Temporal Interference Stimulation, Early Alzheimer's, 40 Participants
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.
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, 2026GovPing 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.
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
Mentioned entities
Related changes
Get daily alerts for ClinicalTrials.gov Studies
Daily digest delivered to your inbox.
Free. Unsubscribe anytime.
Source
About this page
Every important government, regulator, and court update from around the world. One place. Real-time. Free. Our mission
Source document text, dates, docket IDs, and authority are extracted directly from NIH.
The summary, classification, recommended actions, deadlines, and penalty information are AI-generated from the original text and may contain errors. Always verify against the source document.
Classification
Who this affects
Taxonomy
Browse Categories
Get alerts for this source
We'll email you when ClinicalTrials.gov Studies publishes new changes.
Subscribed!
Optional. Filters your digest to exactly the updates that matter to you.