Skip to main content
Occupational Therapy International logoLink to Occupational Therapy International
. 2019 Apr 1;2019:5820952. doi: 10.1155/2019/5820952

Effects of Whole-Body Vibration on Upper Extremity Function and Grip Strength in Patients with Subacute Stroke: A Randomised Single-Blind Controlled Trial

Jin-Young Ahn 1, Hyeongsu Kim 1,, Chan-Bum Park 2,3
PMCID: PMC6466864  PMID: 31065236

Abstract

Background

Whole-body vibration has been used to improve motor function in chronic stroke patients, but its effect on patients with subacute strokes remains unclear.

Objectives

We explored the effect of whole-body vibration on patients with subacute strokes.

Methods

Participants were randomly allocated to a whole-body vibration (WBV) group (n = 30) or an upper- and lower-cycle (ULC) group (n = 30). Both groups received occupational therapy after these interventions. All participants received treatment for 30 min/day, 5 days/week, for 4 weeks. Both groups received the same conventional physical therapy.

Results

The manual function test (MFT) score and grip strength improved after both WBV (p = 0.001 and p = 0.001, respectively) and ULC (p = 0.002 and p = 0.001, respectively), but the improvement was more pronounced (MFT p = 0.016; GS p = 0.023) after WBV.

Conclusions

These findings suggest that the use of WBV and ULC was effective as remedial treatments for improving upper extremity motor function and increasing grip strength for patients with subacute strokes. The improvement was more pronounced for the WBV treatment. This trial is registered with KCT0003246.

1. Introduction

Stroke, which is a leading cause of long-term disability, is often associated with persistent involvement of an upper extremity [1]. The upper extremity function in stroke patients depends on several factors, including paresis severity, degree of spasticity, and extent of motor and sensory loss [2]. Upper extremity paresis after stroke is a leading cause of serious and long-term hand disability [3]. After a stroke, patients exhibit a complex pattern of upper extremity motor impairments resulting in the loss of functional abilities, such as grip and grasp [4], causing pain, joint contracture, and discomfort, which may lead to limb disuse and impede long-term functional recovery [5]. Additionally, because patients use the unaffected side more during arm action, it is necessary to apply therapy to the affected arm [6]. Of the various approaches used to improve motor function, the first is an effort to increase somatosensory input from the paretic hand using somatosensory stimulation to enhance the brain response [7].

Improving upper extremity motor function is important for increasing occupational engagement [8]. Use of vibration stimulation as an intervention has demonstrated improvement in affected upper extremity motor function for stroke patients since 1990 [8, 9].

Upper extremity motor recovery is aided by task-oriented practice [10]. Such training has been used to facilitate motor function [11]; various desired movements are learned, and inappropriate movements are reduced, thereby improving the adaptation of stroke patients [12]. Patients control strategy is improved by task-oriented training [13], which is more effective than traditional therapies [14].

Whole-body vibration (WBV) is a form of somatosensory stimulation used to rehabilitate stroke patients [15]. WBV affects proprioceptive systems [16]. Low-amplitude WBV (<20 Hz) induces muscular relaxation; medium-amplitude WBV (>50 Hz) triggers muscle soreness and haematoma [17]. WBV enhances muscle strength and power, affording neuromuscular adaptations similar to those produced by strengthening exercises [18].

Previous studies on chronic stroke patients showed that WBV improved walking speed, step length, stride length, double-limb support [19], and balance [20] and increased upper extremity function and strength but decreased upper extremity muscle tone [21]. However, although early rehabilitation of stroke patients is very important, no study has yet investigated the effects of WBV on upper extremity motor function and grip strength in subacute stroke patients; thus, we focused on this topic in this study.

