NCT07063264

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)

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
87

participants targeted

Target at P50-P75 for not_applicable

Timeline
Completed

Started Jan 2022

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

Study Start

First participant enrolled

January 12, 2022

Completed
1.1 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

February 20, 2023

Completed
6 months until next milestone

Study Completion

Last participant's last visit for all outcomes

August 23, 2023

Completed
1.8 years until next milestone

First Submitted

Initial submission to the registry

June 3, 2025

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 14, 2025

Completed
Last Updated

July 14, 2025

Status Verified

July 1, 2025

Enrollment Period

1.1 years

First QC Date

June 3, 2025

Last Update Submit

July 2, 2025

Conditions

Keywords

Associative MemoryHigh-Definition Transcranial Direct Current StimulationSlow Wave SleepDLPFC

Outcome Measures

Primary Outcomes (1)

  • face-word assciative memory task score

    In 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.

    1 hour after the end of the afternoon nap

Secondary Outcomes (1)

  • Auditory Verbal Learning Test (AVLT) score

    2 hours after the end of afternoon nap

Study Arms (3)

sleep with active stimulation (Sleep-A)

ACTIVE COMPARATOR

Participants will receive active anode HD-tDCS during slow-wave sleep (SWS) of non-rapid eye movement sleep (NREM) at afternoon nap. An anode stimulation electrode will be placed in F3 (10/20 system) which intended to target the left DLPFC, and four cathodes will be placed at FCz, AFz, F7, and C5 (10/20 system)

Device: high-definition transcranial direct current stimulation (HD-tDCS)

sleep with sham stimulation (Sleep-S)

PLACEBO COMPARATOR

Participants will receive afternoon nap with sham stimulation. A 30-s rising current until 2 mA is reached, with a 30-s decline immediately at the beginning and end of the stimulation section

Device: sham high-definition transcranial direct current stimulation (HD-tDCS)

wake with active stimulation (Wake-A)

SHAM COMPARATOR

Participants will receive active anode HD-tDCS during wakefulness. They will receive HD-tDCS stimulation for 25 minutes while awake, then spent free time in the sleep monitoring room, remaining awake throughout the napping period

Device: high-definition transcranial direct current stimulation (HD-tDCS)

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

sleep with active stimulation (Sleep-A)wake with active stimulation (Wake-A)

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.

sleep with sham stimulation (Sleep-S)

Eligibility Criteria

Age18 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • aged 18-30 years
  • healthy adults

You may not qualify if:

  • 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.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Anhui Medical University

Hefei, Anhui, 230032, China

Location

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
HEALTH SERVICES RESEARCH
Intervention Model
PARALLEL
Sponsor Type
OTHER
Responsible Party
SPONSOR INVESTIGATOR
PI Title
Director of medical psychological department

Study Record Dates

First Submitted

June 3, 2025

First Posted

July 14, 2025

Study Start

January 12, 2022

Primary Completion

February 20, 2023

Study Completion

August 23, 2023

Last Updated

July 14, 2025

Record last verified: 2025-07

Locations