ConductScience.org, home

Library / Trials

Assessment of Transcranial Alternating Current Stimulation's Clinical Efficacy in Treating Cognitive Impairment of Idiopathic Inflammatory Demyelinating Diseases

NCT07087873, Not applicable, Recruiting, Xuanwu Hospital, Beijing

Trial 10

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

FieldValueSource
TitleAssessment of Transcranial Alternating Current Stimulation's Clinical Efficacy in Treating Cognitive Impairment of Idiopathic Inflammatory Demyelinating DiseasesClinicalTrials.gov
NCT numberNCT07087873ClinicalTrials.gov
StatusRecruitingClinicalTrials.gov
PhasesNot applicableClinicalTrials.gov
Enrollment128 participants, estimatedClinicalTrials.gov
Lead sponsorXuanwu Hospital, BeijingClinicalTrials.gov
ConditionsIdiopathic Inflammatory Demyelinating Disorders of the Central Nervous System, MS (Multiple Sclerosis), NMOSD, Acute Disseminated Encephalomyelitis, Transcranial Alternating Current StimulationClinicalTrials.gov
InterventionsNeuroelectrical modulation group, Pseudo-neuromodulation groupClinicalTrials.gov
First posted2025-07-28ClinicalTrials.gov
Last updated2025-07-28ClinicalTrials.gov

Registered outcomes 9

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

ListOutcomeTime frameDescriptionSource
PrimaryExpanded Disability Status Scale, EDSS scoreAt the 5-day point of treatment and 1 month following the end of treatment0-10 points, the higher the score, the more seriousClinicalTrials.gov
PrimarySymbol Digit Modalities Test (SDMT) scaleAt the 5-day point of treatment and 1 month following the end of treatment0-110 points, the higher the score, the better the cognitive functionClinicalTrials.gov
PrimaryScoring results for tasks 1 and 7 in the Alzheimer disease assessment scale-cog(ADAS-cog)At the 5-day point of treatment and 1 month following the end of treatmentthe higher the score, the better the cognitive functionClinicalTrials.gov
SecondaryMini-mental State Examination(MMSE)At the 5-day point of treatment and 1 month following the end of treatment0-30,the higher the score, the better the cognitive functionClinicalTrials.gov
SecondaryMontreal-Cognitive Assessment(MoCA)At the 5-day point of treatment and 1 month following the end of treatment0-30,the higher the score, the better the cognitive functionClinicalTrials.gov
SecondaryStroop Color-Word Test scoreAt the 5-day point of treatment and 1 month following the end of treatmentthe higher the score, the better the cognitive functionClinicalTrials.gov
SecondaryHamilton Depression Scale,HAMDAt the 5-day point of treatment and 1 month following the end of treatmentThe higher the score, the worse the depression.ClinicalTrials.gov
SecondaryHamilton Anxiety Scale,HAMAAt the 5-day point of treatment and 1 month following the end of treatmentThe higher the score, the worse the anxiety.ClinicalTrials.gov
Secondarya subjective questionnaire,adverse effectsFollowing the first day of treatment,Following the second day of treatment,Following the third day of treatment,Following the fourth day of treatment,Following the fifth day of treatmentThe intensity is scored from 0 to 4ClinicalTrials.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 2

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

TestNamed asSource
Symbol CodingPrimary outcomeConductCognition
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)