Effects of Hippotherapy on Postural Stability, in Persons with Multiple Sclerosis: A Pilot Study

Effects of Hippotherapy on Postural Stability, in Persons with Multiple Sclerosis: A Pilot Study

Silkwood-Sherer, Debbie

Purpose: The purpose of this pilot study was to examine the effectiveness of hippotherapy as an intervention for the treatment of postural instability in individuals with multiple sclerosis (MS).

Subjects: A sample of convenience of 15 individuals with MS (24-72 years) were recruited from support groups and assessed for balance deficits.

Methods: This study was a nonequivalent pretest-posttest comparison group design. Nine individuals (4 males, 5 females) received weekly hippotherapy intervention for 14 weeks. The other 6 individuals (2 males, 4 females) served as a comparison group. All participants were assessed with the Berg Balance Scale (BBS) and Tinetti Performance Oriented Mobility Assessment (POMA) at 0, 7, and 14 weeks.

Results: The group receiving hippotherapy showed statistically significant improvement from pretest (0 week) to posttest (14 week) on the BBS (mean increase 9.15 points (x^sup 2^ (2) = 8.82, p = 0.012)) and POMA scores (mean increase 5.13 (x^sup 2^ (2) = 10.38, p = 0.006)). The comparison group had no significant changes on the BBS (mean increase 0.73 (x^sup 2^ (2) = 0.40, p = 0.819)) or POMA (mean decrease 0.13 (x^sup 2^ (2) = 1.41, p = 0.494)). A statistically significant difference was also found between the groups’ final BBS scores (treatment group median = 55.0, comparison group median 41.0), U = 7, r = -0.49.

Discussion: Hippotherapy shows promise for the treatment of balance disorders in persons with MS. Further research is needed to refine protocols and selection criteria.

Key words: hippotherapy, multiple sclerosis, postural stability, balance, task-oriented

(JNPT 2007;31: 77-84)


Impairment of postural stability is one of the greatest deterrents to mobility and autonomy in daily activities for persons with multiple sclerosis (MS).1″5 The causes of poor balance in individuals with MS are well documented and include decreased range of motion, weakness of trunk and lower extremity muscles, spasticity, and fatigue.3-5 Specific sensory deficits that contribute to postural instability are dysfunctions of visual, somatosensory and vestibular systems.4,6-8 Utilizing posturogaphy, Nelson et al9 confirmed that persons with MS (n – 35) have difficulty integrating information from the visual, somatosensory, and vestibular systems. Fifty-eight percent of the 12 individuals whom they classified as having low function balance scores demonstrated either a vestibular dysfunction pattern or a combination of visual-vestibular dysfunction or somatosensory-vestibular dysfunction.9 Thus, postural instability (or poor balance) in persons with MS often results from a combination of impairments of body functions and structures, making treatment of balance in individuals with MS a challenging task.

In the early 1990s trends in the treatment of neurological disorders began to change from a primary focus on impairments to a more goal-directed retraining of functional tasks, or “task-oriented” approach.10 Utilizing the task-oriented approach for treatment of balance problems, the therapist attempts to assist the patient in developing the most effective sensory and motor strategies to maintain postural control while practicing under different functional conditions and with progressive degrees of difficulty.10-12 This taskoriented approach works well for treating balance problems in persons with MS, as the effects of the many impairments are addressed simultaneously in concert with improving functional limitations.

According to Heine,13 hippotherapy can be considered as one such task-oriented multisystem approach to the treatment of persons with neuromuscular disorders including MS. Movement of the horse promotes a disassociation of the pelvis and trunk that, along with the warmth provided by the horse’s body, appears to assist in decreasing tone. Additionally, the horse’s movement displaces the subject’s pelvis through space in a manner similar to the pelvic movement used during gait, but with greater excursion (see Video I).13 Thus greater pelvic displacement increases somatosensory input through the joints and muscles. The movement through space also provides a constantly changing visual flow and increases demands to the vestibular system.13,14 To maintain balance, the client has to adjust to the pelvic movement as well as process the sensory information, thus stimulating righting and equilibrium reactions.14,15

Another advantage of hippotherapy is that while reacting to the movement of the horse, clients learn to “discover” their own solutions to the problems of staying upright on a surface that moves in three dimensions simultaneously. The physical therapist can assist this process by manipulating the environment, thereby randomizing the necessary anticipatory and reactive adjustments for postural control. This manipulation takes the form of changes in speed, direction, the addition of abrupt halts and starts, and asking the client to perform various exercises while atop the moving horse.

