Parkinson disease (PD) is a progressive degenerative neurological disorder of the basal ganglia.1 Because of dopamine deficiency, the brain fails to properly stimulate or inhibit various motor function pathways. Hence, individuals with PD usually encounter difficulty with movements.2 In addition, individuals with PD demonstrate impaired ability in active muscle control, which can potentially result in poor mobility.3 Consequently, this can lead to a pathological gait pattern and affect an individual's quality of life.4 Furthermore, individuals with PD may be affected by other motor symptoms, such as progressive bradykinesia, hypokinesia, tremor, rigidity, and impaired postural control.5 The decline in the movement function of individuals with PD, along with the associated decrease in quality of life, is commonly observed in the development of PD.2 Hence, the disease has large effects on balance, physical function, and gait performance. As a result, it is not uncommon to incorporate balance training and gait reeducation into rehabilitation in order to prevent falls and optimize quality of life for individuals with PD.4
Extensive evidence has shown how the balance and gait of individuals with PD may be improved by various exercise interventions, including physiotherapy, aerobic training, and resistive training.4,6 For instance, land-based interventions are able to improve the gait parameters6–8 and balance9–12 in individuals with PD. The most commonly adopted land-based interventions include trunk mobility training,11 postural stability training,11 treadmill walking,6 progressive strengthening exercises,7 active limb mobilization,8 Tai Chi,9 and gait reeducation.10 In recent decades, aquatic therapy, an alternative to land-based interventions, has been advocated as an effective means of improving balance in individuals with PD.11,12 Aquatic therapy uses the physical properties of water to facilitate improvement. For example, the hydrostatic pressure and warmth of water contribute to pain relief and muscle relaxation,13,14 the turbulence and dragging force of water contribute to a reduction in fall risk,13 and the viscosity and the cushioning effect of water allow patients with neurological deficits to have a longer buffer time for movement control, which may potentially improve balance. The most common aquatic exercises include stretching exercises, trunk mobility exercises,12 Ai Chi,15,16 gait training,17 water resistive strengthening exercises,17,18 and circuit dual-task balance training.17
Although both land- and water-based interventions have been shown to be effective in improving the static and dynamic balance of individuals with PD, Volpe et al12 revealed that individuals with PD who participate in aquatic therapy achieve a greater improvement in balance.12 This may be explained by the aforementioned advantageous physical properties of water. Yet, the optimal design and combination of water-based interventions remain unclear. As a result, a new combination of an evidence-based intervention (Ai Chi), gait training, and balance training was proposed for our study.
Ai Chi applies the concepts of Tai Chi with conventional aquatic exercises.13 With a total of 16 standardized movement katas, Ai Chi involves a series of slow and rhythmic movement patterns performed standing in a pool, with an emphasis on coordination of the lower limbs, upper limbs, and trunk movements synchronized with breathing.13,19 The benefits of Ai Chi are well documented and can be used to compare with land-based Tai Chi. For instance, static and dynamic standing balance can be trained through constant weight shifting, trunk movement, and pivoting on the stance leg. Similarly, Ai Chi allows individuals to experience a reduction in the base of support with progressive complexity and diversity of movement patterns that can reasonably challenge balance.19
Despite studies indicating that aquatic exercises have moderate positive effects in improving static and dynamic balance, there is currently limited evidence exploring the effects of such exercises, and in particular Ai Chi, on lower-limb muscle activation and gait variability among individuals with PD as compared with land-based interventions. In addition, only one study has investigated the effects of aquatic exercise therapy on gait variability using a motion capture system; this study reported no significant differences between the exercise group and the control group.20 Therefore, the current study investigates the effects of a group-based aquatic exercise program (Ai Chi) on gait and balance variability in individuals with PD. To the best of the authors' knowledge, this is the first study to use surface electromyography (sEMG) and inertial measurement units (IMUs) to measure gait variability in individuals with PD post–Ai Chi intervention. Hence, the objective of this pilot study was to investigate the effect of a structured aquatic exercise program (combination of Ai Chi, gait training, and balance training) on balance and gait variability in individuals with PD.
This study was a single-group, quasi-experimental cohort study with pretest and posttest comparison.
Sample size calculations were based on balance and gait parameter effect sizes from previous studies of individuals with PD.21 An a priori sample size calculation based on gait and balance variables, with a 10% dropout rate, 80% power, and α set at .05, showed that we needed at least 10 participants in the intervention group. Thirteen participants with PD were recruited from the Hong Kong Parkinson's Disease Association through convenience sampling. Participants were screened for the following inclusion criteria: (1) diagnosed with idiopathic stage 1-3 PD (Hoehn and Yahr Scale); (2) aged 18 to 75 years; (3) no fear of water; and (4) able to perform movements in water in standing position. Participants were excluded if they were diagnosed with (a) other neurological impairments or cognitive impairments that made them unable to give their own consent for inclusion in the study; (b) any infectious diseases; or (c) skin conditions that contraindicated participation in aquatic exercises.
