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Effects of HD-tDCS During Slow-wave Sleep on Associative Memory

Effects of High-definition Transcranial Direct Current Stimulation During Slow-wave Sleep on Associative Memory

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07063264
Enrollment
87
Registered
2025-07-14
Start date
2022-01-12
Completion date
2023-08-23
Last updated
2025-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy Adults, Transcranial Direct Current Stimulation

Keywords

Associative Memory, High-Definition Transcranial Direct Current Stimulation, Slow Wave Sleep, DLPFC

Brief summary

To evaluate the effects of afternoon naps and high-definition transcranial direct current stimulation (HD-tDCS) over the left dorsolateral prefrontal cortex (DLPFC) in associative memory (AM)

Detailed description

Healthy adults will be randomized into three groups: a sleep with active stimulation (Sleep-A) group will receive active anode HD-tDCS during slow-wave sleep (SWS) of non-rapid eye movement sleep (NREM) at afternoon nap, a sleep with sham stimulation (Sleep-S) group will receive afternoon nap with sham stimulation, and wake with active stimulation (Wake-A) group will receive active anode HD-tDCS during wakefulness. An anode stimulation electrode will be placed in F3 (10/20 system) which intend to target the left DLPFC, and four cathodes will be placed at FCz, AFz, F7, and C5 (10/20 system). The face-word AM task and other multidimensional neuropsychological tasks will be performed before and after afternoon napping.

Interventions

HD-tDCS is described as a non-invasive form of brain stimulation that uses a low-intensity, direct current applied directly to the head through scalp electrodes

Sham HD-tDCS was delivered using the same protocol and current intensity, but the period of active stimulation was only during the ramp-up and ramp-down periods of 30 and 30 seconds.

Sponsors

WANG KAI
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
HEALTH_SERVICES_RESEARCH
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 30 Years
Healthy volunteers
Yes

Inclusion criteria

* aged 18-30 years * healthy adults

Exclusion criteria

* with pacemakers, skull cavities or cracks; * intolerance of high-definition transcranial direct current stimulation (HD-tDCS) adverse reactions; * left-handed; * diagnosed with severe mental disorders, or involved in other experiments.

Design outcomes

Primary

MeasureTime frameDescription
face-word assciative memory task score1 hour after the end of the afternoon napIn the face-cued word association test, participants viewed 20 grayscale photographs of faces on a computer screen, each shown for 3 seconds. Each photograph was paired with a distinct word, which participants read aloud when shown. Participants were instructed to memorize the word linked to each face. One minute later, participants viewed the same 20 faces in a new random order. They were then asked to recall the associated words. Each face was scored as correct or incorrect, and the total number of correct responses formed the AM score.

Secondary

MeasureTime frameDescription
Auditory Verbal Learning Test (AVLT) score2 hours after the end of afternoon napThere are two parts to the test process: learning phase and delayed recall phase. During the learning phase, subjects were asked to listen to a list of words and recall them. During the delayed recall phase, subjects were asked to recall the list of previously learned words again after a period of time. Scoring usually includes recording the number of correct memories the subject has during the learning phase and delayed recall phase, as well as the types of possible errors (such as forgetting, confusion, etc.). Depending on the subject's performance, learning and memory abilities can be assessed. The normal ranges of immediate memory, delayed memory and recognition memory were 10, 8 and 10 respectively. Higher scores mean a better outcome.

Countries

China

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026