Thus a theoretical basis exists for the use of hippotherapy as an intervention tactic for persons with MS. However, there is sparse research on hippotherapy use in adults with neurological disorders.16 The majority of published studies and case reports relate to treatment of children with disabilities.17 22 One barrier to locating literature is a misrepresentation of the term “hippotherapy”. Authors have frequently used the terms “hippotherapy” and “therapeutic riding” interchangeably. Hippotherapy is provided by rehabilitation professionals (physical, occupational, and speech therapists) as a method of attaining functional goals in their clients/patients.23 The client does not control the movement or direction of the horse. Therapeutic riding (taught by trained instructors) is focused on teaching riding skills to persons with disabilities.23,24 Although both interventions have benefits, improper use of these terms in the research literature has made accurate assessment of their outcomes more challenging.

A second problem with hippotherapy research is that early research used small sample sizes, lacked standardized objective measures, and frequently reported results in nonpeer reviewed magazines/journals. Recently researchers have utilized the term hippotherapy accurately and been more systematic in their analysis, but the literature is still plagued by small sample sizes. Collectively these studies have demonstrated that hippotherapy has improved trunk alignment and control,25,26 enhanced symmetrical weight bearing and muscle activity,15,27 increased endurance,28 balance,15,20 coordination and sensory integration, improved motor performance,29 and decreased abnormal tone.30

Only 2 published studies have reported on the effects of using horses as an intervention for adults with MS.14,15 The earliest study by Mackay-Lyons and colleagues14 measured the effects of therapeutic riding on postural sway, gait, and changes in scores of the MS Minimal Record of Disability (MRD) and the Symptom Checklist-90-Revised (SCL-90-R). Although the subjects subjectively reported improvements in function, such as increased endurance and balance, the results of the MRD and postural sway assessments were not significant. There was improvement in relative speed and stride length during free walking and the depression/global severity scales of the SCL-90-R.14

Utilizing a single-subject experimental design, Hammer et al15 investigated the effects of hippotherapy on numerous physical functions (balance, spasticity, functional strength, coordination, pain, and activities of daily living) and the psychological well-being of persons with MS. Ten of the eleven subjects demonstrated improvement in one or more of the variables tested. Results indicated that hippotherapy intervention benefited each subject differently with the most consistent improvements observed in balance (8/11 subjects) and the role-emotional domain of the SF-36.15

Hippotherapy holds promise for enhancing balance and postural control in individuals with MS, but the efficacy of this intervention is still unclear. The supporting literature is based on single-subject designs with no control groups. Without this, it is not possible to verify that improvements in balance are due to the hippotherapy intervention and not fluctuations in the subjects’ MS symptoms. Therefore, the purpose of this study was to assess the effects of individualized hippotherapy intervention on the balance of persons with MS compared with individuals not receiving treatment. The researchers hypothesized that individuals receiving hippotherapy intervention would demonstrate an improvement in balance, while no change would be observed in a comparison group.


This pilot study was a nonequivalent pretest-posttest comparison group design.31 It was approved by the institutional review board of the researchers’ institution as well as the institutional review board of the therapeutic riding facility. All subjects were required to sign informed consent forms before beginning the study. Signed liability forms from the riding center were also required for subjects in the treatment group.


Subjects for this study were individuals with MS recruited through MS support groups of the Michigan Chapter of the National Multiple Sclerosis Society (NMSS). The inclusion criteria to participate in the study were 1) over 18 years of age, 2) ability to stand with or without an assistive device for one minute, 3) no orthopedic or medical problems unrelated to MS, 4) no previous experience with hippotherapy or therapeutic riding, 5) no allergies or aversions to horses, 6) weight less than 240 lbs, and 7) physician referral. Although we did not exclude prior riding experience (before or after the onset of MS), none of the subjects had enough riding experience to be considered proficient in horsemanship skills.

Subjects were placed into two groups. The intervention group consisted of the first 9 individuals who responded to recruitment flyers and were willing to attend weekly hippotherapy sessions at the therapeutic riding center. Although an additional nine individuals were sought to serve as a comparison group only 6 individuals volunteered. Subjects in the comparison group were offered the opportunity to participate in hippotherapy following the study if they wished. No subjects in either group received other forms of rehabilitation during the study.


To make the study as clinically relevant as possible, valid and reliable clinical measurements of balance that had been used for persons with MS were sought.32 Criterion for tool selection was the ability to administer the tool in the treatment surroundings (riding facility) and ease of administration. Additionally the tools could not fatigue subjects and needed to allow rest periods without compromising results. Based on these criteria, the Berg Balance Scale (BBS),33,34 and the Tinetti Performance Oriented Mobility Assessment (POMA)35 were chosen as outcome measures. The Clinical Test for Sensory Interaction on Balance (CTSIB)36,37 was also administered to provide information for intervention on possible sensory adaptation problems of the subjects.

