| Literature DB >> 28386652 |
Kristin Wick1,2, Claudia S Leeger-Aschmann3, Nico D Monn3, Thomas Radtke3, Laura V Ott3, Cornelia E Rebholz3, Sergio Cruz3, Natalie Gerber3, Einat A Schmutz3, Jardena J Puder4,5, Simone Munsch6, Tanja H Kakebeeke7, Oskar G Jenni7, Urs Granacher1, Susi Kriemler8.
Abstract
BACKGROUND: Proficiency in fundamental movement skills (FMS) lays the foundation for being physically active and developing more complex motor skills. Improving these motor skills may provide enhanced opportunities for the development of a variety of perceptual, social, and cognitive skills.Entities:
Keywords: Fundamental Movement Skill; High Effect Size; Locomotor Skill; Motivational Climate; Motor Skill
Mesh:
Year: 2017 PMID: 28386652 PMCID: PMC5603621 DOI: 10.1007/s40279-017-0723-1
Source DB: PubMed Journal: Sports Med ISSN: 0112-1642 Impact factor: 11.136
Intervention characteristics of included studies
| Study | Design | Target population | Setting; participants (mean age ± SD, years) | Assessmenta | Intervention program | Overview resultsb |
|---|---|---|---|---|---|---|
| Alhassan et al. [ | Cluster-randomized controlled trial | Ethnic minority preschoolers | Preschool centers | FMS: TGMD-2 (LMS) | Duration: 6 months | FMS: leaping INT > CON; remaining tests INT ≈ CON |
| Bellows et al. [ | Cluster-randomized controlled trial | Preschool-aged children | Head Start centers | FMS: PDMS-2 (totFMS, OCS, LMS) | Duration: 18 weeks | FMS: INT > CON |
| Bonvin et al. [ | Cluster-randomized controlled trial | Young children aged 2–4 years | Childcare centers | FMS: adapted ZNA (totFMS) | Duration: 9 months | FMS: INT ≈ CON |
| Delic [ | Controlled trial | Kindergarten children | Preschool center | FMS: TGMD | Duration: 10 weeks | FMS: INT > CON |
| Derri et al. [ | Randomized controlled trial | Preschool children | No information about setting | FMS: TGMD (LMS) | Duration: 10 weeks | FMS: galloping, leaping, horizontal jump, skipping INT > CON; remaining tests INT ≈ CON |
| Donath et al.c [ | Cluster-randomized controlled trial | Kindergarten children | Kindergartens | FMS: TGMD-2 (OCS) | Duration: 6 weeks | FMS: total sum score, stationary dribbling INT > CON; remaining tests INT ≈ CON |
| Goodway and Branta [ | Clustered controlled trial | Disadvantaged preschool children | Preschool classes | FMS: TGMD (OCS, LMS) | Duration: 12 weeks | FMS: INT > CON |
| Goodway et al. [ | Cluster-controlled trial | Pre-kindergarten children at risk for DD | Pre-kindergarten | FMS: TGMD (OSC, LMS) | Duration: 9 weeks | FMS: INT > CON |
| Hamilton et al. [ | Clustered controlled trial | Preschool children at risk for DD | Preschool classes | FMS: TGMD (OCS) | Duration: 8 weeks | FMS: INT > CON |
| Hardy et al. [ | Cluster-randomized controlled trial | Preschool-aged children | Preschools and long-day care centers | FMS: TGMD-2 (totFMS, OCS, LMS) | Duration: 20 weeks | FMS: INT ≈ CON |
| Hashemi et al. [ | Controlled trial | Preschool girls from non-affluent families without post-graduate education | Kindergartens | FMS: TGMD-2 (OCS) | Duration: 6 weeks | FMS: INT > CON |
| Hurmeric [ | Cluster-randomized controlled trial | Preschool children | Head Start centers | FMS: TGMD-2 (OCS) | Duration: 8 weeks | FMS: INT1 ≈ INT2 > CON |
| Ignico [ | Clustered controlled trial | Kindergarten children | Elementary school | FMS: TGMD (totFMS) | Duration: 10 weeks | FMS: INT > CON |
| Iivonen et al. [ | Clustered controlled trial | Preschool children | Preschools | FMS: adapted APM Inventory (OCS) | Duration: 8 months | FMS: INT ≈ CON |
| Jones et al. [ | Cluster-randomized controlled trial | Preschool children | Childcare centers | FMS: TGMD-2 (totFMS) | Duration: 20 weeks | FMS: INT > CON |
| Kelly et al. [ | Clustered controlled trial | Preschool children | Motor Development Clinic (INT), Preschool (CON) | FMS: MEAP Test | Duration: 12 weeks | FMS: INT ≈ CON |
| Krombholzc [ | Clustered controlled trial | Preschool children | Childcare centers | FMS: MoTB 3–7 (totFMS) | Duration: 20 months | FMS: INT ≈ CON |
| Piek et al.c [ | Cluster-randomized controlled trial | Young children aged 4–6 years from low socioeconomic area | Primary schools | FMS: BOT-2SF, MABC-2 (totFMS) | Duration: 6 months | FMS: INT ≈ CON |
| Puder et al. [ | Cluster-randomized controlled trial | Preschool children from an area with high proportion of migrants | Preschool | FMS: shuttle run (20 m), obstacle course, balance beam and platform | Duration: 9 months | FMS: shuttle run, obstacle course INT > CON; remaining tests INT ≈ CON |
| Reilly et al. [ | Cluster-randomized controlled trial | Young children | Nurseries | FMS: MABC (totFMS) | Duration: 24 weeks | FMS: INT > CON |
| Robinson and Goodway [ | Cluster-controlled trial | Preschool children at risk for DD | Head Start centers: | FMS: TGMD-2 (OCS) | Duration: 9 weeks | FMS: INT(INT1/2) > CON |
| Roth et al. [ | Cluster-randomized controlled trial | Preschool children | Preschools | FMS: Single items (obstacle course, standing long jump, balancing on one foot, jumping to and fro sideways) − composite | Duration: 11 months | FMS: INT > CON, 1-leg stance, standing long jump, lateral jump INT > CON; obstacle course INT ≈ CON |
| Tsapakidou et al. [ | Controlled trial | Children aged 3.5–5 years | Nursery schools | FMS: TGMD-2 (LMS) | Duration: 2 months | FMS: INT > CON |
| Valentini [ | Controlled trial | Low motor skill functioning children | Early education center | FMS: TGMD (OCS, LMS) | Duration: 12 weeks | FMS: LMS INT > CON, OCS INT ≈ CON |
| Venetsanou and Kambas [ | Controlled trial | Preschool children | Kindergarten | FMS: MOT4-6 (totFMS) | Duration: 20 weeks | FMS: INT > CON |
| Vidoni et al. [ | Cluster-randomized controlled trial | Preschool children | Daycare center | FMS: BOT-2SF (totFMS) | Duration: 11 weeks | FMS: INT > CON |
| Wang [ | Controlled trial | Preschool children | Preschool | FMS: PDMS-2 | Duration: 6 weeks | FMS: LMS INT > CON; remaining tests INT ≈ CON |
| Weiss et al. [ | Controlled trial | Kindergarten children | Kindergarten | FMS: MOT4-6 | Duration: 6 months | FMS: INT > CON |
| Yin et al. [ | Clustered controlled trial | Preschool-aged children | Head Start centers | FMS: LAP-3 (totFMS) | Duration: 18 weeks | FMS: INT1 > CON, INT2 > CON |
| Zask et al. [ | Cluster-randomized controlled trial | Children aged 3–6 years | Preschools | FMS: TGMD-2 (totFMS, LMS) | Duration: 10 months | FMS: INT > CON |
AMP Alle kouluikäisten lasten PsykoMotoriset taidot, BC body composition, BMI body mass index, BOT-2SF Bruininks-Oseretsky test of motor proficiency—version 2 Short Form, CON control group, DD developmental delay, FMS fundamental movement skills, INT intervention group, LAP-3 Learning Achievement Profile 3rd edition, LMS locomotor subscale, MABC-2 Movement assessment battery for children-version 2, MEAP Michigan Educational Assessment Program, MOT4-6 Motorik test for 4- to 6-year-old children, MoTB3-7 motor test battery, N/A not available, OCS object control subscale, PA physical activity, PDMS-2 Peabody Development Motor Scale—2nd edition, SD standard deviation, TGMD-2 Test of Gross Motor Development—2nd edition, totFMS total fundamental movement skill score, ZNA Zurich Neuromotor Assessment
aElectronic Supplementary Material Table S2 gives an overview of all used FMS test batteries within included studies
bFor detailed information see Electronic Supplementary Material Table S5; results depicted are only between groups post-intervention provided from studies; for >, there is a significant difference; for ≈, there is no significant difference
cNumber of participants and mean age ± SD in years only available for post-test period
Fig. 1Study flow chart [33]. CT controlled trial, FMS fundamental movement skills, RCT randomized controlled trial, WoS Web of Science
Fig. 2Effects of fundamental movement skills (FMS) interventions on a total FMS score (40-point scale, higher score is better), b object control subscale (OCS; 20-point scale, higher score is better), and c locomotor subscale (LMS; 20-point scale, higher score is better). CI confidence interval, CON control group, INT intervention group, IV inverse variance, SE standard error, Std standardized, *randomized controlled trial, aadditional information from author
GRADE evidence profiles: fundamental movement skills (FMS) enhancing intervention versus usual care
| Quality assessment | No. of participantsf | Absolute effect (95% CI)f | Quality | Importance | |||||||
|---|---|---|---|---|---|---|---|---|---|---|---|
| No. of studies | Study design | Risk of bias | Inconsistency | Indirectness | Imprecision | Other considerations | INT | CON | |||
|
| |||||||||||
| 16 | RCT and CT | Seriousa,b | Seriousc | Seriousd | Not serious | Publication biase | 2103 | 1847 | SMD 0.46 higher (0.28–0.65 higher) | Very low | Important |
|
| |||||||||||
| 11 | RCT and CT | Seriousa,b | Seriousc | Seriousd | Not serious | Publication biase | 619 | 499 | SMD 1.36 higher (0.80–1.91 higher) | Very low | Important |
|
| |||||||||||
| 10 | RCT and CT | Seriousa,b | Seriousc | Seriousd | Not serious | Publication biase | 796 | 572 | SMD 0.94 higher (0.59–1.30 higher) | Very low | Important |
GRADE Working Group grade of evidence
High quality: We are very confident that the true effect lies close to that of the estimate of the effect
Moderate quality: We are moderately confident in the effect estimate: the true effect is likely to be close to the estimate of the effect, but there is a possibility that it is substantially different
Low quality: Our confidence in the effect is limited: the true effect may be substantially different from the estimate of the effect
Very low quality: We have very little confidence in the effect estimate: the true effect is likely to be substantially different from the estimate of the effect
CI confidence interval, CON control group, CT controlled trial, GRADE Grading of Recommendations Assessment, Development, and Evaluation System, INT intervention group, LMS Locomotor Subscale, OCS Object Control Subscale, RCT randomized controlled trial, SMD standardized mean difference
aSerious because of no clear randomization procedures described
bSerious because of selection bias (unclear or inadequate allocation concealment), detection bias (unclear blinding of data analysts), study integrity (unclear compliance with the intervention)
cSerious because of statistical heterogeneity (I 2 = 83–88%; p < 0.0001)
dSerious because of important differences in implementation across settings
eSerious because publication bias possible
f3 and 1 studies for overall FMS and LMS scores, respectively, could not be included in meta-analyses
Fig. 3Effect sizes of fundamental movement skill (FMS) interventions according to a duration, b methodological quality, and c study execution of included studies. Filled circles illustrate standardized mean differences (SMDbetween) between intervention and control group for single studies. The filled squares represent weighted mean SMDbetween with 95% confidence intervals (CI) of the studies combined. The figures show a statistically significant higher effect sizes on overall FMS in favor of studies with shorter duration (SMDbetween = 1.23, 95% CI 0.86–1.61) compared with studies with longer duration (SMDbetween = 0.32, 95% CI 0.12–0.52); b no statistically significant differences in effect sizes on overall FMS for studies of ‘high’ methodological quality (SMDbetween = 0.59, 95% CI 0.26–0.93) compared with studies with ‘moderate’ (SMDbetween = 1.31, 95% CI 0.74–1.88) and ‘weak’ (SMDbetween = 0.76, 95% CI 0.40–1.11) methodological quality; and c statistically significant higher effect sizes on overall FMS in favor of studies with external experts (SMDbetween = 1.54, 95% CI 0.93–2.15) compared with childcare staff (SMDbetween = 0.41, 95% CI 0.23–0.59)
| Proficiency in fundamental movement skills (FMS) can and should be trained and enhanced at an early age. |
| In this review, interventions tackling FMS improvement in typically developing young children (aged 2–6 years) show clear beneficial effects on overall FMS, locomotion, and object control skills. |
| As there is very little confidence in the effect estimates, and the true effect in this study is most likely different (stronger or weaker) from the effect estimate, more high-quality research with reduced bias is needed. |