Clinical trial registry record

Association of Transcranial Alternating Current Stimulation with Digital Cognitive Training for Cognitive Remediation in Older Adults

A registered study indexed because it matched monitored longevity research terms. Registry status: Recruiting. Registration does not establish safety or effectiveness.

Plain-language guide

Five questions to ask about this record

What this is
A clinical study registration, not a result or recommendation.
Why it may matter
The registry currently reports Recruiting.
Evidence
Registered phase not reported study.
Main limitation
Registration does not prove that the intervention works, is safe, or is available to you.
What changed
Registry metadata was last updated December 13, 2024.
Where to verify
Open the primary registry below for eligibility, locations, contacts, and current status.
Registry ID
NCT06733714
Last registry update
December 13, 2024
Status
Recruiting
Phase
Phase not reported
Sponsor
Universidade Federal do Rio de Janeiro
Enrollment
40
Countries
Brazil
Match confidence
100%
Source feed
ClinicalTrials.gov
Automated source synopsis

A registered study indexed because it matched monitored longevity research terms. Registry status: Recruiting. Registration does not establish safety or effectiveness.

Evidence snapshot

What the source actually supports

Evidence stage
Phase not reported
Study design
RANDOMIZED · PARALLEL · TREATMENT · TRIPLE
Evidence population
Human clinical study registration
Participants
40
Population
ALL · 50 Years
Duration
2024-12-02 to 2027-03-01
Intervention
Transcranial Alternating Current Stimulation; Digital Cognitive Training
Comparator
Not reported
Outcomes measured
MONTREAL COGNITIVE ASSESSMENT (MOCA) — 1 week after intervention; Five digits test (FDT) — 1 week after intervention; Rey-Osterrieth complex figure (ROCF) — 1 week after intervention; Semantic and phonemic verbal fluency — 1 week after intervention; The Rey Auditory Verbal Learning Test (RAVLT) — 1 week after intervention; Visual P300 (Event-Related Potential) — 1 week after intervention; Serum GFAP Analysis — before intervention; Serum Beta-Amyloid Analysis — before intervention; Serum Tau Protein Analysis — before intervention; Prosaccade Task (Eye Tracking) — 1 week after intervention; Antisaccade Task (Eye Tracking) — 1 week after intervention; Visual Search Task (Eye Tracking): — 1 week after intervention
Reported result
No reusable finding-level result is available in this record.

Main limitationThis is a study registration. No reusable structured result is available here, so it cannot show whether the intervention worked or was safe.

Safety and approvalEligibility, adverse-event details, and clinical decisions must be checked in the official registry and with qualified clinicians. Trial registration is not regulatory approval and does not establish that an intervention is available.

Source supportStructured registry protocol metadata; no finding-level conclusion is generated.

Trial stage · Phase not reportedA trial phase describes development stage; it does not establish a positive result.
Phase 1Phase 2Phase 3Phase 4

Registration and recruitment status do not establish safety, efficacy, or regulatory approval.

Why this record appears here · 100% topic match

The title, summary, or source keywords matched one or more topics followed by immortal.life. A higher percentage means a stronger topic match; it does not rate safety, effectiveness, or study quality.

  • Cognitive training · 100%Title contains controlled topic terminology. Summary contains controlled topic terminology. Source terminology contains a controlled topic term. Title supplies ageing or longevity context.

Automated source check 100% · update recency 65%. These figures help sort records; they are not medical ratings.

cognitive training
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