| Literature DB >> 35928511 |
Alexandra M Kasparian1,2, Sherif M Badawy3,4.
Abstract
Background: While Fitbit® devices were initially intended for leisurely, consumer use, there has been recent interest among scientific and medical communities in the prospective use of Fitbit devices for clinical and research purposes. Those who have chronic health conditions are often required to spend considerable amounts of money and time undergoing physiological tests and activity monitoring to support, stabilize, and manage their health. This disease burden is only amplified in pediatric populations. Devices that are used to collect these data can be invasive, uncomfortable, and disconcerting. Using the Fitbit tracker to acquire such biometric data could ease this burden. Our scoping review seeks to summarize the research that has been conducted on the utilization of Fitbit devices in studies of children and adolescents with chronic health conditions and the feasibility, accuracy, and potential benefits of doing so.Entities:
Keywords: Fitbit; children; chronic health conditions; clinical outcomes; physical activity
Year: 2022 PMID: 35928511 PMCID: PMC9343978 DOI: 10.21037/mhealth-21-28
Source DB: PubMed Journal: Mhealth ISSN: 2306-9740
Search terms used for scoping review search on PubMed
| “adolescent” AND “Fitbit” |
| “child” AND “Fitbit” |
| “children” AND “Fitbit” |
| “pediatric” AND “Fitbit” |
| “teen” AND “Fitbit” |
| “teenager” AND “Fitbit” |
Figure 1PRISMA flow diagram of article search, exclusion, and extraction process. During screening, studies were excluded if they did not meet inclusion criteria and/or were review articles (most common reasons were the latter and adult populations). During eligibility, articles were excluded if, after full-text-review, they did not meet inclusion criteria.
Key data fields collected in the data extraction process
| Chronic illness |
| Objectives/aims |
| Author(s) |
| Year of publish |
| Fitbit parameter(s) |
| Fitbit accuracy |
| Study design |
| Fitbit feasibility/acceptability |
| Fitbit advantages, disadvantages, and feedback |
| Activity level changes |
| Clinical/health outcomes |
| Fitbit model |
| Study length |
| Participants (number, gender, age) ( |
Characteristics of studies examined
| Source (chronic illness) | Fitbit model | Study length | Participants | Percent male | Age (years) |
|---|---|---|---|---|---|
| Bian | Charge HR | 8 weeks | 22 | 55 | 14–17 |
| Buchele Harris | Not described | 7 weeks | 116 | 49 | ~10–11 |
| Chen | Flex | 6 months | 40 | 58 | 13–18 |
| DeBoer | Charge HR | Two 68-h periods | 12 | 50 | 5–8 |
| Do | Flex | 16 months | 22 | 45 | 8–14 |
| Dugger | Charge 2 | 10 weeks | 180 | 60 | Mean 7.9 |
| Hakim | Charge | 1 night/participant | 22 | 41 | 3–18 |
| Hasan | Charge 2 | 16 weeks | 23 | 48 | 7–21 |
| Hemphill | Charge 2 | 8 months | 109 | N/A | 9–16 |
| Hooke | One | 25 days | 16 | 31 | 6–15 |
| Jacobsen | Flex | 12 weeks | 14 | 57 | 8–12 |
| Jaimini | Not described | 1 or 3 months | 95 | N/A | 5–17 |
| Kuan | Charge 2 | 1 year | 156 | 58 | 9–16 |
| Le | One | 6 months | 15 | 33 | 15–35 |
| Mendoza | Flex | 10 weeks | 59 | 41 | 14–18 |
| Mittlesteadt | Charge 2 | N/A | 40 | 15 | 9–20 |
| Ovans | Flex | 24 weeks | 15 | 66 | 7–8 |
| Sala | Flex, One | 1 day | 39 | 59 | 4–15 |
| Schoenfelder | Flex | 4 weeks | 11 | 46 | 14–18 |
| Shelley | Flex | N/A | 9 | 44 | Mean 12 |
| Turel | Ultra, one | N/A | 94 | N/A | 10–17 |
| van der Kamp | Zip | 1 week | 30 | N/A | 4–14 |
| Venkataramanan | Not described | 1 or 3 months | 83 | N/A | 5–17 |
| Voss | Charge HR | 1 week | 30 | 47 | 10–18 |
| Yurkiewicz | Not described | 1 year | 33 | 42 | 15–29 |
ADHD, attention-deficit hyperactivity disorder; CHD, congenital heart disease; VTE, venous thromboembolism.
