The Rehabilitative Effect of Archery Exercise Intervention in Patients with Parkinson’s Disease

Chen, Chiu-Ying; Wang, Wei-Ning; Lu, Ming-Kuei; Yang, Yu-Wan; Yu, Tsung; Wu, Trong-Neng; Tsai, Chon-Haw

doi:https://doi.org/10.1155/2023/9175129

Parkinson’s Disease

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Abstract Introduction Materials and Methods Results Discussion Conclusions Data Availability Conflicts of Interest Authors’ Contributions Acknowledgments References Copyright Related Articles

Research Article | Open Access

Volume 2023 | Article ID 9175129 | https://doi.org/10.1155/2023/9175129

The Rehabilitative Effect of Archery Exercise Intervention in Patients with Parkinson’s Disease

Chiu-Ying Chen,^1,2,3Wei-Ning Wang,⁴Ming-Kuei Lu,^5,6,7Yu-Wan Yang,⁵Tsung Yu,⁸Trong-Neng Wu,⁹and Chon-Haw Tsai^5,7,10

Academic Editor: Giovanni Mirabella

Received16 Oct 2022

Revised02 May 2023

Accepted18 May 2023

Published08 Jun 2023

Abstract

Background. Archery exercise exerts a rehabilitative effect on patients with paraplegia and might potentially serve as complementary physiotherapy for patients with Parkinson’s disease. Objective. This study aimed to examine the rehabilitative effects of an archery intervention. Methods. A randomized controlled trial of a 12-week intervention was performed in patients with idiopathic Parkinson’s disease. Thirty-one of the 39 eligible patients recruited from a medical center in Taiwan participated in the trial, of whom 16 were in the experimental group practicing archery exercises and 15 were in the control group at the beginning; twenty-nine completed the whole process. The Purdue pegboard test (PPT), the Unified Parkinson’s Disease Rating Scale I to III (UPDRS I to III), physical fitness test, and timed up and go test (TUG) were used to assess the intervention effects of archery exercise. Results. Compared to the control group, the outcome differences between the posthoc and baseline tests in PPT, UPDRS I to III, lower extremity muscular strength, and TUG in the experimental group (between-group difference in difference’s mean: 2.07, 1.59, 1.36, −2.25, −3.81, −9.10, 3.57, and −1.51, respectively) did show positive changes and their effect sizes examined from Mann–Whitney U tests (η: 0.631, 0.544, 0.555, 0.372, 0.411, 0.470, 0.601, and 0.381, respectively; Ps < 0.05) were medium to large, indicating that the archery intervention exerted promising effects on improving hand flexibility and finger dexterity, activity functions in motor movement, lower extremity muscular strength, and gait and balance ability. Conclusions. Traditional archery exercise was suggested to have a rehabilitative effect for mild to moderate Parkinson’s disease and could be a form of physiotherapy. Nevertheless, studies with larger sample sizes and extended intervention periods are needed to ascertain the long-term effects of archery exercise.

1. Introduction

Parkinson’s disease (PD) is the second most prevalent neurodegenerative disorder after Alzheimer’s disease, and its onset often occurs in the elderly. The estimated global burden of PD has increased from 2.5 million in 1990 to 6.1 million in 2016 and 9.4 million in 2020, and the age-standardized prevalence rates have increased by 21.7% [1, 2]. These changes have resulted in great public health concerns regarding PD prevention and control since society has aged worldwide. Taiwan faces the same challenge, as Taiwan has transformed into an aged society, and up to 40,000 patients have been diagnosed with PD [3]. The symptoms in patients with PD include motor symptoms such as bradykinesia, rigidity, static tremor, and postural instability, and nonmotor symptoms such as sleep disorders, cognitive impairment, anxiety, and depression. Without active treatment and intervention, these symptoms will become more severe as the disease progresses, eventually leading to a loss of daily living activities in patients with PD.

Motor symptoms affect the functional mobility, balance, and gait of patients with PD, which affect many activities of daily living. Pharmacological and neurosurgical treatment of PD may not exert optimal effects on reversing the deteriorating extremity function and mobility of patients with PD [4, 5]; moreover, long-term medication may lead to several motor complications [6].

The use of complementary and alternative medicine and physiotherapy has been recommended as adjuvant strategies to improve motor function, functional mobility, and balance. Tremor and impaired finger dexterity are recognized as early symptoms in patients with PD, and reductions in their amplitude and/or frequency are treatment targets. However, whether complementary approaches are beneficial for improving PD functions is still a highly debated issue [7], and along with medical interventions, exercises have been proposed as promising strategies [8]. Evidence on the effectiveness of a variety of exercises used to improve motor dexterity and reduce tremor has been provided, including treadmill exercise, cycling exercise, aerobic exercise, whole body vibration, stretching exercises, balance training, strength training, curved-walking training, and cued training [9–24]. Some types of exercises designed to enhance specific body functions, such as upper body karate training in a seated situation [25], tango exercises [26], hand movements using a virtual cube pick and place task [27], and limb pure eccentric training [28], were also reported to exert positive effects.

