Cognitive-Integrated Soccer Training and Performance
NCT07284940, Not applicable, Completed, Fan Mao
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Cognitive-Integrated Soccer Training and Performance | ClinicalTrials.gov |
| NCT number | NCT07284940 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 64 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Fan Mao | ClinicalTrials.gov |
| Conditions | Executive Function (Cognition), Soccer Training, Performance, Motor Development | ClinicalTrials.gov |
| Interventions | Cognitively Engaging Soccer Practice, Conventional Soccer Practice | ClinicalTrials.gov |
| First posted | 2025-12-16 | ClinicalTrials.gov |
| Last updated | 2026-07-07 | ClinicalTrials.gov |
Registered outcomes 4
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Video-Based Soccer Decision Accuracy | Baseline, immediately after the 8-week intervention, and 4-week retention follow-up. | Video-based soccer decision accuracy will be used as the primary outcome to assess soccer-specific decision-making performance. Participants will view attacking and transition scenarios from a field-player perspective. Each video will be occluded at a critical decision point, and participants will select the most appropriate action, such as pass, dribble, shoot, switch play, or retain possession. Decision accuracy will be calculated as the percentage of responses that match the expert consensus answer. Higher scores indicate better soccer-specific decision-making performance. | ClinicalTrials.gov |
| Secondary | Dribbling performance time | Baseline, immediately after the 8-week intervention, and 4-week retention follow-up. | Dribbling performance time will be measured as the total time (in seconds) required to complete a standardized cone-dribbling course. | ClinicalTrials.gov |
| Secondary | Reaction time on cognitive tasks (Stroop task and 2-back task) | Baseline, immediately after the 8-week intervention, and 4-week retention follow-up. | Reaction time (in milliseconds) will be recorded for correct responses during computerized Stroop and 2-back tasks. Mean reaction time across trials will be calculated separately for each task at each assessment time point. | ClinicalTrials.gov |
| Secondary | Response accuracy on cognitive tasks (Stroop task and 2-back task) | Baseline, immediately after the 8-week intervention, and 4-week retention follow-up. | Response accuracy will be calculated as the percentage of correct responses during computerized Stroop and 2-back tasks. | 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 2
The papers the trial lists on ClinicalTrials.gov.
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 |
|---|---|---|
| 2-Back Task | Secondary outcome | ConductCognition |
| Stroop Color-Word Test | Secondary 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)