Abstract
Background and objective
While designing the rehabilitation regime of a hemiplegic patient, most physiotherapists focus on the affected/hemiparetic side. The less affected/unaffected side remains unused and loses its properties, i.e., muscle strength, girth, balance, and gait, thus causing deconditioning effects in patients’ overall rehabilitation. To enhance the recovery process, the focus should be drawn to training both sides equally to fasten the recovery process. The rationale behind designing this study was to maintain the integrity of the unaffected side along with rehabilitation of the affected side in hemiplegic patients. Many proven studies focus on bimanual upper-limb training in post-stroke survivors, but there is a lack of literature regarding the same in the lower limbs. This clinical trial was designed to study the effect of bilateral lower-limb training over unilateral lower-limb training on balance and walking in post-stroke survivors.
Methods
40 hemiplegic patients were selected and randomly divided into two groups: Group A (unilateral training group (UTG)) and Group B (bilateral training group (BTG)). Patients in Group A underwent approach-oriented training using the motor relearning program (MRP) and proprioceptive neuromuscular facilitation (PNF) for the affected side, while those in Group B underwent strength training for the lower-limb muscles using DeLorme's principle for the unaffected side and approach-oriented training using the MRP and PNF for the affected side for a period of six weeks, five days per week. A strengthening regimen was designed for the unaffected side, considering the frequency, intensity, time, and type (FITTs) principle provided by the American College of Sports Medicine (ACSM). The static and dynamic balance along with gait parameters were measured using the functional reach test (FRT), one-leg stance test (OLST), Berg balance scale (BBS), Dynamic Gait Index (DGI), gait parameters (stride length, gait velocity, and cadence), and Brunnstrom recovery stages (BRS) at the baseline and post rehabilitation.
Results
Both groups significantly improved following therapy (p<0.05). Group B showed more significant results both statistically and clinically. The enhancement in the FRT (2.25, p<0.03), OLST (5.12. p<0.0001), BBS (0.68, p<0.020), and DGI (1.70, p<0.030) scores indicated improvement in static and dynamic balance in the two groups. Patients showed improvement in the stereotyped sequence of movements indicating recovery on the BRS (4.62, p<0.0001). The overall gait parameters in patients, i.e., gait velocity (6.78, p<0.0001), stride length (3.59, p<0.001) and cadence (6.15, p<0.0001), improved post rehabilitation.
Conclusion
The results of this study showed that the BTG had positive impacts on the postural balance and walking capacities of subacute hemiparetic stroke patients, promoting early recovery in comparison to the UTG. This study also helped to design a strengthening protocol for the unaffected side according to DeLorme’s principle in line with the FITTs principle.
Keywords: rehabilitation, stroke, walking, balance, unilateral training, bilateral training
Introduction
According to the WHO, stroke is the "incoming epidemic of the twenty-first century," defined as "the rapidly expanding clinical evidence of a permanent (or global) impairment of brain function, with symptoms lasting 24 hours or more or leading to death, for no apparent reason other than the vascular origin" [1,2]. In low- and middle-income nations, stroke accounts for 70% of all cases, causes 87% of fatalities, and reduces life expectancy through disability. Modified stroke prevalence rates in rural India range from 84 to 262 per 100,000 people, whereas rates in urban areas range from 334 to 424 per 100,000 people [3].
Based on etiology, stroke is categorized into two disparate variants: ischemic and hemorrhagic. An ischemic variant of stroke evolves whenever the vascularity of the tissues of the brain gets jeopardized as a result of any inherent reason, and it is encountered in a majority of stroke sufferers [4]. However, a hemorrhagic subtype of stroke dawns whenever an artery serving the blood to the brain is disrupted [5]. A large percentage of stroke victims experience hemiplegia (paralysis) or hemiparesis (weakness) on the contralateral side [6]. Aside from this, considerable weakness can be seen on the "seemingly normal" ipsilateral side of the lesion [7,8]. This is because only 75 to 90% of corticospinal fibers cross to the medulla's contralateral side. The remainder transmit ipsilaterally to the spinal cord by the anterior or ventral corticospinal tract. In the spinal cord, some of these fibers cross, while the remainder remain uncrossed, resulting in bilateral paralysis [9].
