Next Article in Journal
Cultivating Self-Compassion to Improve Social Workers’ Professional Quality of Life in Primary Healthcare
Previous Article in Journal
Association Between Sarcopenia and Buttock Pain Among Middle-Aged and Older Chinese People: Evidence from the China Health and Retirement Longitudinal Study
Previous Article in Special Issue
Measurement and Evaluation of Health, Functional Capacity, Physical Fitness, and Daily Habits of Greek Female Healthcare Professionals Working in a Hospital Environment
 
 
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Systematic Review

Effects of Exercise on Balance Function in People with Knee Osteoarthritis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials

1
Beijing Key Laboratory of Sports Performance and Skill Assessment, Beijing Sport University, Beijing 100084, China
2
China Basketball College, Beijing Sport University, Beijing 100084, China
3
Department of Strength and Conditioning Assessment and Monitoring, Beijing Sport University, Beijing 100084, China
4
Institute of Physical Education, Huzhou University, Huzhou 313000, China
5
China Institute of Sport and Health Science, Beijing Sport University, Beijing 100084, China
*
Authors to whom correspondence should be addressed.
These authors contributed equally to this work.
Healthcare 2025, 13(11), 1312; https://doi.org/10.3390/healthcare13111312
Submission received: 27 March 2025 / Revised: 21 May 2025 / Accepted: 27 May 2025 / Published: 1 June 2025
(This article belongs to the Special Issue Exercise Interventions and Testing for Effective Health Promotion)

Abstract

:
Objectives: This study sought to evaluate the impact of exercise on balance function in individuals with knee osteoarthritis (KOA) and determine the most effective exercise protocols for balance enhancement. Methods: A systematic literature search was performed across five major electronic databases (PubMed, Web of Science, EBSCO, Cochrane, Scopus) until 13 September 2024. Statistical synthesis was conducted using weighted mean differences (WMDs) with 95% confidence intervals under a random-effects model. Results: Analysis of 22 studies revealed significant improvements in balance function following exercise interventions. Outcomes measured by the Berg balance scale (BBS, WMD, 2.65, p < 0.00001) and timed up and go test (TUG, WMD, −0.59, p < 0.0001) demonstrated clinically relevant enhancements in KOA populations. Subgroup analyses revealed that multicomponent training (WMD, 6.25, p = 0.003), interventions lasting ≥ 8 weeks (WMD, 4.92, p = 0.002), sessions ≥ 60 min (WMD, 7.42, p = 0.002), frequency ≥ 3 times per week (WMD, 2.83, p = 0.0005), weekly time ≥ 180 min per week (WMD, 7.42, p = 0.002), and patients < 60 years (WMD, 6.71, p = 0.002) were associated with greater improvement in BBS. Conclusions: Exercise significantly improved balance function in KOA patients, with multicomponent training emerging as the most effective intervention. Based on the findings of this meta-analysis, clinicians should recommend that KOA patients engage in exercise at least three times per week, with each session lasting at least 60 min, to achieve a total weekly time of 180 min. These recommendations are particularly relevant for patients less than 60 years, who may experience greater benefits from exercise interventions.

1. Introduction

Knee osteoarthritis (KOA), a progressive joint disorder, exhibits strong age-dependent prevalence patterns. It is characterized by pathological changes such as cartilage degeneration, bone remodeling, osteophytic proliferation, and chronic synovitis. These degenerative cascades clinically present as persistent arthralgia, restricted range of motion, periarticular edema, and progressive functional impairment of the affected joint [1,2]. Epidemiological studies indicate a marked gender disparity, with female populations demonstrating significantly higher susceptibility compared to males [3,4]. The molecular mechanisms underlying osteoarthritis involve the progressive loss of articular chondrocytes due to cartilage damage, leading to reduced joint space, increased bone friction, and subsequent pain and restricted movement [5]. Compared to their healthy counterparts, individuals with KOA typically exhibit poorer physical function, including reduced lower limb muscle strength, impaired balance, and decreased mobility [6,7]. Balance deficits, in particular, have been identified as a significant contributor to mobility limitations and an elevated risk of falls in this population [8].
Exercise has been shown to improve lower limb muscle strength and both static and dynamic balance in older adults, including those at risk of falls [9]. Although cartilage damage in KOA is irreversible and cannot be fully reversed by medication, physiotherapy, or surgery [10], modifiable risk factors such as joint dysfunction and muscle weakness can be targeted through primary and secondary prevention strategies [11]. As a result, non-pharmacological interventions, particularly exercise, are considered central to the management of KOA, aiming to alleviate symptoms and enhance or maintain physical function [10,12,13].
Given the challenges posed by muscle weakness and pain in KOA patients, exercise interventions that address these issues are critical. Strength training, for instance, can mitigate muscle weakness by improving muscle mass and recruitment [14]. Clinical guidelines endorse exercise as a key component of non-pharmacological treatment due to its ease of implementation, low risk of adverse effects, and cost-effectiveness [3]. However, the effects of exercise on balance function in KOA patients remain inconsistent. For example, while a 6-week balance exercise program improved dynamic balance in KOA patients, no significant changes were observed in functional balance scores [15]. Similarly, Tai Chi has been shown to enhance balance function in the elderly with KOA patients, but the overall evidence remains mixed [16].
Falls are a major cause of unintentional injury and mortality among adults aged 65 and older, with balance impairment being a key predictor [17,18,19,20]. Standardized assessments such as the Berg balance scale (BBS) and timed up and go test (TUG) are widely used to evaluate balance function and identify functional limitations [21]. In KOA patients, the loss of balance, proprioception, and postural control can lead to reduced confidence in mobility and an increased risk of falls [22], ultimately compromising their ability to perform daily activities independently [23]. While some studies suggest that balance-based exercises can reduce fall risk in older adults [24], others indicate that balance training alone may not improve muscle strength [25]. Nevertheless, a randomized controlled trial (RCT) has demonstrated that physical activity training can mitigate the negative effects of KOA [26].
Despite the growing body of research, previous studies have often neglected to consider exercise modality, including intervention duration, frequency, session duration, and weekly time, leading to variability in outcomes. To address this gap, we conducted this study to evaluate the impact of exercise on balance function in KOA patients and to identify the optimal exercise modalities for improving balance function in this population.

2. Materials and Methods

This study was conducted in accordance with the Cochrane Handbook for Systematic Reviews of Interventions [27] and the Preferred Reporting Items for Systematic Evaluation and Meta-Analyses guidelines (PRISMA, 2020) [28]. The study protocol was registered with PROSPERO (CRD42024604651).

2.1. Search Strategy

A comprehensive search was performed across multiple electronic databases, including PubMed, Web of Science, EBSCO, Cochrane, and Scopus, up to 13 September 2024. The search strategy utilized a combination of keywords and Medical Subject Headings (MESH) terms such as “exercise”, “balance”, and “knee osteoarthritis” (Table S1). Additionally, the reference lists of identified systematic reviews and meta-analyses were manually screened to ensure no relevant studies were missed. Two independent authors conducted the search and screening process. Any discrepancies between the authors were resolved through discussion with a third author until consensus was reached.

2.2. Eligibility Criteria

The Population, Intervention, Comparison, Outcome (PICO) framework is used to define the inclusion: (a) Population: patients with KOA; (b) Intervention: randomized controlled trials (RCTs) with subjects randomly assigned to either the intervention or control group; (c) Comparison: studies that measured BBS or TUG at baseline and compared results post-intervention; (d) Outcome: the primary outcomes were balance function.
Exclusion criteria were (1) non-English publications; (2) reviews, conference articles, abstracts, or non-original research articles; (3) studies involving animal models; and (4) studies where the control group received any form of exercise intervention.

