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NCT Number: NCT07403864

Effects of Acute Sleep Deprivation on Health

This study will investigate whether various types of regular exercise can provide protective effects against metabolic abnormalities induced by sleep restriction. It will examine responses related to metabolic health, cognitive function, energy expenditure, subjective feelings, and human behaviors, including physical activity and energy intake.

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Key information

About this study

Sleep disturbances are common among the Taiwanese population due to work-related stress, shift work, and academic demands. Poor sleep can impair glucose and lipid metabolism, increasing the risk of cardiovascular disease and type 2 diabetes. This study will investigate whether regular exercise can mitigate these adverse effects. The findings aim to inform diverse exercise intervention strategies tailored to different populations to reduce health risks associated with insufficient sleep.

Participants will be healthy adults aged 20 to 45, categorized according to their habitual activity levels.

  • Sedentary: fewer than 7,000 steps per day and no regular exercise in the past 6 months.
  • Regular Aerobic Exercise: Running or cycling at least 2-3 times per week for the past 6 months.
  • Regular Resistance Exercise: Resistance training performed at least 2-3 times per week for the past 6 months, with minimal aerobic training.

Eligible participants must have regular sleep habits (Pittsburgh Sleep Quality Index [PSQI] ≤ 5), stable body weight (±3% over the past 3 months), no chronic diseases, no smoking or drinking habits, and no special diets.

Prior to the first main trial, participants will complete assessments of V̇O2max and maximal muscle strength within 7 to 14 days before the main trials. They will also record one week of daily physical activity, sleep patterns (including bedtime and wake-up times), and diet (covering two weekdays and one weekend day) to ensure they meet the inclusion criteria.

Day 1:

Physical activity will be restricted to a minimum, with no exercise permitted. Participants may eat freely before 15:00; however, all food intake will be recorded to enable replication prior to the second main trial. Napping is not allowed. Participants will arrive at the laboratory between 18:30 and 19:00. Upon arrival, after a 20-minute rest period, baseline measurements will be conducted, including body composition, waist and hip circumference, vascular function, subjective questionnaires, heart rate variability, food preference, a 20-minute energy metabolism assessment, and cognitive function testing. Subsequently, a standardized dinner will be provided by the researchers and consumed within 25 minutes. Participants will be allowed to wash and prepare between 20:00 and 20:30. From arrival onward, participants will remain seated on the experimental bed throughout the entire laboratory session. Continuous Glucose Monitoring (CGM) will be installed on day 1. Participants will have either an 8-hour sleep opportunity in the laboratory from 23:00 to 07:00 (i.e., normal sleep trial) or a 3-hour sleep opportunity from 03:00 to 07:00 (i.e., partial sleep deprivation trial).

Day 2:

Participants will wake at 07:00. After completing personal hygiene, they will rest for 20 minutes to ensure full wakefulness. At 07:30, a 20-minute resting metabolic rate assessment will be conducted, alongside the collection of heart rate variability and muscle oxygen saturation data. Subsequently, pulse wave velocity measurement, cognitive function tests, and subjective questionnaires will be administered.

This will be followed by a 3-hour oral glucose tolerance test (OGTT), during which 75 g of glucose will be ingested, and muscle oxygen saturation will be continuously monitored. Capillary blood samples will be collected via finger prick at 0, 30, 60, 90, 120, 150, and 180 minutes, alongside continuous glucose monitoring. Resting gas exchange, heart rate variability, and pulse wave velocity will be measured every 60 minutes. Blood pressure and visual analogue scale assessments-including sleep, appetite, and mood-will be recorded every 30 minutes. Cognitive function will be evaluated every 90 minutes.

Upon leaving the laboratory, participants will receive a pedometer and wearable devices. They will be instructed to record their dietary intake (using a food scale and photographic records), sleep patterns, and glucose levels on the experimental day and for the subsequent four consecutive days.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Age between 20-45 years.
  • Body Mass Index (BMI) between 18.5-27 kg/m².
  • No sleep-related medical conditions and good sleep quality, defined as a Pittsburgh Sleep Quality Index (PSQI) score ≤ 5.
  • Usual bedtime between 22:00-01:00, wake-up time between 06:00-09:00, with an average sleep duration of 7 to 9 hours; chronotype classified as "definitely not evening type" (score ≥ 42 on the Morningness-Eveningness Questionnaire), and no changes in sleep patterns over the past 3 months.
  • Without any metabolic or cardiovascular diseases, and not using medications that could affect metabolic responses.
  • No specific dietary habits, such as intermittent fasting or a ketogenic diet.
  • Maintaining a stable weight (no self-reported weight change ± 3 kg) for at least 3 months.
  • Resting blood pressure ≤ 130/80 mmHg.
  • No smoking or excessive alcohol consumption.
  • Not a shift worker.
  • No international travel across time zones has occurred within the past 3 months.

Exclusion criteria

  • Special diets (e.g., intermittent fasting, ketogenic diet)
  • Recent injuries or contraindications to intense exercise.

Treatment and study plan

Normal sleep

Behavioral

Participants will have an 8-hour sleep opportunity in the lab from 23:00 to 07:00.

Partial sleep deprivation

Behavioral

Participants will have a 3-hour sleep opportunity in the lab from 03:00 to 07:00.

Primary outcomes

  1. Glycemic Control

    Time frame: Baseline measurements and continuously at regular intervals throughout the 3-hour OGTT.

    Glucose responses during the 3-hour oral glucose tolerance test (OGTT)

  2. Pulse wave velocity (PWV)

    Time frame: 0 (baseline), 60, 120 and 180 minutes during OGTT

    Pulse wave velocity assessments (i.e., meters per second) will be collected before and during the 3-hour oral glucose tolerance test (OGTT).

  3. Cognitive function (Accuracy)

    Time frame: 0 (baseline), 90 and 180 minutes during OGTT

    Accuracy (i.e., %) in computerized tests will be tested before and during the 3-hour oral glucose tolerance test (OGTT).

  4. Cognitive function (Reaction time)

    Time frame: 0 (baseline), 90 and 180 minutes during OGTT

    Reaction time (i.e., milliseconds) in computerized tests will be tested before and during the 3-hour oral glucose tolerance test (OGTT).

Secondary outcomes

  1. Resting energy expenditure

    Time frame: 0 (baseline), 60, 120 and 180 minutes during OGTT

    Energy expenditure will be collected before and during the 3-hour oral glucose tolerance test (OGTT).

  2. Carbohydrate oxidation

    Time frame: 0 (baseline), 60, 120 and 180 minutes during OGTT

    Carbohydrate oxidation will be collected before and during the 3-hour oral glucose tolerance test (OGTT).

  3. Fat oxidation

    Time frame: 0 (baseline), 60, 120 and 180 minutes during OGTT

    Fat oxidation will be collected before and during the 3-hour oral glucose tolerance test (OGTT).

  4. Heart rate variability

    Time frame: 0 (baseline), 60, 120 and 180 minutes during OGTT

    Heart rate variability will be collected before and during the 3-hour oral glucose tolerance test (OGTT).

  5. Muscle oxygen saturation

    Time frame: 0 minute (baseline) and throughout the entire 3-hour OGTT

    Muscle oxygen saturation data will be collected before and during the 3-hour oral glucose tolerance test (OGTT).

  6. Blood pressure

    Time frame: 0 (baseline), 30, 60, 90, 120,150 and 180 minutes during OGTT

    Blood pressure (mmHg) assessments will be collected before and during the 3-hour oral glucose tolerance test (OGTT).

Sponsors and collaborators

Lead sponsor

National Taiwan Normal University

Other

Registry information

Official study title

Effects of Acute Partial Sleep Deprivation on Metabolic Health and Cognitive Function

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Feb 11, 2026
Registry last updated
Feb 11, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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