One of the most prevalent impairments in persons who have had a stroke is a loss of muscle strength. Muscle weakness leads to activity limitations i.e., walking, sit-to-stand transfers, stair climbing, and upper-limb and lower-limb activities. Strengthening of weak muscles using progressive resistive strength training (PRT) has evidence of positive effects in post-stroke survivors using the DeLorme and Watkins principles where resistance should be gradually raised [10]. The frequency, intensity, time, and type (FITT) principle is provided by the American College of Sports Medicine (ACSM) for stroke patients for strengthening the hemiplegic side, but there is no such consideration for the unaffected side, even though there is enough documentation that post-stroke survivors motor functioning is compromised on the unaffected side, as evidenced by muscular weakness, atrophy, or disuse [11-13].
Combining a bilateral training program with unilateral task-oriented training may be more beneficial for improving arm and hand function in those with chronic paresis than unilateral task-oriented training alone [14]. Bilateral arm training with auditory cueing enhances the functional and motor performance of the affected extremity in stroke survivors [15]. Exercises to strengthen the lower limbs on both sides may assist stroke survivors with getting out of a chair, climbing stairs, walking, and generally improving their quality of life [16]. There is not enough evidence in literature to support whether format, dosage, and strategy are best for enhancing static and dynamic balance as well as the spatial and temporal gait parameters. This dearth in literature is the main purpose of our study by using specific DeLorme’s progressive resistance training on the unaffected side, along with approach-oriented specific training on the affected side. Bilateral training patients are given the task-oriented technique, with the less affected side receiving strength training and the affected side receiving a motor relearning program (MRP) and proprioceptive neuromuscular facilitation (PNF).
Although it is known that the unaffected side begins to lose strength five days after a stroke, limited study has been done on the effects of bilateral lower limb strengthening training, and there is no prescribed strengthening protocol for that side [12]. As a result, both paretic and non-paretic lower limbs were trained in this study, and a fixed regimen for the unaffected side training was designed and implemented.
Materials and methods
Participants
The study included people who had experienced their first stroke and were living in the community between the ages of 45 and 65. This age range was selected to achieve homogeneity and to take into account the age range during which strokes are most common [3]. G. Power 3.1.9.4 program used information from Banerjee and Das (2016) to calculate the number of study participants [3]. The study included 40 patients (20 each in both Groups A and B). The hiring process was placed in a straight line from June 2021 to June 2022. 98 people in total were examined for eligibility. The conduct and reporting of the trial were standardized using Consolidated Standards for the Reporting of Trials (CONSORT) [17]. The inclusion criteria were that the participants had to be of either gender between the age group of 40 to 65 years age group, in the sub-acute stage (one week to six months) of stroke, be able to understand and follow instructions, be willing to participate in the study, and be able to complete the outcome measures. Patients with a history of an old stroke (stroke with no active findings on radiological imaging), transient ischemic attack, or recurrent stroke; patients with any unstable cardiovascular condition, as determined by the physician; patients diagnosed with brainstem stroke and middle cerebral artery stroke; patients diagnosed with the failure of vital organs such as lungs, heart, and kidneys; and those who are currently enrolled in another research trial were excluded from the study. All the participants provided written informed consent. 40 participants were randomized in total, and baseline information is available. Figure 1 shows a flowchart of the study's methodology.
Figure 1. CONSORT flow chart of the study procedure.
CONSORT: Consolidated Standards for the Reporting of Trials
Study design
A randomized clinical trial was performed at the neuro-physiotherapy outpatient department of Ravi Nair Physiotherapy College and Acharya Vinoba Bhave Rural Hospital, Sawangi, Meghe, Wardha, India. Approval was taken from the Committee for Institutional Ethical Committee of the Datta Medical Science, Datta Meghe Institute of Medical Sciences (DMIMS, DU), Sawangi, Meghe, Wardha, India (Ethical permission number: DMIMS[DU]/IEC/2021/248) and Clinical Trial Registration of India (CTRI/2021/05/033621). The included participants diagnosed with subacute stroke were randomized through simple random sampling and allocated through the sequentially numbered opaque sealed envelope (SNOSE) method into Group A (unilateral training group (UTG)) and Group B (bilateral training group (BTG)). Randomization and allocation were done by the primary researcher who is a postgraduate resident in physiotherapy under the guidance of a professor of the neuro-physiotherapy department. Outcomes were assessed before the beginning of the study and immediately after the completion of the study by a postgraduate resident in physiotherapy of the same experience, who was aware of the study and blinded about the intervention. All aspects of the study's enrollment, intervention, and evaluation plans adhered to the established protocol requirements: a suggestion for conducting intervention trials [18].
Intervention
40 hemiplegic patients were selected and randomly divided into two groups: Group A (UTG) and Group B (BTG). Patients in Group A received approach-oriented training for the affected side using MRP and PNF, and Group B received strength training for muscles of the lower limb using DeLorme’s principle for the unaffected side and approach-oriented training for the affected side using MRP and PNF for five days/week for six weeks.
Group A:For five days a week for a period of six weeks, the participants in this group underwent 20 minutes of lower limb training on the affected side only by a physiotherapist. The MRP and PNF (Figure 2) were both part of it, task-specific training and multiplanar motions of the affected lower and upper extremities are included [19].
Figure 2. Intervention provided to the patients in both the groups.
The MRP, PNF, DeLorme's strengthening principle, and FITT principles were used to design the rehabilitation [6,11,19].
PNF: Proprioceptive neuromuscular facilitation; RM: Repetition maximum; MRP: Motor relearning program; FITT: Frequency, intensity, time, and type
Group B:This group got bilateral lower-limb training that comprised a task-oriented strategy for the damaged side, such as the MRP and PNF, as well as strengthening of the less affected side [20,21]. A physiotherapist prescribed strength training for 20 minutes on the side that was less affected, as well as 20 minutes of lower- and upper-limb exercises for the involved side five days a week for six weeks. The hip flexors, abductors and extensors, knee extensors, and ankle dorsiflexors were stengthened [12]. Each muscle was provided strength training for three minutes with a rest period of one minute in between each muscle group. Before training, each muscle group was tested for one repetition maximum (RM) using DeLorme’s boot. Post measurement, the strengthening was provided via a weight cuff tied over the ankle according to the strengthening regimen prescribed by DeLorme. The whole intervention design is displayed in Figure 2 [6,11,19].
Primary outcome measures
The primary outcome measures included balance post intervention. The functional reach test (FRT) is a clinical outcome test that assesses complicated balance in a single task. By measuring the patient's maximum forward reach while standing in a fixed posture, the FRT assesses a patient's stability. One-leg stance test (OLST) or single-leg stance test is a tool that is used to evaluate static posture and balance control. This technique is performed with eyes open and hands on hips. A client is more likely to fall and get an injury if they cannot stand for more than five seconds. Gait parameters, i.e., stride length, cadence, and gait velocity was assessed by 10-meter walk test. Berg balance scale (BBS) is a clinical evaluation that is frequently employed to assess a subject's static and dynamic balance. It is largely acknowledged as the best tool available for actual balancing tests. The 14 basic balance tasks in this evaluation, which take between 15 and 20 minutes to complete, range from standing to one-foot standing while seated. Dynamic Gait Index (DGI) is a tool for evaluating gait, balance, and the risk of falling that has been shown in studies. This requires both frequent steady-state walking and walking while engaging in more demanding activities.
Secondary outcome measures
The Brunnstrom recovery stages (BRS) is a performance-based outcome that is based on the stereotyped sequence of events that take place during the recovery process from a stroke. It has separate components for the upper limb, trunk, and lower limb. For lower-limb evaluation, the patient is tested supine, then sitting, then standing, and if possible, gait is evaluated. The return of function is stated from Stage 1 to Stage 6. The patient’s stage of recovery from the time of the episode helps in early prognosis.
Statistical analysis
Descriptive and inferential statistics were carried out using the chi-square test, Student's paired and unpaired t-tests, and software from SPSS 27.0 (IBM SPSS, Armonk, USA) and GraphPad Prism 7.0 (GraphPad Software, San Diego, USA). The level of significance for the statistical analysis was established at p<0.05. Student’s paired t-tests were used to find the statistical difference between Groups A and B, and it came out to be significant.
Results
In all, 98 patients were enrolled, and eligibility was determined for each. 58 of those patients were left out: 26 people refused to participate, 19 did not meet the requirements for participation, and 13 had additional justifications. The study's 40 patients who met the inclusion requirements formed Group A and Group B. Patients in Group A were 40-63 years old on average, whereas those in Group B were 40-65 years old, with a gender distribution of 12:8 and 11:9 (men: women), respectively. Using the chi-square test, it was determined that there was no statistically significant difference between the two groups' patient ages (p-value=0.91). The baseline characteristics of the subjects are described in Table 1. The patients with the anterior cerebral artery stroke in the subacute phase, i.e., a week to six months from the stroke were in the inclusion criteria.
Table 1. Baseline characteristics.
NS: Not significant
| Baseline Characteristics | Group A | Group B | p-value |
| Age in years | 51.75±7.06 | 51.50±8.40 | 0.91, NS |
| Age Range | 40-63 yrs | 40-64 yrs | |
| Gender | |||
| Male | 12 (60%) | 11 (55%) | 0.54, NS |
| Female | 8 (40%) | 9 (45%) | |
Table 2 indicates the statistical analysis of the measured outcome measures as well as the significant value post rehabilitation between groups. This study found that bilateral lower-limb strengthening exercise benefited hemiparetic stroke patients regain their balance, i.e., Group B showed a larger improvement in outcome measure scores than Group A.
