- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04637178
Predicting the Efficacy of Resistance Exercise Training for Improving Endurance Performance (IDperform)
Identifying Molecular Determinants for the Efficacy of Resistance Training for Improving Endurance Performance in Elite Cyclists
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
For elite endurance athletes, the addition of resistance training to habitual endurance training routines generally leads to improved endurance performance. However, this is not always the case, with several individuals failing to respond in the expected manner. This inter-individual variation is likely associated with inherent cellular and molecular charateristics of skeletal muscle. Indeed, responses to resistance training seem to be associated with muscle biological characteristics such as muscle fiber composition and ribosomal content (during the early phase of resistance training).
The study will investigate the association between muscle fibre composition (type I vs type II muscle fiber proportions) / ribosomal content in m. vastus lateralis and the effects of 10 weeks of resistance training on endurance performance in 52 elite cyclists. Half the participants will perform resistance training in addition to their habitual endurance training routines, the other half will perform endurance training-only. Muscle biopsies will be sampled from m. vastus lateralis before and after the first two weeks of the intervention. For muscle fiber composition, the hypothesis is that larger proportions of type II fibers will be associated with more pronounced benefits of resistance training. For ribosomal content, the hypothesis is that higher rRNA content at baseline and larger increases in rRNA content during the initial part of the intervention will be associated with more pronounced benefits of resistance training. No changes are expected in the non-resistance training control group.
Study Type
Enrollment (Actual)
Phase
- Not Applicable
Contacts and Locations
Study Locations
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Inland Norway
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Lillehammer, Inland Norway, Norway, 2613
- Inland Norway University of Applied Sciences
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion criteria:
- VO2max > 65 ml/kg/min (male participants)
- VO2max > 50 ml/kg/min (female participants)
- >7 hours of endurance training per week for the 6 months leading up to the study
Exclusion criteria:
- having conducted regular resistance training for the last 6 months leading up to the study
Study Plan
How is the study designed?
Design Details
- Primary Purpose: Treatment
- Allocation: Randomized
- Interventional Model: Parallel Assignment
- Masking: Double
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
|---|---|
|
Experimental: Resistance training added to endurance training
Participants (elite cyclists) will conduct heavy-load resistance training twice a week in addition to their habitual endurance training for ten weeks
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Resistance training sessions twice a week for ten weeks
Other Names:
Endurance training for ten weeks (habitual routines)
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Other: Endurance training
Participants (elite cyclists) will conduct habitual endurance training-only for ten weeks
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Endurance training for ten weeks (habitual routines)
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Performance during a 40-minute all-out cycling test
Time Frame: Changes from before the intervention to immediately after the intervention
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Mean power output measured during a 40-minute all-out cycling test
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Changes from before the intervention to immediately after the intervention
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Performance during a 15-minute all-out cycling test
Time Frame: Changes from before the intervention to immediately after the intervention
|
Mean power output measured during a 15-minute all-out cycling test
|
Changes from before the intervention to immediately after the intervention
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Total RNA in muscle tissue (before intervention)
Time Frame: Before the intervention
|
Total RNA content in m. vastus lateralis (ug per mg tissue)
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Before the intervention
|
|
Total RNA in muscle tissue (changes after two weeks)
Time Frame: Changes from before the intervention to immediately after the initial two weeks of resistance training
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Total RNA content in m. vastus lateralis (ug per mg tissue)
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Changes from before the intervention to immediately after the initial two weeks of resistance training
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|
Muscle fiber proportions (before intervention)
Time Frame: Before the intervention
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Muscle fiber proportions in m. vastus lateralis measured using immunohistochemistry
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Before the intervention
|
|
Muscle fiber proportions (changes after two weeks)
Time Frame: Changes from before the intervention to immediately after the initial two weeks of resistance training
|
Muscle fiber proportions in m. vastus lateralis measured using immunohistochemistry
|
Changes from before the intervention to immediately after the initial two weeks of resistance training
|
|
Muscle fiber cross-sectional area (before intervention)
Time Frame: Before the intervention
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Cross-sectional area of muscle fibres in m. vastus lateralis measured using immunohistochemistry
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Before the intervention
|
|
Muscle fiber cross-sectional area (changes after two weeks)
Time Frame: Changes from before the intervention to immediately after the initial two weeks of resistance training
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Cross-sectional area of muscle fibres in m. vastus lateralis measured using immunohistochemistry
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Changes from before the intervention to immediately after the initial two weeks of resistance training
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|
Myonuclear number (before intervention)
Time Frame: Before the intervention
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Myonuclei per muscle fiber in m. vastus lateralis measured using immunohistochemistry
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Before the intervention
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|
Myonuclear number (changes after two weeks)
Time Frame: Changes from before the intervention to immediately after the initial two weeks of resistance training
|
Myonuclei per muscle fiber in m. vastus lateralis measured using immunohistochemistry
|
Changes from before the intervention to immediately after the initial two weeks of resistance training
|
|
rRNA expression (before intervention)
Time Frame: Before the intervention
|
rRNA abundances in m. vastus lateralis measured using qPCR
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Before the intervention
|
|
