NCT03993483

Brief Summary

Recent research suggests that performing resistance exercise training with relatively light loads is equally as effective at increasing muscle mass and muscle strength as performing resistance exercise training with relatively heavy loads. Whether or not performing resistance exercise with relatively heavy loads or light loads is equally as effective between the upper- and lower-body within the same individual has never been investigated. Given the substantial individual variance in resistance exercise training-induced changes in muscle mass and strength, this study is designed to quantify the relative influence that extrinsic training variables (e.g., load), as opposed to intrinsic muscle-based predisposition, has on resistance training-induced changes in muscle mass and muscle strength.

Trial Health

87
On Track

Trial Health Score

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

Enrollment
20

participants targeted

Target at below P25 for not_applicable

Timeline
Completed

Started Jun 2018

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

June 1, 2018

Completed
4 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 5, 2018

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 5, 2018

Completed
9 months until next milestone

First Submitted

Initial submission to the registry

June 17, 2019

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 20, 2019

Completed
Last Updated

June 20, 2019

Status Verified

June 1, 2019

Enrollment Period

4 months

First QC Date

June 17, 2019

Last Update Submit

June 19, 2019

Conditions

Outcome Measures

Primary Outcomes (6)

  • Change in fat-free mass

    Measured by dual x-ray absorptiometry pre- and post-training

    up to 12 weeks

  • Change in vastus lateralis thickness

    Measured by ultrasonography pre- and post-training

    up to 12 weeks

  • Change in vastus lateralis cross sectional area

    Measured by ultrasonography pre- and post-training

    up to 12 weeks

  • Change in biceps brachii thickness

    Measured by ultrasonography pre- and post-training

    up to 12 weeks

  • Change in biceps brachii cross sectional area

    Measured by ultrasonography pre- and post-training

    up to 12 weeks

  • Change in muscle fibre cross sectional area

    Measured by muscle biopsies from the vastus lateralis pre- and post-training

    up to 12 weeks

Study Arms (2)

Higher Load

EXPERIMENTAL

One arm and one leg were randomized (based on limb dominance) to perform unilateral biceps curls (arm) and knee extensions (leg) with relatively higher loads (80 % of their one-repetition maximum).

Behavioral: Unilateral resistance exercise

Lower Load

EXPERIMENTAL

The other arm and leg were randomized (based on limb dominance) to perform unilateral biceps curls (arm) and knee extensions (leg) with relatively higher loads (80 % of their one-repetition maximum).

Behavioral: Unilateral resistance exercise

Interventions

The participants performed three sets of their unilateral resistance exercise (biceps curls and knee extensions) three times per week for 10 weeks.

Higher LoadLower Load

Eligibility Criteria

Age18 Years - 30 Years
Sexmale
Healthy VolunteersYes
Age GroupsAdult (18-64)

You may qualify if:

  • Be between the ages of 18-30 years (inclusive)
  • Be able to maintain a habitual diet and perform resistance exercise three times per week throughout the trial
  • Be in general good health (assessed by Get Active Questionnaire)
  • Understand the study procedures and sign this form providing informed consent to participate in the study.

You may not qualify if:

  • Use of tobacco or related products
  • A history of neuromuscular problems or muscle and/or bone wasting diseases
  • Any acute or chronic illness; cardiac, pulmonary, liver, or kidney abnormalities; insulin- or non-insulin-dependent diabetes or other metabolic disorders (all ascertained through medical questionnaires)
  • Use of medications known to affect protein metabolism (i.e. corticosteroids, non-steroidal anti-inflammatory drugs (prescription use or daily use of over the counter medication), or prescription strength acne medications)

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Exercise Metabolism Research Laboratory, McMaster Univeristy

Hamilton, Ontario, L8S 4K1, Canada

Location

Study Officials

  • Stuart Phillips, PhD

    McMaster University

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
interventional
Phase
not applicable
Allocation
RANDOMIZED
Masking
SINGLE
Who Masked
OUTCOMES ASSESSOR
Masking Details
The histochemistry and ultrasonography were analyzed by blinded study investigators
Purpose
BASIC SCIENCE
Intervention Model
PARALLEL
Model Details: One arm and one leg of each participant were randomized to lift with heavier loads while the other arm and leg of each participant were randomized to lift with lighter loads for 10 weeks.
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Tier 1 Canada Research Chair and Professor

Study Record Dates

First Submitted

June 17, 2019

First Posted

June 20, 2019

Study Start

June 1, 2018

Primary Completion

October 5, 2018

Study Completion

October 5, 2018

Last Updated

June 20, 2019

Record last verified: 2019-06

Data Sharing

IPD Sharing
Will not share

No individual participant data will be made available to other researchers

Locations