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Efficacy of boosting cognition by mimicking slow wave sleep in the awake brain.

Efficacy of boosting cognition by mimicking slow wave sleep in the awake brain in healthy sleepers aged 18 to 35 years.

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ANZCTR
Registry ID
ACTRN12626000304336
Enrollment
5
Registered
2026-03-10
Start date
2025-06-19
Completion date
2027-09-01
Last updated
2026-03-16

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

Conditions

None listed

Brief summary

The aim of this study is to see if the detrimental cognitive effects of 36 hours of sleep deprivation can be offset by applying slow wave oscillations induced by non-invasive brain stimulation to mimic the effects of slow wave sleep. The study will target healthy adults. Effects will be compared to sham stimulation and a brief nap. It is hypothesised that slow wave brain stimulation will protect the brain from the detrimental effects of sleep deprivation, and will provide similar benefits to that provided by a brief nap.

Interventions

Participants will be sleep deprived for 36 hours. Participants will attend the laboratory ~12 hours after waking and will be continually monitored within the laboratory by trained research staff to ensure they do not fall asleep up until the data collection stage at 36 hours sleep deprivation. Prior to attending the laboratory participants will be wearing an actigraphy device on their wrist to provide data on their sleep-wake activity when away from the laboratory. Participants will receive a

Participants will be sleep deprived for 36 hours. Participants will attend the laboratory ~12 hours after waking and will be continually monitored within the laboratory by trained research staff to ensure they do not fall asleep up until the data collection stage at 36 hours sleep deprivation. Prior to attending the laboratory participants will be wearing an actigraphy device on their wrist to provide data on their sleep-wake activity when away from the laboratory. Participants will receive a safe and non-painful form of non-invasive brain stimulation (transcranial alternating current stimulation; tACS) using a NeuroConn DC stimulator. The stimulation will be applied at 2mA for 20 minutes at a frequency of 0.75Hz. Two electrodes will be applied to the frontal region of the scalp to target dorsolateral prefrontal cortex. Stimulation is normally perceived as a scratching or itching sensation. Research staff will monitor the delivery of the stimulation throughout the 20 minutes of stimulation. The device also has inbuilt safety features meaning it will automatically turn off if the connection is compromised or if the impedance under the electrodes is too high. There will be a one-week wash out period between treatments. There are six possible sequence combinations may be allocated to and these are as follows: Intervention - sham - nap Intervention - nap - sham Sham - intervention - nap Sham - nap - intervention Nap - intervention - sham Nap - sham - intervention

Sponsors

The University of Queensland
Lead SponsorUniversity

Study design

Allocation
Randomised controlled trial
Intervention model
Crossover
Primary purpose
Treatment
Masking
Open (masking not used)

Eligibility

Sex/Gender
All
Age
18 Years to 35 Years
Healthy volunteers
Yes

Inclusion criteria

Healthy sleeper (regular sleep schedule with reportedly undisturbed sleep)

Exclusion criteria

Sleep disorders or clinical psychiatric disorders Medications that would interfere with sleep or contraindicate transcranial electric stimulation Excessive consumption of alcohol or caffeine preceding participation

Outcome results

None listed

Source: ANZCTR · Data processed: Mar 20, 2026