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Published on in Vol 8, No 7 (2020): July

Preprints (earlier versions) of this paper are available at https://preprints.jmir.org/preprint/19116, first published .
Effects of a 12-Week Multifaceted Wearable-Based Program for People With Knee Osteoarthritis: Randomized Controlled Trial

Effects of a 12-Week Multifaceted Wearable-Based Program for People With Knee Osteoarthritis: Randomized Controlled Trial

Effects of a 12-Week Multifaceted Wearable-Based Program for People With Knee Osteoarthritis: Randomized Controlled Trial

Authors of this article:

Linda C Li1, 2 Author Orcid Image ;   Lynne M Feehan1 Author Orcid Image ;   Hui Xie2, 3 Author Orcid Image ;   Na Lu2 Author Orcid Image ;   Christopher D Shaw4 Author Orcid Image ;   Diane Gromala4 Author Orcid Image ;   Siyi Zhu2, 5, 6 Author Orcid Image ;   J Antonio Aviña-Zubieta2, 7 Author Orcid Image ;   Alison M Hoens1, 2 Author Orcid Image ;   Cheryl Koehn8 Author Orcid Image ;   Johnathan Tam2 Author Orcid Image ;   Stephanie Therrien2 Author Orcid Image ;   Anne F Townsend9 Author Orcid Image ;   Gregory Noonan10 Author Orcid Image ;   Catherine L Backman2, 11 Author Orcid Image
Article Authors Cited by (31) Tweetations (36) Metrics

    Original Paper

    1Department of Physical Therapy, University of British Columbia, Vancouver, BC, Canada

    2Arthritis Research Canada, Richmond, BC, Canada

    3Faculty of Health Sciences, Simon Fraser University, Burnaby, BC, Canada

    4School of Interactive Art & Technology, Simon Fraser University, Burnaby, BC, Canada

    5Department of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China

    6Rehabilitation Medicine Key Laboratory of Sichuan Province, West China Hospital, Sichuan University, Chengdu, China

    7Department of Medicine, University of British Columbia, Vancouver, BC, Canada

    8Arthritis Consumer Experts, Vancouver, BC, Canada

    9Division of Health Research, Faculty of Health & Medicine, Lancaster University, Lancashire, United Kingdom

    10Mary Pack Arthritis Program, Vancouver General Hospital, Vancouver, BC, Canada

    11Department of Occupational Science & Occupational Therapy, University of British Columbia, Vancouver, BC, Canada

    Corresponding Author:

    Linda C Li, PT, PhD

    Department of Physical Therapy

    University of British Columbia

    2177 Wesbrook Mall

    Vancouver, BC, V6T 1Z3

    Canada

    Phone: 1 6042074020

    Email: lli@arthritisresearch.ca


    Background: Current guidelines emphasize an active lifestyle in the management of knee osteoarthritis (OA), but up to 90% of patients with OA are inactive. In a previous study, we demonstrated that an 8-week physiotherapist (PT)-led counseling intervention, with the use of a Fitbit, improved step count and quality of life in patients with knee OA, compared with a control.

    Objective: This study aimed to examine the effect of a 12-week, multifaceted wearable-based program on physical activity and patient outcomes in patients with knee OA.

    Methods: This was a randomized controlled trial with a delay-control design. The immediate group (IG) received group education, a Fitbit, access to FitViz (a Fitbit-compatible app), and 4 biweekly phone calls from a PT over 8 weeks. Participants then continued using Fitbit and FitViz independently up to week 12. The delay group (DG) received a monthly electronic newsletter in weeks 1 to 12 and started the same intervention in week 14. Participants were assessed in weeks 13, 26, and 39. The primary outcome was time spent in daily moderate-to-vigorous physical activity (MVPA; in bouts ≥10 min) measured with a SenseWear Mini. Secondary outcomes included daily steps, time spent in purposeful activity and sedentary behavior, Knee Injury and OA Outcome Score, Patient Health Questionnaire-9, Partners in Health Scale, Theory of Planned Behavior Questionnaire, and Self-Reported Habit Index.

    Results: We enrolled 51 participants (IG: n=26 and DG: n=25). Compared with the IG, the DG accumulated significantly more MVPA time at baseline. The adjusted mean difference in MVPA was 13.1 min per day (95% CI 1.6 to 24.5). A significant effect was also found in the adjusted mean difference in perceived sitting habit at work (0.7; 95% CI 0.2 to 1.2) and during leisure activities (0.7; 95% CI 0.2 to 1.2). No significant effect was found in the remaining secondary outcomes.

    Conclusions: A 12-week multifaceted program with the use of a wearable device, an app, and PT counseling improved physical activity in people with knee OA.

    Trial Registration: ClinicalTrials.gov NCT02585323; https://clinicaltrials.gov/ct2/show/NCT02585323

    JMIR Mhealth Uhealth 2020;8(7):e19116

    doi:10.2196/19116

    Keywords

    physical activity; counseling; knee osteoarthritis; physiotherapy; wearables 


    Background

    Arthritis is the most common cause of severe chronic pain and disability worldwide [1,2]. Analysis by the Arthritis Alliance of Canada estimates a new diagnosis of osteoarthritis (OA) every 60 seconds [3]. Current evidence supports the use of physical activity to manage OA because of its benefits on pain, mobility, and quality of life [4-6]. Guidelines by the OA Research Society International recommend the use of physical activity and therapeutic exercise as first-line treatment for knee OA [7]. Canadian physical activity guidelines recommend ≥150 min a week of moderate-to-vigorous physical activity (MVPA), performed in bouts of ≥10 min [8]. A study using accelerometers, however, found that over 90% of people with knee OA did not meet the physical activity guidelines [9]. This concurs with a systematic review that only 13% of people with OA accumulated ≥150 min per week of MVPA in bouts of ≥10 min [10].

    Several modifiable factors are associated with low physical activity participation in patients with arthritis. These include lack of motivation [11], doubts about the effectiveness of exercise [12], and lack of health professional advice [13]. To promote an active lifestyle, the use of activity tracking devices has been explored based on the assumption that providing direct feedback on the amount of physical activity encourages people to meet specific targets. A systematic review of 14 randomized controlled trials (RCTs) of accelerometer-based interventions reported a small effect on physical activity participation (standardized mean difference 0.26; 95% CI 0.04 to 0.49). Notably, consumer-grade accelerometers promote physical activity behaviors through the use of behavioral change techniques [14], such as goal setting, self-monitoring, feedback, and rewards [15]. However, effective techniques such as action planning and problem-solving are absent from the use of these devices alone [15]. These techniques require contact with a health professional with counseling experience.

    Our previous study [16] and Lyons et al [17] have demonstrated the feasibility of a physical activity counseling program with the use of a Fitbit (Fitbit Inc), a consumer-grade wearable device. Our subsequent study showed that an 8-week physiotherapist (PT)-led counseling program improved step count and quality of life in people with knee OA, compared with a control [18].

    Study Aim

    In this study, we aimed to assess the effect of a 12-week multifaceted intervention on improving activity participation in people with knee OA. Our primary hypothesis was that, compared with controls, those who received the program would increase mean daily MVPA time as determined by an objective measure. In addition, we explored the effect of the program on OA disease status, depressive symptoms, perceived habitual behaviors, and psychological constructs of being active.


    Study Design

    The Supporting Physical activity & Reducing sedentary behaviour in Arthritis (SuPRA) project was a proof-of-concept RCT with a delay-control design. Participants were randomly assigned to start the intervention either immediately (immediate group [IG]) or 14 weeks (delay group [DG]) after completing the baseline assessment. All participants were reassessed in weeks 13 (primary end point), 26, and 39 (Figure 1).

    ‎
    Figure 1. Consolidated Standards of Reporting Trials flowchart.
    View this figure

    Participants

    Participants were recruited from the Mary Pack Arthritis Program (Vancouver Coastal Health Authority) and the Fraser Health Authority in British Columbia, Canada. We also posted study information on Facebook, Twitter, Kajiji, and Craigslist. Individuals were eligible if they had a diagnosis of knee OA or met 2 criteria for early OA [19]. People with other chronic musculoskeletal conditions or contraindications to be physically active without medical supervision were excluded (Textboxes 1 and 2).

    Inclusion criteria.

    Inclusion criteria

    • Patients who had a physician-confirmed diagnosis of knee osteoarthritis or were aged ≥50 years and had felt pain or discomfort in or around the knee during the previous year lasting >28 separate or consecutive days [19]
    • Patients who had no previous diagnosis of rheumatoid arthritis, psoriatic arthritis, ankylosing spondylitis, polymyalgia rheumatica, connective tissue diseases, fibromyalgia, or gout
    • Patients who had no history of using disease-modifying antirheumatic drugs or gout medications
    • Patients who had no prior knee arthroplasty and not on a waiting list for total knee or hip replacement surgery
    • Patients who did not have surgery in the back, hip, knee, foot, or ankle joints in the past 12 months
    • Patients who had no history of acute injury to the knee in the past 6 months
    • Patients who had an email address and access to the internet daily
    • Patients who were able to attend a 1.5-hour group education session
    Textbox 1. Inclusion criteria.
    Exclusion criteria.

    Exclusion criteria

    • Patients who had previously used a physical activity wearable tracker
    • Patients who received a steroid injection in a knee in the last 6 months
    • Patients who received a hyaluronate injection in a knee in the last 6 months
    • Patients who used medication that may impair activity tolerance (eg, beta blockers)
    • Patients who faced a level of risk by exercising as identified by the Physical Activity Readiness Questionnaire [20]. If a participant did not pass the Physical Activity Readiness Questionnaire, a physician’s note was requested to determine the eligibility
    Textbox 2. Exclusion criteria.

    Randomization and Blinding

    After completing the baseline measures, participants were randomly assigned to the IG or the DG in a 1:1 allocation ratio. Randomization was performed by a research staff not involved in the study using numbers generated by SAS version 9.4 (SAS Institute Inc) in variable block sizes to ensure allocation concealment. Participants were not blinded as they knew whether they received the program during the intervention period. Daily MVPA time (the primary outcome) was measured with a wearable multisensor device couriered to the participant to wear for 7 days. All research personnel processing the objectively measured physical activity data were blinded to the participants’ group assignment. Self-reported measures were completed by the participant via a web-based questionnaire.

    Intervention

    The intervention has 3 components: (1) an in-person session with 20 min of group education and 30 min of individual counseling with a PT, (2) the use of a Fitbit Flex-2 wristband, and (3) PT counseling by phone to review physical activity goals (20-30 min). The in-person session was held in a meeting room at either the Mary Park Arthritis Centre, Fraser Health Authority, or Arthritis Research Canada. Fitbit is a consumer-grade wearable device that tracks and displays steps walked, gross level of physical exertion, and time spent being active. It is easy for users to put on and remove for charging. Fitbit Flex-2 is splash proof but cannot be used during water-based activities (eg, shower, swimming). Participants may record activities not captured by the device on the Fitbit website. Participants could view their physical activity goal attainment on FitViz, a new Fitbit-compatible web-based app developed for this study [21].