2. Materials and Methods

2.1. Participants

We recruited patients with subacute stroke (n = 60) treated at a local rehabilitation centre in the Republic of Korea. The inclusion criteria were (1) that they experienced their first stroke within 6 months prior to recruitment, (2) a score ≥ 26 on the Mini-Mental Status Examination-Korean version, (3) an affected upper extremity score ≤ 2 on the modified Ashworth scale, (4) an affected upper extremity of Brunnstrom stage ≥ 3, (5) Manual Muscle Test (MMT) grade of >2/5 in the hemiparetic shoulder, and (6) a visual analogue pain scale score ≤ 4. The exclusion criteria were (1) another neurological disease, (2) any prestroke musculoskeletal abnormality, and (3) a score < 47 on the star cancellation test for visual spatial neglect. Written informed consent was obtained from all patients. The study was approved by the Institutional Review Board of Konkuk University (7001355-201802-HR-228).

A sample size of 30 of each group was calculated with an alpha of 0.05, power of 80%, an effect size of 0.7, and a drop-out rate of 10%, using the G-power program.

2.2. Procedures

This was a prospective two-group randomised controlled trial. Each of the 60 participants was randomly allocated to a WBV group (n = 30) or an upper- and lower-cycle (ULC) group (n = 30); each subject drew a card from a box containing two cards marked 1 (WBV group) or 2 (ULC group) without looking at the cards.

The WBV group received WBV (Galileo 2000, Germany; 2011 model) for 30 min prior to task-orientated training. Each subject was seated on an armless chair in front of the platform and instructed to flex both shoulders at 90°, slightly bend both elbows, and then bend the trunk forward to allow both hands to be placed on the platform. Each subject was allowed to hold the palms slightly off the platform to minimise discomfort and prevent strong stimulation of the organs, eyes, and head. The WBV protocol featured seven elements at 4 to 7, 8 to 11, 12 to 15, 16 to 19, 12 to 15, 8 to 11, and 4 to 7 Hz. Each element was delivered for 2 min, and 2 min of rest separated the elements. The frequency of each element was increased by 1 Hz weekly. Thus, the frequencies delivered in week 1 were 4, 8, 12, 16, 12, 8, and 4 Hz; those in week 2 were 5, 9, 13, 17, 13, 9, and 5 Hz; those in week 3 were 6, 10, 14, 18, 14, 10, and 6 Hz; and those in week 4 were 7, 11, 15, 19, 15, 11, and 7 Hz to prevent adaptation. The ULC group received ULC training for 30 min before task-oriented training. The intensities (five levels were possible) of both cycles were chosen by the patient. All subjects in both groups received task-orientated training for 30 min after WBV or ULC, including eating (use of a spoon and cup), dressing (donning and removing a shirt), and personal hygiene (use of a toothbrush, comb, and towel). All subjects participated for 60 min/day, 5 days per week, for 4 weeks. All also received conventional physical therapy.

2.3. Outcome Measurements

All subjects were assessed at baseline and after intervention. Motor function was measured using the MFT, and grip strength was measured using a Jamar hydraulic hand dynamometer.

The MFT was developed to assess the impairments in motor function of the affected upper extremity of stroke patients and to statistically analyse the possible recovery processes during rehabilitation. The MFT is composed of 32 test items, which examine arm motions and manipulative activities. The test-retest reliability coefficient and interrater reliability of the MFT were consistently above 0.95. Cronbach's α coefficient as internal consistency of eight items was also 0.95. With respect to the validity of the MFT, it had a correlation of >0.8 with both the Brunnstrom stage and the Stroke Impairment Assessment Set [22].

Grip strength is useful in clinical practice for the assessment of disease and/or rehabilitation progression. The Jamar hydraulic hand dynamometer was used to measure muscle strength (isometric grip strength test). The participant was asked to squeeze the dynamometer as hard as possible with each of his or her hands. Both maximal handgrip force and endurance were assessed. The Jamar dynamometer was found to be highly reliable = 0.98 and valid = 0.99 for measuring hand grip strength [23].

