NCT07815366

Brief Summary

In eccentric cycling exercise (ECC), the cyclist must oppose backwards moving pedals on a specialized motor-driven ergometer. Throughout this process, the force applied on the pedals exceeds the torque generated by the lengthening muscle (negative work), concurrently generating and storing elastic recoil energy . During ECC the cyclist is able to reach fourfold higher forces compared to conventional concentric cycling exercise (CON). At identical work-rates however, ECC is associated with a lower cardiac output 5 and requires up to 80% less oxygen uptake than CON. Hence, ECC is described as a promising and efficient exercise method with low metabolic costs. ECC exhibits greater effectiveness compared to CON, especially in terms of increasing muscle strength, muscle hypertrophy, six-minute walk distance (6MWD). Acute studies during cycle ergometries have proven that ECC is effective to provide exercise at beneficial levels with low metabolic demand, even at low intensities in patients with chronic cardiopulmonary conditions, such as pulmonary hypertension or COPD. However, whether these benefits can be achieved in a real world setting such as an ambulatory rehabilitation is unknown. Therefore, the rational of the study is to evaluate the effectiveness of ECC vs. standard training in healthy individuals during a three-month time period.

Trial Health

75
On Track

Trial Health Score

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

Enrollment
12

participants targeted

Target at below P25 for not_applicable

Timeline
9mo left

Started Sep 2026

Shorter than P25 for not_applicable

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

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 Progress9%
Sep 2026Jul 2027

First Submitted

Initial submission to the registry

September 7, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

September 7, 2026

Completed
4 days until next milestone

First Posted

Study publicly available on registry

September 11, 2026

Completed
8 months until next milestone

Primary Completion

Last participant's last visit for primary outcome

May 1, 2027

Expected
2 months until next milestone

Study Completion

Last participant's last visit for all outcomes

July 1, 2027

Last Updated

September 11, 2026

Status Verified

September 1, 2026

Enrollment Period

8 months

First QC Date

September 7, 2026

Last Update Submit

September 7, 2026

Conditions

Keywords

eccentric cyclingrehabilitationexercise

Outcome Measures

Primary Outcomes (1)

  • Peak work rate

    Peak work rate will be measured using standardized cardiopulmonary exercise testing on a cycling ergometer.

    Pre and post the three month exercise persiod

Secondary Outcomes (4)

  • Peak oxygen uptake

    Pre and post the three month exercise period.

  • Patient reported perceived dyspnea at peak exercise

    Pre and post three month exercise period

  • Patient reported perceived leg fatigue

    Pre and post three month exercise period.

  • Peak quadriceps extension force

    Pre and post three month exercise period.

Study Arms (1)

Eccentric cycling

EXPERIMENTAL

Eccentric cycling for three month

Procedure: Eccentric cycling exercise

Interventions

Participants exercise for three month on an eccentric ergometer

Eccentric cycling

Eligibility Criteria

Sexall
Healthy VolunteersYes
Age GroupsChild (0-17), Adult (18-64), Older Adult (65+)

You may qualify if:

  • Healthy participants without known Cardiopulmonary disease.
  • Provided written informed consent
  • Wiling to voluntarily exercise for 3 month on the eccentric ergometer without a specific indication for rehabilitation

You may not qualify if:

  • Inability to follow the exercise procedure.
  • Vulnerable participants (e.g. minors, participants incapable of judgment or participants under tutelage) will not be included into the study.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Universitätsspital Zürich

Zurich, Canton of Zurich, 8091, Switzerland

Location

MeSH Terms

Conditions

Motor Activity

Condition Hierarchy (Ancestors)

Behavior

Study Design

Study Type
interventional
Phase
not applicable
Allocation
NA
Masking
NONE
Purpose
PREVENTION
Intervention Model
SINGLE GROUP
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Prof. Dr. med.

Study Record Dates

First Submitted

September 7, 2026

First Posted

September 11, 2026

Study Start

September 7, 2026

Primary Completion (Estimated)

May 1, 2027

Study Completion (Estimated)

July 1, 2027

Last Updated

September 11, 2026

Record last verified: 2026-09

Locations