- Research article
- Open Access
The effects of custom-made foot orthoses on foot pain, foot function, gait function, and free-living walking activities in people with psoriatic arthritis (PsA): a pre-experimental trial
Arthritis Research & Therapy volume 24, Article number: 124 (2022)
Foot involvement is a significant concern in psoriatic arthritis (PsA) as it can lead to severe levels of foot pain and disability and reduced mobility and quality of life. Previous studies have shown moderate efficacy for custom-made foot orthoses (CFO) in reducing foot pain and disability in people with rheumatoid arthritis. However, evidence on the efficacy of CFO in people with PsA is lacking.
To explore the effects of CFO on foot function, foot and lower limb pain, gait function, and free-living walking activities (FWA) in people with PsA.
A pre-experimental study including twenty participants with PsA (mean age: 54.10 ± 9.06 years and disease duration: 11.53 ± 10.22 years) was carried out. All the participants received and wore CFO for 7 weeks. Foot and lower limb pain and foot function were measured before and after the intervention using the numerical rating scale (NRS) and the foot function index (FFI). Gait function was assessed by recording spatiotemporal parameters (STPs) during a 10-m walk test using an instrumented gait analysis system (Mobility Lab). Free-living walking activities (step count, free-living cadence, time spent in different ambulatory physical activities (APA)) were recorded over 7 days using an accelerometer-instrumented sock.
The FFI reported scores demonstrated severe baseline levels of foot pain (54.46 ± 14.58 %) and disability (46.65 ± 16.14%). Statistically and clinically significant improvements in foot pain and foot function and large effect sizes (Cohen’s effect size > 1, p < 0.005) were observed after the intervention period. A strong correlation (r = −0.64, p < 0.01) between the CFO wearing time and foot function was demonstrated. However, no significant changes were found for gait STP or free-living walking activities after 7 weeks of CFO use.
Results support the clinical and biomechanical plausibility of using CFO in people with PsA to reduce pain and improve foot function. Large-scale and controlled studies are needed to confirm these findings. Moreover, a multidisciplinary approach including the prescription of exercise therapy and physiotherapy combined with CFO could be required to improve STP and promote APA in people with PsA.
Psoriatic arthritis (PsA) is a chronic inflammatory arthropathy and a complex disease that frequently associates skin psoriasis, musculoskeletal manifestations including axial and/or peripheral arthritis, and several comorbidities such as cardiovascular disease, diabetes, and obesity . Foot and ankle problems are prevalent in people with PsA and are sometimes among the disease’s first and most important musculoskeletal manifestations [2, 3]. Several inflammatory features can be observed in the foot and ankle. These include toe dactylitis referred to as sausage-like toes , Achille’s tendon and plantar fascia enthesitis [4, 5], metatarsophalangeal and distal interphalangeal joint synovitis [6, 7], and tenosynovitis of the tibialis posterior, the common peroneal sheath, the long flexor tendons of flexor digitorum longus, and the flexor hallucis longus [8, 9]. All foot compartments can consequently be affected by PsA, causing pain, swelling, stiffness, tenderness, and in later stages, deformities leading to severe foot disability, reduced mobility, and quality of life [9,10,11].
Quantitative gait analysis, including spatiotemporal, kinematic, and kinetic parameter assessment, has been proven useful in evaluating gait function, disease progression, and/or a given intervention’s effect on patients’ mobility [12, 13]. Gait spatiotemporal parameters (STPs), in particular, are key metrics in gait function evaluation  and are indicators of gait adaptations in people with inflammatory arthritis . Instrumented gait analysis studies in people with PsA demonstrated impairments in gait STP, including reduced cadence, gait speed, stride length, and increased double support time, indicating impaired gait function and ultimately implying difficulties in walking activities [16,17,18].
Walking activities, on the other hand, involve moving in diverse situations and environments (e.g., the patient’s usual environment). A significant part of daily living activities, including transport/commuting, recreation, and domestic/occupational activities, depend mostly on walking. Walking is also the most practical, accessible, prevalent form of physical activity (PA) and the most frequently prescribed activity to meet the recommendations of the international guidelines for PA [19,20,21]. Inherently, gait and walking are closely related. For instance, a reduced gait speed is a significant predictor of decreased daily walking activity, and it could therefore have significant impacts on daily life [22, 23]. The effects of PA and walking on health outcomes are well-established [24, 25]. It has also been reported that PA may benefit disease activity, muscle strength, fatigue, pain, and quality of life in people with PsA . However, a recent systematic review demonstrated low PA levels in people with PsA which could be detrimental to PsA-associated comorbidities (i.e., cardiovascular health) and the disease per se . Importantly a close relationship between foot pain and gait function deficiencies has been demonstrated [27, 28]. This suggests that interventions aiming at improving foot pain and function could eventually improve gait function and promote walking activity and overall PA in people with PsA.
PsA management is mainly based on pharmacological treatments including disease-modifying antirheumatic drugs (DMARDs), Janus kinase inhibitors (JAKi), and biological therapies which have been proven efficient on symptom control and disease activity reduction [29,30,31]. Remarkably, inflammation and foot pain, as well as the related disability, can still be observed in a large proportion of patients on pharmacological therapy [16, 18, 32,33,34]. From a physiopathological perspective, mechanical stress and trauma have been suggested as joint and soft tissue inflammation triggers in PsA [35,36,37]. This could partly explain the high prevalence and persistence of foot and ankle problems, considering the weight-bearing function and the continuous mechanical stress applied to the foot during daily living activities . In this context, experts point out the need for targeted therapies addressing biomechanical abnormalities in the foot to reduce mechanically triggered inflammation and pain in people with PsA with persistent foot problems.
Among such therapies, custom foot orthoses (CFO) are medical devices designed to alter the magnitude and temporal patterns of the reaction forces acting on the plantar foot in order to improve foot and lower limb function and offload painful structures during weight-bearing activities . CFO are common practice in patients with foot problems associated with rheumatic diseases. In people with rheumatoid arthritis (RA), a disease characterized by the high prevalence and severity of foot problems similar to those reported in PsA, the use of CFO showed positive effects on foot pain and disability [40,41,42,43,44,45]. However, to our knowledge, there are no records in the literature on the efficacy of CFO in people with PsA. In addition, despite the similarities in foot problems, RA and PsA are different entities with different clinical presentations making the direct extension of results from RA to PsA inadequate . Therefore, the primary objective of this study is to explore the effects of using CFO for a 7-week period on foot function in people with PsA. The secondary objectives are to explore the effects of CFO on foot pain, the relationship between the CFO wearing time and foot pain and function, and the effects of CFO on gait function (STP) and free-living walking activities (FWA) in people with PsA.