The Berg Balance Test and the POMA were originally designed for assessing balance in the elderly population,33,35 but have been routinely used in clinics to assess the balance and fall risk for individuals with neurological impairments, such as post stroke and traumatic brain injury.38,39 The BBS is a 14 item balance performance battery with a maximum score of 56. It provides information on steady state and anticipatory postural control. Research has demonstrated that the Berg has an interrater reliability of 0.98 and an intrarater reliability of 0.97, within these groups.38,39 Recently, Paltamaa and colleagues40 reported the test-retest reliability for the Berg to be 0.85, with an interrater reliability of 0.99 when using the Berg for ambulatory persons with MS. For consistency of administration in this study during the tandem stance task it was decided that each person would place both the right and left leg behind with the lowest score recorded. Subjects were also asked to stand on each leg during the single leg stance task, again with the lowest score reported.

The POMA like the BBS provides information regarding steady state and anticipatory postural control. It consists of 16 items divided into subtests of balance and gait with a maximum total score of 28. The gait portion of the tool provides challenges to the subjects’ balance not provided by the BBS, in addition to the reactive postural adjustment of the nudge test. Although the reliability of the POMA has not been assessed specifically for persons with MS, it has good test-retest reliability (0.82-0.86), interrater reliability (0.910.93), and concurrent and discriminant validity in the elderly.41 Additionally the tool has good reliability for both novice (students whose k coefficients ranged 0.40-1.00 for all test items) and experienced clinicians with minimal training (k coefficients 0.40-0.75).42

The CTSIB was developed as a clinical tool to simulate the conditions of dynamic posturography developed by Nashner 36.37 jt js utilized to assess the central nervous systems (CNS) ability to integrate the visual, vestibular, and somatosensory systems by altering one or more of the systems during 6 test conditions. Since it has been shown that individuals with MS frequently have difficulty integrating the information from these three systems,9 it was decided to determine whether subjects in this study might have sensory adaptation problems, such as dependency on a specific sense for postural orientation or sensory selection problems. During each test administration the conditions were presented in the following order: standing on a firm surface, eyes open, eyes closed, and with the dome and then on the foam eyes open, eyes closed, dome. Subjects performed each condition 3 times for 30 seconds. Falls, stepping, opening eyes during eyes closed tests, raising arms to maintain balance, or excessive sway (hip strategies) stopped timing of a condition. Conditions not completed for 30 seconds in all 3 trials were recorded as abnormal. If participants demonstrated a sensory dependency or selection problem, then the environment and tasks were altered during their session to either remove or provide inaccurate information through the sensory modality in question, thus forcing the subject to rely on their less preferred senses.12 Results of the CTSIB information for all subjects is included in Table 1 as described by ShumwayCook and Horak.12

Both groups had an initial examination prior to the initiation of hippotherapy treatment, followed by rechecks at 7 and 14 weeks. All assessments were performed by either the primary author (DSS), who has experience in the assessment and treatment of individuals with MS, or the second author (HW) who was a student in the physical therapy program of Central Michigan University. To prevent fatigue from interfering with test results, the intervention group was tested in a barn adjacent to the riding facility prior to a hippotherapy session. The comparison group was assessed in a clinic setting. Although attempts were made to test all individuals at approximately the same time of the day, it was not always possible. This was not a major concern to the researchers, as it has been demonstrated that while fatigue perception in individuals with MS statistically differed between morning and afternoon testing sessions, their balance scores did not significantly differ between times of day.43

During the pretest assessments for each group, one researcher administered each standardized test, while the second observed and scored the test. The researchers then clarified any inconsistencies in interpretation of observations in an effort to improve interrater reliability. The 7 and 14 week retests were performed by either researcher, based on their availability.

Treatment Intervention

Hippotherapy intervention was provided as defined by the American Hippotherapy Association (AHA).24,44 Subjects were not instructed in riding skills, but were placed on the horse so they could respond to changes in the horse’s movement. Horses were led by an experienced horse-handler with two side-walkers for safety. All subjects were required to wear a helmet during each session. In consultation with a certified riding instructor, subjects were matched with a horse whose width and general movement accommodated the subject’s available hip range (specifically abduction) and balance abilities. Six subjects began the study using bareback pads and stirrups, while 3 subjects needed the support of a saddle during the first few weeks of riding. Two of these subjects were able to progress to a bareback pad by the midterm evaluations.

Subjects in the intervention group rode one time per week for 14 weeks in an indoor arena at a therapeutic riding center. Each session was comprised of a 5-minute warm-up, a 30 minute treatment session, and a 5 minute cool-down period. The warm up consisted of a slow walk (90-100 steps/min) without stirrups (dependent on subject’s ability) to stretch the lower extremities, and progressed to a moderate walk (125-130 steps/min) in a large oval pattern in a right and left direction. The cool down periods reversed this process from a moderate walk to a slow walk.

