Neuroathletic Training Effects on Muscle Strength, Balance, and Cognition
NCT07117357, Not applicable, Completed, Ankara Yildirim Beyazıt University
Trial 10
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
| Field | Value | Source |
|---|---|---|
| Title | Neuroathletic Training Effects on Muscle Strength, Balance, and Cognition | ClinicalTrials.gov |
| NCT number | NCT07117357 | ClinicalTrials.gov |
| Status | Completed | ClinicalTrials.gov |
| Phases | Not applicable | ClinicalTrials.gov |
| Enrollment | 52 participants, actual | ClinicalTrials.gov |
| Lead sponsor | Ankara Yildirim Beyazıt University | ClinicalTrials.gov |
| Conditions | Neuroathletic Training, Posterior Chain Muscle Strength, Gluteus Maximus, Hamstrings, Erector Spinae Endurance, Proprioception, Cognitive Performance | ClinicalTrials.gov |
| Interventions | Neuroathletic Training Protocol, Standard Warm-Up Protocol | ClinicalTrials.gov |
| First posted | 2025-08-12 | ClinicalTrials.gov |
| Last updated | 2026-03-10 | ClinicalTrials.gov |
Registered outcomes 8
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description | Source |
|---|---|---|---|---|
| Primary | Gluteus Maximus Muscle Strength (Newton) | Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post | Assessed using a digital handheld dynamometer (Lafayette Manual Muscle Tester, Model 01165) during maximal voluntary isometric contraction in prone hip extension. Three trials are conducted, and the highest value is recorded. | ClinicalTrials.gov |
| Primary | Erector Spinae Endurance (Seconds) | Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post | Evaluated using the Biering-Sørensen Test. Participants maintain a horizontal trunk position with the lower body fixed until fatigue. Time is recorded with a stopwatch. | ClinicalTrials.gov |
| Primary | Knee Joint Proprioception (Degrees) | Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post | Measured using an inclinometer to assess knee joint position sense. Angular deviation from 30° knee flexion target is recorded. The mean error across trials is used as the final score. | ClinicalTrials.gov |
| Primary | Dynamic Balance (Percent Reach Distance) | Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post | Assessed with the Y-Balance Test in three directions: anterior, posteromedial, and posterolateral. Reach distances are normalized to limb length and averaged to calculate dynamic balance performance. | ClinicalTrials.gov |
| Primary | Cognitive Performance - Stroop Test Reaction Time | Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post | Assesses selective attention and cognitive interference using the Stroop Color-Word Test. Reaction time is recorded in milliseconds during the incongruent trial phase. | ClinicalTrials.gov |
| Primary | Cognitive Performance - Stroop Test Error Count | Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post | Assesses accuracy during the Stroop Color-Word Test. The number of errors made during the incongruent trials is recorded. | ClinicalTrials.gov |
| Primary | Cognitive Performance - Trail Making Test Completion Time | Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post | Assesses visual attention and task-switching using Trail Making Test Parts A and B. Time to complete each part is recorded in seconds. | ClinicalTrials.gov |
| Primary | Cognitive Performance - Trail Making Test Error Count | Baseline, Immediately Post-Intervention, 15 Minutes Post, 30 Minutes Post | Assesses accuracy during Trail Making Test Parts A and B. The number of errors committed during each test part is recorded. | 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 4
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 |
| Task Switching Test | Primary outcome | ConductCognition |
| Trail Making Test A | Primary outcome | ConductCognition |
| Trail Making Test B | 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)