    All 8 study PTs completed a 2-day basic training in motivational interviewing at the University of British Columbia [22]. In addition, they attended an orientation session, received a counseling guide, and shadowed at least one education and counseling session before they were paired with a participant.

    Participants in the IG were scheduled to attend a PT-led group education session that focused on physical activity in OA management and strategies to manage joint symptoms. Next, each participant was paired with the next available study PT. During the individual counseling, PTs used the Brief Action Planning approach [23] to guide participants to set specific, measurable, attainable, relevant, and time-bound (SMART) physical activity goals. An example of a SMART goal is “attending a pool exercise class in a community center every Tuesday and Saturday for the next three months.”

    Study PTs then set the parameters on their assigned participants’ FitViz accounts based on the participant’s goals. These parameters included the following: (1) the upper and lower limits of intensity and duration of MVPA (ie, to promote physical activity based on the participant’s goal), (2) the duration when a sedentary behavior should be interrupted (ie, to promote less sitting), and (3) the rest time in between sessions of MVPA (ie, to promote pacing).

    During weeks 1 to 8, the study PT remotely reviewed participants’ progress on FitViz and counseled them to modify their physical activity goals via 4 biweekly phone calls. A counseling guide was provided, and the discussion was documented by the PT. During weeks 9 to 12, participants continued using their Fitbit and FitViz but had no counseling calls with their PTs. However, participants could email their PTs if there were questions related to being physically active. At the end of the program, participants could keep their Fitbit and FitViz account.

    The DG received the same intervention in week 14. During the waiting period, they received monthly emails of arthritis news that were unrelated to physical activity.

    Outcome Measures

    The primary outcome measure was mean daily MVPA time measured with SenseWear Mini (BodyMedia Inc). SenseWear integrates triaxial accelerometer data, physiological sensor data, and personal demographic information to provide estimates of steps and energy expenditure. A strong relationship has been found between SenseWear and indirect calorimetry measures of energy expenditure for activities of daily living (Pearson r=0.85) [24]. The device can be worn 24 hours a day and can capture a full picture of physical activity and off-body time throughout the day [25]. An important feature of SenseWear is its ability to differentiate between sedentary and light physical activities [26]; hence, it is an ideal instrument to assess both active and sedentary behaviors.

    Participants wore a SenseWear Mini over the triceps for 7 days at each assessment. Almeida et al [27] determined that a minimum of 4 days of wear was required to reliably assess energy expenditure from different levels of physical activity in people with rheumatoid arthritis (intraclass correlation coefficient >0.80). We calculated the average MVPA accumulated in bouts (min per day). A bout was defined as ≥10 min at the level of ≥3 metabolic equivalent of the task (MET), with an allowance for interruption of up to 2 min below the threshold [28].

    The secondary outcomes included the following:

    1. Average daily time in purposeful activity performed in ≥4 MET in bouts of ≥10 min, with allowance for interruption of up to 2 min below the threshold (eg, brisk walking) [29].
    2. Average daily step count.
    3. Average daily time in sedentary behavior performed in ≤1.5 MET in bouts of ≥20 min during waking hours [30-33].
    4. Knee Injury and OA Outcome Score (KOOS) [34,35].
    5. Partners in Health Scale (PIHS) [36].
    6. Theory of Planned Behavior Questionnaire [37,38].
    7. Patient Health Questionnaire-9 (PHQ-9) [39].
    8. Self-Reported Habit Index [40,41].

    We used SenseWear to measure purposeful activity time, steps, and sedentary behavior time. The KOOS consists of 5 subscales: pain, symptoms, activities of daily living, sports/recreation, and knee-related quality of life. It was originally developed for people recovering from injuries such as the anterior cruciate ligament and meniscus injury and was validated in patients with OA [34,35]. The PIHS is a 12-item measure designed to assess self-efficacy, knowledge of health conditions and treatment, and self-management behavior, such as adopting a healthy lifestyle (Cronbach α=.82) [36]. Motivation for engaging in physical activity was measured using the Rhodes 7-point Likert-type Theory of Planned Behavior questionnaire [37,38]. The questionnaire consists of 16 items measuring all components of the theory. Previous studies using this measure showed good predictive validity and internal consistency in adult populations [37,38].

    The PHQ-9 consists of 9 questions that correspond to the diagnostic criteria for major depressive disorder. A score greater than 11 indicates a major depressive disorder [39]. The Self-Reported Habit Index is a 12-item scale, rated on a 7-point Likert scale, which measures characteristics of habitual behavior (reliability minimum α=.81) [40,41]. We asked participants to rate their strength of habit for 3 specific activity-related behaviors: sitting during leisure time at home, sitting during usual occupational activities, and walking outside for 10 min. A higher score indicates a stronger habit or behavior that is done frequently and automatically. Demographic variables and comorbid conditions were collected at baseline.

