The Effects of Heavier- and Lighter-load Resistance Training on Arm and Leg Muscle Mass in Young Adult Women (FHALL)

September 27, 2021 updated by: Cameron Mitchell, University of British Columbia

The Effects of Higher- And Lower-Load Resistance Exercise Training on Leg and Arm Skeletal Muscle Mass in Healthy Young Adult Females

When you perform weightlifting, your body makes new proteins within your muscle. These new proteins can increase the size of the fibers within your muscle to make your muscle larger, a process called hypertrophy. The common convention surrounding gains in muscle mass and strength are that higher-loads (i.e. heavier weights) used for fewer repetitions are better for increasing strength and lower-loads (i.e. lighter weights) used for higher repetitions are better for increasing muscle mass. However, recent research has found that when higher- and lower-loads are used when participants exercise until volitional fatigue (i.e. cannot perform another repetition), muscle mass and strength increases are similar regardless of using a higher- or lower-load. Many of these studies have examined this effect in males with fewer studies examining the effects of higher- and lower-load training in females when assessing changes in muscle mass, strength, and muscle endurance.

Further, it has been shown that there is substantial individual variation in response to resistance exercise training where individuals can be broadly categorized as higher- or lower-responders to resistance exercise training. This study aims to explore how the muscle mass, strength, and muscle endurance of females are impacted by both higher- and lower-loads while also exploring how individuals may respond to the training interventions.

Study Overview

Detailed Description

The study will be a total of 12 weeks in total duration. Weeks 1 and 12 will include testing assessments of skeletal muscle mass, muscle strength, and muscle endurance. Weeks 2-11 will be comprised of the resistance training intervention wherein participants will train thrice weekly at the Chan Gunn Pavilion research laboratory at the University of British Columbia.

Resistance training sessions will include unilateral knee extensions and unilateral dumbbell bicep preacher curls with each being performed for three sets. Limbs assigned to train with higher-loads will perform between 8-12 repetitions per set and limbs assigned to train with lower-loads will perform between 20-25 repetitions per set. Participants will rest 90 seconds between sets and 120 seconds between exercises. Each exercise will be performed in its entirety before moving on to the next.

Participants will also be supplemented with whey protein which will be ingested twice daily during the resistance training phase.

Study Type

Interventional

Enrollment (Actual)

16

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

    • British Columbia
      • Vancouver, British Columbia, Canada, V6T 1Z3
        • The University of British Columbia

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 30 years (Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Female

Description

Inclusion Criteria:

  1. Female
  2. 18-30 years of age
  3. Can fluently read and write in English
  4. Able to commit to three training sessions per week for a continuous 10-week period as well as testing one week before and one week after this 10-week training period
  5. All "No" answers on the Canadian Society for Exercise Physiology Get Active questionnaire or doctors' approval to participate

Exclusion Criteria:

  1. Allergic to dairy products or are lactose-intolerant (participants will be supplemented with whey protein twice daily for the 10-week training period)
  2. Allergic to any of the following ingredients which are present in the whey protein concentrate supplement: Bos taurus - Milk, Cocoa, Natural and Artificial Flavours, Xanthan Gum, Sucralose, Non-genetically modified organism Sunflower Lecithin
  3. Any major uncontrolled cardiovascular, muscular, metabolic, and/or neurological disorders
  4. Lung or kidney disease
  5. Medical conditions impacting on their ability to undertake strenuous physical activity
  6. Regular use of any mental health medications that may lead to excessive weight gain (selective serotonin reuptake inhibitors, second generation antipsychotics, antiepileptic drugs)
  7. Participated in consistent resistance exercise training more than twice per month in the previous 12 months
  8. Participated in consistent vigorous aerobic training more than twice per week in the previous 12 months
  9. Significant gain or loss of body mass in the past 6 months (greater than 2 kg)
  10. Current smoker
  11. BMI less than 18 or over 30

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: Basic Science
  • Allocation: Randomized
  • Interventional Model: Parallel Assignment
  • Masking: None (Open Label)

