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Trial · NCT07894809

Audiovisual Conditions During Eight Weeks of BOSU Training in Taekwondo Athletes

NCT07894809, Not applicable, Completed, Inonu University

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. Audiovisual Conditions During Eight Weeks of BOSU Training in Taekwondo Athletes. Trials, record NCT07894809. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT07894809

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
Audiovisual Conditions During Eight Weeks of BOSU Training in Taekwondo Athletes
NCT number
NCT07894809
Status
Completed
Phases
Not applicable
Enrollment
30 participants, actual
Lead sponsor
Inonu University
Conditions
Athletic Performance, Attention, Exercise, Martial Arts
Interventions
BOSU training with high-tempo music and projected competition video, BOSU training with low-tempo music, BOSU training without audiovisual stimulation
First posted
2026-10-26
Last updated
2026-10-26

Source ClinicalTrials.gov

Registered outcomes5

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryTaekwondo-specific electronic impact score: Baldeung Chagi (roundhouse kick)Week 1, week 4 and week 8
Proprietary electronic impact score registered by a Daedo GEN2 electronic trunk protector worn by a live target athlete, in arbitrary device units with an observed upper display bound of 60. Four endpoints are recorded for this technique: the minimum and the maximum of three trials, for the right leg and for the left leg. Higher values indicate a higher registered impact. The score reflects impact intensity, targeting accuracy and technical quality of contact combined and is not a calibrated mechanical force.
PrimaryTaekwondo-specific electronic impact score: Yop Chagi (side kick)Week 1, week 4 and week 8
Proprietary electronic impact score registered by a Daedo GEN2 electronic trunk protector worn by a live target athlete, in arbitrary device units with an observed upper display bound of 60. Four endpoints are recorded for this technique: the minimum and the maximum of three trials, for the right leg and for the left leg. Higher values indicate a higher registered impact. The score reflects impact intensity, targeting accuracy and technical quality of contact combined and is not a calibrated mechanical force.
PrimaryTaekwondo-specific electronic impact score: Dwi Chagi (back kick)Week 1, week 4 and week 8
Proprietary electronic impact score registered by a Daedo GEN2 electronic trunk protector worn by a live target athlete, in arbitrary device units with an observed upper display bound of 60. Four endpoints are recorded for this technique: the minimum and the maximum of three trials, for the right leg and for the left leg. Higher values indicate a higher registered impact. The score reflects impact intensity, targeting accuracy and technical quality of contact combined and is not a calibrated mechanical force.
SecondarySelective attention: d2 Test of Attention concentration performance (CP)Week 1, week 4 and week 8
Paper-and-pencil d2 Test of Attention (14 rows, 20 seconds per row). Concentration performance equals the number of correctly marked target characters minus commission errors; higher scores indicate better selective attention. Other d2 indices were not retained in the dataset.
SecondaryAnaerobic performance: Running-based Anaerobic Sprint Test (RAST)Week 1, week 4 and week 8
Six maximal 35 m sprints separated by 10 seconds of recovery, electronically timed. Derived variables: peak power (W), average power (W), minimum power (W), fatigue index (W/s) and relative peak power (W/kg). Higher power values and a lower fatigue index indicate better anaerobic performance.

Outcomes0

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

None in this release.

Results by group0

Each measurement the trial posted, group by group, in the words and numbers it posted.

None in this release.

Participant flow0

How many started, completed or left each group, period by period.

None in this release.

Adverse events0

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

None in this release.

Adverse event totals0

The totals the trial posted for each group.

None in this release.

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

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.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests1

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

TestNamed as
Cancellation TestSecondary outcome

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.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.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT07894809

GET https://conductscience.org/api/trials/v1/NCT07894809/registered