Does a Multi-ingredient Pre-workout Supplement Enhance Cycling Time Trial Performance?
MIPS
1 other identifier
interventional
12
1 country
1
Brief Summary
The aim of the present study is to test the effect of ingesting a multi-ingredient pre- exercise supplement containing caffeine, creatine, beta-alanine and L-Citrulline compared to a placebo, on endurance exercise performance.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable healthy-volunteers
Started Dec 2021
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 2, 2021
CompletedFirst Submitted
Initial submission to the registry
January 10, 2022
CompletedFirst Posted
Study publicly available on registry
February 9, 2022
CompletedPrimary Completion
Last participant's last visit for primary outcome
August 31, 2022
CompletedStudy Completion
Last participant's last visit for all outcomes
September 30, 2022
CompletedJuly 31, 2025
July 1, 2025
9 months
January 10, 2022
July 28, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Exercise Performance
Work done during 15 min time trial (TT)
15 Minitues
Secondary Outcomes (4)
Alertness
1 Hour
Motivation
1 Hour
Rate of perceived exertion
1 Hour
Gas analysis
1 Hour
Study Arms (2)
Ladder Supplement
EXPERIMENTALLadder Supplement
Placebo
PLACEBO COMPARATORPlacebo
Interventions
Caffeine 200mg L-Theanine 200mg L-Citrulline 6g Creatine 5g Beta-Alanine 1.6g Phosphatidylserine 100mg
Eligibility Criteria
You may not qualify if:
- Any diagnosed metabolic health condition
- Pregnant
- Non-habitual caffeine intake
- Smoker
- No endurance training
- Diagnosed Cardiovascular disease
- Recent history of musculoskeletal injury
- Anti-depressant and anti-anxiety medication
- Age 18-40
- Healthy
- Highly trained endurance athletes (V̇O2max: males \>55 and females \>50 mL⋅kg bm-1⋅min-1)
- Both males and females are allowed to participate. If females are on the oral contraceptive pill they are to be tested on consecutive weeks. If they are not on the oral contraceptive pill, then female subjects are to be tested every 4 weeks, at the same point of their menstrual cycle.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University of Exeterlead
- OpenFit LLCcollaborator
Study Sites (1)
School of Sport and Health Sciences
Exeter, EX4, United Kingdom
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- DOUBLE
- Who Masked
- PARTICIPANT, INVESTIGATOR
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 10, 2022
First Posted
February 9, 2022
Study Start
December 2, 2021
Primary Completion
August 31, 2022
Study Completion
September 30, 2022
Last Updated
July 31, 2025
Record last verified: 2025-07