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Recruiting
NCT07026175
Unravelling Energy Issues Underpinning Low Energy Availability in High Performance Athletes
Conditions: Relative Energy Deficiency in Sport
Sex: All
Ages: 18 Years – 45 Years
Healthy volunteers: Yes
Phase: NA
Enrollment: 20
Sponsor: Australian Catholic University
Location: Australian Catholic University Fitzroy Victoria
Summary
The goal of this clinical trial is to understand how the body responds to short-term, severe low energy availability (LEA) in healthy, weight-bearing endurance athletes aged 18-45 years old. LEA describes a mismatch between an individual's dietary energy intake and the energy cost of their commitments for training and competition. The main questions this trial aims to answer are:
1. What effect does short-term, severe LEA have on sleeping metabolic rate?
2. What effect does short-term, severe LEA have on other body systems identified within the Relative Energy Deficiency in Sport (REDs) Health and Performance Conceptual models?
Researchers will compare a control trial with both a LEA trial achieved through diet restriction and a LEA trial achieved through increased exercise to see if there are differences in the body's response.
Participants will complete three 6-day trials, a minimum of 3-weeks apart, involving:
* Prescribed diet (all food provided)
* Prescribed running and/or cycling exercise
* Two visits to ACU Fitzroy campus for blood tests and exercise testing
* 50 hour stay (two nights and two days) in the ACU metabolic chamber
Eligibility Criteria
Inclusion Criteria:
* 18-45 years old
* Well trained weight-bearing athlete (tier 2-4 1)
* Perform \~45km per week of weight-bearing endurance training, and able to undertake the prescribed exercise in each trial condition
* Pass the ESSA pre-exercise screening tool and/or obtain GP clearance to exercise
Exclusion Criteria:
* Assessment of red status on the REDs Clinical Assessment Tool
* Unable to attend ACU in Fitzroy, Victoria, for the 6 study visits for completion of the study protocol
* Pregnancy
* Use of hormonal contraceptive with the previous 3 months
* Onset of peri/menopause
Source: ClinicalTrials.gov (NCT07026175). StuddyBuddy aggregates publicly available trial information.