| Literature DB >> 35457775 |
Meng Zhang1, Wei Wang2,3, Mingye Li3,4, Haomin Sheng5, Yifei Zhai1.
Abstract
Physical inactivity and sedentary behavior (SB) have attracted growing attention globally since they relate to noninfectious chronic diseases (NCDs) and could further result in the loss of life. This systematic literature review aimed to identify existing evidence on the efficacy of mobile health (mHealth) technology in inducing physical activity and reducing sedentary behavior for physically inactive people. Studies were included if they used a smartphone app in an intervention to improve physical activity and/or sedentary behavior for physically inactive individuals. Interventions could be stand-alone interventions or multi-component interventions, including an app as one of several intervention components. A total of nine studies were included, and all were randomized controlled trials. Two studies involved interventions delivered solely via a mobile application (stand-alone intervention) and seven studies involved interventions that used apps and other intervention strategies (multi-component intervention). Methodological quality was assessed, and the overall quality of the studies was ensured. The pooled data favored intervention in improving physical activity and reducing sedentary behavior. This review provided evidence that mobile health intervention improved physical activity and reduced sedentary behavior among inactive individuals. More beneficial effects can be guaranteed when interventions include multiple components. Further studies that maintain the effectiveness of such interventions are required to maximize user engagement and intervention efficacy.Entities:
Keywords: meta-analysis; mobile health; physical activity; physically inactive people; sedentary behavior
Mesh:
Year: 2022 PMID: 35457775 PMCID: PMC9031730 DOI: 10.3390/ijerph19084905
Source DB: PubMed Journal: Int J Environ Res Public Health ISSN: 1660-4601 Impact factor: 4.614
PICO for research questions.
| Concept | Description of Detail |
|---|---|
| Population | Inactive Population |
| Intervention | Mobile health intervention |
| Comparison | Control group without the mobile health intervention |
| Outcomes | Effects of mobile health intervention on physical activity and sedentary behavior |
Major search terms.
| Concept | Description of Detail |
|---|---|
| Intervention | Application OR App OR Smartphone OR Smart Phone |
| Outcomes | Sedentary OR sedentary behavior OR sedentary behavior OR sitting OR screen time OR inactive OR inactivity |
List of search strings in different digital library.
| Digital Library. | Query String | Scope | Limitation |
|---|---|---|---|
| Web of science | AB = (application OR app OR smartphone OR smartphone OR tablet) AND AB = (sedentary OR sedentary behavior OR sedentary behavior OR sitting OR screen time OR inactive OR inactivity) | Abstract | Limited to journals, English, 2006–2022 |
| CINAHL | AB = (application OR app OR smartphone OR smartphone OR tablet) AND AB = (sedentary OR sedentary behavior OR sedentary behavior OR sitting OR screen time OR inactive OR inactivity) | Abstract | Limited to journals, English, 2006–2022 |
| Scopus | (TITLE-ABS-KEY (application OR app OR smartphone OR smart AND phone OR tablet) AND TITLE-ABS-KEY (sedentary OR sedentary AND behavior OR sedentary AND behavior OR sitting OR screen AND time OR inactive OR inactivity)) AND PUBYEAR > 2006 AND (LIMIT-TO (PUBSTAGE, “final”)) AND (LIMIT-TO (DOCTYPE, “ar”) OR LIMIT-TO (DOCTYPE, “cp”)) AND (LIMIT-TO (LANGUAGE, “English”)) | Title, Abstract and keywords | Limited to journals, English, publication stage: final, 2006–2022 |
| PsychInfo | (application OR app OR smartphone OR smartphone OR tablet).tw. AND (sedentary OR sedentary behavior OR sedentary behavior OR sitting OR screen time OR inactive OR inactivity).tw. | Title and Abstract | Limited to journals, English, human, 2006–2022 |
| PubMed | (application [Title/Abstract] OR app [Title/Abstract] OR smartphone [Title/Abstract] OR smartphone [Title/Abstract] OR tablet [Title/Abstract]) AND (sedentary [Title/Abstract] OR sedentary behavior [Title/Abstract] OR sedentary behavior [Title/Abstract] OR sitting [Title/Abstract] OR screen time [Title/Abstract] OR inactive [Title/Abstract] OR inactivity [Title/Abstract]) | Title and Abstract | Limited to journals, English, human, 2006–2022 |
Figure 1PRISMA flow diagram.
Synthesis of main variables collected from RCTs (n = 9).
| Study | Study Design | Duration | Participant Characteristic | Setting | Intervention | Dependent Variables | Outcome Measure | Comparison Group |
|---|---|---|---|---|---|---|---|---|
| [ | RCT | Intervention exposure: 4 weeks | N = 26 | Home | The SmPh app allows step tacking | App impact on cardiorespiratory fitness of college-going adults | Outcome: | Traditional walking prescription |
| [ | RCT | Intervention exposure: 8 weeks | N = 95 | Home | Three mobile apps shape the user towards more physical activity and fewer daily sedentary time | App impact on daily activity and sedentary time | Outcome: | A diet-tracking control app |
| [ | 2-group | Intervention exposure: 3 week, 20 week follow-up | N = 204 | Home | (i) Behavior treatment; | The effect of Remote coaching supported by mobile tech- nology and financial incentives to improve diet and activity. | Outcome: | No control group |
| [ | 2-group | Intervention exposure: 3-week intervention and a 3 months follow-up | N = 76 | Community, workplace home | (i) Fitbit One to measure steps and provides motivational messages; | The effect of an Internet-based motivational intervention supported by pedometers on physical activity | Outcome: | Without Fitbit one and internet-based motivational intervention |
| [ | 2-group | Intervention exposure: 50-day, 20 week follow-up | N = 76 | Home | (i) Active Team app to encourage friendly rivalry within friendship group; | The effect of an online social networking physical activity intervention with pedometers delivered via Facebook app | Outcome: | Teams allocated to the control condition were placed on a waiting list to receive access to the intervention (app and pedometer) |
| [ | 2-group | Intervention exposure:12 weeks | N = 30 | Home | (i) Initial Brief In-Person Session; | The effect of mobile health intervention in promoting physical activity in Pregnant women | Outcome: | Fitbit Ultra only (accelerometer) |
| [ | 3-group | Intervention exposure:3 months | N = 210 | Home | Use the app and accelerometer for 9 months | The effects of APP on levels of physical activity | Outcome: | Control group: use accelerometer for 9 months |
| [ | 2-group | Intervention exposure: 8 weeks | N = 128 | Home | (i) ERVE smartphone app; | The effects of a smartphone app on physical activity, quality of life, self-efficacy, and exercise motivation for inactive people | Primary outcome: self-efficacy, health-related quality of life, and motivational orientation for exercise | No intervention |
| [ | 2-group RCT | Intervention exposure: 3 months | N = 650 | Primary care center | (i) 5 min of lifestyle counseling before randomization; | The effects of a smartphone app combined with a smart band on weight loss, physical activity, and caloric intake in a population with overweight and obesity | (i) Body weight; | A brief counseling only |
Figure 2Risk of bias summary.
Figure 3Meta-analysis of the effect of mobile health applications among the inactive population on (A) physical activity, (B) physical activity follow-up, and (C) sedentary behavior.
Synthesis of quality assessment of included RCTs (n = 9).