    Adverse Event and Intervention Fidelity Monitoring

    We tracked adverse events (falls as well as cardiovascular and musculoskeletal events) related to their physical activity [42] in the follow-up questionnaire at weeks 13, 26, and 39. Participants were deemed adhering to the 12-week intervention protocol if they (1) attended the education session, (2) used their Fitbit ≥5 days per week in ≥11 weeks, and (3) participated in ≥3 of 4 counseling calls. We monitored participants’ Fitbit wear using FitViz, which wirelessly synchronized physical activity data recorded by a Fitbit 150 times per hour [43]. We calculated the percentage of participants meeting each criterion and all 3 criteria.

    Data Analysis

    Descriptive analysis was used to summarize participant characteristics and comorbid conditions. We performed an intention-to-treat analysis using SAS version 9.4. The analysis of covariance (ANCOVA) was used for the main analysis to estimate an adjusted mean difference comparing time in MVPA (primary outcome) at 13 weeks between groups, adjusting for baseline MVPA and blocking. In a secondary analysis, we used a longitudinal mixed effects model that allowed us to additionally examine the intervention effects at 26 and 39 weeks after intervention initiation. The mixed effects models included the following variables as fixed effects: (1) the randomization group indicator for baseline difference, (2) a set of indicator variables for follow-up assessment time points (weeks 13, 26, and 39) to account for secular trend, and (3) a set of indicator variables for the lengths of time since intervention initiation (weeks 12, 25, or 38) to estimate intervention effects after these amounts of time postintervention initiation. The models additionally included participants as random effects to account for the repeated measures nature of the data. We used the sandwich estimators for linear mixed models [44] to compute empirical standard errors that were robust to model specifications. We examined the secondary outcomes at 13 weeks using ANCOVA and over weeks 26 and 39 using the mixed effects models mentioned earlier.

    Sample Size

    We estimated that our collaboration with health authorities and patient groups allowed the study to recruit 60 eligible participants within 12 months. Our previous study of a similar physical activity counseling program resulted in an estimated MVPA time of 75.5 min per day (SD 54.3) in the intervention group and 50.0 min per day (SD 46.8) in the controls [18]. Assuming approximately 15% attrition, we anticipated that 50 of the 60 participants would complete the study. With a sample size of 50, we would have 74% power at an α level of 0.1 (via a one-sided test).

    Ethics

    The research protocol was approved by the University of British Columbia Behavioural Research Ethics Board (application number: H15-02038) and published in ClinicalTials.gov (NCT02585323).


    Baseline Characteristics

    In the years 2017 to 2019, 253 people indicated an interest to participate, and 221 met the eligibility criteria (Figure 1). Of these, we recruited 51 participants (IG: 23/26, 88% were women; DG: 19/25, 76% were women). Both groups were similar in age (IG: mean 65.0, SD 8.3 years; DG: mean 64.8, SD 9.0 years) and BMI (IG: mean 29.8, SD 9.0 kg/m2; DG: mean 28.9, SD 6.2 kg/m2). Approximately 55% (28/51) of the participants did not meet the Canadian physical activity guidelines at baseline (Table 1).

    Table 1. Baseline characteristics of participants.
    VariablesAll (N=51)Immediate group (n=26)Delay group (n=25)
    Women, n (%)42 (82)23 (89)19 (76)
    Age (years), mean (SD)64.9 (8.5)65.0 (8)64.8 (9)
    Marital status, n (%)

    		Married/common law30 (59)18 (69)12 (48)

    		Separated/divorced10 (20)5 (19)5 (20)

    		Widowed/never married/other11 (22)3 (12)8 (32)
    University degree or trades certificate, n (%)25 (49)14 (54)11 (44)
    Gross annual household income (US $), n (%)

    		≤24,0002 (4)0 (0)2 (8)

    		24,001-40,0006 (12)2 (8)4 (16)

    		40,001-60,0009 (18)4 (15)5 (20)

    		60,001-80,0008 (16)4 (15)4 (16)

    		80,001-100,0007 (14)5 (19)2 (8)

    		>100,0007 (14)3 (12)4 (16)

    		No answer12 (24)8 (31)4 (16)
    Diagnosed with OAa, n (%)

    		Yes37 (73)20 (77)17 (68)

    		No, but met the likely OA criteria14 (28)6 (23)8 (32)
    In general, would you say your health is,n (%)

    		Excellent6 (12)1 (4)5 (20)

    		Very good14 (27)10 (39)4 (16)

    		Good22 (43)11 (42)11 (44)

    		Fair8 (16)3 (12)5 (20)

    		Poor1 (2)1 (4)0 (0)
    Compared with 1 year ago, how would you rate your health in general now? n (%)

    		Much better3 (6)1 (4)2 (8)

    		Somewhat better8 (16)4 (15)4 (16)

    		About the same24 (47)11 (42)13 (52)

    		Somewhat worse16 (31)10 (39)6 (24)

    		Much worse0 (0)0 (0)0 (0)
    Number of comorbid conditions, median (25th, 75th percentile)3.0 (2.0, 5.0)4.0 (3.0, 5.0)3.0 (2.0, 4.0)
    BMI (kg/m2), mean (SD)29.4 (7.7)29.8 (9.0)28.9 (6.2)
    Participants did not meet the Canadian physical activity guideline (≥150 min of MVPAb in bouts of ≥10 min per week), n (%)28 (55)15 (58)13 (52)

    aOA: osteoarthritis.

    bMVPA: moderate-to-vigorous physical activity.

