M5
M5
M5
Environmental Research
and Public Health
Article
Effects of Diet Control and Telemedicine-Based Resistance
Exercise Intervention on Patients with Obesity and Knee
Osteoarthritis: A Randomized Control Trial
Yen-I Hsu 1,2 , Ying-Chou Chen 3 , Chia-Lun Lee 4 and Nai-Jen Chang 1,5,6,7, *
1. Introduction
Obesity is a key public health issue. It promotes the development of osteoarthritis
Copyright: © 2021 by the authors.
(OA), which causes joint stiffness, pain, and declining functional performance [1,2]. In
Licensee MDPI, Basel, Switzerland.
addition, patients with obesity usually lack access to nutritional information and do not
This article is an open access article
know how to manage their nutritional intake to implement a healthy diet [3,4]. European
distributed under the terms and guidelines for obesity management recommend weight reduction as the nonpharmaco-
conditions of the Creative Commons logical treatment for this population [5]. A previous study suggested that a 5% body
Attribution (CC BY) license (https:// weight reduction produced improved clinical symptoms including pain relief and func-
creativecommons.org/licenses/by/ tional mobility improvement [6]. However, adverse effects were observed when sedentary
4.0/). patients with obesity and knee OA were subjected to a very low-energy diet; specifically,
Int. J. Environ. Res. Public Health 2021, 18, 7744. https://doi.org/10.3390/ijerph18157744 https://www.mdpi.com/journal/ijerph
Int. J. Environ. Res. Public Health 2021, 18, 7744 2 of 15
they developed notable bad breath, intolerance to cold, flatulence, and loss of lean body
mass [7].
The American College of Sports Medicine proposed the position that “exercise is
medicine”. Exercise, which includes aerobic and resistance training, is an interventional
recommendation for treating OA [8,9]. Patients with knee OA who underwent an aerobic
exercise intervention reported significantly reduced joint pain and increased joint range
of motion [10]. However, obesity increases knee joint load due to the heavy weight borne
by the knees. Therefore, patients with obesity and comorbid knee OA may experience
increased joint pain during aerobic exercise due to the compressive impact force on the
knee joints, leading to low adherence [11,12]. For strength training, resistance-band training
serves as a relatively cheaper and more convenient alternative to machine-based resistance
training for patients with knee OA [13,14] and patients with sarcopenic obesity [15]. How-
ever, the clinical benefits of these therapeutic exercise programs decline over time, which is
likely due to poor adherence [16]. Engagement in therapeutic exercise among people in
osteoarthritic populations is influenced by a complex interplay between physical, personal,
and social–environmental factors [17]. These barriers to performing therapeutic exercises
include decreased motivation (e.g., patients may only complete exercises when provided
with action coping plans and/or audio/video exercises), pain and physical limitations,
nonpositive therapeutic exercise information, and lack of professional support [18]. In
addition, the limitations of elastic-band training include difficult to load control and quan-
tify the specific an amount of resistance [19]. Therefore, increasing adherence among the
aforementioned population to therapeutic exercise which can be feasibly performed as
graded exercise at home through the provision of instruction is a key strategy [20].
Telemedicine is a promising strategy, particularly for the early stages of a home-based
therapeutic exercise program; it allows for exercise techniques to be corrected for safety, and an
exercise program can be adjusted to suit an individual’s physical ability and goals [21–23]. In
our previous study, a 12-week telemedicine-based elastic band intervention was implemented
with regular follow-up via phone calls or communication software by the clinical staff of a
medical center; the intervention led to improved muscle strength, dynamic balance, and physical
function in patients with comorbid type 2 diabetes mellitus and knee OA [24]. Collectively,
these findings indicate that telemedicine-based elastic band exercise is safe for patients with
various conditions. In addition, systematic reviews and randomized controlled trials examining
people with knee and hip OA have highlighted that e-health technologies such as telehealth
and mobile health may provide more opportunities for interactions with exercise professionals
and increase the exercise adherence of patients, particularly in the OA population [17].
Previous studies have examined patients with obesity and knee OA and compared the ef-
fects of weight loss only [6,25], exercise only [26,27], and weight loss + exercise [12,28–30]. Based
on aforementioned studies, the literature has not examined the feasibility of achieving weight
loss, improving blood biochemical values, and enhancing functional performance through the
provision of nutritional advice and elastic band resistance exercise instructions provided by a
dietitian combined with implementation of follow-up using telemedicine to track participants’
progress, particularly with respect to the aforementioned population with comorbid obesity
and knee OA. Therefore, this study investigated the effects of an individualized nutritional and
elastic band resistance exercise intervention program delivered by a dietitian who specializes
in sports medicine through telemedicine and applied to older patients with obesity and knee
OA. Regarding functional assessments, the Western Ontario and McMaster Universities Os-
teoarthritis scale (WOMAC) scale is a high intraclass correlation coefficient self-questionnaire
used to assess the health status of patients with knee OA [24,31]. The Osteoarthritis Research
Society International recommends the timed up-and-go (TUG) test to assess the dynamic bal-
ance of patients with knee or hip OA [32]. The TUG test is highly reliable for patients with
mild-to-moderate knee OA [24,33].Therefore, the primary outcome was assessed by reviewing
the patients’ body composition and WOMAC scores. The secondary outcomes were assessed
by reviewing the patients’ blood biochemical analysis and TUG test results.
Int. J. Environ. Res. Public Health 2021, 18, 7744 3 of 15
2.2. Participants
Patients who were older than 55 years and had a body mass index (BMI) of 27–35 kg/m2
were included in the study. In the present study, obesity was defined per the definition estab-
lished by the National Health Agency; knee OA was diagnosed when X-ray findings indicated
a Kellgren and Lawrence (K&L) grade ≤3 [35] and visual analog scale ≥4 out of 10 [36]. The
exclusion criteria were as follows: inability to live independently; K&L grade >3; history of
hip or knee replacement surgery; history of myocardial infarction; pregnancy or lactation;
end-stage liver disease and nephropathy; severe heart disease; lung disease; inability to undergo
physical function testing due to conditions such as unstable angina, myocardial infarction, heart
failure, severe heart rhythm disorder or second- or third-degree heart conduction block, cardiac
aneurysm or aortic aneurysm, or myocarditis or pericarditis; chronic obstructive pulmonary
disease accompanied by pulmonary heart disease, untreated or unstable asthma, severe pul-
monary hypertension, or pulmonary embolism; and malignant hypertension. Throughout
the study, all participants’ drug regimens remained unchanged. This study was conducted at
Kaohsiung Chang Gung Memorial Hospital.
2.3. Interventions
2.3.1. Diet Control Group
A clinical dietician provided support to the D group and designed an individualized
nutritional plan for each participant. These participants also received dietary advice (from
the clinical dietitian), health education, and manuals and handouts (covering weight
loss and diet) during their first visit to the medical center. Each participant was asked
by the clinical dietician to follow a balanced low-energy diet of 1200 kcal/day [7] and
update his or her diet record sheet at least three times a week (at least twice and once
on weekdays and weekends, respectively). The clinical dietitian followed up with and
advised the participants through active phone calls or a communication application (e.g.,
LINE, FaceTime) once a week for 12 weeks. While performing active calls or mobile
application, patient’s interventions were actively instructed by the clinical dietitian based
on the individual’s nutritional needs and preferences of each participant.
Figure
Figure 1.
1. Elastic
Elasticband
bandresistance
resistance exercise
exercise intervention.
intervention.
2.3.3.
2.3.3.Combined
CombinedGroup
Group
Both
Boththe
thediet
dietcontrol and
control elastic
and band
elastic resistance
band program
resistance interventions
program (i.e., the
interventions afore-
(i.e., the
mentioned protocols)
aforementioned were were
protocols) applied to thistogroup.
applied this group.
(ANOVA) was performed to test the homogeneity; if the same value (p > 0.05) was obtained,
then ANCOVA was used to analyze the differences between groups; if homogeneity was
not observed (p < 0.05), the Welch test was performed to determine the changes between
groups and a pairwise comparison was performed using Dunnett’s T3 test instead. The
changes from baseline to post-intervention were analyzed using one-way ANOVA, and
post hoc testing was performed using Tukey’s range test. The effect size (Cohen’s d), which
is the difference between pretest and post-test means divided by their common SD, was
calculated and interpreted as small (d = 0.2), medium (d = 0.5), or large (d = 0.8), to show
the magnitude of the effect [45]. Statistical significance was established when p < 0.05.
3. Results
3.1. Study Flow for Participants
A total of 113 outpatient screenings occurred during the enrolment period; 47 patients did
not meet the inclusion criteria, and 66 patients were enrolled. Subsequently, the enrolled patients
were assigned randomly to the D, E, or D + E groups. This study applied an intention-to-treat
analysis. Of the 66 patients, 3 interventions were not completed due to an inability to conduct
follow-up (overseas travel, loss of contact, family refusal). Ultimately, 63 participants (i.e., 21
in each group) completed the intervention (Figure 2). The adherence rates of the participants
who completed the intervention were 83%, 90%, and 87% for the D, E, and D + E groups,
respectively. No significant differences were observed among the three groups with respect to
their baseline data (i.e., age, gender, height, weight, BMI, body fat percentage, K&L classification,
Int. J. Environ. Res. Public Health 2021, 18, x 7 of 16
and medication use; Table 1). Over the entire intervention period, no adverse events related to
the intervention were reported.
Figure
Figure2.2.Consolidated
ConsolidatedStandards
StandardsofofReporting
ReportingTrials
Trialsflow
flowdiagram.
diagram.
Outcomes D E D+E
Body weight (kg)
Baseline 78.37 ± 8.50 78.99 ± 10.78 77.53 ± 10.17
Post-intervention 74.96 ± 8.59 78.63 ± 11.00 74.03 ± 10.11
Change −3.41 ± 0.75 $ −0.36 ± 1.16 −3.50 ± 0.97 $
Effect size 0.4 0.03 0.35
p <0.001 0.168 <0.001
Body mass index (kg/m2 )
Baseline 30.8± 2.57 30.84± 2.47 31.10± 2.60
Post-intervention 29.45± 2.59 30.69± 2.59 29.7± 2.64
Change −1.35 ± 0.33 $ −0.15± 0.46 −1.41± 0.39 $
Effect size 0.52 0.06 0.53
p <0.001 0.161 <0.001
Body fat (%)
Baseline 35.18 ± 6.01 34.64± 6.48 36.20± 5.27