2.3. Data Extraction

Two authors independently extracted data from the included studies. The extracted information included (a) studies characteristics (first author’s name, publication year, sample size); (b) intervention details (intervention type, duration, frequency, session duration, weekly time); (c) participant characteristics (disease duration, age); and (d) pre- and post-intervention balance outcomes [mean and standard deviation (SD)]. In the event of disagreement, a third author was consulted to achieve consensus.

2.4. Methodological Quality Assessment

The methodological quality of the included studies was assessed using the Cochrane Risk of Bias 2 (RoB-2) tool. This tool evaluates domains such as selection bias, performance bias, detection bias, attrition bias, reporting bias, and other biases [29]. Two authors independently conducted the quality assessment, and any disagreements were resolved through discussion with the third author.

2.5. Statistical Analysis

Changes in mean and SD values for BBS and TUG were calculated for each study. When studies reported standard error (SE) or 95% confidence interval (CI), SD values were derived using established methods [27,30]. Data were pooled using the random-effects model to determine the weighted mean difference (WMD) and 95% CI. In case of high heterogeneity (I2 > 60%), meta-regression, subgroup analyses, and sensitivity analyses were conducted to explore potential sources of variability [31].
Subgroup analyses were performed based on intervention type (aerobic exercise, resistance exercise, multicomponent training), duration (<8 weeks, ≥8 weeks), frequency (<3 times per week, ≥3 times per week), session duration (<60 min per session, ≥60 min per session), weekly time (<180 min per week and ≥180 min), and participant age (<60 years, ≥60 years). Forest plots were generated using RevMan.5.4 software, while meta-regression, sensitivity analysis, and funnel plot were performed using Stata 17 software. Statistical significance was set at p < 0.05.

3. Results

3.1. Study Selection

The initial database search yielded 1272 records (Cochrane, n = 464; Scopus, n = 325; Web of Science, n = 313; Embase, n = 109; PubMed, n = 61). Following deduplication procedures, 748 records were retained for preliminary evaluation based on their titles and abstracts. Subsequent detailed assessment identified 48 studies that warranted comprehensive full-text examination. As shown in Table S1, after full-text assessment, 26 studies were excluded for the following reasons: (1) lack of relevant data (n = 5); (2) full text unavailable (n = 3); (3) absence of control group (n = 2); (4) non-target population (n = 1); (5) non-exercise interventions (n = 1); and (6) non-target outcome measures (n = 14). Finally, 22 studies [32,33,34,35,36,37,38,39,40,41,42,43,44,45,46,47,48,49,50,51,52,53] met the inclusion criteria. The complete workflow of this selection methodology is presented in Figure 1.

3.2. Characteristics of the Included Studies

The main characteristics of the included studies are summarized in Table S2. The experimental cohort comprised 31 intervention arms with 608 participants, contrasted by 22 control cohorts encompassing 526 participants. Therapeutic regimens across trials incorporated three principal modalities: aerobic exercise, resistance exercise, or multicomponent training. Implementation durations spanned from 14-day regimens to 24-week programs. Outcome measurement analysis revealed 10 studies employing BBS as the primary metric [32,33,34,35,36,37,38,39,40,41], complemented by 17 studies reporting TUG data [33,36,37,38,39,42,43,44,45,46,47,48,49,50,51,52,53]. Among the included studies, 7 focused exclusively on women [34,39,40,44,51,52,53], while 15 included both men and women [32,33,35,36,37,38,41,42,43,45,46,47,48,49,50]. Demographic characteristics indicated a mean participant age spectrum of 50.7–73.4 years, with all subjects having a radiologically confirmed KOA diagnosis. This cohort encompassed both pre- and post-total knee arthroplasty cases [36,45,46,47,49,52,53]. Of the 31 intervention groups, 1 involved aerobic exercise [50], 20 involved resistance exercise [32,33,34,35,36,38,42,46,47,48,51,52,53], and 9 involved multicomponent training [37,39,40,41,43,44,45,49]. Therapeutic administration frequency was maintained at 2–5 sessions weekly, with one trial omitting this parameter [45]. The mean session duration ranged from 15 to 90 min, with 5 studies not reporting session duration [33,35,44,46,47]. The total weekly time ranged from 75 to 270 min.

3.3. Risk of Bias

The methodological quality was evaluated through the RoB-2 tool, which stratifies bias risk into three tiers: low, high, and unclear. Analytical outcomes revealed a predominance of methodologically robust research, with seven studies demonstrating low bias risk, one exhibiting high risk, and the majority classified as having unclear risk levels (Figure S1).

3.4. Meta-Analysis Results

3.4.1. Effects of Exercise on TUG in KOA Patients

Twenty-four studies provided data on TUG. Exercise significantly improved TUG in KOA patients compared to controls (WMD, −0.59; 95% CI, −0.87 to −0.31, p < 0.0001, I2 = 59%, Figure 2).

3.4.2. Effects of Exercise on BBS in KOA Patients

Exercise significantly improved BBS in KOA patients compared to controls (WMD, 2.65; 95% CI, 1.31 to 4.00, p < 0.00001, I2 = 80%, Figure 3).
Due to the high heterogeneity, subgroup analyses, meta-regression, and sensitivity analyses were conducted.

3.5. Subgroup Analysis

Resistance exercise (WMD, 1.70; 95% CI, 0.78 to 2.63, p = 0.003, I2 = 32%) and multicomponent training (WMD, 6.25; 95% CI, 2.07 to 10.43, p = 0.003, I2 = 94%, Figure 4) significantly improved BBS. Specifically, multicomponent training had a greater effect on improving BBS in KOA patients.
Additionally, analysis by intervention duration showed that interventions lasting <8 weeks (WMD, 1.62; 95% CI, 0.54 to 2.70, p = 0.003, I2 = 42%,) and ≥8 weeks (WMD, 4.92; 95% CI, 1.86 to 7.97, p = 0.002, I2 = 91%, Figure 5) significantly improved BBS. Specifically, interventions lasting ≥8 weeks had a greater effect on improving BBS in KOA patients.
Additionally, interventions performed ≥3 times per week demonstrated significant enhancements in BBS (WMD, 2.83; 95% CI, 1.25 to 4.41, p = 0.0005, I2 = 81%, Figure 6). Conversely, interventions performed <3 times per week failed to achieve significant BBS improvements in KOA patients (WMD, 1.85; 95% CI, −0.64 to 4.33, p = 0.15, I2 = 76%, Figure 6).
Furthermore, both shorter (<60 min per session; WMD, 1.02; 95% CI, 0.10 to 1.94, p = 0.03, I2 = 0%) and extended (≥60 min per session; WMD, 7.42; 95% CI, 2.62 to 12.22, p = 0.002, I2 = 94%, Figure 7) significantly improved BBS. Specifically, prolonged session durations exhibited substantially greater balance enhancement effects compared to shorter protocols.
Moreover, both sub-threshold (<180 min per week; WMD, 0.92; 95% CI, 0.11 to 1.73, p = 0.03, I2 = 0%) and supra-threshold (≥180 min; WMD, 7.42; 95% CI, 2.62 to 12.22, p = 0.002, I2 = 94%, Figure 8) regimens demonstrating significant BBS improvements. Notably, protocols exceeding the 180 min weekly threshold generated greater effects compared to suboptimal dosing regimens.
Finally, exercise significantly improved BBS in KOA patients aged <60 years (WMD, 6.71, 95% CI, 2.4 to11.01, p = 0.002, I2 = 93%) and ≥60 years (WMD, 1.42, 95% CI, 0.65 to 2.20, p = 0.0003, I2 = 16%, Figure 9). Specifically, exercise had a greater effect on improving BBS in KOA patients aged <60 years.

3.6. Meta-Regression

As shown in Table S2, no significant correlations were found between intervention duration (p = 0.631) or frequency (p = 0.852) and BBS. However, significant associations were observed for session duration (p = 0.016), weekly time (p = 0.022), and participant age (p = 0.049).

