Accepted Manuscript Validity of commercial activity trackers in children with congenital heart disease Christine Voss, PhD, Ross F. Gardner, Paige H. Dean, BSc, Kevin C. Harris, MD, MHSc PII:
S0828-282X(16)31147-3
DOI:
10.1016/j.cjca.2016.11.024
Reference:
CJCA 2325
To appear in:
Canadian Journal of Cardiology
Received Date: 12 August 2016 Revised Date:
14 November 2016
Accepted Date: 28 November 2016
Please cite this article as: Voss C, Gardner RF, Dean PH, Harris KC, Validity of commercial activity trackers in children with congenital heart disease, Canadian Journal of Cardiology (2017), doi: 10.1016/ j.cjca.2016.11.024. This is a PDF file of an unedited manuscript that has been accepted for publication. As a service to our customers we are providing this early version of the manuscript. The manuscript will undergo copyediting, typesetting, and review of the resulting proof before it is published in its final form. Please note that during the production process errors may be discovered which could affect the content, and all legal disclaimers that apply to the journal pertain.
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TITLE PAGE
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Validity of commercial activity trackers in children with congenital heart disease
Christine Voss, PhD; Ross F Gardner; Paige H Dean, BSc; Kevin C Harris, MD, MHSc
Dr. Kevin Harris Children’s Heart Centre BC Children’s Hospital 1F27 – 4480 Oak Street Vancouver, BC V6H 3V4 Phone: 604-875-3878 Fax: 604-875-3463 Email:
[email protected]
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Correspondence:
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Division of Cardiology, Department of Pediatrics, University of British Columbia, Canada (all authors)
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Short title: Activity tracker validation in children with CHD
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Word count excluding brief summary, word count, and short title: 4,734
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BRIEF SUMMARY In this validation study of a commercial activity tracker in children, including those with CHD,
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we found that the device provides results that were generally reflective of overall physical activity levels and can identify those meeting physical activity guidelines. These findings are important given the increasing emphasis on physical activity promotion and monitoring in
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children with cardiovascular risk factors.
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ABSTRACT Background: Increasing physical activity levels is a high priority to optimize long-term health in
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children with congenital heart disease (CHD). Commercial activity trackers have been validated in adults and are increasingly used to measure and promote physical activity in pediatric populations, but they have not been validated in children.
Methods: In 30 children with CHD aged 10-18yrs, we assessed the validity of physical activity
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form the wrist-based Fitbit Charge HRTM against hip-based ActiGraph accelerometers under free
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living conditions for 7 days. We assessed the association between devices by intra-class correlation coefficients and Bland-Altman plots. Receiver-operating curves were used to identify Fitbit step cut-points.
Results: There was a strong association between the two devices for daily steps across 138
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analysed person-days (ICC=0.855, p<0.001), but poorer agreement for time spent in physical activity intensities (ICCs<0.7). Daily Fitbit steps of ≥12,500 identified meeting physical activity guidelines defined as ≥60 min MVPA/day. Fitbit devices recorded more steps than
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accelerometers (-2,242 steps/d, 95%LoA of -7,738 to 3,253). Between-device differences were greater in boys vs. girls. Fitbit devices were worn for longer than accelerometers (-36 min/d,
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95%LoA -334 to 261), but overall differences in wear time explained little of the variance in step differences (7%, p=0.048).
Conclusions: Commercial activity trackers provide opportunities to remotely monitor physical activity in children with CHD, but absolute values may differ from accelerometers. These findings are important given the increasing emphasis on physical activity promotion and monitoring in children with cardiovascular risk factors.
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KEY WORDS
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Congenital Heart Disease, Children, Pediatric, Physical Activity, Fitbit, ActiGraph
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INTRODUCTION Physical activity is increasingly recognized as an important behaviour to optimize long-term cardiovascular health and quality of life in children with congenital heart disease (CHD),1,2 who
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are at increased cardiovascular risk.3 Commercial activity trackers hold promise as a tool to measure, prescribe and promote physical activity. Several studies are already taking advantage of commercial trackers to measure and/or promote physical activity in both healthy and clinical
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pediatric populations,4-6 including children with CHD.7 While the validity and reliability of
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commercial trackers has been extensively documented in adults,8 no previous research has established the validity of such devices in children. This is an important shortcoming, given that it is unclear if children’s sporadic bursts of activity9 are adequately quantified by commercial trackers that are designed for adults and optimized to capture walking.10 The objective of the current study was to assess the validity of physical activity from a commercial activity tracker
Sample
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METHODS
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against a research-grade accelerometer under free living conditions in children with CHD.
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We included a convenience sample of 40 participants aged 10-18yrs recruited from the Children’s Heart Centre at BC Children’s Hospital in Vancouver, BC and provincial partnership clinics. We obtained institutional ethics approval, parental consent and participant assent. Cardiac diagnoses were: 1) CHD; categorized as mild, moderate or severe11, 2) cardiac transplant, 3) electrophysiological disorders, or 4) none (e.g. innocent murmur). Nurses measured height (0.1 cm) and weight (0.1 kg). BMI was expressed according to WHO norms12 and categorized according to International Obesity Task Force criteria.13
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Criterion measure: ActiGraph accelerometer We fitted participants with an ActiGraph accelerometer (GT3X+, GT9X; ActiGraph LLC, Pensacola, FL; sampling at 30Hz) to be worn over the right hip and instructed them to wear it
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continuously for the next 7 days and to only remove it for water-based activities,
showering/bathing and sleep. The ActiGraph is widely used to objectively measure physical
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activity in children under free-living conditions.14
Test measure: Fitbit activity tracker
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We chose Fitbit Charge HRTM (Fitbit) for our study. Studies in children have exclusively used Fitbit models (without validation),4-7 and we expected that the appeal of using one of the market leaders would benefit compliance in our study. Wristband size and placement were in accordance with manufacturer’s guidelines. We asked participants to wear the Fitbit continuously during the
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same 7 days as the accelerometer. We created anonymous Fitbit user profiles (online
valid in children).
Data processing
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‘dashboard’) and disabled displays of ‘calories burned’ and ‘distance travelled’ (unlikely to be
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We used ActiLife v.6.13.2 (ActiGraph LLC, Pensacola, FL) to analyse accelerometry files (15s epoch). Valid days were defined as ≥600 min/d wear time (allowing for ≤60min of zero activity) and moderate-to-vigorous physical activity was calculated (MVPA; ≥2296 CPM; includes vigorous).15 Sedentary time was expressed as a percentage relative to wear time.16 Mean physical activity values were based on ≥1 valid days (inclusion criterion for validation analyses); we also used conservative wear time criteria of ≥3 weekdays and ≥1 weekend day(s) to estimate general physical activity levels.17 We defined meeting guidelines as mean daily MVPA ≥60 min/d.18 For
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Fitbit data, we used the ‘Data Export’ function on the ‘dashboard’ to extract steps and physical activity intensities (sedentary, light, fair, and very). MVPA was defined as ‘fair + very’ and sedentary time was expressed relative to wear time. A sub-sample were managed through
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Fitabase (Small Steps Labs LLC, San Diego, CA; www.fitabase.com), a fee-for-service online platform that facilitates access to multiple Fitbit devices simultaneously and provides high
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resolution minute-by-minute data exports.
We created a person-day dataset of matched ActiGraph and Fitbit data on valid accelerometry
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days (≥600 min/d). For a subset of person-days with high-resolution data (n=20), we estimated Fitbit wear time using a modified data analyses package in ‘R’ that processes minute-by-minute accelerometry data (‘accelerometry’, v. 2.2.5, May 2015). First, we re-produced the ActiLife wear time results for accelerometry data by this method, and yielded similar results (815 vs. 809
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min/d). Second, we repeated step 1 using accelerometry steps rather than ‘counts’ to establish that steps can serve as a wear time metric, and yielded similar results (821 vs. 815 min/d). Third, we analysed the minute-by-minute Fitbit steps to determine Fitbit wear time.
