An intradialytic aerobic exercise program ameliorates frailty and improves dialysis adequacy and quality of life among hemodialysis patients: a randomized controlled trial

Article information

Kidney Res Clin Pract. 2022;41(4):462-472
Publication date (electronic) : 2022 March 31
doi : https://doi.org/10.23876/j.krcp.21.284
1College of Nursing, CHA University, Pocheon, Republic of Korea
2Division of Nephrology, Department of Internal Medicine, CHA Bundang Medical Center, CHA University, Seongnam, Republic of Korea
Correspondence: Hye-Ja Park College of Nursing, CHA University, 120 Haeryong-ro, Pocheon 11160, Republic of Korea. E-mail: clara@cha.ac.kr
Co-correspondence: Dong-Ho Yang Division of Nephrology, Department of Internal Medicine, CHA Bundang Medical Center, 11 Yatap-ro, Seongnam 13506, Republic of Korea. E-mail: dhyang@cha.ac.kr
Received 2021 November 27; Revised 2022 January 8; Accepted 2022 February 7.

Abstract

Background

Hemodialysis patients with chronic kidney disease exhibit impaired exercise tolerance and functional decline. Despite the life-saving benefits of adequate dialysis, those declines translate into frailty and deteriorating quality of life (QoL). This study evaluated the effects of an intradialytic aerobic exercise program on frailty, dialysis adequacy, and QoL among hemodialysis patients.

Methods

Patients at an university hospital-affiliated hemodialysis center were randomly assigned to an exercise group (n = 18) or a control group (n = 21). The 12-week aerobic exercise program comprised 40 to 70 minutes of ergometer cycling 3 times/wk and a single education session. The control group completed only the education session. Outcomes were assessed at the time of enrollment, week 4, week 8, and week 12 using Fried’s frailty phenotype measures (gait speed, grip strength, vitality, body mass index, and physical activity), the short physical performance battery (SPPB), Kt/V urea, and the Short Form-36 questionnaire.

Results

There were significant interactions between groups and follow-up times in the frailty score (p < 0.001), gait speed (p < 0.001), SPPB (p < 0.001), and mental QoL (p = 0.03). The intention-to-treat and per-protocol analyses revealed that the exercise group exhibited significant improvements in frailty score (p < 0.001), gait speed (p < 0.001), grip strength (p < 0.001), exhaustion (p = 0.02), SPPB (p = 0.01), dialysis adequacy (p = 0.01), and physical QoL (p = 0.003).

Conclusion

An intradialytic aerobic exercise program could be a safe, feasible, and appropriate additional strategy to routine care among hemodialysis patients for improvements in frailty, dialysis adequacy, and QoL.

Introduction

The survival of patients undergoing hemodialysis has been improved by advances in hemodialysis therapy, standard expert practice, and affordable national healthcare support [1]. However, hemodialysis patients still experience physical and psychosocial burdens from living with chronic kidney disease [2]. Despite the life-saving benefits of adequate dialysis, the uremic milieu continues to impair bodily functions and structures, leading to exercise intolerance, impaired mobility, and disability among hemodialysis patients [3]. Those burdens predispose hemodialysis patients to adverse behaviors, such as a lack of motivation, sedentary lifestyle, and reduced physical activity, which can translate into frailty, which is known to affect approximately one-half of hemodialysis patients [24]. Frailty is a geriatric syndrome characterized as a multidimensional construct (slow gait speed, muscle weakness, exhaustion, weight loss, and low physical activity) [5].

Intradialytic aerobic exercise for hemodialysis patients improves aerobic capacity, muscular functioning, cardiovascular function, walking capacity, dialysis adequacy, and quality of life (QoL) without any adverse effects in clinical practice, although the structure of the intradialytic exercise varied widely in intensity, frequency, and duration [68]. Therefore, intradialytic aerobic exercise is recommended as a safe, feasible, and appropriate way to enhance physical functioning and QoL [9] that is associated with a low dropout rate, no need to find extra time for exercise, good compliance, and supervision by dialysis experts. However, it does have the drawbacks of adding to the workload of dialysis care providers, and its adoption into routine care has been slow [4,6,7]. The coexistence of frailty and dialysis markedly aggravates functional declines and health in all age groups [2]. Low physical activity contributes directly and indirectly to the development of frailty, and increased physical activity can prevent or reverse frailty, a non-permanent progressive condition that reflects physical performance and QoL [10,11]. However, few controlled trials have rigorously explored the effects of an intradialytic aerobic exercise program on the multidimensional nature of frailty among hemodialysis patients in Korea. Therefore, in this study, we evaluated the effects of an intradialytic aerobic exercise program on frailty, dialysis adequacy, and QoL among Korean hemodialysis patients.

Methods

Participants and setting

A sample of 42 hemodialysis patients was enrolled at a university hospital-affiliated hemodialysis center. All participants were undergoing regular hemodialysis (3 times/wk for 3–4 hours per session) with bicarbonate dialysate. The eligibility criteria were the age of ≥18 years, hemodialysis duration of ≥3 months for dialysis adjustment, no perfusion problems through an arteriovenous fistula to maintain adequate blood flow (250 mL/min), no severe hemodialysis-related complications, no history of completing an intradialytic aerobic exercise program (3 times/wk), the ability to use a cycle ergometer while lying in the dialysis bed, and the cognitive ability to read and comprehend the questionnaire. To minimize exercise-related risks, participants were excluded if they had a history of mental illness, any cardiac risk factors (myocardial infarction, angina pain, or uncontrolled hypertension), musculoskeletal risk factors, or a diagnosis of glaucoma during the previous 6 months. The required sample size was 18 patients/group using a repeated-measures within–between interaction model (α = 0.05, 1 – β = 0.8, effect size = 0.35, correlation among repeated measures = 0.5, non-sphericity correction ε = 0.5). To account for dropouts, 42 eligible hemodialysis patients from six sequentially numbered coupled dialysis shifts were enrolled and randomly assigned to either the exercise group (n = 21) or the control group (n = 21). Given the design of the exercise program, the participants, researchers, and dialysis care providers were not blinded. The exercise group completed a 12-week program of intradialytic aerobic exercise and a single education session (n = 18), while the control group completed only the education session (n = 21). In the exercise group, one patient dropped out because of exhaustion after week 4, and two patients missed their dialysis appointments after week 8 (Fig. 1).

Figure 1.

Consolidated standards for reporting trials flow diagram.

Ethical considerations

The study protocol was approved by the Institutional Review Board of Bundang CHA Medical Center (No. BD2015-095) and registered at a primary national clinical trial registration site (https://cris.nih.go.kr/cris/index.jsp; registration No., KCT0006774). All participants provided written informed consent before being enrolled. The researchers provided the participants with information regarding the study’s aims and methods, the right to withdraw at any time without reprisal, and their right to privacy.

Intradialytic aerobic exercise program

An intradialytic aerobic exercise program was developed based on the literature and previous studies [4,1114]. The content of the exercise program was validated by a group of experts: three nephrologists, two dialysis nursing specialists, and a nursing professor with 10-year experience in nephrology nursing (content validity index = 0.95). The researchers performed an initial feasibility study with three hemodialysis patients to standardize the intradialytic cycle ergometer exercise program and ensure its safety; those patients also provided informed consent. The preliminary findings indicated that the intradialytic exercise program, which consisted of warm-up, cycle ergometer exercise, and cool-down stages, was feasible, safe, and tolerable.

The exercise program began with a 50-minute education session called “Exercise guide for patients undergoing hemodialysis,” with sections titled “Exercise and its effects on health,” “Hemodialysis patients can do exercise,” “Types of exercise for people undergoing hemodialysis,” “Principles of exercise,” “Making exercise part of your life,” and “Behavioral change” to boost participant understanding of the intervention [12]. The 12-week aerobic exercise program involved 40 to 70 minutes of ergometer cycling 3 times/wk. Each exercise session comprised a stretching warm-up phase (5 minutes), the main exercise phase (30–60 minutes), and a cool-down phase (5 minutes). During the warm-up phase, the participants completed 10 cycles of neck/arm/hand stretches, shoulder shrugs and rotations, chest and upper back stretching exercises, single knee pulls, front and back leg stretches, and calf stretches [12,13]. During the main phase, the cycle ergometer exercise was safely performed during the first 1 to 1.5 hours of each dialysis session without cardiac decompensation. The leg ergometer (Mbike; Hong Jin Company, Shanghai, China) was fixed at the foot of the patients’ beds to allow them to pedal while remaining in the supine position during dialysis [4]. Exercise intensity was individually determined based on the rate of perceived exertion from the Borg scale, with a gradual increase from very light/light intensity (score of 7–9 for 5 minutes) to somewhat hard/hard intensity (score of 12–15 for 20–50 minutes) and then a decrease again to very light/light intensity (score of 7–9 for 5 minutes) [12,13,15]. Intermittent breaks were permitted during the exercise to prevent exhaustion and blood pressure elevation. The cool-down phase involved 10 cycles of arm, shoulder, and leg stretches in a 5-minute period. The control group completed only the education session after the baseline measurements.

All participants’ exercise durations and intensities during each session were supervised by nephrologists, dialysis nurses, and researchers to ensure that all hemodialysis-related and exercise-related parameters remained stable and safe (blood pressure, heart rate, pulse oxygen saturation, and the overexertion symptoms of fainting, chest pain, dyspnea, abdominal pain, nausea, vomiting, muscle pain, joint pain, etc.), based on the protocols of previous studies [4,14].

Measurements of study outcomes

Demographic, dialytic, and clinical assessments

Data regarding the participants’ demographic characteristics were collected using a self-administered questionnaire. Hemodialysis-related and clinical data were collected from the patients’ electronic medical records at the time of enrollment. Each participant’s Charlson’s comorbidity index was calculated (http://touchcalc.com/calculators/cci_js). Body composition parameters (skeletal muscle mass, body fat, and lower leg muscle) were measured with a body composition analyzer (Inbody S10; InBody Corp., Ltd., Seoul, Korea) using the direct segmental measurement bioelectrical impedance method at the time of enrollment and week 12 of the exercise program.

Frailty stage based on the Fried phenotype and the short physical performance battery measurements

Frailty was assessed using Fried’s frailty phenotype (gait speed, grip strength, vitality, body mass index, and physical activity) [5]. Each factor is scored as 1 (present) or 0 (absent): gait speed of <0.8 m/sec [16], grip strength of <30 kg for men or <20 kg for women [17], vitality score of <55 from the Short Form-36 (SF-36) tool, body mass index of ≤18.5 kg/m2 [5], and light physical activity for <30 minutes on 5 days of the week or moderate physical activity for <150 min/wk [18]. Patients with a score of ≥3 (i.e., three or more factors present) are considered frail [4]. A stopwatch was used to measure the participants’ 4-m gait speeds at a comfortable pace on a flat and straight surface. Maximum handgrip strength was evaluated in kilograms using a handheld dynamometer (JAMAR Hydraulic Hand Dynamometer; Patterson Medical Ltd., Chicago, IL, USA). All measurements were performed 1 hour after the hemodialysis session at the time of enrollment and at weeks 4, 8, and 12.

The validated short physical performance battery (SPPB) is based on scores of 0 to 4 points in three sections (balance, gait speed, and chair stand test), with a maximum score of 12, a minimum score of 0, and scores classified as normal mobility function (≥10 points) and frail mobility function (<10 points) [18]. Cronbach’s alpha value for the SPPB in this study was 0.83. The SPPB values were determined 1 hour after the hemodialysis session at the time of enrollment and at weeks 4, 8, and 12.

Dialysis adequacy

Hemodialysis adequacy was evaluated using Kt/V urea at the time of enrollment and at weeks 4, 8, and 12 of the exercise program.

Quality of life-based on the Short Form-36 questionnaire

Quality Metrics (https://www.qualitymetric.com) provided the validated Korean edition (version 2) of the SF-36 questionnaire (license No. QM027199), which contains eight multi-item scales that generate a physical component summary (PCS) score and a mental component summary (MCS) score. Those scores are transformed linearly into a 0 to 100-point scale, with higher scores indicating better health [19]. The Cronbach’s alpha value was 0.82. The QoL values were evaluated at the time of enrollment and at weeks 4, 8, and 12.

Data analysis

All data were analyzed using IBM SPSS version 23 (IBM Corp., Armonk, NY, USA). Data normality was determined using the Shapiro-Wilk test. The baseline characteristics of the two groups were compared using the chi-square test, Fisher exact test, or unpaired t test. Outcome data were analyzed using the chi-square test, analysis of covariance, and repeated-measures analysis of covariance with Bonferroni correction. If the data failed Mauchly’s sphericity assumption, the results are presented using Greenhouse-Geisser correction method. The Mann-Whitney U test was used for the intention-to-treat analysis with multiple imputations (regression method).

Results

Participant homogeneity

The exercise and control group participants were homogenous except for the significantly lower dialysis vintage in the exercise group (p = 0.004) (Table 1).

Homogeneity test for demographic, dialytic, and clinical characteristics (n = 39)

Changes in the incidence of frailty and body composition parameters

At baseline, the exercise and control groups had similar incidences of frailty. After 12 weeks, the exercise group had less frailty as reflected by Fried’s frailty score (p < 0.001), gait speed (p < 0.001), physical activity (p < 0.001), exhaustion (p = 0.002), and SPPB score (p = 0.002) (Table 2). The body composition parameters showed no significant improvements (Table 2).

Changes in the incidence of frailty and body composition parameters (n = 39)

Within- and between-group interaction effects on frailty, dialysis adequacy, and quality of life

At baseline, the exercise and control groups had similar frailty scores, SPPB scores, and QoL scores. There was a significant interaction in the overall frailty score (p < 0.001), gait speed (p < 0.001), and SPPB score (p < 0.001). The exercise group had a significant interaction in the overall MCS score (p = 0.03) (Table 3).

Within- and between-group interaction effects on frailty, dialysis adequacy, and quality of life (n = 39)

Differences in frailty, dialysis adequacy, and quality of life according to the intention-to-treat and per-protocol analyses

The intention-to-treat and per-protocol analyses revealed that the exercise group exhibited significant improvements in the overall frailty score (p < 0.001, p < 0.001), gait speed (p < 0.001, p < 0.001), grip strength (p < 0.001, p < 0.001), exhaustion (p = 0.02, p = 0.02), SPPB score (p = 0.04, p = 0.01), dialysis adequacy (p = 0.01, p = 0.01), and PCS score (p = 0.005, p = 0.003) (Table 4).

Differencesa in frailty, dialysis adequacy, and QoL according to the intention-to-treat and per-protocol analyses

Discussion

This study determined whether an intradialytic aerobic exercise program could improve frailty, dialysis adequacy, and QoL for hemodialysis patients.

Education and counseling are required to increase physical activity and drive behavioral change in hemodialysis patients [4]. However, a single 50-minute education session about physical activity did not reduce the incidence of frailty in the control group. In contrast, the exercise group had fewer cases of frailty after the program, as shown by Fried’s frailty score (0% vs. 66.7%), as well as its parameters of gait speed (5.6% vs. 66.7%) and exhaustion (38.9% vs. 90.5%) and the SPPB score (0.0% vs. 41.9%). Although this intradialytic aerobic exercise program did not entirely reverse the frailty phenotype, physical exercise could be essential for reducing frailty in hemodialysis patients.

Estimates of body composition can be more informative than the body mass index in hemodialysis patients, especially when considering physical performance rather than nutritional status [20]. We found no significant changes in skeletal muscle, leg muscle, or fat mass values in the exercise or control group. This result is consistent with that of another study, wherein appendicular muscle mass and other body composition parameters did not improve after a 4-month program of cycle ergometer exercise [21]. Additional research is needed to determine whether prolonged exercise or aerobic exercise with various sessions, durations, and intensities might be useful for increasing body muscle in hemodialysis patients.

The only noticeable baseline difference between the exercise and control groups was their baseline dialysis vintage, which influences functioning, frailty, and QoL [3,11]. Because we did not achieve selection balance, dialysis vintage should be considered a confounding variable to determine the within–between interaction effects. The exercise group experienced significant improvements in the average frailty score (f = 0.78), average gait speed (f = 0.93), and SPPB score (f = 0.45) during the 12-week program. These results agree with those of a previous report that a 6-week predialysis exercise training program (20 min/session) improved normal gait speed, fast gait speed, and sit-to-stand performance [22]. Another intradialytic program combining cardiovascular exercise (supine cycle ergometer) and resistance exercise also improved physical capacity in terms of the timed up-and-go, sit-to-stand, and gait speed outcomes [23]. A 4-month intradialytic cycle ergometer exercise program facilitated an increase in walking distance [21]. Gait speed is a sensitive health indicator that has been called the 6th vital sign among hemodialysis patients [16,24]. In the present study, both the exercise and control groups had limited gait speeds at baseline [3,24]. A change of 0.1 m/sec in gait speed reflects a meaningful change [25], and our exercise group exhibited an increase from 0.89 m/sec to 1.21 m/sec, which is sufficient for independent daily living, community ambulation, and crossing the street [3,16,26]. However, although handgrip strength had a significant within–between interaction, there was no significant difference in grip strength at any follow-up time after Bonferroni correction method was applied. In contrast, the previous 4-month intradialytic cycle ergometer program showed an improvement in handgrip strength [21], which could suggest that a longer period of intradialytic aerobic exercise (>12 weeks) is needed to improve handgrip strength and reach a non-frail state. The exercise group in the present study also experienced improvements in the average MCS score during the first 8 weeks (f = 0.29), although the small effect size might indicate a risk of bias. Therefore, large randomized controlled trials are needed to identify the optimal duration and timing of intradialytic cycle ergometer exercise and evaluate the effect on handgrip strength and mental QoL.

