Transcutaneous Electrical Nerve Stimulation Improves Stair Climbing Capacity in People with Knee Osteoarthritis

This study aimed to examine the effect of transcutaneous electrical nerve stimulation (TENS) on stair climbing capacity in individuals with pre-radiographic to mild knee osteoarthritis (OA). This is a secondary analysis of data from a single, participant-blinded, randomized controlled trial with a pre-post design. Participants with pre-radiographic to mild knee OA (mean age, 59.1 years; 72.9% women) were randomly assigned into two groups, a TENS (n = 30) and a sham-TENS groups (n = 29). TENS or sham-TENS treatments were applied to all participants by using the prototype TENS device with pre-specified parameters. The primary outcome measures included valid and reliable functional measures for stair climbing (stair-climb test [SCT]), visual analog scale for knee pain during the SCT, and quadriceps muscle strength. TENS improved SCT time by 0.41 s (95% confidence interval [CI]: 0.07, 0.75). The time reduction in the transition phase explains the TENS therapeutic effect. Post-hoc correlation analyses revealed a non-significant but positive relationship between the pain relief effect and improved 11-step SCT time in the TENS group but not in the sham-TENS group. These results indicate that the TENS intervention may be an option for reducing the burden of early-stage knee OA.


Results
Fifty-nine participants (mean age, 59.1 years; mean body mass index [BMI]: 22.7 kg/m 2 ; 72.9% were women) were included and randomized into the sham-TENS (n = 29) and TENS groups (n = 30). All the participants completed the post-treatment outcome measurements without any adverse events. Data from the results of the insole-based 11-step SCT  in the baseline period from one patient were imputed. Table 1 shows the comparison of participant characteristics between the sham-TENS and TENS groups. Table 2 shows a comparison of changes in outcome measures between the sham-TENS and TENS groups after multiple imputation. The between-group differences in change in knee pain and quadriceps muscle strength were not significantly different. The proportion of treatment responders (i.e., visual analog scale [VAS] pain score improved by ≥30% from baseline to post-treatment) did not differ between the sham-TENS and TENS groups (relative risk to responder in the TENS group: 1.03; 95% confidence interval [CI]: 0.65, 1.62). Although the between-group difference in the change in stopwatch-based 11-SCT time was not significant, that in the insole-based 11-SCT time was 0.41 s (95% CI: − 0.75, −0.07 s), which showed better improvement in the patients in the TENS group than in those in the sham-TENS group. When insole-based 11-SCT time was further divided into three phases (ascending, descending, and transition), the between-group difference in the transition phase time was 0.32 s, which was more improved in patients in the TENS group than in those in the sham-TENS group. The case completed data, excluding one patient in the sham-TENS group, showed similar results (data not shown).
A graphic illustration of these relationships is provided in Fig. 1 to further address the relationship between the pain-relief and therapeutic effect of TENS on the stopwatch- (Fig. 1A) and insole-based 11 SCT times (Fig. 1B). The post-hoc correlation analyses revealed a positive relationship between the change in VAS pain score during SCT and the change in stopwatch-(r = 0.22; 95% CI: −0.15, 0.54) and insole-based 11-SCT times (r = 0.39; 95% CI: 0.04, 0.66) in the TENS group, which were higher than those in the sham-TENS group (stopwatch-based 11-SCT, r = 0.01; 95% CI: −0.35, 0.38; insole-based 11-SCT, r = −0.02; 95% CI: −0.39, 0.36). The interaction effect of group × change in VAS pain score on the insole-based 11-SCT time was marginally significant (p = 0.080).

Discussion
The objective of this study was to examine the therapeutic effects of TENS on stair climbing capacity in individuals with pre-radiographic to mild knee OA. Supporting the first hypothesis, TENS improved the 11-SCT time better than sham-TENS. However, contrary to the second hypothesis, the therapeutic effect of TENS was similar between stair descending and ascending during the 11-SCT. Furthermore, TENS was not superior to sham-TENS in improving knee pain during stair climbing and quadriceps strength, which does not support the third and fourth hypotheses. The improved stair climbing ability by TENS was not due to the reduced knee pain and increased quadriceps muscle strength, although the post-hoc correlation analyses revealed a non-significant   Table 2. Change within-group and difference in change between groups for VAS pain, quadriceps muscle strength, and stair climbing capacity. VAS, visual analog scale; SCT, step stair climb test; 95% CI: confidence interval. *In the sham-TENS group, the missing value of 11-SCT from one patient was imputed using multiple imputation technique. † The mean (95% CI) between-group difference was calculated after adjusting for baseline value. Bold type represents a statistically significant result. www.nature.com/scientificreports www.nature.com/scientificreports/ but positive relationship between the pain relief effect and improved 11-SCT time in the TENS group. The main finding of this study is that TENS improved stair climbing capacity, determined using a sensor-mounted insole, better than sham-TENS in the patients with earlier radiographic OA stage. The time reduction in the transition phase during TENS treatment mostly explained the therapeutic effects (see graphic abstract, Fig. 2). As poor stair climbing capacity is thought to be the first mobility limitation observed in individuals with knee OA 5 , these findings indicate that TENS may be an option for reducing early-stage knee OA-related burden.

Interpretation of the Effects of TENS on Stair Climbing Capacity.
In this study, we found that TENS improved insole-based SCT time by 0.41 s, which is beyond the 95% CI of measurement error. This therapeutic effect on SCT time is not consistent with the findings of a previous study that showed that 12 weeks of TENS treatment in individuals with severe knee OA did not significantly improve SCT time 14 . This discordance may be attributed to the difference in radiographic disease severity. Approximately 85% of the study participants had pre-radiographic knee OA (K&L grade ≤1), who may respond better to therapeutic interventions than those with severe disease 15,16 . Furthermore, insole-based SCT may be more sensitive than stopwatch-based SCT in detecting the efficacy of therapeutic treatment, although the stopwatch-based SCT has high reliability and validity 18 . It should be acknowledged that this study is a secondary analysis from randomized controlled trial (RCT) data without calculation of the required sample size to detect the therapeutic effect of TENS on 11-SCT time. Thus, a type II error may exist, and the non-significant TENS treatment effects on the stopwatch-based 11-SCT time may be attributed to the low statistical power, given that the upper limit of the 95% CI in the stopwatch-based 11-SCT improvement was almost zero.
Contrary to the hypothesis, TENS did not significantly improve the time during stair descending that requires higher internal knee extension moment 3,17 . It is Interesting that the time reduction in the transition phase during TENS treatment mostly explained its therapeutic effects. Although the exact mechanism is unclear, the transition phase involves a quick turn that increases the external knee rotational moment 20 , which may cause knee pain and a subsequent impairment of smooth transition from stair descending to ascending. This preliminary finding warrants validation of the association between knee pain and impaired transition motion, and whether the transition motion responds well to pain-relief treatment.
Theoretically, the TENS treatment reduces pain through selective stimulation for large-diameter, low-threshold non-noxious afferents in dermatomes related to pain 21 and increases quadriceps motor neuron pool excitability 11 . Nevertheless, this study could not detect significant between-group improvements in knee pain during 11-SCT and quadriceps muscle strength immediately after TENS, although the same TENS protocol improved knee pain and walk distance during 6-minute walk test 22 . Further studies would be needed to determine what factors mediate the therapeutic effect of TENS. As improved knee pain was associated with improved 11-SCT time only in the TENS group, the underlying mechanism associated with change in 11-SCT may be different between the sham-TENS and TENS groups.
Significance and Clinical Impact of the Study. TENS was effective in improving mobility during insole-based 11-SCT, including people with pre-radiographic OA, the earliest clinical manifestation associated www.nature.com/scientificreports www.nature.com/scientificreports/ with knee OA 5 . This finding may help clinicians and physical therapists provide effective therapy for patients with early-knee OA who have difficulty performing weight-bearing activities that involve large knee flexion. TENS may be an option for reducing early-stage knee OA-related burden, which should be validated in future clinical trials.
The type of measurement metrics is important for identifying the therapeutic effects of TENS, and this study used both the stopwatch-and insole-based 11-step SCT. The stopwatch-based 11-SCT may not adequately identify the therapeutic effects of TENS, although non-significant results may come from the low sample size. Thus, biomechanically and physiologically more challenging tasks (e.g., 15-step SCT) might be suitable in adequately determining the therapeutic effect by using a stopwatch in the clinical setting. Further studies are warranted to address this question.

Study limitations.
First, this study examined the immediate effects of TENS without follow-up. This study cannot specify optimal TENS treatment protocol. Second, the knee pain intensity on the testing day was quite mild in both groups, although all the participants experienced pain at a mean score of >4 but <9 on a numeric rating scale. As severe knee pain at baseline could influence the pain relief effects of the TENS treatment, the relatively mild pain profile of the included participants may underestimate the pain relief effects of the TENS treatment. Third, the 11-SCT in this study was performed while wearing standard shoes, which may not be used in clinical practice. Data should be interpreted with caution because most clinicians would perform stopwatch-based 11-SCT while the participants wear their own footwear, which might influence the SCT time. Fourth, this study did not calculate the required sample size, as this study is a secondary analysis of RCT data 22 . Finally, the lack of muscle activity data such as electromyography data limited our analysis. As patients are required to use their quadriceps submaximally, the muscle activity during the 11-SCT for quadriceps motor neuron activation may be a better option for identifying the therapeutic effect of TENS.
In conclusion, TENS immediately improved the 11-SCT time better than sham-TENS. However, the therapeutic effect of TENS was similar between stair descending and ascending during the 11-SCT, and the time reduction in the transition phase during the TENS treatment mostly explained its therapeutic effects. The improved stair climbing ability by TENS was not due to the reduced knee pain and increased quadriceps muscle strength, although post-hoc correlation analyses revealed a non-significant positive relationship between the pain relief effect and the improved 11-SCT time in the TENS group. Given that stair climbing is suggested to be the first task that is affected in people with knee OA, TENS intervention may be an option for reducing early-stage knee OA-related burden, which should be validated in future clinical trials.

