Sleep Deprivation
Conditions
Keywords
Sleep Restriction, Women's Health
Brief summary
This study is designed to assess how healthy premenopausal women respond to different patterns of sleep loss at different times in the menstrual cycle.
Detailed description
During a 1.5-week inpatient laboratory protocol, participants will undergo one of two parallel sleep conditions during either the follicular or luteal phase of the menstrual cycle (4 study arms total). Subjects will be randomly assigned to each study arm. During their time in the laboratory, biological samples (e.g., blood) will be collected for assessment of sex steroid hormones and other analyses. Sleep quantity and quality will be monitored and responses on neurobehavioral tests and surveys will be monitored for differences across conditions.
Interventions
BEHAVIORALControlled sleep
Duration and timing of sleep will be assigned and monitored in a controlled laboratory environment.
Sponsors
Brigham and Women's Hospital
National Heart, Lung, and Blood Institute (NHLBI)
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
SINGLE (Subject)
Masking description
Participants may not know to which study arm they are assigned.
Eligibility
Sex/Gender
FEMALE
Age
18 Years to 35 Years
Healthy volunteers
Yes
Inclusion criteria
* Female * 18-35 years old * Regular menstrual cycle between 26-35 days in duration * Not using any form of hormonal contraception for at least the prior 3 months * Regular sleep patterns (7-9 hours/night) * Not taking any medications or supplements * Weight \>110 lb * BMI between 18.5 and 29.5 kg/m2
Exclusion criteria
* Primary sleep disorder * History of shift work * Transmeridian travel in the previous 3 months * Presence of acute or chronic disease, including but not limited to: diabetes, metabolic disorders, psychiatric illness, reproductive disorders * Current pregnancy, \< 6 months postpartum, and/or breastfeeding * Blood donation in the past 8 weeks * Extreme morning or evening chronotype
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| KSS score | The KSS will be administered at frequent intervals over 11 days in a sleep laboratory. Subjects will be in a time-free environment, and not told the sampling frequency. | The Karolinska Sleepiness Score (KSS) measures level of sleepiness on a 9-point Likert scale with 1 = Extremely Alert and 9 = Extremely Sleepy. A linear mixed model analysis will be conducted to compare KSS score at each time point (multiple points across the study) across all 4 study arms. |
| P4/E2 ratio | Biological samples will be collected at frequent intervals over 11 days in a sleep laboratory. Subjects will be in a time-free environment, and not told the sampling frequency. | The ratio of progesterone (P4) and estradiol (E2) in each sample will be calculated as (P4 ng/ml x 1000)/E2 pg/ml. A linear mixed model analysis will be conducted to compare the P4/E2 ratio at each time point (multiple points across the study) across all 4 study arms. |
| Core body temperature | Core body temperature will be collected at frequent intervals over 11 days in a sleep laboratory. Subjects will be in a time-free environment, and not told the sampling frequency. | Core body temperature is measured via rectal thermistor. A linear mixed model analysis will be conducted to compare the core body temperature at each time point (multiple points across the study) across all 4 study arms. |
| PVT lapses in attention | The PVT will be administered at frequent intervals over 11 days in a sleep laboratory. Subjects will be in a time-free environment, and not told the sampling frequency. | The number of lapses in attention will be counted across each Psychomotor Vigilance Task (PVT) session. A linear mixed model analysis will be conducted to compare PVT lapses in attention at each time point (multiple points across the study) across all 4 study arms. |
| PVT mean reaction time | The PVT will be administered at frequent intervals over 11 days in a sleep laboratory. Subjects will be in a time-free environment, and not told the sampling frequency. | The mean reaction time will be calculated across each Psychomotor Vigilance Task (PVT) session. A linear mixed model analysis will be conducted to compare PVT mean reaction time at each time point (multiple points across the study) across all 4 study arms. |
Countries
United States
Contacts
PRINCIPAL_INVESTIGATORMelissa A St. Hilaire, PhD
Brigham and Women's Hospital
Outcome results
None listed