Data were missing for 3.6% of all variables in three patients (7.1%) in the exercise group. The intention-to-treat and per-protocol analyses revealed that the exercise group exhibited significant increments in Kt/V urea (0.12), grip strength (2.03 kg), exhaustion score (5.36), and PCS score (6.29), as well as improvements in Fried’s frailty score (–1.28), gait speed (0.31 m/sec), and SPPB score (1.17). During dialysis, exercise increases blood uremic solute removal by increasing blood flood to low perfusion tissue beds [8]. In the present study, the exercise group had a significant increase in Kt/V urea (+7.37%), and the control group had a decrease in Kt/V urea (–1.32%). This result is consistent with the previous finding that among hemodialysis patients, a 15-minute intradialytic aerobic exercise program safely and effectively improved Kt/V urea by 38% after 8 weeks [14]. Moreover, different types of intradialytic training might improve dialysis adequacy (based on Kt/V urea), cardiorespiratory fitness, and prognosis [6,22,23]. Profound and relentless exhaustion in hemodialysis patients leads to weakness, decreased vitality, and reduced ability to perform daily activities [27]. Furthermore, a 10-point increase in the vital score is associated with a 10% increase in mean survival time [28]. Our exercise group exhibited an increase of 5.36 in vitality score, which is consistent with the finding of a previous report [21]. Therefore, it could be prudent to incorporate exercise programs into the routine care of frail patients who are undergoing hemodialysis.

To determine the participants’ ability to engage in exercise, our nephrologists and dialysis nurses evaluated symptoms such as systolic blood pressure of ≥200 mmHg, diastolic blood pressure of ≥100 mmHg, and Borg score of ≥15, including subjective symptoms such as dizziness, chest tightness, dyspnea, nausea, vomiting, muscle pain, and joint pain [4]. Participants were encouraged to report any issues that they experienced to help identify the support required during or after the intradialytic exercise. Because we observed several episodes of elevated systolic blood pressure during the intradialytic exercise, careful screening and monitoring by nephrologists and dialysis nurses were essential to maintain the participants’ safety, which means that ongoing exercise programs would add to healthcare providers’ work burden. Two participants missed two sessions of the exercise program due to elevation of their systolic blood pressure of ≥190 mmHg during the stretching warm-up phase. Additionally, two participants had an episode of systolic blood pressure elevation to 170 mmHg (from 140 mmHg) during the main exercise phase. After 10 minutes of rest, the high blood pressure had normalized, and the participants safely completed their exercise sessions. In addition, one 48-year-old female participant with intradialytic hypotension experienced improvement in her dialysis-induced hypotension.

The present study has several limitations that warrant consideration. First, we included only patients undergoing treatment at a single hemodialysis center, and the results might not be generalizable to other centers and patient populations. Second, the small effect size for the MCS score improvement (f < 0.35) could indicate a risk of bias. Third, the small sample size precluded the use of factorial statistics for exercise and frailty factors. Fourth, the different statistical measures produced variable efficacies in terms of Kt/V. Because the effects of intradialytic aerobic exercise on Kt/V have been controversial [6], this discrepancy should be checked through further research by modifying the duration, time, and intensity of the intradialytic aerobic exercise program in a larger, multicenter population.

Although the 12-week intradialytic exercise program did not entirely reverse the frailty phenotype, and different statistical measures produced various results, our findings imply that an intradialytic cycle ergometer exercise program could reduce frailty and improve dialysis adequacy and QoL. Intradialytic exercise programs have not been incorporated into routine care due to the practical burden on dialysis health care professionals. A government health policy should be established to correct the lack of trained dialysis health care professionals available to supervise exercise programs and the lack of financial support for ongoing exercise programs.

Notes

Conflicts of interest

All authors have no conflicts of interest to declare.

Authors’ contributions

Conceptualization, Data curation, Investigation, Methodology: All authors

Formal analysis: SK, HJP

Writing–original draft: All authors

Writing–review & editing: All authors

All authors read and approved the final manuscript.

Acknowledgements

The authors owe special thanks to all the hemodialysis patients who participated in this study. We also thank the dialysis care providers at the hospital-affiliated hemodialysis center.

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Article information Continued

Figure 1.

Consolidated standards for reporting trials flow diagram.

Table 1.

Homogeneity test for demographic, dialytic, and clinical characteristics (n = 39)

