| Literature DB >> 32706685 |
Matilda Swee Sun Tang1, Katherine Moore1, Andrew McGavigan1,2, Robyn A Clark3,4, Anand N Ganesan1,2,4.
Abstract
BACKGROUND: Wearable trackers are an increasingly popular tool among healthy adults and are used to facilitate self-monitoring of physical activity.Entities:
Keywords: healthy adults; physical activity; randomized controlled trials; wearable activity tracker
Mesh:
Year: 2020 PMID: 32706685 PMCID: PMC7407266 DOI: 10.2196/15576
Source DB: PubMed Journal: JMIR Mhealth Uhealth ISSN: 2291-5222 Impact factor: 4.773
Figure 1PRISMA Flow Chart.
Characteristics of participants in the included studies.
| Study name, publication year | Sample size | Participant characteristics | Study duration (weeks) | ||
|
|
| Health status | Mean age (years) | Proportion |
|
| Ashe, 2016 [ | 25 | Healthy participants | 40.1 | Women: 100% | 26 |
| Buis, 2017 [ | 40 | Healthy overweight adults | 61.5 | Women: 66%; white ethnicity: 66% | 12 |
| Cadmus-Bertram, 2015 [ | 51 | Healthy and overweight participants | 60.0 | White ethnicity: 92% | 16 |
| Godino, 2013 [ | 466 | Healthy participants | 47.7 | Women: 46%; white ethnicity: 96% | 8 |
| Hurling, 2007 [ | 77 | Healthy participants | 40.3 | Women: 66%; white ethnicity: 99% | 9 |
| Jakicic, 2016 [ | 471 | Healthy overweight adults | 30.9 | Women: 71%; white ethnicity: 77% | 104 |
| Martin, 2015 [ | 49 | Healthy overweight adults | 58.0 | Women: 46%; white ethnicity: 79% | 5 |
| Melton, 2016 [ | 69 | Healthy participants | 19.7 | Women: 100%; black ethnicity: 100% | 6 |
| Poirier, 2007 [ | 264 | Healthy participants | 39.9 | Women: 66%; white ethnicity: 77% | 7 |
| Shrestha, 2013 [ | 28 | Healthy overweight adults | 32.1 | Women: 54% | 26 |
| Thompson, 2014 [ | 49 | Healthy participants | 79.1 | Women: 91%; white ethnicity: 66% | 26 |
| Thorndike, 2014 [ | 104 | Healthy participants | 29.0 | Women: 54% | 12 |
Characteristics of intervention and comparators of included studies.
| Study Name, Year | Intervention Device | Intervention | Comparator |
| Ashe, 2016 [ | Fitbit | 26 weeks of group-based education, social support, individualized physical activity prescription, given Fitbit | 26 weeks: only received health-related information |
| Buis, 2017 [ | Jawbone Up24 | Received a Jawbone Up24 monitor, a tablet with Jawbone Up app installed, and brief weekly telephone counseling | Waitlist control (did not receive any intervention until after their final assessment where they were provided the intervention in full) |
| Cadmus-Bertram, 2015 [ | Fitbit | 16 weeks of Web-Based Tracking Group: Fitbit, instructional session, follow-up call at the fourth week | 16 weeks of standard pedometer |
| Godino, 2013 [ | Combined HR monitor and accelerometer (Actiheart) | 8 weeks of wearing of Actiheart with one of three different types of feedback (simple, visual, contextualized) | 8 weeks of wearing of Actiheart but with no feedback until the end of the trial |
| Hurling, 2007 [ | Wrist-worn accelerometer | 9 weeks of wristworn accelerometer, weekly exercise schedule, email reminders, real-time feedback via the internet | 9 weeks of wrist-worn accelerometer with no feedback |
| Jakicic, 2016 [ | FIT Core; BodyMedia | 24 weeks of enhanced intervention: wearable technology, accompanying web interface to monitor diet and physical activity | 24 weeks of standard intervention: website for self-monitoring of diet and physical activity |
| Martin, 2015 [ | Fitbug Orb | 3-arm study Phase 1 (1 week): blinded run-in Phase 2 (2 weeks): unblinded versus blinded tracking Phase 3 (2 weeks): smart texts versus no texts | Blinded participants with no feedback |
| Melton, 2016 [ | Jawbone UP | 6 weeks of wearing Jawbone UP band and engaging with the application daily with weekly reminders | 6 weeks of using MyFitnessPal application |