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Statistical Analysis
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Descriptive statistics (frequencies (%), mean±SD, median (IQR)) were calculated for applicable variables. Between-sex differences were assessed by independent t-tests, Mann-Whitney U Ranked Sum test, or Pearson’s chi-squared test. Associations and agreement between devices were assessed by intra-class correlation coefficients (ICC) and Bland-Altman plots. The between-device difference (bias and 95% Limits of Agreement, LoA) was defined as ‘criterion measure (accelerometer)’ minus ‘test measure (Fitbit)’. The mean absolute percent error was calculated as ‘mean between-device difference / mean criterion measure *100’. Receiver
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operating curves (ROC) were drawn using Fitbit steps as the classifier and meeting physical activity guidelines (≥60 min/d of MVPA from accelerometry) as the true-status reference; the coordinate with the greatest sum of sensitivity and specificity was used to identify the Fitbit step
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cut-point with discriminatory value.19 Because meaningful between-day variations in physical activity levels are expected within individuals, we treated valid days as independent observations and used a person-day dataset using actual days rather than hypothetical mean days for validation
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analyses. We conducted sensitivity analyses using a reduced dataset (mean values per person) to rule out undue influences of related observations within individuals. Analyses were carried out
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using Stata (v.14.1, Stata Corp LP, College Station, TX) or R (x64 3.3.1, The R Foundation for Statistical Computing) and significance was set at p<0.05.
RESULTS
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Sample characteristics
Thirty participants had at least one day of matching accelerometry and Fitbit data. Four participants did not wear both devices at the time and 6 did not have any valid data, which is
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unsurprising considering that non-compliance with accelerometer wear is commonly observed in adolescents.20,21 There were no significant differences for sample characteristics between the
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analytical sample and those who were excluded, nor were there significant sex-differences (Table 1). Similarly to what was previously reported for children with CHD,22 23% were overweight or obese, which is comparable to national data in healthy children.21 Mean MVPA (based on ≥1 valid day) was 45 min/d, which was similar to national data for similarly aged children and adolescents (~50 min).21 Physical activity levels were not meaningfully different when computed according to conservative wear time inclusion criteria of ≥3 weekdays and
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≥1weekend day (e.g. 47 min/d MVPA, available for n=24 individuals). We acknowledge a lack of expected sex-differences in MVPA, which was likely explained by inter-personal differences and the wide age range of our relatively small sample. Because the aim of the current study was
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to assess the agreement between two devices, we do not consider the heterogeneous physical activity levels of our sample a limitation. We defined adherence to physical activity guidelines as
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mean daily MVPA ≥60 min/d and 25% met physical activity guidelines.
Validity: association and agreement between ActiGraph accelerometer and Fitbit
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We included 138 valid person-days (mean per person: 4.6 days, range: 1-7). We conducted detailed assessments between Fitbit and accelerometer results for physical activity metrics, including steps and time spent in physical activity intensities. The strongest between-device agreement was observed for daily steps (ICC=0.855, p<0.001; Figure 1), which did not vary
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notably between sexes or age groups. However, the Fitbit devices recorded more steps than the accelerometers (10,383±5,321 vs. 8,141±4,023 steps/d; p<0.001). The mean bias was -2,242 steps/d, although between-device differences were highly varied (95%LoA of -7,738 to 3,253;
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Figure 1). The mean absolute percent error was 28%, which is higher than the ≤10% error that is desired for valid step estimates under free-living conditions.23 The mean bias for daily steps was
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greater in boys (-3,320 steps/d; 95%LoA -7,643 – 1,003; 39% MAP) than girls (-1,389 steps/d; 95%LoA -7,133 – 4,356; 18% MAP; Figure 1). An example day illustrating differences in hourly and cumulative steps between devices is found in Figure 2.
