SedentaryNCT07189975
Eccentric Cycling : a Promising Training Modality for Sedentary People
A study testing High intensity eccentric cycling training, Moderate intensity eccentric cycling training and High intensity concentric cycling training in people with Sedentary and Deconditioning, run by University of Liege at 1 site in Belgium.
Trial 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. Read more about this study
- Who is it for?
- Ages 55 to 75 yearsHealthy volunteers can take part
- Conditions the study is for
- Sedentary, Deconditioning, Eccentric Exercise Training
- What is being tested?
- High intensity eccentric cycling training, Moderate intensity eccentric cycling training and High intensity concentric cycling training
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 45 participants
- Where
- 1 siteBelgium
- Study dates
- 20 Apr 2024to 15 Jan 2025
- 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 55 to 75 years
- All sexes
- Healthy volunteers accepted
- Adult, Older adult
Who may be able to join
- Sedentary people (less than 3 hours of physical activity a week)
- No smoker
Who cannot join
- Pain or injury in the 6 previous months in the lower limbes
- Presenting an uncontrolled chronic condition
- Presenting cardiovascular issues
Trial locations and contacts
1 site in 1 country.
About this study
Official title: Effects and Comparison of Eccentric Cycling Trainings Versus Concentric Cycling Training on Muscular and Functional Capacities in Sedentary People
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.
Read more
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.
Read the detailed description
The present study aims to compare the acute and training responses of (1) eccentric HIIT, (2)work-matched continuous eccentric training, and (3) concentric HIIT, 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 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:
- Familiarization Phase (Weeks 2-5)
- Initial Training Phase (Weeks 6-9)
- 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.
- 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.
- 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
- 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
- Sedentary, Deconditioning, Eccentric Exercise Training, Eccentric Cycling Exercise, Elderly, Healthy Participants
- Being tested
- High intensity eccentric cycling training, Moderate intensity eccentric cycling training, High intensity concentric cycling training
- Keywords
- Eccentric cycling, Sedentarity, Elderly, Physical deconditioning, Training modality, Rehabilitation, Eccentric training
- Medical subject headings
- Sedentary Behavior
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
High intensity eccentric cycling trainingOther
This intervention is a high intensity interval training using an eccentric ergocycle
Moderate intensity eccentric cycling trainingOther
This intervention is a moderate intensity continuous training using an eccentric ergocycle
High intensity concentric cycling trainingOther
This intervention is a high intensity interval training using a concentric ergocycle
| Study group | Role | What they receive |
|---|---|---|
| Eccentric Interval | Experimental | Participants in this arm had to follow a high intensity interval training using an eccentric ergocycle Receives: Other: High intensity eccentric cycling training |
| Eccentric continuous | Experimental | Participants in this arm had to follow a moderate intensity continuous training using an eccentric ergocycle Receives: Other: Moderate intensity eccentric cycling training |
| Concentric interval | Experimental | Participants in this arm had to follow a high intensity interval training using a concentric ergocycle Receives: Other: High intensity concentric cycling training |
What is being measured
The primary outcome is the main question the study is designed to answer.
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).
Measured: 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.
Measured: 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.
Measured: 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).
Measured: 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).
Measured: 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
Measured: 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 (%).
Measured: At the begining and the end of the study (week 1 and 14)
Secondary outcomes (5)
Handgrip strength
Handgrip strength of the dominant hand was measured using a handheld isometric dynamometer (Takei Hand Grip Dynamometer, Japan). Participants performed three maximal grip trials, with 30 seconds of rest between each trial. During testing, the arm was kept extended along the body without any auxiliary movements. The best value was retained and expressed in kilograms (kg).
Measured: At week 1 and week 14
Balance error scoring system
Static balance was assessed using the BESS protocol, which includes three stance positions (double-leg, single-leg, and tandem) performed on both firm and foam surfaces. Each position was held for 20 seconds with eyes closed and hands on hips. Errors, such as opening eyes, lifting hands or losing balance were counted, with a maximum of 10 errors per trial.
Measured: Week 1 and 14
Ten times sit to stand test
Functional lower limb strength and mobility were assessed via the TTSST. Participants began seated with arms crossed over their chest and were instructed to stand up and sit down 10 times as quickly as possible. The test started with a countdown and was timed using a stopwatch. Participants performed 3 trials and the best values was retained for analysis and expressed in seconds (s).
Measured: Week 1 and 14
Timed up and go
Mobility and dynamic balance were assessed using the TUAG test. Participants rose from a seated position, walked three meters, turned 180°, returned to the chair, and sat down, performing a second 180° turn. The time to complete the sequence was recorded with a stopwatch. Participants performed 3 trials and the best values was retained for analysis and expressed in seconds (s).
Measured: Week 1 and 14
Six-minute walking test
Aerobic endurance was evaluated via the 6MWT. Participants were instructed to walk as far as possible in six minutes along a 30-meter indoor track, turning around two cones at either end. HR and RPE were monitored throughout the test. The total distance covered was expressed in meters (m).
Measured: Week 1 and 14
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted24 Sep 2025
- Study start20 Apr 2024
- Primary completion15 Jan 2025
- Study completion15 Jan 2025
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (1)Papers the sponsor has linked to this study.
