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FASTER – Fuel Availability and Stress Responses during Endurance Running

FASTER – Fuel Availability and Stress Responses during Endurance Running - FASTER

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
DRKS
Registry ID
DRKS00040864
Enrollment
30
Registered
2026-07-15
Start date
2026-09-01
Completion date
Unknown
Last updated
2026-08-03

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Exercise-induced gastrointestinal, inflammatory, mitochondrial, and muscular stress responses during prolonged running in healthy endurance athletes.

Interventions

Group 1: Moderate carbohydrate intake Participants complete a standardized 4-hour running trial at moderate intensity, corresponding to approximately 60–65% of individually determined VO2peak. During

Sponsors

Sport- und Rehabilitationsmedizin Universitätsklinikum Ulm
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 50 Years

Inclusion criteria

Inclusion criteria: -trained endurance athletes aged 18–50 years regular running-based endurance training of at least 5–6 hours per week for at least two years -previous participation in at least one marathon or a comparable prolonged running event -VO2peak = 50 ml/kg/min in men and = 45 ml/kg/min in women -ability to follow verbal instructions and safely complete the exercise protocol

Exclusion criteria

Exclusion criteria: -orthopedic complaints or injuries currently limiting prolonged running -acute or chronic internal medical diseases -known chronic gastrointestinal diseases or regularly occurring gastrointestinal symptoms during prolonged running -abnormal stool habits outside the normal range, defined as regular formed stool between three times per day and once every three days -known allergies or intolerances to ingredients of the sports nutrition products used, particularly glucose, fructose, maltodextrin, sodium alginate, pectin, sodium bicarbonate, or calcium carbonate -known fructose intolerance or relevant fructose malabsorption -known intolerance to sports gels or carbohydrate-containing sports drinks -pregnancy or breastfeeding -use of medication that may relevantly affect metabolism, immune function, or physical performance

Design outcomes

Primary

MeasureTime frame
Change in I-FABP concentration as a marker of intestinal epithelial cell damage, compared between moderate carbohydrate intake (75 g/h) and high carbohydrate intake (120 g/h) during prolonged running. Assessment: I-FABP will be measured in venous blood samples. Samples will be collected before exercise (T0), immediately after exercise, 1 hour after exercise, and 24 hours after exercise. The primary comparison will be based on the change in I-FABP concentration between the two carbohydrate intake conditions.

Secondary

MeasureTime frame
Changes in the following parameters compared between the two carbohydrate intake conditions: markers of endotoxin-related immune activation: LBP, sCD14 markers of systemic inflammation: IL-6, TNF-a, hsCRP markers of mitochondrial stress responses: mtDNA copy number, cell-free mtDNA markers of muscular stress or muscle damage: CKM, LDH markers of energetic regulation: leptin, ghrelin physiological and perceptual exercise parameters: heart rate, Borg scale/RPE gastrointestinal symptoms during and after exercise capillary blood parameters during exercise, e.g. glucose and/or lactate, depending on the final analysis plan Assessment: Laboratory and molecular secondary endpoints will be assessed from venous blood samples collected at T0, immediately after exercise, 1 hour after exercise, and 24 hours after exercise. Additional capillary blood samples will be collected during exercise after 1, 2, and 3 hours, as well as immediately after exercise, for selected acute parameters. Heart rate and perceived exertion will be repeatedly recorded during the running trial. Gastrointestinal symptoms will be documented during and after exercise using standardized procedures. The sampling schedule is based on the expected kinetics of the investigated markers.

Countries

Austria, Germany, Switzerland

Contacts

Public ContactDaniel Alexander Bizjak

Sport- und Rehabilitationsmedizin Universitätsklinikum Ulm

daniel.bizjak@uniklinik-ulm.de+49731 500-45368

Outcome results

None listed

Source: DRKS (via WHO ICTRP) · Data processed: Aug 10, 2026