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. 2021 May 23;9(6):72. doi: 10.3390/sports9060072

Golf as a Physical Activity to Potentially Reduce the Risk of Falls in Older Adults with Parkinson’s Disease

Rebecca R Bliss 1, Frank C Church 2,*
Editor: Anthony Leicht
PMCID: PMC8224548  PMID: 34070988

Abstract

Advanced age is associated with an increased risk for falls in aging adults. Older adults are also more likely to be diagnosed with Parkinson’s disease (PD), with advanced age as the most significant risk factor. PD is a neurodegenerative disorder with four Cardinal motor symptoms: rigidity, bradykinesia, postural instability, and tremor. Thus, people (person)-with-Parkinson’s disease (PwP) have an even greater risk of falling than non-disorder age-matched peers. Exercise is an activity requiring physical effort, typically carried out to sustain or improve overall health and fitness, and it lowers the risk of falls in the general population. The sport of golf provides a low-impact all-around workout promoting a range of motion, activation of muscles in the upper and lower body, flexibility, and balance. Swinging a golf club offers a unique combination of high amplitude axial rotation, strengthening postural musculature, coordination, and stabilization, demonstrating the potential to impact PD symptoms positively. Golf may be a novel exercise treatment regimen for PD to use in conjunction with traditional medical therapy. We completed a literature review to determine the relationship between the game of golf, PD, and the risk of falls. We concluded that regularly playing golf can lower the risk for falls in community ambulating older adults with PD and demonstrates the potential to improve quality of life for PwP.

Keywords: Parkinson’s disease, golf, older adults, risk of falls, axial mobility, postural instability, bradykinesia, exercise

1. Introduction

1.1. Parkinson’s Disease

Parkinson’s disease (PD) is a chronic neurodegenerative disorder that results from the progressive death of dopaminergic neurons located in the substantia nigra and resultant degeneration of dopaminergic pathways in the basal ganglia [1,2,3]. The loss of dopamine alters both inhibitory and excitatory pathways, resulting in the PD cardinal motor signs: bradykinesia (slowness of movement), tremor (trembling in hands, arms, legs, jaw, and face), impaired balance and posture, and muscle rigidity (stiffness of the limbs and trunk) [4,5,6,7]. Other non-motor PD symptoms may include depression and other psychiatric manifestations; difficulty swallowing and speaking; urinary problems or constipation; sleep disruption; and a myriad of other symptoms not overtly seen or displayed [6,7,8,9,10,11].

PD is both chronic and progressive [12]. Symptoms present gradually over several years and the progression varies from person to person, both in rate of development and the extent to which these symptoms manifest. PD dramatically alters an individual’s movement ability and functional stability, affecting not only physical wellness but also quality of life and psychosocial well-being. PD is second to Alzheimer’s disease as the most common age-related chronic, neurological disorder. Currently, over one million people in the United States are living with PD and ~60,000 new diagnoses are made each year [13].

1.2. Neurodegenerative Diseases and the Positive Impact of Exercise

Neurodegenerative diseases are characterized by progressive nervous system dysfunction [14,15,16]. The most prevalent neurodegenerative disorders include (listed alphabetically) Alzheimer’s disease (AD), amyotrophic lateral sclerosis, Friedreich’s ataxia, Huntington’s disease, multiple sclerosis, Parkinson’s disease (PD), prion disease, spinocerebellar ataxia, and spinal muscular atrophy. With time, neurodegenerative diseases lead to difficulties either with movement (ataxias) or with mental functioning (dementias). There is increasing evidence for a positive role of exercise in improving both the quality of life and symptoms of many neurodegenerative disorders, especially PD and AD [17,18,19,20,21]. Since the etiology of neurodegenerative disorders is both broad and complex, the expected effect of exercise varies among the disorders. Our focus moving forward is centered on PD and reducing the risk of falls using exercise, primarily, from hitting golf balls and playing golf.

1.3. Maintaining Balance in the Presence of Parkinson’s Disease

Posture, balance, and axial mobility are the foundation upon which many day-to-day activities are executed, typically, without conscious thinking. Stopping to bend over and tie your shoes on a walk, or turning to look over your shoulder when driving requires a certain degree of axial movement, flexibility and postural reaction in order to maintain the body’s equilibrium in relation to external forces [22]. Postural instability refers to an impaired ability to maintain posture and balance, compromising the capability to easily and efficiently maintain or change positions [23]. One of the cardinal symptoms of PD, postural instability presents in many patients and worsens as the disease progresses [23,24].

1.4. Can the Game of Golf Reduce Falls in Older Adults with Parkinson’s Disease?

Evidence suggests older adults are at increased risk for falls [25,26]. Likewise, there is additional indication that people (person)-with-Parkinson’s disease (PwP) have a substantially higher risk of falls compared to age-matched non-Parkinson’s people [27,28]. In this narrative review, from our summary of the literature, we suggest that older adults with PD who routinely hit golf balls could possibly lower the chance of falling (Figure 1).

Figure 1.

Figure 1

Playing golf may lessen the risk of falls in older adults with Parkinson’s disease (PD). The goal of this narrative review is to highlight the potential role of golf to reduce falls in older adults with PD. The flow of this paper follows the schematic above by describing Parkinson’s disease, a chronic neurodegenerative disease. Over time, PD develops due to the loss of dopamine-producing neurons in the brain (the chemical structure of dopamine is shown above), which greatly diminishes balance, posture and mobility. Older adults with PD have a substantially increased risk for falls compared to age-matched adults without PD. Our literature review found that golf could be an ideal form of exercise for lowering the risk of falls in older adults in general, but especially for those living with PD. The quote is attributed to Aelius Galenus (Anglicized to Galen). He was a prominent Greek physician-philosopher in the ancient Roman Empire who studied many aspects of medicine including anatomy and neurology [29].

2. Increased Risk of Falling in Older Adults

2.1. Causes of Falls

Falls are one of the leading causes of morbidity and mortality in older adults [25,26]. Importantly, the risk of falling increases with age [26]. The majority of falls typically are caused by a constellation of conditions, including balance and gait deficits, visual impairment, postural hypotension, dementia, neurologic and musculoskeletal disabilities, medications, and environmental hazards (see [30] and references cited therein). In a separate study, Ambrose et al. [31] found that the major risk factors predicting falls were impaired balance and gait, history of previous falls, and polypharmacy. Globally, the most common type of injury reported after a fall were lower extremity fractures including the patella, tibia, fibula, or ankle [32]. However, older adults who have fallen experience increased prevalence of wrist and hip fractures, in addition to potentially serious complications such as head injuries if they are concurrently being treated with oral anticoagulants [33,34,35,36].

Moreland et al. [37] found that lower muscle weakness was a predictor of increased risk of falls in older adults. Balance ability is a key part of our daily life and can be divided into two types: static and dynamic. As we age, controlling balance declines from changes in the vestibular, visual, somatosensory, musculoskeletal, and central nervous systems [38]. In assessing risk for falling in an elderly population, Dunsky et al. [39] recommended both static and dynamic tests used for determination of balance ability.

An algorithm has been developed by the Centers for Disease Control and Prevention [40] to enable health care workers to help older adults with a history of falls: “Multifactorial interventions should include exercise, particularly balance, strength, and gait training; vitamin D supplementation with or without calcium; management of medications, especially psychoactive medications; home environment modification; and management of postural hypotension, vision problems, foot problems, and footwear.”.

2.2. Role of Exercise to Lower the Risk of Falls

Lee et al. [41], presented in a prescription-based format, that older adults would gain many health benefits from aerobic exercise, strength or resistance training, flexibility or stretching exercises, and balance training. In a comprehensive review of over 50 trial studies, Sherrington et al. [42] provided guidelines for how exercise can be used to lower the occurrence of falls in older adults. They suggested that exercise should be ongoing and continual for at least 2 h/week, and both the general and high-risk population groups be targeted for exercise programs [42]. Importantly, they recommended that high-risk individuals not be asked to do brisk walking.

Lesinski et al. [43] designed and implemented a balance training program using healthy community adults; furthermore, those enrolled in this program improved static/dynamic steady-state, proactive, and reactive balance. Normal aging is associated with reduced capacity and loss of strength with musculoskeletal functioning. Furthermore, as we age, we generate more sedentary time. Any increase in physical activity is better than being sedentary. Gschwind et al. [44] evaluated a fall prevention program that contained exercises of balance, strength, and power; combined with cognition, psychosocial well-being, and self-efficacy of falls in healthy older adults.

3. Parkinson’s Disease and the Increased Risk of Falls

3.1. PwP Have an Increased Probability of Falling

PwP are nine times more likely to fall compared to age-matched healthy individuals [45]. PwP have been reported to fall frequently, ~70% report falling yearly, and sadly, 13% report falling weekly [46,47,48]. Due to the average age of PwP (≥65 years old), the same risk factors for falls described in the previous section exists in PD. However, due to many circumstances, PwP must confront a daunting list of issues that predispose them to falls. Shown in Table 1 are some of the compiled risk factors for falls in PwP. These risk factors impact balance, mobility, muscle weakness, and strength, and could affect an individual’s ability to participate in sport. For a more complete review of the various factors that promote falls in older adults with PD, please see [28,45,49] and references cited therein.