3.7. Publication Bias

Funnel plot morphometric evaluation demonstrated skewed distributions in both balance outcomes (Figures S2 and S3). Egger’s test confirmed the absence of small-study effects, with intercept deviations remaining within null hypothesis thresholds (BBS, p = 0.134; TUG, p = 0.084; Table S3).

3.8. Sensitivity Analysis

Sensitivity analyses demonstrated that the overall effect of exercise on BBS (Figure S4) and TUG (Figure S5) in KOA patients remained consistent in direction and significant when any single study was excluded.

4. Discussion

4.1. Main Findings

The systematic evaluation of 22 RCTs demonstrated that exercise produced significant enhancements in balance function, evidenced by improvements in BBS and TUG. Subgroup analyses revealed that multicomponent training, interventions lasting ≥8 weeks, sessions performed ≥3 times per week, session durations ≥60 min, and weekly time ≥180 min were particularly effective in improving BBS. Additionally, patients aged <60 years showed greater improvements in balance function.

4.2. Effects of Exercise on Balance Function in KOA Patients

The findings of this study align with existing evidence supporting exercise as a core component of non-pharmacological management for KOA. Exercise interventions resulted in an overall improvement of 2.65 (WMD) in BBS and a reduction of 0.59 (WMD) in TUG, highlighting their efficacy in enhancing postural stability and balance control. These results are consistent with recommendations from the European Alliance of Associations for Rheumatology (EULAR) [54] and the Hong Kong League Against Osteoarthritis (LLOA) guidelines [55], which advocate for exercise as a first-line treatment for KOA.
The results of a previous study indicated that massage, as one of the non-pharmacological treatments, can improve pain indices and physical function in KOA patients; however, its long-term effects and sustained benefits remain unknown [56]. Although there is insufficient evidence to recommend one form of exercise over another [2], it is reasonable to advocate for exercise as a core treatment for KOA patients. Additionally, when balance function declines, it is accompanied by a decrease in physical function and quality of life, as well as a reduction in the patient’s confidence in engaging in activities or exercise. Gunn et al. [57] found that kinesiophobia is common in symptomatic KOA patients, which may hinder physical activity as patients avoid participating in general exercise that they perceive as “harmful” to their joints. Furthermore, Alghadir et al. [50] demonstrated that retrograde ambulation training significantly enhances quadriceps neuromuscular performance while concurrently reducing pain severity and functional limitations. When compared with healthy individuals, KOA patients have decreased muscle function and functional capacity, and decreased quadriceps strength is a risk factor for KOA patients [7,58]. Previous studies have shown that an increased risk of KOA is associated with weakness of the knee extensor muscles [14,59]. Moreover, quadriceps exercises aim to augment knee joint stability through selective muscle recruitment patterns [60], thereby improving balance performance and reducing fear or avoidance of exercise in KOA patients. It has been shown that exercise can increase the strength of the lower limbs in KOA patients, which reduces internal knee forces, decreases pain, and improves balance function [14].

4.3. Effects of Different Exercise Modalities on Balance Function in KOA Patients

The subgroup analysis provided valuable insights into the optimal exercise modalities for improving balance in KOA patients. According to the intervention type, the majority of interventions for KOA patients aim to enhance postural stability and balance during exercise. Contemporary therapeutic approaches predominantly incorporate three core modalities: aerobic exercise, resistance exercise, and multicomponent training. Previous studies confirm consistent associations between these exercise paradigms and postural stability enhancement, irrespective of intervention specificity [6,61]. Both resistance exercise and multicomponent training have been shown to improve balance function in KOA patients. Our findings indicated that multicomponent training is more beneficial for KOA patients compared to resistance exercise. The benefits of aerobic exercise primarily stem from an increase in oxidative capacity, and when combined with resistance exercise, it significantly enhances balance. A previous meta-analysis suggested that an optimal exercise program for KOA patients should have a singular goal and focus on specific physiological adaptations—whether aerobic capacity, quadriceps torque generation, or neuromuscular coordination [62]. This aligns with our recommendation for multicomponent training.
Previous studies have demonstrated that resistance exercise improves functional capacity and reduces pain in KOA patients [63]. However, Ansanay et al. [33] found that the addition of dexterity and perturbation training to resistance exercises was more effective in improving balance function in KOA patients than resistance exercises alone. Meanwhile, Sadeghi et al. [64] observed that mixed exercise, virtual reality-based game exercise, and balance training significantly improved leg strength and balance in older men, with multicomponent training exhibiting a clinically meaningful superior improvement over the other intervention groups. This is consistent with our results, which indicated that multicomponent training resulted in more significant improvements than resistance exercise. Numerous recommendations, including those of EULAR [54], affirm that combination therapy significantly improves balance function more than monotherapy, and one of the core recommendations is that individualized, multicomponent training management programs should be provided to KOA patients.
Intervention duration played a critical role in determining outcomes. Our results showed that ≥8 weeks of exercise was more effective than <8 weeks of exercise in improving balance function in KOA patients, which aligns with previous studies. Husby et al. [65] showed that 8 weeks of resistance exercise after total knee replacement surgery could maintain the sustained gains from the intervention at the 12-month post-intervention follow-up, as could an additional 8 weeks of strength training. In addition, the results of an RCT comparing the efficacy of Tai Chi and other physical therapies revealed that the benefits of Tai Chi were maintained for up to 52 weeks after a 12-week intervention [66]. Furthermore, Chen et al. [6] documented significant functional gains following three-month exercise regimens in geriatric KOA cohorts. However, Chaipinyo et al. [67] showed that a 4-week home resistance exercise and balance training had no significant improvement in pain and flexibility in KOA patients, which raises the question of whether the lack of improvement is associated with the insufficient intervention duration. Therefore, for KOA patients aiming to better alleviate pain and improve balance, an intervention duration of ≥8 weeks appears to offer more benefits and maintain good functional performance for a relatively long period after the intervention.
Similarly, our results demonstrated that exercising at least three times per week is more effective for improving balance function in KOA patients, which aligns with a previous study, showing that, for optimal results, exercise programs should be supervised and conducted three times a week [62]. According to the American College of Sports Medicine (ACSM) guideline recommendations, resistance exercise should be performed three times a week in elderly patients [68]. Based on our findings, resistance exercise combined with other exercise types is the most suitable exercise for KOA patients to improve balance function, especially when focusing on strengthening the lower limbs, which is most effective at a frequency of three times per week or more. Additionally, to enhance the functional abilities needed for daily life, it is crucial to prioritize balance, strength, and proprioception, necessitating a variety of rehabilitation exercises to restore functional performance [69]. Moreover, Lee et al. [53] showed that progressive dynamic balance training performed five times per week significantly improves balance and quality of life in elderly women who underwent a total knee arthroplasty.
Considering that the subjects were recent surgical patients, simply increasing the duration of a single intervention may not yield better results, as KOA patients or the postoperative population often experience low muscle strength, and over-exercise can lead to fatigue, negatively impacting the effectiveness of the intervention and fostering negative attitudes towards exercise. The results of a trial involving combined balance exercises performed three times per week showed beneficial effects on both static and dynamic balance in individuals following total knee replacement [61].
We cannot solely attribute this improved outcome to three interventions a week. Our results suggested that session duration ≥60 min led to better outcomes. Both healthy older adults and special populations seem to experience greater gains with a session duration of 60 min or more. A previous study demonstrated that multicomponent training significantly improved balance function in healthy older adults who performed approximately 60 min of exercise per session [70]. In addition, a Tai Chi exercise program with 60 min sessions showed improvement in balance function in KOA patients [71]. Furthermore, Mihalko et al. [72] found that a multicomponent training program of 60 min, three times a week, improved balance in adults with overweight KOA. However, longer interventions, such as those exceeding 90 min, should be carefully selected and verified by further experimental studies to determine their potential benefits for KOA patients.
Weekly time also influenced outcomes, with interventions totaling ≥180 min per week showing significant improvements in balance function in KOA patients, aligning with previous studies. The results of an aquatic exercise training study revealed that a weekly 180 min intervention significantly improved lower limb muscle weakness in women with KOA [73]. Since the balance function is closely associated with quadriceps strength, a longer intervention period or cycle can lead to greater muscular gains, enhancing patients’ confidence through improved muscle strength and size. Additionally, Kim et al. [74] showed that a weekly 180 min intervention involving stabilizing and balancing exercises was effective in stimulating the deep stabilizing muscles and proprioception, ultimately improving balance function. This improvement harmonized the muscles around the knee joint, reducing joint load and restoring muscle function. Combined with the above findings, it is evident that, for KOA patients, achieving more than 180 min of exercise per week necessitates both an increase in the frequency of exercise and a reasonable extension of the session duration.
Age was another important factor; patients <60 years showed greater improvements in balance function compared to older adults. The older population with KOA already exhibits weakened lower limb strength, necessitating gradual adaptation to exercise, as rushing may lead to ineffective or detrimental outcomes. A previous review showed that individuals over 40 years of age had a 2% higher risk of developing KOA compared to those under 40 [75]. KOA progressively worsens with age [76], and early intervention, whether during disease progression or post-surgery, can effectively slow the progression of symptoms [75]. A previous study showed that age was significantly negatively correlated with quadriceps thickness but positively correlated with balance function; thus, advancing age leads to increased muscle atrophy, which subsequently impairs balance function in KOA patients [76]. Additionally, a meta-analysis found that, while physical activity positively impacts healthy aging in middle-aged and older adults, this effect diminishes over time [77]. As age increases, KOA patients exhibit inadequate muscle function and peripheral nerve responses, heightened joint instability and ligament laxity, as well as a slower anabolic response to growth factors [78], potentially reducing their sensitivity to exercise at the same intensity.
Considering the substantial evidence that highlights the benefits of exercise in reducing pain and enhancing balance function, KOA patients should be encouraged to incorporate exercise as a key component of their treatment plan. Personal preference, accessibility, and affordability may influence the most suitable approach for individual patients [2]. Therefore, based on the advice of their physician or rehabilitation practitioner, KOA patients should select multicomponent training that suits them, along with the appropriate intervention duration, tailored to their specific circumstances.

