NCT06956963

Brief Summary

The goal of this interventional study is to differentiate the effects of an acute partial sleep deprivation intervention on markers of cardiovascular health, cardio-autonomic function, physical and cognitive performance, as well as overall wellbeing in active vs sedentary individuals. The main aims of the project are:

  • To differentiate the effects of partial sleep deprivation on central hemodynamics (i.e., central blood pressure and arterial stiffness) in active vs sedentary individuals.
  • To differentiate the effects of partial sleep deprivation on physical (i.e., handgrip strength and reactive strength index) and cognitive performance (i.e., reaction time and impulse control) in active vs sedentary individuals.
  • To differentiate the effects of partial sleep deprivation on overall wellbeing (i.e., cardio-autonomic function, inflammation levels, and psychological mood states) in active vs sedentary individuals. Participants will be divided into two groups based on aerobic activity level - active or sedentary - and assessed for markers of cardiovascular health, cardio-autonomic function, physical and cognitive performance, as well as overall wellbeing before and after three days of normal sleep and three days of partially deprived sleep (i.e., 30% reduction in total time in bed).

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
24

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jul 2025

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

April 10, 2025

Completed
24 days until next milestone

First Posted

Study publicly available on registry

May 4, 2025

Completed
3 months until next milestone

Study Start

First participant enrolled

July 21, 2025

Completed
6 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

January 31, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

January 31, 2026

Completed
4 months until next milestone

Results Posted

Study results publicly available

June 8, 2026

Completed
Last Updated

June 8, 2026

Status Verified

June 1, 2026

Enrollment Period

6 months

First QC Date

April 10, 2025

Results QC Date

March 4, 2026

Last Update Submit

June 5, 2026

Conditions

Outcome Measures

Primary Outcomes (1)

  • Arterial Stiffness

    Carotid-femoral pulse wave velocity measured via applanation tonometry

    Following 3-days of Acute Sleep Deprivation (i.e., 30% reduction in total time in bed) as well as following 3-days of Normal Sleep (i.e., 100% habitual time in bed); performed in a randomized order

Study Arms (2)

Normal Sleep

NO INTERVENTION

Acute Partial Sleep Deprivation

EXPERIMENTAL

30% reduction in habitual time in bed

Other: Partial Sleep Deprivation

Interventions

30% reduction in habitual time in bed

Also known as: Reduced Sleep
Acute Partial Sleep Deprivation

Eligibility Criteria

Age18 Years - 39 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Chronically active (≥150 minutes of moderate- and/or ≥75 minutes of vigorous-intensity aerobic exercise per week for the last 3 months) OR
  • Sedentary (≤60 minutes of aerobic exercise per week for the last 3 months)

You may not qualify if:

  • Chronic, uncontrolled disease (cardiovascular, metabolic)
  • Poor sleep (regularly achieving \<7 hours of sleep per night)
  • Musculoskeletal injury in the last 6 months
  • Obese (grade II or higher)
  • Pregnant

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Institute of Sports Sciences and Medicine

Tallahassee, Florida, 32301, United States

Location

Results Point of Contact

Title
Michael Ormsbee, PhD
Organization
Florida State University

Publication Agreements

PI is Sponsor Employee
Yes

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Purpose
OTHER
Intervention Model
CROSSOVER
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Professor

Study Record Dates

First Submitted

April 10, 2025

First Posted

May 4, 2025

Study Start

July 21, 2025

Primary Completion

January 31, 2026

Study Completion

January 31, 2026

Last Updated

June 8, 2026

Results First Posted

June 8, 2026

Record last verified: 2026-06

Locations