Compared with steps, agreement between devices was notably lower for time spent in physical activity intensities (all ICCs<0.66; online supplement Table S1 and Figure S1). Discrepant results are likely explained by methodological differences. For example, the Fitbit records only
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MVPA that is accrued in bouts of ≥10 min duration,24 which is in line with adult physical activity guidelines25 but not current guidelines for children18 and thus not how we calculated MVPA based on accelerometry. This explains person-days where the accelerometer registered
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some MVPA but the Fitbit did not. In contrast, the Fitbit registered substantially more MVPA than the accelerometer on other person-days, which was almost exclusively observed in younger children. The proprietary Fitbit algorithm categorises MVPA as ≥3METs, which in turn is
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derived from estimated caloric expenditure based on movement, age, sex, height and weight.24 Energy cost of activity is greater in children than in adults,26 and it is unclear if and how the
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Fitbit algorithm corrects for this in our younger participants. Fitbit also states that the heart rate feature does ‘a better job of recognizing active minutes’,26 but it is not disclosed how this is done. Sedentary time was the only activity intensity metric that yielded agreement between devices that was comparable to steps (ICC=0.845, p<0.001). However, we faced challenges
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regarding data availability and the need for additional data manipulation when the Fitbit was not worn over night (see online supplement for details) which currently limits the usefulness of this metric. All analyses were performed on person-day datasets that were unadjusted for multiple
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observations per person; we found similar results using a reduced person-level data-set (not
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shown), confirming that no meaningful within-person effects necessitated adjustments.
Diagnostic values of Fitbit devices to identify adherence to physical activity guidelines A ROC curve was created using Fitbit steps as the classifier and meeting physical activity guidelines (≥60 min MVPA based on accelerometry) as the true-status reference (Figure 3). The ROC area under the curve was 0.82 (95%CI 0.74-0.90). The coordinate with the greatest sum of sensitivity and specificity (cut-point that identifies meeting guidelines) was 12,562 steps/d.
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Device wear time analyses and its effect on validity
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Out of a possible 20 participants who had their devices managed through Fitabase, high resolution minute-by-minute Fitbit data were available for 15 participants and 55 person-days. Infrequent Fitbit syncing resulted in some loss of high resolution data. Validation results were
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similar in this sub-sample compared with the entire sample (ICC=0.908; bias -2,236). On average, Fitbits were worn for 36 minutes longer than ActiGraphs (Fitbit 866 min/d vs.
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accelerometer 830 min/d), although differences in wear time were highly varied (95%LoA -334 to 261). Girls wore both devices for longer (844 min/d vs. Fitbit 906 min/d) compared with boys (ActiGraph: 813 min/d vs. Fitbit 821 min/d), although neither sex-difference was statistically significant (ActiGraph p=0.288 and Fitbit p=0.060). Differences in wear time between devices
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tended to be greater in girls (-62 min/d, 95%LoA -294 to 170) than in boys, but the variance was also greater in boys(-7.8 min/d, 95%LoA -360 to 344). Within either device, wear time was not related to steps (ActiGraph r2=0.015, p=0.368; Fitbit r2=0.003, p=0.708). Between-device
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differences in wear time was a significant correlate of between-device differences in steps, but explained only 7% of the variance (r2=0.072, p=0.048). On days were the two devices had
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similar wear time (n=12; ±30 min) the bias in steps was -1,854 (95%LoA -4,815 to 1,107).
DISCUSSION
In children with CHD, we assessed the validity of the Fitbit Charge HRTM - a wrist-worn commercial tracker - to estimate physical activity. We demonstrated a strong correlation between the Fitbit and the ActiGraph for daily steps, and importantly, we identified a cut-point of ~12,500
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Fitbit steps/d to correspond to meeting physical activity guidelines (≥60 minutes MVPA/d from accelerometry), which will have utility for clinical practice and future research.
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Physical activity – a cornerstone of health Physical activity during childhood is of paramount importance for optimal cardio-metabolic health27 and mental well-being,28 and active children are more likely stay active as adults.29 We
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are facing a physical inactivity crisis where fewer than 1 in 10 Canadian children are meeting physical activity guidelines.21 For children with CHD, who are at high cardiovascular risk as a
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consequence of their condition,3 there has been an urgent call for action to promote physical activity to optimize long-term cardiovascular health and quality of life in these individuals.1,2 Innovative strategies are needed to engage these children and their families in health promotion.