Table 2. Mean FRT, OLST, gait velocity, stride length, cadence, BBS, DGI, and BRS pre and post treatment of Groups A and B and inter-group analysis.
FRT: Functional reach test; OLST: One-leg stance test; BBS: Berg balance scale; DGI: Dynamic Gait Index; BRS: Brunnstrom recovery stages
| Outcome measure | Group A | p-value | Group B | p-value | Mean Difference (X±SD) | p-value | |||
| Pre-treatment | Post-treatment | Pre-treatment | Post-treatment | Group A | Group B | ||||
| FRT | 11.55±1.84 | 28.20±3.56 | 0.0001 | 12.65±2.13 | 32±3.74 | 0.0001 | 16.65±4.14 | 19.35±3.39 | 0.030 |
| OLST | 0.85±0.36 | 4.40±0.59 | 0.0001 | 0.90±0.44 | 5.60±0.75 | 0.0001 | 3.55±0.60 | 4.70±0.80 | 0.0001 |
| Gait velocity (m/sec) | 0.03±0.01 | 0.21±0.05 | 0.0001 | 0.04±0.01 | 0.35±0.07 | 0.0001 | 0.17±0.05 | 0.31±0.07 | 0.0001 |
| Stride length (cm) | 19±2.80 | 56.40±8.50 | 0.0001 | 21.60±3.58 | 68.85±7.12 | 0.0001 | 37.40±9.27 | 47.25±7.98 | 0.001 |
| Cadence (steps/min) | 24.60±3.16 | 46.30±5.33 | 0.0001 | 26.15±3.95 | 62.65±9.17 | 0.0001 | 21.70±6.39 | 36.50±8.65 | 0.0001 |
| BBS | 23.85±3.99 | 39.45±4.68 | 0.0001 | 29.80±6.62 | 46.60±3.05 | 0.0001 | 13.60±3.63 | 16.80±6.92 | 0.020 |
| Dynamic Gait Index | 7.65±1.53 | 17.30±2 | 0.0001 | 8.55±1.98 | 19.30±1.71 | 0.0001 | 9.65±2.05 | 10.75±2.02 | 0.030 |
| BRS | 2.50±0.51 | 4.05±0.75 | 0.0001 | 2.45±0.51 | 5.10±0.64 | 0.0001 | 1.55±0.75 | 2.65±0.74 | 0.0001 |
The Figure 3 depicts the pre- and post-treatment scores of the FRT. There was an improvement in both the groups post treatment, but Group B shows more significant results. For inter-group analysis, Student’s unpaired t-test was used, and the results came out to be significant (t-value=2.25, p-value=0.030) for FRT. This indicates an improvement in the dynamic balance of the patients.
Figure 3. Comparison of FRT scores in two groups pre and post treatment.
FRT: Functional reach test
Similarly, in Figure 4, the representation of pre- and post-treatment OLST scores is provided. There were commendable results in Group B, indicating improvement in the static balance of the patient post treatment. For inter-group analysis, Student’s unpaired t-test was used, and the results came out to be significant (t-value=5.12, p-value=0.0001) for OLST.
Figure 4. Comparison of OLST (sec) score in two groups pre and post treatment.
OLST: One-leg stance test
Figure 5 provides the results in gait velocity which were great both clinically and statistically. For inter-group analysis, Student’s unpaired t-test was used, and the results came out to be significant (t-value=6.78, p-value=0.0001) for gait velocity.
Figure 5. Comparison of gait velocity (m/sec) score in two groups pre and post treatment.
Figure 6 provides the results in the improvement of stride length of the patient post rehabilitation. For inter-group analysis, Student’s unpaired t-test was used, and the results came out to be significant (t-value=3.59, p-value=0.0001) for stride length.
Figure 6. Comparison of stride length (cm) in two groups pre and post treatment.
Figure 7 provides the positive effects of the treatment protocol of the patients post rehabilitation on the steps/min, i.e., cadence. This suggested that the treatment provided also enhances gait parameters. For inter-group analysis, Student’s unpaired t-test was used, and the results came out to be significant (t-value=6.15, p-value=0.0001) for cadence score.
Figure 7. Comparison of cadence (steps) in two groups pre and post treatment.
There was an improvement in the patients' balance post rehabilitation. For inter-group analysis, Student’s unpaired t-test was used, and the results came out to be significant (t-value=0.68, p-value=0.020) for the BBS score. It is indicated in Figure 8.
