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RECRUITING NA

Mind After Midnight

NCT07438912 · View on ClinicalTrials.gov ↗

Study Summary

This study examines whether wakefulness during the biological night (2:00-4:00 AM) is associated with increased negative mood, impaired decision-making, and suicidal thoughts. Adults with a history of suicidal ideation in the past six months will complete laboratory and home-based assessments under varying levels of sleep pressure. Participants will be evaluated during late-night wakefulness and under conditions of both higher and lower sleep pressure. The goal of the study is to better understand the biological and behavioral mechanisms that may contribute to elevated suicide risk during nocturnal wakefulness.

Interventions

  • BEHAVIORAL Sleep Pressure Manipulation

Study Locations (1)

Arizona

  • University of Arizona - Center for Sleep, Circadian, and Neuroscience Research — Tucson

Trial Details

FieldValue
Enrollment Target 90 participants
Start Date 2026-03-01
Est. Completion 2029-08-31
Phase NA

Sponsor

University of Arizona

379 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT07438912

The ClinicalTrials.gov registry entry for NCT07438912 describes a study currently listed as recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 90 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University of Arizona, which has 379 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 4 conditions, with Suicidal Ideation appearing as the primary indexed condition, and to 1 intervention — of which Sleep Pressure Manipulation is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT07438912 reports 1 study location spanning 1 distinct geographic area — top geographies include Arizona. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

Frequently Asked Questions

What is clinical trial NCT07438912 about?

NCT07438912 is a clinical study titled "Mind After Midnight". This study examines whether wakefulness during the biological night (2:00-4:00 AM) is associated with increased negative mood, impaired decision-making, and suicidal thoughts. Adults with a history of suicidal ideation in the past six months will complete laboratory and home-based assessments under ...

What is the current status of trial NCT07438912?

This trial is currently recruiting. It is a NA study. The enrollment target is 90 participants. The study started on 2026-03-01. Estimated completion is 2029-08-31.

What conditions does trial NCT07438912 study?

This clinical trial studies the following conditions: Suicidal Ideation, Sleep Deprivation, Circadian Rhythm Disorders, Sleep Wake Disorders. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT07438912?

The interventions under investigation include: Sleep Pressure Manipulation (BEHAVIORAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT07438912?

This trial is sponsored by University of Arizona, which has 379 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT07438912 being conducted?

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

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial