Effect of Dual-Task Aerobic Exercise on Children With Specific Learning Disorder
NCT07054164, Not applicable, Completed, Bezmialem Vakif University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Effect of Dual-Task Aerobic Exercise on Children With Specific Learning Disorder | ClinicalTrials.gov |
| NCT number | NCT07054164 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 30 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Bezmialem Vakif University | ClinicalTrials.gov |
| Conditions | Specific Learning Disorder | ClinicalTrials.gov |
| Interventions | dual-task aerobic exercise, aerobic exercise | ClinicalTrials.gov |
| First posted | 2025-07-08 | ClinicalTrials.gov |
| Last updated | 2025-07-08 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Stroop Test TBAG Form | 8 weeks | The Stroop Test TBAG Form is a neuropsychological test that evaluates complex attention, focused and selective attention, resistance to disruptive stimuli, cognitive inhibition, information processing speed and executive functions. Unit of Measure: Points | ClinicalTrials.gov |
| Secondary | Pediatric Balance Scale (PDS) | 8 weeks | The scale consists of 14 sections in total and each section is evaluated and scored between 0-4 points. The total score gives the PDS score. The score range of the scale is between 0-56 and higher scores indicate better balance performance. | ClinicalTrials.gov |
| Secondary | Biodex Balance System | 8 weeks | The Biodex Balance System is an equipment that can be used for both objective assessment of postural balance and balance training. The device consists of a screen, a circular balance platform, arm support and a printer. | ClinicalTrials.gov |
| Secondary | Quality of Life Inventory for Children (PedsQL) | 8 weeks | It is a scale used to evaluate the general quality of life of children aged 2-18; it consists of a total of 23 items that question children's physical, emotional, psychosocial and school-related problems, and each item is scored between 0-100. | ClinicalTrials.gov |
| Secondary | Body composition measurement | 8 weeks | The Omron BF511 Body Composition Monitor® non-invasive body composition measurement device, which works with the 4-pole bioelectrical impedance method (determines the ratio of fat and muscle tissue in the body with a weak electric current passing through the body), was used to calculate the participants' skeletal muscle mass ratio (%), body fat ratio (%) and basal metabolic rate. | ClinicalTrials.gov |
| Secondary | Body Weight Measurement | 8 weeks | Body weight will be measured using a digital scale with participants wearing light clothing and no shoes. Unit of Measure: Kilograms (kg) | ClinicalTrials.gov |
| Secondary | Height Measurement | 8 weeks | Height will be measured using a stadiometer with participants standing upright without shoes, heels together, and head in the Frankfurt plane. Unit of Measure: Meters (m) | ClinicalTrials.gov |
| Secondary | Body Mass Index (BMI) | 8 weeks | BMI will be calculated using the formula: weight in kilograms divided by the square of height in meters (kg/m²). Unit of Measure: Kilograms per square meter (kg/m²) | 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 0
The papers the trial lists on ClinicalTrials.gov.
| PMID | Listed as | Source |
|---|
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)