2.4. Statistical Analysis

All data were analysed using the Statistical Package for the Social Sciences (SPSS) version 12.0 for Windows (SPSS, Chicago, IL, USA). The WBV and ULC groups were compared employing the χ 2 test, the Mann–Whitney U-test, or the independent t-test. Parameter changes in each group after treatment were compared with the aid of the Wilcoxon signed-rank test, and differences in the changes between the WBV and ULC groups were compared using the Mann–Whitney test. A p value < 0.05 was considered to reflect a statistical significance.

3. Results and Discussion

3.1. Results

The general characteristics of the WBV and ULC groups are shown in Table 1. There was no significant between-group difference in age, sex, type of stroke, days from stroke onset, Mini-Mental Status Examination-Korean version (MMSE-K) or modified Ashworth scale (MAS) scores, or Brunnstrom stage. Also, neither the MFT score (p = 0.22) nor the grip strength (p = 0.57) differed between the WBC and ULC group preintervention.

Table 1.

Characteristics of participants.

Variables WBV group
(n = 30)
ULC group
(n = 30)
Between-group
p values
Age (years), mean ± SD 58.7 ± 7.1 60.7 ± 5.9 0.371
Gender
 Male 18 17 0.712
 Female 12 16
Stroke
 Intracranial hemorrhage 15 16 0.462
 Cerebral infarction 15 14
Time since onset of stroke (days), mean ± SD 95.7 ± 31.5 77.3 ± 30.3 0.741
MMSE-K, mean ± SD 27.2 ± 1.32 27.8 ± 1.66 0.313
MAS, mean ± SD 1.00 ± 0.38 1.20 ± 0.56 0.393
Brunnstrom stage, mean ± SD 2.53 ± 0.52 2.40 ± 0.51 0.543
MFT score, mean ± SD 10.93 ± 4.15 12.40 ± 4.48 0.223
Grip strength (kg), mean ± SD 2.36 ± 2.29 2.92 ± 1.95 0.571

SD: standard deviation, WBV: whole-body vibration, ULC: upper and lower cycle, MMSE-K: Mini-Mental Status Examination-Korean version, MAS: modified Ashworth scale, MFT: manual function test, p < 0.05. 1Independent t-test, 2 χ 2 test, and 3Mann–Whitney U-test.

After intervention, both groups exhibited significant increases in MFT scores (p = 0.001, 0.002, respectively) and grip strength (p = 0.001, 0.001, respectively) compared to the preintervention values (Table 2). Furthermore, the MFT score (p = 0.016) and grip strength (p = 0.023) improved more in the WBV than in the ULC group.

Table 2.

Parameters before and after treatment.

WBV group (mean ± SD) ULC group (mean ± SD) Between-group
p values
Before treatment After treatment p value Before treatment After treatment p value
MFT score 10.93 ± 4.15 17.60 ± 5.54 0.001 12.40 ± 4.48 16.13 ± 5.49 0.002 0.016
Grip strength (kg) 2.36 ± 2.29 4.40 ± 1.39 0.001 2.92 ± 1.95 4.09 ± 1.55 0.001 0.023

SD: standard deviation, WBV: whole-body vibration, ULC: upper and lower cycle, MFT: manual function test, p < 0.05 by Wilcoxon's signed-rank test, p < 0.05 by the Mann–Whitney U-test.

4. Discussion

In this study, we found that the use of WBV on motor function and grip strength in patients with subacute stroke was more effective than the use of ULC. Of course, motor function and grip strength improved in both groups, but it improved more in the WBV group. Therefore, task-oriented training after WBV effectively improved motor function and increased grip strength.

All participants had subacute strokes. Although some recovery may occur spontaneously within the first 3 months after stroke [24], intensive training is essential to improve motor recovery [25]. Active upper extremity movement enhances neuroplasticity [26], improving motor recovery [27]. Early active movements were associated with improvements in both groups.

All participants received task-oriented training, which reduces upper extremity impairment and improves both motor function [28] and individual perceptions of health-related quality of life [29]. Misbah and Muhammad (2017) reported that task-oriented training greatly improved upper extremity function in subacute stroke patients [30].