Study design and participants
A pre-experimental study with pre-test/post-test design was conducted. Potential participants were referred to the research team from the rheumatology out-patient clinics at the Université de Sherbrooke Hotel Dieu University Hospital (CHUS). The first author (RW) screened the potential participants for eligibility via phone interviews. Twenty-two participants with PsA met the inclusion criteria and were then recruited. Inclusion criteria were being between 20 and 70 years of age, having a confirmed diagnosis of PsA by a trained rheumatologist, and having moderate to severe and recurrent foot pain and stable medication over 3 months preceding the recruitment. Patients with diabetes, neurological disease, or any musculoskeletal disease that could impact the normal gait pattern who received an intra-articular corticosteroid injection or any conservative foot treatment such as foot orthoses/footwear intervention within the past 3 months were excluded. The study was approved by the CIUSSS de l'Estrie-CHUS Ethics Board, and all the participants gave their informed consent before data collection.
Data collection procedure
On a first data collection session (T1) at Sherbrooke’s Research Center on Aging, demographic and baseline characteristics were assessed. Then, foot and lower limb pain, global pain, and foot function were measured using self-reported questionnaires. In this same session, all the participants performed three 10-m walking trials at their self-selected speed. Participants were then examined by a trained podiatrist who performed foot casts and designed the CFO. At the CFO delivery visit (T2), the participants’ foot and lower limb pain and foot function were evaluated for a second time. This second pre-intervention measurement was planned considering the T1–T2 delay and the fluctuating nature of pain in PsA. CFO were then dispensed and adjusted if necessary to improve fit and comfort. The participants were directed to wear the CFO for 7 weeks and they were provided with a diary to record daily CFO wearing time, weekly foot pain intensity, and any changes in medication that occurred during the intervention period. At a final follow-up visit scheduled at the end of the 7-week period (T7), foot and lower limb pain and foot function were re-assessed and the instrumented 10-m walking trials were repeated. Free walking activities (FWA) were recorded over seven consecutive days before the CFO first use and after the 7-week intervention period using an instrumented sock (including an IMU at the ankle) that the participants wore during waking hours.
Functional foot orthoses were custom-made for each participant. The CFO were designed by the same experienced podiatrist (GBC) based on a detailed clinical and biomechanical assessment. Foot scans were obtained with the Occipital Structure Sensor 3D scanner (Occipital Inc), the patient in a prone position while the subtalar joint was held in a neutral position. The obtained scan was edited and smoothed using the MSoft software (Techmed3d Inc, Levis, QC, Canada). Three-quarter length CFO were 3D printed in a rigid material (Nylon) using a MultiJet Fusion 3D printer (HP, Palo Alto, CA, USA). The thickness of the CFO ranged between 2 and 3.4 mm depending on the participants’ medial arch weight and height. Most of the orthoses included a medial arch support, a heel stabilizer, and a metatarsal pad. The degrees and types of corrections added to the CFO were determined specifically for each participant based on the clinical examination and were adjusted at the CFO delivery according to each patient’s comfort and tolerance. The participants were taught to wear the CFO progressively during the first 2 weeks to allow for the lower limbs’ muscles and structures to adjust to the CFO, and to wear the orthoses for the next 5 weeks, 7 days a week as often as they could. To document adherence to the CFO, all the participants completed a diary to report the daily wearing time in hours. In addition, the participants were advised to wear the CFO with adapted shoes after the general characteristics (e.g., heel height, malleability of the sole, etc.) of such shoes were explained.
Sociodemographic, baseline characteristics, and control variables
Sex, age, body mass index, professional occupation, and previous history of foot injuries were assessed using a self-reported questionnaire. Disease duration and C-reactive protein (CRP) levels at baseline were obtained from the patients’ medical records. Foot type, foot deformities, and foot pain sites were obtained from the podiatrist’s clinical examination records. Changes in medication during the CFO intervention period were recorded by the participants in the diaries provided to them.
Foot function was measured using the foot function index (FFI). The FFI is a valid, reliable, and responsive self-reported questionnaire widely used in previous studies to evaluate CFO effects on foot function [47, 48]. The FFI is composed of 23 items divided into three subscales measuring foot pain (FFI-P), foot disability (FFI-D), and foot-related activity limitation (FFI-AL). Each item of the FFI is recorded on a zero-to-ten numeric rating scale (NRS) allowing for subscale and total score calculation. Each subscale score is calculated as the sum of all its items divided by its maximum possible total . The total score is obtained as the sum of all subscales’ final percentages divided by the total number of subscales. The values reported are presented as percentages ranging between 0 and 100%, with higher values indicating greater pain, disability, and activity limitation. The minimal clinically important difference (MCID) for the FFI total score was found to be 7 points in patients with plantar fasciitis .
Foot pain intensity was measured using a zero-to-ten NRS which is a valid, reliable, and responsive tool for pain intensity assessment . The MCID reported for the NRS in people with chronic pain is equal to 2 points . Participants were asked to circle the number between 0 and 10 that matched better their average foot pain intensity in the 7 days preceding the data collection. Foot pain was assessed more in detail (e.g., pain walking with foot orthoses, pain walking with shoes, pain at the end of the day, etc.) with the FFI pain subscale. Moreover, to monitor the evolution of foot pain intensity during the intervention period, the patients were asked to report at the end of each week their perceived foot pain in a diary using zero-to-ten NRS. Foot pain and foot function were measured at three time points namely, at first data collection (T1), at CFO delivery (T2), and after the 7-week intervention period (T7). As there were no statistical differences in the FFI and NRS scores between T1 and T2, the average of these two time points was used as a baseline measure while the last time point (T7) represented the final measure.
CFO wearing time
The daily CFO wearing time was recorded in the participants’ diaries and it is reported as the average reported time per week.
Global and lower limb pain
Global pain and pain at the knee, hip, and lower back pain were measured at T1, T2, and T7 using the NRS (0, no pain, to 10, worst imaginable pain). Similarly to foot pain and foot function, data obtained during the first two time points were used as baseline measures.
Gait function was assessed using an instrumented gait analysis system. Gait spatiotemporal parameters (STPs) including cadence, gait cycle duration, gait speed, stride length, double support, swing time, foot strike angle, and stride time variability were recorded using the Mobility Lab system (APDM Wearable Technologies) during the 10-m walk test (10MWT). Mobility Lab is a research-grade system proven to accurately and reliably estimate STP [52,53,54]. Mobility Lab uses a set of six OPAL inertial measurement units (IMUs) and a software that allows for automated and easy extraction of STP. All the participants performed three trials of the 10MWT. To do so, they walked over a 14-m straight walkway with the Mobility Lab’s IMUs fixed with elastics straps on the chest, the lower back, both wrists, and feet. The 10MWT trials were performed at the participants’ comfortable speed and the average of the three trials was calculated.