    Comparison of the Immediate Group With Delay Group

    Table 2 and Figure 2 present the results of the primary outcome from 4 time points. At baseline, the mean MVPA time was 31.0 min per day (SD 37.3) for the IG and 71.3 min per day (SD 99.8) for the DG. The DG accumulated significantly more MVPA time—2 outliners accumulated a mean of >300 min per day (Figure 3). At 13 weeks (the primary end point), the IG accumulated a mean MVPA of 37.7 min per day (SD 30.5), whereas the DG had 49.4 min per day (SD 63.6). The adjusted mean difference in time spent in MVPA between groups following the intervention at 13 weeks was 13.1 min per day (95% CI 1.6 to 24.5), favoring the IG. Analyses adjusted for blocking yielded nearly identical results; thus, it was removed from subsequent analyses. A secondary analysis using a mixed effects model revealed smaller intervention effects at 12 weeks (9.4 min per day; 95% CI −3.0 to 21.7), 25 weeks (−3.0 min per day; 95% CI −34.9 to 29.0), and 38 weeks (0.2 min per day; 95% CI −44.0 to 44.4) postprogram initiation (Table 3).

    Table 2. Participant outcomes and results of the primary analysis.
    MeasuresImmediate group, mean (SD)Delay group, mean (SD)Adjusted difference in mean change at T0-T1
    Baseline (T0; n=26)13 weeks (T1; n=24)26 weeks (T2; n=22)39 weeks (T3; n=20)Baseline (T0; n=25)13 weeks (T1; n=24)26 weeks (T2; n=22)39 weeks (T3; n=23)Mean difference (95% CI)P value
    Time in MVPAa,b (min)31.0 (37.3)37.7 (30.5)37.0 (32.3)34.0 (25.2)71.3 (99.8)49.4 (63.6)74.6 (102.1)54.8 (66.2)13.1 (1.6 to 24.5).03
    Time in purposeful activityc (min)11.1 (19.5)13.3 (20.0)13.7 (18.8)12.8 (16.8)42.1 (80.2)23.1 (37.1)36.5 (62.6)22.0 (42.3)1.6 (−3.0 to 6.1).50
    Daily steps6294.0 (3418.0)7133.3 (3603.3)6381.6 (3492.0)5845.3 (2575.5)7030.1 (3921.6)6232.7 (3086.1)8162.3 (6642.3)7445.1 (4713.2)1106.5 (−19.9 to 2232.9).05
    Sedentary timed (min)567.5 (183.1)531.4 (173.5)492.5 (156.6)502.8 (135.3)551.1 (234.9)558.3 (224.9)499.5 (248.9)483.1 (225.4)−29.5 (−75.8 to 16.7).21
    Knee Injury and Osteoarthritis Outcome Score (0-100; higher=better)
    Symptoms68.5 (10.7)69.3 (12.7)65.4 (45.8)68.4 (16.3)e65.7 (12.3)66.9 (14.9)f72.2 (16.8)g72.5 (13.3)g−1.4 (−7.8 to 4.9).66
    Pain72.6 (13.5)73.1 (15.3)72.5 (18.3)72.1 (19.8)e65.1 (13.7)65.9 (15.6)f74.8 (15.4)g72.8 (13.2)g2.5 (−4.2 to 9.5).49
    Activity of daily living75.5 (14.7)75.0 (13.1)77.7 (18.9)74.8 (20.7)e72.2 (15.8)70.3 (16.9)f80.3 (13.1)g80.0 (14.0)g2.8 (−3.3 to 8.8).37
    Sports and recreation47.9 (23.7)47.1 (22.4)50.5 (30.1)51.6 (30.4)e46.8 (25.4)52.5 (22.7)f62.5 (22.5)g55.8 (26.3)g−3.8 (−14.9 to 7.2).50
    Quality of life44.0 (16.0)48.7 (17.5)49.4 (15.7)49.3 (19.1)e47.5 (16.0)46.9 (13.6)f54.7 (14.7)g54.4 (14.6)g1.4 (−5.0 to 7.9).66
    Partners in Health (0-96; higher=better)76.8 (11.0)76.7 (11.5)78.9 (9.0)81.0 (7.0)e78.0 (12.0)81.6 (9.6)f82.6 (9.3)g82.6 (10.0)g−2.3 (−6.6 to 1.9).28
    Patient Health Questionnaire-9 (0-27; lower=better)5.2 (4.6)4.0 (3.0)3.6 (3.3)4.2 (4.1)e5.4 (5.3)4.7 (4.9)f4.5 (5.2)g4.5 (5.3)g−0.4 (−1.7 to 0.8).47
    Self-Reported Habit Index (1-7; higher=stronger habit)
    Sitting at work subscale5.0 (1.4)5.2 (1.6)4.7 (2.1)5.0 (1.9)e4.5 (2.1)4.4 (2.0)f4.3 (2.1)g4.1 (2.1)g0.7 (0.2 to 1.2).004
    Sitting at leisure subscale4.8 (1.1)5.1 (1.1)5.0 (1.1)5.5 (1.1)e5.1 (1.4)4.7 (1.6)f4.4 (1.9)g4.7 (1.7)g0.7 (0.2 to 1.2).006
    Walking subscale4.3 (1.8)4.4 (1.6)4.6 (1.8)4.7 (1.8)e4.8 (2.0)4.6 (2.0)f4.8 (1.6)g4.6 (1.8)g0.3 (−0.3 to 0.9).27
    Theory of Planned Behavior Questionnaire (1-7; higher=more positive)
    Attitude toward physical activity6.0 (0.6)5.9 (0.7)6.0 (0.5)6.0 (0.5)e6.1 (0.6)6.1 (0.7)f6.2 (0.6)g6.1 (0.7)g−0.1 (−0.4 to 0.2).63
    Subjective norm6.2 (0.6)6.2 (0.8)6.1 (0.8)6.2 (1.1)e6.3 (0.8)6.2 (0.7)f6.3 (0.8)g6.3 (0.7)g0.2 (−0.1 to 0.5).13
    Perceived control5.8 (1.0)5.6 (1.4)5.6(1.5)5.7 (1.4)e6.1 (0.7)5.8 (1.2)f6.2 (1.0)g6.2 (0.9)g0.1 (−0.6 to 0.8).80
    Intention6.2 (0.8)5.9 (1.0)5.7 (1.1)5.8 (0.8)e6.3 (0.8)6.4 (0.6)f6.4 (0.6)g6.3 (0.9)g0.1 (−0.1 to 0.3).22