Post-intervention 33.97 ± 6.47 33.48± 6.46 34.32± 5.50
Change −1.20 ± 0.81 −1.17± 0.75 −1.87± 0.78 #,$
Effect size 0.19 0.18 0.35
p <0.001 <0.001 <0.001
Soft lean mass (kg)
Baseline 46.29 ± 6.25 47.05 ± 8.41 45.64 ± 8.97
Post-intervention 45.05 ± 6.38 47.83 ± 8.53 44.46 ± 8.55
Change −1.23 ± 0.65 $ 0.78 ± 0.64 −1.18 ± 1.56 $
Effect size 0.2 0.1 0.13
p <0.001 <0.001 0.002
Lower-limb muscle mass (kg)
Baseline 17.59 ± 2.62 17.37 ± 3.2 17.34 ± 3.57
Post-intervention 16.85 ± 2.60 17.89 ± 3.37 17.17 ± 3.43
Change −0.75 ± 0.40 $ 0.52 ± 0.35 −0.17 ± 0.55 #,$
Effect size 0.28 0.16 0.05
p <0.001 <0.001 <0.001
Results are expressed as means ± standard deviations. Change was calculated by subtracting the baseline value
from the postintervention value; p: pairwise test; effect size indicates Cohen’s d; $ indicates vs. E group (p < 0.05);
# indicates vs. D group (p < 0.05); D: diet control group; E: resistance exercise group; D + E: diet control and
Outcomes D E D+E
Total Score
Baseline 34.57 ± 7.69 30.24 ± 6.06 38.86 ± 7.98
Post-intervention 25.33 ± 6.55 22.62 ± 5.41 25.81 ± 6.61
Change −9.24 ± 3.59 −7.62 ± 2.64 −13.05 ± 4.09 #,$
Effect size 1.29 1.33 1.78
p <0.001 <0.001 <0.001
Pain
Baseline 6.48 ± 2.21 6.05 ± 1.99 7.43 ± 2.01
Post-intervention 4.33 ± 1.65 4.14 ± 1.46 4.48 ± 1.44
Change −2.14 ± 1.28 −1.90 ± 1.48 −2.95 ± 1.12 $
Effect size 1.1 1.09 1.69
p <0.001 <0.001 <0.001
Stiffness
Baseline 2.91 ± 1.09 1.33 ± 1.15 2.86 ± 1.59
Post-intervention 1.86 ± 0.66 0.90 ± 0.83 1.38 ± 0.97
Change −1.05 ± 0.81 −0.43 ± 0.68 −1.48 ± 1.03 $
Effect size 1.17 0.21 1.12
p <0.001 <0.001 <0.001
Physical Function
Baseline 25.19 ± 5.62 22.86 ± 4.30 28.57 ± 5.76
Post-intervention 19.43 ± 5.29 17.76 ± 3.82 19.95 ± 4.79
Change −5.76 ± 2.84 −5.10 ± 1.70 −8.62 ± 3.58 #,$
Effect size 1.06 1.25 1.63
p <0.001 <0.001 <0.001
Results are expressed as means ± standard deviations. Change is calculated by subtracting the baseline value
from the postintervention value; p, pairwise test; Effect size indicates Cohen’s d; $ indicates vs. E group (p < 0.05);
# indicates vs. D group (p < 0.05); D, diet control group; E, resistance exercise group; D + E, diet control and
For the stiffness subscale, significant postintervention differences were observed among
the groups (F =3.764, p = 0.029). In the pairwise comparison test, all three groups (p < 0.001)
exhibited significant improvements relative to their baseline data. Furthermore, the changes
in the D + E group (p = 0.001) represented significant improvements relative to the E group.
The stiffness scores of the D, E, and D + E groups improved by 32.16%, 29.64%, and 39.83%,
respectively. MCIDs were observed in all three groups.
For the physical function subscale, significant postintervention differences were ob-
served among the groups (F =3.989, p = 0.024). In the pairwise comparison test, all three
groups (p < 0.001) exhibited significant improvements relative to their baseline data. Fur-
thermore, the changes in the D + E group represented significantly improvements relative
to the D (p < 0.001) and E (p = 0.005) groups. The physical function scores of the D, E, and D
+ E groups improved by 23.05%, 21.54%, and 29.72%, respectively. MCIDs were observed
in all three groups.
Outcomes D E D+E
Total cholesterol (mg/dL)
Baseline 177.17 ± 23.35 169.95 ± 25.06 177.48 ± 27.04
Post-intervention 160.10 ± 20.16 165.81 ± 26.89 151.52 ± 18.03
Change −17.57 ± 18.07 −4.14 ± 13.40 −25.95 ± 23.27 $
Effect size 0.78 0.16 1.13
p <0.001 0.175 <0.001
LDL (mg/dL)
Baseline 99.47 ± 24.19 94.47 ± 24.19 97.57 ± 24.10
Post-intervention 84.38 ± 18.69 91.76 ± 24.32 79.52 ± 14.27
Change −15.24 ± 15.17 $ −2.71 ± 13.94 −18.05 ± 19.78 $
Effect size 0.7 0.11 0.91
p <0.001 0.325 <0.001
Triglycerides (mg/dL)
Baseline 145.40 ± 52.95 128.81 ± 62.68 140.62 ± 54.57
Post-intervention 110.75 ± 48.77 118.05 ± 47.68 97.33 ± 35.79
Change −34.65 ± 16.17 −10.76 ± 48.92 −43.29 ± 26.37 $
Effect size 0.68 0.19 0.94
p <0.001 0.325 <0.001
Results are expressed as means ± standard deviations. Change was calculated by subtracting the baseline value
from the postintervention value; p: pairwise test; effect size indicates Cohen’s d; $ indicates vs. E group (p < 0.05);
D: diet control group; E: resistance exercise group; D + E: diet control and resistance exercise group.
For LDL, significant postintervention differences were observed among the groups
(F = 5.946, p = 0.004). In the pairwise comparison test, the D + E (p < 0.001) and D (p < 0.001)
groups exhibited significant improvements relative to their baseline data; however, such
improvements were not observed in the E group (p = 0.383). Furthermore, the changes in
the D + E (p = 0.01) and D (p = 0.044) groups represented significant improvements relative
to the E group.
For triglycerides, significant postintervention differences were observed among the
groups (F = 6.035, p = 0.004). In the pairwise comparison test, the D + E (p < 0.001) and
D (p < 0.001) groups exhibited significant improvements relative to their baseline data;
however, such improvements were not observed in the E group (p = 0.325). Furthermore,
the changes in the D + E group (p = 0.007) represented significant improvements relative to
the E group.
Outcomes D E D+E
TUG(s)
Baseline 11.25 ± 2.15 10.51 ± 1.97 10.98 ± 1.98
Post-intervention 9.92 ± 1.68 9.59 ± 1.56 9.37 ± 1.61
Change −1.33 ± 0.59 −0.92 ± 0.67 −1.61 ± 0.52 $
Effect size 0.69 0.52 0.89
p <0.001 <0.001 < 0.001
Results are expressed as means ± standard deviations. Change was calculated by subtracting the baseline value
from the postintervention value; p: pairwise test; effect size indicates Cohen’s d; $ indicates vs. E group (p < 0.05);
D: diet control group; E: resistance exercise group; D + E: diet control and resistance exercise group.
Int. J. Environ. Res. Public Health 2021, 18, 7744 11 of 15
4. Discussion
To the best of our knowledge, this was the first prospective study in which patients
with obesity and knee OA received home-based nutritional consultation combined with
telemedicine-based exercise intervention. Individualized diet control interventions com-
bined with telemedicine-based resistance exercise interventions, which were supervised by
a clinical dietitian, significantly improved body composition (i.e., reduction in BMI and
body fat percentage), improved blood biochemistry values (i.e., reduction in total choles-
terol, LDL, and triglyceride levels), and enhanced lower-limb functional performance (i.e.,
improvements in WOMAC and TUG results) in the investigated population. The adherence
rates of the patients who completed the intervention were 83%, 90%, and 87% in the D, E,
and D + E groups, respectively. The high compliance can be attributed to the consistent
follow-up with the clinical dietician and the convenience of exercising at home, which
indicate that this method is feasible and effective. The adherence levels observed in all
groups were higher than those reported in previous studies [16,46].
Regarding body composition changes, most weight-loss methods for patients with
obesity and knee OA involve meal replacements. Although studies involving meal re-
placements have successfully achieved >10% body weight reductions, the rapid weight
loss has also led to reductions in participants’ lean body mass by 11%–17% of their body
weight [47–49]. In contrast, in the present study, each participant followed an individual-
ized, balanced low-energy diet of 1200 kcal/day that was developed by a clinical dietitian.
Each participant also engaged in follow-up and regularly consulted with the clinical di-
etitian through phone calls or online real-time communication once a week for 12 weeks;
therefore, we were able to regularly monitor individuals’ nutritional status and control
their energy intake such that their body weight could be reduced gradually. In addition,
the percentage of participants who lost more than 5% of their body weight was 33.3%, and
47.6% in the E and D + E groups. A previous systematic review reported that a weekly
reduction of body weight by 0.25% can improve the disability status of individuals with
overweight or obesity with knee OA [50]. Moreover, we discovered that the participants
in the D group experienced not only decreases in their body weight, body fat percentage,
BMI, and soft lean mass, but also their muscle mass (which was expected). In the D + E
group, no significant decrease in muscle mass was observed, which indicates that resistance
exercise is essential for weight loss because it can slow muscle mass loss. In other words,
implementing a weight-loss intervention that does not incorporate exercises will lead to
the loss of muscle mass in the lower limbs and, consequently, increase the risk of knee
joint impact injuries resulting from insufficient quadriceps muscle strength. Elastic band
resistance exercises help to initiate muscle anabolism and improve the protein synthesis
rate of the limb muscles. In the present study, soft lean mass and lower-limb muscle mass
increased significantly in the E group. These results were consistent with those reported in
a previous study [15]. Therefore, we recommend a combined telemedicine-based interven-
tion for patients with obesity and knee OA because this intervention allows for weight loss
without the loss of lower-limb muscle mass.
Regarding functional performance, the D + E group achieved the most significant
improvements in overall WOMAC scores (33.52%) and physical function subscale (29.72%),
and these improvements met the MCID threshold. Similarly to the present study, previous
studies have indicated that elastic band resistance exercises improved the WOMAC scores
of patients with and without obesity who have OA [13,51,52]. In addition, the D + E
group exhibited significant improvements on the TUG test relative to the E group. This
finding may have contributed to the decreased pain that was reported. The three groups
experienced significant pain relief benefits after completing their interventions. Pain
and physical activity are mutually influential [24]. A study of home-based balance and
low-resistance exercise training verified that healthy older adults in the community who
participated in a supervised exercise training program took an average of 8.7–9.91 s to
complete the TUG test [53]. In the present study, after receiving telemedicine support from
clinical staff and completing the interventions, the patients with obesity and knee OA took
Int. J. Environ. Res. Public Health 2021, 18, 7744 12 of 15
9.37–9.92 s to complete the TUG test; these results are similar to those achieved by healthy
older adults (8.4–9.1 s). This finding indicated a significant improvement that met the
MCID threshold [42].
For blood biochemistry values, the three groups exhibited decreased total cholesterol
levels. In addition, the D + E group exhibited lower LDL and triglyceride levels relative to
the E group, indicating the effectiveness of regular diet control supervised by a dietician
through telemedicine. Blood lipid level (particularly LDL level) influences a patient’s
cardiovascular risk [54]. Previous studies have indicated that resistance exercise training
aids the control of blood lipid levels [55,56]. Furthermore, a high triglyceride level increases
endogenous LDL [57]. Collectively, these findings indicate that regular diet control and
resistance exercise can greatly benefit patients at high risk of cardiovascular disease (e.g.,
those with obesity).
The primary contribution of the present study is its demonstration of the feasibility
of implementing diet control through nutritional consultation and improving functional
performance through a supervised resistance exercise program for the investigated popula-
tion; this was achieved via phone consultations provided by clinical staff over a 12-week
follow-up period after the participants’ first visit to the outpatient department. However,
the study had several limitations that can be addressed in future studies. First, we enrolled
participants from only a single medical center, and the positive outcomes could have been
achieved primarily because a clinical dietitian with a sports medicine background aided
in follow-up and tracked the health status and exercise adherence of the participants via
phone calls or a communication application; in a regional hospital or small clinic, this
protocol may be difficult to replicate. Second, other intervention-related dependent vari-
ables were not assessed. Changes in physical activity levels assessed through wearable
technology (e.g., daily walking steps, speed), performance-based measures of physical
function, and quality of life for this population were not tracked, and physical or occupa-
tional activities unrelated to the study could have introduced bias into the results. The OA
participants were also not precisely assessed for intra-articular joint condition (e.g., carti-
laginous wear) by magnetic resonance imaging [58] and biomechanics changes (e.g., gait,
joint loading) [59]. Third, a potential placebo effect was not accounted for, since there is no
sham exercise. Fourth, the severe OA participants (i.e., K&L grade >3) were excluded. The
generalizability of the results to all patients with obesity and knee OA is low. Fifth, we did
not verify whether the participants’ family members actively supervised the interventions,
which is a factor that could also have introduced bias into the results. Sixth, limitations
of BIA in morbidly obese patients may exist. Obese individuals have a relatively high
amount of extracellular water and total body water, which may lead to underestimation
of fat mass and overestimation of fat-free mass [60]. Therefore, adoption of total body
DXA scanning for the precise measurement of body composition is suggested, but the
safety of repeated measurements, the cost, and technical expertise are limiting [61]. A last,
long-term follow-up should be conducted to determine, especially after the conclusion
of interventions, whether our strategy changed the dieting and exercise behavior of the
investigated population and produced long-term effects.
5. Conclusions
Supervised by a clinical dietitian, a 12-week individualized diet control intervention
combined with a telemedicine-based elastic band resistance exercise intervention led to
significant reductions in BMI, body fat, total cholesterol, LDL, and triglyceride levels
and enhanced lower-limb functional performance in patients with obesity and mild-to-
moderate knee OA. We recommend the application of this strategy by medical centers.
Author Contributions: Y.-I.H.; N.-J.C. conceived and designed the experiments; Y.-I.H.; Y.-C.C.; N.-
J.C. performed the experiments; Y.-I.H.; Y.-C.C.; C.-L.L.; N.-J.C. interpreted the data and participated
in drafting the text and figures. All authors have read and agree to the published version of the
manuscript.
Int. J. Environ. Res. Public Health 2021, 18, 7744 13 of 15
Funding: This research was supported by the Department of Medical Research, Kaohsiung Chang
Gung Memorial Hospital (Project Number: CMRPG8H0581). This work was also in part supported
by the NSYSU-KMU joint research project [NSYSUKMU110-P004].
Institutional Review Board Statement: The study was conducted according to the guidelines of the
Declaration of Helsinki, and approved by the Institutional Review Board of the Chang Gung Medical
Foundation (Approval No. 201800607B0).
Informed Consent Statement: Informed consent was obtained from all subjects involved in the
study.
Data Availability Statement: Data are contained within the article.
Acknowledgments: We would like to thank all our participants for their time and effort. We also
thank researchers for assistance with statistical analyses, from the Biostatistics Center, Kaohsiung
Chang Gung Memorial Hospital.
Conflicts of Interest: The authors declare no conflict of interest.
References
1. Largo, R.; Herrero-Beaumont, G. Joint obesity as a pathogenic factor in osteoarthritis. Osteoarthr. Cartil. 2021. [CrossRef]
2. Salih, S.; Sutton, P. Obesity, knee osteoarthritis and knee arthroplasty: A review. BMC Sports Sci. Med. Rehabil. 2013, 5, 1–6.
[CrossRef]
3. Lim, S.; Smith, C.A.; Costello, M.F.; MacMillan, F.; Moran, L.; Ee, C. Barriers and facilitators to weight management in overweight
and obese women living in Australia with PCOS: A qualitative study. BMC Endocr. Disord. 2019, 19, 1–9. [CrossRef] [PubMed]
4. Lopez-Hernandez, L.; Martinez-Arnau, F.M.; Perez-Ros, P.; Drehmer, E.; Pablos, A. Improved nutritional knowledge in the obese
adult population modifies eating habits and serum and anthropometric markers. Nutrients 2020, 12, 3355. [CrossRef] [PubMed]
5. Yumuk, V.; Tsigos, C.; Fried, M.; Schindler, K.; Busetto, L.; Micic, D.; Toplak, H. Obesity management task force of the european
association for the study of European guidelines for obesity management in adults. Obes. Facts 2015, 8, 402–424. [CrossRef]
[PubMed]
6. Christensen, R.; Bartels, E.M.; Astrup, A.; Bliddal, H. Effect of weight reduction in obese patients diagnosed with knee osteoarthri-
tis: A systematic review and meta-analysis. Ann. Rheum. Dis. 2007, 66, 433–439. [CrossRef] [PubMed]
7. Christensen, P.; Bliddal, H.; Riecke, B.F.; Leeds, A.R.; Astrup, A.; Christensen, R. Comparison of a low-energy diet and a very
low-energy diet in sedentary obese individuals: A pragmatic randomized controlled trial. Clin. Obes. 2011, 1, 31–40. [CrossRef]
[PubMed]
8. Fransen, M.; McConnell, S.; Harmer, A.R.; Van der Esch, M.; Simic, M.; Bennell, K.L. Exercise for osteoarthritis of the knee.
Cochrane Database Syst. Rev. 2015, 1, CD004376. [CrossRef]
9. Vincent, K.R.; Vincent, H.K. Resistance exercise for knee osteoarthritis. PM&R 2012, 4, S45–S52.
10. Alrushud, A.S.; Rushton, A.B.; Kanavaki, A.M.; Greig, C.A. Effect of physical activity and dietary restriction interventions on
weight loss and the musculoskeletal function of overweight and obese older adults with knee osteoarthritis: A systematic review
and mixed method data synthesis. BMJ Open 2017, 7, e014537. [CrossRef]
11. Blagojevic, M.; Jinks, C.; Jeffery, A.; Jordan, K. Risk factors for onset of osteoarthritis of the knee in older adults: A systematic
review and meta-analysis. Osteoarthr. Cartil. 2010, 18, 24–33. [CrossRef]
12. Messier, S.P.; Mihalko, S.L.; Legault, C.; Miller, G.D.; Nicklas, B.J.; DeVita, P.; Beavers, D.P.; Hunter, D.J.; Lyles, M.F.; Eckstein, F.;
et al. Effects of intensive diet and exercise on knee joint loads, inflammation, and clinical outcomes among overweight and obese
adults with knee osteoarthritis: The IDEA randomized clinical trial. JAMA 2013, 310, 1263–1273. [CrossRef]
13. Chang, T.-F.; Liou, T.-H.; Chen, C.-H.; Huang, Y.-C.; Chang, K.-H. Effects of elastic-band exercise on lower-extremity function
among female patients with osteoarthritis of the knee. Disabil. Rehabil. 2012, 34, 1727–1735. [CrossRef]
14. Rogers, M.W.; Tamulevicius, N.; Semple, S.J.; Krkeljas, Z. Efficacy of home-based kinesthesia, balance & agility exercise training
among persons with symptomatic knee osteoarthritis. J. Sports Sci. Med. 2012, 11, 751–758. [PubMed]
15. Liao, C.-D.; Tsauo, J.-Y.; Huang, S.-W.; Ku, J.-W.; Hsiao, D.-J.; Liou, T.-H. Effects of elastic band exercise on lean mass and physical
capacity in older women with sarcopenic obesity: A randomized controlled trial. Sci. Rep. 2018, 8, 2317. [CrossRef] [PubMed]
16. Uthman, O.A.; van der Windt, D.A.; Jordan, J.L.; Dziedzic, K.S.; Healey, E.L.; Peat, G.M.; Foster, N.E. Exercise for lower limb
osteoarthritis: Systematic review incorporating trial sequential analysis and network meta-analysis. BMJ 2013, 347, f5555.
[CrossRef]
17. Holden, M.A.; Button, K.; Collins, N.J.; Henrotin, Y.; Hinman, R.S.; Larsen, J.B.; Metcalf, B.; Master, H.; Skou, S.T.; Thoma, L.M.;
et al. Guidance for implementing best practice therapeutic exercise for people with knee and hip osteoarthritis: What does the
current evidence base tell us? Arthritis Care Res. 2020. [CrossRef] [PubMed]
18. Kanavaki, A.M.; Rushton, A.; Efstathiou, N.; Alrushud, A.; Klocke, R.; Abhishek, A.; Duda, J.L. Barriers and facilitators of physical
activity in knee and hip osteoarthritis: A systematic review of qualitative evidence. BMJ Open 2017, 7, e017042. [CrossRef]
[PubMed]
Int. J. Environ. Res. Public Health 2021, 18, 7744 14 of 15
19. Phil, P.; Ellenbecker, T.S. Strength Band Training, 2nd ed.; Human Kinetics: Champaign, IL, USA, 2010.
20. Nicolson, P.J.A.; Bennell, K.L.; Dobson, F.L.; Van Ginckel, A.; Holden, M.A.; Hinman, R.S. Interventions to increase adherence to
therapeutic exercise in older adults with low back pain and/or hip/knee osteoarthritis: A systematic review and meta-analysis.
Br. J. Sports Med. 2017, 51, 791–799. [CrossRef] [PubMed]
21. Schafer, A.G.M.; Zalpour, C.; von Piekartz, H.; Hall, T.M.; Paelke, V. The efficacy of electronic health-supported home exercise
interventions for patients with osteoarthritis of the knee: Systematic review. J. Med. Internet Res. 2018, 20, e9465. [CrossRef]
22. 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. [CrossRef]
23. 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. [CrossRef]
24. Chen, S.M.; Shen, F.C.; Chen, J.F.; Chang, W.D.; Chang, N.J. Effects of resistance exercise on glycated hemoglobin and functional
performance in older patients with comorbid diabetes mellitus and knee osteoarthritis: A randomized trial. Int. J. Environ. Res.
Public Health 2019, 17, 224. [CrossRef]
25. Toda, Y.; Toda, T.; Takemura, S.; Wada, T.; Morimoto, T.; Ogawa, R. Change in body fat, but not body weight or metabolic
correlates of obesity, is related to symptomatic relief of obese patients with knee osteoarthritis after a weight control program. J.
Rheumatol. 1998, 25, 2181–2186.
26. Waller, B.; Munukka, M.; Rantalainen, T.; Lammentausta, E.; Nieminen, M.T.; Kiviranta, I.; Kautiainen, H.; Hakkinen, A.; Kujala,
U.M.; Heinonen, A. Effects of high intensity resistance aquatic training on body composition and walking speed in women with
mild knee osteoarthritis: A 4-month RCT with 12-month follow-up. Osteoarthr. Cartil. 2017, 25, 1238–1246. [CrossRef]
27. 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.; et al.
Comparative effectiveness of tai chi versus physical therapy for knee osteoarthritis: A randomized trial. Ann. Intern. Med. 2016,
165, 77–86. [CrossRef]
28. Messier, S.P.; Loeser, R.F.; Miller, G.D.; Morgan, T.M.; Rejeski, W.J.; Sevick, M.A.; Ettinger, W.H., Jr.; Pahor, M.; Williamson, J.D.
Exercise and dietary weight loss in overweight and obese older adults with knee osteoarthritis: The arthritis, diet, and activity
promotion trial. Arthritis Rheum. 2004, 50, 1501–1510. [CrossRef] [PubMed]
29. Munugoda, I.P.; Beavers, D.P.; Wirth, W.; Aitken, D.A.; Loeser, R.F.; Miller, G.D.; Lyles, M.; Carr, J.J.; Guermazi, A.; Hunter, D.J.;
et al. The effect of weight loss on the progression of meniscal extrusion and size in knee osteoarthritis: A post-hoc analysis of the
Intensive Diet and Exercise for Arthritis (IDEA) trial. Osteoarthr. Cartil. 2020, 28, 410–417. [CrossRef] [PubMed]
30. Beavers, D.P.; Beavers, K.M.; Loeser, R.F.; Walton, N.R.; Lyles, M.F.; Nicklas, B.J.; Shapses, S.A.; Newman, J.J.; Messier, S.P. The
independent and combined effects of intensive weight loss and exercise training on bone mineral density in overweight and
obese older adults with osteoarthritis. Osteoarthr. Cartil. 2014, 22, 726–733. [CrossRef] [PubMed]
31. Davis, A.M.; Perruccio, A.V.; Canizares, M.; Hawker, G.A.; Roos, E.M.; Maillefert, J.-F.; Lohmander, L.S. Comparative, validity
and responsiveness of the HOOS-PS and KOOS-PS to the WOMAC physical function subscale in total joint replacement for
osteoarthritis. Osteoarthr. Cartil. 2009, 17, 843–847. [CrossRef] [PubMed]
32. Dobson, F.; Hinman, R.S.; Roos, E.M.; Abbott, J.H.; Stratford, P.; Davis, A.M.; Buchbinder, R.; Snyder-Mackler, L.; Henrotin, Y.;
Thumboo, J.; et al. OARSI recommended performance-based tests to assess physical function in people diagnosed with hip or
knee osteoarthritis. Osteoarthr. Cartil. 2013, 21, 1042–1052. [CrossRef] [PubMed]
33. Alghadir, A.; Anwer, S.; Brismee, 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, 1–7. [CrossRef] [PubMed]
34. World Medical Association. World medical association declaration of Helsinki: Ethical principles for medical research involving
human subjects. JAMA 2013, 310, 2191–2194. [CrossRef] [PubMed]
35. Kohn, M.D.; Sassoon, A.A.; Fernando, N.D. Classifications in brief: Kellgren-lawrence classification of osteoarthritis. Clin. Orthop.
Relat. Res. 2016, 474, 1886–1893. [CrossRef]
36. Arendt-Nielsen, L.; Nie, H.; Laursen, M.B.; Laursen, B.S.; Madeleine, P.; Simonsen, O.H.; Graven-Nielsen, T. Sensitization in
patients with painful knee osteoarthritis. Pain 2010, 149, 573–581. [CrossRef]
37. Arab, A.; Askari, G.; Golshiri, P.; Feizi, A.; Hekmatnia, A.; Iraj, B.; Nourian, M. The effect of a lifestyle modification education on
adiposity measures in overweight and obese nonalcoholic fatty liver disease patients. Int. J. Prev. Med. 2017, 8, 10. [PubMed]
38. Lee, L.C.; Hsu, P.S.; Hsieh, K.C.; Chen, Y.Y.; Chu, L.P.; Lu, H.K.; Chiu, Y.C.; Li, L.; Lai, C.L. Standing 8-electrode bioelectrical
impedance analysis as an alternative method to estimate visceral fat area and body fat mass in Athletes. Int. J. Gen. Med. 2021, 14,
539–548. [CrossRef]
39. Escobar, A.; Quintana, J.; Bilbao, A.; Arostegui, I.; Lafuente, I.; Vidaurreta, I. Responsiveness and clinically important differences
for the WOMAC and SF-36 after total knee replacement. Osteoarthr. Cartil. 2007, 15, 273–280. [CrossRef]
40. Collins, N.J.; Misra, D.; Felson, D.T.; Crossley, K.M.; Roos, E.M. Measures of knee function: International knee documentation
committee (IKDC) subjective knee evaluation form, knee injury and osteoarthritis outcome score (KOOS), knee injury and
osteoarthritis outcome score physical function short form (KOOS-PS), knee outcome survey activities of daily living scale
(kos-adl), lysholm knee scoring scale, oxford knee score (OKS), western ontario and McMaster universities osteoarthritis index
(WOMAC), activity rating scale (ARS), and tegner activity score (TAS). Arthritis Care Res. 2011, 63, S208–S228.
Int. J. Environ. Res. Public Health 2021, 18, 7744 15 of 15
41. Basaran, S.; Guzel, R.; Seydaoglu, G.; Guler-Uysal, F. Validity, reliability, and comparison of the WOMAC osteoarthritis index and
Lequesne algofunctional index in Turkish patients with hip or knee osteoarthritis. Clin. Rheumatol. 2010, 29, 749–756. [CrossRef]
42. Wright, A.A.; Cook, C.E.; Baxter, G.D.; Dockerty, J.D.; Abbott, J.H. A comparison of 3 methodological approaches to defining
major clinically important improvement of 4 performance measures in patients with hip osteoarthritis. J. Orthop. Sports Phys.
Ther. 2011, 41, 319–327. [CrossRef] [PubMed]
43. 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. [CrossRef]
44. Lee, S.; Lee, D.K. What is the proper way to apply the multiple comparison test? Korean J. Anesthesiol. 2020, 73, 572. [CrossRef]
45. Lakens, D. Calculating and reporting effect sizes to facilitate cumulative science: A practical primer for t-tests and ANOVAs.