4.4. Strengths and Limitations

Three studies [16,79,80] investigated the effects of exercise on balance function (BBS and/or TUG) in KOA patients. However, these studies share a critical limitation: they do not differentiate between exercise modalities. Specifically, aerobic exercise, resistance exercise, and multicomponent training were analyzed collectively, which obscures the specific benefits of each intervention type. While existing evidence supports the general association between exercise and improved balance function in KOA patients, these studies fail to provide actionable guidance for clinical practice. For instance, they do not clarify whether aerobic exercise, resistance exercise, or multicomponent training is more effective. Furthermore, key parameters such as optimal session duration, weekly frequency, and total weekly exercise volume remain unaddressed. These gaps underscore the necessity of our study, which aims to deliver detailed, evidence-based exercise prescriptions tailored to balance improvement in KOA patients.
This study advances the existing literature by addressing three key strengths. First, we provide a comprehensive evaluation of how distinct exercise protocols influence balance function in KOA patients, offering specific recommendations for optimizing exercise prescriptions. Additionally, the inclusion of subgroup analyses allows us to identify specific exercise parameters, such as intervention duration, session duration, frequency, and weekly time, that are most effective in improving balance function. This provides valuable insights for clinical practice. Finally, our results demonstrate that multicomponent training confers the greatest balance benefits, providing clear clinical guidance for exercise prescription in this population.
This study has several limitations. First, the included studies did not differentiate patients who had undergone total knee arthroplasty and those who had not, which may have influenced the results. Second, some included studies lacked detailed information on exercise intensity, limiting the ability to assess their impact on outcomes. Third, the heterogeneity in exercise modalities and intervention details across studies may have contributed to variability in the results. Moreover, we recognize the importance of the minimal clinically important difference (MCID) in interpreting the clinical relevance of our results. However, it is crucial to note that there is currently no gold standard for MCID values specific to balance function (BBS and TUG) in KOA patients. Although previous studies reported the MCID values for KOA patients [81,82], these values do not directly apply to our research due to differences in participant characteristics, such as surgical status and disease grading. These differences can significantly impact the determination of MCID values. Finally, the subjective nature of quality assessment and the significant heterogeneity observed in the meta-analysis necessitate cautious interpretation of the findings.

5. Conclusions

Exercise significantly improved balance function in KOA patients, with multicomponent training emerging as the most effective intervention. The synthesis of evidence from this meta-analysis supports the implementation of structured exercise protocols for managing KOA, advocating regimens that include at least three weekly sessions of at least 60 min each. This prescription framework aims to achieve a cumulative weekly exercise volume of 180 min to optimize neuromuscular adaptation and biomechanical stability in affected populations. These recommendations are particularly relevant for patients less than 60 years, who may experience greater benefits from exercise interventions. Future research should focus on standardizing exercise protocols and exploring the long-term effects of different exercise modalities on balance and functional outcomes in KOA patients.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/healthcare13111312/s1, Figure S1: Results of Cochrane risk of bias tool; Figure S2: Funnel plot of BBS; Figure S3: Funnel plot of TUG; Figure S4: Sensitivity analysis of BBS; Figure S5: Sensitivity analysis of TUG; Table S1. Search strategies; Table S2. Excluded studies list; Table S3: Characteristics of studies included in this meta-analysis; Table S4: Results of meta-regression; Table S5: Results of Egger’s test.

Author Contributions

Conceptualization, X.W. and L.Y.; methodology, X.W., Z.C. and Y.L. (Yuanyuan Lv); software, X.W. and Z.C.; validation, Y.L. (Yin Liang) and H.S.; formal analysis, X.W. and Z.C.; investigation, X.W., Z.C., Y.L. (Yin Liang), H.S. and T.W.; resources, L.Y.; data curation, Y.L. (Yin Liang) and H.S.; writing—original draft preparation, X.W.; writing—review and editing, X.W., Z.C., Y.L. (Yin Liang), H.S., T.W., Y.L. (Yuanyuan Lv) and L.Y.; visualization, X.W. and Z.C.; supervision, L.Y.; project administration, L.Y.; funding acquisition, L.Y. All authors have read and agreed to the published version of the manuscript.

Funding

This research was funded by the Humanities and Social Science Fund of the Ministry of Education of China, grant number 24YJC890065.

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

All data generated or analyzed during this study are included in the article/Supplementary Material.

Conflicts of Interest

The authors declare no conflicts of interest.