Table 1.

Risk factors for falls in Parkinson’s disease.

Risk Factor Reference(s) Cited
Exercise/Sports-Related:
Balance-mobility [47,48,50,51,52]
Decreased arm swing [48]
Gait disturbances [28,47,50]
Inability to get up from a sitting position [28,53]
Orthostasis [28,47]
PD-specific clinical symptoms:
Bradykinesia [53]
Dyskinesia [51]
Freezing [51,52,54,55,56,57]
Rigidity [50,58]
General Neurological/PD-Related:
Advanced age [53,59]
Cognition [57,60,61]
Depression and anxiety [48,50,62]
Disease severity [51,52,56]

3.2. Exercise Has Proven Beneficial in Reducing Falls in Parkinson’s Disease

Fall prevention programs using exercise and motor training have been devised to reduce falls in PD [63,64]. Two clinical trials targeting balance resulted in a statistically significant reduction in falls [65,66]. Alternatively, under similar exercise conditions, two other studies did not find a statistically significant reduction in falls [67,68]. Under supervision, Tai Chi exercise focused on flexibility and leg strengthening, resulted in improved anticipatory balance in PwP [69,70]. Three separate studies focused on gait and balance training [71], strategies of fall prevention [72], and balance and strengthening with fall prevention advice [73] showed improvement in fall reduction following therapy. We are making progress in understanding the complex clinical picture of falls in PD [74,75]. Although positive results have been reported, there is clearly a need for additional exercise programs to help reduce falls in PD. We turn our attention to golf. Several components of the game of golf with PD and falls are discussed moving forward.

4. Golf as an Exercise to Reduce Falls in Older Adults

4.1. Overview of Golf Compared to PD-Specific Exercises

Positive research results have shown the effect of exercise on the alleviation of physical and neurological PD symptoms [76,77,78,79,80,81,82,83,84,85]. This has led to the development of PD-specific exercise programs designed to improve cardinal physical symptoms. Examples of PD-specific exercise programs include PWR! Moves, Rock Steady Boxing and Dance for PD programs, power walking with poles, stationary biking, tai chi, and yoga [86,87,88,89,90,91,92].

The game of golf is not only physical exercise but, as a game of constant strategy, it provides an opportunity for continual cognitive involvement, and it is a sport of camaraderie and social support [93,94,95,96,97,98,99]. However, the unique combination of axial rotation, muscle strengthening, cognitive, and social components obtained through playing golf has yet to be fully explored as an exercise treatment regimen to reduce the risk of falls for older adults with PD.

4.2. The Golf Swing

Golf is a sport that offers an all-around low-impact exercise [100,101,102]. The golf swing is a whole-body goal-oriented task that requires an extension, axial mobility, weight shift, coordination, transition of the body (over the base of support), and focus on visual-motor integration to allow the golf club to hit the golf ball [103,104]. The golf swing can be split up into five segments: (i) back swing (ball address to top of back swing); (ii) forward swing [top of swing to club horizontal (early part of down swing)]; (iii) forward swing acceleration [horizontal club to impact (late part of down swing)]; (iv) early follow through (impact to horizontal club); and (v) late follow through (horizontal to completion of swing) [105,106,107]. The complete golf swing not only promotes full range of bodily motion and axial rotation flexibility but activates many muscles in the body [100,101,102,103,104,105,106,107,108,109,110,111]. Shown in Figure 2 are the various major muscles used in the golf swing [107].

Figure 2.

Figure 2

The major muscles used in the golf swing. Shown in (A) (far-left panels) are the major muscles used for the back swing, (B) (left-middle panels) are the major muscles used for the forward acceleration phase of the down swing, and (C) (right-middle panels) and (D) (far-right panels) are the major muscles used for the early and late phases of the follow through, respectively. Muscles highlighted above were from the work of McHardy and Pollard [107].

Essential to the proper execution of the golf swing is the axial skeleton [22,112]. The axial skeleton (highlighted in blue in Figure 3) includes all the bones along the body’s long axis, including the skull, laryngeal skeleton, vertebral column, and thoracic cage. The appendicular skeleton includes all the bones from the upper and lower limbs and the shoulder and pelvic girdle; these bones “append” to the axial skeleton. The axial structures form the supporting platform for the movement of the head and the limbs. Thus, axial mobility can alter our ability to move adjacent joints comprising the shoulder and the pelvic complexes [22,112]. From practicing the golf swing, one could improve spinal rotation to increase axial mobility. Therefore, we speculate that routinely practicing the golf swing could counter inadequate spinal rotation caused by reduced axial mobility, which is one of PD’s consequences.

Figure 3.

Figure 3

The axial skeleton region (highlighted in blue) along with the surrounding neurovascular and muscle supporting structures. This figure was prepared with permission from Human Anatomy Atlas (Version 2021) [iPhone software. from www.visiblebody.com (accessed on 7 April 2021)].

4.3. Playing Golf Promotes Wellness and Reduces Falls in Older Adults

Tsang and Hui-Chen [113] found that older golfers had better static and dynamic balance control compared to the control group of older healthy non-golfers. Next, Gao et al. [114] suggested that the combined precision and repetitive nature of the golf swing and walking the golf course favored older golfers to have better balance and more confidence when compared to the control group of older healthy non-golfers. Comparing experienced older golfers to older Tai Chi practitioners, Tsang and Hui-Chen [115] reported that both groups had better joint proprioception and balance control during weight shifting compared to age-matched controls. Furthermore, both older golfers and Tai Chi test subjects were comparable in balance control to healthy college-aged control subjects [115].

Du Bois et al. [116] gave golf lessons to two older adults who were non-golfers and they measured significant increase in strength and power along with improved balance and posture. Martinez-Bustelo et al. [117] measured quadriceps symmetry in active, sedentary, and institutionalized lifestyle in females over 80 years of age. The active group were golfers and they had increased muscular function compared to the other groups [117]. Du Bois et al. [118] used a 12-week comprehensive golf training program to study the physical abilities, dynamic balance, and hip muscle performance of older military veterans. They found that the older military veterans showed improved physical performance and dynamic balance from playing golf [118].

In a direct comparison of golf to Tai Chi for patients with moderate PD, Johnson et al. [119] reported golf was associated with greater improvements in balance and mobility than Tai Chi. Murray et al. [98] reviewed golf and health. Besides finding improved physical health and mental well-being in golfers, they also suggested that playing golf contributes to muscle strengthening, improved balance and fall prevention [98]. Collectively, these studies reinforce the hypothesis that golf [(a) repetitively hitting golf balls; (b) playing a round of golf; and (c) walking while you play golf] strengthens the body, improves posture, coordination and axial rotation, and enhances balance. These studies imply that older adults who routinely practice/play golf should be less likely to fall.

5. Golf Could Improve Functional Ability in Older Adults with Parkinson’s Disease

5.1. Comparing Regular Physical Activity to Playing Golf

Individuals with PD who exercise consistently have been shown to preserve function, slow disease progression [120], demonstrate positive effects on mobility, and improve health-related quality of life [121]. Regular physical activity has also been shown to have a positive correlation with improved functional capacity, posture, and balance with reduced risk for falls in PwP [122]. As previously described, golf offers the potential to improve axial rigidity, bradykinesia and postural instability due to qualities inherent to the swing and game of golf itself. Furthermore, components of strategy, social engagement, and focus on task offer potential to address non-motor symptoms and improve beneficial carryover for PwP. We now highlight specific aspects of the golf swing for improving postural instability in PD, and we describe some golf-specific activities for PwP.

5.2. Postural Instability: Anticipatory Movements and Bradykinesia

Postural instability in PD is a leading cause of falls throughout the disease progression, and in advanced stages, can lead to a loss of independence [123,124]. This is of particular concern because postural instability does not always respond positively to medications used to manage symptoms of PD, highlighting the importance of identifying salient strategies to heighten postural reaction [123,125]. King and Horak [126] examined lateral stepping strategies in individuals with PD (both on and off medication) and found that individuals with PD had a reduced ability to recruit anticipatory postural adjustments (APAs) characterizing their steps as smaller, and slower with increased prevalence for falls as compared to age norms. Medication did not significantly impact falls or stepping strategy. Furthermore, Lin et al. [127] showed that bradykinetic APAs and varied force production may contribute to walking hesitation and potentially increase falls in PwP. A study by Dijkstra et al. [128] showed that reduced amplitude during weight shift was associated with freezing of gait, a pronounced sign of postural instability in advanced stages. The golf swing has a forceful and quick weight shift that is applied laterally during the early down swing and followed by a sustained weight shift onto the opposite limb during the follow through [108]. We reason that this action has potential to address bradykinesia in PD with anticipated movement in a lateral direction, and potentially improve postural instability with repetition.

5.3. Postural Instability: Axial Rigidity and Coordination

A forward flexed posture, truncal rigidity, and limited trunk mobility are common tenets in a PwP and further contribute to postural instability [123]. Coactivation of agonist and antagonist muscles on both sides of the body contributes to increased stiffness in the lower legs, hips and trunk leading to ineffective balance recovery [129]. Carpenter et al. [130] used EMG electrodes to assess muscle activation with multidirectional perturbations. They concluded that individuals with PD demonstrated reactive strategies responding to disequilibrium [130]; however, these strategies were inefficient at preventing loss of balance due to a stiffening response in the ankles, trunk, and hips. Components of the golf swing require extensive thoracolumbar rotation while controlling the momentum and weight of the golf club to be performed successfully. We propose this coupling of the golf club with rotational movement offers potential to improve axial mobility and trunk rotation in PwP who play golf regularly. Use of the golf club simultaneously offers a force for overpressure to achieve increased stretch and potential for an added perturbation as the golfer controls the movement of the golf club.

Activation of spinal extensors during the golf downswing and follow through complement the need to strengthen antigravity musculature to address stooped posture. Furthermore, neuromuscular coordination between spinal extensors and oblique musculature as the golfer transitions from backswing to down swing offer opportunities for the PwP to practice selective trunk engagement with attention to muscle coordination, potentially limiting the prevalence of co-contraction of trunk musculature during the golf swing. This is of importance because multiple studies have shown that PwP have difficulty with multi-segmental coordination, particularly, coordinating the arm, hand, and trunk movements with reaching tasks [131,132]. Individuals with PD may be challenged switching from one movement to a different movement. Thus, the transitional movement between set up, back swing and down swing of the golf club may facilitate opportunities for PwP to practice weight shift and transitional movements.

5.4. Motivation and External Engagement

Several studies have demonstrated the benefit of PwP exercising with increased intensity in addition to use of cues to augment motor learning [133,134,135]. This can be challenging to achieve without the guidance of a physical therapist or exercise instructor specializing in PD. Although golf does not replace these components of an individual’s healthcare team, golf offers opportunity to utilize external feedback of how far or fast the ball moves to improve the individual’s ability to assess their own performance and adjust accordingly. Motivation to hit the ball far on a long drive may facilitate increased weight shift, amplitude, and power beyond what the individual may have completed without the external cue of a ball.

The importance of movement and exercise are becoming increasingly understood as an important strategy for minimizing disease progression in people with PD. However, creating a habit of daily exercise can be a challenge for individuals with chronic disease who may be impacted by non-motor symptoms of reduced motivation or depression. A report by Chong et al. [136] found that even in individuals who were not clinically depressed, individuals with PD were less motivated than controls if rewards were low. Golf offers the opportunity to increase motivation with the use of a goal, social engagement, and connection with the outdoors. Interestingly, Johnson et al. [119] found that participants with PD were more likely to continue with golf (86%) as compared to Tai Chi (33%) at the end of the study. Furthermore, a full game of golf requires strategy and planning, offering the potential to improve cognitive skills including executive function, which can be impacted in PD.

5.5. Hitting Golf Balls and Playing Golf

Gary Smith has PD and is using golf as part of his exercise therapy (from Golf Channel, “Comeback: Smith battles Parkinson’s disease with golf” https://www.golfchannel.com/video/comeback-smith-battles-parkinsons-disease-golf/ (accessed on 16 April 2021)). He started by hitting 100 golf balls/day at a TopGolf facility and over the past several years, his medical therapy has not advanced. Typically, increases in medication dosages imply disease progression.

Four strategies for hitting golf balls are described below (Table 2). While reports of golf reducing falls in older adults are both positive and encouraging, they comprise a handful of publications (with only one study pertaining to PD) [113,114,115,116,117,118,119]. Thus, based on these previous studies, current understanding of PD, and the biomechanics of a golf swing, we speculate and offer some expected goals/outcomes for PwP while using the golf plans detailed in Table 2.

Table 2.

Golf exercise routines for Parkinson’s disease.

Be safe, be careful, and realize that most PwP typically have gait and balance issues
To ensure safety, the benefit of a new exercise program will only work if you have (i) talked with your neurologist; (ii) worked out a plan with your physical therapist or personal trainer that includes stretching exercises for pre- and post-golf and discussion on the optimal dose and frequency as you prepare for a new exercise; (iii) if you know how to play golf and you are starting anew, welcome back; and (iv) if you are a beginner golfer, welcome, and have fun.
Plan #1: Practice the golf swing at home
This plan requires only a couple of golf clubs, a golf mat to swing on and likely plastic golf balls (and possibly a net to capture balls). If weather permits, practice outside. The goal is to swing the golf club 100 times/day for 3–5 days per week.
Plan #2: Hitting golf balls at a golf driving range
The next level is going to a golf driving range, where you are hitting real golf balls and likely have a few more golf clubs. Similar goal, try to hit 100 golf balls/day for 3–5 days per week.
Plan #3: Play a round of golf at a local golf course/club
The third level is to play a round of golf, playing either 9 holes or 18 holes at a local golf course. If you are able to walk, you enhance the exercise routine. Try to play once (or twice) per week. Golf has many rules, yet it is a very honorable and social sport. You can enjoy it playing alone or with friends. Two downsides to golf include the time it takes to play 9 or 18 holes of golf, and it is not without significant equipment and clothes expenditures. However, plans #1 and #2 described above are much more reasonable in terms of time and cost.
Plan #4: Virtual Golf
“Park Place Golf Club” is designed specifically for Parkinson’s disease. This is a virtual 18-hole golf and fitness training program that provides instructional golf videos paired with functional fitness workouts where you can track your progress. Park Place Virtual Golf was created by Taunya Foerster [from https://parkplacegolfclub.com (accessed on 16 April 2021)].
Learning how to play golf
“Golf for Beginners: So You Want To Play Golf” [from https://www.golfdigest.com/gallery/golf-beginners-tips/amp (accessed on 16 April 2021)];
“Beginner Basics” [from https://schools.golfdigest.com/series/will-robins-beginner-basics-rsuzob7 (accessed on 16 April 2021)];
“The best way to learn golf now” [from https://www.golfdigest. com/story/how-to-play-golf-now/amp (accessed on 16 April 2021)];
“A Beginner’s Golf Guide: What every new golfer should know when picking up the game” [from https://www.golfdigest.com/story/the-complete-beginner-s-guide-to-golf (accessed on 16 April 2021)];
“Golf 101: Dos and don’ts for beginners” [from https://golf.com/instruction/golf-101-dos-and-donts-for-beginners/ (accessed on 16 April 2021)];
“How to Play Golf | The Beginner’s Guide” [from https://golfworkoutprogram.com/how-to-play-golf/ (accessed on 16 April 2021)].

Plan #1 involves practicing the golf swing at home. As described above (see Figure 2 and Figure 3), the proper golf swing utilizes many muscles in the upper and lower body. Furthermore, the mechanics of the golf swing offer potential to improve anticipatory postural adjustments and weight shift ability, in addition to coordination, strength, and mobility of trunk musculature. These components may provide a helpful mechanism to reduce the risk for falls (See Section 5.1 and Section 5.2 above for discussion at length of these concepts and related research). With repetition, balance and coordination should improve. Current literature and anecdotal accounts are limited and describe a varied frequency from 2 x/week [119] to 5–7 x/week [see Gary Smith noted above]. Therefore, we propose an exercise dose and frequency of hitting 100 golf balls 3–5 x/week (a typical hour at the driving range involves hitting 50–100 golf balls), although more research is needed to determine optimal dose and frequency.

Plan #2 involves hitting golf balls at a golf driving range. In addition to the benefits discussed in the previous plan, the golfer will now have additional feedback on how far the golf ball travels. As previously discussed in Section 5.4 above, use of external cues may enhance motor learning performance in a PwP [133,134,135] and motivate the golfer to move beyond self-selected effort.

Plan #3 and plan #4 have PwP playing a round of golf on a real surface and virtually, respectively. These golf plans both add components of strategy, cognitive engagement, and a social setting for PwP, allowing the sport to have a positive impact that is multidimensional with potential to address non-motor symptoms in addition to the benefits previously discussed. Playing on a real golf course offers the opportunity to walk on uneven surfaces which may further optimize dynamic balance [114]. With time and continued practice, the golfer with PD should realize improved posture, coordination, balance, and enhanced axial spine rotation (as discussed in Section 5.3 above).

The golf plans described here offer a framework for another exercise strategy for PwP to gain strength, improve balance, coordination, posture, and axial rotation, thereby, potentially reducing their risk of falls. While golf may be considered an expensive sport, plan #1 and plan #2 provide relatively inexpensive options to improve access and allow PwP to benefit from the full-body exercise workout that swinging a golf club provides. Other sports, such as boxing, tai chi, dance, yoga, and pickleball, were also once considered relatively expensive sports that were not easily accessible or available to adapt for PD. However, all of these exercises have inspired community programs and become widely used by PwP to improve quality of life and offer relief from their motor symptoms. Our goal is to “plant-a-seed” for golf, inspire further research, give rise to community programs, and hopefully, watch the game of golf grow in use by PwP as an engaging past time that may prevent falls associated with complications from PD.

6. Conclusions

PD is a chronic neurodegenerative disorder featuring the development and progression of both motor and non-motor defects. This narrative review presents golf as a physical activity to lower the risk of falls in community ambulating older adults with PD. Our literature review has shown that many types of exercise can lessen the risk of falls in older adults. The biomechanics of the golf swing supports the concept of strengthening the upper and lower body, increasing the process of balance, enhancing axial mobility, and improving coordination and posture, all of which should help anyone with PD. Golf also has the potential to improve the quality of life for PwP. Although further study is needed, playing golf regularly may be beneficial in reducing the risk of falls in older adults with PD.

Acknowledgments

F.C.C. dedicates this review article to the memory of Todd R. Klaenhammer (1951–2021) who was an amazing scientist/advisor/academic role model, wonderful husband to Amy and proud parent to Ellen, good friend, and occasional golf partner. F.C.C. thanks Nigel Mackman, Kim Griffin, Jr., and Walter D. Bach, Jr. for their camaraderie during our weekly golf outings and for support of his journey with Parkinson’s disease. Finally, F.C.C. acknowledges Russell R. Broaddus, the Joe W. and Evelyn M. Grisham Distinguished Professor and Department Chair, in the Department of Pathology and Laboratory Medicine at UNC School of Medicine, for continued support of his Parkinson’s disease research/scholarship.

Author Contributions

Conceptualization, F.C.C. and R.R.B.; writing—original draft preparation, R.R.B. and F.C.C.; writing—review and editing, R.R.B. and F.C.C.; visualization, F.C.C. and R.R.B.; project administration, F.C.C. Both authors have read and agreed to the published version of the manuscript.

Funding

No external funding was received for this research.

Institutional Review Board Statement

Not Applicable.

Informed Consent Statement

Not Applicable.

Data Availability Statement

Not Applicable.

Conflicts of Interest

The authors declare no conflict of interest.

