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Role of Photic and Non-photic Time Cues in Resetting Circadian Rhythms (LipidPRC)

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Mass General Brigham

Status

Enrolling

Conditions

Light Exposure
Meal Timing

Treatments

Behavioral: Bright Light
Behavioral: 12-h meal window
Behavioral: Dim light
Behavioral: Time-restricted eating

Study type

Interventional

Funder types

Other

Identifiers

NCT05276739
2021P000757

Details and patient eligibility

About

The aim of this study is to determine the principal time cue (light or meals) for resetting circadian rhythms in melatonin and metabolic outcomes.

Full description

The objective of this proposal is to construct and compare PRCs describing the relationship between the timing of light exposure and meals across the 24-hour day and the size and direction of shift in circadian rhythms of circulating lipids and melatonin in humans. Completion of the work will provide mechanistic insight on the role of photic and non-photic cues mediating entrainment of circadian rhythms in humans besides that of melatonin. In this proposal, we will use the same experimental paradigm that we have successfully used previously to characterize and compare PRCs for shifts in melatonin in response to light exposure of different durations and spectra, and as used in our pilot trials demonstrating a robust PRC of lipid circadian rhythms in response to combined photic and non-photic stimuli across the day. We will achieve our objective using a randomized controlled trial in young healthy adults (n=48, 18-30 years) that systematically manipulates the timing of 6.5-hour bright light exposure and 6.5-hour time restricted eating across the 24-hour circadian cycle to specifically:

Aim 1: Determine if light is the primary time cue for resetting melatonin but not lipid circadian rhythms. Hypothesis: The resetting response of circadian rhythms in melatonin but not cholesterol and triglycerides is dependent upon the circadian phase at which a 6.5-hour bright light exposure occurs.

Aim 2: Determine if meal timing is the primary time cue for resetting lipid but not melatonin circadian rhythms. Hypothesis: The resetting response of circadian rhythms in cholesterol and triglycerides but not melatonin is dependent upon the circadian phase at which a 6.5-hour time restricted eating occurs.

Aim 3 (Exploratory): Evaluate the acute effects of eating across the 24-hour day on circulating lipid levels. Hypothesis: The acute effects of 6.5-hour time restricted eating on circulating cholesterol and triglycerides levels are dependent on the circadian phase at which meals are eaten.

Enrollment

48 estimated patients

Sex

All

Ages

18 to 30 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • Aged between 18-30 years
  • Healthy (no medical, psychiatric or sleep disorders;
  • Non-smoking for at least 6 months;
  • Body Mass Index of >18 or <30 kg/m2;
  • Able to maintain 8-hour consistent sleep schedule during the study
  • Able to refrain from caffeine, alcohol, medication and supplements during the study

Exclusion criteria

  • History of alcohol or substance abuse;
  • Positive result on drugs of abuse urine toxicology;
  • Current or past history of sleep disorders, including but not limited to obstructive sleep apnea, narcolepsy, insomnia, or any significant sleep complaint
  • Psychiatric disorder, or first degree relative with a psychiatric disorder
  • Recent acute or chronic medical disorder
  • Use of drugs or medication (birth control OK) likely to affect sleep, alertness or light sensitivity, as determined by the investigators
  • Visual disorder, including but not limited to color blindness, or family history of glaucoma
  • Pregnancy or lactation
  • Shift work (past 3 years)
  • Transmeridian travel (2 or more time zones) in the past 3 months
  • Any other reason as determine by the Principal Investigator

Trial design

Primary purpose

Basic Science

Allocation

Randomized

Interventional model

Parallel Assignment

Masking

Single Blind

48 participants in 3 patient groups

Bright light
Experimental group
Description:
Participants will receive a 6.5-hour 10,000 lux light pulse (4100K fluorescent light) centered within the 16-hour wake episode (start 4.75 hour after wake and end 11.25 hour after wake). Participants will receive 4 identical meals (equal calories and macronutrient content), over a 12-hour interval (meals at 2, 6, 10, and 14 hours after waking) centered within the 16-hour wake episode.
Treatment:
Behavioral: 12-h meal window
Behavioral: Bright Light
Time-restricted eating
Experimental group
Description:
Participants will consume 4 identical meals, as in the other groups, except that the meal window will be restricted to 6.5 hours instead of 12 hours (meals at 4.75, 6.9, 9.1, 11.25 hours after waking) centered within the 16-hour wake episode. Participants will remain in dim light (\<3 lux) throughout the 16-hour wake episode.
Treatment:
Behavioral: Dim light
Behavioral: Time-restricted eating
Control
Sham Comparator group
Description:
Participants will receive 4 identical meals (equal calories and macronutrient content), over a 12-hour interval (meals at 2, 6, 10, and 14 hours after waking) centered within the 16-hour wake episode. Participants will remain in dim light (\<3 lux) throughout the 16-hour wake episode.
Treatment:
Behavioral: Dim light
Behavioral: 12-h meal window

Trial contacts and locations

1

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Central trial contact

Shadab A Rahman, PhD, MPH; Leilah K Grant, PhD

Data sourced from clinicaltrials.gov

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