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Mind After Midnight

The Mind After Midnight: Mechanistic Examination of Nocturnal Wakefulness as a Suicide Risk Factor

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT07438912
Acronym
MaM
Enrollment
90
Registered
2026-02-27
Start date
2026-03-06
Completion date
2029-08-31
Last updated
2026-05-22

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

Conditions

Circadian Rhythm Disorders, Sleep Deprivation, Sleep Wake Disorders, Suicidal Ideation

Keywords

Nocturnal Wakefulness, Suicide Risk, Circadian Misalignment, Impulsivity, Mood Regulation, Biological Night, Sleep Pressure, Decision-Making

Brief 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.

Detailed description

Suicide risk is elevated during the biological night, particularly between 2:00 and 4:00 AM. Observational and epidemiologic data suggest that nocturnal wakefulness is associated with increased negative affect, impaired decision-making, and greater suicidal ideation. The "Mind After Midnight" hypothesis proposes that wakefulness during the biological night exposes individuals to a combination of circadian vulnerability and homeostatic sleep pressure that contributes to emotional and cognitive dysregulation. This study will recruit approximately 90 adults with a history of suicidal ideation in the past six months. Participants will complete both home-based and laboratory-based procedures. Laboratory assessments will evaluate mood, hopelessness, suicidal ideation, impulsivity, and decision-making at different times of day, including 2:00-4:00 AM. To examine the role of homeostatic sleep pressure, participants will complete late-night assessments under two conditions: (1) high sleep pressure (remaining awake until 2:00 AM) and (2) low sleep pressure (sleeping and being awakened at 2:00 AM). Circadian factors will be assessed using behavioral measures and physiologic markers, including melatonin. The goal of the study is to experimentally test whether nocturnal wakefulness contributes to suicide-associated cognitive and affective processes and to identify underlying chronobiological mechanisms.

Interventions

BEHAVIORALSleep Pressure Manipulation

Participants undergo an experimental manipulation of homeostatic sleep pressure involving controlled wakefulness or scheduled awakening during the biological night. Mood, suicidal ideation, impulsivity, and decision-making are assessed during overnight laboratory sessions.

Sponsors

University of Arizona
Lead SponsorOTHER
National Institute of Mental Health (NIMH)
CollaboratorNIH

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE

Masking description

This study is open-label. Participants and study personnel are aware of the assigned sleep pressure condition (high sleep pressure or low sleep pressure), as the experimental manipulation involves remaining awake or being awakened during the biological night.

Intervention model description

Participants will complete laboratory assessments under two experimental sleep pressure conditions in a within-subject crossover design. In one condition, participants will remain awake until 2:00 AM (high sleep pressure). In the other condition, participants will sleep and be awakened at 2:00 AM (low sleep pressure). Mood, suicidal ideation, and decision-making will be assessed during the biological night under both conditions.

Eligibility

Sex/Gender
ALL
Age
18 Years to 55 Years
Healthy volunteers
No

Inclusion criteria

* Age 18-55 years * History of suicidal ideation within the past 6 months * Habitual bedtime between 9:00 PM and 1:00 AM * Habitual wake time between 6:00 AM and 9:00 AM * Ability to provide informed consent

Exclusion criteria

* Current suicidal intent requiring immediate clinical intervention * Diagnosis of a primary sleep disorder (e.g., untreated obstructive sleep apnea, narcolepsy) * Bipolar disorder or psychotic disorder * Substance use disorder within the past 3 months * Use of medications that significantly affect sleep or circadian rhythms * Night shift work or transmeridian travel within the past month * Medical or neurological condition that would interfere with participation * Pregnancy

Design outcomes

Primary

MeasureTime frameDescription
Feelings of HopelessnessVisit 1(day 2, night 2), Visit 2 (day 2, night 2)Total score on the BECK Hopelessness scale (BHS)
Impaired Executive FunctionVisit 1(day 2, night 2), Visit 2 (day 2, night 2)BART total score
Negative MoodVisit 1(day 2, night 2), Visit 2 (day 2, night 2)PANAS negative affect score

Countries

United States

Contacts

CONTACTDenisse Armenta
armentamd@arizona.edu5206261737
CONTACTDarilyn Rivera-Collazo, MS
darilyn@arizona.edu5206264746
PRINCIPAL_INVESTIGATORMichael A Grandner, PhD

University of Arizona

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: May 23, 2026