Abbreviations

The following abbreviations are used in this manuscript:
KOAKnee osteoarthritis
BBSBerg balance scale
TUGTimed up and go test
RCTRandomized controlled trial
PRISMAPreferred Reporting Items for Systematic Evaluation and Meta-Analyses
MESHMedical Subject Headings
SDStandard deviation
SEStandard error
CIConfidence interval
WMDWeighted mean difference
EULAREuropean Alliance of Associations for Rheumatology
LLOAHong Kong League Against Osteoarthritis
ACSMAmerican College of Sports Medicine

References

  1. Yohannes, A.M.; Caton, S. Management of depression in older people with osteoarthritis: A systematic review. Aging Ment. Health 2010, 14, 637–651. [Google Scholar] [CrossRef]
  2. Kolasinski, S.L.; Neogi, T.; Hochberg, M.C.; Oatis, C.; Guyatt, G.; Block, J.; Callahan, L.; Copenhaver, C.; Dodge, C.; Felson, D.; et al. 2019 American College of Rheumatology/Arthritis Foundation Guideline for the Management of Osteoarthritis of the Hand, Hip, and Knee. Arthritis Rheumatol. 2020, 72, 220–233. [Google Scholar] [CrossRef]
  3. McAlindon, T.E.; Bannuru, R.; Sullivan, M.C.; Arden, N.K.; Berenbaum, F.; Bierma-Zeinstra, S.M.; Hawker, G.A.; Henrotin, Y.; Hunter, D.J.; Kawaguchi, H.; et al. OARSI guidelines for the non-surgical management of knee osteoarthritis. Osteoarthr. Cartil. 2014, 22, 363–388. [Google Scholar] [CrossRef] [PubMed]
  4. Lawrence, R.C.; Felson, D.T.; Helmick, C.G.; Arnold, L.M.; Choi, H.; Deyo, R.A.; Gabriel, S.; Hirsch, R.; Hochberg, M.C.; Hunder, G.G.; et al. Estimates of the prevalence of arthritis and other rheumatic conditions in the United States. Part II. Arthritis Rheum. 2008, 58, 26–35. [Google Scholar] [CrossRef] [PubMed]
  5. Xia, B.; Di, C.; Zhang, J.; Hu, S.; Jin, H.; Tong, P. Osteoarthritis pathogenesis: A review of molecular mechanisms. Calcif. Tissue Int. 2014, 95, 495–505. [Google Scholar] [CrossRef]
  6. Chen, H.; Zheng, X.; Huang, H.; Liu, C.; Wan, Q.; Shang, S. The effects of a home-based exercise intervention on elderly patients with knee osteoarthritis: A quasi-experimental study. BMC Musculoskelet. Disord. 2019, 20, 160. [Google Scholar] [CrossRef] [PubMed]
  7. Fisher, N.M.; Pendergast, D.R. Reduced muscle function in patients with osteoarthritis. Scand. J. Rehabil. Med. 1997, 29, 213–221. [Google Scholar] [CrossRef]
  8. Williams, S.B.; Brand, C.A.; Hill, K.D.; Hunt, S.B.; Moran, H. Feasibility and outcomes of a home-based exercise program on improving balance and gait stability in women with lower-limb osteoarthritis or rheumatoid arthritis: A pilot study. Arch. Phys. Med. Rehabil. 2010, 91, 106–114. [Google Scholar] [CrossRef]
  9. Yang, Y.; Wang, K.; Liu, H.; Qu, J.; Wang, Y.; Chen, P.; Zhang, T.; Luo, J. The impact of Otago exercise programme on the prevention of falls in older adult: A systematic review. Front. Public. Health 2022, 10, 953593. [Google Scholar] [CrossRef]
  10. Mort, J.S.; Billington, C.J. Articular cartilage and changes in arthritis: Matrix degradation. Arthritis Res. 2001, 3, 337–341. [Google Scholar] [CrossRef]
  11. Roos, E.M.; Arden, N.K. Strategies for the prevention of knee osteoarthritis. Nat. Rev. Rheumatol. 2016, 12, 92–101. [Google Scholar] [CrossRef]
  12. Zhang, W.; Moskowitz, R.W.; Nuki, G.; Abramson, S.; Altman, R.D.; Arden, N.; Bierma-Zeinstra, S.; Brandt, K.D.; Croft, P.; Doherty, M.; et al. OARSI recommendations for the management of hip and knee osteoarthritis, Part II: OARSI evidence-based, expert consensus guidelines. Osteoarthr. Cartil. 2008, 16, 137–162. [Google Scholar] [CrossRef] [PubMed]
  13. Hunter, D.J.; Bierma-Zeinstra, S. Osteoarthritis. Lancet 2019, 393, 1745–1759. [Google Scholar] [CrossRef] [PubMed]
  14. Fransen, M.; McConnell, S.; Harmer, A.R.; Van der Esch, M.; Simic, M.; Bennell, K.L. Exercise for osteoarthritis of the knee: A Cochrane systematic review. Br. J. Sports Med. 2015, 49, 1554–1557. [Google Scholar] [CrossRef] [PubMed]
  15. Tirasci, E.; Sarpel, T.; Coskun Benlidayi, I.; Deniz, V. The effect of balance exercises on central sensitization in patients with knee osteoarthritis. Rheumatol. Int. 2024, 44, 795–804. [Google Scholar] [CrossRef]
  16. You, Y.; Liu, J.; Tang, M.; Wang, D.; Ma, X. Effects of Tai Chi exercise on improving walking function and posture control in elderly patients with knee osteoarthritis: A systematic review and meta-analysis. Medicine 2021, 100, e25655. [Google Scholar] [CrossRef]
  17. Kramarow, E.; Chen, L.H.; Hedegaard, H.; Warner, M. Deaths from Unintentional Injury Among Adults Aged 65 and Over: United States, 2000–2013; NCHS Data Brief; National Center for Health Statistics: Hyattsville, MD, USA, 2015; p. 199.
  18. Fortinsky, R.H.; Baker, D.; Gottschalk, M.; King, M.; Trella, P.; Tinetti, M.E. Extent of implementation of evidence-based fall prevention practices for older patients in home health care. J. Am. Geriatr. Soc. 2008, 56, 737–743. [Google Scholar] [CrossRef]
  19. Berg, K.O.; Maki, B.E.; Williams, J.I.; Holliday, P.J.; Wood-Dauphinee, S.L. Clinical and laboratory measures of postural balance in an elderly population. Arch. Phys. Med. Rehabil. 1992, 73, 1073–1080. [Google Scholar]
  20. Keskin, D.; Borman, P.; Ersöz, M.; Kurtaran, A.; Bodur, H.; Akyüz, M. The risk factors related to falling in elderly females. Geriatr. Nurs. 2008, 29, 58–63. [Google Scholar] [CrossRef]
  21. Arnold, C.M.; Gyurcsik, N.C. Risk factors for falls in older adults with lower extremity arthritis: A conceptual framework of current knowledge and future directions. Physiother. Can. 2012, 64, 302–314. [Google Scholar] [CrossRef]
  22. Nnodim, J.O.; Yung, R.L. Balance and its Clinical Assessment in Older Adults—A Review. J. Geriatr. Med. Gerontol. 2015, 1, 3. [Google Scholar] [CrossRef]
  23. Fransen, M.; McConnell, S. Land-based exercise for osteoarthritis of the knee: A metaanalysis of randomized controlled trials. J. Rheumatol. 2009, 36, 1109–1117. [Google Scholar] [CrossRef] [PubMed]
  24. 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. [Google Scholar] [CrossRef]
  25. Pirayeh, N.; Kazemi, K.; Rahimi, F.; Mostafaee, N.; Shaterzadeh-Yazdi, M.J. The Effect of Balance Training on Functional Outcomes in Patients with Knee Osteoarthritis: A Systematic Review. Med. J. Islam. Repub. Iran. 2022, 36, 107. [Google Scholar] [CrossRef]
  26. Gomiero, A.B.; Kayo, A.; Abraão, M.; Peccin, M.S.; Grande, A.J.; Trevisani, V.F. Sensory-motor training versus resistance training among patients with knee osteoarthritis: Randomized single-blind controlled trial. Sao Paulo Med. J. 2018, 136, 44–50. [Google Scholar] [CrossRef] [PubMed]
  27. Zhou, Y.; Ren, H.; Hou, X.; Dong, X.; Zhang, S.; Lv, Y.; Li, C.; Yu, L. The effect of exercise on balance function in stroke patients: A systematic review and meta-analysis of randomized controlled trials. J. Neurol. 2024, 271, 4751–4768. [Google Scholar] [CrossRef] [PubMed]
  28. Page, M.J.; McKenzie, J.E.; Bossuyt, P.M.; Boutron, I.; Hoffmann, T.C.; Mulrow, C.D.; Shamseer, L.; Tetzlaff, J.M.; Akl, E.A.; Brennan, S.E.; et al. The PRISMA 2020 statement: An updated guideline for reporting systematic reviews. BMJ 2021, 372, n71. [Google Scholar] [CrossRef]
  29. Li, G.; Tao, X.; Lei, B.; Hou, X.; Yang, X.; Wang, L.; Zhang, S.; Lv, Y.; Wang, T.; Yu, L. Effects of exercise on post-stroke cognitive function: A systematic review and meta-analysis of randomized controlled trials. Top. Stroke Rehabil. 2024, 31, 645–666. [Google Scholar] [CrossRef]
  30. Wu, W.; Chen, Z.; Zhou, H.; Wang, L.; Li, X.; Lv, Y.; Sun, T.; Yu, L. Effects of Acute Ingestion of Caffeine Capsules on Muscle Strength and Muscle Endurance: A Systematic Review and Meta-Analysis. Nutrients 2024, 16, 1146. [Google Scholar] [CrossRef]
  31. Qiu, B.; Zhou, Y.; Tao, X.; Hou, X.; Du, L.; Lv, Y.; Yu, L. The effect of exercise on flow-mediated dilation in people with type 2 diabetes mellitus: A systematic review and meta-analysis of randomized controlled trials. Front. Endocrinol. 2024, 15, 1347399. [Google Scholar] [CrossRef]
  32. Özlü, A.; Ünver, G.; Tuna, H.U.; Menekşeoǧlu, A.K. The Effect of a Virtual Reality-Mediated Gamified Rehabilitation Program on Pain, Disability, Function, and Balance in Knee Osteoarthritis: A Prospective Randomized Controlled Study. Games Health J. 2023, 12, 118–124. [Google Scholar] [CrossRef] [PubMed]
  33. Ansanay, R.L.; Tinduh, D.; Kusharyaningsih, R.H. The effect of dexterity and perturbation exercise on knee osteoarthritis through functional balance and power improvement of quadriceps and hamstring. Indian J. Forensic Med. Toxicol. 2020, 14, 2307–2312. [Google Scholar]
  34. Yousefian Molla, R.; Sadeghi, H.; Kahlaee, A.H. The Effect of Early Progressive Resistive Exercise Therapy on Balance Control of Patients with Total Knee Arthroplasty. Top. Geriatr. Rehabil. 2017, 33, 286–294. [Google Scholar] [CrossRef]
