Changes in Energy Expenditure in Response to Physical Activity in Healthy Adults (VITAL)

April 7, 2026 updated by: Medical University of Bialystok

Assessment of Changes in Energy Expanditure in Response to Short-term Physical Activity Measured by Indirect Calorymetry in Healthy Individuals

This study investigates how short, high-intensity body-weight exercises affect energy use in healthy young adults. The focus is on resting metabolic rate (RMR), total energy expenditure (TEE) and excess post-exercise oxygen consumption (EPOC), measured with a portable indirect calorimetry system (COSMED K5). Participants will be 14 volunteers, seven women and seven men aged 18 to 30 years, recruited from the academic community of the Medical University of Białystok. Each subject will first undergo basic screening, including ECG, blood pressure, and body composition. Measurements will be taken in three phases. In the resting phase, RMR will be recorded after fifteen minutes of quiet sitting. In the exercise phase, participants will perform squats, burpees, or a plank for one minute at maximum effort or sustained position while energy use is continuously monitored. In the recovery phase, EPOC will be measured immediately after exercise to capture short-term changes. Oxygen uptake, ventilation, heart rate, and oxygen saturation will be tracked throughout the session. Environmental conditions such as room temperature and humidity will be standardized, and participants will avoid caffeine, alcohol, and heavy physical activity at least 24 hours before testing. The main aim is to determine whether even one minute of exercise can meaningfully alter EPOC steady state parameters, and to compare the energy cost of different exercise types. The data will be analyzed in relation to anthropometric variables and cardiopulmonary function. Results are expected to improve understanding of short-term energy dynamics and may support more precise recommendations in pulmonary rehabilitation, cardiology, sports medicine, and nutrition. By providing reliable measurements of caloric cost in simple exercises, the study can help design safer and more effective training, rehabilitation, and weight control programs.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Study Type

Observational

Enrollment (Estimated)

20

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Contact Backup

Study Locations

    • Podlaskie Voivodeship
      • Bialystok, Podlaskie Voivodeship, Poland, 15-540
        • Recruiting
        • II Departemnt of Lung Diseases, Lung Cancer, and Internal Medicine
        • Contact:

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

  • Adult

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Healthy volunteers aged 18 to 30 years will be recruited from the academic community of the Medical University of Białystok, primarily students affiliated with the Student Research Group at the II Department of Pulmonary Diseases, Lung Cancer and Internal Medicine. Participants must be free of chronic diseases, musculoskeletal injuries, and active infections, and must meet standard medical screening criteria before enrollment.

Description

Inclusion Criteria:

  • Age 18-30 years
  • Healthy volunteers without chronic diseases
  • Normal resting ECG (regular sinus rhythm, 60-90 bpm)
  • Normal blood pressure according to ESC guidelines
  • Ability and willingness to provide written informed consent

Exclusion Criteria:

  • Chronic diseases or musculoskeletal injury within the past 6 months
  • Use of tobacco or nicotine products within the past 6 months
  • Blood donation >20 mL (except diagnostic) within the past 6 months
  • Use of narcotics, sedatives, or dietary supplements (e.g., creatine) within the past 2 weeks
  • Active infection, fever, or acute illness at the time of study
  • Inability to comply with study instructions (dietary restrictions, abstinence from alcohol/caffeine, exercise restrictions)

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Differences Between Pre- and Post-exercise Energy Expenditure Measurement
Time Frame: Baseline and immediately post-exercise (within 10-15 minutes).
Resting metabolic rate (RMR) will be measured in kcal/min using the COSMED K5 portable indirect calorimetry system. Each participant will undergo a baseline measurement after 15 minutes of seated rest. Immediately following one minute of physical activity (squats, burpees, or plank) with continuous measurement of energy expenditure, then during restitution EPOC will be measured (in lO₂ or kcal) until values stabilize. The primary outcome is the difference between post-exercise energy expenditure and baseline, reflecting the acute impact of short-duration, high-intensity activity on energy metabolism in healthy young adults.
Baseline and immediately post-exercise (within 10-15 minutes).

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Total Energy Expenditure (TEE) During Exercise
Time Frame: From the beginning to the end of performing the exercise (1 minute).
Resting metabolic rate (RMR) will be measured in kcal/min using the COSMED K5 portable indirect calorimetry system. Each participant will undergo a baseline measurement after 15 minutes of seated rest. Immediately following one minute of physical activity (squats, burpees, or plank) with continuous measurement of energy expenditure, then during restitution EPOC will be measured (in lO₂ or kcal) until values stabilize. The secondary outcome is a measure of energy expenditure during one minute of high-intensity activity in healthy young adults.
From the beginning to the end of performing the exercise (1 minute).

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

September 1, 2025

Primary Completion (Estimated)

November 1, 2026

Study Completion (Estimated)

December 1, 2026

Study Registration Dates

First Submitted

April 7, 2026

First Submitted That Met QC Criteria

April 7, 2026

First Posted (Actual)

April 14, 2026

Study Record Updates

Last Update Posted (Actual)

April 14, 2026

Last Update Submitted That Met QC Criteria

April 7, 2026

Last Verified

June 1, 2025

More Information

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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