
33. McHugh ML. Interrater reliability: the kappa statistic. Biochem Med (Zagreb). 2012;22(3):276–282.
34. Cashin AG, McAuley JH. Clinimetrics: Physiotherapy Evidence Database (PEDro) Scale. J Physiother. 2019;66(1):59.
35. Casady RL, Nichols-Larsen DS. The effect of
hippotherapy on ten children with
cerebral palsy . Pediatr Phys Ther. 2004;16(3):165–172.
36. Ribeiro MF, Espindula AP, Lage JB, et al. Analysis of the electromyographic activity of lower limb and motor function in
hippotherapy practitioners with
cerebral palsy . J Bodyw Mov Ther. 2019;23(1):39–47.
37. McGibbon NH, Benda W, Duncan BR, Silkwood-Sherer D. Immediate and long-term effects of
hippotherapy on symmetry of adductor muscle activity and functional ability in children with spastic
cerebral palsy . Arch Phys Med Rehabil. 2009;90(6):966–974.
38. Žalienė L, Mockevičienė D, Kreivinienė B, Razbadauskas A, Kleiva Ž, Kirkutis A. Short-term and long-term effects of riding for children with
cerebral palsy gross motor functions. Biomed Res Int. 2018;2018:4190249.
39. Bohannon R, Smith M. Interrater reliability of a modified Ashworth scale of muscle
spasticity . Phys Ther. 1987;67(2):206–207.
40. Scholtes VA, Becher JG, Beelen A, Lankhorst GJ. Clinical assessment of
spasticity in children with
cerebral palsy : a critical review of available instruments. Dev Med Child Neurol. 2006;48(1):64–73.