Motor-Cognitive Integrated Intervention for Children With Developmental Coordination Disorder
NCT07486856, Not applicable, Completed, Shanghai University of Sport
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Motor-Cognitive Integrated Intervention for Children With Developmental Coordination Disorder | ClinicalTrials.gov |
| NCT number | NCT07486856 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 20 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Shanghai University of Sport | ClinicalTrials.gov |
| Conditions | Developmental Coordination Disorder | ClinicalTrials.gov |
| Interventions | Action Observation and Motor Imagery (AOMI) Training, Fundamental Movement Skills (FMS) Training, General Physical Activities | ClinicalTrials.gov |
| First posted | 2026-03-23 | ClinicalTrials.gov |
| Last updated | 2026-03-25 | ClinicalTrials.gov |
Registered outcomes 13
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Change in Inhibitory Control Assessed by the Stroop Task | Baseline (pre-intervention) and post-intervention (10 weeks). | A computerized task evaluating automated response inhibition under conflict. Stimuli are four Chinese color words presented in congruent or incongruent font colors (1:1 ratio). Participants must ignore the meaning and respond only to the font color. The task consists of 68 trials. Performance is assessed via RT and accuracy. | ClinicalTrials.gov |
| Primary | Change in Cognitive Flexibility Assessed by the More-Odd Shifting | Baseline (pre-intervention) and post-intervention (10 weeks). | A computerized task evaluating rule-switching ability. Stimuli (digits 1-9, excluding 5) require magnitude, parity, or color-cued judgments. Task 1 and 2 are single-rule blocks (58 trials each). Task 3 is a mixed-rule block (59 trials) producing switch and non-switch conditions. Performance is evaluated via Reaction Time (RT) and accuracy. | ClinicalTrials.gov |
| Primary | Change in Spatial Working Memory Assessed by the 16-Grid Paradigm | Baseline (pre-intervention) and post-intervention (10 weeks). | A computerized task assessing spatial information retention and updating in a 4x4 grid. 4 black squares are presented (1000ms), followed by a blank screen (1000ms), and a target stimulus. Participants judge whether the target is the original pattern rotated by 90°. The task consists of 90 trials divided into 4 blocks. | ClinicalTrials.gov |
| Secondary | Change in Gross Motor Skills Assessed by the BOT-2 | Baseline (pre-intervention) and post-intervention (10 weeks). | The Bruininks-Oseretsky Test of Motor Proficiency, Second Edition (BOT-2) evaluates gross motor skills, including balance, bilateral coordination, and running speed. The Total Motor Composite standard score will be reported. The standard score ranges from a minimum of 20 to a maximum of 80. Higher scores indicate better gross motor proficiency and coordination. | ClinicalTrials.gov |
| Secondary | Change in Gross Motor Development Assessed by the TGMD-3 | Baseline (pre-intervention) and post-intervention (10 weeks). | The Test of Gross Motor Development - Third Edition (TGMD-3) evaluates fundamental locomotor and object control skills. The total score is calculated based on the performance criteria of the skills. The total score ranges from a minimum of 0 to a maximum of 100. Higher scores indicate better overall gross motor development. | ClinicalTrials.gov |
| Secondary | Change in Dynamic Postural Control Assessed by the Y-Balance | Baseline (pre-intervention) and post-intervention (10 weeks). | Measures maximum controlled reach distance in three directions while maintaining a single-leg stance. | ClinicalTrials.gov |
| Secondary | Change in Static Postural Control Assessed by the Single-Leg Stance Test with Eyes Closed | Baseline (pre-intervention) and post-intervention 10weeks | Participants stand on one leg with their eyes closed. The duration (in seconds) they can successfully maintain balance is recorded to evaluate static postural control and proprioceptive integration capacity. | ClinicalTrials.gov |
| Secondary | Change in Lower Limb Coordination Assessed by the Side Hop Test | Baseline (pre-intervention) and post-intervention 10 weeks | Participants perform continuous lateral jumps back and forth over a set distance within a limited time. The total number of successful jumps is recorded to reflect lower limb coordination and rapid posture adjustment ability. | ClinicalTrials.gov |
| Secondary | Change in Sprinting Speed Assessed by the 50-Meter Dash | Baseline (pre-intervention) and post-intervention (10 weeks). | The time taken (in seconds) to complete a 50-meter sprint is recorded to evaluate physical speed and acceleration capabilities. | ClinicalTrials.gov |
| Secondary | Change in Coordination and Cardiopulmonary Endurance Assessed by the 1-Minute Jump Rope Test | Baseline (pre-intervention) and post-intervention (10 weeks). | The number of valid jumps completed within one minute is recorded to reflect whole-body coordination and cardiopulmonary endurance levels. | ClinicalTrials.gov |
| Secondary | Change in Lower Limb Explosive Power Assessed by the Standing Long Jump | Baseline (pre-intervention) and post-intervention (10 weeks). | The maximum valid horizontal jump distance (in centimeters) is recorded to evaluate the explosive power of the lower limbs. | ClinicalTrials.gov |
| Secondary | Change in Core Muscle Endurance Assessed by the 1-Minute Sit-Up Test | Baseline (pre-intervention) and post-intervention (10 weeks). | The number of correctly performed sit-ups completed in one minute is recorded to evaluate trunk and core muscle endurance. | ClinicalTrials.gov |
| Secondary | Change in Flexibility Assessed by the Sit-and-Reach Test | Baseline (pre-intervention) and post-intervention (10 weeks). | The maximum forward reach distance (in centimeters) is recorded to evaluate the flexibility of the lower back and hamstring muscles. | 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 1
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|---|---|
| 42869961 | DERIVED | 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 1
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 |
|---|---|---|
| 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)