Front. Psychol. 2013, 4, 863. [CrossRef] [PubMed]
46. Hunter, D.; Beavers, D.; Eckstein, F.; Guermazi, A.; Loeser, R.F.; Nicklas, B.; Mihalko, S.; Miller, G.; Lyles, M.; DeVita, P. The
intensive diet and exercise for arthritis (IDEA) trial: 18-month radiographic and MRI outcomes. Osteoarthr. Cartil. 2015, 23,
1090–1098. [CrossRef] [PubMed]
47. Christensen, P.; Henriksen, M.; Bartels, E.M.; Leeds, A.R.; Meinert Larsen, T.; Gudbergsen, H.; Riecke, B.F.; Astrup, A.; Heitmann,
B.L.; Boesen, M. Long-term weight-loss maintenance in obese patients with knee osteoarthritis: A randomized trial. Am. J. Clin.
Nutr. 2017, 106, 755–763. [CrossRef] [PubMed]
48. Riecke, B.F.; Christensen, R.; Christensen, P.; Leeds, A.R.; Boesen, M.; Lohmander, L.S.; Astrup, A.; Bliddal, H. Comparing two
low-energy diets for the treatment of knee osteoarthritis symptoms in obese patients: A pragmatic randomized clinical trial.
Osteoarthr. Cartil. 2010, 18, 746–754. [CrossRef] [PubMed]
49. Luppino, F.S.; de Wit, L.M.; Bouvy, P.F.; Stijnen, T.; Cuijpers, P.; Penninx, B.W.; Zitman, F.G. Overweight, obesity, and depression:
A systematic review and meta-analysis of longitudinal studies. Arch. Gen. Psychiatry 2010, 67, 220–229. [CrossRef]
50. Hall, M.; Castelein, B.; Wittoek, R.; Calders, P.; Van Ginckel, A. Diet-induced weight loss alone or combined with exercise in
overweight or obese people with knee osteoarthritis: A systematic review and meta-analysis. Semin. Arthritis Rheum. 2019, 48,
765–777. [CrossRef]
51. Fukumoto, Y.; Tateuchi, H.; Ikezoe, T.; Tsukagoshi, R.; Akiyama, H.; So, K.; Kuroda, Y.; Ichihashi, N. Effects of high-velocity
resistance training on muscle function, muscle properties, and physical performance in individuals with hip osteoarthritis: A
randomized controlled trial. Clin. Rehabil. 2014, 28, 48–58. [CrossRef]
52. Rogers, M.W.; Tamulevicius, N.; Coetsee, M.F.; Curry, B.F.; Semple, S.J. Knee osteoarthritis and the efficacy of kinesthesia, balance
& agility exercise training: A pilot study. Int. J. Exerc. Sci. 2011, 4, 124–132.
53. Lacroix, A.; Kressig, R.W.; Muehlbauer, T.; Gschwind, Y.J.; Pfenninger, B.; Bruegger, O.; Granacher, U. Effects of a supervised
versus an unsupervised combined balance and strength training program on balance and muscle power in healthy older adults:
A randomized controlled trial. Gerontology 2016, 62, 275–288. [CrossRef] [PubMed]
54. Toft-Petersen, A.P.; Tilsted, H.H.; Aarøe, J.; Rasmussen, K.; Christensen, T.; Griffin, B.A.; Aardestrup, I.V.; Andreasen, A.;
Schmidt, E.B. Small dense LDL particles-a predictor of coronary artery disease evaluated by invasive and CT-based techniques: A
case-control study. Lipids Health Dis. 2011, 10, 21. [CrossRef] [PubMed]
55. Choi, H.; Shim, J.-S.; Lee, M.H.; Yoon, Y.M.; Choi, D.P.; Kim, H.C. Comparison of formulas for calculating low-density lipoprotein
cholesterol in general population and high-risk patients with cardiovascular disease. Korean Circ. J. 2016, 46, 688–698. [CrossRef]
[PubMed]
56. Kim, H.-S.; Kim, D.-G. Effect of long-term resistance exercise on body composition, blood lipid factors, and vascular compliance
in the hypertensive elderly men. J. Exerc. Rehabil. 2013, 9, 271–277. [CrossRef] [PubMed]
57. Sacks, F.M.; Lichtenstein, A.H.; Wu, J.H.; Appel, L.J.; Creager, M.A.; Kris-Etherton, P.M.; Miller, M.; Rimm, E.B.; Rudel, L.L.;
Robinson, J.G. Dietary fats and cardiovascular disease: A presidential advisory from the American Heart Association. Circulation
2017, 136, e1–e23. [CrossRef] [PubMed]
58. Du, J.Y.; Sivasundaram, L.; Trivedi, N.N.; Voos, J.E.; Victoroff, B.N. Obesity is preferentially associated with patellofemoral
compartment wear: A magnetic resonance imaging assessment. J. Am. Acad. Orthop. Surg. 2021, 29, e722–e731. [CrossRef]
59. Messier, S.P.; Beavers, D.P.; Mihalko, S.L.; Miller, G.D.; Lyles, M.F.; Hunter, D.J.; Carr, J.J.; Eckstein, F.; Guermazi, A.; Loeser, R.F.;
et al. The effects of intensive dietary weight loss and exercise on gait in overweight and obese adults with knee osteoarthritis.
The intensive diet and exercise for arthritis (IDEA) trial. J. Biomech. 2020, 98, 109477. [CrossRef]
60. Coppini, L.Z.; Waitzberg, D.L.; Campos, A.C. Limitations and validation of bioelectrical impedance analysis in morbidly obese
patients. Curr. Opin. Clin. Nutr. Metab. Care 2005, 8, 329–332. [CrossRef]
61. Marra, M.; Sammarco, R.; De Lorenzo, A.; Iellamo, F.; Siervo, M.; Pietrobelli, A.; Donini, L.M.; Santarpia, L.; Cataldi, M.; Pasanisi,
F.; et al. Assessment of body composition in health and disease using bioelectrical impedance analysis (BIA) and dual energy
X-ray absorptiometry (DXA): A critical overview. Contrast Media Mol. Imaging 2019, 2019, 1–9. [CrossRef]