Footnotes

Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  • 1.Kalia L., Lang A. Parkinson’s Disease. Lancet. 2015;386:896–912. doi: 10.1016/S0140-6736(14)61393-3. [DOI] [PubMed] [Google Scholar]
  • 2.Poewe W., Seppi K., Tanner C.M., Halliday G.M., Brundin P., Volkmann J., Schrag A.-E., Lang A.E. Parkinson Disease. Nat. Rev. Dis. Primers. 2017;3:17013. doi: 10.1038/nrdp.2017.13. [DOI] [PubMed] [Google Scholar]
  • 3.Ahlskog J.E. The New Parkinson’s Disease Treatment Book: Partnering with Your Doctor to Get the Most from Your Medications. Oxford University Press; Oxford, UK: 2015. [Google Scholar]
  • 4.Santens P., Boon P., Van Roost D., Caemaert J. The pathophysiology of motor symptoms in Parkinson’s disease. Acta Neurol. Belg. 2003;103:103. [PubMed] [Google Scholar]
  • 5.Fox S.H., Katzenschlager R., Lim S.Y., Barton B., de Bie R.M., Seppi K., Coelho M., Sampaio C., Movement Disorder Society Evidence-Based Medicine Committee International Parkinson and Movement Disorder Society Evidence-Based Medicine Review: Update on Treatments for the Motor Symptoms of Parkinson’s Disease. Mov. Disord. 2018;33:1248–1266. doi: 10.1002/mds.27372. [DOI] [PubMed] [Google Scholar]
  • 6.Berganzo K., Tijero B., Gonzalez-Eizaguirre A., Somme J., Lezcano E., Gabilondo I., Fernandez M., Zarranz J., Gómez-Esteban J. Motor and Non-Motor Symptoms of Parkinson’s Disease and Their Impact on Quality of Life and on Different Clinical Subgroups. Neurología. 2016;31:585–591. doi: 10.1016/j.nrl.2014.10.010. [DOI] [PubMed] [Google Scholar]
  • 7.Church F. Treatment Options for Motor and Non-Motor Symptoms of Parkinson’s Disease. Biomolecules. 2021;11:612. doi: 10.3390/biom11040612. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8.Vuletić V. Non-Motor Symptoms in Parkinson’s Disease. Mind Brain. 2020:109–118. doi: 10.1007/978-3-030-38606-1_9. [DOI] [Google Scholar]
  • 9.Schapira A.H., Chaudhuri K.R., Jenner P. Non-Motor Features of Parkinson Disease. Nat. Rev. Neurosci. 2017;18:435. doi: 10.1038/nrn.2017.62. [DOI] [PubMed] [Google Scholar]
  • 10.Chaudhuri K.R., Schapira A.H. Non-Motor Symptoms of Parkinson’s Disease: Dopaminergic Pathophysiology and Treatment. Lancet Neurol. 2009;8:464–474. doi: 10.1016/S1474-4422(09)70068-7. [DOI] [PubMed] [Google Scholar]
  • 11.Chaudhuri K.R., Healy D.G., Schapira A.H. Non-Motor Symptoms of Parkinson’s Disease: Diagnosis and Management. Lancet Neurol. 2006;5:235–245. doi: 10.1016/S1474-4422(06)70373-8. [DOI] [PubMed] [Google Scholar]
  • 12.Maiti P., Manna J., Dunbar G.L. Current Understanding of the Molecular Mechanisms in Parkinson’s Disease: Targets for Potential Treatments. Transl. Neurodegener. 2017;6:28. doi: 10.1186/s40035-017-0099-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13.Parkinson’s Foundation Statistics. Parkinson’s Foundation; Miami, FL, USA: 2019. [Google Scholar]
  • 14.Rekatsina M., Paladini A., Piroli A., Zis P., Pergolizzi J.V., Varrassi G. Pathophysiology and Therapeutic Perspectives of Oxidative Stress and Neurodegenerative Diseases: A Narrative Review. Adv. Ther. 2020;37:113–139. doi: 10.1007/s12325-019-01148-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 15.Lázaro D.F., Bellucci A., Brundin P., Outeiro T.F. Editorial: Protein Misfolding and Spreading Pathology in Neurodegenerative Diseases. Front. Mol. Neurosci. 2020;12:312. doi: 10.3389/fnmol.2019.00312. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 16.Hung C.-W., Chen Y.-C., Hsieh W.-L., Chiou S.-H., Kao C.-L. Ageing and neurodegenerative diseases. Ageing Res. Rev. 2010;9:S36–S46. doi: 10.1016/j.arr.2010.08.006. [DOI] [PubMed] [Google Scholar]
  • 17.Quan H., Koltai E., Suzuki K., Aguiar A.S., Jr., Pinho R., Boldogh I., Berkes I., Radak Z. Exercise, Redox System and Neurodegenerative Diseases. Biochim. Biophys. Acta (BBA) Mol. Basis Dis. 2020;1866:165778. doi: 10.1016/j.bbadis.2020.165778. [DOI] [PubMed] [Google Scholar]
  • 18.Paillard T., Rolland Y., de Souto Barreto P. Protective Effects of Physical Exercise in Alzheimer’s Disease and Parkinson’s Disease: A Narrative Review. J. Clin. Neurol. 2015;11:212. doi: 10.3988/jcn.2015.11.3.212. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19.Marques-Aleixo I., Beleza J., Sampaio A., Stevanović J., Coxito P., Gonçalves I., Ascensão A., Magalhães J. Preventive and Therapeutic Potential of Physical Exercise in Neurodegenerative Diseases. Antioxid. Redox Signal. 2021;34:674–693. doi: 10.1089/ars.2020.8075. [DOI] [PubMed] [Google Scholar]
  • 20.Campos C., Rocha N.B.F., Lattari E., Paes F., Nardi A.E., Machado S. Exercise-induced neuroprotective effects on neurodegenerative diseases: The key role of trophic factors. Expert Rev. Neurother. 2016;16:723–734. doi: 10.1080/14737175.2016.1179582. [DOI] [PubMed] [Google Scholar]
  • 21.Liu Y., Yan T., Chu J.M.-T., Chen Y., Dunnett S., Ho Y.-S., Wong G.T.-C., Chang R.C.-C. The beneficial effects of physical exercise in the brain and related pathophysiological mechanisms in neurodegenerative diseases. Lab. Investig. 2019;99:943–957. doi: 10.1038/s41374-019-0232-y. [DOI] [PubMed] [Google Scholar]
  • 22.Schenkman M., Shipp K.M., Chandler J., Studenski S.A., Kuchibhatla M. Relationships Between Mobility of Axial Structures and Physical Performance. Phys. Ther. 1996;76:276–285. doi: 10.1093/ptj/76.3.276. [DOI] [PubMed] [Google Scholar]
  • 23.Duchesne C., Lungu O.V., Nadeau A., Robillard M., Bore A., Bobeuf F., Lafontaine A., Gheysen F., Bherer L., Doyon J. Enhancing both motor and cognitive functioning in Parkinson’s disease: Aerobic exercise as a rehabilitative intervention. Brain Cogn. 2015;99:68–77. doi: 10.1016/j.bandc.2015.07.005. [DOI] [PubMed] [Google Scholar]
  • 24.Hirsch M.A., Farley B.G. Exercise and Neuroplasticity in Persons Living with Parkinson’s Disease. Eur. J. Phys. Rehabil. Med. 2009;45:215–229. [PubMed] [Google Scholar]
  • 25.Alamgir H., Muazzam S., Nasrullah M. Unintentional falls mortality among elderly in the United States: Time for action. Injury. 2012;43:2065–2071. doi: 10.1016/j.injury.2011.12.001. [DOI] [PubMed] [Google Scholar]
  • 26.Rubenstein L.Z. Falls in older people: Epidemiology, risk factors and strategies for prevention. Age Ageing. 2006;35(Suppl. 2):ii37–ii41. doi: 10.1093/ageing/afl084. [DOI] [PubMed] [Google Scholar]
  • 27.Dibble L.E., Lange M. Predicting Falls in Individuals with Parkinson Disease: A Reconsideration of Clinical Balance Measures. J. Neurol. Phys. Ther. 2006;30:60–67. doi: 10.1097/01.NPT.0000282569.70920.dc. [DOI] [PubMed] [Google Scholar]
  • 28.Dennison A.C., Noorigian J.V., Robinson K.M., Fisman D.N., Cianci H.J., Moberg P., Bunting-Perry L., Martine R., Duda J., Stern M.B. Falling in Parkinson Disease: Identifying and Prioritizing Risk Factors in Recurrent Fallers. Am. J. Phys. Med. Rehabil. 2007;86:621–632. doi: 10.1097/PHM.0b013e311611583. [DOI] [PubMed] [Google Scholar]
  • 29.Siegel R.E. Galen on the Affected Parts. Translation from the Greek Text with Explanatory Notes. Med. Hist. 1977;21:212. [Google Scholar]
  • 30.Tinetti M.E., Speechley M., Ginter S.F. Risk Factors for Falls among Elderly Persons Living in the Community. N. Engl. J. Med. 1988;319:1701–1707. doi: 10.1056/NEJM198812293192604. [DOI] [PubMed] [Google Scholar]
  • 31.Ambrose A.F., Paul G., Hausdorff J.M. Risk factors for falls among older adults: A review of the literature. Maturitas. 2013;75:51–61. doi: 10.1016/j.maturitas.2013.02.009. [DOI] [PubMed] [Google Scholar]
  • 32.James S.L., Lucchesi L.R., Bisignano C., Castle C.D., Dingels Z.V., Fox J.T., Hamilton E.B., Henry N.J., Krohn K.J., Liu Z., et al. The global burden of falls: Global, regional and national estimates of morbidity and mortality from the Global Burden of Disease Study. Inj. Prev. 2020;26:i3–i11. doi: 10.1136/injuryprev-2019-043286. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 33.Gregg E.W., Pereira M.A., Caspersen C.J. Physical Activity, Falls, and Fractures Among Older Adults: A Review of the Epidemiologic Evidence. J. Am. Geriatr. Soc. 2000;48:883–893. doi: 10.1111/j.1532-5415.2000.tb06884.x. [DOI] [PubMed] [Google Scholar]
  • 34.Tow B.P.B., Chua B.S.Y., Fook-Chong S., Howe T.S. Concurrent fractures of the hip and wrist: A matched analysis of elderly patients. Injury. 2009;40:385–387. doi: 10.1016/j.injury.2008.09.013. [DOI] [PubMed] [Google Scholar]
  • 35.Ensrud K.E. Epidemiology of Fracture Risk with Advancing Age. J. Gerontol. Ser. A Biol. Sci. Med. Sci. 2013;68:1236–1242. doi: 10.1093/gerona/glt092. [DOI] [PubMed] [Google Scholar]
