Eccentric Cycling : a Promising Training Modality for Sedentary People
NCT ID: NCT07189975
Last Updated: 2025-09-24
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
NA
45 participants
INTERVENTIONAL
2024-04-20
2025-01-15
Brief Summary
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It is hypothesized that eccentric interval training will produce comparable or superior improvements in functional outcomes relative to concentric interval training, but at a lower metabolic and perceptual cost. Furthermore, eccentric interval training is expected to yield greater physiological benefits than continuous eccentric training for a similar perceived and metabolic load.
Forty-three sedentary healthy adults (23 men and 20 women) were recruited for this study based on predefined inclusion and exclusion criteria. Participants were randomly (stratified randomization) allocated into one of three training groups.
Participants attended the laboratory on 28 occasions over a 14-week period, with two sessions per week.
Participants in the EI and EC groups trained using an eccentric ergometer, while the CI group trained on a concentric ergometer. Baseline and post-intervention assessments were conducted during weeks 1 and 14, respectively. These included a maximal incremental cycling test to determine VO₂ peak and concentric MAP, followed by six functional performance assessments.
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Detailed Description
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It is hypothesized that eccentric HIIT will produce comparable or superior improvements in functional outcomes relative to concentric HIIT, but at a lower metabolic and perceptual cost. Furthermore, eccentric HIIT is expected to yield greater physiological benefits than continuous eccentric training for a similar perceived and metabolic load.
Forty-three healthy adults (23 men and 20 women) were recruited for this study based on predefined inclusion and exclusion criteria. Participants were randomly (stratified randomization) allocated into one of three training groups:
* Eccentric Interval Group (EI): n = 15 (8 men, 7 women); age = 62.6 ± 3.9 years old (yo)
* Eccentric Continuous Group (EC): n = 15 (8 men, 7 women); age = 61.6 ± 6.3 yo
* Concentric Interval Group (CI): n = 13 (7 men, 6 women); age = 60.5 ± 5.1 yo All participants were unaccustomed to eccentric cycling and engaged in no more than 2 hours of recreational physical activity per week. Individuals with recent lower limb injuries or chronic medical conditions were excluded. Prior to participation, all individuals were fully informed of the study procedures, potential risks, and provided written informed consent. The study protocol received ethical approval from the Ethics Committee of the University of Liège (Ref. 2023/72), and all procedures conformed to the Declaration of Helsinki.
Participants in the EI and EC groups trained using an eccentric ergometer, while the CI group trained on a concentric ergometer. Baseline and post-intervention assessments were conducted during weeks 1 and 14, respectively. These included a maximal incremental cycling test to determine VO₂peak and concentric MAP (cMAP), followed by six functional performance assessments.
The training protocol consisted of three consecutive 4-week phases:
1. Familiarization Phase (Weeks 2-5)
2. Initial Training Phase (Weeks 6-9)
3. Progressive Training Phase (Weeks 10-13) with increased training intensity.
At the first and final visits, participants underwent a concentric incremental cycling test to determine VO₂peak and cMAP. The test began with a standardized 2-minute warm-up at 30 watts (W) and a cadence of 60 revolutions per minute (rpm). The workload was then increased every minute by 15 W for women and 20 W for men until volitional exhaustion.
Participants were instructed to maintain a cadence above 60 rpm and were verbally encouraged throughout the test.
The 12-week training intervention was structured into three consecutive phases: (1) familiarization, (2) initial training, and (3) progressive training. All participants completed two supervised sessions per week, either on a recumbent eccentric ergometer (Cyclus 2, RBM Elektronik-Automation GmbH, Germany) or a seated concentric cycle ergometer (Technogym, Italy), depending on group allocation.
1. Phase 1 (T1) - Familiarization (Weeks 2-5) During the familiarization phase, all groups completed work-matched sessions adapted to their respective contraction modality (eccentric or concentric cycling). Based on the findings of Lipski et al., a conversion ratio of 1.5 was used to estimate eccentric MAP (eMAP) from cMAP, such that 100% eMAP was considered equivalent to 150% of cMAP.
Training intensity and duration were progressively increased across the four weeks. Participants began with 5 minutes of cycling at 30% of their cMAP and progressed to 30 minutes by the end of the phase.
2. Phase 2 (T2) - Initial Training (Weeks 6-9)
In the second phase, all groups trained at an intensity equivalent to 80% of their modality-specific MAP for 30 minutes per session:
* EI Group: 10 x 2' training/1' rest at 120% of cMAP (\~80% of eMAP)
* EC Group: 30' at 80% of cMAP
* CI Group: 10 x 2' training/1' rest at 80% of cMAP
3. Phase 3 (T3) - Progressive Training (Weeks 10-13)
Training intensity was further increased to 90% of each group's modality-specific MAP:
* EI Group: 10 x 2' training/1' rest at 135% of cMAP (\~90% of eMAP)
* EC Group: 30' at 90% of cMAP
* CI Group: 10 x 2' training/1' rest at 90% of cMAP This progressive overload aimed to enhance aerobic capacity and muscular adaptations in a contraction-specific manner. All sessions remained isocaloric and time-matched across groups to allow for valid comparisons.
Heart rate, rating of perceived exertion, cognitive demand / fatigue and muscle soreness were monitored during each training session.
A battery of six functional tests was performed pre- and post-intervention to evaluate intra-group improvements and inter-group differences. All tests were administered by the same trained evaluator to minimize inter-rater variability. Standardized instructions and verbal encouragement were provided to ensure consistency across participants. These tests include : maximal isometric force, handgrip strength, balance, ten times sit-to-stand time, timed up and go and six-minute walking test.
Conditions
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Study Design
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RANDOMIZED
PARALLEL
TREATMENT
NONE
Study Groups
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Eccentric Interval
Participants in this arm had to follow a high intensity interval training using an eccentric ergocycle
High intensity eccentric cycling training
This intervention is a high intensity interval training using an eccentric ergocycle
Eccentric continuous
Participants in this arm had to follow a moderate intensity continuous training using an eccentric ergocycle
Moderate intensity eccentric cycling training
This intervention is a moderate intensity continuous training using an eccentric ergocycle
Concentric interval
Participants in this arm had to follow a high intensity interval training using a concentric ergocycle
High intensity concentric cycling training
This intervention is a high intensity interval training using a concentric ergocycle
Interventions
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High intensity eccentric cycling training
This intervention is a high intensity interval training using an eccentric ergocycle
Moderate intensity eccentric cycling training
This intervention is a moderate intensity continuous training using an eccentric ergocycle
High intensity concentric cycling training
This intervention is a high intensity interval training using a concentric ergocycle
Eligibility Criteria
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Inclusion Criteria
* No smoker
Exclusion Criteria
* Presenting an uncontrolled chronic condition
* Presenting cardiovascular issues
55 Years
75 Years
ALL
Yes
Sponsors
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University of Liege
OTHER
Responsible Party
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Vandenbroeck Benoit
Principal Investigator
Principal Investigators
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Stéphanie HODY, PhD
Role: STUDY_DIRECTOR
ULiege - Supervisor
Jean-François Kaux, Prof
Role: STUDY_DIRECTOR
ULiege - Co-supervisor
Locations
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Liege University
Liège, , Belgium
Countries
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Provided Documents
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Document Type: Study Protocol and Statistical Analysis Plan
Other Identifiers
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B7072023000019 - 2023/72
Identifier Type: -
Identifier Source: org_study_id
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