Pedal power after knee surgery? trial tests home cycling

NCT ID NCT07838012

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Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
Registered, but not yet taking participants.
By invitation only
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Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
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Expanded access (paused)
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Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
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First seen Sep 24, 2026 · Last updated Sep 25, 2026 · Updated 1 time

Summary

Researchers are testing whether adding early home-based stationary cycling to standard exercises after knee replacement is practical and acceptable. The pilot trial enrolls 24 adults scheduled for partial or total knee replacement. Participants are randomly assigned to either standard home exercises alone or standard exercises plus 30 minutes of stationary cycling at home at least five days a week for eight weeks, starting two weeks after surgery. The study measures recruitment, adherence, and participant feedback to plan a larger trial.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
early home-based stationary cycling added to standard postoperative exercises
What this could lead to
If the cycling programme proves practical, it could shape a larger trial testing whether early cycling improves recovery, pain, and function after knee replacement.
What could go wrong
This is a small pilot study with 24 participants, so it cannot show whether cycling actually improves outcomes. It only checks whether the programme can be delivered and tolerated. Results may not apply to all knee replacement patients.

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Study facts

What this study's own registry entry says, in plain language.

Phase

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

About 24 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

Sep 2026

An estimate. Start dates often move.

Expected to finish

Mar 2028

An estimate. End dates often move.

Lead sponsor

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

18 years and older

Sex

Anyone

Healthy volunteers

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

Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.

Inclusion Criteria: * Scheduled for unilateral primary medial unicompartmental knee arthroplasty (UKA) or total knee arthroplasty (TKA). * Age ≥ 18 years. * Able to speak and read Danish. * Daily access to a stationary bike during the intervention period, or willingness to use a stationary bike provided by the study through an external rental company for the duration of the intervention. Due to logistical constraints, loan bikes can only be provided to participants residing within approximately one hour of transport from Aarhus or Silkeborg. Participants living outside this area may participate if they have access to a stationary bike. * Ability to use a smartphone with internet connectivity (required for completion of electronic questionnaires and using SENS motion application) or a tablet and having an email address enabling completion of electronic questionnaires. Exclusion Criteria: * Previous surgery in either lower limb within 3 months before the date of knee arthroplasty or planned surgery in either lower limb within 3 months after the date of knee arthroplasty. * Inflammatory joint disease * Previous osteotomy around the knee or tibial condyle fracture that has been treated with osteosynthesis in the affected knee. * Medical or physical conditions that would prevent safe participation in the cycling intervention (e.g., unstable cardiovascular, pulmonary, or chronic neurodegenerative disorders). * Active cancer treatment, if this treatment would interfere with safe participation or adherence to the cycling protocol. * Preoperative reduced knee flexion preventing full pedal rotation on a stationary bike. * Current or recent history of alcohol and/or substance misuse, as identified during the anaesthetic pre-assessment and documented in the electronic patient record. * Cognitive impairment (e.g. dementia) or diagnosed psychiatric disorder that would prevent the patient from understanding or adhering to the cycling protocol.

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Conditions

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