In addition to the usual exercise interventions described above, Qigong [29, 30], Tai Chi [31], Wuqinxi [32, 33], yoga [34], Irish set dancing [35], active theatre therapy [36, 37], and archery [15] were proposed as complementary therapeutic methods for improving the motor function of patients with PD, and empirical evidence showed more or less favorable effects not only on motor function but also on psychological well-being (e.g., the reduction in depression, apathy, and anxiety). Although archery training was much less applied, it appeared to be a promising approach for improving upper extremity functions.

Archery is a static sport with a stable sequence of movements throughout the shot. The movements include standing in a proper position with postural stability, pushing the bow, drawing the bow string with a three-finger hook, sighting the target, relaxing the flexor group muscles of the forearm, and actively contracting the extensors to release the arrow [38–40]. An archer should control relevant muscles to achieve a good shot; due to the nature of the archery, this exercise is assumed to have the potential to maintain or improve the extremity functions of patients with PD. However, very few intervention programs have applied archery in the rehabilitation of patients with PD and lack sufficient evidence on its effect; therefore, this study aimed to examine the effects of an archery intervention using a random-controlled trial.

2. Materials and Methods

2.1. Study Design and Participants

A randomized controlled trial of a 12-week archery training course was designed to improve the impairments associated with Parkinson’s disease (PD). The clinical diagnosis of PD was based on the UK Brain Bank Criteria [41] and determined by neurologists with movement disorder expertise in China Medical University Hospital, Taichung, Taiwan. The criteria for eligibility were as follows: aged 40 years or older, on a stable medication regime, with a Hoehn and Yahr scale score ranging from 1 to 4, and no significant impairment in cognitive function assessed from the Chinese version of Cognitive Abilities Screening Instrument (CASI C-2.0) [42]. The exclusion criteria were as follows: unable to fully participate in the 12-week study period, already enrolled in another pharmaceutical or exercise intervention, extremity dysfunction severely affecting movement, frailty, severe impairments in vision, and any conditions considered by their neurologists unsafe and unsuitable to participate in the trial, for example, severe comorbidities such as diabetes and heart disease.

After receiving approval from the Research Ethics Committee of China Medical University and Hospital (CRREC-106-083 AR-1), we started this study on December 7, 2017. Initially, 59 volunteers were recruited; and among the volunteers, 16 were unable to fully participate in the trial, and one already participated in another study. Therefore, 39 participants provided written informed consent, and a random assignment approach was then applied to allocate them into the experimental group (n = 20) and the control group (n = 19). During the pretest task for collecting baseline data, four of the participants in each group withdrew. During and after the 12-week course, one participant in the archery exercise intervention group withdrew and one participant in the control group was unable to complete the post-test task. Figure 1 shows the flowchart of participant inclusion throughout the study period.

2.2. Intervention

The participants in the experimental group were assigned to take the archery training course. The course was designed by three archery trainers after discussion with the neurologists to provide participants with PD appropriate movements of drawing the bow and releasing the arrow. The trainers were traditional archery coaches with professional licenses issued by the Taiwan National Archery Association. This archery training aimed to improve the functions of the upper extremities; as patients with PD had stepping problems in terms of balance and stability, sitting postures were adopted for the participants’ safety. Participants in the experimental group were assigned to two classes with approximately 10 participants in a class. Each trainer was assigned to instruct 3-4 participants who were all on medication and carefully directed each participant’s performance on arching actions. Three-stage archery training was designed during the 12-week intervention. Basic arching (1st stage), advanced shooting (2nd stage), and integrative practice (3rd) were arranged in the first three weeks, the next four weeks, and the final five weeks, respectively. Each archery practice lasted for two hours and was held once a week in the Student Activity Center of the China Medical University next to its affiliated hospital. Before starting the archery practices, sitting posture exercises for warming up and stretching the upper extremities and finger skeletal muscles using elastic bands were led by coaches for approximately 15 minutes. For participant safety, a physical therapist was assigned to accompany them and observe their ongoing activities to avoid injury. Each participant was provided an elastic band and encouraged to practice the upper extremity and finger stretching actions at home to improve their archery skills. A telephone interview was conducted once a month to provide care and support to participants.

Participants in the control group received standard care. The care included a face-to-face personal interview educating them on how to stretch the upper extremities (UE) and finger skeletal muscles and self-care in daily living activities by delivering a pamphlet.