- Other trials for SedentaryStudies of the same condition, open and under way.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
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
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 45 participants (actual)
Sponsor and investigators
- Lead sponsor
- University of Liege
- Sponsor type
- University, hospital or other
- Responsible party
- Principal investigator, Vandenbroeck Benoit, University of Liege
- Investigators
- Stéphanie HODY, PhD, Study director, ULiege - SupervisorJean-François Kaux, Prof, Study director, ULiege - Co-supervisor
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT07189975
- Sponsor's protocol ID
- B7072023000019 - 2023/72
- Status last verified
- Sep 2025
- First submitted
- 25 Aug 2025
- Last updated
- 24 Sep 2025
- Results posted
- No
- Data monitoring committee
- No
- FDA-regulated drug
- No
- FDA-regulated device
- No
- Individual data sharing
- No
Publications
Vandenbroeck B, Kaux JF, Schleich F, Monseur J, Hody S. Interval eccentric cycling : a promising training modality for sedentary people. Eur J Appl Physiol. 2026 Jul 15. doi: 10.1007/s00421-026-06345-z. Online ahead of print.
PubMed 42455306
Study at a glance
From the registry record, last updated by the sponsor on 24 Sep 2025. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Effects and Comparison of Eccentric Cycling Trainings Versus Concentric Cycling Training on Muscular and Functional Capacities in Sedentary People
- ClinicalTrials.gov ID
- NCT07189975
- Acronym / sponsor ID
- B7072023000019 - 2023/72
- Conditions
- Sedentary, Deconditioning, Eccentric Exercise Training, Eccentric Cycling Exercise, Elderly, Healthy Participants
- Keywords
- Eccentric cycling, Sedentarity, Elderly, Physical deconditioning, Training modality, Rehabilitation, Eccentric training
- Study type
- Interventional
- Recruitment status
- Completed
- Enrolment
- 45 participants (actual)
- Lead sponsor
- University of LiegeUniversity, hospital or other
- Study start
- 20 Apr 2024 (actual)
- Primary completion
- 15 Jan 2025 (actual)
- Study completion
- 15 Jan 2025 (actual)
- First posted
- 24 Sep 2025 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
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.
Detailed description
The present study aims to compare the acute and training responses of (1) eccentric HIIT, (2)work-matched continuous eccentric training, and (3) concentric HIIT, 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 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:
- Familiarization Phase (Weeks 2-5)
- Initial Training Phase (Weeks 6-9)
- 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.
- 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.
- 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
- 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.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 3
| Arm | Type | Receives |
|---|---|---|
| Eccentric Interval | Experimental | Other: High intensity eccentric cycling trainingParticipants in this arm had to follow a high intensity interval training using an eccentric ergocycle |
| Eccentric continuous | Experimental | Other: Moderate intensity eccentric cycling trainingParticipants in this arm had to follow a moderate intensity continuous training using an eccentric ergocycle |
| Concentric interval | Experimental | Other: High intensity concentric cycling trainingParticipants in this arm had to follow a high intensity interval training using a concentric ergocycle |
Who may qualify
- Ages
- 55 to 75 years
- Sex
- All
- Healthy volunteers
- Accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (2 listed)
- Sedentary people (less than 3 hours of physical activity a week)
- No smoker
Key exclusion criteria (3 listed)
- Pain or injury in the 6 previous months in the lower limbes
- Presenting an uncontrolled chronic condition
- Presenting cardiovascular issues
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| High intensity eccentric cycling trainingThis intervention is a high intensity interval training using an eccentric ergocycle | Other | Eccentric Interval |
| Moderate intensity eccentric cycling trainingThis intervention is a moderate intensity continuous training using an eccentric ergocycle | Other | Eccentric continuous |
| High intensity concentric cycling trainingThis intervention is a high intensity interval training using a concentric ergocycle | Other | Concentric interval |
Primary outcome
Maximal Isometric Force
Time frame: At enrollment and at the end of treatment at 14 weeks
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).
Maximal Aerobic Power
Time frame: At the begining and the end of study (week 1 and 14)
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.
Peak oxygen consumption
Time frame: At the begining and the end of the study (week 1 and 14)
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.
Weight
Time frame: At the begining and the end of the study (week 1 and 14)
Study participants were weighed during their first session of participation. This measurement was taken on a Tanita balance and is expressed in kilograms (kg).
Height
Time frame: At the begining and the end of the study (week 1 and 14)
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).
Body mass index
Time frame: At the begining and the end of the study (week 1 and 14)
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
Body fat index
Time frame: At the begining and the end of the study (week 1 and 14)
The body fat percentage of each participant was measured using Tanita scales and expressed as a percentage (%).
5 secondary outcomes
Handgrip strength
Time frame: At week 1 and week 14
Balance error scoring system
Time frame: Week 1 and 14
Ten times sit to stand test
Time frame: Week 1 and 14
Timed up and go
Time frame: Week 1 and 14
Six-minute walking test
Time frame: Week 1 and 14
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Sep 2025.
- Derived from this study: PubMed 42455306Vandenbroeck B, Kaux JF, Schleich F, Monseur J, Hody S. Interval eccentric cycling : a promising training modality for sedentary people. Eur J Appl Physiol. 2026 Jul 15. doi: 10.1007/s00421-026-06345-z. Online ahead of print.
- Individual participant dataSharing planned: No
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
Stéphanie HODY, PhD study director
ULiege - Supervisor
Jean-François Kaux, Prof study director
ULiege - Co-supervisor
1 site in 1 country: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A study testing High intensity eccentric cycling training, Moderate intensity eccentric cycling training and High intensity concentric cycling training in people with Sedentary and Deconditioning, run by University of Liege at 1 site in Belgium.
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: finished, as of the sponsor's last update on 24 Sep 2025. 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 Belgium. 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?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
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?
Maximal Isometric Force (time frame: At enrollment and at the end of treatment at 14 weeks). The study lists 7 primary outcomes in all. It is what the study was designed to measure, not a finding.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT07189975, which also lists 1 linked publication.
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 24 Sep 2025.