In the previous studies, WBV effectively improved motor function in stroke patients [31, 32]. WBV induced tonic vibration reflexes affected the proprioceptive systems of primary and secondary afferent fibers [18]. The WBV with frequency < 20 Hz induced muscular relaxation [19].

Our study had several limitations. First, the sample size was small, and the results thus cannot be generalised. Second, we did not schedule follow-up after interventions ended; long-term outcomes were not explored.

5. Conclusions

These findings suggest that the use of WBV and ULC was effective as remedial treatments for improving upper extremity motor function and increasing grip strength for patients with subacute strokes. The improvement was more pronounced for the WBV treatment.

Acknowledgments

This paper was supported by Konkuk University in 2018.

Data Availability

(1) The data used to support the findings of this study were supplied under license and so cannot be made freely available. Requests for access to these data should be made to mubul@kku.ac.kr. (2) The data used to support the findings of this study are currently under embargo while the research findings are commercialized. Requests for data, 12 months after publication of this article, will be considered by the corresponding author. (3) The data used to support the findings of this study may be released upon application to Dr. Kim, who can be contacted at mubul@kku.ac.kr.

Conflicts of Interest

The authors declare that there is no conflict of interest regarding the publication of this paper.

References

  • 1.Broeks J. G., Lankhorst G. J., Rumping K., Prevo A. J. H. The long-term outcome of arm function after stroke: results of a follow-up study. Disability and Rehabilitation. 2009;21(8):357–364. doi: 10.1080/096382899297459. [DOI] [PubMed] [Google Scholar]
  • 2.Hewett T. E., Ford K. R., Levine P., Page S. J. Reaching kinematics to measure motor changes after mental practice in stroke. Topics in Stroke Rehabilitation. 2014;14(4):23–29. doi: 10.1310/tsr1404-23. [DOI] [PubMed] [Google Scholar]
  • 3.Teasell R., Foley N., Pereira S., Sequeira K., Miller T. Evidence to practice: botulinum toxin in the treatment of spasticity post stroke. Topics in Stroke Rehabilitation. 2015;19(2):115–121. doi: 10.1310/tsr1902-115. [DOI] [PubMed] [Google Scholar]
  • 4.Page S. J., Levine P., Leonard A., Szaflarski J. P., Kissela B. M. Modified constraint-induced therapy in chronic stroke: results of a single-blinded randomized controlled trial. Physical Therapy. 2008;88(3):333–340. doi: 10.2522/ptj.20060029. [DOI] [PubMed] [Google Scholar]
  • 5.Cirstea M. C., Levin M. F. Improvement of arm movement patterns and endpoint control depends on type of feedback during practice in stroke survivors. Neurorehabilitation and Neural Repair. 2007;21(5):398–411. doi: 10.1177/1545968306298414. [DOI] [PubMed] [Google Scholar]
  • 6.Feys H. M., de Weerdt W. J., Selz B. E., et al. Effect of a therapeutic intervention for the hemiplegic upper limb in the acute phase after stroke: a single-blind, randomized, controlled multicenter trial. Stroke. 1998;29(4):785–792. doi: 10.1161/01.STR.29.4.785. [DOI] [PubMed] [Google Scholar]
  • 7.O'Dell M. W., Lin C.-C. D., Harrison V. Stroke rehabilitation: strategies to enhance motor recovery. Annual Review of Medicine. 2009;60(1):55–68. doi: 10.1146/annurev.med.60.042707.104248. [DOI] [PubMed] [Google Scholar]
  • 8.Caliandro P., Celletti C., Padua L., et al. Focal muscle vibration in the treatment of upper limb spasticity : a pilot randomized controlled trial in patients with chronic stroke. Archives of Physical Medicine and Rehabilitation. 2012;93(9):1656–1661. doi: 10.1016/j.apmr.2012.04.002. [DOI] [PubMed] [Google Scholar]
