Impact of Night Shift Work on 24-hour Blood Glucose Levels
NCT ID: NCT05559762
Last Updated: 2025-03-10
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.
COMPLETED
22 participants
OBSERVATIONAL
2022-11-08
2023-07-30
Brief Summary
Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.
Related Clinical Trials
Explore similar clinical trials based on study characteristics and research focus.
Evaluation of Glucose Monitoring Methods: Characterizing Glycemic Control in Subjects With Diabetes
NCT00805506
Sleep Effectiveness and Insulin and Glucose Homeostasis
NCT01887691
Effects of Standing on Glycemia in Prediabetic Adults
NCT01884792
The Effects of Normobaric Hypoxia on Blood Glucose Levels.
NCT01302782
Effects of Exercise and Energy Balance on 24-hour Blood Glucose Control
NCT03350997
Detailed Description
Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.
Conditions
See the medical conditions and disease areas that this research is targeting or investigating.
Study Design
Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.
COHORT
PROSPECTIVE
Study Groups
Review each arm or cohort in the study, along with the interventions and objectives associated with them.
Day Shift
Nurses regularly working 12hr day shifts
No interventions assigned to this group
Night Shift
Nurses regularly working night shift
No interventions assigned to this group
Eligibility Criteria
Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.
Inclusion Criteria
* Free from presence of uncontrolled chronic illness and specifically prediabetes, Type 1 or Type 2 diabetes (but not including history of gestational diabetes) and not currently taking any glucose-lowering or steroid medication
* Not currently pregnant or breastfeeding
* English speaking and able to provide informed consent
* Must own and know how to operate a Smartphone
* Must be willing and able to wear two small sensors attached by adhesive for the study duration, the Fibion SENS activity monitor and the Dexcom G6 continuous glucose monitor
* Must regularly consume food during shifts and refrain from actively attempting weight loss during the study duration
* Must work only one job at the time of study participation
18 Years
65 Years
ALL
No
Sponsors
Meet the organizations funding or collaborating on the study and learn about their roles.
Providence St Joseph Health
UNKNOWN
Lincoln Memorial University
OTHER
Responsible Party
Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.
Lindsey Miller
Associate Professor
Principal Investigators
Learn about the lead researchers overseeing the trial and their institutional affiliations.
Lindsey Miller
Role: PRINCIPAL_INVESTIGATOR
Lincoln Memorial University
Locations
Explore where the study is taking place and check the recruitment status at each participating site.
Providence Sacred Heart Hospital
Spokane, Washington, United States
Countries
Review the countries where the study has at least one active or historical site.
Other Identifiers
Review additional registry numbers or institutional identifiers associated with this trial.
STUDY2022000529
Identifier Type: -
Identifier Source: org_study_id
More Related Trials
Additional clinical trials that may be relevant based on similarity analysis.