  • 36.Franko J., Kish K.J., O’Connell B.G., Subramanian S., Yuschak J.V. Advanced Age and Preinjury Warfarin Anticoagulation Increase the Risk of Mortality After Head Trauma. J. Trauma Inj. Infect. Crit. Care. 2006;61:107–110. doi: 10.1097/01.ta.0000224220.89528.fc. [DOI] [PubMed] [Google Scholar]
  • 37.Moreland J.D., Richardson J.A., Goldsmith C.H., Clase C.M. Muscle Weakness and Falls in Older Adults: A Systematic Review and Meta-Analysis. J. Am. Geriatr. Soc. 2004;52:1121–1129. doi: 10.1111/j.1532-5415.2004.52310.x. [DOI] [PubMed] [Google Scholar]
  • 38.Borges E.G.D.S., Vale R.G.D.S., Cader S.A., Leal S., Miguel F., Pernambuco C.S., Dantas E.H. Postural balance and falls in elderly nursing home residents enrolled in a ballroom dancing program. Arch. Gerontol. Geriatr. 2014;59:312–316. doi: 10.1016/j.archger.2014.03.013. [DOI] [PubMed] [Google Scholar]
  • 39.Dunsky A., Zeev A., Netz Y. Balance Performance Is Task Specific in Older Adults. BioMed Res. Int. 2017;2017:6987017. doi: 10.1155/2017/6987017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 40.Moncada L.V.V., Mire L.G. Preventing Falls in Older Persons. Am. Fam. Phys. 2017;96:240–247. [PubMed] [Google Scholar]
  • 41.Lee P.G., Jackson E.A., Richardson C.R. Exercise Prescriptions in Older Adults. Am. Fam. Phys. 2017;95:425–432. [PubMed] [Google Scholar]
  • 42.Sherrington C., Tiedemann A., Fairhall N., Close J.C., Lord S.R. Exercise to prevent falls in older adults: An updated meta-analysis and best practice recommendations. NSW Public Health Bull. 2011;22:78–83. doi: 10.1071/NB10056. [DOI] [PubMed] [Google Scholar]
  • 43.Lesinski M., Hortobágyi T., Muehlbauer T., Gollhofer A., Granacher U. Effects of Balance Training on Balance Performance in Healthy Older Adults: A Systematic Review and Meta-Analysis. Sports Med. 2015;45:1721–1738. doi: 10.1007/s40279-015-0375-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44.Gschwind Y.J., Kressig R.W., Lacroix A., Muehlbauer T., Pfenninger B., Granacher U. A best practice fall prevention exercise program to improve balance, strength/power, and psychosocial health in older adults: Study protocol for a randomized controlled trial. BMC Geriatr. 2013;13:105. doi: 10.1186/1471-2318-13-105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 45.Bloem B.R., Grimbergen Y.A., Cramer M., Willemsen M., Zwinderman A.H. Prospective Assessment of Falls in Parkinson’s Disease. J. Neurol. 2001;248:950–958. doi: 10.1007/s004150170047. [DOI] [PubMed] [Google Scholar]
  • 46.Stolze H., Klebe S., Zechlin C., Baecker C., Friege L., Deuschl G. Falls in Frequent Neurologicaldiseases. J. Neurol. 2004;251:79–84. doi: 10.1007/s00415-004-0276-8. [DOI] [PubMed] [Google Scholar]
  • 47.Gray P., Hildebrand K. Fall Risk Factors in Parkinson’s Disease. J. Neurosci. Nurs. 2000;32:222–228. doi: 10.1097/01376517-200008000-00006. [DOI] [PubMed] [Google Scholar]
  • 48.Wood B.H., Bilclough J.A., Bowron A., Walker R.W. Incidence and Prediction of Falls in Parkinson’s Disease: A Prospective Multidisciplinary Study. J. Neurol. Neurosurg. Psychiatry. 2002;72:721–725. doi: 10.1136/jnnp.72.6.721. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 49.Almeida L.R.S., Paul S.S., Valenca G.T. Recurrent Falls in People with Parkinson’s Disease. Diagn. Manag. Parkinson’s Dis. 2020;1:157–183. [Google Scholar]
  • 50.Ashburn A., Stack E., Pickering R.M., Ward C.D. A Community-Dwelling Sample of People with Parkinson’s Disease: Characteristics of Fallers and Non-Fallers. Age Ageing. 2001;30:47–52. doi: 10.1093/ageing/30.1.47. [DOI] [PubMed] [Google Scholar]
  • 51.Almeida L.R., Sherrington C., Allen N.E., Paul S.S., Valenca G.T., Oliveira-Filho J., Canning C.G. Disability is an Independent Predictor of Falls and Recurrent Falls in People with Parkinson’s Disease without a History of Falls: A One-Year Prospective Study. J. Park. Dis. 2015;5:855–864. doi: 10.3233/JPD-150651. [DOI] [PubMed] [Google Scholar]
  • 52.Almeida L.R., Valenca G.T., Negreiros N.N., Pinto E.B., Oliveira-Filho J. Predictors of Recurrent Falls in People with Parkinson’s Disease and Proposal for a Predictive Tool. J. Park. Dis. 2017;7:313–324. doi: 10.3233/JPD-160934. [DOI] [PubMed] [Google Scholar]
  • 53.Koller W.C., Glatt S., Vetere-Overfield B., Hassanein R. Falls and Parkinson’s Disease. Clin. Neuropharmacol. 1989;12:98–105. doi: 10.1097/00002826-198904000-00003. [DOI] [PubMed] [Google Scholar]
  • 54.Okuma Y. Freezing of Gait and Falls in Parkinson’s Disease. J. Parkinson’s Dis. 2014;4:255–260. doi: 10.3233/JPD-130282. [DOI] [PubMed] [Google Scholar]
  • 55.Bloem B.R., Hausdorff J.M., Visser J.E., Giladi N. Falls and Freezing of Gait in Parkinson’s Disease: A Review of Two Interconnected, Episodic Phenomena. Mov. Disord. 2004;19:871–884. doi: 10.1002/mds.20115. [DOI] [PubMed] [Google Scholar]
  • 56.Cole M.H., Rippey J., Naughton G.A., Silburn P.A. Use of a Short-Form Balance Confidence Scale to Predict Future Recurrent Falls in People with Parkinson Disease. Arch. Phys. Med. Rehabil. 2016;97:152–156. doi: 10.1016/j.apmr.2015.07.027. [DOI] [PubMed] [Google Scholar]
  • 57.Camicioli R., Majumdar S.R. Relationship between Mild Cognitive Impairment and Falls in Older People with and without Parkinson’s Disease: 1-Year Prospective Cohort Study. Gait Posture. 2010;32:87–91. doi: 10.1016/j.gaitpost.2010.03.013. [DOI] [PubMed] [Google Scholar]
  • 58.McKay J.L., Hackney M.E., Factor S.A., Ting L.H. Lower Limb Rigidity Is Associated with Frequent Falls in Parkinson’s Disease. Mov. Disord. Clin. Pract. 2019;6:446–451. doi: 10.1002/mdc3.12784. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 59.Adkin A.L., Frank J.S., Jog M.S. Fear of Falling and Postural Control in Parkinson’s Disease. Mov. Disord. 2003;18:496–502. doi: 10.1002/mds.10396. [DOI] [PubMed] [Google Scholar]
  • 60.Mak M.K., Wong A., Pang M.Y. Impaired Executive Function Can Predict Recurrent Falls in Parkinson’s Disease. Arch. Phys. Med. Rehabil. 2014;95:2390–2395. doi: 10.1016/j.apmr.2014.08.006. [DOI] [PubMed] [Google Scholar]
  • 61.Öztürk E.A., Koçer B.G. Can Recurrent Falls Be Predicted in Parkinson’s Disease? Ankara Üniversitesi Tıp Fakültesi Mecmuası. 2017;70:1–6. doi: 10.1501/Tıpfak_000000971. [DOI] [Google Scholar]
  • 62.Gazibara T., Tepavcevic D.K., Svetel M., Tomic A., Stankovic I., Kostic V.S., Pekmezovic T. Recurrent falls in Parkinson’s disease after one year of follow-up: A nested case-control study. Arch. Gerontol. Geriatr. 2016;65:17–24. doi: 10.1016/j.archger.2016.02.006. [DOI] [PubMed] [Google Scholar]
  • 63.Allen N.E., Sherrington C., Paul S.S., Canning C.G. Balance and Falls in Parkinson’s Disease: A Meta-Analysis of the Effect of Exercise and Motor Training. Mov. Disord. 2011;26:1605–1615. doi: 10.1002/mds.23790. [DOI] [PubMed] [Google Scholar]
  • 64.Shen X., Wong-Yu I.S., Mak M.K. Effects of Exercise on Falls, Balance, and Gait Ability in Parkinson’s Disease: A Meta-Analysis. Neurorehabilit. Neural Repair. 2016;30:512–527. doi: 10.1177/1545968315613447. [DOI] [PubMed] [Google Scholar]
  • 65.Mirelman A., Rochester L., Maidan I., Del Din S., Alcock L., Nieuwhof F., Rikkert M.O., Bloem B.R., Pelosin E., Avanzino L., et al. Addition of a non-immersive virtual reality component to treadmill training to reduce fall risk in older adults (V-TIME): A randomised controlled trial. Lancet. 2016;388:1170–1182. doi: 10.1016/S0140-6736(16)31325-3. [DOI] [PubMed] [Google Scholar]
  • 66.Sparrow D., DeAngelis T.R., Hendron K., Thomas C.A., Saint-Hilaire M., Ellis T. Highly Challenging Balance Program Reduces Fall Rate in Parkinson Disease. J. Neurol. Phys. Ther. 2016;40:24–30. doi: 10.1097/NPT.0000000000000111. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67.Ashburn A., Fazakarley L., Ballinger C., Pickering R., McLellan L.D., Fitton C. A randomised controlled trial of a home based exercise programme to reduce the risk of falling among people with Parkinson’s disease. J. Neurol. Neurosurg. Psychiatry. 2006;78:678–684. doi: 10.1136/jnnp.2006.099333. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68.Goodwin V.A., Richards S.H., Henley W., Ewings P., Taylor A.H., Campbell J.L. An Exercise Intervention to Prevent Falls in People with Parkinson’s Disease: A Pragmatic Randomised Controlled Trial. J. Neurol. Neurosurg. Psychiatry. 2011;82:1232–1238. doi: 10.1136/jnnp-2011-300919. [DOI] [PubMed] [Google Scholar]
