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RecruitingNCT07232628TriatLEAUpdated Nov 18, 2025

Energy Availability and Its Impact in Elite Triathletes

An observational study in Low Energy Availability and Relative Energy Deficiency in Sport, sponsored by Bispebjerg Hospital. Recruiting at 1 site in Denmark. Open to participants aged 18 Years and older, including healthy volunteers. Per ClinicalTrials.gov, last updated 2025-11-18.

Sponsored by Bispebjerg Hospital · Observational

From the registry’s dates

  • Started Oct 2025; still recruiting 1 year 1 month later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
40
Ages
18 Years and older
Sex
All
01

Study summary

This study investigates how energy availability affects performance, injury risk, and training outcomes in elite triathletes. Over two competitive seasons (2026-2027), 40 elite and sub-elite triathletes will be monitored through physiological tests, blood samples, and questionnaires. The goal is to identify markers of low energy availability and understand its impact on health and athletic performance. The study is observational and does not involve experimental treatments. Participants continue their regular training and diet while undergoing periodic assessments.

Read the detailed description

Low energy availability (LEA) is a condition where the energy intake of an athlete is insufficient to support both training demands and essential physiological functions. LEA is common among endurance athletes, including triathletes, due to high training volumes and sometimes intentional dietary restrictions. Prolonged LEA can lead to hormonal imbalances, impaired bone health, reduced immune function, and increased injury risk. This study aims to explore the prevalence and consequences of LEA in elite triathletes over two seasons.

The study is a 2-year exploratory cohort study conducted at the Institute of Sports Medicine, Bispebjerg Hospital, Copenhagen. Forty elite or sub-elite triathletes (men and women, aged 18+) who train more than 15 hours per week will be enrolled. Participants will undergo five comprehensive test days spaced across the off-season, pre-season, and in-season periods of 2025-2027. These test days include blood sampling, DXA scans, MR imaging, muscle strength and stiffness assessments, VO₂ max testing, and dietary and activity monitoring.

The primary outcome is the change in the thyroid hormone triiodothyronine (T3), a known marker of LEA. Secondary outcomes include bone density, muscle mass, metabolic rate, performance metrics (e.g., running economy, VO₂ max), and injury incidence. Energy availability will be assessed via validated questionnaires (LEAF-Q for females, LEAM-Q for males), dietary logs (MyFood24), and training data from wearable devices.

Monthly injury reports and quarterly dietary assessments will be collected. Blood samples will be analyzed for hormones (e.g., cortisol, testosterone, GH, IGF-1, TSH, T3, T4), bone turnover markers (CTX, PINP, osteocalcin), immune parameters, and nutritional status (e.g., vitamin D, iron, B12). Some samples will be stored in a coded biobank until 2029 for future analysis.

Participants will receive no financial compensation but will be reimbursed for public transport. All procedures are non-invasive or minimally invasive and carry low risk. The study has been approved by the relevant ethics committee (Approval No. H-25043062), and informed consent will be obtained from all participants.

Results will be published in peer-reviewed journals and presented at scientific conferences. If not accepted for publication, results will be made publicly available via ClinicalTrials.gov and the EU Clinical Trials Register.

02

Conditions studied

  • Low Energy Availability
  • Relative Energy Deficiency in Sport

Keywords

  • RED-S
  • injury risk
  • performance
  • triathlon
  • biomarker
03

In context

Relative Energy Deficiency in Sport

20 studies on the registry are indexed under Relative Energy Deficiency in Sport; 9 are open to participants now.

This study's planned enrollment of 40 is close to the median of 42 across 10 observational studies indexed under Relative Energy Deficiency in Sport.

Browse Relative Energy Deficiency in Sport studies →

Lead sponsor

Bispebjerg Hospital is the lead sponsor of 289 studies on the registry; 29 are open to participants now.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Accepts healthy volunteers
Yes
Sampling method
Non-probability sample

Study population

Elite triathletes with a weekly training volume of more than 15 hours

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Age ≥18 years
  • Healthy individuals
  • Training ≥15 hours/week in triathlon

Exclusion criteria

Exclusion Criteria:

  • Smokers
  • Use of prohibited substances (WADA list) without medical justification
  • Existing injuries or illnesses that could worsen due to participation
05

Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
40 participants (estimated)
Patient registry
No
Biospecimen retention
Samples without dna

