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Exercise TrainingNCT04295590

Impact of Augmenting Exercise Intensity vs. Frequency

A study testing Frequency comparison and Intensity comparison in people with Exercise Training, run by Brendon Gurd, PhD at 1 site in Canada.

Unknown status

Status not confirmed. The sponsor has not verified this record for over two years, so it may be out of date.

Official record
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Trial summary

The purpose of this study is to compare the impact of augmenting exercise intensity and augmenting exercise frequency on peak work rate. Participants will complete exercise tests and provide 8 skeletal muscle samples following a within-subjects randomized crossover design utilizing single-leg cycling. Read more about this study

Who is it for?
Ages 18 to 30 yearsHealthy volunteers can take part
Conditions the study is for
Exercise Training
What is being tested?
Frequency comparison and Intensity comparison
Could I receive a placebo?
No, everyone receives an active treatment
How many people
16 participants
Where
1 siteCanada
Study dates
30 Sep 2019to 10 Apr 2020
Phase
Interventional
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 30 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Recreational active (<3 hours per week of aerobic exercise)
  • Willing to provide skeletal muscle biopsies

Who cannot join

  • Cardiovascular or metabolic disease
  • Athletes or individuals exceeding 3 hours per week of aerobic exercise
  • Smokers

Trial locations and contacts

1 site in 1 country.

Canada1 site
  • Queen's Muscle Physiology Lab in the School of Kinesiology and Health Studies at Queen's University

    Kingston, Ontario, K7L 3N6

Other trials in Canada

About this study

Official title: Impact of Augmenting Exercise Intensity vs. Frequency on Peak Work Rate

The purpose of this study is to compare the impact of augmenting exercise intensity and augmenting exercise frequency on peak work rate. Participants will complete exercise tests and provide 8 skeletal muscle samples following a within-subjects randomized crossover design utilizing single-leg cycling. Both training periods will be 4 weeks long and skeletal muscle biopsies will be collected from both legs before and after each training period. All exercise sessions will be supervised, take place in the investigator's laboratory, and occur on stationary bikes.

Being tested
Frequency comparison, Intensity comparison

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • Frequency comparisonBehavioural

    One leg assigned to low-frequency low-intensity (3 days per week of 11 x 1 min @ 73% peak work rate interspersed with 1-minute periods of active recovery). The other leg assigned to high-frequency low-intensity (5 days per week of 11 x 1 min @ 73% peak work rate interspersed with 1-minute periods of active recovery).

  • Intensity comparisonBehavioural

    One leg assigned to low-frequency low-intensity (3 days per week of 11 x 1 min @ 73% peak work rate interspersed with 1-minute periods of active recovery). The other leg assigned to low-frequency high-intensity (3 days per week of 8 x 1 min @ 100% peak work rate interspersed with 1-minute periods of active recovery).

Study groups in NCT04295590
Study groupRoleWhat they receive
Frequency then IntensityExperimentalTraining period 1: Frequency comparison Training period 2: Intensity comparison
Receives: Behavioral: Frequency comparison; Behavioral: Intensity comparison
Intensity then FrequencyExperimentalTraining period 1: Intensity comparison Training period 2: Frequency comparison
Receives: Behavioral: Frequency comparison; Behavioral: Intensity comparison

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Peak work rate

    Change in Highest work rate achieved (30s period) during incremental exercise tests

    Measured: Before exercise training on two days (~7 and 6 days before first training session; ~24 hours apart), and after exercise on two days (~48-96 hours after the last training session; ~24 hours apart)

Secondary outcomes (2)
  1. Peak oxygen uptake

    Change in Highest oxygen uptake achieved (30s period) during incremental exercise tests

    Measured: Before exercise training on two days (~7 and 6 days before first training session; ~24 hours apart), and after exercise on two days (~48-96 hours after the last training session; ~24 hours apart)

  2. Maximal citrate synthase activity

    Change in maximal citrate synthase activity

    Measured: Before exercise training (~7 days before first training session), and after exercise training (~48-72 hours after the last training session)

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted4 Mar 2020
  2. Study start30 Sep 2019
  3. Primary completion10 Apr 2020 (estimated)
  4. Study completion10 Apr 2020 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase N/A
Primary purpose
Basic science
Allocation
Randomised
Intervention model
Crossover
Masking
Single blind
Who is masked
Outcomes assessor
Enrolment
16 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT04295590
Sponsor's protocol ID
UCD Study
Status last verified
Mar 2020
First submitted
2 Mar 2020
Last updated
4 Mar 2020
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

Questions about this trial

What is this clinical trial studying?

A study testing Frequency comparison and Intensity comparison in people with Exercise Training, run by Brendon Gurd, PhD at 1 site in Canada.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 2 inclusion and 3 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: status not confirmed, as of the sponsor's last update on 4 Mar 2020. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Canada. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

Are results available for this study?

Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Peak work rate (time frame: Before exercise training on two days (~7 and 6 days before first training session; ~24 hours apart), and after exercise on two days (~48-96 hours after the last training session; ~24 hours apart)). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 4 Mar 2020; AzTrials last refreshed its copy on 1 Nov 2026.

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