  • 9.Cardinale M., Wakeling J. Whole body vibration exercise: are vibrations good for you? British Journal of Sports Medicine. 2005;39(9):585–589. doi: 10.1136/bjsm.2005.016857. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10.Langhorne P., Coupar F., Pollock A. Motor recovery after stroke: a systematic review. Lancet Neurology. 2009;8(8):741–754. doi: 10.1016/S1474-4422(09)70150-4. [DOI] [PubMed] [Google Scholar]
  • 11.Yang Y. R., Wang R. Y., Lin K. H., Chu M. Y., Chan R. C. Task-oriented progressive resistance strength training improves muscle strength and functional performance in individuals with stroke. Clinical Rehabilitation. 2016;20(10):860–870. doi: 10.1177/0269215506070701. [DOI] [PubMed] [Google Scholar]
  • 12.Carr J. H., Shepherd R. B. Stroke Rehabilitation: Guidelines for Exercise and Training to Optimize Motor Skill. 1st. London: Butterworth Helenemann; 2003. [Google Scholar]
  • 13.Kim B. H., Lee S. M., Bae Y. H., Yu J. H., Kim T. H. The effect of a task-oriented training on trunk control ability, balance and gait of stroke patients. Journal of Physical Therapy Science. 2012;24(6):519–522. doi: 10.1589/jpts.24.519. [DOI] [Google Scholar]
  • 14.Rensink M., Schuurmans M., Lindeman E., Hafsteinsdóttir T. Task-oriented training in rehabilitation after stroke: systematic review. Journal of Advanced Nursing. 2009;65(4):737–754. doi: 10.1111/j.1365-2648.2008.04925.x. [DOI] [PubMed] [Google Scholar]
  • 15.van Nes I. J. W., Latour H., Schils F., Meijer R., van Kuijk A., Geurts A. C. H. Long-term effects of 6-week whole-body vibration on balance recovery and activities of daily living in the postacute phase of stroke. Stroke. 2006;37(9):2331–2335. doi: 10.1161/01.STR.0000236494.62957.f3. [DOI] [PubMed] [Google Scholar]
  • 16.Cardinale M., Rittweger J. Vibration exercise makes your muscles and bones stronger: fact or fiction? The Journal of the British Menopause Society. 2016;12(1):12–18. doi: 10.1258/136218006775997261. [DOI] [PubMed] [Google Scholar]
  • 17.Rittweger J., Mutschelknauss M., Felsenberg D. Acute changes in neuromuscular excitability after exhaustive whole body vibration exercise as compared to exhaustion by squatting exercise. Clinical Physiology and Functional Imaging. 2003;23(2):81–86. doi: 10.1046/j.1475-097X.2003.00473.x. [DOI] [PubMed] [Google Scholar]
  • 18.Cardinale M., Lim J. Electromyography activity of vastus lateralis muscle during whole-body vibrations of different frequencies. Journal of Strength and Conditioning Research. 2003;17(3):621–624. doi: 10.1519/1533-4287(2003)017<0621:eaovlm>2.0.co;2. [DOI] [PubMed] [Google Scholar]
  • 19.Choi E. T., Kim Y. N., Cho W. S., Lee D. K. The effects of visual control whole body vibration exercise on balance and gait function of stroke patients. Journal of Physical Therapy Science. 2016;28(11):3149–3152. doi: 10.1589/jpts.28.3149. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20.Uhm Y. H., Yang D. J. The effects of whole body vibration combined biofeedback postural control training on the balance ability and gait ability in stroke patients. Journal of Physical Therapy Science. 2017;29(11):2022–2025. doi: 10.1589/jpts.29.2022. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21.Lee J. S., Kim C. Y., Kim H. D. Short-term effects of whole-body vibration combined with task-related training on upper extremity function, spasticity, and grip strength in subjects with poststroke hemiplegia: a pilot randomized controlled trial. American Journal of Physical Medicine & Rehabilitation. 2016;95(8):608–617. doi: 10.1097/PHM.0000000000000454. [DOI] [PubMed] [Google Scholar]
