Myocene Sensivity to Cycling Intensities
Muscular Response to Short vs. Prolonged Cycling: A Crossover Trial on Low-Frequency Fatigue Sensitivity
1 other identifier
interventional
20
0 countries
N/A
Brief Summary
This study aims to address this gap by assessing LFF following different efforts in cycling, aiming to identify a pattern. Also, we expect that this study helps to clarify to which efforts (prolonged vs short) are more likely to trigger substantial changes in LFF responses.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for not_applicable
Started Apr 2025
Shorter than P25 for not_applicable
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
First Submitted
Initial submission to the registry
March 24, 2025
CompletedStudy Start
First participant enrolled
April 1, 2025
CompletedFirst Posted
Study publicly available on registry
April 6, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
May 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
July 1, 2025
CompletedApril 6, 2025
April 1, 2025
1 month
March 24, 2025
April 2, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
low-frequency fatigue
Low-frequency fatigue assessed using Myocene software, which computes the median value of the ratio between high and low frequency stimulations
Baseline, 30 minutes post, 24 hours post
Study Arms (2)
4 minutes all-out
EXPERIMENTAL4 minute time trial all-out
30 minute all-out
EXPERIMENTAL30 minute cycling all-out
Interventions
Low frequency fatigue will be measured using Myocene
Eligibility Criteria
You may qualify if:
- Road cyclists
You may not qualify if:
- Injured or recently injured participants
Contact the study team to confirm eligibility.
Sponsors & Collaborators
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- NON RANDOMIZED
- Masking
- NONE
- Purpose
- DIAGNOSTIC
- Intervention Model
- CROSSOVER
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
March 24, 2025
First Posted
April 6, 2025
Study Start
April 1, 2025
Primary Completion
May 1, 2025
Study Completion
July 1, 2025
Last Updated
April 6, 2025
Record last verified: 2025-04