Free-living walking activities (FWA)
FWA including step count, free-living cadence, and time spent in ambulatory physical activity (APA) intensity-based categories were measured using an instrumented sock (Sensoria Inc, Redmond, WA, USA) including a 9-axis IMU positioned at the ankle. The instrumented sock connects automatically, without any manipulation needed from the participants, via Bluetooth to a smartwatch (Apple Watch, series 3) where the raw inertial measures of motion (3D accelerometer) are stored. The data are then transferred to a computer where they are processed to extract walking activities’ specific outcomes (see Additional file 1 for signal processing and step identification description). Step count was assessed as the total number of steps per day. Furthermore, to describe the step accumulation pattern throughout the day, the number of steps was assessed for each of the following active event categories based on the number of consecutive steps within each category: 0 to 20 steps, 20 to 60 steps, 60 to 120 steps, 120 to 300 steps, 300 to 600 steps, and more than 600 steps. Free-living cadence included cadence averaged for total wearing time (mean cadence/day). Moreover, as cadence may vary depending on the number of consecutive steps performed, it was also assessed for each of the above active event categories. APA intensity-based categories were determined using cadence data. They included stepping activities (0 to 59 steps/min), slow walking (60 to 79 step/min), medium walking (80 to 99 step/min), moderate intensity APA (MAPA) (100 to 119 step/min), and vigorous APA (VAPA) ( > 120 step/min), as previously defined [55, 56]. The time spent in each of the last three categories was calculated only for purposeful walking (i.e., events composed of more than 60 steps). Free-living walking activities were assessed over a period of 7 consecutive days before and after the intervention. To do so, the participants were instructed to wear the instrumented sock during waking hours while they perform daily activities. Only valid days defined as days with at least 8 h of recordings and only valid participants with a minimum of one valid day were included in the analyses. Adherence to the instrumented sock use was tested by the system itself and by asking the participants to record the daily wearing time in a diary. To avoid influencing the participant’s physical activity, they were only told that the study would assess the effects of CFO on foot pain, foot function, and gait STP.
Sample size and statistical analysis
Given the exploratory nature of this study, the sample size was calculated assuming a large effect size (0.8) for the pre-post differences in the FFI total score. Using a two-tailed paired T-test, a significance level α of 5%, a power of 90%, and assuming a 15% dropout rate, a total sample size of 22 participants was required. The Shapiro-Wilk test was used to examine data distribution and parametric and nonparametric statistical tests were used depending on data distribution. Paired t-tests (or the Wilcoxon signed-rank test) were used to assess the differences in foot pain, foot function, and global and lower limb pain between baseline and T7. Cohen’s effect size was calculated to quantify the magnitude of these differences. A one-way repeated measures ANOVA was conducted to determine whether there was a statistically significant difference in weekly recorded foot pain intensity and CFO wearing time over the 7-week intervention period. Spearman correlation coefficients were calculated to assess the relationships between the CFO wearing time, foot pain, and foot function at T7. As a 2-week adaptation period was required, correlation analyses were performed using the average CFO wearing time per week calculated for the last 5 weeks of the intervention period. Correlation coefficients were considered weak, moderate, and strong for values between 0.1 and 0.3, 0.3 and 0.5, and > 0.5, respectively . The pre-post differences in gait function and free-living walking activities were assessed using the Wilcoxon signed-rank test. The significance level was set at 0.05. The statistical analyses were performed using SPSS version 26 (IBM statistics Corporation, Armonk, NY).
The participant flow throughout the study is presented in Additional file 2. Twenty-seven participants were initially screened, five were excluded as two did not meet inclusion criteria and three declined to participate. Twenty-two participants met the inclusion criteria and participated in the study. Of these, one participant was excluded after the podiatry examination because the CFO was considered not clinically appropriate. Another patient was excluded because of an acute arthritis flare during follow-up. From September 2019 to August 2021, twenty participants completed the study and were included in the analyses.
Demographic and baseline clinical characteristics
Demographic and baseline clinical characteristics are presented in Table 1. The study sample was composed of 5 males and 15 females with a mean age of 54.10 ± 9.06 years, a mean BMI of 29.3 ± 4.5 kg/m2, and a mean disease duration of 11.53 ± 10.22 years. The CRP baseline levels were within the normative ranges for 75% of the patients. Two participants recorded changes in medication during the intervention period (Table 1). The first participant started taking NSAIDs at the end of the fourth week for generalized body pain, and the second received a new biological therapy starting at week 4.
Foot function and global and lower limb pain
Figure 1 presents the FFI (Fig. 1a) and NRS (Fig. 1b) scores at baseline and after 7 weeks of using the CFO. All the FFI sub-scores and total score decreased at T7 indicating a significant improvement in foot pain (54.46 ± 14.58% at baseline and 34.01 ± 18.94 at T7), foot disability (46.26 ± 19.91% at baseline and 24.13 ± 18.84 at T7), and foot-related activity limitation (41.54 ± 31.35% at baseline and 12.26 ± 17.57 at T7). The mean pre-post difference in the FFI total score was 22.30 ± 24.76% (p = 0.004) and a large effect size (d = 1.25) was reported. A significant improvement in foot pain was also demonstrated through the NRS score which decreased by 2.30 ± 2.98 points and a large effect size was reported (d = 1.19, p = 0.004). Global pain was also significantly decreased with a mean difference of 1.95 ± 2.77 and a large effect size (d = 0.90, p = 0.006). Regarding lower limb pain, while there were no significant changes in knee and lower back pain, hip pain significantly improved with a mean difference of 1.88 ± 3.38 points and a moderate effect size (d = 0.67, 0.031) (Table 2).
Seventeen participants recorded the weekly foot pain intensity and CFO wearing time using the provided diaries. The CFO weekly wearing time and the evolution of foot pain are presented in Fig. 2a and b. As it can be observed, there was a tendency for foot pain to decrease during the first 4 weeks and a plateau was observed after this period. The same tendency was also observed for wear time which increased progressively during the first 4 weeks and remained almost stable afterward. The one-way repeated measures ANOVA showed statistically significant changes in weekly foot pain intensity over time F (2.13, 32.02) = 20.28, p = 0.001, and CFO wearing time F (2.27, 34.17) = 5.92, p = 0.005. Post hoc tests (with Bonferroni adjustment) showed no significant differences in foot pain between the different time points. However, the differences between week 1 and week 7 (mean difference = 1.81, p = 0.09) and weeks 2 and 7 (mean difference = 1.43, p = 0.06) were almost significant. Regarding CFO wearing time, post hoc analysis showed a significant decrease between the first week and all the other time points (p < 0.05). Correlation coefficients showed significant correlations between the CFO wearing time (hours/week) and foot pain (r = −0.57, p = 0.023), disability (r = −0.68, p = 0.005), activity limitation (r = −0.49, p = 0.047), and the FFI total score (r = −0.64, p = 0.01) at T7 (Fig. 3).
Spatiotemporal gait parameters measured before and after the intervention period are presented in Table 2. Results show a slight but significant increase and decrease in double support time and swing time, respectively, at T7. However, for all the remaining STP including cadence, gait cycle duration, gait speed, stride length, and foot strike angle, there were no significant differences at T7 compared to baseline. Similarly, no significant changes were reported for the effects of CFO on stride time variability.
Free-living walking activities (FWA)
Free-living walking activities are presented in Figs. 4, 5, and 6. Out of the 20 participants, four were excluded from the FWA analyses because they did not accumulate at least one valid day of recordings (i.e., recording time > 8 h) at baseline and T7. Consequently, the results presented in this section include data from 16 participants. On average, the patients accumulated a total of 10.79 ± 1.18 h and 9.99 ± 1.02 h of recorded time at baseline and T7, respectively, with no significant differences between baseline and T7 (p = 0.09). The average active time was 3.9 ± 1.7 h at baseline and 3.5 ± 1.6 h at T7 (p = 0.08). The average number of steps per day was 6460 ± 2818 steps/day at baseline and 5836 ± 3079 steps/day at the end of the intervention period with no significant differences between the two time points (p = 0.18) (Fig. 4a). The pattern of accumulating these steps is presented in Fig. 4b. As can be observed, the total number of steps was accumulated in short active events composed of 20 to 300 consecutive steps (Fig. 4b). The daily average free-living cadence was 96.68 ± 5.85 steps/min and 96.03 ± 5.58 steps/min before and after the intervention, respectively (p = 0.79) (Fig. 5a). Results show that cadence increases considerably for active events of more than 20 steps compared to those of less than 20 steps (Fig. 5b). For active events composed of 20 to 600 consecutive steps, the mean cadence was 96.65 ± 1.10 steps/min at baseline and 96.38 ± 1.02 steps/min at T7. Results also show that cadence reaches and crosses 100 step/min only for active events composed of more than 600 consecutive steps, for an average of 100.94 ± 11.06 steps/min at baseline and 101.75 ± 8.73 steps/min at T7 with no significant differences between the two time points (p = 0.44).
Figure 6 presents minutes spent in APA intensity-based categories including stepping activities (Fig. 6a) and slow, medium, brisk walking, and vigorous APA (Fig. 6b). Out of 234.1 min of active time recorded at baseline, 183.7 min (78 %) were spent in stepping activities and 50.4 min (22 %) were spent in purposeful walking. This same pattern was observed at T7: out of 210.2 min of active time, 164.3 min (78 %) were spent in stepping activities and 45.0 min (22%) spent purposeful walking with no significant differences between the two time points. Participants accumulated 25.9 ± 19.4 min and 18.7 ± 11.6 min of medium and brisk walking at baseline and 21.5 ± 15.0 19 min and 19.1 ± 13.9 min at T7. Time spent in vigorous APA was 1.2 ± 2.0 min at baseline and 0.8 ± 1.4 min at the final follow-up (p = 0.52).
The primary purpose of this study was to explore the effects of wearing CFO for a 7-week period on foot function in people with PsA. As a secondary objective, we sought to assess the effects of CFO on foot pain, gait function (instrumented gait STP analysis), and FWA and to assess the relationship between the CFO wearing time and foot pain and function in people with PsA with foot involvement.
Foot pain and foot function
The main findings showed a significant improvement in foot pain (NRS and FFI) and foot function (FFI) after using the CFO for a 7-week intervention period. The FFI total score decreased by 22.30%, and a large effect size (d = 1.25) was reported. Interestingly, after only 7 weeks of intervention, this improvement was clinically significant for 70% of the participants since the pre-post differences in their FFI total scores were higher than the MCID previously reported for the FFI total score .
Research in people with RA has shown some efficacy of CFO on foot pain which is consistent with our findings [41,42,43]. However, conflicting results regarding the effects of CFO on foot function have been reported. Indeed, while some studies endorsed the effectiveness of CFO on foot function [44, 46], others reported no significant effects for this outcome [58,59,60]. Several factors could explain such discrepancies. First, the orthoses type can differ between the studies according to the targeted therapeutical aim (e.g., palliative vs functional). Moreover, foot casting and manufacturing materials and techniques can vary from one study to another depending on the latest advances in technologies and on the national practice guidelines making between-studies comparison difficult. In our study, we used functional CFO in all the participants. The materials and techniques of foot casting and manufacturing were standardized for all the participants. However, the degrees and types of corrections were specific for each participant’s needs and tolerance. The CFO were also adjusted at delivery and during the following 2 weeks to increase comfort and acceptance if needed. This could explain the positive effects on pain and foot function observed in this study. Furthermore, there was no consensus regarding the previous studies’ intervention durations and control conditions. Some trials used placebo orthoses while others used shoes only as a control condition. As the former are usually made from thick and cushioned materials, they cannot be considered as not having therapeutic effects, thereby attenuating the CFO effects. In contrast, using shoes-only as a control could overestimate the effect of CFO .
Importantly, the CFO wearing time was not documented in all the previous studies which can compromise their conclusions as a lack of effectiveness could partially be related to insufficient use of the orthoses. In our study, a sufficient wearing time (8h/day) was reported and a strong correlation between the CFO wearing time and the FFI total score was demonstrated. These findings are similar to those reported in a few studies in people with RA that did report wearing time [44, 46, 60]. This observation highlights the relevance of monitoring this variable in future studies and the importance of continuous and regular wearing of the CFO.
Apart from the intervention characteristics, sampling groups and individual characteristics such as age, sex distribution, disease duration, and baseline levels of foot pain and disability are also important considerations as they may influence the effectiveness of CFO. For instance, data from a previous study  showed that shorter disease duration, younger age, and higher baseline values of foot pain and disability predicted improved outcomes after CFO use. In the present study, the participants had a mean age of 54.10 ± 9.06, a median disease duration of 6 years, a high prevalence of foot pain, and severe levels of disability at baseline. Therefore, it is not unexpected that the CFO helped relieve pain and improve perceived foot function. In addition to foot pain and disability, the findings showed a significant decrease in global and hip pain. However, the differences were not clinically significant (mean differences < 2 points). Knee and lower back pain also improved but the differences did not reach the significance level. Although there is evidence that CFO could have beneficial effects on lower limb pain [63,64,65,66], further studies using specific tools to assess knee, hip, and lower back pain in detail are needed to confirm the beneficial effects of CFO on these outcomes.
Gait STPs are indicators of functional capacity and overall health and autonomy, making them the most relevant and most often measured biomechanical parameters for gait analysis in healthy and pathological populations [13, 67]. We noticed a lack of scientific evidence regarding the effects of CFO on gait STPs in people with arthritic foot diseases. For instance, studies in people with RA showed only a minimal or no effect of CFO for increasing gait speed, cadence, and stride length [42, 68, 69] and some studies showed that wearing the CFO allowed for an improvement of gait stability [45, 70].
Our findings showed that gait STPs were altered compared to the normative values reported for healthy adults [71, 72]. However, there were no significant changes in STP and gait stability after the intervention except for a negligible effect on double support and swing time. These results could be potentially attributed to the short-term nature of our intervention period and the long disease duration reported in this study. Gait impairments demonstrated in participants with PsA may be acquired over many years. Consequently, the patients can develop antalgic walking strategies that may require more extended intervention periods to improve. In addition, the patients could have developed fear-avoidance beliefs which have been reported as significant predictors of poorer response to CFO in other patient populations . Another possible explanation for the lack of STP response could be that PsA may be more responsive to CFO treatment in earlier stages of the disease. Therefore, long-term studies including patients with early disease would be more relevant to assess the effects of CFO on gait STP properly.
Furthermore, although the 10MWT is reliable and responsive in patients with major gait impairments secondary to neurological diseases such as stroke and Parkinson , it might not have been responsive in this study because of the relatively milder gait impairment related to PsA and the short intervention’s duration and follow-up period . Longer time/distance tests should also be considered when assessing gait in people with PsA as gait impairments reported in this population could be attributed to common features of inflammatory arthritis such as muscle weakness, reduced range of motion, and deformities [76,77,78] and they may be more significant during sustained walking activities.
Free-living walking activities
The benefits of physical activity on health are undeniable. Results from a recent systematic review  suggest that physical activity may positively affect disease activity, muscle strength, fatigue, pain, quality of life, and cardiovascular risk in people with PsA. Therefore, promoting physical activity in this population should be a health care priority. Walking is a practical, accessible, and low-skill mode of physical activity that plays a major role in occupational and social activities of everyday living . The findings of this study reported decreased step counts with large standard deviations (6460 steps/day at baseline and 5836 steps/day at T7) which are below the recommended 10,000 steps/day . Similarly, the daily averaged free-living cadence was 96.67 ± 5.85 steps/min at baseline and 96.03 ± 5.85 steps/min at T7 which is below the naturally selected free-living walking speed (100 steps/min) reported for healthy individuals [56, 81]. Besides, the reported time spent in brisk walking did not achieve the minimum of daily 30 min of moderate-intensity physical activity recommended by the international guidelines for PA activity . These results indicate decreased PA levels in participants with PsA with foot problems which is consistent with what is reported in a previous systematic review . Future studies comparing PA levels between participants with PsA and matched healthy controls are needed to confirm these results.
We postulated that by alleviating pain, the use of CFO would positively impact walking activities in people with PsA. Nevertheless, neither the number of steps/day, free-living cadence, nor the time spent in the different intensity-based APA changed after using the CFO. Again, the short-term nature of this study could have not fully reflected the effects of CFO. Besides, free-living cadence is a measure of ambulatory behavior  that is likely influenced by psychoaffective factors that have not been assessed in this study. In a previous study in people with PsA, beliefs about PA (e.g., fear of exacerbating pain) have been shown to be associated with activity level . This suggests that future studies should address the patient’s behavior which is complex and may require using a multidisciplinary approach including behavioral change strategies, advice, education, prescription of exercise therapy, and CFO to promote physical activity in people with PsA. In addition, as this study was carried out over nearly 2 years, natural environmental factors such as seasons/weather, and the occurrence of the COVID-19 pandemic, might have influenced the patients’ PA [84, 85].
Lastly, it should be mentioned that only 16 participants were included in the FWA analyses and there might be not enough power to detect significant changes. Also, the average recorded time was nearly 1 h lower at T7 compared to baseline (10.79 h vs 9.99). This could have contributed to the obtained results. To our knowledge, only one study investigated the effects of CFO on physical activity  in a population of people with RA. Using a self-reported questionnaire, their results showed that a 6-month CFO use improved light-intensity physical activity but not moderate- and vigorous-intensity activities . However, these findings cannot be compared to those demonstrated in the present study because of the different approaches used for PA measurement since using self-reported measures could overestimate PA compared to objective measurements .
This study has limitations that should be mentioned. First, there was no control group to control for the placebo effect and the natural evolution of the disease. Future studies are encouraged to use prefabricated, sham orthoses and/or a shoe-only condition as comparators to overcome this limitation. The choice of the control condition should be made according to the study aims (e.g., using prefabricated orthoses as a control condition if the aim is to assess the intervention’s cost-effectiveness). Moreover, if sham orthoses are to be used, researchers are encouraged to document the credibility and the biomechanical effects of these devices. Second, the follow-up duration may have been too short to show changes in outcomes such as gait parameters and FWA that may necessitate a longer time to improve. Moreover, the small sample size and the high proportion of female participants which is not representative of the gender distribution usually seen in PsA could compromise the generalizability of our findings.
The use of CFO for a 7-week period improved foot pain and related disability in people with PsA. This suggests that CFO may be used in conjunction with pharmacological therapy to relieve pain and improve perceived foot function. However, the results should be confirmed in larger and controlled studies. The effects of CFO on gait function and free-living walking activities were not evident in this study due to the small sample size, short follow-up period, and personal and environmental factors that have not been measured. Future RCTs with larger sample sizes and longer intervention durations are needed for any conclusions to be drawn.
Availability of data and materials
The dataset used and analyzed during the current study is available from firstname.lastname@example.org on reasonable request.
Ambulatory physical activity
Body mass index
Custom foot orthoses
Disease-modifying antirheumatic drug
Foot function index
Free-living walking activities
Gait cycle time
Minimal clinically important difference
Numerical rating scale
10-m walk test
Perez-Chada LM, Merola JF. Comorbidities associated with psoriatic arthritis: review and update. Clin Immunol Orlando Fla. 2020;214:108397.
Bezza A, Niamane R, Amine B, El Maghraoui A, Bensabbah R, Hajjaj-Hassouni N. Involvement of the foot in patients with psoriatic arthritis. A review of 26 cases. Joint Bone Spine. 2004;71(6):546–9.
Nordbø ECA, Aamodt G, Ihlebæk CM. Subjective health complaints in individuals with psoriasis and psoriatic arthritis: associations with the severity of the skin condition and illness perceptions - a cross-sectional study. Int J Behav Med. 2017;24(3):438–46.
Gladman DD, Ziouzina O, Thavaneswaran A, Chandran V. Dactylitis in psoriatic arthritis: prevalence and response to therapy in the biologic era. J Rheumatol. 2013;40(8):1357–9.
Polachek A, Li S, Chandran V, Gladman DD. Clinical enthesitis in a prospective longitudinal psoriatic arthritis cohort: incidence, prevalence, characteristics, and outcome. Arthritis Care Res. 2017;69(11):1685–91.
Bagel J, Schwartzman S. Enthesitis and dactylitis in psoriatic disease: a guide for dermatologists. Am J Clin Dermatol. 2018;19(6):839–52.
Freeston JE, Coates LC, Nam JL, Moverley AR, Hensor EMA, Wakefield RJ, et al. Is there subclinical synovitis in early psoriatic arthritis? A clinical comparison with gray-scale and power Doppler ultrasound. Arthritis Care Res. 2014;66(3):432–9.
Suzuki T. Power Doppler ultrasonographic assessment of the ankle in patients with inflammatory rheumatic diseases. World J Orthop. 2014;5(5):574–84.
Patience A, Helliwell PS, Siddle HJ. Focussing on the foot in psoriatic arthritis: pathology and management options. Expert Rev Clin Immunol. 2018;14(1):21–8.
Hyslop E, McInnes IB, Woodburn J, Turner DE. Foot problems in psoriatic arthritis: high burden and low care provision. Ann Rheum Dis. 2010;69(5):928.
Carter K, Walmsley S, Chessman D, Rome K, Turner DE. Perspectives of patients and health professionals on the experience of living with psoriatic arthritis-related foot problems: a qualitative investigation. Clin Rheumatol. 2019;38(6):1605–13.
Simon SR. Quantification of human motion: gait analysis-benefits and limitations to its application to clinical problems. J Biomech. 2004;37(12):1869–80.
Cimolin V, Galli M. Summary measures for clinical gait analysis: a literature review. Gait Posture. 2014;39(4):1005–10.
Roberts M, Mongeon D, Prince F. Biomechanical parameters for gait analysis: a systematic review of healthy human gait. Phys Ther Rehabil. 2017;4(1):6.
Carroll M, Parmar P, Dalbeth N, Boocock M, Rome K. Gait characteristics associated with the foot and ankle in inflammatory arthritis: a systematic review and meta-analysis. BMC Musculoskelet Disord. 2015; [cited 2021 Jun 12];16. Available from: https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4455329/.
Woodburn J, Hyslop E, Barn R, McInnes IB, Turner DE. Achilles tendon biomechanics in psoriatic arthritis patients with ultrasound proven enthesitis. Scand J Rheumatol. 2013;42(4):299–302.
Hyslop E. Biomechanics of enthesitis of the foot in psoriatic arthritis [Internet] [Ph.D.]. 2013. Glasgow Caledonian University; [cited 2018 Oct 1]. Available from: https://ethos.bl.uk/OrderDetails.do;jsessionid=B5D1850DF9C83E5734657DB70A62054C?uin=uk.bl.ethos.601641
Wilkins RA, Siddle HJ, Redmond AC, Helliwell PS. Plantar forefoot pressures in psoriatic arthritis-related dactylitis: an exploratory study. Clin Rheumatol. 2016;35(9):2333–8.
Schutz Y, Nguyen DMT, Byrne NM, Hills AP. Effectiveness of three different walking prescription durations on total physical activity in normal- and overweight women. Obes Facts. 2014;7(4):264–73.
Hulteen RM, Smith JJ, Morgan PJ, Barnett LM, Hallal PC, Colyvas K, et al. Global participation in sport and leisure-time physical activities: a systematic review and meta-analysis. Prev Med. 2017;95:14–25.
Zaleski AL, Taylor BA, Panza GA, Wu Y, Pescatello LS, Thompson PD, et al. Coming of age: considerations in the prescription of exercise for older adults. Methodist DeBakey Cardiovasc J. 2016;12(2):98–104.
Hirata S, Ono R, Yamada M, Takikawa S, Nishiyama T, Hasuda K, et al. Ambulatory physical activity, disease severity, and employment status in adult women with osteoarthritis of the hip. J Rheumatol. 2006;33(5):939–45.
Lennon N, Church C, Shields T, Shrader MW, Henley J, Niiler T, et al. Factors associated with walking activity in adults with cerebral palsy. Gait & Posture. 2021;90(4):43–7.
Hamer M, Chida Y. Walking and primary prevention: a meta-analysis of prospective cohort studies. Br J Sports Med. 2008;42(4):238–43.
Lee IM, Skerrett PJ. Physical activity and all-cause mortality: what is the dose-response relation? Med Sci Sports Exerc. 2001;33(6 Suppl):S459–71 discussion S493-494.
Kessler J, Chouk M, Ruban T, Prati C, Wendling D, Verhoeven F. Psoriatic arthritis and physical activity: a systematic review. Clin Rheumatol. 2021;40(11):4379–89.
Riskowski JL, Hagedorn TJ, Dufour AB, Hannan MT. Associations of region-specific foot pain and foot biomechanics: the Framingham foot study. J Gerontol A Biol Sci Med Sci. 2015;70(10):1281–8.
Štefan L, Kasović M, Zvonar M. Gait speed as a screening tool for foot pain and the risk of falls in community-dwelling older women: a cross-sectional study. Clin Interv Aging. 2020;15:1569–74.
Perrotta FM, Marchesoni A, Lubrano E. Minimal disease activity and remission in psoriatic arthritis patients treated with anti-TNF-α drugs. J Rheumatol. 2016;43(2):350–5.
Hagège B, Tan E, Gayraud M, Fautrel B, Gossec L, Mitrovic S. Remission and low disease activity in psoriatic arthritis publications: a systematic literature review with meta-analysis. Rheumatology. 2020;59(8):1818–25.
Gossec L, Baraliakos X, Kerschbaumer A, de Wit M, McInnes I, Dougados M, et al. EULAR recommendations for the management of psoriatic arthritis with pharmacological therapies: 2019 update. Ann Rheum Dis. 2020;79(6):700–12.
Delle Sedie A, Riente L, Filippucci E, Scirè CA, Iagnocco A, Meenagh G, et al. Ultrasound imaging for the rheumatologist. XXXII. Sonographic assessment of the foot in patients with psoriatic arthritis. Clin Exp Rheumatol. 2011;29(2):217–22.
Healy PJ, Groves C, Chandramohan M, Helliwell PS. MRI changes in psoriatic dactylitis--extent of pathology, relationship to tenderness and correlation with clinical indices. Rheumatol Oxf Engl. 2008;47(1):92–5.
Galluzzo E, Lischi DM, Taglione E, Lombardini F, Pasero G, Perri G, et al. Sonographic analysis of the ankle in patients with psoriatic arthritis. Scand J Rheumatol. 2000;29(1):52–5.
Eder L, Law T, Chandran V, Shanmugarajah S, Shen H, Rosen CF, et al. Association between environmental factors and onset of psoriatic arthritis in patients with psoriasis. Arthritis Care Res. 2011;63(8):1091–7.
Cambré I, Gaublomme D, Burssens A, Jacques P, Schryvers N, De Muynck A, et al. Mechanical strain determines the site-specific localization of inflammation and tissue damage in arthritis. Nat Commun. 2018;9(1):4613.
McGonagle D, Tan AL, Benjamin M. The biomechanical link between skin and joint disease in psoriasis and psoriatic arthritis: what every dermatologist needs to know. Ann Rheum Dis. 2008;67(1):1–4.
van Deursen R. Mechanical loading and off-loading of the plantar surface of the diabetic foot. Clin Infect Dis. 2004;39(Supplement_2):S87–91.
Kirby K. Evolution of foot orthoses in sports. In: Athletic footwear and orthoses in sports medicine; 2010. p. 19–35.
Gijon-Nogueron G, Ramos-Petersen L, Ortega-Avila AB, Morales-Asencio JM, Garcia-Mayor S. Effectiveness of foot orthoses in patients with rheumatoid arthritis related to disability and pain: a systematic review and meta-analysis. Qual Life Res. 2018;27(12):3059–69.
da Conceição CS, Gomes Neto M, Mendes SMD, Sá KN, Baptista AF. Systematic review and meta-analysis of effects of foot orthoses on pain and disability in rheumatoid arthritis patients. Disabil Rehabil. 2015;37(14):1209–13.
Hennessy K, Woodburn J, Steultjens MPM. Custom foot orthoses for rheumatoid arthritis: a systematic review. Arthritis Care Res. 2012;64(3):311–20.
Rome K, Clark H, Gray J, McMeekin P, Plant M, Dixon J. Clinical effectiveness and cost-effectiveness of foot orthoses for people with established rheumatoid arthritis: an exploratory clinical trial. Scand J Rheumatol. 2017;46(3):187–93.
Woodburn J, Barker S, Helliwell PS. A randomized controlled trial of foot orthoses in rheumatoid arthritis. J Rheumatol. 2002;29(7):1377–83.
Gaino JZ, Bértolo MB, Nunes CS, de Barbosa CM, Landim SF, Sachetto Z, et al. The effect of foot orthoses on balance, foot function, and mobility in rheumatoid arthritis: a randomized controlled clinical trial. Clin Rehabil. 2021;35(7):1011–20.
Merola JF, Espinoza LR, Fleischmann R. Distinguishing rheumatoid arthritis from psoriatic arthritis. RMD Open. 2018;4(2):e000656.
Budiman-Mak E, Conrad KJ, Roach KE. The foot function index: a measure of foot pain and disability. J Clin Epidemiol. 1991;44(6):561–70.
Budiman-Mak E, Conrad KJ, Mazza J, Stuck RM. A review of the foot function index and the foot function index – revised. J Foot Ankle Res. 2013;6(1):5.
Landorf KB, Radford JA. Minimal important difference: values for the foot health status questionnaire, foot function index and visual analogue scale. Foot. 2008;18(1):15–9.
Ferreira-Valente MA, Pais-Ribeiro JL, Jensen MP. Validity of four pain intensity rating scales. Pain. 2011;152(10):2399–404.
Farrar JT, Young JP, LaMoreaux L, Werth JL, Poole MR. Clinical importance of changes in chronic pain intensity measured on an 11-point numerical pain rating scale. Pain. 2001;94(2):149–58.
Morris R, Stuart S, McBarron G, Fino PC, Mancini M, Curtze C. Validity of mobility lab (version 2) for gait assessment in young adults, older adults and Parkinson’s disease. Physiol Meas. 2019;40(9):095003.
Schmitz-Hübsch T, Brandt AU, Pfueller C, Zange L, Seidel A, Kühn AA, et al. Accuracy and repeatability of two methods of gait analysis - GaitRiteTM und mobility LabTM - in subjects with cerebellar ataxia. Gait Posture. 2016;48:194–201.
Washabaugh EP, Kalyanaraman T, Adamczyk PG, Claflin ES, Krishnan C. Validity and repeatability of inertial measurement units for measuring gait parameters. Gait Posture. 2017;55:87–93.
Tudor-Locke C, Camhi SM, Leonardi C, Johnson WD, Katzmarzyk PT, Earnest CP, et al. Patterns of adult stepping cadence in the 2005-2006 NHANES. Prev Med. 2011;53(3):178–81.
Tudor-Locke C, Rowe DA. Using cadence to study free-living ambulatory behaviour. Sports Med Auckl NZ. 2012;42(5):381–98.
Cohen J. Statistical power analysis for the behavioral sciences. 2nd ed. New York: Routledge; 1988. p. 567.
Cho NS, Hwang JH, Chang HJ, Koh EM, Park HS. Randomized controlled trial for clinical effects of varying types of insoles combined with specialized shoes in patients with rheumatoid arthritis of the foot. Clin Rehabil. 2009;23(6):512–21.
Conrad KJ, Budiman-Mak E, Roach KE, Hedeker D, Caraballada R, Burks D, et al. Impacts of foot orthoses on pain and disability in rheumatoid arthritics. J Clin Epidemiol. 1996;49(1):1–7.
Moreira E, Jones A, Oliveira HA, Jennings F, Fernandes A, Natour J. Effectiveness of insole use in rheumatoid feet: a randomized controlled trial. Scand J Rheumatol. 2016;45(5):363–70.
Bonanno DR, Landorf KB, Murley GS, Menz HB. Selecting control interventions for use in orthotic trials: the methodological benefits of sham orthoses. Contemp Clin Trials. 2015;42:257.
van der Leeden M, Fiedler K, Jonkman A, Dahmen R, Roorda LD, van Schaardenburg D, et al. Factors predicting the outcome of customised foot orthoses in patients with rheumatoid arthritis: a prospective cohort study. J Foot Ankle Res. 2011;4:8–8.