    aMVPA: moderate-to-vigorous physical activity.

    bMVPA was performed at ≥3 metabolic equivalent of tasks and in bouts ≥10 min.

    cPurposeful activity was performed at ≥4 METs and in bouts ≥10 min.

    dSedentary behavior was performed at ≤1.5 METs in bouts ≥20 min.

    en=19.

    fn=22.

    gn=24.

    ‎
    Figure 2. Time in moderate-to-vigorous physical activity.
    View this figure
    ‎
    Figure 3. Boxplot of time in moderate-to-vigorous physical activity at baseline and 13 weeks.
    View this figure
    Table 3. Results of mixed effects models.
    MeasuresIntervention effect postprogram initiation (95% CI)Secular trend (95% CI)

    		12 weeks25 weeks38 weeksT2a effect vs T1bT3c effect vs T1
    Time in MVPAd,e (min)9.4 (−3.0 to 21.7)−3.0 (−34.9 to 29.0)0.2 (−44.0 to 44.4)11.9 (−12.4 to 36.1)6.4 (−29.7 to 42.5)
    Time in purposeful activityf (min)1.5 (−8.4 to 11.5)−9.0 (−33.5 to 15.5)−6.8 (−42.3 to 28.6)10.0 (−8.0 to 28.0)6.9 (−21.3 to 35.1)
    Daily steps1461.2 (433.8 to 2488.6)715.0 (−1995.9 to 3425.9)71.4 (−4063.6 to 4206.3)101.7 (−2142.6 to 2346.0)336.9 (−3261.7 to 3935.4)
    Sedentary timeg (min)−32.2 (−78.1 to 13.7)−62.6 (−162.8 to 37.6)−63.4 (−217.6 to 90.8)−19.8 (−83.7 to 44.1)−7.6 (−117.0 to 101.9)

    		Symptoms−2.2 (−8.2 to 3.4)−12.4 (−22.6 to −2.2)−21.1 (−36.8 to −5.4)6.1 (0.2 to 11.9)16.5 (6.2 to 26.9)

    		Pain0.3 (−6.2 to 6.8)−7.8 (−19.7 to 4.1)−15.1 (−33.1 to 3.0)7.5 (1.3 to 13.8)13.7 (2.0 to 25.4)

    		Activity of daily living1.1 (−5.0 to 7.1)−4.6 (−16.2 to 7.0)−13.2 (−32.0 to 5.6)8.1 (2.7 to 13.6)13.5 (2.1 to 24.9)

    		Sports and recreation−7.4 (−18.7 to 3.9)−21.2 (−42.4 to 0.1)−27.2 (−59.2 to 4.9)16.5 (5.1 to 27.9)23.6 (2.5 to 44.7)

    		Quality of life2.4 (−4.6 to 9.3)−2.1 (−13.6 to 9.4)−6.9 (−24.8 to 11.0)4.8 (−3.2 to 12.7)9.0 (−3.2 to 21.2)
    Partners in Health (0-96; higher=better)−1.7 (−5.7 to 2.4)−3.8 (−10.9 to 3.3)−4.2 (−15.2 to 6.8)3.4 (−1.1 to 7.9)5.6 (−2.7 to 13.9)
    Patient Health Questionnaire-9 (0-27; lower=better)−0.9 (−2.4 to 0.6)−1.3 (−4.0 to 1.3)−1.3 (−5.5 to 2.9)0.1 (−1.2 to 1.5)0.6 (−2.2 to 3.3)

    		Sitting at work subscale0.4 (−0.3 to 1.1)0.3 (−1.1 to 1.6)0.6 (−1.5 to 2.7)−0.5 (−1.2 to 0.3)−0.5 (−1.9 to 0.9)

    		Sitting at leisure subscale0.6 (0.1 to 1.0)1.4 (0.5 to 2.4)2.4 (0.9 to 3.9)−1.0 (−1.6 to −0.4)−1.5 (−2.5 to −0.4)

    		Walking subscale0.3 (−0.3 to 0.9)0.4 (−0.6 to 1.4)0.7 (−1.1 to 2.4)0 (−0.6 to 0.5)−0.3 (−1.4 to 0.8)

    		Beliefs toward physical activity−0.1 (−0.4 to 0.2)−0.2 (−0.7 to 0.3)−0.3 (−1.1 to 0.4)0.2 (−0.1 to 0.4)0.2 (−0.4 to 0.7)

    		Subjective norm0.1 (−0.3 to 0.5)0.0 (−0.6 to 0.6)0.1 (−0.9 to 1.1)0.0 (−0.4 to 0.4)0.0 (−0.6 to 0.6)

    		Perceived control0.0 (−0.6 to 0.7)−0.4 (−1.6 to 0.7)−0.7 (−2.5 to 1.1)0.3 (−0.3 to 1.0)0.8 (−0.3 to 2.0)

    		Intention−0.4 (−0.7 to −0.1)−1.1 (−1.7 to −0.4)−1.5 (−2.6 to −0.5)0.4 (0.1 to 0.7)1.0 (0.3 to 1.7)

    aT2: 26-week assessment.

    bT1: 13-week assessment.

    cT3: 39-week assessment.

    dMVPA: moderate-to-vigorous physical activity.

    eMVPA was performed at ≥3 metabolic equivalent of tasks and in bouts of ≥10 min.

    fPurposeful activity was performed at ≥4 METS and in bouts of ≥10 min.

    gSedentary behavior was performed at ≤1.5 METS in bouts of ≥20 min.

    For the secondary outcome, a trend favoring the IG, but not statistically significant, was found from baseline to 13 weeks in purposeful activity time (1.6 min per day; 95% CI −3.0 to 6.1), step count (1106.5; 95% CI −19.9 to 2232.9), and sedentary time (−29.5 min per day; 95% CI −75.8 to 16.7). The results from the KOOS, PIHS, and PHQ-9 were also not statistically significant (Table 2). We found a small effect in perceived sitting habit while at work (0.7; 95% CI 0.2 to 1.2) or during leisure activities (0.7; 95% CI 0.2 to 1.2).

    Secondary analysis demonstrated an effect attributable to being in the program for daily steps at 12 weeks (1461.2; 95% CI 433.8 to 2488.6; Table 3). Knee symptoms (measured by the KOOS symptoms subscale), perceived sitting habit during leisure activities, and intention to be physically active also showed statistically significant effects attributable to being in the program for different durations, although statistically significant secular trends were also observed over the assessment period.

    Intervention Adherence and Adverse Events

    Intervention adherence in the IG was 100% (26/26) for education session attendance, 96% (25/26) for PT counseling phone calls, and 81% (21/26) for Fitbit use (Table 4). In all, 81% (21/26) of participants met all 3 fidelity criteria. Adherence rates were similar in the DG when participants received the program in week 13. During the 4 weeks when the PT counseling ended, 2 participants each from the IG and the DG contacted their study PT via email with further questions regarding their physical activity.

    After starting the program, 10 of the 51 participants reported adverse events because of physical activity; of those, 7 reported muscle pain (IG: n=5 and DG: n=2). Falls were reported by 3 in the IG; of those, 2 fell while being physically active (1 had an ankle sprain). Three participants from the DG also reported a fall; 1 occurred while being physically active. Of the remaining 2 participants who had a fall, 1 sustained a vertebral compression fracture.

    Table 4. Summary of intervention adherence.
    Adherence criterionImmediate group (n=26), n (%)Delay group (n=25), n (%)All (N=51), n (%)
    Attended the initial session with group education and met with a physiotherapist to set physical activity goals26 (100)25 (100)51 (100)
    Completed ≥3 of 4 counseling phone calls with a physiotherapist25 (96)22 (88)47 (92)
    Met Fitbit use criteriaa ≥11 weeks out of the 12-week intervention period21 (81)20 (80)41 (80)
    Met 2 of 3 criteria25 (96)24 (96)49 (96)
    Met all 3 criteria21 (81)18 (72)39 (77)

    aParticipants had steps recorded in their Fitbit ≥5 days per week.


    Principal Findings

    More than 1 in 6 people in the United States are using wearable devices to monitor their health [45], but the integration of these tools in chronic disease management is at an early stage. This study demonstrated the potential of a multifaceted wearable-based program for promoting MVPA in people with knee OA. We found an effect in the adjusted mean difference in time spent in MVPA between groups after the 12-week program. Furthermore, the mixed effects model analysis suggests a significant effect in daily steps attributable to the program.

    These results, however, should be viewed in the context that the DG accumulated significantly more daily MVPA time than the IG at baseline, and the observed effect was primarily driven by a decline in daily MVPA time in the DG at week 13. More than 80% of participants rated their health as “good,” “very good,” or “excellent” at baseline, suggesting that they might have few health constraints to be physically active. Nonetheless, the results extend those of our previous RCT on a similar program, whereby a significant improvement in participation in physical activity was found in people with knee OA at the end of an 8-week intervention [18]. We also found a small effect on the awareness of sitting habits at work and during leisure activities at 13 weeks. The reason for this observation is unclear, but it is likely too small to be clinically important.

    Our results contribute to the literature on physical activity promotion in arthritis management. Recommendations by the European League Against Rheumatism endorse the use of behavior change techniques to promote physical activity among people with arthritis [46]. The 2019 American College of Rheumatology/Arthritis Foundation guidelines further highlight the involvement of health professionals, including PTs, to deliver nonpharmacological treatment [47]. The optimal approach for supporting an active lifestyle in people with arthritis remains to be unclear, but research in healthy adults has shown that low-dose health coaching had little effect on physical activity behavior [48]. Although PTs are skilled in exercise prescription, a recent survey in Canada revealed up to 71% of the respondents wished to acquire further training in physical activity counseling.[49] This suggests an opportunity for professional development for PTs to master skills in counseling techniques that match their patients’ readiness to acquire a health-related behavior. In our study, training on motivational interviewing and the opportunity to shadow a PT with experience in counseling participants are essential to the program. The PTs’ written record for each interaction with participants allowed us to ensure that counseling followed the Brief Action Planning approach. Participants continuing to use their Fitbits suggests that the behavior of self-monitoring was sustained even after the PT counseling ended. Future research can refine and compare different implementation strategies of physical activity counseling for this population.

    Strengths and Limitations

    A strength of this study was intervention fidelity, with an overall intervention adherence of 81%. There is no consensus on what constitutes good intervention adherence, but 80% to 100% has been deemed as high fidelity in delivery [50]. Furthermore, more than 80% of participants adhered to Fitbit use over the 12-week period, indicating that it is feasible to transition individuals from a multifaceted program to a wearable-only intervention after the initial 8-week counseling from a PT.

    This study has some limitations. With the use of a delay-control design in which the participants in the control arm received the program after a 13-week delay, the efficacy of the counseling program could only be unequivocally assessed at 13 weeks. At 26 and 39 weeks, both groups had already received the intervention, and there was an absence of a control group at these 2 time points, which can cause intervention effect estimates at 26 and 39 weeks to be less robust and more susceptible to small sample bias. Hence, the long-term effects of the program remain unclear. Furthermore, the results may not be generalizable to men because 82% of the participants were women.

    Conclusions

    Supporting a physically active lifestyle is a core component of physiotherapy practice. The Exercise is Medicine initiative advocates for the creation and worldwide implementation of effective physical activity promotion strategies in treatment plans for patients [51]. With the ubiquitous use of wearables, health professionals can leverage the use of these tools to motivate, monitor, and counsel people with arthritis to reach physical activity goals. To this end, we have shown that a 12-week multifaceted counseling program, with the use of a wearable device, can improve physical activity participation in people with knee OA.

    Acknowledgments

    The authors would like to thank Navi Grewal, Morgan Barber, Ankit Gupta, Juliane Chien, Eric C Sayre, Hussein Mamdani, and Amrit Sandhu for their important contributions to this project. The authors would also like to thank Jacob McIvor for his support with the SenseWear Mini data processing. LCL was supported by the Harold Robinson/Arthritis Society Chair in Arthritic Diseases award, the Canada Research Chair Program, and the Michael Smith Foundation for Health Research Scholar Award. HX was supported by the Maureen and Milan Ilich/Merck Chair in Statistics for Arthritis and Musculoskeletal Diseases award. JAAZ was supported by the BC Lupus Society Research Scholar and the Walter & Marilyn Booth Research Scholar. DG was supported by the Canada Research Chair Program during the study. SuPRA project was funded by the Canadian Institutes of Health Research (CIHR; KAL-135772) and Preventing Complications from Inflammatory Skin, Joint and Bowel Conditions, a CIHR team grant (THC-135235). The latter provided funding for the development of FitViz and statistical analysis for the RCT. The funders had no role in the study design, collection, analysis, and interpretation of data; in the writing of the manuscript; and in the decision to submit the manuscript for publication.

    Authors' Contributions

    LCL, LMF, CDS, DG, AMH, CK, JAAZ, AFT, GN, and CLB obtained funding. LCL, LMF, HX, CDS, DG, AMH, JAAZ, AFT, GN, and CLB contributed to the study design and proposal. LCL contributed to study oversight. LCL, SZ, JT, and ST contributed to data collection. LCL, LMF, HX, and NL analyzed the data. LCL, LMF, HX, NL, and AMH interpreted the data. LCL, LMF, HX, NL, CDS, DG, SZ, JAAZ, AMH, CK, JT, ST, AFT, GN, and CLB reviewed the manuscript.

    Conflicts of Interest

    None declared.

    ‎
    Multimedia Appendix 1

    CONSORT checklist.

    PDF File (Adobe PDF File), 735 KB
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    ‎
    ANCOVA: analysis of covariance
    CIHR: Canadian Institutes of Health Research
    DG: delay group
    IG: immediate group
    KOOS: Knee Injury and Osteoarthritis Outcome Score
    MET: metabolic equivalent of task
    MVPA: moderate-to-vigorous physical activity
    OA: osteoarthritis
    PHQ-9: Patient Health Questionnaire-9
    PIHS: Partners in Health Scale
    PT: physiotherapist
    RCT: randomized controlled trial
    SMART goal: specific, measurable, attainable, relevant, and time-bound goal
    SuPRA: Supporting Physical activity & Reducing sedentary behaviour in Arthritis

    Edited by G Eysenbach; submitted 04.04.20; peer-reviewed by R Warty, AS Aslam, G Signorelli; comments to author 27.04.20; revised version received 01.05.20; accepted 03.06.20; published 03.07.20

    Copyright

    ©Linda C Li, Lynne M Feehan, Hui Xie, Na Lu, Christopher D Shaw, Diane Gromala, Siyi Zhu, J Antonio Aviña-Zubieta, Alison M Hoens, Cheryl Koehn, Johnathan Tam, Stephanie Therrien, Anne F Townsend, Gregory Noonan, Catherine L Backman. Originally published in JMIR mHealth and uHealth (http://mhealth.jmir.org), 03.07.2020.

    This is an open-access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work, first published in JMIR mHealth and uHealth, is properly cited. The complete bibliographic information, a link to the original publication on http://mhealth.jmir.org/, as well as this copyright and license information must be included.