2.3. Outcome Measures

The primary outcome measure was tests of UE impairment and activity using the Purdue pegboard test (PPT). The test involves two abilities: gross movements of arms, hands, and fingers and fine motor extremity ability, through which finger dexterity and arm and hand coordination are assessed. Participants were asked to place as many pegs as they can and the number was recorded when time elapsed. The related information on PPT and its execution could be reached in elsewhere [43–45]. The secondary outcomes were several measures on assessing the progression of PD symptoms. Parts I to III of the Unified Parkinson’s Disease Rating Scale (UPDRS) were used to evaluate the effects of the intervention. UPDRS consists of four parts, each of which consists of a 5-point ranking subscale. The first 4-item subscale is designed to assess intelligence, behavior, and emotions, including mentation, thought disorder, depression, and motivation/initiative. The second 13-item subscale is designed to assess daily living abilities, including speech, salivation, swallowing, handwriting, cutting ford, dressing, hygiene, turning in bed, falling, freezing, walking, tremor, and sensory symptoms. The third 27-item subscale is designed to assess motor ability, including speech; facial expression; resting tremor of the face, lips, chin, right hand, left hand, right foot, and left foot; action tremor of the hands (right and left); rigidity of the neck, upper extremities (right and left), and lower extremities (right and left); finger taps (right and left); hand grips (right and left); hand pronate/supinate (right and left); leg agility (right and left), rising from a chair; posture; gait; postural stability; and bradykinesia. The assessed score ranges from 0 to 4 points; the higher the score, the more severe the symptoms [46, 47]. Changes in body composition, limb muscular strength and endurance, limb flexibility, cardiorespiratory endurance, agility, and balance ability were also assessed using a physical fitness test suitable for the elderly. In addition, gait and balance were assessed using the timed up and go (TUG) test [48]. A logbook was delivered to participants to remind them to track medication records and the status of “on” and “off” drug effects.

2.4. Statistical Methods

The statistical analyses in this study were conducted using SPSS 25.0 for Windows. The chi-square and Fisher’s exact tests were used to compare the discrete variables’ distributions between the experimental and control groups; the Mann–Whitney U test was used to compare the continuous variables’ distributions. The Wilcoxon signed-rank test and Mann–Whitney U test were used to examine the differences between the post-test and pretest in the outcome measures within and between groups, respectively. The effect size statistic was also provided, where a value less than 0.3 indicates a small effect, 0.3 to 0.5 indicates a medium effect, and greater than 0.5 indicates a large effect [49].

3. Results

At baseline (before implementing the archery intervention), equal distributions of sociodemographic characteristics and factors that may be associated with PD progression were observed between the experimental and control groups (Table 1). The mean age of patients with PD in the experimental group was 69.4 years (SD: 7.3), which was slightly older than that in the control group (67.2 years, SD: 10.7). More participants were male than female (over 50%), had at least a high school diploma, and most were married and in families with income levels ranging from 20,000 to 59,999 New Taiwan Dollar (NTD, symbol: NT$). The mean duration from the initial PD diagnosis was approximately 5 years; most patients were diagnosed with stage 2 PD, followed by stage 3. More than 60% reported a weekly exercise time >4 hours, and the drug that the patients took most was the levodopa. In addition, no differences in the UE impairments and activity functions at baseline were observed between the two groups, as shown in Table 2, in which the primary outcome (PPT) and the secondary outcomes (UPDRS, a physical fitness test for body composition, limb muscle strength and endurance, limb flexibility, cardiorespiratory endurance, and agility, and a TUG test for gait and balance abilities) were examined.

During the intervention, two subjects discontinued participation, and finally, 15 subjects in the experimental group and 14 subjects in the control group completed the post-test outcomes. The potential effects of this archery intervention on improving the physical functions of participants with PD are shown in Table 3, in which the comparison of the primary and secondary outcomes showed differences between baseline and posthoc tests, including differences within and between groups. The mean values of the differences between the post-test and baseline (post-test record minus pretest record) in the primary outcomes of right hand, left hand, and both hand PPTs within the experimental group indicated significant positive improvement (mean (SD): 1.77 (1.45), 1.06 (1.40), and 1.02 (1.19), respectively; Ps < 0.05), and the corresponding η values were greater than 0.5, showing large effects (η: 0.802, 0.609, 0.668, respectively). The mean values of the differences in the secondary outcomes, namely, UPDRS I to III, extremity flexibility (upper and lower), lower extremity muscular strength, cardio endurance, and TUG test, also showed significant positive improvements with large effects. All differences in outcomes between the post-test and baseline within the control group were insignificant, although most of the differences suggested that their corresponding functions tended to regress. Significant differences with medium to large effects in the differences between the post-test and baseline in the outcomes of PPT, UPDRS I to III, lower extremity muscle strength, and TUG tests between the experimental and control groups were observed (between-group difference’s mean: 2.07, 1.59, 1.36, −2.25, −3.81, −9.10, 3.57, and −1.51 and effect size: 0.631, 0.544, 0.555, 0.372, 0.411, 0.470, 0.601, and 0.381, respectively; Ps < 0.05), suggesting that the archery intervention exerted promising effects on improving hand flexibility and finger dexterity, activity functions in motor movement, lower extremity muscular strength, and gait and balance abilities.