Characteristic Exercise group Control group χ2 or t p-value
Demographic characteristic
 No. of patients 18 21
 Age (yr) 57.61 ± 13.69 56.76 ± 12.32 0.20 0.84
 Sex
  Male 10 (55.6) 10 (47.6) 0.24 0.62
  Female 8 (44.4) 11 (52.4)
 Spouse
  Yes 17 (94.4) 18 (85.7) 0.80 0.61a
  No 1 (5.6) 3 (14.3)
 Educational level
  ≤High school 10 (55.6) 16 (76.2) 1.86 0.17
  ≥College 8 (44.4) 5 (23.8)
 Job
  Full time 3 (16.7) 3 (14.3) 1.42 0.49
  Part time 3 (16.7) 7 (33.3)
  None 12 (66.7) 11 (52.4)
 Religion
  Yes 14 (77.8) 12 (57.1) 1.86 0.31a
  No 4 (22.2) 9 (42.9)
 Health insurance
  National 15 (83.3) 16 (76.2) 0.30 0.70a
  Medicaid 3 (16.7) 5 (23.8)
 Monthly income ($)
  <2,000 12 (66.7) 18 (85.7) 1.98 0.26a
  ≥2,000 6 (33.3) 3 (14.3)
Dialysis-related characteristic
 Hemodialysis vintage (yr) 2.38 ± 2.72 5.74 ± 3.99 –3.10 0.004
 Dialysis duration/session (min) 223.61 ± 17.81 228.10 ± 19.14 0.75 0.46
 Blood flow rate (mL/min) 281.67 ± 23.58 276.19 ± 24.39 0.71 0.48
 Dialysate flow rate (mL/min) 516.67 ± 70.71 571.43 ± 130.93 1.67 0.11
 Dialyzer efficacy
  High 12 (66.7) 17 (81.0) 2.26 0.32a
  Medium 5 (27.8) 2 (9.5)
  Low 1 (5.6) 2 (9.5)
 Fistula type
  Arteriovenous fistula 16 (88.9) 16 (76.2) 
  Arteriovenous graft 2 (11.1) 5 (23.8) 1.06 0.42a
Clinical characteristic
 Hemoglobin (g/dL) 10.70 ± 1.18 10.25 ± 1.04 –1.27 0.21
 Albumin (g/dL) 3.87 ± 0.18 3.77 ± 0.49 –0.92 0.37
 Calcium (mg/dL) 8.65 ± 0.65 8.77 ± 0.67 –0.58 0.57
 Phosphorus (mg/dL) 5.04 ± 1.32 4.81 ± 1.50 0.48 0.62
 Potassium (mEq/L) 5.10 ± 0.71 4.69 ± 0.68 1.80 0.08
 Creatinine (mg/dL) 10.09 ± 2.44 10.38 ± 2.21 –0.38 0.71
 Urea reduction ratio (%) 74.78 ± 3.83 74.98 ± 4.00 0.16 0.88
 Cause of renal failure
  Diabetes 7 (38.9) 11 (52.4) 0.82 0.70a
  Hypertension 7 (38.9) 6 (28.6)
  Others 4 (22.2) 4 (15.1)
 Charlson comorbidity index 5.33 ± 2.35 5.14 ± 2.26 0.26 0.80
 Dry body weight (kg) 58.95 ± 10.30 56.57 ± 9.95 0.73 0.47

Data are expressed as number only, mean ± standard deviation, or numer (%).

a

Fisher exact test.

Table 2.

Changes in the incidence of frailty and body composition parameters (n = 39)

Variable Baseline
In 12 wk
Exercise group (n = 18) Control group (n = 21) χ2 or F p-value Exercise group (n = 18) Control group (n = 21) χ2 or F p-value
Frailty (score)
 Not frail, 0-2 10 (55.6) 9 (42.9) 0.63 0.53 18 (100) 7 (33.3) 18.72 <0.001a
 Frail, 3-5 8 (44.4) 12 (57.1) 0 (0) 14 (66.7)
Frailty phenotype
 Gait speed (m/sec)
  Not frail, ≥0.8 12 (66.7) 11 (52.4) 0.82 0.52 17 (94.4) 7 (33.3) 15.29 <0.001a
  Frail, <0.8 6 (33.3) 10 (47.6) 1 (5.6) 14 (66.7)
 Grip strength (kg)
  Not frail, M: ≥30 and F: ≥20 6 (33.3) 12 (57.1) 2.21 0.20 10 (55.6) 7 (33.3) 1.95 0.21
  Frail, M: <30 and F: <20 12 (66.7) 9 (42.9) 8 (44.4) 14 (66.7)
 Physical activity
  Not frail 10 (55.6) 7 (33.3) 1.95 0.21 18 (100) 7 (33.3) 18.72 <0.001a
  Frail 8 (44.4) 14 (66.7) 0 (0) 14 (66.7)
 Exhaustion (vitality, score)
  Not frail, ≥55 6 (33.3) 5 (23.8) 0.43 0.72a 11 (61.1) 2 (9.5) 11.61 0.002a
  Frail, <55 12 (66.7) 16 (76.2) 7 (38.9) 19 (90.5)
 Weight loss, BMI (kg/m2)
  Not frail, >18.5 16 (88.9) 17 (81.0) 0.47 0.67a 17 (94.4) 17 (81.0) 1.58 0.35a
  Frail, ≤18.5 2 (11.1) 4 (19.0) 1 (5.6) 4 (19.0)
SPPB (score)
 Not frail, 10–12 14 (77.8) 14 (66.7) 0.59 0.497a 18 (100) 12 (57.1) 10.03 0.002a
 Frail, <10 4 (22.2) 7 (33.3) 0 (0) 9 (41.9)
Skeletal muscle mass (kg) 25.46 ± 4.80 24.32 ± 4.16 0.15 0.71 25.47 ± 4.85 23.17 ± 4.71 0.79 0.37b
Body fat (%) 21.17 ± 7.85 22.21 ± 9.99 0.03 0.86 21.82 ± 7.84 24.11 ± 9.23 0.43 0.52b
Lower leg muscles (kg) 15.42 ± 3.70 14.16 ± 3.51 1.23 0.27 13.79 ± 3.10 12.51 ± 2.59 0.80 0.38b