Utility of commercial activity trackers in children in clinical practice and research
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Exercise training programs are effective at improving physical activity levels in children with CHD,30 but access to such programs is typically limited to those residing near metropolitan areas. Considering the relevance of technology for our young patients, the role of commercial activity
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trackers for remote / home-based physical activity promotion is already being explored.4,6,7
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Commercial trackers such as the Fitbit offer several advantages over research-grade activity devices: 1) aesthetically pleasing and user-friendly hardware; 2) appealing user-experience through the online ‘dashboard’; 3) cost-effective and readily available; 4) no specialist software and/or data processing expertise necessary; 5) wrist-based, a preferred device location in children and youth.31 In addition, services such as Fitabase can streamline the remote management of multiple users at once. This is important to effectively facilitate exercise prescription, where
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continuous remote monitoring of participant activity levels are needed in order to provide tailored feedback and recommendations.
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Validity of Fitbit devices in children The target consumer group for commercial trackers are adults, whose most common activity is walking.32 Fitbit algorithms are “designed to look for motion patterns most indicative of people
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walking”.10 No previous research has validated the Fitbit in children, but adult studies
consistently demonstrate good validity for steps under free-living conditions.8,33-35 Children
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engage in sporadic bouts of high intensity activity,9 and it is unclear to what extent, if any, these differences in activity patterns may impact algorithms to accurately identify physical activity. We found agreement between devices was most consistent for daily steps – a physical activity metric that most closely resembles total activity rather than intensity. The poorer agreement for time spent in physical activity intensities is in part explained by the Fitbit only recording MVPA
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bouts of ≥10 min duration (in line with adult guidelines),24 and the interpretation of Fitbit MVPA being further complicated by undisclosed proprietary algorithms drawing on estimates of caloric
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expenditure that may not be valid in children.
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Sex differences in Fitbit validity: wear time or physical activity? Between-device step differences in steps were nearly twice as great in boys as in girls. We investigated whether this was explained by poorer compliance in boys. Girls tended to wear both devices for longer than boys, but it is the girls who were less consistent with wearing both devices equally, and clearly favouring the Fitbit. Regardless, wear time differences overall explained only a small portion of the variance in step differences (7%), and a sub-analyses of person-days with similar device wear time still registered a substantial between-device step
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difference (-1,854). Thus, we do not believe that device wear time is an important factor affecting our validation results.
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Physical activity volume and patterns could instead play a role in our observed sex-differences. Our physical activity data hints at well-documented sex-differences in physical activity, with boys generally being more active than girls.36 In addition to more sporadic bursts of high
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intensity activity in children compared with adults,9 boys commonly play games, whereas girls frequently walk for leisure.37 Walking is an activity that Fitbits are optimized to capture,10 which
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could explain the more favourable step results in girls. The notion that boys may engage more in higher intensity, sustained play/games is supported by our finding that between-device agreement for MVPA was good for boys (ICC=0.824), but poorer for the sample overall (ICC=0.657; Table S1).
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Strengths, limitations and future directions
This is the first validation study of commercial activity trackers in children. Our analyses identified the daily Fitbit steps as the most suitable metric for use in children, in line what has
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been found for adults.8 Our sample was a convenience sample of patients attending pediatric
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cardiology clinics and most had CHD. We previously found that our CHD patients are as active as healthy Canadians of the same age and sex, and thus believe the current findings are of relevance to the wider pediatric community.
We acknowledge that there was considerable variance in our results. For example, we found that while the Fitbit recorded on average 2,242 more steps than accelerometers did, 95%LoA indicated that there was considerable variability. A certain degree of variance is to be expected in
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a context where children are tasked with collecting behavioural data under free living conditions, and are acceptable in light of the strong correlations we observed.