The 30 minute treatment sessions were individually designed by the primary researcher, an AHA registered therapist in hippotherapy, based on the results of the examination information. Notes were kept on all sessions by the researchers and modifications to activities and exercises were made based on the subject’s response to treatment. Although sessions were individualized, similar activities were performed by all participants. For example, all participants began their sessions sitting forward. In this position the subject performed trunk rotation by placing one hand on the horses’ shoulders and the other on the hind quarters. This was done in both directions to provide a stretch to trunk and adductor muscles. To practice anticipatory challenges, subjects were asked to raise their arms overhead or out to the side while sitting forward.

All subjects experienced changes in direction, such as weaving among cones, riding 10 and 20 meter circles moving both right and left, serpentine patterns, changing direction on the diagonal, figure 8’s, sudden stops and starts, walking over ground poles, as well as changes in speed of the horse, from a slow walk to a medium walk to a trot (150 steps/min), if tolerated. Each time the horse changed direction and/or speed a postural adjustment was required by the subject. Subjects who could tolerate advanced challenges to their postural control were asked to change positions on the horse (see Video 2), such as standing in their stirrups with hands on the horses shoulders (2 point-position), sitting side-ways, and riding backward.

Information from the CTSIB was used to further manipulate the activities by either taking away the sense upon which the subject was most reliant, or providing inaccurate information through that sense. For example subject 5, who demonstrated visual dependency, would sidebend her trunk to the left whenever she closed her eyes while sitting on the moving horse. To improve her postural control without relying on her visual input we had her close her eyes and made small circles around barrels in a direction that caused her to lean to the right based on the vestibular and somatosensory information she was receiving. This resulted in a correction of her trunk to neutral alignment in a frontal plane (see Video 3). She was also asked to sit sideways on the horse facing the walls of the riding arena. This provided her with visual flow that conflicted with her vestibular and somatosensory information. If the subject was allowed to sit sideways facing the center of the arena, she tended to use a fixed visual point to decrease the conflict, thus continuing to rely upon her visual system. After 6 sessions the subject was able to independently maintain neutral trunk alignment with eyes closed while on a moving horse.

Data Analysis

SPSS 13.0 statistical software was used for data analyses. Nonparametric statistical tests were utilized due to the small sample size and the ordinal scales of the assessment tools.31 Friedman’s Two-Way Analysis of Variance Test (ANOVA) was used to calculate the pre-mid-post test within group scores for both the Berg and POMA. For the intervention group Wilcoxon’s signed-rank test was used to determine when the greatest changes in balance scores occurred. A Mann Whitney U was used to determine between group comparisons of balance, as well as to determine any differences between the groups in relation to age and number of years with MS. Chi-Square analysis was used for the nominal data of gender and type of MS. All statistical analyses were calculated using alpha levels of 0.05.

One-tailed analysis was used when comparing the midterm and posttest assessments between the groups, since it was expected that the intervention would improve the subjects’ balance scores. Two-tailed analysis was used for the pretest and demographic comparisons.31

Post test data for one subject in the intervention group was not used in the final analysis because this individual began steroid treatments in week 13. Post test data for a second person in the intervention group was not collected, as this individual did not complete the study due to an exacerbation that began during week 9. Finally one subject in the comparison group did not attend the final testing session. The final number of subjects in the intervention group was 7 with 5 individuals in the comparison group.


Demographic data for the groups is listed in Table 1. Ages of participants in the intervention group ranged from 24-72 years (mean 42.4, SD = 14.2), while members of the comparison group ranged from 36-63 years (mean 47.7, SD = 9.3). The mean number of years that individuals in the intervention group had been diagnosed with MS was 9.9 (SD = 8.2), and 12.6 (SD = 7.6) years for the comparison group. There were no statistical differences between the groups with regard to gender (p = 1.00), type of MS (p = 1.00), age (p = 0.549), or years with MS (p = 0.507).

Table 2 provides the raw data from the Berg and POMA assessments for each subject, while average means for both groups are presented in Figure 1. Friedman’s ANOVA revealed no statistical differences between the pretest, midterm or posttest for the Berg (x^sup 2^(2) = 0.40, p = 0.819) or the POMA (x^sup 2^(2) = 1.41,P = 0.494) in the comparison group. Statistically significant differences in scores for the Berg (x^sup 2^(2) = 8.82, p = 0.012) and the POMA (x^sup 2^(2) = 10.38, p = 0.006) were found in the intervention group. The most significant change occurred between the pre and midterm tests (Berg pretest Md = 35 and midterm Md = 50, T = O, p = 0.016, r = -0.790 and POMA pretest Md = 17 and midterm Md = 20, T = 0, p = 0.016, r = 0.789) (Table 3).

