- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05768841
Prevalence of Mental Health Issues in Endurance Athletes.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This study is an exploratory descriptive survey study.
The study protocol will be largely replicated from the IOC consensus paper and the questionnaires based according to SMHAT 1 with an athlete-specific screening tool (APSQ) and further eleven subsequent disorder-specific screening tools:
Eleven disorder specific screening tools:
- General Anxiety Disorder-7 (GAD-7): assesses the presence of symptoms of anxiety.
- Patient Health Questionnaire-9 (PHQ-9): assesses the presence of symptoms of depression.
- Athlete Sleep Screening Questionnaire (ASSQ): assesses the presence of sleep disturbance.
- Alcohol Use Disorders Identification Test Consumption (AUDIT-C): assesses the presence of alcohol misuse.
- Cutting Down, Annoyance by Criticism, Guilty Feeling, and Eye-openers Adapted to Include Drugs (CAGE-AID): assesses the presence of substance misuse, being slightly adapted for the SMHAT (no focus on alcohol use as already explored with the AUDIT-C; additional question to explore which substance was used).
- Brief Eating Disorder in Athletes Questionnaire (BEDA-Q): assesses the presence of disordered eating.
- ADHD
- Bipolar disorder
- PTSD
- Gambling
- Psychosis
Additionally questions to assess exercise addiction will be used as it has been shown that exercise addiction may be particularly prevalent in endurance athletes.
Further questions about age, gender, country of origin, training data, past medical history and medication will be asked as well as a few specific questions about there thoughts on mental health issues as per IOC consensus paper
Study Type
Enrollment (Estimated)
Contacts and Locations
Study Contact
- Name: Volker Scheer, Prof
- Phone Number: +33 4 25 36 79 54
- Email: contact@ultrasportsscience.org
Study Locations
-
-
-
Pierre-Bénite, France, 69310
- Recruiting
- Ultra Sports Science Foundation
-
Contact:
- Volker Scheer, Prof
- Phone Number: +33 (0)4 25 36 79 54
- Email: contact@ultrasportsscience.org
-
-
Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Sampling Method
Study Population
Description
Inclusion Criteria:
- endurance athletes (marathon runners, ultramarathon runners and triathletes)
- over the age of 16
- all genders
- recreational athletes (non- elite)
- elite athletes (professional, international, college level)
Exclusion Criteria:
- athletes that that are not competing or have not competed in an official endurance race
- athletes that are younger than 16 years of age.
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
Intervention / Treatment |
---|---|
endurance athletes
participants that have or are participating in endurance sports
|
survey on mental health issues in endurance athletes
|
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of participants with mental health issues
Time Frame: March-September 2023
|
Number of participants with mental health issues
|
March-September 2023
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Number of participants with risk factors associated with mental health issues
Time Frame: March-September 2023
|
Number of participants with risk factors associated with mental health issues
|
March-September 2023
|
Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Volker Scheer, Prof, Ultra Sports Science Foundation
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Estimated)
Study Completion (Estimated)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Actual)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- VS1
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
IPD Plan Description
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
Studies a U.S. FDA-regulated device product
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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