Methods
Study design and participants. This study was a secondary analysis of data from a RCT that examined the effects of TENS on knee pain and physical function in individuals with painful knee OA 22 . The institutional ethics committee of Kyoto University Graduate School and Faculty of Medicine approved the study (approval No. C1349). The study was conducted in compliance with Good Clinical Practice, the ethical standards of the responsible committee on human experimentation (institutional and national) and the Declaration of Helsinki 1975. Written informed consent was obtained from all participants before their enrollment. The required sample size in the RCT was calculated on the basis of the data from a previous clinical trial to detect the therapeutic effects of TENS. Details for sample size calculation were provided in the original RCT study 22 . Community-dwelling adults who reported knee pain within the last month were identified through a website. Subjects interested in this study answered a questionnaire concerning their physical condition, and those who met the inclusion criteria were invited to the university in February 2018 to participate in the study. The eligibility criteria included (1) age of ≥50 years; (2) Kellgren and Lawrence (K&L) grade of ≤2 in one or both knees as evaluated using weight-bearing anteroposterior radiographs, and (3) mean pain score of ≥4 but ≤9 on a numeric rating scale (0-10 total points) in the last month. The participants were excluded if they (1) had a history of knee surgery or intra-articular corticosteroid or hyaluronic acid injection within the last 6 months, (2) had a history of knee joint replacement or tibial osteotomy, (3) were receiving physical therapy, (4) had pain in any other major joints (e.g. back, hip, or ankle) with a greater effect than their knee pain on the current ability limits, (5) had severe medical conditions (e.g., chronic obstructive pulmonary disease, cardiovascular disease, arteriosclerosis obliterans, cerebrovascular accident, lumbar disk herniation, and rheumatoid arthritis), (6) did not usually use stairs in daily living, and (7) did not have the ability to walk and climb stairs without an ambulatory assistive device and handrail. Although the original RCT excluded patients with K&L grade 2 after data assessment 22 , this secondary study included these patients to increase its statistical power.
Randomization. The participants were randomly allocated to one of the two groups, the TENS or sham-TENS group, by using stratified and block randomization 22 . Studies have shown that female patients have a lower sensory threshold and respond to electrical stimulation differently from male patients; 7,8 thus, blocks were stratified by sex. Details for randomization were provided in the original RCT study 22 . TENS Intervention. The TENS and sham-TENS treatments were applied to index knee of all participants using the prototype TENS device (HV-F710, Omron Healthcare Co., Ltd., Kyoto, Japan) with pre-specified parameters (sweep mode from 1 to 250 Hz, symmetrical biphasic pulse, and a 60-μs pulse width). Sweep mode was chosen because low and high frequency TENS demonstrate analgesic effects in different mechanism, and the combination of these frequencies is supposed to be more effective in reducing pain than alone 23 . The index knee was defined as the more painful knee at inclusion. The intensity in the TENS group was gradually increased and limited by the participant's perception of a "strong but comfortable, non-painful tingle" immediately below (2020) 10:7294 | https://doi.org/10.1038/s41598-020-64176-0 www.nature.com/scientificreports www.nature.com/scientificreports/ the visible motor threshold. The participants in the sham-TENS group received sham stimulation at the same sites. TENS and sham-TENS were applied just before functional assessments explained in original RCT study 22 . Treatment time was not strictly set because previous Cochrane review showed similar therapeutic effects on knee pain and functional outcomes regardless of treatment time of ≤20 min, 30 to 40 min, and 60 ≥ min 24 . The TENS units were turned off when all the functional assessments were completed, for a total application time of around 60 minutes. Trained physical therapists with clinical experience in the musculoskeletal field performed the procedures. More information on the treatment procedure was provided in the original RCT 22 . Outcome measurement. The participants were assessed by the same assessor at baseline and during the treatment period. The primary outcome measures included valid and reliable functional measures for stair climbing, VAS for knee pain during SCT, and quadriceps muscle strength.
Instrumentation. Footwear influences balance performance 25,26 and walking speed 26 ; thus, all the participants wore standard shoes (LD AROUND M, Mizuno, Tokyo, Japan) with a pressure sensor (Force register sensors Model 402, Interlink Electronics Inc., CA, USA) to avoid any potential bias from the participants' wearing of their own footwear 27 . Fifteen sensors were attached in the shoe insole to enable detection of the precise initial contact and foot off time point during the SCT. During stair climbing, forefoot contact without heel contact was expected, and a pilot study for healthy adults indeed confirmed the forefoot initial contact during stair descending (data not shown). In-shoe foot pressure sensors can more precisely detect foot contact than single foot sensor. Furthermore, this method allows examination of the stair climbing capacity using actual stairs outside the motion laboratory. The sensors were connected to a flexible circuit board containing a microcontroller and micro-SD card placed on the participants' lower legs 27 . Although the footwear was novel for each participant, all the subjects reported that the shoes were comfortable and caused no pain. Data were sampled at 100 Hz.