Participants who met the inclusion and exclusion criteria were invited to participate on a voluntary basis. An information session was arranged for each participant, and an information sheet was provided. All participants gave written informed consent to participate in the study, which was collected after the information session. The study's protocols were approved by the Departmental Research Committee of the Hong Kong Polytechnic University's Department of Rehabilitation Sciences (reference no.: HSEARS20190611001).
Preintervention assessment was scheduled 1 week before the study was initiated. The assessment was performed by a physiotherapist with 10 years of experience, and the tests were performed by the same person on each occasion to improve reliability. The tests consisted of assessments on gait and balance, which were performed over 2 days to minimize fatigue. The gait assessment was conducted in the Gait and Motion Analysis Laboratory, and the balance assessment was performed in the Neuro-rehabilitation Laboratory at the Hong Kong Polytechnic University, where the room temperature was controlled at 25.5 °C. Balance and gait assessments were performed within 3 hours of the participant taking their prescribed medication in order to avoid motor fluctuations. All participants reported that they were in the “on phase,” and for each participant, the time since medication was the same at the pretest and posttest assessments.
All the participants then underwent aquatic training twice a week for 6 weeks (12 sessions in total), with each session lasting 60 minutes. One participant was lost to follow-up due to a change in medical status. All participants were required to avoid participation in other exercise or therapeutic interventions during the study period. Postintervention assessment was sc-heduled 1 week after the intervention was completed, using the same settings as in the preintervention assessment (Figure 1).
Gait Measurement. Participants were first asked to perform the Timed Up and Go (TUG) test, followed by the Ten Meter Walk Test (10MWT) at their usual speed,22 with IMUs and sEMG electrodes in situ. The IMUs collected acceleration data for motion tracking by referencing each sensor for comparison.23 sEMG is a measurement of the change in electrical potential across the muscle fiber membrane.24 The locations of the IMUs and sEMG electrodes are listed in Table 1. The 10MWT was videotaped in both vertical and horizontal planes.
TABLE 1 -
Locations of sEMG Electrodes and MVC Testing Procedures
||Location of the Electrode
||MVC Testing Procedure
||Midpoint between ASIS and patella
||Participants laid in supine position with tested hip flexed 45° and supported. Investigator resisted isometric knee extension for 5 s.
||Midpoint between gluteal fold and knee crease, 2 cm lateral from central line
||Participants laid in prone position with tested knee flexed 90°. Investigator resisted isometric knee flexion for 5 s.
||Belly of TA
||Participants laid in supine position with tested ankle in neutral. Investigator resisted isometric dorsiflexion for 5 s.
||Belly of GME, 2 cm lateral from the central line
||Participants performed heel-off in single-leg standing position and sustained for 5 s.
Abbreviations: ASIS, anterior superior iliac spine; BF, biceps femoris; GME, gastrocnemius; MVC, maximum voluntary contraction; RF, rectus femoris; sEMG, surface electromyography; TA, tibialis anterior.
The sEMG activities and IMU signals were recorded using Akto sensors of the Myon system (SX230 surface EMG sensor, Biometrics Ltd, Newport, United Kingdom) and a customized data logger at a 1000-Hz sampling rate. The raw sEMG signals were digitized using a bandpass filter (at 20-300 Hz) and a root-mean-square sliding window (50-millisecond constant) (MatLab 2017a; Mathematical computing software; The MathWorks, Inc, Natick, Massachusetts). The sEMG signals were then exported using LabView8.6 (National Instruments Corporation, Austin, Texas). In the 10MWT, the gait parameters and muscle activities of the first and last 2 m were not processed so that the effects of acceleration and deceleration were eliminated. Only the gait parameters and muscle activation of the mid-6 m of the 10MWT were determined using our customized programs. The amplitudes of the sEMG signals for the corresponding muscles were then calculated and averaged. The maximum voluntary contraction (MVC) data collected were also processed in the same way, with the first 5 seconds of contraction being taken for data processing. The percent maximum voluntary contraction (%MVC) was then generated and compared between pre- and postintervention assessments.
Surface Electromyography. The sEMG signals were analyzed to measure activities of the bilateral rectus femoris (RF), biceps femoris (BF), tibialis anterior (TA), and gastrocnemius (GME), as these are the 4 key muscles involved in gait to generate movements at the hip, knee, and ankle joints (Figure 2).25 The electrodes were placed 2.5 cm apart to avoid interference.26 Participants were asked to perform an MVC for 5 seconds to normalize sEMG under the instruction of an investigator. Table 1 provides details of the locations of the sEMG electrodes and the MVC procedures. The data are represented by mean %MVC.
Spatiotemporal Parameters. Gait speed, cadence, stride duration, step duration, swing duration, and double support duration were calculated by IMU recording. The IMU sensors were placed at the S2 spinous process, 2 cm above the femoral lateral epicondyle (Figure 3A) and 2 cm above the lateral malleolus (Figure 3B). Stride length was deduced from videotapes, analyzed by ImageJ (National Institutes of Health, Java 1.8.0_172; Bethesda, Maryland).
Balance Measurement. Both static and dynamic balance performance was assessed. To simulate the participants' daily activities involving balance, 3 balance assessments were used: Four Square Step Test (FSST), Five Times Sit-to-Stand (FTSTS) test, and Sensory Organization Test (SOT).
Timed Up and Go Test. Participants were required to move from sitting to standing from a chair, walk at their usual walking speed for 3 m, and return to sit on the chair.27 The process was timed as a functional assessment of gait and mobility. The TUG total score and the interexaminer, test-retest, and intraexaminer reliabilities were classified as excellent (0.95 ≤ intraclass correlation coefficient [ICC] ≤ 0.99).28 The sensitivity and specificity of the TUG test in identifying fallers have been found to be 41% and 73%, respectively.29
Four Square Step Test. Participants stepped on 4 squares sequentially in a cross configuration illustrated on the floor. They were asked to start at the bottom left square and step in a clockwise manner and then in a counterclockwise direction, without turning their body. The interrater and test-retest reliability was excellent (r = 0.916-0.999, ICC2,2 = 0.96-0.99).30 The sensitivity of this test is 85%, with a specificity of 88% to 100%, and a positive predictive value of 86% for the identification of subjects with risk factors for falls.31
Five Times Sit-to-Stand Test. In this test, the participants were asked to sit against the back of a chair and then move from sitting to standing at their fastest speed 5 times with their arms folded across their chest. The duration of the sequence of movements was counted to quantify quadriceps strength.32 Interrater and test-retest reliability for the FTSTS test was high (ICC: 0.99 and 0.76, respectively).33 The sensitivity and specificity of the test are reported to be 75% and 68%, respectively, to quantify functional lower extremity strength.33
Sensory Organization Test. Performance of the sensory systems of static balance was measured by the SOT with Bertec's Computerized Dynamic Posturography using a force plate (CDP/IVR; Bertec, Columbus, Ohio). The SOT identifies an individual's ability in using visual, somatosensory, and vestibular information to effectively maintain balance and posture. The SOT, a test of sensory integration for balance control, is recognized as a criterion standard to measure postural sway and identify fall risk in older people.34
The exercise intervention took place at an indoor swimming pool located at the Young Men's Christian Association (YMCA) of Hong Kong. The water depth was 1.2 m, and the water temperature was 28.5 °C to 29.5 °C. The program was supervised and implemented by a qualified physiotherapist with more than 10 years of aquatic physiotherapy experience and expertise in Ai Chi. The ratio of physiotherapists to participants was 1:10. Each session lasted for 60 minutes.
Ai Chi Intervention. Ai Chi combines slow and coordinated rhythmic movements involving the upper and lower limbs and the trunk of the body while standing in a pool. Sixteen movement patterns were included in the intervention (Figure 4). Most of the Ai Chi movements were performed at shoulder depth immersion while the participants stood in a mini-squat position (Figure 5). Further combinations of deep breathing, trunk movements, and limb movements were also incorporated into the Ai Chi program. For each session, additional patterns were added such that all 16 Ai Chi movements were completed by the end of the 12 sessions.
The pre- and postintervention data were analyzed by the software SPSS Statistics 23 (IBM, Armonk, New York). Changes of outcomes between baseline and postintervention assessments in each group were compared. The data were first preanalyzed for normality using the Shapiro-Wilk test. Parametric data (FSST, SOT, TUG, speed, cadence, step duration, stride duration, stance-phase duration, double support, mean %MVC of RF [left], TA [left and right], BF [left], and GMR [left and right]) were compared with paired t tests. Nonparametric data (FTSTS, step length, stride length, swing-phase duration, RF [right], BF [right]) were compared with the Wilcoxon signed rank test. The level of significance was set at P < .05.
Characteristics of the Participants
The demographic characteristics of the 10 participants (3 males and 7 females) are shown in Table 2. The results for the 10 individuals were analyzed, with all of the participants completing at least 9 of the 12 sessions. The mean age was 65.4 years (SD = 7.2). The mean duration of being diagnosed with PD was 46 months (SD = 23.9). All of the individuals attended at least 9 of the 12 sessions (75% attendance) of the intervention. There were no adverse events reported in this study.
TABLE 2 -
Descriptive Characteristics of the Participantsa
||Aquatic Group (N = 10)
||n = 3
||n = 7
|Mean of both legs
|Diagnosis time, mo
||n = 8
||n = 1
||n = 1
||n = 4
|Fall history in past month
||n = 1
|Fall history in past year
||n = 5
|No. of days of exercise per week
|Hours of walking each day
|Hours of sitting each day
Abbreviations: BMI, body mass index; HY stage, Hoehn and Yahr stage.
aData are presented as means (SDs).
The results of the FTSTS test, FSST, and SOT are reported in Table 3. There were significant reductions in the FTSTS (Z = −2.80, P = .005) and FSST (t = 4.50, P = .001) scores postintervention. These findings indicate that Ai Chi may improve dynamic balance, as shown by the faster performance of the FTSTS test and FSST. The SOT with computerized dynamic posturography showed significant increases in the composite (t = −3.33, P = .009), vision (t = −5.69, P < .001), and vestibular (t = −3.41, P = .008) scores; however, no significant changes were found in the somatosensation and visual preference scores. These results demonstrated improvements in overall equilibrium performance and improved performance in 2 of the sensory systems (vision and vestibular). Such findings could provide additional evidence that Ai Chi may improve overall static balance for individuals with PD, impacting the vision and vestibular functions in particular.
TABLE 3 -
Results for the FTSTS Test, FSST, and SOTa
||Aquatic Group (N = 10)
Abbreviations: FSST, Four Square Step Test; FTSTS, Five Times Sit-To-Stand; SOT, Sensory Organization Test.
aData are presented as means (SDs).
bStatistically significant at P < .05.
The TUG results and the spatiotemporal gait parameters are presented in Table 4. There were significant reductions in the TUG scores (t = 4.02, P = .003). There were no significant differences in gait parameters detected postintervention. As such, the effects of Ai Chi on balance were more significant than its effects on gait parameters in individuals with PD.
TABLE 4 -
Results for the TUG Test and Gait Parametersa
||Aquatic Group (N = 10)
|Cadence, steps per min
|Step length, m
|Stride length, m
|Step duration, s
|Stride duration, s
|Swing phase, s
|Stance phase, s
|Double support, s
Abbreviation: TUG, Timed-Up and Go.
aData are presented as means (SDs).
bStatistically significant at P < .05.
The results for the mean %MVC of RF, TA, BF, and GME are reported in Table 5 There was a significant reduction in the mean %MVC of the left hamstring (t = 3.06, P = .01). In general, all of the studied muscle groups showed a reduction in muscle activity, although the right GME exhibited an insignificant increase. The trends of the mean %MVC of the muscles are shown in Figure 6. The results revealed that Ai Chi could have effects on muscle activity during gait, despite most of the studied muscle groups showing insignificant changes.
TABLE 5 -
Results for the Mean %MVC of RF, TA, BF, and GME of Gaita
||Aquatic Group (N = 10)
Abbreviations: BF, biceps femoris; GME, gastrocnemius; %MVC, percent maximum voluntary contraction; RF, rectus femoris; TA, tibialis anterior.
aData are presented as means (SDs).
bStatistically significant at P < .05.
Effect of Ai Chi on Balance
This study investigated the effect of Ai Chi on balance and gait in individuals with PD. The FTSTS, FSTS, and SOT results indicated a positive effect, showing a significant improvement in both static and dynamic balance. An improvement in static balance was indicated by a significant increase in all of the SOT scores, albeit with large SDs, which may reflect a large amount of variation in the group being studied. The improvement in somatosensory function was statistically insignificant, which may be due to a high preintervention score (99/100). An improvement in dynamic balance was shown by a significant decrease in the time taken to complete the FSST and FTSTS test. The smaller SDs posttest for the FTSTS test and FSST may help show decreased variability in performance after the intervention.
Evidence of Ai Chi improving balance and mobility is well supported by previous studies.15,16,35 When Ai Chi has been compared with conventional land-based physiotherapy, studies have reported that Ai Chi could improve balance and physical function to a higher degree.15,35 The results of our study echo those of studies that have shown improvements in the balance and gait of individuals with PD after a structured aquatic therapy program, including Ai Chi, as measured by the SOT, TUG test, FTSTS test, and FSST. The aquatic therapy program adopted in those studies15,16,35 consisted of 20 to 25 sessions of Ai Chi practice, while our study consisted of 12 sessions only. Our study showed that a shorter period of intervention (12 sessions) could also achieve significant benefits in balance.