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It is a limitation that we did not assess the validity of the Fitbit against a direct measure of physical activity (e.g. direct observation) and/or energy expenditure (e.g. indirect calorimetry), but instead against a widely used accelerometer14 and associated MVPA cut-points that are based
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on indirect calorimetry in children.15 Adult validation studies reported different device
performance between controlled, laboratory-based treadmill walking and running versus free-
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living conditions;8,35 thus, validation under free-living conditions is clearly warranted. However, (unknown) differences in device wear time can impact validation studies under such conditions. We used algorithms to identify non-wear from a lack of movement signal, but different devices may have different thresholds as to what acceleration signal constitutes a step, for example. More
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direct measures of wear time are desirable, such as skin sensors in the newer ActiGraph models (optimized for wrist placement). For Fitbits, the continuous heart rate feature has potential to identify wear time, but access to the fee-for-service Fitabase and advanced data processing skill
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are required.
We did not assess intra- or inter-device reliability of the Fitbit, but this has been reported
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elsewhere.e.g. 38 There are currently no published studies of the Fitbit Charge HRTM, likely due to the discrepancy between the fast-paced release of new commercial trackers and the lag in research and peer-reviewed scientific publication. Fewer adult studies have assessed the newer wrist-based Fitbit models, and although they performed well, they were typically inferior to the hip-based models.e.g. 35 It is possible that hip-based Fitbit models yield more comparable results
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to the ActiGraph in children. However, children favour wrist-based over hip-based devices,31 and the importance of compliance should be carefully evaluated against the need for accuracy.
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CONCLUSION In children with CHD, commercial activity trackers can provide general estimates of physical activity using daily step counts, and a cut-point of ~12,500 Fitbit steps/d relates to meeting
ACKNOWLEDGEMENTS
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prescribe and monitor physical activity in children.
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physical activity guidelines (defined as ≥60 min MVPA/d). Fitbits may be useful to remotely
We are grateful to the participants and their families who participated in this research. We thank the nurses, administrative staff and research staff at the Children’s Heart Centre and our
FUNDING SOURCES
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partnership clinics for their support.
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We received funding form the Heart and Stroke Foundation of Canada (F1504) and the Child &
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Family Research Institute, University of British Columbia.
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33. Tully MA, McBride C, Heron L, Hunter RF. The validation of Fibit Zip physical activity monitor as a measure of free-living physical activity. BMC Res Notes. 2014; 7:952. 34. Ferguson T, Rowlands AV, Olds T, Maher C. The validity of consumer-level, activity monitors in healthy adults worn in free-living conditions: a cross-sectional study. Int J Behav Nutr Phys Act. 2015; 12:42. 35. Kooiman TJ, Dontje ML, Sprenger SR, et al. Reliability and validity of ten consumer activity trackers. BMC Sports Sci Med Rehabil. 2015; 7:24. 36. Nader PR, Bradley RH, Houts RM, McRitchie SL, O'Brien M. Moderate-to-vigorous physical activity from ages 9 to 15 years. JAMA. 2008; 300:295-305.
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37. Fakhouri TH, Hughes JP, Burt VL, et al. Physical activity in U.S. youth aged 12-15 years, 2012. NCHS Data Brief. 2014:1-8.
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38. Dontje ML, De Groot M, Lengton RR, Van der Schans CP, Krijnen WP. Measuring steps with the Fitbit activity tracker: An inter-device reliability study. J Med Eng Tech. 2015; 39:286-90.
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Figure 1. Association between daily steps measured by accelerometer and Fitbit
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Scatter plot (A) and Bland-Altman plot (B) for the overall sample (n=138 person-days, n=30 individuals). Note the strong correlation between the two devices (A, dotted line), while a significant bias suggests that the Fitbit measured more steps than the accelerometer. There was systematic bias, whereby the differences between devices were greater at higher total steps. Note the outliers likely indicate that the accelerometer was worn for longer than the Fitbit, which we confirmed in wear time analyses.
Figure 2. Example day of a participant’s hourly steps by accelerometer and Fitbit Note how the Fitbit registers more steps at almost every hour of the day, which significantly amplifies the total cumulative steps for the day.
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Figure 3. Receiver-operating curve identifying a Fitbit step cut-point. Fibit steps ≥12,500 steps/d identify those who meet physical activity guidelines (defined as ≥60 min/d based on accelerometry).
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