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Enrolling by invitationNCT06801210Updated Aug 28, 2026

The Weight of Victory: Exploring Short- and Long-term Health Outcomes in Former Male & Female Elite Athletes From Weight-sensitive Sports

An observational study in Musculoskeletal Health, Fertility and Mental Health, sponsored by Norwegian School of Sport Sciences. Enrolling by invitation at 1 site in Norway. Open to participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2026-08-28.

Primary conditionPsychological Well-Being(the registry's first term)UnverifiedIs this wrong?Psychological Well-Being is a broad heading, used only when no more specific condition is named. No better condition is named, so the registry's term is kept.

Sponsored by Norwegian School of Sport Sciences · Observational

Study type
Observational
Model
Other
Time perspective
Cross-sectional
Enrollment
1,500
Ages
18 Years and older
Sex
All
01

Study summary

The health of former elite athletes has been identified as a critical research gap where there is limited knowledge about both short- and long-term consequences after ending their careers. The transition phase from an active elite career to everyday life has been shown to be particularly problematic, yet this issue has been little studied among former Norwegian elite athletes. Furthermore, questions remain regarding the health of athletes from weight-sensitive sports, such as weight-class, aesthetic, and certain endurance sports. These athletes face specific challenges related to maintaining a certain physique and frequent changes in body weight during their active careers. This group has been shown to be vulnerable to a range of problematic health outcomes related to low energy availability, and little is known about the long-term effects of a career involving this.

Therefore, the overall purpose of the project is to map the mental and physical health of former elite athletes. At the same time, there will be a particular focus on the differences between weight-sensitive and less weight-sensitive sports, different types of sports, gender, as well as previous dieting and eating behaviors.

Read the detailed description

The project will be a quantitative cross-sectional study that includes former elite athletes from both weight-sensitive and less weight-sensitive sports, as well as a sample from the general population for comparison. Information will be collected via an electronic questionnaire that surveys a range of physical and mental health variables among the participants. In addition, behavioral variables related to impulse control, eating and dieting patterns, and weight regulation will be assessed.

Furthermore, the project is expected to contribute new knowledge by identifying health challenges and the explanatory variables for these challenges among former elite athletes. Thus, the project can inform the development of targeted preventive measures, interventions, and policy changes that can improve health and quality of life both during and after athletes' careers and be of significant importance for future athletes.

02

Conditions studied

  • Musculoskeletal Health
  • Fertility
  • Mental Health
  • Quality of Life
  • Body Image
  • Disordered Eating

Keywords

  • Elite athletes
  • Mental health
  • Somatic health
  • Disordered eating
  • Musculoskeletal health
  • Quality of life
  • Anxiety and depression
  • Behavioral
  • Reproductive health
  • Fertility
  • Harassment
  • Body acceptance
  • Personality traits
  • Weight regulation
03

In context

Psychological Well-Being Unverified

2,193 studies on the registry are indexed under Psychological Well-Being; 728 are open to participants now.

This study's planned enrollment of 1,500 is above the median of 300 across 358 observational studies indexed under Psychological Well-Being.

Browse Psychological Well-Being studies →

Lead sponsor

Norwegian School of Sport Sciences is the lead sponsor of 46 studies on the registry; 6 are open to participants now.

Compared within Psychological Well-Being, the registry's first condition term, which may not be this study's main condition. Counted across the registry records on this site, refreshed daily. How we classify →

04

Who can participate

Ages eligible
18 Years and older
Sexes eligible
All
Sampling method
Non-probability sample

Study population

Former male and female Norwegian elite athletes and a age matched controls from the general population

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

  • Represented the national team at senior and/or junior level, (Non-organized sports) competed at national and/or international level. , >1 year since retirement , >18 years old,and a proficient level of Norwegian reading and writing skills

Exclusion criteria

Exclusion Criteria:

-

05

Study design

Observational model
Other
Time perspective
Cross-sectional
Enrollment
1,500 participants (estimated)
Patient registry
No

Groups and cohorts

  • Former elite athletes from weight-sensitive sports

    Former elite athletes from weight-sensitive sports. Including former elite athletes from weight-class, gravitational, aesthetic, and certain endurance type of sports.

  • Former elite athletes from less weight-sensitive sports

    Former elite athletes from less weight-sensitive sports. Including team sports (e.g. handball, soccer, basketball)

  • General population

    An age matched reference group for the groups of former elite athletes. Includes a sample from the general population without a background as an elite athlete.

06

What researchers measure

Primary outcomes

  1. Symptoms of eating disorders (Eating Disorder Examination Questionnaire, EDE-Q)

    This outcome measure will use the Eating Disorder Examination Questionnaire (EDE-Q) to assess the frequency and severity of eating disorder symptoms. The EDE-Q is a validated self-report questionnaire covering dietary restraint, eating concern, shape concern, and weight concern

    Time frame: January 2025 to June 2025

  2. Pain, function, and overall well-being connected to musculoskeletal status (Musculoskeletal Health Questionnaire, MSK-HQ)

    This outcome measure will use the Musculoskeletal Health Questionnaire (MSK-HQ) to assess self-reported musculoskeletal health. The MSK-HQ is a validated instrument covering key domains such as pain, function, and overall well-being in individuals with musculoskeletal conditions. It provides a comprehensive overview of the patient's musculoskeletal status, including symptoms and the impact on daily activities.