Specific task items from the BBS were analyzed. These included standing with eyes closed, standing with feet together, forward reach, retrieving an object from the floor, turning 360°, alternating stool touch and standing on one foot. There were no statistically significant changes in any of the items for the comparison group. In contrast the mean rank change (1.50 to 2.07) of the alternating stool touch task showed significant change (x^sup 2^(2) = 4.67, p = 0.037) for the intervention group.

Between group comparisons revealed no statistical difference between the pretest Berg (p = 0.813) or POMA (p = 0.906) scores. There was also no statistically significant difference between the midterm scores for either assessment (Berg p = 0.204, POMAp = 0.104). A statistically significant difference was found between the posttest Berg scores (p = 0.043), but not the POMA (p = 0.070) (Fig. 1, Table 3).


Consistent with the findings of Hammer et al,15 the group receiving hippotherapy had statistically significant improvement in scores on both standard balance tests (BBS and POMA) following intervention. The comparison group demonstrated no improvement in scores, although small fluctuations between the three testing sessions were observed for all members. This may have been caused by the many factors (ie heat sensitivity and fatigue) that can influence the ability of a person with MS on any day. With the exception of subject 5’s BBS scores, the intervention group improved or maintained their tests scores throughout the 14 weeks. This suggests that hippotherapy intervention may have had an effect on postural stability, since score fluctuations were not observed. The effect sizes in Table 3 also demonstrate that the differences between the groups became progressively larger as one group received intervention. The final effect sizes of -0.43 and -0.49 for the POMA and BBS respectively, suggests hippotherapy intervention appeared to have a medium effect on the changes in mean rank scores.45

It is important to determine if positive changes in balance scores are clinically and functionally relevant. Cattaneo and colleagues46 found that a combination of balance, assistive device use and ambulation were the best predictors of fall risk in persons with MS. However, the single best predictor was the Equiscale test, a balance test derived from components of the POMA and BBS. Although fall risk was not specifically measured, based on Cattaneo et al’s findings it is logical that the improvement in balance scores of the subjects who received hippotherapy correlates to a potential decrease in fall risk.

It is also important to compare hippotherapy treatment to other physical therapy interventions. Smedal et al47 demonstrated improved BBS scores for 2 patients with MS following intense NDT training of 1 hour per day, 5 days a week. Lord et al48 compared the use of neurofacilitation and task oriented approaches. Both groups had improved BBS scores, but there was no difference between the two techniques after 15 to 19 sessions. Our intervention group had similar improvements in BBS scores to the individuals in Lord’s study, and better gains than observed in the Smedal study. The primary difference is that the improvement occurred with less intervention (thirteen 40 minute sessions). Although direct comparisons cannot be made, and a specific study comparing techniques needs to be undertaken, it appears hippotherapy intervention may be equivalent to other traditional PT approaches and an option for improving postural stability in persons with MS.

In this study, the post intervention POMA scores were not significantly different between the groups, despite the significant within group improvement of the intervention group. There are several possible explanations for this effect. Although not statistically different, the comparison group’s POMA mean score and rank were higher than the intervention group’s at initial assessment. The intervention groups’ considerable improvement over their own pretest POMA scores was not large enough to overcome the pretest difference. This may be because the POMA’s incremental scale is narrower than the BBS making it less sensitive. Tesio and colleagues49 have also suggested the POMA may be too redundant and easy for persons with MS.

The intervention group’s average scores for the last 7 weeks of treatment did not show a significant change, although subjects maintained the observed improvement of the first 7 weeks. The subjects’ skills may have stabilized, but this is more likely an example of Schmidt and Lee’s50 logarithmic law of practice. This law states that skill improvement is linearly related to the amount of improvement left to attain. Large gains in skill seen early in the intervention with smaller incremental changes later are consistent with this law of practice. Another possible explanation is a ceiling effect of the testing tools.39,43 Several of the subjects in the intervention group (subjects 2,3,4) were near or at the maximum score for both scales during their initial examination. This did not allow any improvement in their balance to be measured by either tool. This finding is consistent with Hammer et al’s15 observations.

It was expected that balance would improve after hippotherapy, since riding is considered a balance-demanding activity.16 The movement of the horse, combined with appropriate equipment selection, is purported to provide input to the motor, visual, somatosensory (proprioceptive, tactile), and vestibular systems of the individual subjects.13 Individuals with impaired nervous systems tend to have fewer movement strategies and therefore become more cautious limiting their interaction with the environment.51 A therapist directing a hippotherapy session can manipulate the movement of the horse, tasks, and environment in such a way that the individual’s preferred movement patterns are not adequate to maintain postural control. By affecting several subsystems simultaneously the subjects had to explore more appropriate movement strategies to prevent loss of dynamic stability. This could include a reorganization of how the individual used and weighted sensory information while receiving conflicting sensory input.51 Hippotherapy treatments not only allowed the subjects an opportunity to develop, refine, and practice motor patterns, but also permitted concurrent practice in the integration of sensory information in a controlled environment as a whole task activity.52~54 Research has also demonstrated that discovery learning and random practice are more effective for long-term retention of a task.53,54 In this study, the therapists manipulated the environment by varying the movement, direction, and speed of the horse as well as the subject’s position on the horse, allowing the subjects to practice postural control and balance under a variety of unpredictable conditions. This more accurately simulates the random use of balance and postural control of everyday tasks.

This study has limitations. Subjects were not randomly assigned to groups. Those who volunteered for hippotherapy intervention may have been more motivated than the comparison group members who were recruited later. The small number of subjects necessitated the use of nonparametric analysis and makes it difficult to generalize this information to individuals with different types of MS. There was potential for bias since the researchers were not masked to subject participation. During the examination procedures the researchers were careful to utilize the same instructions with all participants. However, there was the potential for a Hawthorne effect since the intervention group was examined at the riding center, while the comparison group was evaluated in a clinical setting.31 Variables that may have affected outcome between the groups, such as cognitive impairments that might affect motor learning, fatigue, or level of motor and sensory impairments, were not controlled. Finally, the Berg and POMA did not appear to be sensitive enough to measure improvement for subjects with mild balance problems.

Additional research is needed regarding the use of this therapeutic intervention. Suggestions to improve this study would be a larger sample size to improve the homogeneity of the subjects and the use of masked evaluators. Measurement tools such as timed tandem stance, one-leg stance, and functional self-generated perturbations (functional reach and step test) have been shown to be better measures of balance for ambulatory individuals with mild balance difficulties,43 and their inclusion in future research is suggested. A timed walk test might provide more meaningful information than the gait component of the POMA. Timing of these tests would allow for the use of parametric data analysis. The Dynamic Gait Index (DGl) to measure gait under conflicting sensory input might provide information on how well the intervention transfers to a functional task.32 Finally, the addition of a second postintervention assessment after one month of no intervention could provide information on the retention of improved postural stability.


The results of this pilot study demonstrated a statistically significant improvement in balance as measured by the Berg Balance Scale and POMA following 7 weeks of hippotherapy intervention. The comparison group had no improvement in balance. The intervention also produced a between group difference in the BBS scores by 14 weeks, suggesting that improvements in the intervention group may have been caused by the hippotherapy treatments. The small number of participants and the use of nonparametric analysis of the data make it difficult to state with confidence that hippotherapy would improve balance for all persons with MS. However, this study does strengthen the literature supporting the use of hippotherapy as a possible intervention for balance disorders in persons with MS. A multicenter study using timed balance tests in addition to the BBS and DGI would be a logical step for future research.


1. National Multiple Sclerosis Society. The Library & Literature Page. Gait or walking problems the basic facts. Available at: http://www.nmss.org/ Brochures-On%20Gait.asp. Accessed May, 23 2006.

2. Ford HL, Gery E, Johnson MH, Tennant A. Health status and quality of life of people, with multiple sclerosis. Di.iabil Kehabil. 2001;23:516521.

3. Calebresi PA. Diagnosis and management of multiple sclerosis. Am Fam Physician. 2004;70:1935-1944.

4. Paty DW, Poser CM. Clinical symptoms and signs of multiple sclerosis. In: Poser CM, ed. The Diagnosis of Multiple Sclerosis. New York: Thieme-Stratton; 1984:27^3.

5. Miller AE. Clinic features: In: Cook S, ed. Handbook of Multiple Sclerosis. New York: M Dekker; 1990:169-186.

6. Ruelen JPH, Sanders ACM, Hogenhuis LAH. Eye movement disorders in multiple sclerosis and optic neuritis. Brain. 1983:106:121-140.

7. Grenman R. Involvement of the audiovestibular system in multiple sclerosis. An otoneurologic and audiologic study. Ada Otolatyngol Suppl. 1985:420:1-95.

8. Williams NP, Roland PS, YeIHn W. Vestibular evaluation in patients with early multiple sclerosis. Am J Otol. 1997:18:93-100.