  35. Sayers, S.P.; Gibson, K.; Cook, C.R. Effect of high-speed power training on muscle performance, function, and pain in older adults with knee osteoarthritis: A pilot investigation. Arthritis Care Res. 2012, 64, 46–53. [Google Scholar] [CrossRef] [PubMed]
  36. Blasco, J.M.; Acosta-Ballester, Y.; Martínez-Garrido, I.; García-Molina, P.; Igual-Camacho, C.; Roig-Casasús, S. The effects of preoperative balance training on balance and functional outcome after total knee replacement: A randomized controlled trial. Clin. Rehabil. 2020, 34, 182–193. [Google Scholar] [CrossRef]
  37. Xiao, C.; Zhuang, Y.; Kang, Y. Effects of Wu Qin xi Qigong exercise on physical functioning in elderly people with knee osteoarthritis: A randomized controlled trial. Geriatr. Gerontol. Int. 2020, 20, 899–903. [Google Scholar] [CrossRef]
  38. Domínguez-Navarro, F.; Silvestre-Muñoz, A.; Igual-Camacho, C.; Díaz-Díaz, B.; Torrella, J.V.; Rodrigo, J.; Payá-Rubio, A.; Roig-Casasús, S.; Blasco, J.M. A randomized controlled trial assessing the effects of preoperative strengthening plus balance training on balance and functional outcome up to 1 year following total knee replacement. Knee Surg. Sports Traumatol. Arthrosc. 2021, 29, 838–848. [Google Scholar] [CrossRef]
  39. Song, J.; Wei, L.; Cheng, K.; Lin, Q.; Xia, P.; Wang, X.; Wang, X.; Yang, T.; Chen, B.; Ding, A.; et al. The Effect of Modified Tai Chi Exercises on the Physical Function and Quality of Life in Elderly Women with Knee Osteoarthritis. Front. Aging Neurosci. 2022, 14, 860762. [Google Scholar] [CrossRef]
  40. Assar, S.; Gandomi, F.; Mozafari, M.; Sohaili, F. The effect of Total resistance exercise vs. aquatic training on self-reported knee instability, pain, and stiffness in women with knee osteoarthritis: A randomized controlled trial. BMC Sports Sci. Med. Rehabil. 2020, 12, 27. [Google Scholar] [CrossRef]
  41. Zhang, S.; Guo, G.; Li, X.; Yao, F.; Wu, Z.; Zhu, Q.; Fang, M. The Effectiveness of Traditional Chinese Yijinjing Qigong Exercise for the Patients with Knee Osteoarthritis on the Pain, Dysfunction, and Mood Disorder: A Pilot Randomized Controlled Trial. Front. Med. 2022, 8, 792436. [Google Scholar] [CrossRef]
  42. Joshi, S.; Kolke, S. Effects of progressive neuromuscular training on pain, function, and balance in patients with knee osteoarthritis: A randomised controlled trial. Eur. J. Physiother. 2023, 25, 179–186. [Google Scholar] [CrossRef]
  43. Joshi, S.; Singh, S.K.; Vij, J.S. Effect of retrowalking, a non-pharmacological treatment on pain, disability, balance and gait in knee osteoarthritis: A randomized controlled trial. Indian J. Public Health Res. Dev. 2019, 10, 214–219. [Google Scholar] [CrossRef]
  44. López, L.L.; Benítez, P.O.; López, J.C.; Martos, I.C.; Torres, J.R.; Santiago, M.G.; Valenza, M.C. Effectiveness of an individualized comprehensive rehabilitation program in women with chronic knee osteoarthritis: A randomized controlled trial. Menopause 2022, 29, 687–692. [Google Scholar] [CrossRef]
  45. Liao, C.D.; Liou, T.H.; Huang, Y.Y.; Huang, Y.C. Effects of balance training on functional outcome after total knee replacement in patients with knee osteoarthritis: A randomized controlled trial. Clin. Rehabil. 2013, 27, 697–709. [Google Scholar] [CrossRef]
  46. Skoffer, B.; Maribo, T.; Mechlenburg, I.; Korsgaard, C.G.; Søballe, K.; Dalgas, U. Efficacy of preoperative progressive resistance training in patients undergoing total knee arthroplasty: 12-month follow-up data from a randomized controlled trial. Clin. Rehabil. 2020, 34, 82–90. [Google Scholar] [CrossRef]
  47. Liao, C.D.; Lin, L.F.; Huang, Y.C.; Huang, S.W.; Chou, L.C.; Liou, T.H. Functional outcomes of outpatient balance training following total knee replacement in patients with knee osteoarthritis: A randomized controlled trial. Clin. Rehabil. 2015, 29, 855–867. [Google Scholar] [CrossRef]
  48. Nigam, A.; Satpute, K.H.; Hall, T.M. Long term efficacy of mobilisation with movement on pain and functional status in patients with knee osteoarthritis: A randomised clinical trial. Clin. Rehabil. 2021, 35, 80–89. [Google Scholar] [CrossRef] [PubMed]
  49. Pournajaf, S.; Goffredo, M.; Pellicciari, L.; Piscitelli, D.; Criscuolo, S.; Le Pera, D.; Damiani, C.; Franceschini, M.; Franceschini, M. Effect of balance training using virtual reality-based serious games in individuals with total knee replacement: A randomized controlled trial. Ann. Phys. Rehabil. Med. 2022, 65, 101609. [Google Scholar] [CrossRef] [PubMed]
  50. Alghadir, A.H.; Anwer, S.; Sarkar, B.; Paul, A.K.; Anwar, D. Effect of 6-week retro or forward walking program on pain, functional disability, quadriceps muscle strength, and performance in individuals with knee osteoarthritis: A randomized controlled trial (retro-walking trial). BMC Musculoskelet. Disord. 2019, 20, 159. [Google Scholar] [CrossRef]
  51. An, J.; Son, Y.W.; Lee, B.H. Effect of Combined Kinematic Chain Exercise on Physical Function, Balance Ability, and Gait in Patients with Total Knee Arthroplasty: A Single-Blind Randomized Controlled Trial. Int. J. Environ. Res. Public Health 2023, 20, 3524. [Google Scholar] [CrossRef]
  52. Lee, J.Y.; Kim, J.H.; Lee, B.H. Effect of dynamic balance exercises based on visual feedback on physical function, balance ability, and depression in women after bilateral total knee arthroplasty: A randomized controlled trial. Int. J. Environ. Res. Public Health 2020, 17, 3203. [Google Scholar] [CrossRef] [PubMed]
  53. Lee, H.G.; An, J.; Lee, B.H. The effect of progressive dynamic balance training on physical function, the ability to balance and quality of life among elderly women who underwent a total knee arthroplasty: A double-blind randomized control trial. Int. J. Environ. Res. Public Health 2021, 18, 2513. [Google Scholar] [CrossRef]
  54. Moseng, T.; Vlieland, T.P.M.V.; Battista, S.; Beckwée, D.; Boyadzhieva, V.; Conaghan, P.G.; Costa, D.; Doherty, M.; Finney, A.G.; Georgiev, T.; et al. EULAR recommendations for the non-pharmacological core management of hip and knee osteoarthritis: 2023 update. Ann. Rheum. Dis. 2024, 83, 730–740. [Google Scholar] [CrossRef]
  55. Kan, H.; Chan, P.; Chiu, K.; Yan, C.; Yeung, S.; Ng, Y.; Shiu, K.; Ho, T. Non-surgical treatment of knee osteoarthritis. Hong Kong Med. J. 2019, 25, 127–133. [Google Scholar] [CrossRef] [PubMed]
  56. Perlman, A.I.; Sabina, A.; Williams, A.L.; Njike, V.Y.; Katz, D.L. Massage therapy for osteoarthritis of the knee: A randomized controlled trial. Arch. Intern. Med. 2006, 166, 2533–2538. [Google Scholar] [CrossRef]
  57. Gunn, A.H.; Schwartz, T.A.; Arbeeva, L.S.; Callahan, L.F.; Golightly, Y.; Goode, A.; Hill, C.H.; Huffman, K.; Iversen, M.D.; Pathak, A.; et al. Fear of Movement and Associated Factors Among Adults with Symptomatic Knee Osteoarthritis. Arthritis Care Res. 2017, 69, 1826–1833. [Google Scholar] [CrossRef]
  58. Slemenda, C.; Heilman, D.K.; Brandt, K.D.; Katz, B.P.; Mazzuca, S.A.; Braunstein, E.M.; Byrd, D. Reduced quadriceps strength relative to body weight: A risk factor for knee osteoarthritis in women? Arthritis Rheum. 1998, 41, 1951–1959. [Google Scholar]
  59. Øiestad, B.E.; Juhl, C.B.; Eitzen, I.; Thorlund, J.B. Knee extensor muscle weakness is a risk factor for development of knee osteoarthritis. A systematic review and meta-analysis. Osteoarthr. Cartil. 2015, 23, 171–177. [Google Scholar] [CrossRef] [PubMed]
  60. Feng, Y.; Wu, Y.; Liu, H.; Bao, T.; Wang, C.; Wang, Z.; Huang, J.; Jiang, Y.; He, C.; Zhu, S. Effect of the telemedicine-supported multicomponent exercise therapy in patients with knee osteoarthritis: Study protocol for a randomized controlled trial. Trials 2023, 24, 729. [Google Scholar] [CrossRef]
  61. An, J.; Cheon, S.J.; Lee, B.H. The Effect of Combined Balance Exercise on Knee Range of Motion, Balance, Gait, and Functional Outcomes in Acute Phase Following Total Knee Arthroplasty: A Single-Blind Randomized Controlled Trial. Medicina 2024, 60, 1389. [Google Scholar] [CrossRef]
  62. Juhl, C.; Christensen, R.; Roos, E.M.; Zhang, W.; Lund, H. Impact of exercise type and dose on pain and disability in knee osteoarthritis: A systematic review and meta-regression analysis of randomized controlled trials. Arthritis Rheumatol. 2014, 66, 622–636. [Google Scholar] [CrossRef] [PubMed]
  63. Gür, H.; Cakin, N.; Akova, B.; Okay, E.; Küçükoğlu, S. Concentric versus combined concentric-eccentric isokinetic training: Effects on functional capacity and symptoms in patients with osteoarthrosis of the knee. Arch. Phys. Med. Rehabil. 2002, 83, 308–316. [Google Scholar] [CrossRef] [PubMed]