  • 69.Song R., Grabowska W., Park M., Osypiuk K., Vergara-Diaz G., Bonato P., Hausdorff J., Fox M., Sudarsky L., Macklin E. The Impact of Tai Chi and Qigong Mind-Body Exercises on Motor and Non-Motor Function and Quality of Life in Parkinson’s Disease: A Systematic Review and Meta-Analysis. Parkinsonism Relat. Disord. 2017;41:3–13. doi: 10.1016/j.parkreldis.2017.05.019. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 70.Fuzhong L., Peter H., Kathleen F., Elizabeth E., Ronald S., Johnny G., Gianni M., Sara S. Tai Chi and Postural Stability in Patients with Parkinson’s Disease. N. Engl. J. Med. 2012;366:511–519. doi: 10.1056/NEJMoa1107911. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 71.Shen X., Mak M.K. Technology-Assisted Balance and Gait Training Reduces Falls in Patients with Parkinson’s Disease: A Randomized Controlled Trial with 12-Month Follow-Up. Neurorehabilit. Neural Repair. 2015;29:103–111. doi: 10.1177/1545968314537559. [DOI] [PubMed] [Google Scholar]
  • 72.Morris M.E., Menz H.B., McGinley J.L., Watts J.J., Huxham F.E., Murphy A.T., Danoudis M.E., Iansek R. A Randomized Controlled Trial to Reduce Falls in People with Parkinson’s Disease. Neurorehabilit. Neural Repair. 2015;29:777–785. doi: 10.1177/1545968314565511. [DOI] [PubMed] [Google Scholar]
  • 73.Canning C.G., Sherrington C., Lord S.R., Close J.C., Heritier S., Heller G.Z., Howard K., Allen N.E., Latt M.D., Murray S.M., et al. Exercise for falls prevention in Parkinson disease: A randomized controlled trial. Neurology. 2015;84:304–312. doi: 10.1212/WNL.0000000000001155. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74.van der Marck M.A., Klok M.P.C., Okun M.S., Giladi N., Munneke M., Bloem B.R., Force N.F.T. Consensus-Based Clinical Practice Recommendations for the Examination and Management of Falls in Patients with Parkinson’s Disease. Parkinsonism Relat. Disord. 2014;20:360–369. doi: 10.1016/j.parkreldis.2013.10.030. [DOI] [PubMed] [Google Scholar]
  • 75.Fasano A., Canning C.G., Hausdorff J.M., Lord S., Rochester L. Falls in Parkinson’s Disease: A Complex and Evolving Picture. Mov. Disord. 2017;32:1524–1536. doi: 10.1002/mds.27195. [DOI] [PubMed] [Google Scholar]
  • 76.Amara A.W., Memon A.A. Effects of Exercise on Non-motor Symptoms in Parkinson’s Disease. Clin. Ther. 2018;40:8–15. doi: 10.1016/j.clinthera.2017.11.004. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77.Crowley E.K., Nolan Y.M., Sullivan A.M. Exercise as Therapy for Parkinson’s? Aging. 2018;10:1536. doi: 10.18632/aging.101503. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 78.Crowley E., Nolan Y., Sullivan A. Exercise as a therapeutic intervention for motor and non-motor symptoms in Parkinson’s disease: Evidence from rodent models. Prog. Neurobiol. 2019;172:2–22. doi: 10.1016/j.pneurobio.2018.11.003. [DOI] [PubMed] [Google Scholar]
  • 79.De Carvalho A.O., Filho A.S.S., Murillo-Rodriguez E., Rocha N.B., Carta M.G., Machado S. Physical Exercise for Parkinson’s Disease: Clinical and Experimental Evidence. Clin. Pr. Epidemiol. Ment. Health. 2018;14:89–98. doi: 10.2174/1745017901814010089. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80.Ebersbach G., Grust U., Ebersbach A., Wegner B., Gandor F., Kühn A.A. Amplitude-Oriented Exercise in Parkinson’s Disease: A Randomized Study Comparing Lsvt-Big and a Short Training Protocol. J. Neural Transm. 2015;122:253–256. doi: 10.1007/s00702-014-1245-8. [DOI] [PubMed] [Google Scholar]
  • 81.El-Sayes J., Harasym D., Turco C.V., Locke M.B., Nelson A.J. Exercise-Induced Neuroplasticity: A Mechanistic Model and Prospects for Promoting Plasticity. Neuroscientist. 2018;25:65–85. doi: 10.1177/1073858418771538. [DOI] [PubMed] [Google Scholar]
  • 82.Ellis T., Rochester L. Mobilizing Parkinson’s Disease: The Future of Exercise. J. Park. Dis. 2018;8:S95–S100. doi: 10.3233/JPD-181489. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83.Petzinger G.M., Fisher B.E., Van Leeuwen J.E., Vukovic M., Akopian G., Meshul C.K., Holschneider D.P., Nacca A., Walsh J.P., Jakowec M.W. Enhancing Neuroplasticity in the Basal Ganglia: The Role of Exercise in Parkinson’s Disease. Mov. Disord. 2010;25:S141–S145. doi: 10.1002/mds.22782. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84.Schenkman M., Moore C.G., Kohrt W.M., Hall D.A., Delitto A., Comella C.L., Josbeno D.A., Christiansen C.L., Berman B.D., Kluger B.M. Effect of High-Intensity Treadmill Exercise on Motor Symptoms in Patients with De Novo Parkinson Disease: A Phase 2 Randomized Clinical Trial. JAMA Neurol. 2018;75:219–226. doi: 10.1001/jamaneurol.2017.3517. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85.Silveira C.R., Roy E.A., Intzandt B.N., Almeida Q.J. Aerobic exercise is more effective than goal-based exercise for the treatment of cognition in Parkinson’s disease. Brain Cogn. 2018;122:1–8. doi: 10.1016/j.bandc.2018.01.002. [DOI] [PubMed] [Google Scholar]
  • 86.Hall M.-F.E., Church F.C. Integrative Medicine and Health Therapy for Parkinson Disease. Top. Geriatr. Rehabil. 2020;36:176–186. doi: 10.1097/TGR.0000000000000278. [DOI] [Google Scholar]
  • 87.David F.J., Rafferty M.R., Robichaud J.A., Prodoehl J., Kohrt W.M., Vaillancourt D.E., Corcos D.M. Progressive Resistance Exercise and Parkinson’s Disease: A Review of Potential Mechanisms. Parkinson’s Dis. 2012;2012:124527. doi: 10.1155/2012/124527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 88.Lamotte G., Rafferty M.R., Prodoehl J., Kohrt W.M., Comella C.L., Simuni T., Corcos D.M. Effects of Endurance Exercise Training on the Motor and Non-Motor Features of Parkinson’s Disease: A Review. J. Parkinson’s Dis. 2015;5:21–41. doi: 10.3233/JPD-140425. [DOI] [PubMed] [Google Scholar]
  • 89.Ahlskog J.E. Does vigorous exercise have a neuroprotective effect in Parkinson disease? Neurology. 2011;77:288–294. doi: 10.1212/WNL.0b013e318225ab66. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 90.van der Kolk N.M., de Vries N.M., Kessels R.P., Joosten H., Zwinderman A.H., Post B., Bloem B.R. Effectiveness of Home-Based and Remotely Supervised Aerobic Exercise in Parkinson’s Disease: A Double-Blind, Randomised Controlled Trial. Lancet Neurol. 2019;18:998–1008. doi: 10.1016/S1474-4422(19)30285-6. [DOI] [PubMed] [Google Scholar]
  • 91.Ridgel A.L., Vitek J.L., Alberts J.L. Forced, Not Voluntary, Exercise Improves Motor Function in Parkinson’s Disease Patients. Neurorehabilit. Neural Repair. 2009;23:600–608. doi: 10.1177/1545968308328726. [DOI] [PubMed] [Google Scholar]
  • 92.Ferrazzoli D., Ortelli P., Cucca A., Bakdounes L., Canesi M., Volpe D. Motor-Cognitive Approach and Aerobic Training: A Synergism for Rehabilitative Intervention in Parkinson’s Disease. Neurodegener. Dis. Manag. 2020;10:41–55. doi: 10.2217/nmt-2019-0025. [DOI] [PubMed] [Google Scholar]
  • 93.Sell T.C., Abt J.P., Lephart S.M. Physical Activity-Related Benefits of Walking During Golf. In: Crews D., Lutz. R., editors. Science and Golf V: Proceedings of the World Scientific Congress of Golf (V) World Scientific Congress of Golf Trust; Mesa, AZ, USA: 2008. [Google Scholar]
  • 94.Cann A.P., Vandervoort A.A., Lindsay D.M. Optimizing the Benefits versus Risks of Golf Participation by Older People. J. Geriatr. Phys. Ther. 2005;28:85–92. doi: 10.1519/00139143-200512000-00004. [DOI] [PubMed] [Google Scholar]
  • 95.Luscombe J., Murray A.D., Jenkins E., Archibald D. A rapid review to identify physical activity accrued while playing golf. BMJ Open. 2017;7:018993. doi: 10.1136/bmjopen-2017-018993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 96.Farahmand B., Broman G., De Faire U., Vågerö D., Ahlbom A. Golf: A Game of Life and Death–Reduced Mortality in Swedish Golf Players. Scand. J. Med. Sci. Sports. 2009;19:419–424. doi: 10.1111/j.1600-0838.2008.00814.x. [DOI] [PubMed] [Google Scholar]
  • 97.Stenner B.J., Mosewich A.D., Buckley J.D. An exploratory investigation into the reasons why older people play golf. Qual. Res. Sport Exerc. Health. 2016;8:257–272. doi: 10.1080/2159676X.2016.1148773. [DOI] [Google Scholar]
  • 98.Murray A.D., Daines L., Archibald D., Hawkes R.A., Schiphorst C., Kelly P., Grant L., Mutrie N. The relationships between golf and health: A scoping review. Br. J. Sports Med. 2017;51:12–19. doi: 10.1136/bjsports-2016-096625. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 99.Vaile P.A. The Soul of Golf. N. Am. Rev. 1910;192:359–368. [Google Scholar]
  • 100.Mun F., Suh S.W., Park H.-J., Choi A. Kinematic relationship between rotation of lumbar spine and hip joints during golf swing in professional golfers. Biomed. Eng. Online. 2015;14:41. doi: 10.1186/s12938-015-0041-5. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 101.Adlington G.S. Proper Swing Technique and Biomechanics of Golf. Clin. Sports Med. 1996;15:9–26. doi: 10.1016/S0278-5919(20)30155-1. [DOI] [PubMed] [Google Scholar]