rRNA expression (changes after two weeks)
Time Frame: Changes from before the intervention to immediately after the initial two weeks of resistance training
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rRNA abundances in m. vastus lateralis measured using qPCR
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Changes from before the intervention to immediately after the initial two weeks of resistance training
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mRNA expression (before intervention)
Time Frame: Before the intervention
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mRNA abundances in m. vastus lateralis measured using qPCR
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Before the intervention
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mRNA expression (changes after two weeks)
Time Frame: Changes from before the intervention to immediately after the initial two weeks of resistance training
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mRNA abundances in m. vastus lateralis measured using qPCR
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Changes from before the intervention to immediately after the initial two weeks of resistance training
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Maximal concentric force production
Time Frame: Changes from before the intervention to immediately after the intervention
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Maximal concentric force production measured using a seated leg press test
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Changes from before the intervention to immediately after the intervention
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Sprint performance
Time Frame: Changes from before the intervention to immediately after the intervention
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Mean power output measured during a 10-second all-out cycling sprint
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Changes from before the intervention to immediately after the intervention
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Maximal oxygen consumption
Time Frame: Changes from before the intervention to immediately after the intervention
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Maximal oxygen consumption measured during an incremental cycling exercise test to exhaustion
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Changes from before the intervention to immediately after the intervention
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Maximal aerobic power output
Time Frame: Changes from before the intervention to immediately after the intervention
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Maximal aerobic power output measured as mean power output during the last minute of an incremental cycling exercise test to exhaustion
|
Changes from before the intervention to immediately after the intervention
|
|
Power output at lactate threshold
Time Frame: Changes from before the intervention to immediately after the intervention
|
Power output at 4 mmol blood lactate concentration measured during an incremental cycling exercise test (with 5 minute steps)
|
Changes from before the intervention to immediately after the intervention
|
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Gross efficiency
Time Frame: Changes from before the intervention to immediately after the intervention
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Contribution of total energy turnover to power output in the fresh and fatigued state
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Changes from before the intervention to immediately after the intervention
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Fractional utilization of VO2max (incremental test)
Time Frame: Changes from before the intervention to immediately after the intervention
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Fractional utilization of VO2max measured at 4 mmol blood lactate concentrations measured during an incremental cycling exercise test (with 5 minute steps)
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Changes from before the intervention to immediately after the intervention
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Fractional utilization of VO2max (15-minute performance test)
Time Frame: Changes from before the intervention to immediately after the intervention
|
Fractional utilization of VO2max measured during a 15-minute performance test
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Changes from before the intervention to immediately after the intervention
|
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Hemoglobin mass
Time Frame: Changes from before the intervention to immediately after the intervention
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Hemoglobin mass measured using CO rebreathing (g)
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Changes from before the intervention to immediately after the intervention
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Blood volume
Time Frame: Changes from before the intervention to immediately after the intervention
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Blood volume measured using CO rebreathing
|
Changes from before the intervention to immediately after the intervention
|
|
Plasma volume
Time Frame: Changes from before the intervention to immediately after the intervention
|
Plasma volume measured using CO rebreathing
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Changes from before the intervention to immediately after the intervention
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Red blood cell volume
Time Frame: Changes from before the intervention to immediately after the intervention
|
Red blood cell volume measured using CO rebreathing
|
Changes from before the intervention to immediately after the intervention
|
|
Hematocrit
Time Frame: Changes from before the intervention to immediately after the intervention
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Hematocrit measured using centrifugation
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Changes from before the intervention to immediately after the intervention
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Other Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Endurance training volume
Time Frame: Throughout study completion (daily), an average of ten weeks
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Self-reported endurance training volume measured as time-spent in different exercise intensity zones
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Throughout study completion (daily), an average of ten weeks
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Resistance training volume
Time Frame: Throughout study completion (daily), an average of ten weeks
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Self-reported resistance training volume measured as load x repetitions
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Throughout study completion (daily), an average of ten weeks
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Collaborators and Investigators
Study record dates
Study Major Dates
Study Start (Actual)
Primary Completion (Actual)
Study Completion (Actual)
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
Keywords
Other Study ID Numbers
- Trainome 2020#025-2
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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