Clinical Trials Directory

Trials / Enrolling By Invitation

Enrolling By InvitationNCT05656768

Sleep and Circadian Contributions to Nighttime Blood Pressure

Status
Enrolling By Invitation
Phase
N/A
Study type
Interventional
Enrollment
1,427 (estimated)
Sponsor
University of Alabama at Birmingham · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Broadly, this study (SCN-BP) seeks to examine sleep and circadian factors that contribute to blood pressure levels at night.

Detailed description

SCN-BP is imbedded in a parent grant titled "Improving the Detection of Hypertension (IDH-MEGA)" and examines a variety of sleep (e.g., sleep duration, timing, and the presence of sleep disorder) and circadian factors in Aims 1 and 2. In Aim 3, the investigators will conduct a 30-hour constant routine protocol to directly examine endogenous circadian and blood pressure rhythms. Aims 1 and 2 are purely observation. The study design design described below pertains the intervention piece of this study (Aim 3).

Conditions

Interventions

TypeNameDescription
OTHERConstant Routine ProtocolA constant routine protocol is used to directly examine markers of circadian rhythmicity (e.g., melatonin and core body temperature). A constant routine protocol requires an individual to remain in a dimly lit room, in a constant semi-recumbent posture, and remain awake for more than 24 hours. It is one of two gold-standard research protocols for examining circadian rhythms in humans.

Timeline

Start date
2023-06-01
Primary completion
2028-12-30
Completion
2028-12-30
First posted
2022-12-19
Last updated
2026-01-29

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT05656768. Inclusion in this directory is not an endorsement.