- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT07378007
Characteristics of Performance in Collegiate Cheerleaders and Dancers
January 28, 2026 updated by: Michael J. Ormsbee, Florida State University
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.
Study Overview
Status
Recruiting
Conditions
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.
Study Type
Observational
Enrollment (Estimated)
65
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
- Name: Hannah Eberhardt
- Phone Number: 8648879769
- Email: he24a@fsu.edu
Study Contact Backup
- Name: Michael J Ormsbee
Study Locations
-
-
Florida
-
Tallahassee, Florida, United States, 32301
- Recruiting
- Institute of Sports Sciences and Medicine (ISSM)
-
Contact:
- Hannah Eberhardt
- Phone Number: (864) 887-9769
- Email: he24a@fsu.edu
-
Contact:
- Michael J Ormsbee
- Email: mormsbee@fsu.edu
-
-
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
Yes
Sampling Method
Non-Probability Sample
Study Population
Current members of the Florida State University Cheer and Dance teams
Description
Inclusion Criteria:
- 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)
Exclusion Criteria:
- 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
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
Cohorts and Interventions
Group / Cohort |
|---|
|
Division I Collegiate Cheerleaders and Dancers
Normal weight obese or normal weight lean
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Energy Availability (kcals/kg FFM)
Time Frame: 7 days
|
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.
|
7 days
|
|
Physical Fitness
Time Frame: Day of study enrollment
|
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).
|
Day of study enrollment
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Subjective Sleep
Time Frame: Day of study enrollment
|
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.
|
Day of study enrollment
|
|
Body Composition
Time Frame: Day of study enrollment
|
Body Composition will be assessed via Air Displacement Plethysmography on the first day of study enrollment.
|
Day of study enrollment
|
|
Muscle Quality - Echo Intensity
Time Frame: Day of study enrollment
|
Ultrasound echo intensity will be used to assess intramuscular fat.
|
Day of study enrollment
|
|
Nutrition Knowledge
Time Frame: Day of study enrollment
|
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.
|
Day of study enrollment
|
|
Muscle Quality - Muscle Thickness
Time Frame: day of study enrollment
|
Muscle thickness of the rectus femoris will be assessed via ultrasound
|
day of study enrollment
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
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)
August 3, 2025
Primary Completion (Estimated)
May 1, 2026
Study Completion (Estimated)
May 1, 2026
Study Registration Dates
First Submitted
January 14, 2026
First Submitted That Met QC Criteria
January 28, 2026
First Posted (Actual)
January 30, 2026
Study Record Updates
Last Update Posted (Actual)
January 30, 2026
Last Update Submitted That Met QC Criteria
January 28, 2026
Last Verified
January 1, 2026
More Information
Terms related to this study
Keywords
Other Study ID Numbers
- CDNWO00006460
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
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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