Blood Pressure Clinical Trial
Official title:
Night Shift Work, On-shift Napping, and Endothelial Function: A Pilot Study
Verified date | January 2024 |
Source | University of Pittsburgh |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
Cardiovascular disease (CVD) and CVD risk factors such as high blood pressure (BP) are disproportionately higher among night shift workers, including those who work in public safety and healthcare. The purpose of this pilot study is to assess feasibility of collecting data germane to key indicators of cardiovascular health (i.e., ambulatory blood pressure) repeatedly during a simulated night shift protocol. The primary outcome measure will be the number of participants for which at least 70% of required ambulatory BP measures were collected. A result of at least 10 participants/subjects will be considered feasible.
Status | Completed |
Enrollment | 10 |
Est. completion date | March 4, 2023 |
Est. primary completion date | March 4, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years to 100 Years |
Eligibility | Inclusion Criteria: All participants will be working aged adults (18 years of age or older). Investigators are interested in enrolling public safety workers and healthcare workers given how often this group works night shifts. Criteria that participants will need to address: 1. 18 years of age or older; 2. Currently licensed or certified as an EMS clinician, other public safety shift worker, or other type of healthcare clinicians and actively working in Western Pennsylvania as an EMT, Paramedic, Flight Nurse/Paramedic, other EMS clinician, firefighter, or other type of healthcare clinician (e.g., nurse, physician, physician assistants, patient care technician, or other healthcare clinician); 3. a 'no' answer to #2 above is not a criterion for exclusion. Exclusion Criteria: 1. Having ever been diagnosed with the following: hypertension, cardiovascular disease, myocardial infarction, stroke/TIA, chronic kidney disease, liver disease, adrenal disease, thyroid disease, rheumatologic disease, hematologic disease, cancer of any type, dementia/memory loss, organ transplantation; major sleep problem; heavy alcohol use; sleep apnea or other diagnosis that is related to problems with breathing or the airway; 2. Current pregnancy; 3. Insomnia is NOT a criterion for exclusion. |
Country | Name | City | State |
---|---|---|---|
United States | University of Pittsburgh | Pittsburgh | Pennsylvania |
Lead Sponsor | Collaborator |
---|---|
University of Pittsburgh |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Number of Participants for which at least 70% of required Ambulatory BP readings were collected | A result of at least 10 participants will be considered feasible | 48 continuous hours for each arm/condition | |
Secondary | Average blood pressure while awake during simulated night shift | The mean and standard deviation of blood pressure measurements taken while participant is awake during the 12-hour simulated night shift | 12 continuous hours for each arm/condition | |
Secondary | Average blood pressure while napping during simulated night shift | The mean and standard deviation of blood pressure measurements taken while participant is napping (sleeping) during the 12-hour simulated night shift that includes the 45-minute nap condition. | 45 minutes | |
Secondary | Average Reactive Hyperemia Index (RHI) at baseline | The mean and standard deviation RHI score for the endothelial dysfunction measurement assessed at baseline | 20-30 minutes for each arm/condition | |
Secondary | Average Reactive Hyperemia Index (RHI) after simulated night shift | The mean and standard deviation RHI score for the endothelial dysfunction measurement assessed after the 12-hour simulated night shift | 20-30 minutes for each arm/condition |
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