NCT05945641

Brief Summary

Local muscle endurance (LME) is the ability of a muscle(s) to resist fatigue and is needed for daily activities of life such as climbing stairs, lifting/moving objects, and in sport contexts like rock climbing, mixed martial arts, cross-fit, kayaking and canoeing. Therefore, the investigators want learn how to improve LME and understand what in human bodies changes during exercise training to cause these changes. The investigators know that lifting weights improves muscle strength which is believed to improve LME. Specifically lifting less heavy weights (LLRET) for more repetitions leads to greater gains in LME opposed to heavier weights for fewer repetitions. Therefore, lifting less heavy weights likely causes greater changes in our muscles than lifting heavier weights that cause improvements in LME. Aerobic exercise preformed at high intensities in an interval format (HIIT) may also help improve LME by increasing our muscle's ability to produce energy during exercise. Therefore, the investigators want to see which of LLRET or HIIT leads to greater improvements in LME.

Trial Health

57
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Sep 2023

Geographic Reach
1 country

1 active site

Status
recruiting

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

June 9, 2023

Completed
1 month until next milestone

First Posted

Study publicly available on registry

July 14, 2023

Completed
3 months until next milestone

Study Start

First participant enrolled

September 27, 2023

Completed
1.5 years until next milestone

Primary Completion

Last participant's last visit for primary outcome

April 1, 2025

Completed
1 month until next milestone

Study Completion

Last participant's last visit for all outcomes

May 1, 2025

Completed
Last Updated

March 30, 2025

Status Verified

May 1, 2024

Enrollment Period

1.5 years

First QC Date

June 9, 2023

Last Update Submit

March 25, 2025

Conditions

Keywords

Muscle StrengthLocal Muscle EnduranceMuscle HypertrophyMitochondrial ContentMitochondrial FunctionMuscle CapillarizationHigh-Intensity Interval TrainingSprint Interval TrainingLow Load Resistance TrainingResistance TrainingInterval TrainingKnee ExtensionMuscle Endurance

Outcome Measures

Primary Outcomes (4)

  • Change in repetitions completed for 30% pre-training 1- Repetition maximum (Single leg Knee extension)

    The number of single leg knee extension repetitions that one can complete at 30% of their pre-training 1-RM

    Change from baseline to 6 weeks

  • Change in Repetitions completed for 30% pre-training 1- Repetition maximum (Single leg Knee extension)

    The number of single leg knee extension repetitions that one can complete at 30% of their pre-training 1-RM

    Change from baseline to 12 weeks

  • Change in CFPE index (Capillary to fiber ratio normalized to fiber perimeter)

    Mean number of capillaries touching each muscle fibre (normalized to the fibre perimeter). Assessed using imaging of muscle samples gathered via muscle biopsies.

    Change from baseline to 12 weeks

  • Change in Maximal Citrate synthase (CS) Activity

    Indicator of Mitochondrial content and function in skeletal muscle.

    Change from baseline to 12 weeks

Secondary Outcomes (17)

  • Change in Single leg Knee extension 1- Repetition maximum (weight lifted)

    Change from baseline to 6 weeks

  • Change in Single leg Knee extension 1- Repetition maximum (weight lifted)

    Change from baseline to 12 weeks

  • Change in Single leg Knee extension Isometric Maximum Voluntary Contraction

    Change from baseline to 6 weeks

  • Change in Single leg Knee extension Isometric Maximum Voluntary Contraction

    Change from baseline to 12 weeks

  • Change in Single leg Knee Flexion Isometric Maximum Voluntary Contraction

    Change from baseline to 6 weeks

  • +12 more secondary outcomes

Study Arms (2)

Low Load Resistance Training

EXPERIMENTAL

LLRET - 12 weeks (2-3 times/week) 3 sets of Knee extension exercise (single leg) done at 30%1- RM. Performed to failure with 3 minutes of rest between sets, weight lifted will be adjusted throughout the study to keep repetitions completed in a 20-30 repetition range.

Behavioral: Low Load Resistance training

Sprint/High Intensity Interval Training

EXPERIMENTAL

SIT/HIIT- 12 weeks (2-3 times/week), mix of SIT and HIIT (8-15 sets/session). SIT -30 second Super Maximal "Wingate style intervals" performed on a Kicking ergometer (single leg) with 4 minutes rest provided between sets (number of interval ranges from 4-5), load determined from DEXA leg lean mass and will not be altered throughout training. HIIT - 1-minute Submaximal efforts (90% single leg kicking ergometer VO2Peak Wattage) performed on a kicking ergometer (single leg) with 1 minute rest provided between sets (number of interval ranges from 8-10), if all sets completed wattage will be increased by 5watts for the next training session.

Behavioral: Sprint/High Intensity Interval Training

Interventions

Performing single leg knee extension exercise with using equivalent to \~30%1-RM to failure,

Also known as: LLRET
Low Load Resistance Training

Performing repeated submaximal/maximal 30second-60 seconds (1-3 minute rest between) aerobic intervals on a Kicking ergometer (modified bike that allows cycling to be performed with one leg using a kicking motion).

Also known as: SIT/HIIT
Sprint/High Intensity Interval Training

Eligibility Criteria

Age19 Years - 30 Years
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Able to understand and communicate in English
  • years of age
  • All "No" answers on the CSEP Get Active questionnaire or doctors' approval to participate
  • Untrained participants: no structured resistance and/or endurance training over the past 12-months (i.e., \>2 hours per week of structured/periodized training)

You may not qualify if:

  • BMI lower than 18 or greater than 30
  • Current use of cigarettes or other nicotine devices
  • Any major uncontrolled cardiovascular, muscular, metabolic, and/or neurological disorders
  • Any medical condition impacting the ability to participate in maximal exercise
  • Type one or type two diabetes
  • Diagnosis of cancer or undergoing cancer treatment in the past 12 months
  • Taking blood-thinning medication or the presence of a bleeding disorder
  • Drug therapy with any drugs that alter skeletal muscle metabolism (i.e., Metformin, Benzodiazepines)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Univeristy if British Columbia

Vancouver, British Columbia, V6T 1Z3, Canada

RECRUITING

MeSH Terms

Conditions

Hypertrophy

Interventions

High-Intensity Interval Training

Condition Hierarchy (Ancestors)

Pathological Conditions, AnatomicalPathological Conditions, Signs and Symptoms

Intervention Hierarchy (Ancestors)

Physical Conditioning, HumanExerciseMotor ActivityMovementMusculoskeletal Physiological PhenomenaMusculoskeletal and Neural Physiological Phenomena

Central Study Contacts

Lucas A Wiens, BSc

CONTACT

Cameron J Mitchell, PhD

CONTACT

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
NONE
Masking Details
Since the interventions are exercise interventions it is not possible to blind either the participants or Investigator to which condition each participants leg receives. However, the legs will be randomly assigned to their conditions (neither the participant nor the Investigator will determine this.)
Purpose
PREVENTION
Intervention Model
PARALLEL
Model Details: Within subject Design: Each participant will have one leg randomly assigned to each training condition. Training for each leg will occur over the same 12 week training period.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Principal Investigator

Study Record Dates

First Submitted

June 9, 2023

First Posted

July 14, 2023

Study Start

September 27, 2023

Primary Completion

April 1, 2025

Study Completion

May 1, 2025

Last Updated

March 30, 2025

Record last verified: 2024-05

Data Sharing

IPD Sharing
Will share

Individual participant data will be held by Lucas Wiens and will be released upon request to other researchers.

Shared Documents
STUDY PROTOCOL, SAP, ICF, CSR
Time Frame
Data will be made available after publication/completion of the project. Data will remain available for at least 10 years following the completion of this project.
Access Criteria
Data will only be released to researchers who have valid association with an institution or private laboratory.

Locations