Objectives, methods, and reported accuracy of Fitbit of studies examined
| Source (chronic illness) | Objectives | Fitbit data collected | Fitbit accuracy | Study design |
|---|---|---|---|---|
| Bian | Explore correlation between self-rated sleep data, Fitbit sleep and PA data, and asthma impact | Steps, calories, distance, heart rate, sleep data (time in bed, awakenings) | Poor long-term sleep and PA accuracy; accurate step accuracy (cited Klassen | 8 weeks wearing Fitbit; questionnaires; monetary compensation |
| Buchele Harris | Determine intervention impacts on attention | Steps, calories, distance, heart rate | Not reported | 4-week intervention; wore Fitbit, daily 6-minute CBPA break in intervention group; attention tests |
| Chen | Evaluate intervention effects and feasibility on physical activity | Steps, calories, distance, activity, sleep minutes | Not reported | 6 months wearing Fitbit; 3-month intervention program; text messages |
| DeBoer | Assess safety and effectiveness of artificial pancreas system | Total steps, steps/min, heart rate | Not reported | Given artificial pancreas system and usual insulin pump/glucose monitor; hypoglycemic events and glucose levels monitored; wore Fitbit |
| Do | Assess sleep quality and relationship between sleep, activity, and psychosocial well-being | Steps/day, sleep efficiency, total sleep time | Sleep overreported | Baseline biometric data collected; questionnaires; 12-week intervention; 16 weeks wearing Fitbit |
| Dugger | Report obesogenic behaviors leading to BMI increase | Steps, moderate/vigorous physical activity, sedentary time, total sleep, sleep onset and offset time | Reliable and valid for heart rate and sleep (cited de Zambotti | 10 weeks wearing Fitbit; either 1) 6-week health/academic program, 4–6 weeks academic program, or no program |
| Hakim | Compare Fitbit measurements to polysomnography | Total sleep time, total wake time, number awakenings | Total sleep time overestimated; total waking time underestimated | 1 night wearing Fitbit during polysomnography |
| Hasan | Assess adherence to prescribed physical activity after VTE; evaluate QOL and biomarker changes pre- and post-intervention | Steps, distance, active minutes, hourly activity | May underestimate total activity | 16 weeks wearing Fitbit; formed physical activity and education groups; PA group had 4 weeks normal PA, 8 weeks coached PA, 4 weeks choice PA |
| Hemphill | Measure change in physical activity due to COVID-19 | Steps | Not reported | Data collected from previously ongoing study; 24 months wearing Fitbit |
| Hooke | Explore if Fitbit coaching increases steps per day | Steps/day | Not reported | 2-week intervention; wore Fitbit and Fitbit coaching; daily emails and Fitbit feedback |
| Jacobsen | Evaluate feasibility, benefits, and safety of physical activity intervention | Steps | Fitbit data matched daily activity logs | 12-week intervention; physical activity program; wore Fitbit; participant and parent surveys |
| Jaimini | Assess effects of asthma on patients using intervention physiological data | Activity, sleep | Not reported | 1- or 3-month intervention; wore Fitbit, Microlife Peak Flow Meter, and Foobot collecting data; mobile app questionnaires |
| Kuan | Evaluate seasonal variation in physical activity | Steps/day | Steps overestimated | 1 year wearing Fitbit; wore hip monitor 7 days, physical activity questionnaire |
| Le | Assess feasibility and health impact of intervention | Steps, calories, distance, overall movement, flights stairs | Not reported | 6-month intervention; wore Fitbit daily; surveys and physical evaluations |