Effect of Ai Chi on Gait. An improvement in gait performance was also shown by the significant reduction in the time taken to complete the TUG test. It should be noted that while there was a change in TUG score, the participants' gait speed remained unchanged; this can be interpreted as an improvement in turning and sit-to-stand efficiency specifically resulting from an Ai Chi program. A previous study on gait performance after an underwater gait training exercise program reported similar, but minimal, improvements in gait variability in both aquatic and land-based exercise groups17; in that study, spatiotemporal gait variables, such as step length and step time, were measured by a motion capture system. The results of that prior study correspond with those of our study, showing no significant improvement in gait parameters measured after a 6-week aquatic exercise intervention (2 sessions per week, 45 minutes per session). The lack of significant findings on gait parameters may be related to task specificity.17 Given the variability in the dosage of gait training, the results in regard to gait parameters have been inconsistent. An optimal dosing has yet to be determined. However, many studies have revealed the benefit of gait training when implemented for 20 to 60 minutes, 3 to 5 days per week, for 4 to 12 weeks, which is consistent with our Ai Chi training dosages.20 It is important to note that various gait training dosages may need to be adopted to optimize gait parameters.
The sEMG electrodes recorded an insignificant change among the targeted muscle groups; however, a decreasing trend of muscle activation was observed. There are 2 possible reasons that might explain this reduction. First, the co-contraction of muscles was reduced because of impaired muscle activity in individuals with PD. There is a tendency for individuals with PD to develop an abnormal muscle activation that is an earlier, longer, and larger antagonist leg muscle activity, while the paired agonist muscles are activated concurrently.36 Co-contraction could lead to joint stiffness, which may result in balance deficits. A reduction in co-contraction could be one of the rehabilitation goals to optimize balance.37 A significant improvement in balance was observed post–Ai Chi intervention, which could suggest a reduction in co-contraction as the underlying mechanism in improving balance. Despite the improvement, the dosages of exercise prescription were insufficient to make a significant difference in terms of mean %MVC. Reducing co-contraction is a process of neuromuscular remodulation and thus longer sessions may provide better therapeutic adaptations than shorter sessions.11 A second possible reason for the decreasing trend of muscle activation was that less power was generated by the muscles. The spatiotemporal changes, although insignificant, showed a decreasing trend in gait parameters. Cadence increased, while stride length, stride duration, stance-phase duration, swing-phase duration, and double support duration decreased, resulting in a shuffling gait. Therefore, less muscle activation was required with smaller steps.
Possible Mechanisms by Which Aquatic Exercise Improves Balance Ability of Individuals With PD
The properties of water and the characteristics of Ai Chi play an important role in improving balance in individuals with PD as shown in our results.
Hydrostatic Pressure. In our study, under head-out-of-water immersion, hydrostatic pressure can cause a shift of blood volume in humans from the lower limbs and abdomen to the thorax.38 This shift of blood increases central venous pressure, left ventricular end-diastolic volume, stroke volume, and cardiac output and decreases systemic vascular resistance at rest and during submaximal exercise.39 This increases the rate of blood circulation and hence the delivery of oxygen, with enhanced removal of toxins in muscle metabolism. As a result, individuals report less muscle fatigue when exercising in water.
Viscosity. The resistance of movement underwater is caused by the drag force between the water molecules themselves and between the water molecules and the object moving through the water. Therefore, resistance is proportional to movement velocity. Viscosity challenges the proximal stability and strength of the distal extremities. Moreover, turbulence flow, generated by high-velocity movement via water, could disturb stability for individuals with PD.40 Proprioception, balance responses, and core stability may be challenged when trained underwater. In addition, the resistance of water from the drag force could act as a support for individuals with PD following loss of balance and falls during training. This could reduce the injury rate and the fear of falls in individuals with PD.35 With the use of water dumbbells and noodles, individuals with PD can perform a variety of movements, which further challenge balance and muscle control. Hence, our Ai Chi program can be progressed with an increase in speed to level up the drag force.
Buoyancy. Buoyancy off-loads the body weight of an individual. The body weight borne by the lower extremities is directly associated with the depth of immersion.38 By adjusting the immersion level, stress to the weight-bearing joints and muscles is reduced to an optimal level that is suitable for training.17 Buoyancy may create a torque when the center of buoyancy is not in situ with the center of gravity. If the movement is in the same direction as the torque, it could assist the movements of individuals with PD. It allows a higher degree of movements for our Ai Chi program.