The between-group differences in the outcomes between the post-test and baseline were analyzed using Mann–Whitney U tests to obtain more information on the effects of this archery intervention on each secondary outcome assessed using the UPDRS subscales (I to III). As shown in Figure 2, among UPDRS I items, the decreased depression score (mean ± SD: −1.00 ± 1.25) of the experimental group was significantly different () from the increased depression score (mean ± SD: 0.11 ± 1.72) of the control group, and the effect size was medium (η = 0.426). Among UPDRS II items, the severity in the function of handwriting was significantly decreased to a greater extent in the experimental group (mean ± SD: −0.43 ± 0.70) than in the control group (mean ± SD: −0.07 ± 0.48) (), and the effect size was medium (η = 0.372); improvements in the functions of turning in bed and facial expressions were observed in the experimental group, but the functions in the control group were worse; both between-group differences were significant (mean ± SD: −0.40 ± 0.54 v.s. 0.36 ± 0.63, ; −0.27 ± 0.62 v.s. 0.14 ± 0.50, , respectively), where the effect size for turning in bed was large (η = 0.551) and for facial expression was medium (η = 0.388). Among the UPDRS III items, the severity of right upper extremity, finger taps of the left hand, and left leg agility were significantly decreased in the experimental group but increased in the control group, and these between-group differences were significant (mean ± SD: −0.43 ± 1.03 v.s. 0.29 ± 0.61, ; −0.30 ± 0.62 v.s. 0.29 ± 0.61, ; −0.50 ± 0.82 v.s. 0.50 ± 0.65, , respectively). The results also found a large effect for left leg agility (η = 0.584) and medium effects for the right upper extremity (η = 0.396) and for the left-hand finger taps (η = 0.414).

4. Discussion

During the archery intervention, no adverse events occurred, indicating that performing archery exercise while in a sitting posture is a safe intervention for patients with Parkinson’s disease. Based on the results of the present study, archery exercise exerted a positive effect in improving several motor functions of patients with mild to moderate PD. One of the study strengths is the randomized controlled design and stratification of patients by PD disease stage (Hoehn and Yahr stages 1 to 4) to control for the confounding effects of unequal distribution of disease severity between the experimental and control groups on the intervention outcomes. The results in Tables 1 and 2 indicated comparable characteristics between groups before initiating the archery exercise course. Nevertheless, as most of the participants in this study were patients with stage 2 and 3 PD, the implication is that the effect of this archery rehabilitation intervention has limitations for patients with stage 4 PD and/or with severe symptoms.

Archery was one of the first sports introduced in the medical treatment of paraplegics and tetraplegics and was documented to be an ideal remedial exercise for training muscle groups of the arm, shoulder, and trunk muscles mainly used in archery [15]. To our knowledge, no rehabilitation program using archery exercises to help patients with PD has been developed; our study is the first to describe its effect by performing a randomized controlled trial.

The electrical activity of the muscle groups involved in the archery exercise was monitored using electromyography in an experimental study [15] and revealed that deltoids on both sides for securing horizontal and vertical positions of the arms, the biceps of the right arm for drawing and the left triceps for holding the bow in extension, the trapezius and rhomboid for bracing the shoulders while loading pulling the bow in horizontal draw, and latissimus dorsi and serratus anterior of the trunk muscles were all involved during the archery exercise. In addition, the palm of the hand, all finger muscles, and extensions of the wrist involved in the hook attachment and before the release of the arrow were exercised while performing the archery intervention. While a patient with PD focused on succeeding in shooting the target point from attaching the hook to the bow string, drawing the bow string back, twisting the hand, to releasing the arrow during the archery exercise, all involved muscle groups were activated and thus had the potential to enhance strength.

As patients with PD expressed many ambitions in pursuing success in shooting at the target point while performing the archery intervention in our study, this 12-week intervention of practicing archery actions along with using elastic bands to repeatedly activate their fingers, arm, trunk, and leg muscles helped patients with PD alleviate their symptoms, stabilize their gait and balance, and improve their extremity functions. These improvements were documented in the results of the present study, in which significantly greater differences in the post- and pretest numbers of placed nails (the changes of the primary outcomes of the three PPT tests) were observed between the experimental group and the control group (see Table 3), indicating that the archery intervention improves the functions of arms, hands, and finger dexterity in patients with PD. Significantly lower differences in post-and pretest scores of UPDRS I to III (the lower the value, the better the function) were observed for the experimental group than the control group (see Table 3), indicating that the archery intervention improved several motor functions required for daily living that mainly involve the upper and lower extremities, such as hand writing, turning in bed, facial expressions, right upper extremity, left finger taps, and left leg agility in particular (see Figure 2). Our findings are similar to the effects found in studies using other complementary therapies [29–37]. Additionally, participants in the experimental group improved their mentation, behavior, and mood (as assessed using UPDRS I) after the archery intervention, suggesting that practicing the archery exercise may have the potential to induce joyful feelings or even self-fulfillment feelings in patients with PD who succeeded in shooting the target point repeatedly, which in turn decreased their depressive symptoms. It is worth noting that similar to other complementary approaches such as Wuqinxi exercise [32, 33], yoga [34], and active theatre [36, 37], the archery approach also helps to improve psychological well-being.