Baghaei Roodsari R, Esteki A, Aminian G, Ebrahimi I, Mousavi ME, Majdoleslami B, et al. The effect of orthotic devices on knee adduction moment, pain and function in medial compartment knee osteoarthritis: a literature review. Disabil Rehabil Assist Technol. 2017;12(5):441–9.
Castro-Méndez A, Munuera PV, Albornoz-Cabello M. The short-term effect of custom-made foot orthoses in subjects with excessive foot pronation and lower back pain: a randomized, double-blinded, clinical trial. Prosthetics Orthot Int. 2013;37(5):384–90.
Gélis A, Coudeyre E, Hudry C, Pelissier J, Revel M, Rannou F. Is there an evidence-based efficacy for the use of foot orthotics in knee and hip osteoarthritis? Elaboration of French clinical practice guidelines. Joint Bone Spine. 2008;75(6):714–20.
Kong L, Zhou X, Huang Q, Zhu Q, Zheng Y, Tang C, et al. The effects of shoes and insoles for low back pain: a systematic review and meta-analysis of randomized controlled trials. Res Sports Med Print. 2020;28(4):572–87.
Sagawa Y, Turcot K, Armand S, Thevenon A, Vuillerme N, Watelain E. Biomechanics and physiological parameters during gait in lower-limb amputees: a systematic review. Gait Posture. 2011;33(4):511–26.
Maddali Bongi S, Del Rosso A, Mikhaylova S, Landi G, Ferretti B, Cavigli E, et al. A comparison of two podiatric protocols for metatarsalgia in patients with rheumatoid arthritis and osteoarthritis. Clin Exp Rheumatol. 2014;32(6):855–63.
MacSween A, Brydson G, Hamilton J. The effect of custom moulded ethyl vinyl acetate foot orthoses on the gait of patients with rheumatoid arthritis. Foot. 1999;9(3):128–33.
Cameron-Fiddes V, Santos D. The effects of foot orthoses on walking stability in patients with early rheumatoid arthritis. Podiatry Rev. 2012;69(5):04–8.
Hollman JH, McDade EM, Petersen RC. Normative spatiotemporal gait parameters in older adults. Gait Posture. 2011;34(1):111–8.
König N, Taylor WR, Baumann CR, Wenderoth N, Singh NB. Revealing the quality of movement: a meta-analysis review to quantify the thresholds to pathological variability during standing and walking. Neurosci Biobehav Rev. 2016;68:111–9.
Whittaker GA, Landorf KB, Munteanu SE, Menz HB. Predictors of response to foot orthoses and corticosteroid injection for plantar heel pain. J Foot Ankle Res. 2020;13(1):60.
Scrivener K, Sherrington C, Schurr K. A systematic review of the responsiveness of lower limb physical performance measures in inpatient care after stroke. BMC Neurol. 2013;13:4.
Husted JA, Cook RJ, Farewell VT, Gladman DD. Methods for assessing responsiveness: a critical review and recommendations. J Clin Epidemiol. 2000;53(5):459–68.
Carroll M, Joyce W, Brenton-Rule A, Dalbeth N, Rome K. Assessment of foot and ankle muscle strength using hand held dynamometry in patients with established rheumatoid arthritis. J Foot Ankle Res. 2013;6(1):10.
Baan H, Dubbeldam R, Nene AV, van de Laar MAFJ. Gait analysis of the lower limb in patients with rheumatoid arthritis: a systematic review. Semin Arthritis Rheum. 2012;41(6):768–788.e8.
An HJ, Tizaoui K, Terrazzino S, Cargnin S, Lee KH, Nam SW, et al. Sarcopenia in autoimmune and rheumatic diseases: a comprehensive review. Int J Mol Sci. 2020;21(16):5678.
Harries T, Rettie R. Walking as a social practice: dispersed walking and the organisation of everyday practices. Sociol Health Illn. 2016;38(6):874–83.
Le-Masurier GC, Sidman CL, Corbin CB. Accumulating 10,000 steps: does this meet current physical activity guidelines? Res Q Exerc Sport. 2003;74(4):389–94.
Murtagh EM, Mair JL, Aguiar E, Tudor-Locke C, Murphy MH. Outdoor walking speeds of apparently healthy adults: a systematic review and meta-analysis. Sports Med Auckl NZ. 2021;51(1):125–41.
Bull FC, Al-Ansari SS, Biddle S, Borodulin K, Buman MP, Cardon G, et al. World Health Organization 2020 guidelines on physical activity and sedentary behaviour. Br J Sports Med. 2020;54(24):1451–62.
Larkin L, Gallagher S, Fraser AD, Kennedy N. Relationship between self-efficacy, beliefs, and physical activity in inflammatory arthritis. Hong Kong Physiother J. 2016;34:33–40.
Lesser IA, Nienhuis CP. The impact of COVID-19 on physical activity behavior and well-being of Canadians. Int J Environ Res Public Health. 2020;17(11):3899.
Tucker P, Gilliland J. The effect of season and weather on physical activity: a systematic review. Public Health. 2007;121(12):909–22.
Hishikawa N, Toyama S, Sawada K, Kawasaki T, Ohashi S, Ikoma K, et al. Foot orthosis treatment improves physical activity but not muscle quantity in patients with concurrent rheumatoid arthritis and sarcopenia. Mod Rheumatol. 2021;31(5):997–1003.
Dyrstad SM, Hansen BH, Holme IM, Anderssen SA. Comparison of self-reported versus accelerometer-measured physical activity. Med Sci Sports Exerc. 2014;46(1):99–106.
The authors would like to thank the rheumatologists of the CHU Hôtel Dieu of Sherbrooke for their contribution to the participants’ recruitment.
This research was funded by the Canadian MSK Rehab Research Network and supported through a donation from Janssen Pharmaceutical companies to Fondation pour la recherche et l'enseignement en orthopédie de Sherbrooke.
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The study was approved by the Institutional Review Board of the CIUSSS de l'Estrie-CHUS (2019-3182), and all the participants gave their informed consent to participate in the study.
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Walha, R., Dagenais, P., Gaudreault, N. et al. The effects of custom-made foot orthoses on foot pain, foot function, gait function, and free-living walking activities in people with psoriatic arthritis (PsA): a pre-experimental trial. Arthritis Res Ther 24, 124 (2022). https://doi.org/10.1186/s13075-022-02808-8
- Psoriatic arthritis
- Custom foot orthoses
- Foot pain
- Foot function
- Spatiotemporal parameters
- Free-living walking activities