Eccentric Cycling : a Promising Training Modality for Sedentary People
Effects and Comparison of Eccentric Cycling Trainings Versus Concentric Cycling Training on Muscular and Functional Capacities in Sedentary People
1 other identifier
interventional
45
1 country
1
Brief Summary
The present study aims to compare the acute and training responses of (1) eccentric high intensity interval training (EI), (2)work-matched continuous eccentric training (EC), and (3) concentric high intensity interval training (CI), all performed on cycle ergometers. The variables of interest include ratings of perceived exertion (RPE), cognitive demand (Fat), heart rate (HR), maximal oxygen consumption (VO₂max), maximal aerobic power (MAP), and various functional and health-related parameters. 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for not_applicable
Started Apr 2024
Shorter than P25 for not_applicable
1 active site
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
Study Start
First participant enrolled
April 20, 2024
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 15, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
January 15, 2025
CompletedFirst Submitted
Initial submission to the registry
August 25, 2025
CompletedFirst Posted
Study publicly available on registry
September 24, 2025
CompletedSeptember 24, 2025
September 1, 2025
9 months
August 25, 2025
September 19, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (7)
Maximal Isometric Force
Maximal isometric knee extensors strength of the dominant leg was assessed using a MicroFET2 handheld dynamometer (Hoggan Scientific, USA) secured to an immovable frame. Participants were seated with hips at 85° and knees at 90° flexion. After a warm-up involving five minutes of low-intensity cycling and three submaximal isometric contractions (50-90% effort), participants completed five maximal voluntary contractions, each lasting five seconds with 30 seconds of rest between efforts. The highest recorded value was retained for analysis and expressed in newton-meters (Nm).
At enrollment and at the end of treatment at 14 weeks
Maximal Aerobic Power
At the first and final visits, participants underwent a concentric incremental cycling test to determine their maximal aerobic power (expressed in watt (W)). The test began with a standardized 2-minute warm-up at 30 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. The higher value was recorded as their MAP. Participants were instructed to maintain a cadence above 60 rpm and were verbally encouraged throughout the test.
At the begining and the end of study (week 1 and 14)
Peak oxygen consumption
At the first and final visits, participants underwent a concentric incremental cycling test to determine VO₂ peak (expressed in mililiters per minute per kilogram (mL/min/kg)). 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. The higher value of VO₂ was recorded as their VO₂ peak. Participants were instructed to maintain a cadence above 60 rpm and were verbally encouraged throughout the test.
At the begining and the end of the study (week 1 and 14)
Weight
Study participants were weighed during their first session of participation. This measurement was taken on a Tanita balance and is expressed in kilograms (kg).
At the begining and the end of the study (week 1 and 14)
Height
Participants were measured during their first session of participation in the study. This measurement was taken using a wall-mounted height gauge and is expressed in meters (m).
At the begining and the end of the study (week 1 and 14)
Body mass index
The body mass index (BMI) of the participants was calculated based on their previously measured weight and height. The following formula was used: weight (kg)/height (m)², and BMI is expressed in kg/m\^2
At the begining and the end of the study (week 1 and 14)
Body fat index
The body fat percentage of each participant was measured using Tanita scales and expressed as a percentage (%).
At the begining and the end of the study (week 1 and 14)
Secondary Outcomes (5)
Handgrip strength
At week 1 and week 14
Balance error scoring system
Week 1 and 14
Ten times sit to stand test
Week 1 and 14
Timed up and go
Week 1 and 14
Six-minute walking test
Week 1 and 14
Other Outcomes (4)
Rating of perceived exertion
Throughout all the training sessions (week 2 to week 13)
Heart Rate
Throughout the training sessions, from week 2 to week 15
Cognitive demand
At the end of each training session, from week 2 to week 15
- +1 more other outcomes
Study Arms (3)
Eccentric Interval
EXPERIMENTALParticipants in this arm had to follow a high intensity interval training using an eccentric ergocycle
Eccentric continuous
EXPERIMENTALParticipants in this arm had to follow a moderate intensity continuous training using an eccentric ergocycle
Concentric interval
EXPERIMENTALParticipants in this arm had to follow a high intensity interval training using a concentric ergocycle
Interventions
This intervention is a high intensity interval training using an eccentric ergocycle
This intervention is a moderate intensity continuous training using an eccentric ergocycle
This intervention is a high intensity interval training using a concentric ergocycle
Eligibility Criteria
You may qualify if:
- Sedentary people (less than 3 hours of physical activity a week)
- No smoker
You may not qualify if:
- Pain or injury in the 6 previous months in the lower limbes
- Presenting an uncontrolled chronic condition
- Presenting cardiovascular issues
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Liege University
Liège, 4000, Belgium
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- STUDY DIRECTOR
Stéphanie HODY, PhD
ULiege - Supervisor
- STUDY DIRECTOR
Jean-François Kaux, Prof
ULiege - Co-supervisor
Study Design
- Study Type
- interventional
- Phase
- not applicable
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- PARALLEL
- Sponsor Type
- OTHER
- Responsible Party
- PRINCIPAL INVESTIGATOR
- PI Title
- Principal Investigator
Study Record Dates
First Submitted
August 25, 2025
First Posted
September 24, 2025
Study Start
April 20, 2024
Primary Completion
January 15, 2025
Study Completion
January 15, 2025
Last Updated
September 24, 2025
Record last verified: 2025-09
Data Sharing
- IPD Sharing
- Will not share