9. Nelson SR, DiFabio RP, Anderson JH. Vestibular and sensory interaction deficits assessed by dynamic platform posturography in patients with multiple sclerosis. Ann Otol Rhinol Laryngol. 1995:104:62-68.

10. Heriza C. Motor development: traditional and contemporary theories. In: Contemporary Management of Motor Control Problems. Proceedings of the II Step Conference. Alexandria: APTA, 1991:99-126.

11. Montgomery PC. Perceptual Issues in Motor Control. In: Contemporary Management of Motor Control Problems. Proceedings of the II Step Conference. Alexandria: APTA; 1991:175-184.

12. Shumway-Cook A, Horak FB. Balance rehabilitation in the neurological patient. Course Syllabus. Seattle: NERA, 1992. Cited in: ShumwayCook A, Woollacott MH. Motor Control: Theory and Practical Applications, 2nd ed. Baltimore: Williams & Wilkins; 2001:285-287.

13. Heine B. Hippotherapy. A multisystem approach to the treatment of neuromuscular disorders. Aust J Physiother. 1997;43:145-149.

14. Mackay-Lyons M, Conway C, Roberts W. Effects of therapeutic riding on patients with multiple sclerosis: A preliminary trial. Phvsiother Can. 1988:40:104-109.

15. Hammer A, Nilsagård Y, Forsberg A, et al. Evaluation of therapeutic riding (Sweden)/hippotherapy (United Stated). A single-subject experimental design study replicated in eleven patients with multiple sclerosis. Physiother Theory Pract. 2005:21:51-77.

16. Pauw J. Therapeutic horseback riding studies: problems experienced by researchers. Physiotherapy. 2000:86:523-527.

17. Wheeler A. Hippotherapy as a specific treatment: A review of literature. In: Engel BT, ed. Therapeutic Riding II: Strategies for Rehabilitation. Durango, CO: Barbara Engel Therapy Services; 1997:25-29.

18. Bertoti D. Effects of therapeutic horseback riding on posture in children with cerebral palsy. Phys Ther. 1988;68:1505-1512.

19. Hansen K. A group case study: hippotherapy as a means of improving gross motor function in children with cerebral palsy. In: Engel BT, ed. Therapeutic Riding II: Strategies for Rehabilitation. Durango, CO: Barbara Engel Therapy Services; 1997:233-240.

20. Biery MJ, Kauffman N. The effects of therapeutic horseback riding on balance. Adapted P Act Q. 1989;6:l-29.

21. Wingate L. Feasibility of horseback riding as a therapeutic and integrative program for handicapped children. Phys Ther. 1982;62:184-I86.

22. McKinnon J, Noh S, Laliberte D, Lariviere J, Allan D. Therapeutic horseback riding: a review of the literature. Phs Occup Ther Pediatr. 1995:15:1-15.

23. Silkwood-Sherer D. The difference lies in the perspective. NARHA ‘s Stride. 2003:9:14-16.

24. Meregillano G. Hippotherapy. Phvs Med Rehahil CHn N Am. 2004; 15: 843-854.

25. Haehl V, Giuliani C, Lewis C. Influence of hippotherapy on the kinematics and functional performance of two children with cerebral palsy. Pediatr Phys Ther. 1999; 11:89-101.

26. MacPhail HEA, Edwards J. Golding J, et al. Trunk postural reactions in children with and without cerebral palsy during therapeutic horseback riding. Pediatr Phys Ther. 1998; 10:143-147.

27. Benda W, McGibbon NH, Grant KL. Improvements in muscle symmetry in children with cerebral palsy after equine-assisted therapy (hippotherapy). J A Item Complement Med. 2003;9:817-825.

28. McGibbon N, Andrade C, Widener G, Cintas H. Effect of an equinemovement therapy program on gait, energy expenditure, and motor function in children with spastic cerebral palsy: a pilot study. Dev Med Child Neural. 1998;40:754-762.

29. Casady RL, Nichols-Larsen DS. The effect of hippotherapy on ten children with cerebral palsy. Pediatr Phys Ther. 2004;16:165-172.

30. Lechner HE, Feldhaus S, Gudmundsen L, et al. The short term effect of hippotherapy on spasticity in patients with spinal cord injury. Spinal Cord. 2003;41:502-505.

31. Portney LG, Watkins MP. Foundations of Clinical Research: Applications to Practice. Upper Saddle River, NJ: Prentice Hall, Inc.; 2000: 473-490.

32. Cattaneo D, Regola A, Meotti M. Validity of six balance disorder scales in persons with multiple sclerosis. Disabil Rehabil. 2006:30:789-795.

33. Berg KO, Wood-Dauphinee SL, Williams JI,. Gayton D. Measuring balance in the elderly: preliminary development of an instrument. Physiother Can. 1989;41:304-311.

