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Low Energy AvailabilityNCT07378007

Characteristics of Performance in Collegiate Cheerleaders and Dancers

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Withdrawn

Withdrawn.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 investigate performance differences between collegiate cheerleaders and dancers classified as normal weight obese and those classified as normal weight lean. The study will assess differences in physical performance, lifestyle behaviors, muscle quality, and nutrition-related factors between groups. Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
How many people
0 participants
Where
1 siteUnited States
Study dates
3 Aug 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 to 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Study population: Current members of the Florida State University Cheer and Dance teams

Who may be able to join

  • Must be a part of either the Florida State University dance or cheer team
  • Sex: Female
  • Age: 18-30
  • BMI: Normal (18.5 - 24.9 kg/m2)

Who cannot join

  • Not biologically female
  • Have a diagnosed and unresolved eating disorder
  • Not weight stable (defined as a gain/loss of more than ~7.7 lbs in the past 2 months)
  • Participants who are pregnant or who become pregnant during the study

Trial locations and contacts

1 site in 1 country.

United States1 site
  • Institute of Sports Sciences and Medicine (ISSM)

    Tallahassee, Florida, 32301

Other trials in United States

About this study

Official title: Body Composition and Characteristics of Performance in Collegiate Cheerleaders and Dancers

This study aims to investigate performance differences between collegiate cheerleaders and dancers classified as normal weight obese and those classified as normal weight lean. The study will assess differences in physical performance, lifestyle behaviors, muscle quality, and nutrition-related factors between groups. Performance testing, body composition assessment, and questionnaire-based measures will be used to characterize these relationships.

Read the detailed description

This study focuses on understanding body composition-related differences in performance among collegiate cheerleaders and dancers, a population that relies heavily on strength, power, and aesthetic presentation for successful performance. Obesity is commonly classified using body mass index (BMI); however, BMI may fail to identify individuals with excess adiposity, particularly in athletic populations. One such classification is normal-weight obesity, which describes individuals with a normal BMI but elevated body fat percentage and increased risk for impaired muscle function and reduced physical performance. Aesthetic athletes, including cheerleaders and dancers, may be particularly susceptible to this condition due to sport-specific performance demands and body composition expectations. This study aims to determine whether performance outcomes differ between normal weight obese and normal weight lean cheerleaders and dancers, with specific focus on measures of power, strength, and muscle quality. In addition, the study examines differences in lifestyle behaviors, compositional and functional muscle characteristics of the upper leg, and nutrition-related factors between groups. By integrating body composition assessment, physical performance testing, and questionnaire-based measures, this study seeks to better characterize normal-weight obesity in this population. Ultimately, the findings may help clarify how body composition and lifestyle factors relate to performance in collegiate cheer and dance athletes.

Keywords
Body Composition, Energy Availability, Physical Fitness, Division I Collegiate Cheerleaders and Dancers, Nutrition

What participants receive

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

Study groups in NCT07378007
Study groupRoleWhat they receive
Division I Collegiate Cheerleaders and DancersNormal weight obese or normal weight lean

What is being measured

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

  1. Energy Availability (kcals/kg FFM)

    Energy availability will be assess by subtracting exercise energy expenditure from energy intake relative to fat free mass. This will be assessed daily for 7 continuous days.

    Measured: 7 days

  2. Physical Fitness

    Physical fitness will be assessed via maximal jump height (in inches) using a double leg (and single leg counter movement jump and a maximal isokinetic leg extension and leg curl (expressed in kgs).

    Measured: Day of study enrollment

Secondary outcomes (5)
  1. Subjective Sleep

    The Pittsburgh Sleep Quality Index (PSQI) will be used to assess subjective sleep quality, while the Athlete Sleep Behavior Questionnaire (ASBQ) will be used to assess subjective sleep behavior. A score of >42 on the ASBQ indicates poor sleep behavior. A score >5 on the PSQI indicates poor sleep quality.

    Measured: Day of study enrollment

  2. Body Composition

    Body Composition will be assessed via Air Displacement Plethysmography on the first day of study enrollment.

    Measured: Day of study enrollment

  3. Muscle Quality - Echo Intensity

    Ultrasound echo intensity will be used to assess intramuscular fat.

    Measured: Day of study enrollment

  4. Nutrition Knowledge

    Knowledge of nutrition based on the Abbreviated Nutrition for Sports Knowledge Questionnaire (ANSKQ). The maximum score is 100%. The minimum score is 0%. Higher scores indicate better nutrition knowledge.

    Measured: Day of study enrollment

  5. Muscle Quality - Muscle Thickness

    Muscle thickness of the rectus femoris will be assessed via ultrasound

    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 posted30 Jan 2026
  2. Study start3 Aug 2025
  3. Primary completion1 May 2026
  4. Study completion1 May 2026

Why it stopped: Study was not initiated due to insufficient participant recruitment, limited institutional/team support, and inadequate research staffing to conduct the protocol as planned.

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
NCT07378007
Sponsor's protocol ID
CDNWO00006460
Status last verified
Jul 2026
First submitted
14 Jan 2026
Last updated
6 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 4 inclusion and 4 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 6 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 (kcals/kg FFM) (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 6 Jul 2026.

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