  64. Sadeghi, H.; Jehu, D.A.; Daneshjoo, A.; Shakoor, E.; Razeghi, M.; Amani, A.; Hakim, M.N.; Yusof, A. Effects of 8 Weeks of Balance Training, Virtual Reality Training, and Combined Exercise on Lower Limb Muscle Strength, Balance, and Functional Mobility Among Older Men: A Randomized Controlled Trial. Sports Health 2021, 13, 606–612. [Google Scholar] [CrossRef]
  65. Husby, V.S.; Foss, O.A.; Husby, O.S.; Winther, S.B. Randomized controlled trial of maximal strength training vs. standard rehabilitation following total knee arthroplasty. Eur. J. Phys. Rehabil. Med. 2018, 54, 371–379. [Google Scholar] [CrossRef] [PubMed]
  66. Wang, C.; Schmid, C.H.; Iversen, M.D.; Harvey, W.F.; Fielding, R.A.; Driban, J.B.; Price, L.L.; Wong, J.B.; Reid, K.F.; Rones, R. Comparative Effectiveness of Tai Chi Versus Physical Therapy for Knee Osteoarthritis: A Randomized Trial. Ann. Intern. Med. 2016, 165, 77–86. [Google Scholar] [CrossRef]
  67. Chaipinyo, K.; Karoonsupcharoen, O. No difference between home-based strength training and home-based balance training on pain in patients with knee osteoarthritis: A randomised trial. Aust. J. Physiother. 2009, 55, 25–30. [Google Scholar] [CrossRef]
  68. American College of Sports Medicine Position Stand. Progression models in resistance training for healthy adults. Med. Sci. Sports Exerc. 2009, 41, 687–708. [Google Scholar] [CrossRef]
  69. Kehlet, H.; Søballe, K. Fast-track hip and knee replacement--what are the issues? Acta Orthop. 2010, 81, 271–272. [Google Scholar] [CrossRef]
  70. Forte, P.; Encarnação, S.G.; Branquinho, L.; Barbosa, T.M.; Monteiro, A.M.; Pecos-Martín, D. The Effects of an 8-Month Multicomponent Training Program in Body Composition, Functional Fitness, and Sleep Quality in Aged People: A Randomized Controlled Trial. J. Clin. Med. 2024, 13, 6603. [Google Scholar] [CrossRef]
  71. Kalebota, N.; Žerjavić, N.L.; Durmiš, K.K.; Milošević, M.; Andreić, A.; Končar, B.; Vedriš, M.; Turković, P.; Žura, N.; Žagar, I.; et al. Effects of Tai Chi exercise on pain, functional status, and quality of life in patients with osteoarthritis or inflammatory arthritis. Turk. J. Phys. Med. Rehabil. 2024, 70, 300–308. [Google Scholar] [CrossRef]
  72. Mihalko, S.L.; Cox, P.; Beavers, D.P.; Miller, G.D.; Nicklas, B.J.; Lyles, M.; Hunter, D.J.; Eckstein, F.; Guermazi, A.; Loeser, R.F.; et al. Effect of intensive diet and exercise on self-efficacy in overweight and obese adults with knee osteoarthritis: The IDEA randomized clinical trial. Transl. Behav. Med. 2019, 9, 227–235. [Google Scholar] [CrossRef] [PubMed]
  73. Ha, G.C.; Yoon, J.R.; Yoo, C.G.; Kang, S.J.; Ko, K.J. Effects of 12-week aquatic exercise on cardiorespiratory fitness, knee isokinetic function, and Western Ontario and McMaster University osteoarthritis index in patients with knee osteoarthritis women. J. Exerc. Rehabil. 2018, 14, 870–876. [Google Scholar] [CrossRef]
  74. Kim, J.-Y.; Lee, D.-W.; Jeong, M.-B. Effect of a Telerehabilitation Exercise Program on the Gait, Knee function and Quality of life In Patients with Knee Osteoarthritis. J. Korean Soc. Phys. Med. 2020, 15, 143–152. [Google Scholar] [CrossRef]
  75. Dong, Y.; Yan, Y.; Zhou, J.; Zhou, Q.; Wei, H. Evidence on risk factors for knee osteoarthritis in middle-older aged: A systematic review and meta analysis. J. Orthop. Surg. Res. 2023, 18, 634. [Google Scholar] [CrossRef]
  76. Koca, I.; Boyaci, A.; Tutoglu, A.; Boyaci, N.; Ozkur, A. The Relationship between Quadriceps Thickness, Radiological Staging, and Clinical Parameters in Knee Osteoarthritis. J. Phys. Ther. Sci. 2014, 26, 931–936. [Google Scholar] [CrossRef]
  77. Lin, Y.H.; Chen, Y.C.; Tseng, Y.C.; Tsai, S.T.; Tseng, Y.H. Physical activity and successful aging among middle-aged and older adults: A systematic review and meta-analysis of cohort studies. Aging 2020, 12, 7704–7716. [Google Scholar] [CrossRef] [PubMed]
  78. Arden, N.; Nevitt, M.C. Osteoarthritis: Epidemiology. Best Pract. Res. Clin. Rheumatol. 2006, 20, 3–25. [Google Scholar] [CrossRef]
  79. Prabhakar, A.J.; Shruthi, R.; Thomas, D.T.; Nayak, P.; Joshua, A.M.; Prabhu, S.; Kamat, Y.D. Effectiveness of balance training on pain and functional outcomes in knee osteoarthritis: A systematic review and meta-analysis. F1000Research 2023, 11, 598. [Google Scholar] [CrossRef] [PubMed]
  80. Tan, B.; Yan, Y.; Zhou, Q.; Ran, Q.; Chen, H.; Sun, S.; Lu, W.; Chen, W.; Wang, J. Kinesitherapy for Knee Osteoarthritis Patients Physical and Psychological Health Based on “Traditional Chinese Exercise” Management Modalities: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Orthop. Surg. 2024, 16, 3–16. [Google Scholar] [CrossRef]
  81. Alghadir, A.; Anwer, S.; Brismée, J.M. The reliability and minimal detectable change of Timed Up and Go test in individuals with grade 1-3 knee osteoarthritis. BMC Musculoskelet. Disord. 2015, 16, 174. [Google Scholar] [CrossRef]
  82. Mostafaee, N.; Pirayeh, N.; Moosavi, S.S. Reliability, validity, responsiveness and minimal important changes of common clinical standing balance tests in individuals with knee osteoarthritis. Physiother. Theory Pract. 2025, 1–9. [Google Scholar] [CrossRef] [PubMed]
Figure 1. PRISMA flowchart of study selection.
Figure 1. PRISMA flowchart of study selection.
Healthcare 13 01312 g001
Figure 2. Meta-analysis results of the effect of exercise on TUG in KOA patients [33,36,37,38,39,42,43,44,45,46,47,48,49,50,51,52,53]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Figure 2. Meta-analysis results of the effect of exercise on TUG in KOA patients [33,36,37,38,39,42,43,44,45,46,47,48,49,50,51,52,53]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Healthcare 13 01312 g002
Figure 3. Meta-analysis results of the effect of exercise on BBS in KOA patients [32,33,34,35,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Figure 3. Meta-analysis results of the effect of exercise on BBS in KOA patients [32,33,34,35,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Healthcare 13 01312 g003
Figure 4. Meta-analysis results of the effect of types of intervention on BBS in KOA patients [32,33,34,35,36,38,39,40,41,42,43,44,45,46,47,48,49,51,52,53]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Figure 4. Meta-analysis results of the effect of types of intervention on BBS in KOA patients [32,33,34,35,36,38,39,40,41,42,43,44,45,46,47,48,49,51,52,53]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Healthcare 13 01312 g004
Figure 5. Meta-analysis results of the effect of intervention duration on BBS in KOA patients [32,33,34,35,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Figure 5. Meta-analysis results of the effect of intervention duration on BBS in KOA patients [32,33,34,35,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Healthcare 13 01312 g005
Figure 6. Meta-analysis results of the effect of frequency of intervention on BBS in KOA patients [32,33,34,35,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Figure 6. Meta-analysis results of the effect of frequency of intervention on BBS in KOA patients [32,33,34,35,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Healthcare 13 01312 g006
Figure 7. Meta-analysis results of the effect of duration of intervention per session on BBS in KOA patients [32,34,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Figure 7. Meta-analysis results of the effect of duration of intervention per session on BBS in KOA patients [32,34,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Healthcare 13 01312 g007
Figure 8. Meta-analysis results of the effect of duration of intervention per week on BBS in KOA patients [32,34,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Figure 8. Meta-analysis results of the effect of duration of intervention per week on BBS in KOA patients [32,34,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Healthcare 13 01312 g008
Figure 9. Meta-analysis results of the effect of different age groups on BBS in KOA patients [32,33,34,35,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Figure 9. Meta-analysis results of the effect of different age groups on BBS in KOA patients [32,33,34,35,36,37,38,39,40,41]. The pooled estimates were obtained from random effects analysis. Diamonds indicated the effect size of each study summarized as WMD. The size of the shaded squares was proportional to the percentage weight of each study. Horizontal lines represented the 95% CI and the vertical line represented the overall effect.
Healthcare 13 01312 g009
Disclaimer/Publisher’s Note: The statements, opinions and data contained in all publications are solely those of the individual author(s) and contributor(s) and not of MDPI and/or the editor(s). MDPI and/or the editor(s) disclaim responsibility for any injury to people or property resulting from any ideas, methods, instructions or products referred to in the content.