  • 102.Myers J., Lephart S., Tsai Y.-S., Sell T., Smoliga J., Jolly J. The role of upper torso and pelvis rotation in driving performance during the golf swing. J. Sports Sci. 2008;26:181–188. doi: 10.1080/02640410701373543. [DOI] [PubMed] [Google Scholar]
  • 103.Nesbit S.M., Serrano M. Work and power analysis of the golf swing. J. Sports Sci. Med. 2005;4:520–533. [PMC free article] [PubMed] [Google Scholar]
  • 104.Nesbit S.M., McGinnis R. Kinematic Analyses of the Golf Swing Hub Path and its Role in Golfer/Club Kinetic Transfers. J. Sports Sci. Med. 2009;8:235–246. [PMC free article] [PubMed] [Google Scholar]
  • 105.Meister D.W., Ladd A., Butler E.E., Zhao B., Rogers A.P., Ray C.J., Rose J. Rotational Biomechanics of the Elite Golf Swing: Benchmarks for Amateurs. J. Appl. Biomech. 2011;27:242–251. doi: 10.1123/jab.27.3.242. [DOI] [PubMed] [Google Scholar]
  • 106.Gluck G.S., Bendo J.A., Spivak J. The lumbar spine and low back pain in golf: A literature review of swing biomechanics and injury prevention. Spine J. 2008;8:778–788. doi: 10.1016/j.spinee.2007.07.388. [DOI] [PubMed] [Google Scholar]
  • 107.McHardy A., Pollard H., Garbutt P.J. Muscle activity during the golf swing * Commentary. Br. J. Sports Med. 2005;39:799–804. doi: 10.1136/bjsm.2005.020271. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 108.Hume A.P.P.A., Keogh J., Reid D. The Role of Biomechanics in Maximising Distance and Accuracy of Golf Shots. Sports Med. 2005;35:429–449. doi: 10.2165/00007256-200535050-00005. [DOI] [PubMed] [Google Scholar]
  • 109.Choi A., Kang T.G., Mun J.H. Biomechanical Evaluation of Dynamic Balance Control Ability During Golf Swing. J. Med. Biol. Eng. 2016;36:430–439. doi: 10.1007/s40846-016-0141-0. [DOI] [Google Scholar]
  • 110.Mitchell K., Banks S., Morgan D., Sugaya H. Shoulder Motions During the Golf Swing in Male Amateur Golfers. J. Orthop. Sports Phys. Ther. 2003;33:196–203. doi: 10.2519/jospt.2003.33.4.196. [DOI] [PubMed] [Google Scholar]
  • 111.Ball K., Best R. Centre of pressure patterns in the golf swing: Individual-based analysis. Sports Biomech. 2012;11:175–189. doi: 10.1080/14763141.2012.673007. [DOI] [PubMed] [Google Scholar]
  • 112.Neumann D.A. Kinesiology of the Musculoskeletal System. 3rd ed. Elsevier; Amsterdam, The Netherlands: 2015. Axial Skeleton: Muscle and Joint Interactions; pp. 379–422. [Google Scholar]
  • 113.Tsang W.W., Hui-Chan C.W. Static and Dynamic Balance Control in Older Golfers. J. Aging Phys. Act. 2010;18:1–13. doi: 10.1123/japa.18.1.1. [DOI] [PubMed] [Google Scholar]
  • 114.Gao K.L., Hui-Chan C.W.Y., Tsang W.W.N. Golfers have better balance control and confidence than healthy controls. Graefe’s Arch. Clin. Exp. Ophthalmol. 2011;111:2805–2812. doi: 10.1007/s00421-011-1910-7. [DOI] [PubMed] [Google Scholar]
  • 115.Tsang W.W., Hui-Chan C.W. Effects of Exercise on Joint Sense and Balance in Elderly Men: Tai Chi versus Golf. Med. Sci. Sports Exerc. 2004;36:658–667. doi: 10.1249/01.MSS.0000122077.87090.2E. [DOI] [PubMed] [Google Scholar]
  • 116.Du Bois A.M., Marcione N.A., Castle S.C., Salem G.J. Golf as Therapeutic Exercise for Older Adults; Proceedings of the World Scientific Congress of Golf; Abbotsford, BC, Canada. 11–13 July 2008. [Google Scholar]
  • 117.Bustelo S.M., Simon B., Warner M., Jácome A., Wootton J., Welch D., Samuel D. Between-side symmetry of quadriceps thickness using ultrasound imaging in female golfers and non-golfers aged over 80 years. Osteoarthr. Cartil. 2016;24:S65. doi: 10.1016/j.joca.2016.01.144. [DOI] [Google Scholar]
  • 118.Du Bois A., Marcione N., Powers C., Flanagan S., Schroeder T., Castle S., Moore J., Salem G.J. The Effects of a Comprehensive Golf Training Program on Measures of Physical Performance and Dynamic Balance in Older Military Veterans. Int. J. Golf Sci. 2021;9 in press. [Google Scholar]
  • 119.Johnson R., Plummer L., Chan J., Willis A.M. Feasibility and Tolerability Randomized Clinical Trial of Golf Versus Tai Chi for People with Moderate Parkinson’s Disease (1962) Neurology. 2021;96:15 Supplement. [Google Scholar]
  • 120.Sacheli M.A., Murray D.K., Vafai N., Cherkasova M.V., Dinelle K., Shahinfard E., Neilson N., McKenzie J., Schulzer M., Appel-Cresswell S. Habitual Exercisers Versus Sedentary Subjects with Parkinson’s Disease: Multimodal Pet and Fmri Study. Mov. Disord. 2018;33:1945–1950. doi: 10.1002/mds.27498. [DOI] [PubMed] [Google Scholar]
  • 121.Rafferty M.R., Schmidt P.N., Luo S.T., Li K., Marras C., Davis T.L., Guttman M., Cubillos F., Simuni T. Regular Exercise, Quality of Life, and Mobility in Parkinson’s Disease: A Longitudinal Analysis of National Parkinson Foundation Quality Improvement Initiative Data. J. Parkinson’s Dis. 2017;7:193–202. doi: 10.3233/JPD-160912. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 122.Lauzé M., Daneault J.-F., Duval C. The Effects of Physical Activity in Parkinson’s Disease: A Review. J. Park. Dis. 2016;6:685–698. doi: 10.3233/JPD-160790. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 123.Palakurthi B., Burugupally S.P. Postural Instability in Parkinson’s Disease: A Review. Brain Sci. 2019;9:239. doi: 10.3390/brainsci9090239. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 124.Kim S.D., Allen N.E., Canning C.G., Fung V.S.C. Postural Instability in Patients with Parkinson’s Disease. CNS Drugs. 2013;27:97–112. doi: 10.1007/s40263-012-0012-3. [DOI] [PubMed] [Google Scholar]
  • 125.Levy G., Louis E.D., Côté L., Pérez M., Mejia-Santana H., Andrews H., Harris J., Waters C., Ford B., Frucht S., et al. Contribution of Aging to the Severity of Different Motor Signs in Parkinson Disease. Arch. Neurol. 2005;62:467–472. doi: 10.1001/archneur.62.3.467. [DOI] [PubMed] [Google Scholar]
  • 126.King L.A., Horak F.B. Lateral Stepping for Postural Correction in Parkinson’s Disease. Arch. Phys. Med. Rehabil. 2008;89:492–499. doi: 10.1016/j.apmr.2007.11.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 127.Lin C.-C., Creath R.A., Rogers M.W. Variability of Anticipatory Postural Adjustments During Gait Initiation in Individuals with Parkinson Disease. J. Neurol. Phys. Ther. 2016;40:40–46. doi: 10.1097/NPT.0000000000000112. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 128.Dijkstra B.W., Gilat M., Lizama L.E.C., Mancini M., Bergmans B., Verschueren S.M., Nieuwboer A. Impaired Weight-Shift Amplitude in People with Parkinson’s Disease with Freezing of Gait. J. Park. Dis. 2021:1–14. doi: 10.3233/jpd-202370. [DOI] [PubMed] [Google Scholar]
  • 129.Horak F., Nutt J., Nashner L. Postural inflexibility in parkinsonian subjects. J. Neurol. Sci. 1992;111:46–58. doi: 10.1016/0022-510X(92)90111-W. [DOI] [PubMed] [Google Scholar]
  • 130.Carpenter M.G., Allum J.H.J., Honegger F., Adkin A.L., Bloem B.R. Postural abnormalities to multidirectional stance perturbations in Parkinson’s disease. J. Neurol. Neurosurg. Psychiatry. 2004;75:1245–1254. doi: 10.1136/jnnp.2003.021147. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 131.Bertram C.P., Lemay M., Stelmach G.E. The effect of Parkinson’s disease on the control of multi-segmental coordination. Brain Cogn. 2005;57:16–20. doi: 10.1016/j.bandc.2004.08.014. [DOI] [PubMed] [Google Scholar]
  • 132.Wang J., Bohan M., Leis B.C., Stelmach G.E. Altered coordination patterns in parkinsonian patients during trunk-assisted prehension. Parkinsonism Relat. Disord. 2006;12:211–222. doi: 10.1016/j.parkreldis.2005.11.008. [DOI] [PubMed] [Google Scholar]
  • 133.Nieuwboer A., Rochester L., Müncks L., Swinnen S.P. Motor Learning in Parkinson’s Disease: Limitations and Potential for Rehabilitation. Parkinsonism Relat. Disord. 2009;15:S53–S58. doi: 10.1016/S1353-8020(09)70781-3. [DOI] [PubMed] [Google Scholar]
  • 134.Georgiou N., Bradshaw J.L., Iansek R., Phillips J.G., Mattingley J.B., Bradshaw J.A. Reduction in External Cues and Movement Sequencing in Parkinson’s Disease. J. Neurol. Neurosurg. Psychiatry. 1994;57:368–370. doi: 10.1136/jnnp.57.3.368. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 135.Rocha P.A., Porfírio G.M., Ferraz H.B., Trevisani V.F. Effects of External Cues on Gait Parameters of Parkinson’s Disease Patients: A Systematic Review. Clin. Neurol. Neurosurg. 2014;124:127–134. doi: 10.1016/j.clineuro.2014.06.026. [DOI] [PubMed] [Google Scholar]
  • 136.Chong T.T.-J., Bonnelle V., Manohar S., Veromann K.-R., Muhammed K., Tofaris G.K., Hu M., Husain M. Dopamine Enhances Willingness to Exert Effort for Reward in Parkinson’s Disease. Cortex. 2015;69:40–46. doi: 10.1016/j.cortex.2015.04.003. [DOI] [PMC free article] [PubMed] [Google Scholar]

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