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Temporal Interference Stimulation, Early Alzheimer's, 40 Participants

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Summary

NIH registered a randomized, double-blind, sham-controlled clinical trial (NCT07543094) evaluating Temporal Interference Stimulation (TIS) — a non-invasive brain stimulation technique — for cognitive function in patients with early-stage Alzheimer's disease. Forty participants will be enrolled and randomly assigned to receive either active TIS or sham stimulation over a 2-week intervention period, with follow-up assessments at 12 weeks.

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What changed

NIH registered a new clinical trial (NCT07543094) on ClinicalTrials.gov investigating the efficacy and safety of Temporal Interference Stimulation (TIS) for cognitive function in early-stage Alzheimer's disease. The study will enroll 40 participants randomized to active TIS or sham stimulation over a 2-week period, with assessments at baseline, post-treatment, and 12 weeks after treatment.

Affected parties include clinical investigators conducting Alzheimer's disease research, patients meeting early-stage Alzheimer's criteria, and sponsors of neuromodulation device studies. ClinicalTrials.gov registration is mandatory for applicable trials under FDA regulations — sponsors and investigators should confirm registration status and ensure trial information is current and accurate.

Archived snapshot

Apr 22, 2026

GovPing captured this document from the original source. If the source has since changed or been removed, this is the text as it existed at that time.

← ClinicalTrials.gov Studies

A Randomized, Double-Blind, Controlled Trial to Evaluate the Efficacy and Safety of Temporal Interference Stimulation on Cognitive Function in Patients With Early-Stage Alzheimer's Disease

N/A NCT07543094 Kind: NA Apr 21, 2026

Abstract

This study aims to investigate the efficacy and safety of a novel non-invasive brain stimulation technique-Temporal Interference Stimulation (TIS)-in patients with early-stage Alzheimer's disease. A total of 40 participants will be randomly assigned to either the TIS group or the sham stimulation group. The intervention will last for 2 weeks, with cognitive and safety assessments at baseline, post-treatment, and 12 weeks after treatment.

Conditions: Alzheimer Disease

Interventions: Temporal Interference Stimulation, Sham Stimulation

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Last updated

Classification

Agency
NIH
Published
April 21st, 2026
Instrument
Notice
Branch
Executive
Legal weight
Non-binding
Stage
Final
Change scope
Minor
Document ID
NCT07543094

Who this affects

Applies to
Healthcare providers Clinical investigators Patients
Industry sector
6211 Healthcare Providers
Activity scope
Clinical trial registration Neuromodulation research Alzheimer's disease research
Geographic scope
United States US

Taxonomy

Primary area
Healthcare
Operational domain
Clinical Operations
Topics
Medical Devices Pharmaceuticals

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