    Time frame: From January 2025 to June 2025

  3. Menstrual function and history & fertility function and history (The Low Energy Availability in Males Questionnaire, LEAM-Q, Low Energy Availability in Females Questionnaire, LEAF-Q, and The Norwegian Mother, Father and Child Cohort Study, MoBa)

    Items from The validated Low Energy Availability in Females Questionnaire (LEAF-Q) will be included to assess menstrual function (Melin et al., 2014). Items from The Low Energy Availability in Males Questionnaire (LEAM-Q) (Lundy et al., 2022) will be included for assessing reproductive health among the male participants. In addition, questions from The Norwegian Mother, Father and Child Cohort Study (MoBa) will be included to cover fertility status.

    Time frame: From January 2025 to June 2025

Secondary outcomes

  1. Symptoms of Psychological Distress (Symptom Checklist-10, SCL-10)

    This outcome measure will use the Symptom Checklist-10 (SCL-10) to assess the frequency and severity of common mental distress symptoms. The SCL-10 is a validated, abbreviated version of the SCL family of instruments (e.g., SCL-25, SCL-90) that covers core areas such as anxiety, depression, and somatic complaints. It provides an overall indication of the level of psychological distress and can be used for both screening and monitoring changes over time.

    Time frame: From January 2025 to June 2025

  2. Alchohol and drug use (Alcohol Use Disorders Identification Test - Consumption, AUDIT-C and Drug Use Disorders Identification Test, DUDIT)

    The AUDIT-C assesses alcohol consumption, drinking behaviors, and alcohol-related issues (Babor et al., 2001). The Drug Use Disorders Identification Test (DUDIT) will be included. The DUDIT assesses symptoms of substance abuse, as well as harmful use, and drug dependence.

    Time frame: From January 2025 to June 2025

  3. Satisfaction With Life (Satisfaction With Life Scale, SWLS)

    This outcome measure will use the Satisfaction With Life Scale (SWLS) to evaluate individuals' overall assessments of their own life satisfaction. The SWLS is a validated, brief questionnaire comprising five statements that respondents rate based on their level of agreement. It captures the cognitive judgment of one's life quality, providing a reliable indicator of subjective well-being and overall life satisfaction.

    Time frame: From January 2025 to June 2025

  4. Cognitive Function (PROMIS® v2.0 Cognitive Function-Short Form 6a)

    This outcome measure will utilize the PROMIS® v2.0 Cognitive Function-Short Form 6a to assess individuals' self-reported cognitive abilities. The PROMIS Cognitive Function-Short Form 6a is a validated, brief questionnaire designed to evaluate various aspects of cognitive performance, including memory, concentration, and mental clarity

    Time frame: From January 2025 to June 2025

  5. Body Appreciation and Muscle Dysmorphic Disorder Symptoms (Body Appreciation Scale-2, BAS-2, and the Muscle Dysmorphic Disorder Inventory, MDDI)

    The Body appreciation scale-2 (BAS-2) is a 10-item measure of an individual's acceptance, opinions and respect of their own body, The questionnaire is validated. Body satisfaction will be measured with the inclusion of the Muscle Dysmorphic Disorder Inventory (MDDI). The MDDI is a 13-item self-report measure which have three sub-scales assessing clinical features associated with muscle dysmorphia (MD), including drive for size, functional impairment, and appearance intolerance

    Time frame: From January 2025 to June 2025

Other outcomes

  1. Experiences of harassment, maltreatment, and abuse.

    To assess harassment, maltreatment and abuse a modified version of the questionnaire developed by Sølvberg et al (2022) will be included. This version will include questions regarding the participants experiences with harassment in their active career, and will include questions on physical, psychological, sexual (contact and non-contact), and neglecting harassment and/or abuse. Reference: Sølvberg N, Torstveit MK, Rosenvinge JH, Pettersen G, Sundgot-Borgen J. Sexual Harassment and Abuse among Young Elite Athletes, Recreational Athletes, and Reference Students: A Prospective Study. Med Sci Sports Exerc. 2022 Nov 1;54(11):1869-1878. doi: 10.1249/MSS.0000000000002972. Epub 2022 Jun 24. PMID: 35763597; PMCID: PMC9584052.

    Time frame: From January 2025 to June 2025

07

Study locations

1 site
08

References and documents

Individual participant data

Plan to share: Undecided

No publications or documents are linked to this record.

09

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Started Jun 2025 (actual). Primary completion is estimated for Aug 2026, 14 months after the start.

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

Registered
Jan 16, 2025
First posted
Jan 30, 2025
StartActual
Jun 5, 2025
Primary completionEst.
Aug 31, 2026
CompletionEst.
Aug 31, 2026
Last update
Aug 28, 2026
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 Aug 28, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT06801210
Lead sponsor
Norwegian School of Sport Sciences
Responsible party
Professor Jorunn Sundgot-Borgen (Professor, Norwegian School of Sport Sciences) — Principal investigator
First posted
Jan 30, 2025
Start date
Jun 5, 2025
Primary completion
Aug 31, 2026 (estimated)
Completion
Aug 31, 2026 (estimated)
Last update
Aug 28, 2026

Oversight

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

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