Figure 8. Comparison of total BBS score in two groups pre and post treatment.
BBS: Berg balance scale
For inter-group analysis, Student’s unpaired t-test was used, and the results came out to be significant (t-value=1.70, p-value=0.030) for the DGI score indicated in Figure 9.
Figure 9. Comparison of DGI scores in two groups pre and post treatment.
DGI: Dynamic Gait Index
There was refinement in the movement pattern from the stereotyped movement pattern indicated by BRS (see Figure 10). For inter-group analysis, Student’s unpaired t-test was used, and the results came out to be significant (t-value=4.62, p-value=0.0001) for the BRS score.
Figure 10. Comparison of BRS Score in two groups pre and post treatment.
BRS: Brunnstrom recovery stages
Discussion
The goal of stroke rehabilitation is to enable individuals who have had a stroke to return to having as close to a normal life as possible by reclaiming their daily skills. Different therapeutic options have been used to help people who have suffered from a stroke to improve their quality of life. While developing the rehabilitation regimen for a hemiplegic patient, most physiotherapists focus on the affected/hemiparetic side. The less affected/not affected side stays unused and loses its properties, thus causing deconditioning effects in the overall rehabilitation of patients. To enhance the recovery process, emphasis should be placed on training both. The rationale for this study was to maintain the integrity of the unaffected side as well as the rehabilitate the impacted side in hemiplegic patients.
We believe this study is the first to document the key benefits of strengthening the unaffected lower limb to enhance balance and gait in stroke survivors. Strength impairment on the unaffected side was stated in 1995 when individuals with stroke had muscle strength impairment which was more proximally than distally for both upper limbs and lower limbs. These correlations provide support for the inclusion of bilateral strength training activities in the management of post-stroke survivors [12]. Static balance and proprioception are instantly impacted by strengthening training as an intervention strategy in healthy adults. It is suggested that strengthening exercises for the gluteus medius should be targeted since the group of subjects who received strengthening training in their weak areas fared substantially better than the group who received relaxation therapy in their strong areas [22].
In a systemic review of a similar nature on the upper limb in 2020, it was found that training both arms may be more helpful than training only one in hastening the recovery of upper-limb function after stroke [23]. In a similar study in 2021, six weeks of bilateral training illustrated a drastic improvement showing the importance of training both sides in patients with hemiplegia [24]. A study in 2018 showed the positive effects of bilateral lower limb strengthening on the balance and walking in hemiplegic patients. It also showed that the non-paretic limb strength also a has significant effect on balance [25].
The FRT was 32±3.74 cm in all of the participants of Group B while in Group A, it was 28.20±3.56. Recurrent falls were linked to a score of 17.78 cm in a previous study, which has been utilized to look into the effects of balance and falls in patients after stroke suggesting an improvement in dynamic balance [26,27]. The OLST, which is used to assess static posture and balance control, provided a significant result in our study. As the suggested normative value indicates, the inability to stand for less than five seconds suggested a greater risk of injury from a fall. Most of our subjects approached the normative value post six weeks of intervention. Walking speed, which is frequently decreased in stroke patients, is crucial for evaluating gait. In healthy people, the average walking speed is 1.3 m/s, whereas, in people with hemiplegia, it ranges from 0.23-0.73 m/s [28,29]. Both groups improved their gait velocity as a result of our research, with Group B showing a mean of 0.35, indicating normative values for hemiplegic patients. The majority of the patients in both groups showed improvement in stride length. The mean came out to be 68.85 cm. Bytyci and Henein stated that a stride length of 64 cm accurately predicts the occurrence of future clinical issues, suggesting that it could be used to guide individuals to the best possible exercise and assistance [30]. In this clinical trial, 17 participants in Group B and 11 in Group A achieved more than 64 cm stride length. Similar effects were found in cadence, suggesting an improvement in overall gait. The improvement in stride length can be correlated with the improvement in cadence [30]. It is in line with previous research, which states that in addition to traditional therapy after a stroke, bilateral isokinetic strengthening exercise appears to be useful in strengthening muscles on both sides and enhancing gait, balance, and functional characteristics [31].
The majority of the patients (34 out of 40) in the current study complained of a lack of balance. The BBS is a recognized tool to measure the static and dynamic balance in stroke patients. The mean BBS score for all of the participants of Group B was 46.60±3.05, indicating that most of them (17 out of 20) were at minimal risk of falling as, according to previous studies, scores of 45 have been linked to an increased risk of falling [32,33]. In an original article, it is stated that the most effective treatment for increasing strength seems to be progressive resistance training [34]. It greatly boosts strength when it is properly targeted, thereby improving the balance and reducing the gait deviations [34,35]. The BRS in our subjects also improved post treatment, which is also found out in similar studies [36].
In our study, FRT, OLST, gait parameters, BBS, DGI, and BRS of the lower limb showed more improvement in the BTG post rehabilitation. Training both sides aided in both early recovery and the creation of a foundation for future studies on how emphasizing the unaffected side can enhance the capabilities of the affected side. As a result, physiotherapists should use bilateral lower-limb training to efficiently restore balance and rehabilitate gait in post-stroke survivors to achieve the highest level of self-independence.
Limitations and future scope
It is important to recognize the study's several shortcomings. As this was a time-bound study, follow up was not possible, suggesting the long-term effects were not assessed. Sub-acute stroke survivors were included. Thus, generalization of results was not possible. This study's randomized controlled design and standardized training regimen with pre-established exercises are its greatest strengths. All of the evaluations were carried out by the same independent physiotherapist, which lessened the risk to internal validity. The narrow age range can be seen as a strength because a bigger age range would probably have resulted in considerably greater variance in the outcomes.
The results of this study demonstrate the benefits of strengthening the unaffected side combined with approach-oriented training for the affected side in post-stroke survivors. A similar study with different patients in acute and chronic stages of stroke can be done in the future. This study also helped to design a set strengthening regimen for the unaffected side of hemiparetic patients, further enabling many new types of research.
Conclusions
Reduction in muscle strength post stroke is one of the causes of delayed recovery. In this randomized clinical trial, we found that both groups improved in terms of static and dynamic balance, gait parameters, and overall stroke-specific index of disability. When both groups were compared, the BTG showed more significant results clinically and statistically on comparison of all the outcome measures, i.e., FRT, OLST, gait parameters, BBS, DGI, and BRS of the lower limb. Training both sides not only helped in early recovery but also helped to establish a base for further research on how focusing on the unaffected side helps to improve the competencies of the affected side. As a result, physiotherapists should use bilateral lower-limb training to efficiently restore balance and rehabilitate gait in post-stroke survivors to achieve the highest level of independence.
The content published in Cureus is the result of clinical experience and/or research by independent individuals or organizations. Cureus is not responsible for the scientific accuracy or reliability of data or conclusions published herein. All content published within Cureus is intended only for educational, research and reference purposes. Additionally, articles published within Cureus should not be deemed a suitable substitute for the advice of a qualified health care professional. Do not disregard or avoid professional medical advice due to content published within Cureus.
The authors have declared that no competing interests exist.
Human Ethics
Consent was obtained or waived by all participants in this study. Institutional Ethics Committee, Datta Meghe Institute of Medical Sciences (Deemed to be University), Sawangi (Meghe), Wardha, India issued approval DMIMS(DU)/IEC/2021/248. The following study project has been approved by the institutional ethics committee to be carried out at Ravi Nair Physiotherapy College, Sawangi (Meghe), Wardha, India. This approval has been given upon the understanding that the research project would be conducted in conformity with the ethical standards established by the Central Ethics Committee on Human Research (CECHR).
Animal Ethics
Animal subjects: All authors have confirmed that this study did not involve animal subjects or tissue.
References
- 1.Stroke prevention--medical and lifestyle measures. Sarikaya H, Ferro J, Arnold M. Eur Neurol. 2015;73:150–157. doi: 10.1159/000367652. [DOI] [PubMed] [Google Scholar]
- 2.World Health Organization (WHO) Definition of Stroke. [ Jan; 2021 ]. https://www.publichealth.com.ng/world-health-organization-who-definition-of-stroke/ https://www.publichealth.com.ng/world-health-organization-who-definition-of-stroke/
- 3.Fifty years of stroke researches in India. Banerjee TK, Das SK. Ann Indian Acad Neurol. 2016;19:1–8. doi: 10.4103/0972-2327.168631. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Hui C, Tadi P, Patti L. Ischemic Stroke. StatPearls Publishing. Treasure Island, USA: StatPearls Publishing; 2022. Ischemic Stroke. [PubMed] [Google Scholar]
- 5.Unnithan AKA, M Das J, Mehta P. Hemorrhagic Stroke. In. Treasure Island. Treasure Island, USA: StatPearls Publishing; 2022. Hemorrhagic Stroke; p. 2022. [PubMed] [Google Scholar]
- 6.O’Sullivan SB, Schmitz TJ, Fulk GD. Philadelphia, USA: F.A. Davis Company; 2019. Physical Rehabilitation. [Google Scholar]
- 7.Longitudinal changes in muscle strength and mass after acute stroke. Carin-Levy G, Greig C, Young A, Lewis S, Hannan J, Mead G. Cerebrovasc Dis. 2006;21:201–207. doi: 10.1159/000090792. [DOI] [PubMed] [Google Scholar]
- 8.The distribution of muscle weakness in upper motoneuron lesions affecting the lower limb. Adams RW, Gandevia SC, Skuse NF. Brain. 1990;113:1459–1476. doi: 10.1093/brain/113.5.1459. [DOI] [PubMed] [Google Scholar]
- 9.The pyramidal tract. Davidoff RA. Neurology. 1990;40:332–339. doi: 10.1212/wnl.40.2.332. [DOI] [PubMed] [Google Scholar]
- 10.Progressive resistance training after stroke: effects on muscle strength, muscle tone, gait performance and perceived participation. Flansbjer UB, Miller M, Downham D, Lexell J. J Rehabil Med. 2008;40:42–48. doi: 10.2340/16501977-0129. [DOI] [PubMed] [Google Scholar]
- 11.Liguori G. ACSMs Guidelines for Exercise Testing and Prescription. https://www.acsm.org/education-resources/books/guidelines-exercise-testing-prescription. Wolters Kulwer; 2021. ACSMs Guidelines for Exercise Testing and Prescription. ACSM_CMS. Accessed: September 27, 2022. [Google Scholar]
- 12.Post-stroke hemiplegia; crural muscle strength and structure. Sjöström M, Fugl-Meyer AR, Nordin G, Wählby L. Scand J Rehabil Med Suppl. 1980;7:53–67. [PubMed] [Google Scholar]
- 13.Limb muscle strength is impaired bilaterally after stroke. Bohannon RW, Andrews AW. J Phys Ther Sci. 1995;7:1–7. [Google Scholar]
- 14.Sequencing bilateral and unilateral task-oriented training versus task oriented training alone to improve arm function in individuals with chronic stroke. McCombe Waller S, Whitall J, Jenkins T, Magder LS, Hanley DF, Goldberg A, Luft AR. BMC Neurol. 2014;14:236. doi: 10.1186/s12883-014-0236-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Repetitive bilateral arm training with rhythmic auditory cueing improves motor function in chronic hemiparetic stroke. Whitall J, McCombe Waller S, Silver KH, Macko RF. https://www.ahajournals.org/doi/10.1161/01.str.31.10.2390?url_ver=Z39.88-2003&rfr_id=ori:rid:crossref.org&rfr_dat=cr_pub%20%200pubmed. Stroke. 2000;31:2390–2395. doi: 10.1161/01.str.31.10.2390. [DOI] [PubMed] [Google Scholar]
- 16.Dynamic muscle strength training in stroke patients: effects on knee extension torque, electromyographic activity, and motor function. Engardt M, Knutsson E, Jonsson M, Sternhag M. Arch Phys Med Rehabil. 1995;76:419–425. doi: 10.1016/s0003-9993(95)80570-2. [DOI] [PubMed] [Google Scholar]
- 17.Consolidated standards of reporting trials (CONSORT) and the completeness of reporting of randomised controlled trials (RCTs) published in medical journals. Turner L, Shamseer L, Altman DG, et al. Cochrane Database Syst Rev. 2012;11:0. doi: 10.1002/14651858.MR000030.pub2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 18.SPIRIT 2013 statement: defining standard protocol items for clinical trials. Chan AW, Tetzlaff JM, Altman DG, et al. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5114123/pdf/nihms6040.pdf. Ann Intern Med. 2013;158:200–207. doi: 10.7326/0003-4819-158-3-201302050-00583. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.Carr JH, Shepherd RB. UK: Butterworth-Heinemann; [ Jan; 2021 ]. 2003. Stroke rehabilitation: guidelines for exercise and training to optimize motor skill 2002. [Google Scholar]
