Under construction – not a live service
Sign in
CompletedNo phase

Protocol for Rapid Onset of Mobilization in Patients With Traumatic Spinal Cord Injury

Key facts

Who runs it
Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Where
Canada1 site in 1 countryChoose a country to see its sites
Trial code
Status
Completed
People taking part
45 people enrolled
Started
1 Apr 2021
Ended
31 Aug 2024
Type of study
Interventional
Treatments tested
  • Leg ergometer
Record updated
26 November 2025

Who can take part

Age
18 years and older
Sex
Women and men
Healthy volunteers
Cannot take part

The registry criteria, word for word

Show all 11 criteriaShow less

Who can take part

  • Blunt traumatic spinal cord injury
  • Neurological level of injury from C0 to L2
  • American Spinal Injury Association impairment scale grade A, B or C
  • Spine surgery performed within 48 hours of injury

Who cannot take part

  • Inability to walk independently prior to injury
  • Condition limiting patient's ability to engage into cycling
  • Medical condition that might interfere with patient's safety if cycling
  • Pre-existing neurological disorder
  • Moderate or severe brain injury
  • Complete spinal cord transection
  • Unwilling or unable to comply with scheduled follow-up

This trial has no sites in United States.

It has sites in one country. Choose a country to see its sites.

About the trial

What the trial wants to find out

PROMPT-SCI (Protocol for Rapid Onset of Mobilization in Patients with Traumatic SCI) is a single-site single-arm proof-of-concept trial. Forty-five patients aged 18 years or older who have sustained a severe traumatic SCI (American Spinal Injury Association Impairment Scale grade A, B or C) from C0 to L1 and undergoing spinal surgery within 48 hours of the injury will be included. Participants will receive daily 30-minute sessions of in-bed leg cycling for 14 consecutive days, initiated within 48 hours after spinal surgery. The feasibility outcomes consist of the 1) absence of serious adverse events associated with cycling sessions, 2) completion of at least 1 full session within 48 hours after spinal surgery for at least 90% of participants, and 3) completion of at least 11 sessions for at least 80% of participants. Patient outcomes 6 weeks and 6 months after injury will be measured from neurofunctional assessments, quality of life questionnaires and inpatient length of stay. Feasibility and patient outcomes will be analysed with descriptive statistics. Patient outcomes will also be compared to a matched historical cohort not receiving in-bed cycling.

The group in the trial

  • Early in-bed leg cyclingTreatment being tested

    Treatment: Leg ergometer

Data and sources

Registry record
Listed on ClinicalTrials.gov.
Official title
Protocol for Rapid Onset of Mobilization in Patients With Traumatic Spinal Cord Injury (PROMPT-SCI)
Publications
Record updated
26 November 2025