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Low Energy AvailabilityNCT07347522

Body Composition and Lifestyle Factors in ROTC

An observational study of Low Energy Availability and Physical Performance, run by Florida State University at 1 site in United States.

Withdrawn

Withdrawn. The study stopped before anyone enrolled.

Official record
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Trial summary

This study aims to investigates the relationships between body composition, sleep, diet, and physical fitness in ROTC cadets. Further, it aims to evaluate the accuracy of body composition screening methods and identify lifestyle factors linked to performance. Read more about this study

Who is it for?
Ages 18 years and olderHealthy volunteers can take part
How many people
0 participants
Where
1 siteUnited States
Study dates
1 Oct 2025to 1 May 2026
Phase
Observational
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 years and older
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

Study population: Current members of local Reserve Officer Training Corps Cadets (ROTC) programs.

Who may be able to join

  • currently enrolled as a Reserve Officer Training Corps Cadets
  • 18 years or older

Who cannot join

  • pregnancy
  • injuries preventing full participation in ROTC training or activities

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Institute of Sports Sciences and Medicine

    Tallahassee, Florida, 32306

Other trials in United States

About this study

Official title: Associations Between Body Composition, Energy Availability, and Lifestyle Factors in Reserve Officer Training Corps Cadets

This study aims to investigates the relationships between body composition, sleep, diet, and physical fitness in ROTC cadets. Further, it aims to evaluate the accuracy of body composition screening methods and identify lifestyle factors linked to performance. Methods include body composition testing, surveys, accelerometry, and fitness score collection from cadets.

Read the detailed description

This study focuses on understanding health and performance among students enrolled in Reserve Officers' Training Corps (ROTC). ROTC cadets are a population expected to maintain both academic and military-readiness demands. Many cadets must balance early-morning training, full course loads, part-time jobs, and social obligations, all of which can influence their sleep habits, nutrition choices, and physical fitness. At the same time, the assessment of body composition is an important part of military standards, yet the tools used to evaluate it vary widely and may not always reflect an individual's true physiological status. To explore these interconnected factors, this study examines patterns in cadets' body composition alongside their dietary practices, sleep behaviors, and physical fitness. By doing so, it seeks to clarify how everyday lifestyle factors may support or hinder readiness and whether commonly used body composition screening methods align with more precise measurements. Ultimately, the goal is to provide a clearer picture of the health challenges and needs of ROTC cadets and to help inform strategies that promote performance, well-being, and long-term resilience in this unique group.

Keywords
body composition, energy availability, physical fitness, Reserve Officer Training Corp, nutrition

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

Study groups in NCT07347522
Study groupRoleWhat they receive
Reserve Officer Training Corps CadetsLow Energy Availability or Non-Low Energy Availability

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Energy Availability

    Measured: 7 days

  2. Physical Fitness

    Measured: Day of study enrollment

Secondary outcomes (4)
  1. Subjective Sleep

    Measured: Day of study enrollment

  2. Body Composition

    Measured: Day of study enrollment

  3. Muscle quality

    Ultrasound echo intensity and muscle thickness

    Measured: day of study enrollment

  4. Nutrition Knowledge

    Knowledge of nutrition based on survey scores

    Measured: day of study enrollment

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted16 Jan 2026
  2. Study start1 Oct 2025
  3. Primary completion1 May 2026 (estimated)
  4. Study completion1 May 2026 (estimated)

Why it stopped: The study did not enroll participants

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Observational
Observational model
Cohort
Time perspective
Prospective
Enrolment
0 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT07347522
Sponsor's protocol ID
STUDY00006460
Status last verified
Jan 2026
First submitted
9 Jan 2026
Last updated
13 Jul 2026
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
Undecided

Questions about this trial

What is this clinical trial studying?

An observational study of Low Energy Availability and Physical Performance, run by Florida State University at 1 site in United States.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 2 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: withdrawn, as of the sponsor's last update on 13 Jul 2026. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in United States. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

The study was withdrawn before enrolling participants, so there are no results.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Energy Availability (time frame: 7 days). The study lists 2 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 13 Jul 2026.

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