- 20.Outcomes of progressive resistance strength training following stroke: a systematic review. Morris SL, Dodd KJ, Morris ME. Clin Rehabil. 2004;18:27–39. doi: 10.1191/0269215504cr699oa. [DOI] [PubMed] [Google Scholar]
- 21.Thomas L. DeLorme and the science of progressive resistance exercise. Todd JS, Shurley JP, Todd TC. J Strength Cond Res. 2012;26:2913–2923. doi: 10.1519/JSC.0b013e31825adcb4. [DOI] [PubMed] [Google Scholar]
- 22.Effect of weak-part strengthening training and strong-part relaxation therapy on static balance, muscle strength asymmetry, and proprioception in the gluteus medius: immediate effect analysis. Choi EB, Jung YJ, Lee D, Hong JH, Yu JH, Kim JS, Kim S-G. J Korean Soc Phys Med. 2022;17:11–20. [Google Scholar]
- 23.The modulatory effects of bilateral arm training (BAT) on the brain in stroke patients: a systematic review. Wu J, Cheng H, Zhang J, Bai Z, Cai S. Neurol Sci. 2021;42:501–511. doi: 10.1007/s10072-020-04854-z. [DOI] [PubMed] [Google Scholar]
- 24.Bilateral arm training vs unilateral arm training for severely affected patients with stroke: exploratory single-blinded randomized controlled trial. Renner CI, Brendel C, Hummelsheim H. Arch Phys Med Rehabil. 2020;101:1120–1130. doi: 10.1016/j.apmr.2020.02.007. [DOI] [PubMed] [Google Scholar]
- 25.Effect of bilateral lower limb strengthening exercise on balance and walking in hemiparetic patients after stroke: a randomized controlled trial. Jeon HJ, Hwang BY. J Phys Ther Sci. 2018;30:277–281. doi: 10.1589/jpts.30.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 26.Functional reach: predictive validity in a sample of elderly male veterans. Duncan PW, Studenski S, Chandler J, Prescott B. J Gerontol. 1992;47:0–8. doi: 10.1093/geronj/47.3.m93. [DOI] [PubMed] [Google Scholar]
- 27.Reliability and validity of the modified functional reach test at the sub-acute stage post-stroke. Katz-Leurer M, Fisher I, Neeb M, Schwartz I, Carmeli E. Disabil Rehabil. 2009;31:243–248. doi: 10.1080/09638280801927830. [DOI] [PubMed] [Google Scholar]
- 28.One-leg standing test for elderly populations. Michikawa T, Nishiwaki Y, Takebayashi T, Toyama Y. J Orthop Sci. 2009;14:675–685. doi: 10.1007/s00776-009-1371-6. [DOI] [PubMed] [Google Scholar]
- 29.Functional gait of patients with stroke after strength training: a systematic review of randomised controlled trials. Mwansa MR, Himalowa S, Kunda R. Int J Health Sci Res. 2021;11:144–158. [Google Scholar]
- 30.Stride length predicts adverse clinical events in older adults: a systematic review and meta-analysis. Bytyçi I, Henein MY. J Clin Med. 2021;10:2670. doi: 10.3390/jcm10122670. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Effects of the bilateral isokinetic strengthening training on functional parameters, gait, and the quality of life in patients with stroke. Büyükvural Şen S, Özbudak Demir S, Ekiz T, Özgirgin N. https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4659126/pdf/ijcem0008-16871.pdf. Int J Clin Exp Med. 2015;8:16871–16879. [PMC free article] [PubMed] [Google Scholar]
- 32.Predicting the probability for falls in community-dwelling older adults. Shumway-Cook A, Baldwin M, Polissar NL, Gruber W. Phys Ther. 1997;77:812–819. doi: 10.1093/ptj/77.8.812. [DOI] [PubMed] [Google Scholar]
- 33.Rating scale analysis of the Berg Balance Scale. Kornetti DL, Fritz SL, Chiu YP, Light KE, Velozo CA. Arch Phys Med Rehabil. 2004;85:1128–1135. doi: 10.1016/j.apmr.2003.11.019. [DOI] [PubMed] [Google Scholar]
- 34.Muscle strengthening for hemiparesis after stroke: a meta-analysis. Wist S, Clivaz J, Sattelmayer M. Ann Phys Rehabil Med. 2016;59:114–124. doi: 10.1016/j.rehab.2016.02.001. [DOI] [PubMed] [Google Scholar]
- 35.Comparison of the effects between isokinetic and isotonic strength training in subacute stroke patients. Chen CL, Chang KJ, Wu PY, Chi CH, Chang ST, Cheng YY. J Stroke Cerebrovasc Dis. 2015;24:1317–1323. doi: 10.1016/j.jstrokecerebrovasdis.2015.02.002. [DOI] [PubMed] [Google Scholar]
- 36.Improving the utility of the Brunnstrom recovery stages in patients with stroke: validation and quantification. Huang CY, Lin GH, Huang YJ, et al. Medicine (Baltimore) 2016;95:0. doi: 10.1097/MD.0000000000004508. [DOI] [PMC free article] [PubMed] [Google Scholar]










