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Efficacy of the MovinCog Intervention in Children

Efficacy of the MovinCog Intervention in Children: A Randomized, Placebo-controlled Trial

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03255499
Enrollment
1000
Registered
2017-08-21
Start date
2017-09-10
Completion date
2021-12-31
Last updated
2020-11-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cognitive Change, Learning Disabilities, Learning Disorders

Keywords

cognitive training, physical exercise, brain dynamics, cognitive abilities, physiological markers

Brief summary

This study aims to test the efficacy of the MovinCog Intervention to enhance cognitive abilities in children 7-15 yrs. The intervention consists of two parts: a physical exercise regimen, based on high-intensity training, and a cognitive training component. The design will contrast the intervention with an active control group, matched for expectancy effects.

Detailed description

Specifically, the investigators will compare both components together (exercise and cognitive training) against either one of the components (exercise alone, or cognitive training alone) and against an active control group. The study will include measures of scholastic aptitude, as well as of working memory and cognitive control (primary outcome measures), two cognitive abilities that are critical to daily life activities, and that respond well to training. In addition, the investigators will measure physiological responses to training, to monitor changes associated with exercise (secondary outcome measures). Finally, the investigators will relate training-specific improvements with transfer gains, to better model the interaction between training and transfer. This will provide a comprehensive understanding of the dynamics associated with the intervention.

Interventions

BEHAVIORALExercise

Exercise

BEHAVIORALCognitive

Cognitive

BEHAVIORALActive control

Active control, including a blend of computer games, board games, quizzes, trivia

Sponsors

University of Auckland, New Zealand
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
DOUBLE (Subject, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
7 Years to 15 Years
Healthy volunteers
Yes

Inclusion criteria

* Age 7-15

Exclusion criteria

* Age outside inclusion criteria * History of seizures, brain trauma

Design outcomes

Primary

MeasureTime frameDescription
Change from baseline working memory capacity at 10 weeksBaseline and 10-week posttestConstructs measured by multiple tasks (bds, corsi, n-back)
Change from baseline cognitive control at 10 weeksBaseline and 10-week posttestConstructs measured by multiple tasks (flanker, go/no-go, stroop)
Change from baseline scholastic aptitude at 10 weeksBaseline and 10-week posttestConstructs measured by multiple national (New Zealand), standardized tests

Secondary

MeasureTime frameDescription
Change from baseline resting heart rate at 10 weeksBaseline and 10-week posttestMeasured by monitor
BDNF polymorphism measured by genetic saliva kitBaselineEffect of BDNF polymorphism on primary outcomes

Countries

New Zealand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026