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Active Breaks and Executive Function in Scholars

Active-breaks, Learning, Creativity and Emotional Health in Preadolescent Students (ACTISTOP)

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07538453
Acronym
ACTISTOP
Enrollment
114
Registered
2026-04-20
Start date
2026-03-26
Completion date
2026-06-01
Last updated
2026-04-20

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

Conditions

Creativity, Executive Function (Cognition), Psychological Wellbeing

Keywords

cognition, attention, creativity, exercise, memory, sedentarism, physical activity, Inhibition, emotions

Brief summary

This study aims to examine whether short bouts of exercise (10 minutes) performed during the school day can improve thinking skills, creativity and emotional wellbeing in primary school children. Specifically, children aged 11-12 years will be randomly assigned to perform either a short aerobic exercise break, a strength-based exercise break, or a seated control activity. The study will evaluate how these 10 minutes activity breaks influence attention, working memory, creativity, and emotional wellbeing state after completing cognitively demanding tasks. The findings will help to identify effective strategies to integrate physical activity into the classroom to enhance learning and overall well-being in school settings.

Detailed description

This study investigates the effects of short classroom-based physical activity breaks on cognitive performance, creativity and emotional wellbeing in primary school children aged 11 to 12 years. Many children spend long periods sitting during the school day, which may negatively affect attention, learning, and overall health. Introducing brief "active breaks" during class time has been proposed as a practical strategy to interrupt sedentary behavior and promote both physical and cognitive benefits. In this study, participants will be randomly assigned to one of three groups: an aerobic exercise group, a strength-based (neuromuscular) exercise group, or a control group that remains seated and watches a low-demand video. All interventions will last approximately 10 minutes and will be delivered in a standardized format including a warm-up, main activity, and cool-down. To better reflect real classroom conditions, participants will perform academic tasks (e.g., reading and mathematics) prior to the intervention to induce cognitive fatigue. At baseline, before and after the intervention, children will complete a series of simple tasks and questionnaires designed to assess key aspects of cognitive function, such as attention, working memory, and inhibitory control, as well as creativity and emotional state. In addition, participants will undergo physical fitness assessments (e.g., strength, cardiorespiratory fitness, and body composition). These measures will be used as potential moderating variables or to explore associations between physical fitness levels and cognitive and emotional responses to the activity breaks. The main objective of the study is to determine whether these short activity breaks can produce immediate improvements in cognitive, creativity and emotional outcomes, and whether different types of exercise (aerobic vs. strength-based) have distinct effects. The results of this study may help schools and educators design effective, evidence-based strategies to integrate physical activity into daily classroom routines, with the goal of improving students' learning, wellbeing, and overall development.

Interventions

A 10-min active break format was selected to maximize feasibility within school settings. All conditions followed an identical temporal structure consisting of a 1-min warm-up, an 8-min main activity phase, and a 1-min cool-down delivered through standardized instructional videos that guided students in reproducing and observing the correct technique and execution of the exercises.

Sponsors

Universitat Jaume I
Lead SponsorOTHER

Study design

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

Masking description

Researchers responsible for outcomes assessment, data processing, and statistical analyses will remain blinded throughout the study

Intervention model description

This study is a three-arm randomized controlled trial with a parallel-group design. Participants will be randomly allocated to one out of three groups: an aerobic exercise active break, a strength-based active break, or a non exercise group (control condition). Outcomes will be assessed at 3 time points (baseline, post-cognitive fatigue, and post-intervention) to evaluate the acute effects of the intervention.

Eligibility

Sex/Gender
ALL
Age
11 Years to 12 Years
Healthy volunteers
Yes

Inclusion criteria

* Students enrolled in the 5th and 6th grades of primary education in the city of Castellón, with continuous academic progression and no history of grade retention. * Students without diagnosed physical, neurological, or cognitive disorders.

Exclusion criteria

* Students with a history of grade retention. * Students with diagnosed learning difficulties or neurodevelopmental disorders. * Students presenting any medical or psychiatric disease. * Students undergoing chronic pharmacological treatment.

Design outcomes

Primary

MeasureTime frameDescription
Self-perceived emotional stateExample assessment timeline: baseline assessment (9:00 a.m.); pre-intervention assessment (following cognitively demanding tasks; 10:00 a.m.); and post-intervention assessment (immediately after the active break protocol; 10:25 a.m.).Assessed using a paper-based measure following the Russell's circumplex model of affect, which conceptualizes emotions according to two primary dimensions: activation level (0 = low to 10 = high) and well-being or happiness level (0 = low to 10 = high).
Executive FunctionExample assessment timeline: baseline assessment (9:00 a.m.); pre-intervention assessment (following cognitively demanding tasks; 10:00 a.m.); and post-intervention assessment (immediately after the active break protocol; 10:25 a.m.).The Eriksen Flanker Task and forward and backward digit span tests will be administered online and in paper format, respectively.
CreativityExample assessment timeline: baseline assessment (9:00 a.m.); pre-intervention assessment (following cognitively demanding tasks; 10:00 a.m.); and post-intervention assessment (immediately after the active break protocol; 10:25 a.m.).Guilford's divergent thinking test will be administered in paper format.

Secondary

MeasureTime frameDescription
Socioeconomic statusMeasured once (one-week before the intervention)Socioeconomic status will be assessed using the Family Affluence Scale III (FAS III), a self-reported questionnaire with higher scores indicating higher family affluence.
Sleep PatternMeasured once (one-week before the intervention)Sleep quality will be assessed using the Pittsburgh Sleep Quality Index (PSQI), a self-reported questionnaire with a global score ranging from 0 to 21, where higher scores indicate poorer sleep quality.
Self-reported Physical FitnessMeasured once (one-week before the intervention)Self-reported physical fitness will be assessed using the International Fitness Scale (IFIS), which evaluates overall fitness, cardiorespiratory fitness, muscular strength, speed-agility, and flexibility using a 5-point Likert scale (1 = very poor to 5 = very good), where higher scores indicate better perceived physical fitness.
Diet PatternMeasured once (one-week before the intervention)Adherence to the Mediterranean diet will be assessed using the Mediterranean Diet Quality Index for children and adolescents (KIDMED), with scores ranging from -4 to 12, where higher scores indicate better adherence to the Mediterranean diet.
Physical Activity EnjoymentMeasured once (one-week before the intervention)Enjoyment of physical activity will be assessed using the Physical Activity Enjoyment Scale (PACES), consisting of 16 items rated on a 5-point Likert scale (1 to 5), with total scores ranging from 16 to 80, where higher scores indicate greater enjoyment of physical activity.
Affective StateMeasured once (one-week before the intervention)Negative affect will be assessed using the Negative Affect subscale of the Positive and Negative Affect Schedule (PANAS), which consists of 10 items rated on a 5-point Likert scale (1 = very slightly or not at all to 5 = extremely), with total scores ranging from 10 to 50, where higher scores indicate greater negative affect.
Sedentary BehaviorMeasured once (one-week before the intervention)Sedentary behavior will be assessed using the Children and Adolescents Physical Activity and Sedentary Questionnaire (CAPAS-Q), which estimates daily time spent in sedentary activities. Results are expressed in minutes per day, where higher values indicate greater sedentary behavior.
Resting Heart RateMeasured once (one-week before the intervention)Resting heart rate will be assessed using a heart rate monitor, expressed in beats per minute (bpm), with lower values indicating better cardiovascular fitness.
Systolic Blood PressureMeasured once (one-week before the intervention)Systolic blood pressure will be measured using an automated sphygmomanometer and expressed in millimeters of mercury (mmHg).
Diastolic Blood PressureMeasured once (one-week before the intervention)Diastolic blood pressure will be measured using an automated sphygmomanometer and expressed in millimeters of mercury (mmHg).
Daily physical activityDuring one week before the intervention procedure.Students will wear an accelerometer (GENEActiv; Activinsights Ltd, Kimbolton, UK) during one week.
Handgrip Strength TestMeasured once (one-week before the intervention)Upper-body muscular strength will be assessed using the handgrip strength test with a dynamometer, expressed in kilograms (kg), where higher values indicate greater muscular strength.
20-m Shuttle Run TestMeasured once (one-week before the intervention)Cardiorespiratory fitness will be assessed using the 20-m shuttle run test, with performance expressed as the number of completed stages or laps, where higher values indicate better cardiorespiratory fitness.
Standing Long Jump TestMeasured once (one-week before the intervention)Lower-body muscular power will be assessed using the standing long jump test, expressed in centimeters (cm), where greater distances indicate higher muscular power.
4x10-m Shuttle Run TestMeasured once (one-week before the intervention)Speed and agility will be assessed using the 4 × 10-m shuttle run test, with performance expressed in seconds (s), where lower times indicate better performance.
Body WeightMeasured once (one-week before the intervention)Body weight will be measured using electrical bioimpedance (Tanita DC-360 portable S) and expressed in kilograms (kg).
HeightMeasured once (one-week before the intervention)Height will be measured using a stadiometer (SECA 213) and expressed in centimeters (cm).
Body Mass Index (BMI)Measured once (one-week before the intervention)Body mass index (BMI) will be calculated from weight and height measurements and expressed in kilograms per square meter (kg/m²).
Body Fat PercentageMeasured once (one-week before the intervention)Body fat percentage will be assessed using electrical bioimpedance (Tanita DC-360 portable S) and expressed as a percentage (%), where higher values indicate higher adiposity.

Countries

Spain

Contacts

CONTACTDiego Moliner-Urdiales, PhD
dmoliner@uji.es+34 964 729782
CONTACTCarlos Babiloni-Lopez, PhD
cbabilon@uji.es+34 964 729840
PRINCIPAL_INVESTIGATORDiego Moliner-Urdiales, PhD

Universitat Jaume I

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Apr 21, 2026