| Mendoza | Promote physical activity in cancer survivors via intervention; assess Fitbit feasibility | Steps, energy expended, distance, minutes of high activity | Not reported | 10-week intervention; wore Fitbit, Facebook support group; post-intervention health and feasibility questionnaires |
| Mittlesteadt | Investigate Fitbit ability to detect seizure events | Heart rate | Data collected is second-order; unreliable sleep data; physiological data underestimated (cited Montgomery-Downs | Wore Fitbit; compared data to EEG data to assess seizure detection |
| Ovans | Assess impact of intervention on physical activity, quality of life, and fatigue | Steps/day | Accurate and reliable physical activity tracking (cited Diaz et al, 2015) | 12-week intervention; wore Fitbit; physical therapy sessions |
| Sala | Assess Fitbit accuracy in ambulation (wrist and hip) | Steps, distance | Wrist Fitbit steps inaccurate, hip Fitbit steps accurate | Wore Fitbit on wrist and hip; stood for 3 minutes, ambulated, sat for 3 minutes |
| Schoenfelder | Assess intervention feasibility/acceptability | Steps, energy expended, distance | Accurate step measurements (cited Evenson | 4 weeks wearing Fitbit; joined Facebook group; text messages and questionnaires |
| Shelley | Explore physical activity perceptions and assess Fitbit acceptability | Not reported | Not reported | Wore Fitbit; interviews |
| Turel | Examine association between obesity and cardiometabolic deficit to suggest intervention(s) | Sleep duration, time asleep, time awake | Sleep duration accurate | Surveys; wore Fitbit; blood test; studied Fitbit sleep measurement validity |
| van der Kamp | Assess daily physical activity in children with exercise-induced bronchoconstriction | Steps, minutes in different activity intensities | Possible inexactness due to infrequent collection rate | 1 week wearing Fitbit; daily questionnaires |
| Venkataramanan | Determine triggers to asthma using intervention physiological data | Activity, sleep | Stated Fitbit reliability | 1- or 3-month intervention; wore Fitbit, Microlife Peak Flow Meter, and Foobot collecting data; mobile app questionnaires |
| Voss | Assess validity of Fitbit data collection compared to ActiGraph | Steps minutes in different activity intensities | Steps accurate; assumed inaccurate distance | Wore ActiGraph for 7 days; wore Fitbit for 7 days; statistical analysis |
| Yurkiewicz | Investigate effect of wearable devices on health-related quality of life | Steps, calories, sleep | Not reported | 6 months wearing Fitbit, pre- and post-wearing surveys |
PA, physical activity; ADHD, attention-deficit hyperactivity disorder; CHD, congenital heart disease; BMI, body mass index; QOL, quality of life; VTE, venous thromboembolism.
Study objectives as related to respectively researched chronic health conditions
| Chronic illness (number of studies evaluated) | Seeking clinical outcome(s) | Exploring disease-related health effects | Researching Fitbit use in disease treatment |
|---|---|---|---|
| ADHD (n=2) | ✓ | ||
| Asthma (n=4) | ✓ | ✓ | |
| Cancer (n=5) | ✓ | ||
| CP (n=1) | ✓ | ||
| CHD (n=4) | ✓ | ✓ | ✓ |
| CF (n=1) | ✓ | ||
| Diabetes (n=1) | ✓ | ||
| Epilepsy (n=2) | ✓ | ✓ | ✓ |
| Obesity (n=3) | ✓ | ✓ | |
| Sleep apnea (n=1) | ✓ | ||
| VTE (n=1) | ✓ |
ADHD, attention-deficit hyperactivity disorder; CP, cerebral palsy; CHD, congenital heart disease; CF, cystic fibrosis; VTE, venous thromboembolism.
Feasibility, overall feedback, and outcomes of studies examined
| Source (chronic illness) | Demonstrated feasibility and acceptability | Advantages (A), disadvantages (D), feedback (F) | Activity changes | Clinical/health outcomes |
|---|---|---|---|---|
| Bian | Not reported | A: continuous, non-obstructive, low-cost | No change | Found potential inverse relationship between sleep quality and pediatric asthma impact—means worse sleep greater asthma impact; Fitbit potential to predict asthma symptoms |
| Buchele Harris | Not reported | Not reported | Activity increase | Improved processing speed, focused attention, concentration, attention span |
| Chen | Not reported | F: 91% participants shared Fitbit data with healthcare providers | Activity increase | Improved BMI, diastolic BP, PA, TV/computer time, consumption of fruit, vegetables, soda/sweet drinks, self-efficacy, and dietary self-efficacy; potential to improve health outcomes and reduce obesity/overweightness |
| DeBoer | Not reported | D: not designed for children (limitation) | Activity increased with artificial pancreas system | Not reported |
| Do | Feasible | F: 75% used app throughout day, 100% found Fitbit helpful in PA tracking, 88% found Fitbit helpful in diet tracking | Older participants with initially low activity more likely to increase activity | Improved sleep quality; demonstrated children with epilepsy have comparable sleep and activity patterns to children without epilepsy despite reported fatigue/sleep problems |
| Dugger | Not reported | A: long wear-time; D: consumer device limits data | Activity (sp. MVPA) increase; sedentary time decrease | Decrease in obesogenic behaviors (improved sleep, screen time, diet, PA) |
| hakim | Not reported | A: accessible | No change | Not reported |
| Hasan | Not reported | D: hard to use | No change | Improved PTS scores; lower frequency of PTS development; lower QOL |
| Hemphill | Not reported | Not reported | Activity decrease | Demonstrated possibly detrimental effects of decreased PA in at-risk population; severe impacts dependent on pandemic length; mean steps in 2019/2020 below Canadian national standard |
| Hooke | Feasible | F: families enjoyed and interested in future purchase | Increased steps per day during intervention | Increased steps associated with decreased fatigue |
| Jacobsen | Not reported | Not reported | Exercise capacity increase; VO2max increase | Parents reported improved HRQOL, social, school, psychosocial, and physical function |
| Jaimini | 66% intervention compliance, thus suitable | Not reported | No change | Improved asthma control levels |
| Kuan | Initially high acceptability; 60% adherence at completion | D: technical difficulties; skin irritations including rash and eczema | No change | Demonstrated PA increase in late spring/autumn, decrease in winter/summer; most common activities were walking and running; 11% participants met PA guidelines |
| Le | Feasible | D: fell off during exercise; F: suggested better attachment; would recommend Fitbit to survivors; 20% suggested Fitbit use in therapy; 80% after therapy | Increased MVPA by average 50 min/week | Increased number of participants meeting CDC PA recommendations |
| Mendoza | Acceptable | A: popular device, well-designed, affordable, easy, and can set goals | Activity increase | Increased motivation |
| Mittlesteadt | Compliance ensured via monitoring | A: well-known, affordable, discreet; D: syncing issues, non-compliance, wrist too small, second-order data; F: family interest in consumer device to detect seizures | No change | Not reported |
| Ovans | Intervention feasible | A: no adverse effects, cost-effective | Non-significant increase in average steps | Increased level of perceived wellness; decreased fatigue, increased quality of life |
| Sala | A: low-cost | No change | Not reported | |
| Schoenfelder | Feasible and acceptable, high adherence | Not reported | Activity increase; increase in average steps | Increased awareness of activity and ADHD symptoms; decreased average ADHD symptoms |
| Shelley | Acceptable and compliant | A: feels like regular watch, comfortable, sleek, compliance, continuity, potential activity motivator | No change | Not reported |
| Turel | Not reported | Not reported | No change | Found negative correlation between videogame addiction and sleep time, negative correlation between low sleep time and obesity; demonstrated obesity correlated to high BP, low HDL’s, high triglycerides, high insulin resistance; demonstrated adverse link between health and videogames |
| van der Kamp | 10% participants low compliance | D: low data collection frequency | Found children with EIB have less (intense) activity than those without EIB | Not reported |
| Venkataramanan | 63% intervention adherence | D: low charge could reduce measurements | Sedentary time decrease | Determined asthma triggers were pollen and PM2.5 (particulate matter) |
| Voss | Feasible and acceptable | A: at-home PA, fashionable, easy use/user-friendly, cost-effective, accessible, wrist-based technology preferred; D: non-compliance with wristwear common in adolescents; made for adults, thus pediatric accuracy unclear | No change | Demonstrated PA guideline to be ~12,500 steps/day; found participant MVPA comparable to national average; demonstrated boys more active than girls |
| Yurkiewicz | Acceptable | F: 85% enjoyed wearing | Majority felt more active | Increased number of participants meeting CDC PA recommendations |
ADHD, attention-deficit hyperactivity disorder; CHD, congenital heart disease; BMI, body mass index; PA, physical activity; PTS, postthrombotic symdrome; QOL, quality of life; MVPA, moderate to vigorous physical activity; VTE, venous thromboembolism; EIB, exercise-induced bronchoconstriction; CDC, Centers for Disease Control and Prevention.