The differences in outcomes indicated a significant increase in the lower extremity muscle strength, as assessed using physical fitness tests, and a significant decrease in the time required to complete the TUG test before and after the test in the experimental group compared to those in the control group (see Table 3), which also suggested that the archery intervention exerted a positive effect on increasing the muscle strength of the legs. A potential explanation for this finding is that practicing archery in a seated posture requires patients with PD to strengthen their lower extremity muscles to stabilize their upper extremities and trunk while they hold up the bow and arrows before releasing a shot. The strength of the muscles involved in performing a successful shot might be increased through archery exercises, which may in turn improve the gait and balance of patients with PD.

In the archery intervention, the use of an elastic band at home by the PD participants to practice the actions involved in the archery classes may have a potential influence on the positive effects of this archery intervention. Figure 3 shows an important part of the practice, in which a trainee was encouraged to practice the archery movement with one of the legs raised, the left leg in particular, by using an elastic band at home to stabilize their shooting actions for successfully reaching the target center in class. Figure 4 shows the actual shooting practices in class. By performing these actions, the strength of the muscle groups involved in the action, namely, the arms, the right forearm, in particular, hands and fingers, was expected to be increased. The dexterity of the hands and fingers was also improved by the practice of buckling the string and gripping the bow with bent fingers using hand muscles. The aforementioned practices may explain the improved functions of the arms, hands, and finger dexterity assessed using the PPT and improved hand writing, decreased rigidity of the right upper extremity, and improved tapping function of the left finger assessed using UPDRS. In addition, a practicing archer with a seating posture that is asked to leave the body a distance from the back of the chair (see Figure 4) might also potentially improve the agility of the left leg and strengthen the trunk muscles. By stabilizing and balancing the whole body to achieve a good shot, the strength of the involved muscles would be enhanced by the aforementioned practices.

5. Conclusions

With the advantage of using a random clinical trial design, this study suggested that traditional archery exercise exerts positive effects on ameliorating a depressed mood and improving the motor functions of arms, hands, and legs and finger dexterity in patients with PD, such as hand writing, turning in bed, decreased rigidity of the right upper extremity, tapping movement of the left fingers, and agility of the left leg in particular. The strength of leg muscles and the gait and balance were also significantly improved. Nevertheless, due to the small number of eligible participants with PD and the short period of intervention (3 months) in this study, these conclusions should be interpreted with caution. Further studies using an RCT design that recruit more participants are needed to achieve sufficient statistical power, and the time of the intervention should be increased to ascertain the long-term effects of the traditional archery exercise.

Data Availability

The data are not available because based on Taiwan Personal Data Protection Act and Human Subjects Research Act, the study participants were assured that their data would remain confidential and would not be shared.

Conflicts of Interest

The authors declare that they have no conflicts of interest.

Authors’ Contributions

CHT and CYC conceptualized and designed the study. WNW, TY, and TNW contributed to the conceptualization and design. WNW assisted in performing the intervention program and data collection. MKL, YWY, and CHT provided professional and administrative support, performed the assessment and contributed to data collection and interpretation of the results. CYC and WNW analyzed the data and interpreted the results. CYC drafted the initial manuscript and CHT revised the manuscript for important intellectual content and provided overall supervision of the study.

Acknowledgments

The authors would like to thank the archery coaches Yu-Te Lin, Kuei-Hua Tung, Chido Chu, and Jyun-Hong Dong from Full-Win Traditional Archery School, Taipei, Taiwan, for their assistance in implementing the archery training course for the study participants and neurological nurses and doctors in the Department of Neurology, China Medical University Hospital for their assistance in the recruitment of the study subjects. The authors would also like to thank Yang Orthopedics Clinic Keelung, Taiwan (106426BM), the Ministry of Science and Technology, Taiwan (MOST 112-2321-B-039-007- & MOST 111-2314-B-039-080-), and China Medical University Hospital, Taiwan (DMR 112-215 & DMR 111-223) for their sponsorships by providing financial and administrational support to this study.