Temperature. The warm temperature of pool water may cause vasodilation, increase peripheral blood supply, and increase the delivery of oxygen while enhancing the removal of toxins in muscle metabolism. Thus, our program can potentially cause a momentary reduction of muscle tone, generate muscle relaxation, reduce rigidity, and consequently maximize training effects.40
Characteristics of Ai Chi. Stiffness and rigidity are common symptoms of PD. It is common for individuals with PD to present with a stooped posture.41 Stooped posture, described as rounded shoulders, decreased low back curve, or a forward lean of the head or whole body, decreases the magnitude and speed of the center of pressure displacements, thereby leading to a decreased stability margin.6 Stooped posture may be addressed in Ai Chi through stretching the shortened muscles and engaging the weak muscles. Ai Chi, which involves thoracic extension, pectoralis muscles stretching, and retraction of the scapula, could address prolonged stooped posture in individuals with PD. With better postural alignment, less effort is required to maintain balance, and muscles achieve optimal length, leading to better coordination of muscles and hence improved balance ability.6
Also, Ai Chi includes a series of weight-shifting and trunk and limb movements performed in an unstable aquatic environment. This could induce the recruitment of muscles that contribute to static and dynamic standing balance. Our Ai Chi training could therefore improve balance ability.
Possible Mechanisms by Which Aquatic Exercise Affects the Gait Pattern of Individuals With PD
This study showed no improvement in gait spatiotemporal parameters. This could be explained by the different environments of water and land. Although exercises performed underwater, such as stride hop and forward reaching with single-leg standing, challenge the balance and gait ability of individuals with PD, their effects are mainly aided by the physical properties of water. However, water properties such as viscosity and drag are absent on land. There is no evidence to conclude that the training effect of walking underwater reflects gait performance on land.
There are a few limitations of this study. First, there was no comparison group and there was no randomization in this study, which increase the threat to the internal validity of the study. Second, the sample size was small and therefore medium and small changes were not detected, which affect the generalizability of the results. Third, most of the individuals were female and classified as Hoehn and Yahr stage 1; therefore, a conclusion could not be drawn on the effect of Ai Chi on individuals in the later stages of PD. Fourth, although the participants showed improvement in terms of balance measures, they comprised a group of highly active individuals, which may be an important consideration in assessing the applicability of the results. Fifth, the intervention was conducted at the “on stage” of medication use; it is suggested that future studies investigate the effect of an aquatic Ai Chi program on individuals with PD at the “off” medication stage. Finally, the lack of patient self-reports may limit the translation of the study's results into meaningful change for individuals with PD in terms of quality of life, balance confidence, or other aspects of health.
This study revealed that a 6-week Ai Chi exercise program could significantly improve the balance of individuals with PD. The change in gait performance after Ai Chi was insignificant. There is a need for further investigation of the effectiveness of Ai Chi for individuals with PD, with particular consideration of the later stages of PD, the intervention dosages, and the effects at the off-medication stage. Overall, the study shows that a 6-week Ai Chi program is sufficient to show an improvement in balance and should be recommended for individuals with PD.
The authors express their profound gratitude to Prof Margaret Mak for assisting with the recruitment of participants from the Hong Kong Parkinson's Disease Association. The authors also acknowledge the work of Mr Wan Tsz Pat and Mr Cyrus Tsoi in implementing the data collection process and the intervention. The authors thank Mr Calvin Yuen and Mr Man Cheung for their statistical advice and all those who participated in the study. Special credit is also given to the Young Men's Christian Association (YMCA) of Hong Kong for providing the venue for the study.
1. Pompeu JE, Gimenes RO, Pereira RP, Rocha SL, Santos MA. Effects of aquatic physical therapy on balance and gait of patients with Parkinson's disease
. J Health Sci Inst. 2013;31:201–204.
2. Latif S, Jahangeer M, Maknoon Razia D, et al. Dopamine in Parkinson's disease
. Clin Chim Acta. 2021;522:114–126. doi:10.1016/j.cca.2021.08.009
3. Warlop T, Detrembleur C, Stoquart G, Lejeune T, Jeanjean A. Gait complexity and regularity are differently modulated by treadmill walking in Parkinson's disease
and healthy population. Front Physiol. 2018;9:68. doi:10.3389/fphys.2018.00068
4. Uehara A, Kawamoto H, Sankai Y. Development of gait assist method for Parkinson's disease
patients with FOG in walking. Paper presented at: the 55th Annual Conference of the Society of Instrument and Control Engineers of Japan (SICE); September 20-23, 2016.