| Poirier, 2007 [ | Variety of activity trackers | 2-arm study 6 weeks of walking program, Walkadoo, and wireless activity tracker 1 week of follow-up with wearing of activity tracker for at least 10 hours a day | 2-arm study 6 weeks of not wearing activity trackers and maintaining daily activity routine 1 week of follow-up wearing of activity tracker for 10 hours a day |
| Shrestha, 2013 [ | Polar FA20 accelerometer | 1 time 1.5-hour lifestyle instruction and 26 weeks of continuous accelerometer use and feedback | 26 weeks of self-directed exercise and/or US Army mandated physical training |
| Thompson, 2014 [ | Fitbit | 26 weeks of accelerometer use and feedback, weekly brief telephone counseling sessions focused on accelerometer feedback, 6 in-person brief counseling sessions | 26 weeks of accelerometer without feedback |
| Thorndike, 2014 [ | Fitbit e3 | 2-arm study Phase 1: 6 weeks RCTa comparing daily steps displaying feedback about steps and energy consumed Phase 2: 6 weeks non-RCT team steps competition where all participants wore monitors with feedback | 2-arm study Phase 1: 6 weeks blinded monitor Phase 2: 6 weeks non-RCT team steps competition where all participants wore monitor with feedback |
aRCT: randomized controlled trial.
Figure 2Forest plot of standardized mean difference (95% CI) in the effect of wearable trackers on physical activity.
Figure 3Forest plot of standardized mean difference (95% Cl) in the effect of wearable trackers on steps/day.
Figure 4Forest plot of standardized mean difference (95% Cl) in the effect of wearable trackers on weight loss for intervention and control group.
Figure 5Forest plot of standardized mean difference (95% CI) in the effect of wearable trackers on physical activity in overweight adults.
Figure 6Forest plot of standardized mean difference (95% CI) in the effect of wearable trackers on healthy adults.
Figure 7GRADE Working Group grades of evidence summary.
Risk of bias (Cochrane Critical Appraisal Skills Program Toola).
|
| Q1 | Q2 | Q3 | Q4 | Q5 | Q6 | Q7 | Total score/7 | Quality Score, % |
| Ashe, 2016 [ | Lb | L | Hc | Ud | H | L | L | 4.5 | 64 |
| Buis, 2017 [ | L | L | U | U | U | L | L | 5.5 | 79 |
| Cadmus-Bertram, 2015 [ | L | L | L | U | U | U | H | 4.5 | 64 |
| Godino, 2013 [ | L | L | L | U | L | L | L | 6.5 | 93 |
| Hurling, 2007 [ | L | L | L | U | H | L | L | 5.5 | 79 |
| Jakicic, 2016 [ | L | L | L | U | L | L | L | 6.5 | 93 |
| Martin, 2015 [ | L | L | L | U | H | L | L | 5.5 | 79 |
| Melton, 2016 [ | L | L | L | L | U | L | L | 6.5 | 93 |
| Poirier, 2007 [ | L | L | H | U | L | L | L | 5.5 | 79 |
| Shrestha, 2013 [ | L | H | L | L | L | L | L | 6 | 86 |
| Thorndike, 2014 [ | L | U | L | L | H | U | L | 5 | 71 |
| Thompson, 2014 [ | L | H | L | U | L | L | L | 6 | 86 |
| Category Score (%) | 100 | 88 | 79 | 45 | 54 | 88 | 100 |
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aCochrane risk of bias tool. Q1: Were there selection bias (biased allocation to interventions) due to inadequate generation of a randomized sequence? Q2: Were there selective bias (biased allocation to interventions) due to inadequate concealment of allocations prior to assignment? Q3: Were there reporting bias due to selective outcome report? Q4: Were there bias due to problems not covered elsewhere in the table? Q5: Were there performance bias due to knowledge of the allocated interventions by participants and personnel during the study? Q6: Were there detection bias due to knowledge of the allocated interventions by outcome assessors? Q7: Were there attribution bias due to amount, nature, or handling or incomplete outcome data?
bL: low risk.
cH: high risk.
dU: unclear risk.