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Cardiometabolic Outcomes With Light Exposure During Sleep

Cardiometabolic Outcomes With Light Exposure During Sleep

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05317559
Enrollment
20
Registered
2022-04-08
Start date
2014-02-28
Completion date
2018-07-31
Last updated
2022-04-08

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

Conditions

Light

Keywords

light, sleep, metabolism, sympathetic nervous system, insulin resistance

Brief summary

This study tested the hypothesis that acute exposure to light during nighttime sleep adversely affects cardiometabolic function.

Detailed description

This study tested the hypothesis that acute exposure to light during sleep adversely affects next morning glucose homeostasis and whether this effect occurs via reduced sleep quality, melatonin suppression, or sympathetic nervous system (SNS) activation during sleep. Twenty young adults participated in this parallel-group study design. The room light condition (n=10) included one night of sleep in dim light (\< 3 lux) followed by one night of sleep with overhead room lighting (100 lux). The dim light condition (n=10) included two consecutive nights of sleep in dim light.

Interventions

BEHAVIORALroom light

The room light condition (n=10) included one night of sleep in dim light (\< 3 lux) followed by one night of sleep with overhead room lighting (100 lux). The dim light condition (n=10) included two consecutive nights of sleep in dim light.

Sponsors

Northwestern University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
BASIC_SCIENCE
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 40 Years
Healthy volunteers
Yes

Inclusion criteria

* healthy adults * ages 18-40 years * habitual sleep duration of 6.5-8.5 hours * habitual sleep onset of 9:00 pm-1:00 am

Exclusion criteria

* any sleep disorder as assessed by history and screening questionnaires for obstructive sleep apnea (Berlin) and excessive daytime sleepiness (ESS \>12), and by PSG to exclude sleep apnea (apnea hypopnea index ≥ 15), periodic leg movements (movement arousal index ≥ 15), or REM sleep behavior disorder; * history of a cognitive or neurological disorder; * history of a major psychiatric disorder, including but not limited to mood/anxiety, eating, and alcohol/substance abuse disorders; * depressed mood (Beck Depression Inventory II score ≥ 20); * diabetes or other endocrine disorders; * any gastrointestinal disease requiring dietary adjustment; * blindness or significant vision loss; * any unstable or serious medical conditions; * current or recent (within the past month) of psychoactive, hypnotic, stimulant or analgesic medications; * shift work or other types of self-imposed irregular sleep schedules; * obesity (body mass index \> 30 kg/m2); * history of habitual smoking (6 or more cigarettes per week) or drinking (7 or more alcoholic beverages per week) or caffeine consumption greater than 300 mg per day; * current use of light therapy; * use of any other legal or illicit substance that may affect sleep and/or appetite; * allergy to heparin. * Due to the metabolic stress associated with pregnancy and breastfeeding, patients who were pregnant or breastfeeding were also excluded.

Design outcomes

Primary

MeasureTime frameDescription
Matsuda IndexDay 2OGTT
HOMA-IRDay 2Fasting

Secondary

MeasureTime frameDescription
Heart RateNight 2beat to beat
Sleep StagesNight 1Stage N1, N2, N3
Blood pressureDay 2diastolic/systolic
Slow Wave ActivityNight 1Spectral power in the Slow Wave Activity (0.5 to 4 Hz)

Other

MeasureTime frameDescription
subjective sleepinessDay 2sleepiness level
MelatoninDay 2pg/ml
hungerDay 2hunger level

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026