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Clinical Trials in Israel / NCT05393830
Recruiting Not applicable

The Effect of Sleep Loss on Emotion Regulation

NCT05393830 · tracked via the Priya Life Science Israel tracker
Phase
Not applicable
Started
2023-05-11
Last updated
2026-04-14

Condition(s) studied

SleepInsomniaSleep Deprivation

Investigational drug(s) / intervention(s)

Sleep Restriction

Sleep Restriction: Three nights of sleep restricted to 4 hours per night.

Study summary

The study is designed to investigate the impact of three nights of sleep restricted to 4 hours per night, on the processing and regulation of emotional information compared to Insomnia Disorder and control. The investigators will address and attempt to answer two questions.

(i) How do three nights of reduced sleep or a diagnosis of Insomnia Disorder affect the processing and regulation of emotional information compared to typical, undisturbed sleep? (ii) What overlapping and distinct neural mechanisms are engaged and associated with behavioral effects when attempting to process and regulate emotions in a sleep restricted state or with a clinical diagnosis of Insomnia Disorder? This study will investigate sleep's role in emotion processing and regulation. The findings will help further understanding of the role of sleep in healthy emotional functioning.

Eligibility

Sex
ALL
Min age
18 Years
Max age
40 Years
Healthy volunteers
Accepted
Inclusion Criteria: * willing and able to follow the protocol * willing and able to meet inclusion criteria for fMRI scanning * willing to refrain from alcohol and recreational drugs for the duration of the protocol * normal or corrected to normal vision is required Exclusion Criteria: * left-handedness or ambidexterity * the use of any drugs that could affect either sleep or cognitive functioning (e.g., prescription sleeping pills or antidepressants)

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Beth Israel Deaconess Medical Center Boston Massachusetts Recruiting

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Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT05393830 on ClinicalTrials.gov ↗ ← All trials in Israel