Predicting the Efficacy of Resistance Exercise Training for Improving Endurance Performance (IDperform)

February 26, 2021 updated by: Inland Norway University of Applied Sciences

Identifying Molecular Determinants for the Efficacy of Resistance Training for Improving Endurance Performance in Elite Cyclists

The overall objective of the study is to identify molecular determinants of the efficacy of resistance training for improving endruance performance in elite cyclists

Study Overview

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

Interventional

Enrollment (Actual)

25

Phase

  • Not Applicable

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

    • Inland Norway
      • Lillehammer, Inland Norway, Norway, 2613
        • Inland Norway University of Applied Sciences

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

18 years to 45 years (Adult)

Accepts Healthy Volunteers

Yes

Genders Eligible for Study

All

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

This section provides details of the study plan, including how the study is designed and what the study is measuring.

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
Resistance training sessions twice a week for ten weeks
Other Names:
  • Heavy-load strength training
Endurance training for ten weeks (habitual routines)
Other: Endurance training
Participants (elite cyclists) will conduct habitual endurance training-only for ten weeks
Endurance training for ten weeks (habitual routines)

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
Mean power output measured during a 40-minute all-out cycling test
Changes from before the intervention to immediately after the intervention
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)
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
Total RNA content in m. vastus lateralis (ug per mg tissue)
Changes from before the intervention to immediately after the initial two weeks of resistance training
Muscle fiber proportions (before intervention)
Time Frame: Before the intervention
Muscle fiber proportions in m. vastus lateralis measured using immunohistochemistry
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
Cross-sectional area of muscle fibres in m. vastus lateralis measured using immunohistochemistry
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
Cross-sectional area of muscle fibres in m. vastus lateralis measured using immunohistochemistry
Changes from before the intervention to immediately after the initial two weeks of resistance training
Myonuclear number (before intervention)
Time Frame: Before the intervention
Myonuclei per muscle fiber in m. vastus lateralis measured using immunohistochemistry
Before the intervention
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
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
rRNA abundances in m. vastus lateralis measured using qPCR
Changes from before the intervention to immediately after the initial two weeks of resistance training
mRNA expression (before intervention)
Time Frame: Before the intervention
mRNA abundances in m. vastus lateralis measured using qPCR
Before the intervention
mRNA expression (changes after two weeks)
Time Frame: Changes from before the intervention to immediately after the initial two weeks of resistance training
mRNA abundances in m. vastus lateralis measured using qPCR
Changes from before the intervention to immediately after the initial two weeks of resistance training
Maximal concentric force production
Time Frame: Changes from before the intervention to immediately after the intervention
Maximal concentric force production measured using a seated leg press test
Changes from before the intervention to immediately after the intervention
Sprint performance
Time Frame: Changes from before the intervention to immediately after the intervention
Mean power output measured during a 10-second all-out cycling sprint
Changes from before the intervention to immediately after the intervention
Maximal oxygen consumption
Time Frame: Changes from before the intervention to immediately after the intervention
Maximal oxygen consumption measured during an incremental cycling exercise test to exhaustion
Changes from before the intervention to immediately after the intervention
Maximal aerobic power output
Time Frame: Changes from before the intervention to immediately after the intervention
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
Gross efficiency
Time Frame: Changes from before the intervention to immediately after the intervention
Contribution of total energy turnover to power output in the fresh and fatigued state
Changes from before the intervention to immediately after the intervention
Fractional utilization of VO2max (incremental test)
Time Frame: Changes from before the intervention to immediately after the intervention
Fractional utilization of VO2max measured at 4 mmol blood lactate concentrations measured during an incremental cycling exercise test (with 5 minute steps)
Changes from before the intervention to immediately after the intervention
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
Changes from before the intervention to immediately after the intervention
Hemoglobin mass
Time Frame: Changes from before the intervention to immediately after the intervention
Hemoglobin mass measured using CO rebreathing (g)
Changes from before the intervention to immediately after the intervention
Blood volume
Time Frame: Changes from before the intervention to immediately after the intervention
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
Changes from before the intervention to immediately after the intervention
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
Hematocrit measured using centrifugation
Changes from before the intervention to immediately after the intervention

Other Outcome Measures

Outcome Measure
Measure Description
Time Frame
Endurance training volume
Time Frame: Throughout study completion (daily), an average of ten weeks
Self-reported endurance training volume measured as time-spent in different exercise intensity zones
Throughout study completion (daily), an average of ten weeks
Resistance training volume
Time Frame: Throughout study completion (daily), an average of ten weeks
Self-reported resistance training volume measured as load x repetitions
Throughout study completion (daily), an average of ten weeks

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start (Actual)

November 16, 2020

Primary Completion (Actual)

February 26, 2021

Study Completion (Actual)

February 26, 2021

Study Registration Dates

First Submitted

November 12, 2020

First Submitted That Met QC Criteria

November 18, 2020

First Posted (Actual)

November 19, 2020

Study Record Updates

Last Update Posted (Actual)

March 1, 2021

Last Update Submitted That Met QC Criteria

February 26, 2021

Last Verified

November 1, 2020

More Information

Terms related to this study

Drug and device information, study documents

Studies a U.S. FDA-regulated drug product

No

Studies a U.S. FDA-regulated device product

No

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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