Procedure for the 11-Step Stair-Climb Test. Each participant underwent the SCT in accordance with
the OARSI recommended method 28 , while wearing pressure sensor-mounted standard shoes. To exclude the influence of the participants' clothes on the stopwatch operability, the participants' pants were rolled up to the knee level. The 11-SCT with a regular stairwell was selected because it represents the type and size of stairs that subjects likely need to manage during daily activities, and some previous studies that examined reliability also used 11-SCT 29,30 . The participants descended and ascended a flight of stairs, which consisted of 11 steps with step height, width, and tread of 17, 135, and 29 cm, respectively. Although the standard SCT starts from the ascending stairs, the 11-SCT in this study started from descending stairs because of environmental constraints. The pilot study confirmed that the 11-SCT time in the 6 healthy adults (mean age: 24.3 years) did not significantly differ between starting ascending and descending (data not shown). A trained physical therapist (KS) measured the time required to perform 11-SCT in all the participants' test and retest sessions by using a stopwatch (TD-392, Tanita Corp., Tokyo, Japan). On the trained physical therapist's "start" command, each participant was instructed to walk as quickly and safely as possible without running 31 and was subsequently retested to ensure that their physical condition was stable over the testing period. The use of any walking aid or handrail was prohibited. The participants performed one practice trial for familiarization and to verify their safety. Stopwatch-based 11-SCT time was defined as the time from the therapist's command to "start" to the subject reaching the point where both feet were on the top platform. The stopwatch and insole measurements were performed simultaneously.
To determine insole-based 11-SCT time, vertical ground reaction force (GRF) was calculated from the sensor-mounted shoe data as previously described 27 . Subsequently, initial contact and foot off were defined as the time point where the vertical GRF exceeded and was <1% of the threshold of the estimated maximum GRF using MATLAB version R2017a (MathWorks Inc., Natick, MA, USA). The insole-based 11-SCT time was defined as the time from the initial foot off on the top platform to the point of foot contact in both feet on the top platform. By using the initial contact and foot off data, the insole-based 11-SCT time was further divided into three phases, namely descending, ascending, and transition. The transition phase was defined as the time between initial contact to staircase landing after descending and initial contact to the first step during ascending. The test-retest reliability was excellent for the stopwatch-based (intraclass correlation coefficient [ICC 1,1 ], 0.952 s; 95% CI, 0.560, 0.985 s) and insole-based 11-SCT times (ICC 1,1 , 0.929 s; 95% CI, 0.883, 0.957 s). The minimal detectable changes (MDC 95 ) for stopwatch-and insole-based 11-SCT times were 0.102 s and 0.089 s, respectively.
Knee Pain Intensity during Stair-Climb Test. Knee pain during SCT was evaluated after the 11-SCT by using the VAS (0-100 mm). Each participant was asked the following "Please mark on where you think the level of pain you experienced during stair climbing. " The participants recorded their level of knee pain by drawing a vertical mark between the ends of a 100-mm horizontal line. The 0-and the 100-mm end represented no pain and most extreme pain, respectively. The distance from the 0-mm end to the drawn mark was recorded to the first decimal place.
Quadriceps muscle strength. The maximum isometric quadriceps (Nm/kg) in both legs were measured using a hand-held dynamometer (HHD; μTas F-1, Anima Corp., Tokyo, Japan) in accordance with a method previously validated for use on community-dwelling elderly fallers 32 . The participants were instructed to remain seated in an upright position. The knee was placed in 90° flexion, with the HHD attached 10 cm proximal to the lateral malleolus and held in place with an inelastic strap that was looped around the therapy bed and fastened. The length of the straps allowed for an isometric contraction to be performed, with the knee at 90° flexion during testing. The participants were instructed to extend their leg for 5 s. Strong verbal encouragement was provided to ensure maximum effort. To provide moment value (Nm), the lever arm (length of tibia) between the knee joint