healthy participants
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - Athlete at OSP - Written consent of the subject or legal representatives to participate in the present study and for the disclosure of pseudonymized data in the context of documentation and analysis;
Exclusion criteria
Exclusion criteria: - Psychiatric disorder with risk of eating disorder - BMI < 10th age related percentile in adolescents or BMI < 18,5 kg/m2 in adults - metabolic condition - further severe disease restricting study participation
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Exploratory feasibility project, therefore no definition of primary and secondary endpoints. - Weight, BMI; fat-free mass, blood pressure, resting heart rate. - Measurement of electrophysiological biomarkers (heart rate, pulse and electrodermal activity using wearables) - Assessment of stress and recovery after exercise - Assessment of performance in own discipline evaluated by trainers - Muscular adaptation, strength measurement - Routine blood values in the OSP: blood count, CRP, liver values, kidney values, CK profile, urea profile - Additional blood values for the study: vitamin B12, holotranscobalamin, ferritin, transferrin saturation, Na, K, Ca, Ph, Mg. - Additional blood sample for immunophenotyping - Stool samples for microbiome testing (cytometry, sequencing, short chain fatty acids, metabolome). - Self-assessment of sleep quality on a Likert scale. - 72h nutrition protocol - Nutritional analysis of energy and nutrient intake - Information on duration and frequency of exercise - Demographic information | — |
Secondary
| Measure | Time frame |
|---|---|
| Exploratory feasibility project, therefore no definition of primary and secondary endpoints. | — |
Countries
Germany
Contacts
Klinik für Pädiatrie m. S. Onkologie/Hämatologie/SZT, AG Integrative Medizin/Seifert