Clinical Trials Directory

Trials / Completed

CompletedNCT02484846

Impaired Vigilance, and Its Effects on Cognition and Behavior

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
50 (actual)
Sponsor
Stanford University · Academic / Other
Sex
All
Age
18 Years – 45 Years
Healthy volunteers
Accepted

Summary

Fifty healthy, young participants (10 male, 40 female) completed two 3-hour study sessions that were at least five days apart. The first session was a baseline. The sleep intervention took place on the night prior to Session 2, where the amount of time in bed was manipulated to be 60-130% of the individual's habitual sleep time. Within both sessions, subjective (Stanford Sleepiness Scale, SSS) and objective (Psychomotor Vigilance Test, PVT) alertness were measured. During the middle of each session, a 40-minute ad libitum meal opportunity allowed participants to eat from eight different food items. Food healthfulness, caloric density, distribution and number of calories were measured and compared to alertness levels.

Conditions

Interventions

TypeNameDescription
BEHAVIORALTime in bedHabitual time spent in bed for the purpose of sleep was determined at baseline. This was used to calculated the experimental time in bed the subject was to spent on the one night prior to the second lab visit.

Timeline

Start date
2011-02-01
Primary completion
2012-03-01
Completion
2012-03-01
First posted
2015-06-30
Last updated
2015-06-30

Source: ClinicalTrials.gov record NCT02484846. Inclusion in this directory is not an endorsement.