Data are expressed as number (%) or mean ± standard deviation.

BMI, body mass index; F, female; M, male; SPPB, short physical performance battery.

a

Fisher exact test,

b

analysis of covariance adjusted for dialysis vintage.

Table 3.

Within- and between-group interaction effects on frailty, dialysis adequacy, and quality of life (n = 39)

Variable Time (wk) Exercise group (n = 18) Control group (n = 21) F p-value Repeated measures of ANCOVA
F p-value η₂ (f)
Frailty (score)a Baseline 2.22 ± 1.22 2.52 ± 0.87 0.35 0.56 Time 1.80 0.17d 0.048
4th 1.33 ± 1.14c 2.95 ± 1.02 17.52 <0.001 Group 18.55 <0.001 0.340
8th 1.11 ± 0.90c 3.05 ± 1.02 26.47 <0.001 T*G 21.74 <0.001d 0.376 (0.78)
12th 0.94 ± 0.93c 3.10 ± 1.04 34.71 <0.001
Gait speed (m/sec) Baseline 0.89 ± 0.22 0.83 ± 0.24 0.21 0.65 Time 8.18 0.003d 0.185
4th 1.14 ± 0.30c 0.76 ± 0.22 11.88 0.001 Group 12.64 0.001 0.260
8th 1.18 ± 0.31c 0.72 ± 0.19 20.23 <0.001 T*G 32.2 <0.001d 0.464 (0.93)
12th 1.21 ± 0.31c 0.71 ± 0.19 24.26 <0.001
Grip strength (kg) Baseline 23.58 ± 9.79 26.10 ± 8.83 1.27 0.27 Time 1.92 0.15d 0.051
4th 24.00 ± 9.16 21.13 ± 9.51 0.18 0.68 Group 0.05 0.83 0.001
8th 25.28 ± 8.45 22.40 ± 9.78 0.52 0.48 T*G 9.73 <0.001d 0.213 (0.52)
12th 25.61 ± 8.88 22.07 ± 8.41 0.75 0.39
Exhaustion (vitality in SF-36, score) Baseline 48.46 ± 12.80 46.24 ± 10.79 1.27 0.27 Time 1.17 0.33 0.031
4th 53.16 ± 12.06 44.11 ± 9.78 7.60 0.009 Group 9.96 0.003 0.217
8th 53.66 ± 8.99 41.68 ± 8.34 15.08 <0.001 T*G 2.27 0.09 0.059 (0.25)
12th 53.82 ± 10.06 43.26 ± 6.80 12.38 0.001
Weight loss (BMI, kg/m2) Baseline 21.55 ± 2.31 21.68 ± 3.06 0.03 0.88 Time 3.35 0.05d 0.085
4th 21.53 ± 2.16 21.68 ± 3.02 0.03 0.86 Group 0.03 0.88 0.001
8th 21.53 ± 2.01 21.64 ± 2.77 0.04 0.84 T*G 1.67 0.20d 0.044 (0.21)
12th 21.58 ± 1.98 21.79 ± 3.01 0.24 0.63
SPPB (score)b Baseline 10.67 ± 1.61 10.10 ± 2.02 0.07 0.79 Time 4.31 0.03d 0.009
4th 11.56 ± 0.98c 9.52 ± 2.06 8.73 0.005 Group 8.73 0.006 0.142
8th 11.72 ± 0.67c 9.86 ± 2.20 6.96 0.01 T*G 28.81 <0.001d 0.168 (0.45)
12th 11.83 ± 0.51c 9.76 ± 2.28 9.89 0.003
Kt/V urea Baseline 1.64 ± 0.19 1.67 ± 0.19 0.14 0.71 Time 0.46 0.67d 0.013
4th 1.68 ± 0.24 1.71 ± 0.24 0.05 0.82 Group 0.29 0.59 0.008
8th 1.70 ± 0.23 1.71 ± 0.28 0.14 0.71 T*G 2.85 0.05d 0.073 (0.28)
12th 1.76 ± 0.30 1.64 ± 0.18 2.40 0.13
Physical component summary Baseline 45.51 ± 6.48 44.50 ± 8.76 1.30 0.26 Time 5.59 0.003d 0.134
4th 49.41 ± 4.94 43.81 ± 7.38 8.35 0.007 Group 8.52 0.006 0.191
8th 50.31 ± 4.50 44.76 ± 6.88 7.41 0.01 T*G 1.98 0.13d 0.052 (0.23)
12th 51.80 ± 4.51 42.79 ± 8.38 10.95 0.002
Mental component summary Baseline 50.35 ± 11.04 49.81 ± 9.17 0.12 0.73 Time 0.90 0.97 0.003
4th 53.98 ± 7.83c 45.22 ± 8.64 9.41 0.004 Group 5.11 0.03 0.124
8th 53.24 ± 7.28c 44.95 ± 8.65 7.66 0.009 T*G 3.04 0.03 0.078 (0.29)
12th 53.23 ± 8.60 48.95 ± 8.14 2.92 0.10

Data are expressed as mean ± standard deviation.

BMI, body mass index; Kt/V, K = dialyzer’s capacity to clear urea at the blood flow rate, t = treatment time, V = distribution volume of urea; SF-36, Short Form-36 tool; SPPB, short physical performance battery; T*G, time*group.

F is effect size calculated using the analysis of covariance (ANCOVA) model adjusted for dialysis vintage in G*Power (small = 0.10, medium = 0.25, large = 0.40); F-score calculated using ANCOVA adjusted by dialysis vintage (exercise group vs. control group).

Score range:

a

0–5,

b

0–12.

c

Statistically significant based on Bonferroni correction (p < 0.013);

d

Greenhouse-Geisser correction according to Mauchly’s sphericity test (p < 0.05).

Table 4.

Differencesa in frailty, dialysis adequacy, and QoL according to the intention-to-treat and per-protocol analyses

Variable Intention-to-treat analysis (n = 42)
Per-protocol analysis (n = 39)
Exercise group (n = 21) Control group (n = 21) zb p-value Exercise group (n = 18) Control group (n = 21) zb p-value
Frailty score –1.26 ± 0.96 0.57 ± 0.81 –5.08 <0.001 –1.28 ± 1.02 0.57 ± 0.81 –4.84 <0.001
 Slowness (gait speed, m/sec) 0.27 ± 0.22 –0.11 ± 0.15 –4.77 <0.001 0.31 ± 0.19 –0.11 ± 0.15 –5.21 <0.001
 Weakness (grip strength, kg) 1.58 ± 3.94 –4.02 ± 4.52 –4.03 <0.001 2.03 ± 3.79 –4.02 ± 4.52 –4.05 <0.001
 Exhaustion (vitality, score) 4.57 ± 7.74 –2.98 ± 9.91 –2.30 0.02 5.36 ± 8.09 –2.98 ±9.91 –2.42 0.02
 Weight loss (BMI, kg/m2) 0.18 ± 1.20 0.48 ± 1.79 –0.57 0.57 0.03 ± 1.07 0.48 ± 1.79 0.42 0.69
SPPB (0–12, score) 0.88 ± 1.43 –0.33 ± 1.68 –2.06 0.04 1.17 ± 1.29 –0.33 ± 1.68 –2.67 0.01
Dialysis adequacy (Kt/V urea) 0.13 ± 0.22 –0.03 ± 0.13 –2.48 0.01 0.12 ± 0.21 –0.03 ± 0.13 –2.48 0.01
QoL
 PCS 5.69 ± 5.58 –1.72 ± 9.04 –2.79 0.005 6.29 ± 5.62 –1.72 ± 9.04 –2.86 0.003
 MCS 2.49 ± 7.28 –0.86 ± 9.41 –1.59 0.11 2.88 ± 7.79 –0.86 ± 9.41 –1.54 0.13

Data are expressed as mean ± standard deviation.

BMI, body mass index; Kt/V, K = dialyzer’s capacity to clear urea at the blood flow rate, t = treatment time, V = distribution volume of urea; SPPB, short physical performance battery; MCS, mental component summary; PCS, physical component summary; QoL, quality of life.

a

Value at the 12th week – value at baseline.

b

z-score calculated using the Mann-Whitney U test.