Effect of a School Intervention With Physical Activity on Executive Functions
NCT06496503, Not applicable, Completed, State University of Londrina
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Effect of a School Intervention With Physical Activity on Executive Functions | ClinicalTrials.gov |
| NCT number | NCT06496503 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 100 participants, actual | ClinicalTrials.gov |
| Lead sponsor | State University of Londrina | ClinicalTrials.gov |
| Conditions | Healthy Lifestyle | ClinicalTrials.gov |
| Interventions | Physical activity Protocol | ClinicalTrials.gov |
| First posted | 2024-07-11 | ClinicalTrials.gov |
| Last updated | 2025-05-14 | ClinicalTrials.gov |
Registered outcomes 3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Executive Functions | Will be assessed pre-protocol, after 12 weeks, and 8 weeks after the end of the intervention. | The executive functions will be assessed pre-protocol, after 12 weeks, and 8 weeks after the end of the intervention (follow-up period). Executive functions will be investigated in the domains of working memory, using the Corsi Block Test (Corsi, 1972; Kessels et al., 2000), and inhibitory control, investigated by the Stroop Test (Stroop, 1935; MacLeod, 1991). For both tests there will be familiarization and reproducibility of measurements for both the children and evaluator. The evaluation will be carried out by a single evaluator blind to group allocation. | ClinicalTrials.gov |
| Secondary | Cardiorespiratory fitness | Will be assessed pre-protocol, after 12 weeks, and 8 weeks after the end of the intervention. | The test will be conducted in the field with cones at a distance of 20 meters and a pre-recorded audio track to indicate the speed of each stage. The first stage starts at 8.5 km/h, with an increase of 0.5 km/h every minute, which indicates a change of stage. The test is considered to end when the child is unable to maintain the imposed speed or complete a stage with less than two errors (Léger et al., 1998). The prescription of training will be dependent on the individual results for each child based on the last stage completed in the progressive test. At baseline, two field tests will be performed, the first one being a familiarization test and the second being considered as the value prior to the training. In addition, reproducibility of measurements will be tested to indicate the reliability of the results. | ClinicalTrials.gov |
| Other | Motor Coordination | Will be assessed pre-protocol, after 12 weeks, and 8 weeks after the end of the intervention. | To evaluate general motor coordination, the Körperkoordinationstest Für Kinder (KTK) test will be applied (Kiphard; Schiling, 1974, apud Moreira et al., 2019; Nascimento et al., 2019). For all tests involving the KTK battery, there will be familiarization and reproducibility of measurements for both children and the evaluator. The evaluation will be carried out by a single evaluator blind to group allocation. | ClinicalTrials.gov |
Outcomes 0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as | Source |
|---|
Results by group 0
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units | Source |
|---|
Participant flow 0
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted | Source |
|---|
Adverse events 0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
| Type | Event | Organ system | Group | Affected | At risk | Events | Source |
|---|
Adverse event totals 0
The totals the trial posted for each group.
| Total | Group | Affected | At risk | Source |
|---|
Papers 20
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 2034749 | BACKGROUND | PubMed |
| 3184250 | BACKGROUND | PubMed |
| 11296689 | BACKGROUND | PubMed |
| 11394996 | BACKGROUND | PubMed |
| 16150004 | BACKGROUND | PubMed |
| 17399884 | BACKGROUND | PubMed |
| 17695343 | BACKGROUND | PubMed |
| 18949660 | BACKGROUND | PubMed |
| 19120425 | BACKGROUND | PubMed |
| 20332511 | BACKGROUND | PubMed |
| 21299297 | BACKGROUND | PubMed |
| 21852486 | BACKGROUND | PubMed |
| 22777140 | BACKGROUND | PubMed |
| 23020641 | BACKGROUND | PubMed |
| 25311901 | BACKGROUND | PubMed |
| 29054748 | BACKGROUND | PubMed |
| 31241688 | BACKGROUND | PubMed |
| 31803092 | BACKGROUND | PubMed |
| 33612080 | BACKGROUND | PubMed |
| 35409571 | BACKGROUND | PubMed |
Grants 0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
| Project | Title | Principal investigators | Organization | Funder | Fiscal years | Source |
|---|
Trial comparisons 0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
| Comparison | Source |
|---|
Tests 2
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
| Test | Named as | Source |
|---|---|---|
| Corsi Block-Tapping Test | Primary outcome | ConductCognition |
| Stroop Color-Word Test | Primary outcome | ConductCognition |
Source 5
| Field | Value | Source |
|---|---|---|
| Release | trials-2026-11-12-0.4.0 | ClinicalTrials.gov |
| Release manifest SHA-256 | 0f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4 | ClinicalTrials.gov |
| Registry capture | 2026-11-12 | ClinicalTrials.gov |
| Results copy, AACT | 2026-03-23 | ClinicalTrials.gov |
| NIH clinical studies file | 2026-11-13 | ClinicalTrials.gov |
Release trials-2026-11-12-0.4.0
ClinicalTrials.gov's posted results, through CTTI's AACT: ClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299 ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
ClinicalTrials.gov: none stated ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
NIH RePORTER's clinical studies and project files: Public domain (NIH RePORTER)