References

N. Maserejian, L. Vinikoor-Imler, and A. Dilley, “Estimation of the 2020 global population of Parkinson’s disease (PD) [abstract],” Movement Disorders, vol. 35, no. 1, pp. S79–S80, 2020.
View at: Google Scholar
E. R. Dorsey, A. Elbaz, E. Nichols et al., “Global, regional, and national burden of Parkinson's disease, 1990–2016: a systematic analysis for the Global Burden of Disease Study 2016,” The Lancet Neurology, vol. 17, no. 11, pp. 939–953, 2018.
View at: Publisher Site | Google Scholar
W. M. Liu, R. M. Wu, J. W. Lin, Y. C. Liu, C. H. Chang, and C. H. Lin, “Time trends in the prevalence and incidence of Parkinson's disease in Taiwan: a nationwide, population-based study,” Journal of the Formosan Medical Association, vol. 115, no. 7, pp. 531–538, 2016.
View at: Publisher Site | Google Scholar
S. H. Fox, R. Katzenschlager, S. Y. Lim et al., “The Movement Disorder Society evidence‐based medicine review update: treatments for the motor symptoms of Parkinson's disease,” Movement Disorders, vol. 26, no. 3, pp. S2–S41, 2011.
View at: Publisher Site | Google Scholar
O. Rascol, P. Payoux, J. Ferreira, and C. Brefel-Courbon, “The management of patients with early Parkinson's disease,” Parkinsonism & Related Disorders, vol. 9, no. 1, pp. 61–67, 2002.
View at: Publisher Site | Google Scholar
K. R. Chaudhuri, P. Odin, A. Antonini, and P. Martinez-Martin, “Parkinson’s disease: the non-motor issues,” Parkinsonism & Related Disorders, vol. 17, no. 10, pp. 717–723, 2011.
View at: Publisher Site | Google Scholar
G. Mirabella, “Is art therapy a reliable tool for rehabilitating people suffering from brain/mental diseases?” Journal of Alternative & Complementary Medicine, vol. 21, no. 4, pp. 196–199, 2015.
View at: Publisher Site | Google Scholar
C. Voelcker-Rehage, D. F. Kutz, and C. Voelcker-Rehage, “Exercise-induced changes in basal ganglia volume and their relation to cognitive performance,” Journal of Neurology and Neuromedicine, vol. 1, no. 5, pp. 19–24, 2016.
View at: Publisher Site | Google Scholar
J. Mehrholz, J. Kugler, A. Storch, M. Pohl, K. Hirsch, and B. Elsner, “Treadmill training for patients with Parkinson's disease,” Cochrane Database of Systematic Reviews, vol. 2015, no. 9, Article ID CD007830, 2015.
View at: Publisher Site | Google Scholar
G. Ebersbach, D. Edler, O. Kaufhold, and J. Wissel, “Whole body vibration versus conventional physiotherapy to improve balance and gait in Parkinson’s disease,” Archives of Physical Medicine and Rehabilitation, vol. 89, no. 3, pp. 399–403, 2008.
View at: Publisher Site | Google Scholar
S. Farashi, L. Kiani, and S. Bashirian, “Effect of exercise on Parkinson’s disease tremor: a meta-analysis study,” Tremor and Other Hyperkinetic Movements, vol. 11, no. 1, pp. 15–10, 2021.
View at: Publisher Site | Google Scholar
C. Youm, Y. Kim, B. Noh, M. Lee, J. Kim, and S. M. Cheon, “Impact of trunk resistance and stretching exercise on fall-related factors in patients with Parkinson’s disease: a randomized controlled pilot study,” Sensors, vol. 20, no. 15, p. 4106, 2020.
View at: Publisher Site | Google Scholar
F. Y. Cheng, Y. R. Yang, Y. R. Wu, S. J. Cheng, and R. Y. Wang, “Effects of curved-walking training on curved-walking performance and freezing of gait in individuals with Parkinson's disease: a randomized controlled trial,” Parkinsonism & Related Disorders, vol. 43, pp. 20–26, 2017.
View at: Publisher Site | Google Scholar
N. E. Allen, J. Song, S. S. Paul et al., “An interactive videogame for arm and hand exercise in people with Parkinson's disease: a randomized controlled trial,” Parkinsonism & Related Disorders, vol. 41, pp. 66–72, 2017.
View at: Publisher Site | Google Scholar
L. Guttmann and N. C. Mehra, “Experimental studies on the value of archery in paraplegia,” Spinal Cord, vol. 11, no. 2, pp. 159–165, 1973.
View at: Publisher Site | Google Scholar
I. S. Wong-Yu and M. K. Mak, “Task-and context-specific balance training program enhances dynamic balance and functional performance in parkinsonian nonfallers: a randomized controlled trial with six-month follow-up,” Archives of Physical Medicine and Rehabilitation, vol. 96, no. 12, pp. 2103–2111, 2015.
View at: Publisher Site | Google Scholar
A. Nieuwboer, G. Kwakkel, L. Rochester et al., “Cueing training in the home improves gait-related mobility in Parkinson’s disease: the RESCUE trial,” Journal of Neurology, Neurosurgery & Psychiatry, vol. 78, no. 2, pp. 134–140, 2007.
View at: Publisher Site | Google Scholar
A. Carvalho, D. Barbirato, N. Araujo et al., “Comparison of strength training, aerobic training, and additional physical therapy as supplementary treatments for Parkinson’s disease: pilot study,” Clinical Interventions in Aging, vol. 10, pp. 183–191, 2015.
View at: Publisher Site | Google Scholar
A. L. Ridgel, J. L. Vitek, and J. L. Alberts, “Forced, not voluntary, exercise improves motor function in Parkinson's disease patients,” Neurorehabilitation and Neural Repair, vol. 23, no. 6, pp. 600–608, 2009.
View at: Publisher Site | Google Scholar
M. D. Sage and Q. J. Almeida, “Symptom and gait changes after sensory attention focused exercise vs aerobic training in Parkinson's disease,” Movement Disorders, vol. 24, no. 8, pp. 1132–1138, 2009.
View at: Publisher Site | Google Scholar
K. Tanaka, R. F. Santos, F. Stella, L. T. B. Gobbi, and S. Gobbi, “Benefits of physical exercise on executive functions in older people with Parkinson’s disease,” Brain and Cognition, vol. 69, no. 2, pp. 435–441, 2009.
View at: Publisher Site | Google Scholar
D. K. White, R. C. Wagenaar, T. D. Ellis, and L. Tickle-Degnen, “Changes in walking activity and endurance following rehabilitation for people with Parkinson disease,” Archives of Physical Medicine and Rehabilitation, vol. 90, no. 1, pp. 43–50, 2009.
View at: Publisher Site | Google Scholar
Y. R. Yang, Y. Y. Lee, S. J. Cheng, and R. Y. Wang, “Downhill walking training in individuals with Parkinson's disease: a randomized controlled trial,” American Journal of Physical Medicine & Rehabilitation, vol. 89, no. 9, pp. 706–714, 2010.
View at: Publisher Site | Google Scholar
A. Ashburn, L. Fazakarley, C. Ballinger, R. Pickering, L. D. McLellan, and C. Fitton, “A randomised controlled trial of a home based exercise programme to reduce the risk of falling among people with Parkinson’s disease,” Journal of Neurology, Neurosurgery & Psychiatry, vol. 78, no. 7, pp. 678–684, 2006.
View at: Publisher Site | Google Scholar
S. S. Palmer, J. A. Mortimer, D. D. Webster, R. Bistevins, and G. L. Dickinson, “Exercise therapy for Parkinson’s disease,” Archives of Physical Medicine and Rehabilitation, vol. 67, no. 10, pp. 741–745, 1986.
View at: Publisher Site | Google Scholar
R. P. Duncan and G. M. Earhart, “Randomized controlled trial of community-based dancing to modify disease progression in Parkinson disease,” Neurorehabilitation and Neural Repair, vol. 26, no. 2, pp. 132–143, 2012.
View at: Publisher Site | Google Scholar
I. Cikajlo and K. Peterlin Potisk, “Advantages of using 3D virtual reality based training in persons with Parkinson’s disease: a parallel study,” Journal of NeuroEngineering and Rehabilitation, vol. 16, no. 1, p. 119, 2019.
View at: Publisher Site | Google Scholar
L. E. Dibble, T. F. Hale, R. L. Marcus, J. P. Gerber, and P. C. LaStayo, “High intensity eccentric resistance training decreases bradykinesia and improves quality of life in persons with Parkinson's disease: a preliminary study,” Parkinsonism & Related Disorders, vol. 15, no. 10, pp. 752–757, 2009.
View at: Publisher Site | Google Scholar
T. Schmitz-Hübsch, D. Pyfer, K. Kielwein, R. Fimmers, T. Klockgether, and U. Wüllner, “Qigong exercise for the symptoms of Parkinson's disease: a randomized, controlled pilot study,” Movement Disorders, vol. 21, no. 4, pp. 543–548, 2006.
View at: Publisher Site | Google Scholar
D. Burini, B. Farabollini, S. Iacucci et al., “A randomised controlled cross-over trial of aerobic training versus Qigong in advanced Parkinson's disease,” Europa Medicophysica, vol. 42, no. 3, pp. 231–238, 2006.
View at: Google Scholar
M. E. Hackney and G. M. Earhart, “Tai Chi improves balance and mobility in people with Parkinson disease,” Gait & Posture, vol. 28, no. 3, pp. 456–460, 2008.
View at: Publisher Site | Google Scholar
T. Wang, G. Xiao, Z. Li et al., “Wuqinxi exercise improves hand dexterity in patients with Parkinson’s disease,” Evidence-based Complementary and Alternative Medicine, vol. 2020, Article ID 8352176, pp. 1–9, 2020.
View at: Publisher Site | Google Scholar
M. Shen, Y. L. Pi, Z. Li et al., “The feasibility and positive effects of Wuqinxi exercise on the cognitive and motor functions of patients with Parkinson’s disease: a pilot study,” Evidence-based Complementary and Alternative Medicine, vol. 2021, Article ID 8833736, 7 pages, 2021.
View at: Publisher Site | Google Scholar
M. Ban, X. Yue, P. Dou, and P. Zhang, “The effects of yoga on patients with Parkinson’s disease: a meta-analysis of randomized controlled trials,” Behavioural Neurology, vol. 2021, Article ID 5582488, 11 pages, 2021.
View at: Publisher Site | Google Scholar
D. Volpe, M. Signorini, A. Marchetto, T. Lynch, and M. E. Morris, “A comparison of Irish set dancing and exercises for people with Parkinson’s disease: a phase II feasibility study,” BMC Geriatrics, vol. 13, no. 1, Article ID 54, 2013.
View at: Publisher Site | Google Scholar
G. Mirabella, P. De Vita, M. Fragola et al., “Theatre is a valid add-on therapeutic intervention for emotional rehabilitation of Parkinson’s Disease patients,” Parkinson's Disease, vol. 2017, Article ID 7436725, pp. 1–11, 2017.
View at: Publisher Site | Google Scholar
N. Modugno, S. Iaconelli, M. Fiorlli, F. Lena, I. Kusch, and G. Mirabella, “Active theater as a complementary therapy for Parkinson's disease rehabilitation: a pilot study,” The Scientific World Journal, vol. 10, pp. 2301–2313, 2010.
View at: Publisher Site | Google Scholar
H. Ertan, B. Kentel, S. T. Tümer, and F. Korkusuz, “Activation patterns in forearm muscles during archery shooting,” Human Movement Science, vol. 22, no. 1, pp. 37–45, 2003.
View at: Publisher Site | Google Scholar
H. Ertan, S. Yagcioglu, A. Yılmaz, P. Ungan, and F. Korkusuz, “Accuracy in archery shooting is linked to the amplitude of the ERP N1 to the snap of clicker,” Montenegrin Journal of Sports Science and Medicine, vol. 10, no. 1, pp. 37–44, 2021.
View at: Publisher Site | Google Scholar
P. Leroyer, J. Van Hoecke, and J. N. Helal, “Biomechanical study of the final push‐pull in archery,” Journal of Sports Sciences, vol. 11, no. 1, pp. 63–69, 1993.
View at: Publisher Site | Google Scholar
W. R. Gibb, J. M. Fearnley, and A. J. Lees, “The anatomy and pigmentation of the human substantia nigra in relation to selective neuronal vulnerability,” Advances in Neurology, vol. 53, pp. 31–34, 1990.
View at: Google Scholar
K. N. Lin, P. N. Wang, C. Y. Liu, W. T. Chen, Y. C. Lee, and H. C. Liu, “Cutoff scores of the cognitive abilities screening instrument, Chinese version in screening of dementia,” Dementia and Geriatric Cognitive Disorders, vol. 14, no. 4, pp. 176–182, 2002.
View at: Publisher Site | Google Scholar
E. L. Proud, B. Bilney, K. J. Miller, M. E. Morris, and J. L. McGinley, “Measuring hand dexterity in people with Parkinson’s disease: reliability of pegboard tests,” American Journal of Occupational Therapy, vol. 73, no. 4, pp. 7304205050p1–7304205050p8, 2019.
View at: Publisher Site | Google Scholar
E. L. Proud, K. J. Miller, B. Bilney, M. E. Morris, and J. L. McGinley, “Construct validity of the 9-Hole Peg Test and Purdue Pegboard Test in people with mild to moderately severe Parkinson’s disease,” Physiotherapy, vol. 107, pp. 202–208, 2020.
View at: Publisher Site | Google Scholar
I. Lawson, “Purdue pegboard test,” Occupational Medicine, vol. 69, no. 5, pp. 376-377, 2019.
View at: Publisher Site | Google Scholar
S. Fahn, R. L. Elton, and The UPDRS Development Committee, “The unified Parkinson’s disease rating scale,” in Recent Developments in Parkinson's Disease, S. Fahn, C. D. Marsden, D. B. Calne, and M. Goldstein, Eds., vol. 2, pp. 153–163, MacMillan Healthcare Information, NJ, USA, 1987.
View at: Google Scholar
C. G. Goetz and G. T. Stebbins, “Assuring interrater reliability for the UPDRS motor section: utility of the UPDRS teaching tape,” Movement Disorders, vol. 19, no. 12, pp. 1453–1456, 2004.
View at: Publisher Site | Google Scholar
B. Silva, C. D. C. M. Faria, M. P. Santos, and A. Swarowsky, “Assessing timed up and go in Parkinson’s disease: reliability and validity of timed up and go assessment of biomechanical strategies,” Journal of Rehabilitation Medicine, vol. 49, no. 9, pp. 723–731, 2017.
View at: Publisher Site | Google Scholar
J. Cohen, Statistical Power Analysis in the Behavioral Sciences, Routledge, New York City, NY, USA, 2nd edition, 1988.

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Copyright © 2023 Chiu-Ying Chen et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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