CClinicalTrials.gg
Active, not recruitingNCT05946616MEM_MODUpdated Sep 15, 2026

Spectral Characteristics of Memory Transformation

An interventional study of Transcranial alternating current stimulation (tACS) combined with behavioral intervention and Inactive (sham) stimulation combined with behavioral intervention in Healthy, sponsored by Medical University of South Carolina. Active, not recruiting at 1 site in United States. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2026-09-15.

Sponsored by Medical University of South Carolina · Not applicable, Interventional, and Basic science

Phase
Not applicable
Study type
Interventional
Enrollment
30
Allocation
Randomized
Ages
18 Years and older
Sex
All
01

Study summary

Sometimes, it is necessary to re-learn a previously learned movement behavior, for example, a bad posture during the golf drive or while playing the piano. Unlearning or relearning an intensively trained behavior is particularly important if the behavior is hampering recovery, for example, in chronic pain or after a stroke. With this pilot study, the brain mechanisms that control the change of pre-existing stable memories of a motor skill will be tested with electroencephalography (EEG). Non-invasive brain stimulation will be used to modulate these brain mechanisms and test if it is possible to change the pre-existing motor memory and the learning of a new motor skill.

02

Conditions studied

  • Healthy
03

In context

Lead sponsor

Medical University of South Carolina is the lead sponsor of 852 studies on the registry; 165 are open to participants now.

Of its 128 completed or terminated interventional studies of FDA-regulated products, 101 (79%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes

Inclusion criteria

  • Age 18 years or older (2/3 of the final sample will be ≥60years of age)
  • No previous stroke, brain tumor, neurodegenerative disease, or trauma to the head
  • Ability to give consent for study participation
  • who have access to a personal computer with internet

Exclusion criteria

Exclusion Criteria:

    • Pregnancy

      • Inability to use all ten fingers to type on a standard computer keyboard
      • Uncorrected vision, hindering perception of visual cues presented on a standard computer screen
      • Medication use at the time of study that may interfere with learning or the effect of tACS, including but not limited to carbamazepine, flunarizine, sulpiride, rivastigmine, dextromethorphan;
      • Neuromuscular disorders affecting hand and finger movements necessary for 10-finger keyboard typing
      • Presence of neurological or psychiatric disorders
      • Presence of scalp injury or disease
      • Prior history of seizures
      • Prior intracranial surgery
      • Prior brain radiotherapy
      • Prior history of intracranial tumor, intracranial infection, or cerebrovascular malformation
      • Metal in head or neck
      • Contraindications to MRI (such as severe claustrophobia, implanted medical devices)
05

Study design

Phase
Not applicable
Primary purpose
Basic science
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Participant)
Enrollment
30 participants (estimated)

Study arms

  • Experimental
    Active non-invasive brain stimulation during behavioral memory interference

    Non-invasive brain stimulation with transcranial alternating current stimulation will be applied during a memory interference intervention.

    Other: Transcranial alternating current stimulation (tACS) combined with behavioral intervention

  • Sham comparator
    Sham stimulation during behavioral memory interference

    Inactive (sham) stimulation will be applied during a memory interference intervention.

    Other: Inactive (sham) stimulation combined with behavioral intervention

Interventions

  • OtherTranscranial alternating current stimulation (tACS) combined with behavioral intervention

    Transcranial alternating current stimulation (tACS) combined with behavioral intervention (memory interference).

  • OtherInactive (sham) stimulation combined with behavioral intervention

    Inactive (sham) stimulation combined with behavioral intervention (memory interference)

06

What researchers measure

Primary outcomes

  1. Behavioral: interference rate

    Change in performance precision of a previously learned sensorimotor skill

    Time frame: before - after one single intervention (1 hour)

  2. Neural: brain connectivity change

    Change in EEG-derived markers of brain activation and connectivity

    Time frame: before - after one single intervention (1 hour)

Secondary outcomes

  1. Behavioral: interference rate

    Change in performance precision of a previously learned sensorimotor skill

    Time frame: before - after one single intervention (24 hour follow-up)

  2. Neural: brain connectivity change

    Change in EEG-derived markers of brain activation and connectivity

    Time frame: before - after one single intervention (24 hour follow-up)

07

Study locations

1 site
  • Medical University of South Carolina
    Charleston, South Carolina 29425, United States
08

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Sep 15, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT05946616
Lead sponsor
Medical University of South Carolina
Responsible party
Kirstin-Friederike Heise (Assistant Professor-Faculty, Medical University of South Carolina) — Principal investigator
First posted
Jul 14, 2023
Start date
Jul 1, 2023
Primary completion
Dec 31, 2026 (estimated)
Completion
Dec 31, 2026 (estimated)
Last update
Sep 15, 2026

Study contacts

Kirstin-Friederike Heise, PhD
principal investigator · Medical University of South Carolina

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is active, not recruiting, as verified in Sep 2026. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion