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Turkish Adaptation and Validation of the Adolescents and Adults Coordination Questionnaire

NCT07754487, Not yet recruiting, Gulser CINBAZ

Trial 8

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

FieldValueSource
TitleTurkish Adaptation and Validation of the Adolescents and Adults Coordination QuestionnaireClinicalTrials.gov
NCT numberNCT07754487ClinicalTrials.gov
StatusNot yet recruitingClinicalTrials.gov
Enrollment120 participants, estimatedClinicalTrials.gov
Lead sponsorGulser CINBAZClinicalTrials.gov
ConditionsMotor Coordination AssessmentClinicalTrials.gov
First posted2026-08-10ClinicalTrials.gov
Last updated2026-08-10ClinicalTrials.gov

Registered outcomes 7

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

ListOutcomeTime frameDescriptionSource
PrimaryTurkish AAC-Q ScoreAssessments will be performed at baseline and repeated 7-10 days later to evaluate test-retest reliability.
The Turkish version of the Adolescents and Adults Coordination Questionnaire (AAC-Q) is a 12-item self-report questionnaire designed to assess coordination difficulties in adolescents and adults. Each item is scored on a 5-point Likert scale, with higher scores indicating greater coordination difficulties.
ClinicalTrials.gov
PrimaryAdult Executive Functioning Inventory (ADEXI)Assessments will be performed at baseline
Executive functioning will be assessed using the Adult Executive Functioning Inventory (ADEXI), a 14-item self-report questionnaire evaluating working memory and inhibition. Higher scores indicate greater executive functioning difficulties.
ClinicalTrials.gov
SecondaryLower Extremity Motor Coordination TestAssessments will be performed at baseline
Lower extremity motor coordination will be evaluated using the Lower Extremity Motor Coordination Test. Participants will alternately touch two targets with the great toe for 20 seconds while seated. The average number of correct touches from two trials will be recorded.
ClinicalTrials.gov
SecondaryStar Excursion Balance TestAssessments will be performed at baseline
Dynamic balance will be assessed using the Star Excursion Balance Test. Participants will reach in the anterior, posteromedial, and posterolateral directions while maintaining single-leg stance. The average reach distance from three trials in each direction will be recorded.
ClinicalTrials.gov
SecondaryNine-Hole Peg TestAssessments will be performed at baselineManual dexterity and upper extremity coordination will be assessed using the Nine-Hole Peg Test. The time required to place and remove nine pegs will be recorded separately for each hand.ClinicalTrials.gov
SecondaryRuler Drop TestAssessments will be performed at baselineReaction time will be evaluated using the Ruler Drop Test. Participants will catch a falling ruler as quickly as possible, and the catching distance will be recorded as an indicator of reaction time.ClinicalTrials.gov
SecondaryStroop TestAssessments will be performed at baselineExecutive function, selective attention, cognitive flexibility, and resistance to interference will be assessed using the Stroop Test (Çapa Form). Completion time and error rate will be recorded.ClinicalTrials.gov

Outcomes 0

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

TypeOutcomeTime framePopulationUnitsMeasured asSource

Results by group 0

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

OutcomeGroupCategoryValueSpreadUnitsSource

Participant flow 0

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

PeriodMilestoneGroupParticipantsUnits countedSource

Adverse events 0

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

TypeEventOrgan systemGroupAffectedAt riskEventsSource

Adverse event totals 0

The totals the trial posted for each group.

TotalGroupAffectedAt riskSource

Papers 0

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource

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.

ProjectTitlePrincipal investigatorsOrganizationFunderFiscal yearsSource

Trial comparisons 0

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

ComparisonSource

Tests 1

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

TestNamed asSource
Stroop Color-Word TestSecondary outcomeConductCognition

Source 5

FieldValueSource
Releasetrials-2026-11-12-0.4.0ClinicalTrials.gov
Release manifest SHA-2560f4a8d8c48aee2a7573ae0fa94ecbeab70c1adbe449bbc95c424bc7d3e97b9d4ClinicalTrials.gov
Registry capture2026-11-12ClinicalTrials.gov
Results copy, AACT2026-03-23ClinicalTrials.gov
NIH clinical studies file2026-11-13ClinicalTrials.gov

The same record as JSON

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)