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Sleep, Stress and Learning: an Experimental Pilot Study

Sleep, Stress and Learning: an Experimental Pilot Study

Status
UNKNOWN
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03657901
Acronym
Sleepstress
Enrollment
20
Registered
2018-09-05
Start date
2018-06-01
Completion date
2018-12-31
Last updated
2018-09-05

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

Conditions

Stress, Sleep

Brief summary

To investigate the efficiency and effect of a programmed slow-breathing exercise in the evening to the heart rate variability, sleep quality and memory performance over night.

Detailed description

Background Stress and increased alertness in the evening are major reasons for sleep onset problems, poor sleep and insomnia symptoms. For instance, increased amount of REM, and decreased amount of slow wave sleep may result. Also, the function of sleep in memory consolidation may suffer. They also affect the sleep structure and continuity during the night. They are highly prevalent phenomena among the entire population, including healthy adults and children. However, at the physiological level, the concept of evening alertness is still understudied and often neglected. Recent advances show that breathing exercise is an efficient tool to reduce stress. However, its use specifically prior to sleep onset and with measurement sleep stages and their microstructures with sleep EEG has been little been studied before. The overall objective of this study is to explore interrelations of stress, learning and sleep quality.

Interventions

BEHAVIORALMusic listening

Guided music listening for 30 minutes before sleep onset

BEHAVIORALSlow breathing

Guided slow breathing for 30 minutes before sleep onset

Sponsors

University of Helsinki
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Intervention model description

Randomized control trial with a cross-over design.

Eligibility

Sex/Gender
ALL
Age
20 Years to 45 Years
Healthy volunteers
Yes

Inclusion criteria

* age 20-45

Exclusion criteria

* chronic disease requiring daily medication, acute sickness (e.g. a flu), jet lag from a recent travel, current diagnosed sleep disorder (such as snoring or insomnia) and any use of medication affecting autonomic nervous system function or sleep.

Design outcomes

Primary

MeasureTime frameDescription
Sleep structureChange from night 1 to night 2Percent distribution of different sleep stages

Secondary

MeasureTime frameDescription
Sleep spindle durationChange from night 1 to night 2Duration of sleep spindles in seconds
Sleep spindle powerChange from night 1 to night 2Amplitude of sleep spindles in microvolts

Countries

Finland

Outcome results

None listed

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