5. Tysnes OB, Storstein A. Epidemiology of Parkinson's disease
. J Neural Transm (Vienna). 2017;124(8):901–905. doi:10.1007/s00702-017-1686-y
6. Miyai I, Fujimoto Y, Ueda Y, et al. Treadmill training with body weight support: its effect on Parkinson's disease
. Arch Phys Med Rehabil. 2000;81(7):849–852. doi:10.1053/apmr.2000.4439
7. Ellis T, de Goede CJ, Feldman RG, Wolters EC, Kwakkel G, Wagenaar RC. Efficacy of a physical therapy program in patients with Parkinson's disease
: a randomized controlled trial. Arch Phys Med Rehabil. 2005;86(4):626–632. doi:10.1016/j.apmr.2004.08.008
8. Peppe A, Chiavalon C, Pasqualetti P, Crovato D, Caltagirone C. Does gait analysis quantify motor rehabilitation efficacy in Parkinson's disease
patients? Gait Posture. 2007;26(3):452–462. doi:10.1016/j.gaitpost.2006.11.207
9. Li F, Harmer P, Fitzgerald K, et al. Tai chi and postural stability in patients with Parkinson's disease
. N Engl J Med. 2012;366(6):511–519. doi:10.1056/NEJMoa1107911
10. Shen X, Mak MK. Technology-assisted balance and gait training reduces falls in patients with Parkinson's disease
: a randomized controlled trial with 12-month follow-up. Neurorehabil Neural Repair. 2015;29(2):103–111. doi:10.1177/1545968314537559
11. Vivas J, Arias P, Cudeiro J. Aquatic therapy versus conventional land-based therapy for Parkinson's disease
: an open-label pilot study. Arch Phys Med Rehabil. 2011;92(8):1202–1210. doi:10.1016/j.apmr.2011.03.017
12. Volpe D, Giantin MG, Maestri R, Frazzitta G. Comparing the effects of hydrotherapy and land-based therapy on balance in patients with Parkinson's disease
: a randomized controlled pilot study. Clin Rehabil. 2014;28(12):1210–1217. doi:10.1177/0269215514536060
13. So BCL, Kong ISY, Lee RKL, et al. The effect of Ai Chi aquatic therapy on individuals with knee osteoarthritis: a pilot study. J Phys Ther Sci. 2017;29(5):884–890. doi:10.1589/jpts.29.884
14. Marinho-Buzelli AR, Bonnyman AM, Verrier MC. The effects of aquatic therapy on mobility of individuals with neurological diseases: a systematic review. Clin Rehabil. 2015;29(8):741–751. doi:10.1177/0269215514556297
15. Pérez-de la Cruz S. A bicentric controlled study on the effects of aquatic Ai Chi in Parkinson disease. Complement Ther Med. 2018;36:147–153. doi:10.1016/j.ctim.2017.12.001
16. Pérez-de la Cruz S, García Luengo AV, Lambeck J. Effects of an Ai Chi fall prevention programme for patients with Parkinson's disease
. Neurologia. 2016;31(3):176–182. doi:10.1016/j.nrl.2015.05.009
17. Carroll LM, Volpe D, Morris ME, Saunders J, Clifford AM. Aquatic exercise therapy for people with Parkinson disease: a randomized controlled trial. Arch Phys Med Rehabil. 2017;98(4):631–638. doi:10.1016/j.apmr.2016.12.006
18. Ayan C, Cancela J. Feasibility of 2 different water-based exercise training programs in patients with Parkinson's disease
: a pilot study. Arch Phys Med Rehabil. 2012;93(10):1709–1714. doi:10.1016/j.apmr.2012.03.029
19. Lambeck J, Bommer A. Ai Chi: applications in clinical practice. In: Becker BE, Cole A, eds. Comprehensive Aquatic Therapy. 3rd ed. Washington State University: Butterworth-Heinemann; 2011:171–191.
20. Osborne JA, Botkin R, Colon-Semenza C, et al. Physical therapist management of Parkinson disease: a clinical practice guideline from the American Physical Therapy Association. Phys Ther. 2022;102(4):pzab302. doi:10.1093/ptj/pzab302
21. Shen X, Wong-Yu ISK, Mak MKY. Effects of exercise on falls, balance, and gait ability in Parkinson's disease
: a meta-analysis. Neurorehabil Neural Repair. 2016;30(6):512–527. doi:10.1177/1545968315613447
22. Steffen T, Seney M. Test-retest reliability and minimal detectable change on balance and ambulation tests, the 36-item Short-Form Health Survey, and the Unified Parkinson Disease Rating Scale in people with parkinsonism. Phys Ther. 2008;88(6):733–746. doi:10.2522/ptj.20070214
23. Yang W, Bajenov A, Shen Y. Improving low-cost inertial-measurement-unit (IMU)-based motion tracking accuracy for a biomorphic hyper-redundant snake robot. Robotics Biomim. 2017;4(1):16. doi:10.1186/s40638-017-0069-z
24. Stylianou AP. Local Muscle Fatigue of Elbow Flexors: SEMG Analysis, and Effects on Motor Control Performance. ProQuest Dissertations Publishing; 2004.
25. Peikenkamp K, Stief T. Effect of motor imagery of the human gait on sEMG—activities of the lower limb muscles. J Biomech. 2012;45:S246–S246.
26. McGill S, Juker D, Kropf P. Appropriately placed surface EMG electrodes reflect deep muscle activity (psoas, quadratus lumborum, abdominal wall) in the lumbar spine. J Biomech. 1996;29(11):1503–1507. doi:10.1016/0021-9290(96)84547-7
27. Podsiadlo D, Richardson S. The Timed “Up & Go”: a test of basic functional mobility for frail elderly persons. J Am Geriatr Soc. 1991;39(2):142–148. doi:10.1111/j.1532-5415.1991.tb01616.x
28. Da Silva BA, Faria CDCM, Santos MP, Swarowsky A. Assessing timed up and go in Parkinson's disease
: reliability and validity of timed up and go assessment of biomechanical strategies. J Rehabil Med. 2017;49(9):723–731. doi:10.2340/16501977-2254
29. Vance RC, Healy DG, Galvin R, French HP. Dual tasking with the Timed “Up & Go” test improves detection of risk of falls in people with Parkinson disease. Phys Ther. 2015;95(1):95–102. doi:10.2522/ptj.20130386
30. Boddy A, Mitchell K, Ellison J, Brewer W, Perry LA. Reliability and validity of modified Four Square Step Test (mFSST) performance in individuals with Parkinson's disease
. Physiother Theory Pract. 2022:1–6. doi:10.1080/09593985.2022.2031360
31. Dite W, Temple VA. A clinical test of stepping and change of direction to identify multiple falling older adults. Arch Phys Med Rehabil. 2002;83(11):1566–1571. doi:10.1053/apmr.2002.35469
32. Bohannon RW. Sit-to-Stand Test for measuring performance of lower extremity muscles. Percept Mot Skills. 1995;80(1):163–166. doi:10.2466/pms.19126.96.36.199
33. Duncan RP, Leddy AL, Earhart GM. Five Times Sit-to-Stand Test performance in Parkinson's disease
. Arch Phys Med Rehabil. 2011;92(9):1431–1436. doi:10.1016/j.apmr.2011.04.008
34. Freeman L, Gera G, Horak FB, Blackinton MT, Besch M, King L. Instrumented Test of Sensory Integration for Balance: a validation study. J Geriatr Phys Ther. 2018;41(2):77–84. doi:10.1519/JPT.0000000000000110
35. Kurt EE, Büyükturan B, Büyükturan Ö, Erdem HR, Tuncay F. Effects of Ai Chi on balance, quality of life, functional mobility, and motor impairment in patients with Parkinson's disease
. Disabil Rehabil. 2018;40(7):791–797. doi:10.1080/09638288.2016.1276972
36. Lang KC, Hackney ME, Ting LH, McKay JL. Antagonist muscle activity during reactive balance responses is elevated in Parkinson's disease
and in balance impairment. PLoS One. 2019;14(1):e0211137. doi:10.1371/journal.pone.0211137
37. Hortobágyi T, Devita P. Mechanisms responsible for the age-associated increase in coactivation of antagonist muscles. Exerc Sport Sci Rev. 2006;34(1):29–35. doi:10.1097/00003677-200601000-00007
38. Hall J, Bisson D, O'Hare P. The physiology of immersion. Physiotherapy. 1990;76(9):517–521. doi:10.1016/S0031-9406(10)63019-2
39. McGowan CM, Goff L, Stubbs N. Animal Physiotherapy. John Wiley & Sons Inc; 2007.
40. Rodriguez P, Cancela JM, Ayan C, do Nascimento C, Seijo-Martinez M. Effects of aquatic physical exercise on the kinematic gait pattern in patients with Parkinson's disease
: a pilot study. Rev Neurol. 2013;56(6):315–320.
41. Kawami Y, Marumoto K, Shiomi Y, et al. The effect of comprehensive physiotherapy-based rehabilitation on stooped posture in Parkinson's disease
. J Phys Ther Sci. 2018;30(12):1440–1445. doi:10.1589/jpts.30.1440