Dietary Intervention to Mitigate Adverse Consequences of Night Work

Part of paid clinical trials in Boston, Massachusetts.

Sponsor
Brigham and Women's Hospital
Study ID
NCT04868526
Status
Recruiting

Conditions

  • Dietary Habits

Eligibility Criteria

Sex
ALL
Age
18 Years - 45 Years
Healthy Volunteers
Accepted

Interventions

  • dietary intervention — BEHAVIORAL
    Research participants will be assigned to two dietary conditions.

Study Details

The goal of this clinical trial is to test whether our dietary intervention can prevent or lessen the negative health effects of night shift work in healthy participants. Participants will: * complete 2 inpatient stays * be provided with identical meals * have frequent blood draws * provide urine, saliva, stool and rectal swab samples

Key Dates

Start date
Mar 29, 2023
Status verified
Nov 2025
Primary completion
Sep 1, 2026
Completion
Sep 1, 2026

Study Design

Enrollment
24 participants (estimated)
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE

Arms

  • Experimental: Control-Dietary Intervention
    Control condition first, then the Dietary intervention. Since this is a single blind study, the details of the dietary interventions cannot be released during recruitment stage but will be made public once enrollment closes.
  • Experimental: Dietary intervention-Control
    Dietary intervention first, then the Control condition. Since this is a single blind study, the details of the dietary interventions cannot be released during recruitment stage but will be made public once enrollment closes.

Primary Outcome Measure

Change in glucose tolerance from Baseline to Test Day [ Time Frame: Baseline (Day 2) and Test Day (Day 4) ]

Central Contacts

Locations (1)

FacilityCityStateZIPSite coordinators
Brigham and Women's HospitalBostonMassachusetts02115
Han-Chow Koh, PhD
6172780924
Frank Scheer, PhD (PRINCIPAL_INVESTIGATOR)
Han-Chow Koh, PhD (SUB_INVESTIGATOR)
Jingyi Qian, PhD (SUB_INVESTIGATOR)

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