| [ | [ | [ | [ | [ | [ | [ | [ | [ | |
| Title and abstract | |||||||||
| (a) identification as randomized trial in title; (b) structured summary | 1 | 1 | 1 | 0.5 | 1 | 1 | 1 | 1 | 1 |
| Introduction | |||||||||
| (a) scientific background/rationale; (b) specific objectives/hypotheses | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| Methods | |||||||||
| Trial design: (a) description of trial design; (b) changes in methods after trial commencement | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 |
| Participants | |||||||||
| (a) eligibility criteria; (b) settings and locations of data collection | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| Interventions | |||||||||
| Descriptions of sufficient details to allow replication | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| Outcomes | |||||||||
| (a) pre-specified primary and secondary outcomes; (b) changes to outcomes after trial commencement | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 | 0.5 |
| Sample size | |||||||||
| (a) how sample size was determined; (b) if applicable, interim analysis/stopping guidelines | 0.5 | 0.5 | 0 | 0 | 0 | 0 | 0.5 | 0.5 | 0.5 |
| Randomization—sequence generation | |||||||||
| (a) method used; (b) type of randomization including any type of restriction | 0.5 | 1 | 1 | 0 | 0.5 | 0.5 | 0 | 0.5 | 0.5 |
| Allocation concealment mechanism | |||||||||
| Implementation of random allocation sequence, including concealment | 1 | 1 | 1 | 0 | 1 | 1 | 0 | 1 | 1 |
| Implementation | |||||||||
| Who generated random allocation sequence, who enrolled participants, who assigned participants | 0 | 1 | 0 | 0 | 0.5 | 1 | 0 | 1 | 1 |
| Blinding | |||||||||
| (a) if done, who was blinded and how; (b) if relevant, similarity of interventions | 0 | 0.5 | 0 | 0 | 0.5 | NA | NA | NA | NA |
| Statistical methods | |||||||||
| Statistical methods used (a) for primary outcomes; (b) additional analyses | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| Results | |||||||||
| | 1 | 1 | 1 | 0.5 | 1 | 1 | 1 | 1 | 1 |
| Recruitment | |||||||||
| (a) dates of recruitment and follow-up; (b) why the trial ended | 0.5, NA | 0.5, NA | 0.5, NA | 0.5,NA | 0.5,NA | 0.5,NA | 0.5,NA | 0.5,NA | 0.5,NA |
| Baseline data | |||||||||
| A table with baseline demographic and clinical characteristics for each group | 1 | 1 | 1 | 0 | 1 | 1 | 1 | 1 | 1 |
| Numbers analyzed | |||||||||
| For each group, number of participants included in each analyses | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| Outcomes and Estimation | |||||||||
| (a) results for each group, and the estimated effect size and its precision; (b) absolute and relative effect sizes for binary outcomes | 0.5, NA | 0.5, NA | 0, NA | 0, NA | 0.5, NA | 0.5, NA | 0.5, NA | 0.5, NA | 0.5, NA |
| Ancillary analyses | |||||||||
| Results of any other analyses performed, distinguishing pre-specified from exploratory | 1 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | 0 |
| Harms | |||||||||
| Harms or unintended effects in each group | 0 | 1 | 0 | 0 | 0 | 1 | 1 | 0 | 0 |
| Discussion | |||||||||
| Limitations Trial limitations/bias/multiplicity of analyses | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| Generalisability | |||||||||
| Generalisability (external validity/applicability) of findings | 0 | 1 | 1 | 1 | 0 | 0 | 0 | 0 | 0 |
| Interpretation | |||||||||
| Consistent with results and balanced | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 | 1 |
| Other information | |||||||||
| RegistrationRegistration number and name of registry | 1 | 1 | 0 | 0 | 1 | 0 | 1 | 0 | 1 |
| Protocol | |||||||||
| Where full trial protocol can be accessed | 0 | 1 | 0 | 0 | 1 | 1 | 1 | 0 | 1 |
| Funding | |||||||||
| Sources of funding/ role of funders | 0 | 1 | 1 | 1 | 1 | 0 | 1 | 1 | 1 |
| Study quality score attainable | 24 | 24 | 24 | 24 | 24 | 23 | 23 | 23 | 23 |
| Study quality score | 16 | 21.5 | 15.5 | 11.5 | 19 | 17 | 17.5 | 16 | 18 |
| Study quality percentage | 66.7 | 87.8 | 63.2 | 46.9 | 77.6 | 70.8 | 76.1 | 69.6 | 78.2 |
| Study quality rating | High | high | mid | low | high | High | High | High | High |