Share and Cite

MDPI and ACS Style

Wang, X.; Chen, Z.; Liang, Y.; Su, H.; Wang, T.; Lv, Y.; Yu, L. Effects of Exercise on Balance Function in People with Knee Osteoarthritis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Healthcare 2025, 13, 1312. https://doi.org/10.3390/healthcare13111312

AMA Style

Wang X, Chen Z, Liang Y, Su H, Wang T, Lv Y, Yu L. Effects of Exercise on Balance Function in People with Knee Osteoarthritis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Healthcare. 2025; 13(11):1312. https://doi.org/10.3390/healthcare13111312

Chicago/Turabian Style

Wang, Xingyue, Zhuying Chen, Yin Liang, Hao Su, Tongling Wang, Yuanyuan Lv, and Laikang Yu. 2025. "Effects of Exercise on Balance Function in People with Knee Osteoarthritis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials" Healthcare 13, no. 11: 1312. https://doi.org/10.3390/healthcare13111312

APA Style

Wang, X., Chen, Z., Liang, Y., Su, H., Wang, T., Lv, Y., & Yu, L. (2025). Effects of Exercise on Balance Function in People with Knee Osteoarthritis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials. Healthcare, 13(11), 1312. https://doi.org/10.3390/healthcare13111312

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop