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NCT05393830 · ClinicalTrials.gov registry record · NA

The Effect of Sleep Loss on Emotion Regulation

A NA study of Insomnia and Sleep, sponsored by Beth Israel Deaconess Medical Center.

Recruiting
Registry status
NA
Development phase
90
Enrollment target
1
Study location

NCT05393830 is a NA study of Insomnia and Sleep that is actively recruiting participants, run by Beth Israel Deaconess Medical Center. The registered enrollment target is 90 participants, below the 170-participant average among 151 other Insomnia trials with a reported enrollment target (47% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT05393830, a NA study of Insomnia and Sleep, is actively recruiting participants, sponsored by Beth Israel Deaconess Medical Center.

RECRUITING
Registry status
NA
Development phase
90 participants
Enrollment target
1
Study location

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.

Interventions

  • BEHAVIORAL Sleep Restriction

Study Locations (1)

Massachusetts

  • Beth Israel Deaconess Medical Center - Boston

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2023-05-11
Est. Completion 2027-07-31
Phase NA

What the Registry Record Tells You About NCT05393830

The ClinicalTrials.gov registry entry for NCT05393830 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 170-participant average among 151 other Insomnia trials with a reported enrollment target (47% lower). The listed sponsor is Beth Israel Deaconess Medical Center, which has 488 total studies on file at ClinicalTrials.gov.

The record links to 3 conditions, with Insomnia appearing as the primary indexed condition, and to 1 intervention - of which Sleep Restriction is the first listed.

NCT05393830 reports 1 study location spanning 1 distinct geographic area - top geographies include Massachusetts.

Frequently Asked Questions

What is clinical trial NCT05393830 about?

NCT05393830 is a clinical study titled "The Effect of Sleep Loss on Emotion Regulation". 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 ...

What is the current status of trial NCT05393830?

This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2023-05-11. Estimated completion is 2027-07-31.

What conditions does trial NCT05393830 study?

This clinical trial studies the following conditions: Insomnia, Sleep, Sleep Deprivation.

What interventions are being tested in trial NCT05393830?

The interventions under investigation include: Sleep Restriction (BEHAVIORAL).

Who is sponsoring clinical trial NCT05393830?

This trial is sponsored by Beth Israel Deaconess Medical Center, which has 488 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT05393830 being conducted?

This trial has 1 study location across Massachusetts. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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