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Olfactory Decision-making and Deprived Sleep

Not Applicable
Completed
Conditions
Sleep Deprivation
Interventions
Behavioral: Sleep deprivation
Registration Number
NCT05093413
Lead Sponsor
Northwestern University
Brief Summary

This research study will use magnetic resonance imaging (MRI) and olfactory stimuli to better understand the connection between sleep deprivation, brain activity, and olfaction in humans.

Detailed Description

Not available

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
46
Inclusion Criteria
  • At least 18 years old
  • Fluent English speakers
Exclusion Criteria
  • History of neurological conditions (e.g., epilepsy, dementia, multiple sclerosis, brain tumors, etc.)
  • History of psychiatric conditions (e.g., general anxiety disorder, depression, schizophrenia, obsessive-compulsive disorder, post-traumatic stress disorder, attention deficit hyperactivity disorder, alcoholism, etc.)
  • Significant medical illnesses (e.g., cancer, meningitis, chronic obstructive pulmonary disease, cardiovascular disease, etc.)
  • Cerebrovascular risk factors (e.g., hypertension, diabetes, elevated cholesterol, etc.)
  • Use of psychoactive medications (e.g., barbiturates, benzodiazepines, chloral hydrate, haloperidol, lithium, carbamazepine, phenytoin, citalopram, escitalopram, fluoxetine, diazepam, etc.)
  • Smell or taste dysfunction
  • History of severe allergies requiring hospitalization for treatment
  • History of severe asthma requiring hospitalization for treatment
  • Habitual smoking
  • History of eating disorders (e.g., anorexia nervosa, bulimia nervosa, binge-eating disorder, etc.)
  • Dieting or fasting
  • History of sleep disorders (e.g., obstructive sleep apnea, narcolepsy, insomnia, etc.) Magnetic implants (e.g., shunts or stents, aneurysm clips, surgical clips, cochlear implants, metal bone/joint pins, plates and screws, eyelid spring or wires, etc.)
  • Electronic implants (e.g., implanted cardiac defibrillator, cardiac pacemaker, deep brain/spinal cord or nerve stimulator, internal electrodes/wires, medication infusion devices, etc.)
  • History of metal working without proper eye protection, or injury with metal shrapnel or metal slivers
  • Left-handedness
  • Claustrophobia

Study & Design

Study Type
INTERVENTIONAL
Study Design
CROSSOVER
Arm && Interventions
GroupInterventionDescription
Sleep deprived first; Fully slept secondSleep deprivationParticipants will be sleep deprived during the first experimental visit and fully slept during the second experimental visit
Fully slept first; Sleep deprived secondSleep deprivationParticipants will be fully slept during the first experimental visit and sleep deprived during the second experimental visit
Primary Outcome Measures
NameTimeMethod
Behavior an olfactory perceptual decision-making taskUp to 24 hours after the intervention

Food-like perceptual responses to binary food-nonfood odor mixtures

Secondary Outcome Measures
NameTimeMethod
Resting-state functional magnetic resonance imagingUp to 24 hours after the intervention

Resting-state activity determined by functional magnetic resonance imaging

Trial Locations

Locations (1)

Northwestern University

🇺🇸

Chicago, Illinois, United States

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