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Active Young, Healthy Mind. The YoungFitT Project

NCT06406283, Not applicable, Unknown, University of Barcelona

Trial 10

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

FieldValueSource
TitleActive Young, Healthy Mind. The YoungFitT ProjectClinicalTrials.gov
NCT numberNCT06406283ClinicalTrials.gov
StatusUnknownClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment219 participants, estimatedClinicalTrials.gov
Lead sponsorUniversity of BarcelonaClinicalTrials.gov
ConditionsUniversity StudentsClinicalTrials.gov
InterventionsHigh-Intensity Functional Training (HIFT), Mindfulness-Based Stress Reduction Program (MBSR), QigongClinicalTrials.gov
First posted2024-05-09ClinicalTrials.gov
Last updated2024-05-09ClinicalTrials.gov

Registered outcomes 35

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

ListOutcomeTime frameDescriptionSource
PrimaryChanges in immediate verbal attentionBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Direct Digit Span, subtest from the Wechsler Adult Intelligence Scale - Third Edition (WAIS-III). Span. Direct score. Range 0-9. Higher scores indicate better performance.ClinicalTrials.gov
PrimaryChanges in processing speedBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Symbol-Digit Coding subtest from the Wechsler Adult Intelligence Scale - Third Edition (WAIS-III). Direct score. Range 0-133. Higher scores indicate better performance.ClinicalTrials.gov
PrimaryChanges in visual attentionBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Trail Making Test Part A. Seconds to complete the numerical sequence. Direct score. More time indicates worse performance.ClinicalTrials.gov
PrimaryChanges in verbal memoryBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Rey Auditory Verbal Learning Test. Direct score. Range 0-75. Higher scores indicate better performance.ClinicalTrials.gov
PrimaryChanges in visual memoryBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Rey-Osterrieth Complex Figure. The memory drawing accuracy at 3-5 minutes. Direct score. Range 0-36. Higher scores indicate better performance.ClinicalTrials.gov
PrimaryChanges in Executive Function - FlexibilityBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Trail Making Test Part B. Seconds to complete the alphanumeric sequence. Direct score. More time indicates worse performance.ClinicalTrials.gov
PrimaryChanges in Executive Function - InhibitionBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)
Stroop Color and Word Test. Interference of the Stroop Color and Word Test. Interference is calculated as follows: CW - ((W \* C) / (W + C)). Higher scores indicate better performance. Negative values are possible, meaning a bad performance.
ClinicalTrials.gov
PrimaryChanges in Executive Function - Verbal FluencyBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)
Phonetic Fluency is measured using the Controlled Oral Word Association Test, spanish adaptation, and semantic fluency test using the category Animal. The total number of evoked words starting with the letters P, M, and R (60 seconds for each letter) and animals (60 seconds). Direct score. Higher scores indicate better performance.
ClinicalTrials.gov
PrimaryChange in verbal digit working memoryBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Backward Digit Span subtest from the Wechsler Adult Intelligence Scale - Third Edition (WAIS-III). Span. Direct score. Range 0-8. Higher scores indicate better performance.ClinicalTrials.gov
PrimaryChanges in Verbal ComprehensionBaseline (2 weeks before)Vocabulary subtest from the Wechsler Adult Intelligence Scale - Third Edition (WAIS-III). Direct score. Range 0-66. Higher scores indicate better performance.ClinicalTrials.gov
PrimaryChanges in Psychological symptomsBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)90 Symptoms Inventory (90-SCL-R). Direct scores from 0 to 4. Higher scores indicate more symptomatology.ClinicalTrials.gov
PrimaryChanges in Self-esteemBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Rosenberg Self-esteem scale (RSE). Direct scores from 10 to 40. Higher scores indicate higher self-esteem.ClinicalTrials.gov
PrimaryChanges in Depression, anxiety and stressBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Depression, Anxiety and Stress Scale-21 (DASS-21). Direct score. Range 0-126. Higher scores indicate more global symptomsClinicalTrials.gov
PrimaryChanges in MindfulnessBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Five facet mindfulness questionnaire (FFMQ). Direct scores from 39 to 195. Higher scores indicate more Mindfulness levels.ClinicalTrials.gov
PrimaryChanges in Self-efficacyBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)General self-efficacy scale (GSE). Direct scores from 10 to 40. Higher scores indicate more self-eficacy.ClinicalTrials.gov
PrimaryChanges in Sleep qualityBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Pittsburgh Sleep Quality Index (PSQI). Direct score. Range 0-21. Lower scores indicate better sleep quality.ClinicalTrials.gov
PrimaryChanges in DietBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Mediterranean Diet Assessment Tool (PREDIMED). Direct score. Range 0-14. Higher scores indicate more adherence to a Mediterranean diet.ClinicalTrials.gov
SecondaryChanges in Physical activityBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)
International Physical Activity Questionnaire (IPAQ). Total physical activity measured in MET-min/week through the International Physical Activity Questionnaire - Short Form. Direct score. Higher scores indicate more physical activity.
ClinicalTrials.gov
SecondaryChanges in Anthropometric Measurements - HeightBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Height in metersClinicalTrials.gov
SecondaryChanges in Anthropometric Measurements - WeightBaseline (2 weeks before) & follow-up (2 weeks after completing interventions)Weight in KgClinicalTrials.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 1

The papers the trial lists on ClinicalTrials.gov.

PMIDListed asSource
40748900DERIVEDPubMed

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 9

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

TestNamed asSource
Category FluencyPrimary outcomeConductCognition
Complex Figure Copy and RecallPrimary outcomeConductCognition
Digit Span TestPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition
Trail Making Test APrimary outcomeConductCognition
Trail Making Test BPrimary outcomeConductCognition
Verbal FluencyPrimary outcomeConductCognition
Verbal LearningPrimary outcomeConductCognition
Vocabulary TestPrimary 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)