34. Berg KO, Wood-Dauphinee SL, Williams JI, Maki B. Measuring balance in the elderly: validation of an instrument. Can J Publ Hlth. 1992:83:87-92.

35. Tinetti M. Performance-oriented assessment of mobility problems in elderly patients. J Am Geriatr Soc. 1986;34:119-126.

36. Shumway-Cook A, Horak F. Assessing the influence of sensory interaction of balance. Suggestion from the field. Phvs Ther. 1986;66:15481550.

37. Horak F. Clinical measurement of postural control in adults. Phys Ther. 1987:67:1881-1885.

38. Berg KO, Wood-Dauphinee SL, Williams JI. The balance scale: reliability assessment with elderly residents and patients with an acute stroke. Scand J Rehabil Med. 1995;27:27-39.

39. Newstead A, Hinman M, Toberlin J. Reliability of the Berg Balance Scale and Balance master limits of stability tests for individuals with brain injury. JNPT. 2005;29:18-23.

40. Paltamaa J, West H, Sarasoja T, Wikström J, Mälkiä E. Reliability of physical functioning measures in ambulatory subjects with MS. Physiother Res Int. 2005;10:93-109.

41. Faber MJ, Bosscher RJ, van Wieringen PCW. Clinemetric properties of the performance oriented mobility assessment. Phvs Ther. 2006;86:944-954.

42. Cipriany-Dacko LM, Innerst D, Johannsen J, Rude V. Interrater reliability of the Tinetti balance scores in novice and experienced physical therapy clinicians. Arch Phys Med Rehahil. 1997;78:1160-1164.

43. Frzovic D, Morris ME, Vowels L. Clinical tests of standing balance: performance of persons with multiple sclerosis. Arch Phys Med Rehabil. 2000;81:215-221.

44. American Hippotherapy Association. The present use of hippotherapy in the United States page. Available at: htpp://www.americanhippotherapy association.org/aha_hpot_A-use.htm. Accessed May 23, 2006.

45. Field A. Discovering Statistics Using SPSS, 2nd ed. Thousand Oaks, CA: SAGE Publications Ltd; 2005:31-33.

46. Cattaneo D, Nuzzo C, Fascia T, et al. Risk of falls in subjects with multiple sclerosis. Arch Phys Med Rehabil. 2002;83:864-867.

47. Smedal T, Lygren H, Myhr KM, et al. Balance and gait improved in patients with MS after physiotherapy based on the Bobath concept. Physio/her Res Im. 2006; 11:104-116.

48. Lord SE, Wade DT, Halligan PW. A comparison of two physiotherapy treatment approaches to improve walking in multiple sclerosis: a pilot randomized controlled study. Clin Rehahil. 1998:12:477-486.

49. Tesio L, Perucca L, Franchignoni FP, Battaglia MA. A short measure of balance in multiple sclerosis: validation through rasch analysis. Functional Neural. 1997; 12:255-265.

50. Schmidt RA, Lee TD. Motor Control and Learning: A Behavioral Emphasis. Champaign, IL: Human Kinetics; 2005. Cited in: Shumway-Cook A, Woollacott MH. Motor Control: Translating Research into Clinical Practice, 3rd ed. Baltimore: Lippincott Williams & Wilkins; 2007:35.

51. Shumway-Cook A, Woollacott MH. Abnormal postural control. In: Shumway-Cook A, Woollacott MH. Motor Control: Theory and Practical Applications, 2nd ed. Baltimore: Williams & Wilkins; 2001:248-270.

52. Horak FB. Assumptions underlying motor control for neurological rehabilitation. In: Contemporary Management of Motor Control Problems. Proceedings of the Il Step Conference. Alexandria: APTA; 1991: 11-27.

53. Nicholson DE. Motor learning. In: Fredericks CM, Saladin LK, ed. Pathophysiology of Motor Systems: Principles and Clinical Presentations. Philadelphia: FA Davis Company; 1996:238-251.

54. Schmidt RA. Motor learning principles for physical therapists. In: Contemporary Management of Motor Control Problems. Proceedings of the II Step Conference. Alexandria: APTA; 1991:49-63.

Debbie Silkwood-Sherer, PT, MS, and Heather Warmbier, MPT

Graduate Program in Physical Therapy, Central Michigan University, Mt. Pleasant, Michigan

Address correspondence to: Debbie Silkwood-Sherer, E-mail: silkwld@cmich.edu

Copyright © 2007 by Lippincott Williams & Wilkins

ISSN: 1557-0576/07/3102-0077

DOl: 10.1097/NPT.Ob013e31806769f7

Copyright Neurology Report Jun 2007

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