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Comparison of Two Non-invasive Neuromodulation Techniques as Synergistic Therapy to Cognitive Stimulation in Amnestic Mild Cognitive Impairment (aMCI)

NCT06467253, Not applicable, Recruiting, Instituto Nacional de Psiquiatría Dr. Ramón de la Fuente

Trial 10

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

FieldValueSource
TitleComparison of Two Non-invasive Neuromodulation Techniques as Synergistic Therapy to Cognitive Stimulation in Amnestic Mild Cognitive Impairment (aMCI)ClinicalTrials.gov
NCT numberNCT06467253ClinicalTrials.gov
StatusRecruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment60 participants, estimatedClinicalTrials.gov
Lead sponsorInstituto Nacional de Psiquiatría Dr. Ramón de la FuenteClinicalTrials.gov
ConditionsMild Cognitive ImpairmentClinicalTrials.gov
Interventions1. rTMS + CS, 2. rTMS Sham + CS, 3. tDCS + CS, 4. tDCS Sham + CSClinicalTrials.gov
First posted2024-06-20ClinicalTrials.gov
Last updated2024-06-20ClinicalTrials.gov

Registered outcomes 29

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

ListOutcomeTime frameDescriptionSource
PrimaryChanges in orientationBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Barcelona Test. Score ranges from 10 or less to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in languageBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the WAIS-IV vocabulary test. Score ranges from 1 to 19. Direct scores are converted to standardized scores. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in languageBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Barcelona Test. Score ranges from 10 or less to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in verbal memoryBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Barcelona Test. Score ranges from 10 or less to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in verbal memoryBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by Neuropsi Attention and Memory. Score ranges from 1 to 19. Direct scores are converted to standardized scores. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in visual memoryBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Barcelona Test. Score ranges from 10 or less to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in visual memoryBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by Neuropsi Attention and Memory. Score ranges from 1 to 19. Direct scores are converted to standardized scores. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in visual-constructive abilitiesBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Barcelona Test. Score ranges from 10 or less to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in visual-constructive abilitiesBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by Neuropsi Attention and Memory. Score ranges from 10 or less to 95. Direct scores are converted to standardized scores. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in processing speedBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Barcelona Test. Score ranges from 10 or less to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in processing speedBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Trail Making Test version A and B. Score ranges from 5 to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in abstractionBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Barcelona Test. Score ranges from 10 or less to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in verbal fluencyBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by a verbal fluency test (semantic: animals and phonologic: F, A, S). Score ranges from 5 to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in interferenceBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Stroop Test. Score ranges from 5 to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in working memoryBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by the Barcelona Test. Score ranges from 10 or less to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in working memoryBaseline, after maintenance (15 weeks), and in follow-up phase (1 year later).Measured by Trail Making Test version A and B. Score ranges from 5 to 95. Direct scores are converted to percentile. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in Global Cognitive FunctionBaseline, after first phase (3 weeks), after maintenance (15 weeks) and in follow-up phase (1 year later).Measured by Montreal Cognitive Assessment. Score ranges from 0 to 30 points. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in Global Cognitive FunctionBaseline, after first phase (3 weeks), after maintenance (15 weeks) and in follow-up phase (1 year later).Measured by Screen for Cognitive Impairment in Psychiatry. Direct scores ranges from 37 to 115 points. Higher scores mean better outcomes.ClinicalTrials.gov
PrimaryChanges in memory regarding situations and activities of daily lifeBaseline, after first phase (3 weeks), after maintenance (15 weeks) and in follow-up phase (1 year later)Measure by Everyday Memory Questionnaire. Score ranges from 0 to 56. Higher scores mean worse outcomes.ClinicalTrials.gov
PrimaryChanges in Global Clinical ImpressionBaseline, after first phase (3 weeks), after maintenance (15 weeks) and in follow-up phase (1 year later).Measure by Clinical Impression Scale. Score ranges from 0 to 7. Higher scores mean worse outcomes.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 5

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

TestNamed asSource
Sternberg Memory ScanningPrimary outcomeConductCognition
Stroop Color-Word TestPrimary outcomeConductCognition
Trail Making Test APrimary outcomeConductCognition
Trail Making Test BPrimary outcomeConductCognition
Verbal FluencyPrimary 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)