ICU patients may benefit from short bursts of bed cycling
NCT ID NCT05279547
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests two ways of cycling while lying in a hospital bed for patients in the intensive care unit (ICU). One method is steady cycling for 10-20 minutes, and the other is short bursts of harder cycling mixed with easier pedaling. The goal is to see which approach better activates leg muscles and is safe for patients who are weak from being in the ICU.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- bed-cycling exercise
- What this could lead to
- If successful, this study could point toward better exercise routines for ICU patients to prevent muscle weakness.
- What could go wrong
- This is a small pilot study, so results may not apply to all ICU patients. The main goal is to test safety and feasibility, not to prove a treatment works.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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About 100 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2023
- Expected to finish
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Dec 2028
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Full cooperatively adult patients indicated by the Adequacy Score of standardized 5 questions (SQ5) = 5/5 * Patients mechanically ventilated for longer than 48 hours during the same ICU admission * Patients are expected to remain in the ICU for more than an additional 48 hours starting from study enrollment * Patients able to perform active cycling for \> 10 consecutive minutes Exclusion Criteria: * Pre-existing functional limitations * Low limb injuries or conditions that would preclude in-bed cycling such as a body habitus unable to fit the bike * Extreme obesity (body mass index \>35 kg/m2) * Neurologically unstable * Acute surgery * Palliative goals of care * Temperature \> 40 °C * An anticipated fatal outcome * Evidence of coronary ischaemia, for example, chest pain or electrocardiogram changes * Resting heart rate \<40 or \>120 beats per minute * Mean arterial pressure \<60 or \>120 mmHg * Peripheral capillary oxygen saturation \< 90% * Wounds, trauma or surgery of leg precluding cycle ergometry * Wounds, trauma or surgery of pelvis precluding cycle ergometry * Wounds, trauma or surgery of lumbar spine precluding cycle ergometry * Coagulation disorder (international normalised ratio \> 1.8, or platelets \< 50,000 mcL) * Intracranial pressure \>20 mm Hg * Femoral access other than femoral central line * Acute deep vein thrombosis * Pulmonary embolism * \>20 mcg/min of noradrenaline * inotropic or vasopressor support comparable to a dose of noradrenaline \>20mcg/min * Fraction of inspired oxygen \> 55% * Arterial partial pressure of oxygen (PaO2) \<65 torr (\<8.66 kPa) * Positive end-expiratory pressure \> 10 cmH2O * Respiratory rate \> 30 breaths per minutes with adequate ventilatory support * Minute ventilation \>150 mL/kg body weight
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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University Hospital Leuven
RECRUITINGLeuven, 3000, Belgium
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