Skip to main content
OpenTrials
Completed

NCT Number: NCT03391505

Acute Effects of Physical Activity On Memory, Cognitive Performance and Brain Activity

The overall aim of the study is to investigate the effects of an acute bout of physical activity on cognitive performance and long-term memory in elementary school children. Elaborating, the study seeks to investigate the effect of the intensity of the physical activity on cognitive performance and long-term memory in preadolescent children.

Completed

Looking for future studies?

Notify Me

Key information

Age range

10 year–14 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

University of Southern Denmark

Odense, 5700, Denmark

About this study

Based on a power analysis a total population of 100 children (four school classes) will be invited to participate in a 10-day protocol. The children will be randomly allocated, within their cluster (classes) and stratified for gender and soccer level, to one of 3 intervention groups. The groups consist of: A small-sides soccer game group (SSG), a walking soccer group (WSG) and a rest group watching soccer on TV (RES). At day 1 the children will complete a screening of their physical characteristics (height, weight, fat percentages, lean muscle mass and fitness status). On day 2 the children will complete a screening and a familiarization to the cognitive tasks used (cognitive performance and long-term memory) and the brain activity measuring devices (transportable EEG systems). On day 3 the children will complete the interventions, which first consist a long-term memory task, where the children will be asked to remember forty different pictures. Immediately after exposure to the forty pictures, the children will participate in 2 x 10 minutes of their respective interventions with 5 minutes break in between. During the break, the children will complete a short questionnaire to address their flow. Furthermore, during the intervention they will be equipped with heart rate monitors to quantify the physical demands of the intervention. Immediately after completing the 2 x 10 minutes interventions the children will be equipped with a transportable EEG system, and undergo a cognitive test (the Flanker task) to address their cognitive performance. The EEG recordings are used to measure the P3 amplitude and latency, biomarkers for cognitive performance. While equipping the children with the EEG system, the children will complete questionnaires about their participation. At day 10 the children will try to remember as many pictures of the forty pictures as possible to address the effect of the interventions on their long-term memory.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Informed consent from the childrens´ legal guardians.
  • Physical, linguistic and mental competencies to complete the intervention and testing.

Exclusion criteria

  • Use of prescription-only drugs that kan affect learning ability.
  • Smoking.
  • Neurological diseases inclusive damages to the spinal cord.
  • Children who is not evaluated to being cable of completing the protocol among these psychological diseases or psychological unstable children.

Treatment and study plan

Small-sided soccer game

Behavioral

The small-sided soccer game consists of a single bout (two times ten minutes) of small-sided soccer game (3v3) interspersed with a five minutes break.

Other names: SSG

Walking soccer game

Behavioral

The walking soccer game consists of a single bout (two times ten minutes) of small-sided walking soccer game (3v3) interspersed with a five minutes break.

Other names: WSG

Rest group watching soccer

Behavioral

The rest group watching soccer consists of watching a soccer game on a laptop (two times ten minutes) interspersed with a five minutes break.

Other names: RES

Primary outcomes

  1. Event-related brain potentials (P300)

    Time frame: 1 day

    Electroencephalographic measures (mV) of the neuroelectric system that occur in response to, or in or in preparation for, a discrete event.

  2. Cognitive Response Speed Performance

    Time frame: 1 day

    Measures of response speed (ms) during the computer-based Flanker task

  3. Cognitive Response Accuracy Performance

    Time frame: 1 day

    Measures of response accuracy (%) during the computer-based Flanker task

  4. Long-term Memory Accuracy Performance

    Time frame: 7 days

    Measures of response accuracy (%) during a tablet-based visual memory task

Secondary outcomes

  1. Height

    Time frame: 1 day

    Measures of height (cm) with a Tanita Leicester portable altimeter

  2. Weight

    Time frame: 1 day

    Measures weight (kg) with an InBody 230 multifrequency body composition analyser

  3. Fat Percentage

    Time frame: 1 day

    Measures fat percentage (%) with an InBody 230 multifrequency body composition

  4. Lean Body Mass

    Time frame: 1 day

    Measures of lean body mass (kg) with an InBody 230 multifrequency body composition

  5. Fitness Status

    Time frame: 1 day

    Measures of distance covered during an maximal exercise test

  6. Maximal Heart Rate

    Time frame: 1 day

    Measures of maximal heart rate with heart rate monitors during an maximal exercise test

  7. Flow

    Time frame: 1 day

    Measures of flow with a danish translation og the flow questionnaire (Rheinberg et al., 2003) during the intervention

  8. Motivation

    Time frame: 1 day

    Measures of motivation with the Intrinsic Motivation Inventory (IMI) questionnaire (McAuley et al., 1987) after the intervention

  9. Enjoyment

    Time frame: 1 day

    Measures of self-perceived enjoyment with the Physical Activity Enjoyment Scale (PACES) (Kendzierski et al., 1991) questionnaire after the intervention

  10. Intervention intensity

    Time frame: 1 day

    Measures of heart rate with heart rate monitors during the intervention

Sponsors and collaborators

Lead sponsor

University of Southern Denmark

Other

Collaborators

  • University of Copenhagen

Registry information

Important dates

Study start
2018
Primary completion
2018
Study completion
2018
First posted
Jan 5, 2018
Registry last updated
May 8, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.