  • 22.Miyamoto S., Kondo T., Suzukamo Y., Michimata A., Izumi S.-I. Reliability and validity of the manual function test in patients with stroke. American Journal of Physical Medicine & Rehabilitation. 2009;88(3):247–255. doi: 10.1097/PHM.0b013e3181951133. [DOI] [PubMed] [Google Scholar]
  • 23.Bellace J. V., Healy D., Besser M. P., Byron T., Hohman L. Validity of the Dexter Evaluation System’s Jamar dynamometer attachment for assessment of hand grip strength in a normal population. Journal of Hand Therapy. 2000;13(1):46–51. doi: 10.1016/S0894-1130(00)80052-6. [DOI] [PubMed] [Google Scholar]
  • 24.Maulden S. A., Gassaway J., Horn S. D., Smout R. J., Dejong G. Timing of initiation of rehabilitation after stroke. Archives of Physical Medicine and Rehabilitation. 2005;86(12):34–40. doi: 10.1016/j.apmr.2005.08.119. [DOI] [PubMed] [Google Scholar]
  • 25.Nudo R. J., Friel K. M. Cortical plasticity after stroke: implications for rehabilitation. Revue Neurologique. 1999;155(9):713–717. [PubMed] [Google Scholar]
  • 26.French B., Thomas L., Leathley M., et al. Does repetitive task training improve functional activity after stroke? A Cochrane systematic review and meta-analysis. Journal of Rehabilitation Medicine. 2010;42(1):9–14. doi: 10.2340/16501977-0473. [DOI] [PubMed] [Google Scholar]
  • 27.Woldag H., Hummelsheim H. Evidence-based physiotherapeutic concepts for improving arm and hand function in stroke patients: a review. Journal of Neurology. 2002;249(5):518–528. doi: 10.1007/s004150200058. [DOI] [PubMed] [Google Scholar]
  • 28.Kwakkel G., Kollen B., Lindeman E. Understanding the pattern of functional recovery after stroke: facts and theories. Restorative Neurology and Neuroscience. 2004;22(3–5):281–299. [PubMed] [Google Scholar]
  • 29.Wolf S. L., Winstein C. J., Miller J. P., et al. Effect of constraint-induced movement therapy on upper extremity function 3 to 9 months after stroke: the EXCITE randomized clinical trial. JAMA. 2006;296(17):2095–2104. doi: 10.1001/jama.296.17.2095. [DOI] [PubMed] [Google Scholar]
  • 30.Misbah M., Muhammad U. Effectiveness of task oriented training in improving upper limb function after stroke. RMJ. 2017;42(3):341–343. [Google Scholar]
  • 31.Choi W., Han D., Kim J., Lee S. Whole-body vibration combined with treadmill training improves walking performance in post-stroke patients: a randomized controlled trial. Medical Science Monitor. 2017;23:4918–4925. doi: 10.12659/MSM.904474. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32.Silva A. T., Dias M. P. F., Calixto R., Jr, et al. Acute effects of whole-body vibration on the motor function of patients with stroke. American Journal of Physical Medicine & Rehabilitation. 2014;93(4):310–319. doi: 10.1097/PHM.0000000000000042. [DOI] [PubMed] [Google Scholar]

Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Data Availability Statement

(1) The data used to support the findings of this study were supplied under license and so cannot be made freely available. Requests for access to these data should be made to mubul@kku.ac.kr. (2) The data used to support the findings of this study are currently under embargo while the research findings are commercialized. Requests for data, 12 months after publication of this article, will be considered by the corresponding author. (3) The data used to support the findings of this study may be released upon application to Dr. Kim, who can be contacted at mubul@kku.ac.kr.


Articles from Occupational Therapy International are provided here courtesy of Hindawi Ltd. and John Wiley and Sons, Inc.

RESOURCES