Groups and cohorts

  • Triathletes

    Elite triathletes

06

What researchers measure

Primary outcomes

  1. T3

    Plasma triiodothyronine (T3) levels

    Time frame: Two years - from off-season 2025 until in-season 2027

Secondary outcomes

  1. RER

    Resting energy expenditure by indirect calorimetry

    Time frame: Two years - from off-season 2025 until in-season 2027

  2. Bone mineral density

    Bone mineral density by DXA scanning

    Time frame: Two years - from off-season 2025 until in-season 2027

  3. Fat free mass

    Fat free mass by DXA scanning

    Time frame: Two years - from off-season 2025 until in-season 2027

  4. Appendicular fat free mass

    Appendicular fat free mass by DXA scanning

    Time frame: Two years - from off-season 2025 until in-season 2027

  5. Fat mass

    Fat mass by DXA scanning

    Time frame: Two years - from off-season 2025 until in-season 2027

  6. Tendon thickness

    Patella and Achilles tendon thickness by ultrasound

    Time frame: Two years - from off-season 2025 until in-season 2027

  7. Tendon vascularisation

    Color doppler by ultrasound of Patella and Achilles tendons

    Time frame: Two years - from off-season 2025 until in-season 2027

  8. Tendon stiffness

    Patella and Achilles tendon stiffness by MyotonPro measurement

    Time frame: Two years - from off-season 2025 until in-season 2027

  9. Quadriceps muscle strength

    Concentric muscle strength by Biodex dynamometer

    Time frame: Two years - from off-season 2025 until in-season 2027

  10. Hamstring muscle strength

    Concentric muscle strength by Biodex dynamometer

    Time frame: Two years - from off-season 2025 until in-season 2027

  11. Peak muscle power

    Measured during counter movement jump on force-plate

    Time frame: Two years - from off-season 2025 until in-season 2027

  12. Jump height

    Measured during counter movement jump on force-plate

    Time frame: Two years - from off-season 2025 until in-season 2027

  13. Running economy

    Measured on treadmill with direct measurement of oxygen uptake

    Time frame: Two years - from off-season 2025 until in-season 2027

  14. Biking economy

    Measured on ergometer bike with direct measurement of oxygen uptake

    Time frame: Two years - from off-season 2025 until in-season 2027

  15. Maximal oxygen uptake

    Measured on ergometer bike with direct measurement of oxygen uptake

    Time frame: Two years - from off-season 2025 until in-season 2027

  16. Calorie intake

    Measured on three-day dietary registrations

    Time frame: Two years - from off-season 2025 until in-season 2027

  17. Exercise energy expenditure

    Measured by tracking devices

    Time frame: Two years - from off-season 2025 until in-season 2027

  18. Risk of low energy availability

    Evaluated by questionnaires - LEAF-Q for females, and LEAM-Q for males

    Time frame: Two years - from off-season 2025 until in-season 2027

  19. Risk of eating disorder

    Evaluated by EDE-Q questionnaire

    Time frame: Two years - from off-season 2025 until in-season 2027

  20. Injury prevalence

    Evaluated through monthly injury diary

    Time frame: Two years - from off-season 2025 until in-season 2027

  21. Time loss due to injuries

    Evaluated through monthly injury diary

    Time frame: Two years - from off-season 2025 until in-season 2027

  22. Biomarkers

    Biomarkers related to metabolism, stress hormones, sex hormones, immune system, muscle breakdown, organ function, bone turnover, lipid profile, minerals, haemoglobin and iron status measured from blood samples

    Time frame: Two years - from off-season 2025 until in-season 2027

07

Study locations

1 of 1 sites recruiting
  • Institute of Sports Medicine Copenhagen, Bispebjerg Hospital
    Copenhagen, Denmark
    Recruiting
08

References and documents

Related links

Individual participant data

Plan to share: Undecided

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Oct 2025 (actual). Primary completion is estimated for Nov 2027, 25 months after the start.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 14, 2025
First posted
Nov 18, 2025
StartActual
Oct 1, 2025
Primary completionEst.
Nov 30, 2027
CompletionEst.
Jun 2028
Last update
Nov 18, 2025
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Nov 18, 2025, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07232628
Responsible party
Jakob Agergaard (Senior Researcher, Ph.D., Bispebjerg Hospital) — Principal investigator
First posted
Nov 18, 2025
Start date
Oct 1, 2025
Primary completion
Nov 30, 2027 (estimated)
Completion
Jun 2028 (estimated)
Last update
Nov 18, 2025

Study contacts

Jakob Agergaard, Ph.D.
Contact
jakob.agergaard@regionh.dk
+45 38 63 58 73

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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