Arms and Interventions

Participant Group / Arm
Intervention / Treatment
Active Comparator: Higher-load limbs
This treatment arm will have participants performing resistance training with loads of ~80% of an individuals one-repetition maximum. Each participant will have one arm and one leg assigned to this condition.
This intervention will have one arm and one leg of each participant training with ~80% of their one repetition maximum
Active Comparator: Lower-load limbs
This treatment arm will have participants performing resistance training with loads of ~30% of an individuals one-repetition maximum. Each participant will have one arm and one leg assigned to this condition.
This intervention will have one arm and one leg of each participant training with ~30% of their one repetition maximum

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in upper- and lower-body skeletal muscle mass between weeks 1 and 12
Time Frame: Weeks 1 and 12
The total skeletal muscle mass measured in each individual arm and leg quantified using dual-energy x-ray absorptiometry scanning
Weeks 1 and 12

Secondary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Change in unilateral dumbbell bicep preacher curl one repetition maximum between weeks 1 and 12
Time Frame: Weeks 1 and 12
The maximum amount of weight that an individual can move for one full repetition during the unilateral dumbbell bicep preacher curl exercise
Weeks 1 and 12
Change in unilateral knee extension one repetition maximum between weeks 1 and 12
Time Frame: Weeks 1 and 12
The maximum amount of weight that an individual can move for one full repetition during the unilateral knee extension exercise
Weeks 1 and 12
Change in unilateral dumbbell bicep preacher curl relative muscle endurance between weeks 1 and 12
Time Frame: Weeks 1 and 12
The maximum number of repetitions that can be completed with 30% and 80% of the individuals current one repetition maximum for the unilateral dumbbell bicep preacher curl exercise
Weeks 1 and 12
Change in unilateral dumbbell bicep preacher curl absolute muscle endurance between weeks 1 and 12
Time Frame: Weeks 1 and 12
The maximum number of repetitions that can be completed with 30% and 80% of the individuals baseline one repetition maximum for the unilateral dumbbell bicep preacher curl exercise
Weeks 1 and 12
Change in unilateral knee extension relative muscle endurance between weeks 1 and 12
Time Frame: Weeks 1 and 12
The maximum number of repetitions that can be completed with 30% and 80% of the individuals current one repetition maximum for the unilateral knee extension exercise
Weeks 1 and 12
Change in unilateral knee extension absolute muscle endurance between weeks 1 and 12
Time Frame: Weeks 1 and 12
The maximum number of repetitions that can be completed with 30% and 80% of the individuals baseline one repetition maximum for the unilateral knee extension exercise
Weeks 1 and 12
Change in Vastus Lateralis and Biceps Brachii Cross Sectional Area between weeks 1 and 12
Time Frame: Weeks 1 and 12
The cross sectional area of the vastus lateralis and biceps brachii muscles measured using ultrasonography
Weeks 1 and 12
Change in Vastus Lateralis and Biceps Brachii Muscle Thickness between weeks 1 and 12
Time Frame: Weeks 1 and 12
The thickness of the vastus lateralis and biceps brachii muscles measured using ultrasonography
Weeks 1 and 12
Change in Vastus Lateralis Pennation Angle between weeks 1 and 12
Time Frame: Weeks 1 and 12
The pennation angle of the vastus lateralis muscle fibers measured using ultrasonography
Weeks 1 and 12
Change in Vastus Lateralis Fascicle Length between weeks 1 and 12
Time Frame: Weeks 1 and 12
The length of the fascicles of the vastus lateralis muscle measured using ultrasonography
Weeks 1 and 12

Collaborators and Investigators

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

Investigators

  • Principal Investigator: Cameron J Mitchell, PhD, University of British Columbia

Publications and helpful links

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

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)

January 5, 2021

Primary Completion (Actual)

August 12, 2021

Study Completion (Actual)

August 12, 2021

Study Registration Dates

First Submitted

September 4, 2020

First Submitted That Met QC Criteria

September 11, 2020

First Posted (Actual)

September 14, 2020

Study Record Updates

Last Update Posted (Actual)

September 29, 2021

Last Update Submitted That Met QC Criteria

September 27, 2021

Last Verified

September 1, 2021

More Information

Terms related to this study

Additional Relevant MeSH Terms

Other Study ID Numbers

  • H20-01570

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

No

IPD Plan Description

A plan has not yet been made to make individual participant data available to other researchers

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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