Sleep Restriction and Parental History of Hypertension

Status: Recruiting
Location: See location...
Intervention Type: Behavioral
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

The purpose of this study is to research the effects of partial sleep deprivation (sleep restriction) in a group of individuals whose parents have high blood pressure compared to a group of individuals whose parents have normal blood pressure.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 35
Healthy Volunteers: t
View:

• Healthy adults aged 18-35 years

• Absence of any significant medical or psychiatric disease (as per the investigators' judgment)

• Nonsmoker

• Nonpregnant

• History of normal sleep duration (reported average sleep duration between 7-9 hours/night and no habitual napping)

• Hypertension status information available for both biological parents

• Ability to understand study procedures and to comply with them for the entire length of the study

• Ability to understand English and provide informed consent

Locations
United States
Minnesota
Mayo Clinic in Rochester
RECRUITING
Rochester
Contact Information
Primary
Sabah Munir
Munir.Sabah@mayo.edu
(507)255-0151
Time Frame
Start Date: 2025-02-20
Estimated Completion Date: 2029-04
Participants
Target number of participants: 44
Treatments
Experimental: Study Sequence AB
Sleep restriction condition in the first period and normal sleep condition in the second period. Each period will consist of a 10-day inpatient visit comprising a 3-day/2-night baseline, followed by a 5-day/5-night experimental phase, and a 2-day/2-night recovery phase.
Experimental: Study Sequence BA
Normal sleep condition in the first period and sleep restriction condition in the second period. Each period will consist of a 10-day inpatient visit comprising a 3-day/2-night baseline, followed by a 5-day/5-night experimental phase, and a 2-day/2-night recovery phase.
Related Therapeutic Areas
Sponsors
Leads: Mayo Clinic
Collaborators: National Heart, Lung, and Blood Institute (NHLBI)

This content was sourced from clinicaltrials.gov

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