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Pedaling in bed: new study tests quicker spine surgery recovery

NCT ID NCT07506720

Symptom relief Sponsor: Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal Source: ClinicalTrials.gov ↗

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
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 Results may not be published yet.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
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study looks at whether using a special stationary bike while lying in bed, the day after spine surgery, helps people get moving sooner. About 88 adults having elective spine surgery will either get standard care or add a 30-minute in-bed cycling session. Researchers will track how much time they spend in bed and how long they stay in the hospital.

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

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 88 people

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

Started

Aug 2025

Expected to finish

Jan 2029

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 Male or female ≥ 18 years old. Postoperative #0 following elective spinal surgery: decompression with or without fusion, or fusion. Patient able to walk independently before surgery (does not require assistance from another person and does not use a wheelchair). Patient admitted directly from the operating room to the ward. Hemodynamically stable: Systolic blood pressure (SBP): ≥ 90 mmHg and \< 140 mmHg Oxygen saturation \> 94% Heart rate: 50-100 bpm Patient approved for surgery after preoperative internal medicine evaluation. Patient alert and conscious. Valid informed consent obtained. Exclusion Criteria Non-ambulatory preoperatively. Body Mass Index (BMI) \> 40 kg/m². Acute neurological spinal trauma. Non-neurological musculoskeletal impairment of the lower limbs (e.g., severe osteoarthritis, hip fracture, amputation) limiting the ability to pedal in bed. Uncontrolled comorbidities preventing surgery or intervention (cardiovascular, respiratory, diabetes). Expected hospital stay of less than 2 days after surgery. Surgery-related complications: acute neurological deficit, dural tear, cerebrospinal fluid (CSF) leak, residual spinal instability. Transfer to intensive care unit or hemodynamic instability. Persistent hemodynamic instability: SBP \< 90 mmHg or \> 200 mmHg, oxygen saturation \< 88%, heart rate \< 50 or \> 100 bpm, temperature \> 38°C. Capillary blood glucose outside target values: \< 4.0 or \> 7.0 mmol/L fasting or pre-meal, \< 5.0 and \> 10.0 mmol/L 2 hours post-meal. Patient confused, disoriented, or agitated. Patient already evaluated by physiotherapy for discharge planning or intensive functional rehabilitation. Patient in isolation. Patient already discharged.

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Conditions

The condition(s) this trial relates to.

Kinesiophobia vertebral column disorder

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

Post surgery patients Recovery method SPINE

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. 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

  • Montreal Sacred Heart Hospital

    RECRUITING

    Montreal, Quebec, H4J 1C5, Canada

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