Hopital du Sacre-Coeur de Montreal
Montreal, Quebec, h4j1c5, Canada
Location contact
Andreane Richard-Denis, MD, MSc
PRINCIPAL_INVESTIGATOR
Jean-Marc Mac-Thiong, MD, PhD
PRINCIPAL_INVESTIGATOR
Lara Chawa
CONTACT
1+514-338-2222
NCT Number: NCT07798310
This longitudinal cohort study will investigate the clinical benefits of early acute exercise therapy after mild spinal cord injury (SCI). We hypothesize that early acute exercise therapy after mild SCI will improve neurofunctional recovery (walking, functional independence, motor and sensory recovery) and quality of life one year after the SCI, while decreasing complications during acute care and reducing the care burden (shorter hospital stay and home discharge more likely). For this study, 107 participants with mild SCI will be recruited. Participants will perform daily 30-minute sessions of seated cycling throughout acute care, starting within 2 days of their surgery to decompress the spinal cord. Neurofunctional recovery, quality of life, acute complications and care burden for the participants performing early acute cycling will be compared to a control cohort of patients with mild SCI who did not receive exercise therapy during acute care.
Trial opening soon.
Get Notified18 year and older
All sexes
Interventional
Not applicable
Montreal, Quebec, h4j1c5, Canada
Andreane Richard-Denis, MD, MSc
PRINCIPAL_INVESTIGATOR
Jean-Marc Mac-Thiong, MD, PhD
PRINCIPAL_INVESTIGATOR
Lara Chawa
CONTACT
1+514-338-2222
GOALS: This longitudinal cohort study will investigate the clinical benefits of early acute exercise therapy after mild spinal cord injury (SCI).
Primary hypothesis: Recovering independent walking 1 year after a mild SCI is more likely with early acute exercise therapy, in comparison with a historical cohort not exposed to early acute exercise therapy. We have determined that an increase in the percentage of individuals recovering independent walking in the community from 35% to 55% would be considered as a clinically meaningful increase.
Secondary hypothesis: Acute complications, neurological recovery, functional independence, quality of life and care pathway are improved with early acute exercise therapy.
METHODS: For this 5-year study, 107 participants with mild acute traumatic SCI will be recruited. Participants will perform daily 30-minute sessions of seated cycling throughout acute care, starting within 2 days of their surgery to decompress the spinal cord. The immediate response to cycling will be monitored from physiological (hemodynamic and respiratory) and electrophysiological (electromyography and H-reflex testing in lower extremities) assessments. Independent walking in the community (primary outcome) is defined by the ability to walk 100 meters outdoors without technical aids or only with leg orthosis. Secondary outcomes include all complications occurring during acute care (particularly early spasticity, pneumonia, urinary tract infection and pressure injury) and the care pathway (discharge destination and length of stay), as well as neurological recovery, functional independence and quality of life 1 year after the SCI. Outcomes will be compared to a control cohort of patients with mild SCI who did not receive exercise therapy during acute care, and the association with electrophysiological measures will be assessed.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Seated cycling using motorized under desk exerciser
Time frame: 1 year
Ambulation in the community
Time frame: perioperatively/periprocedurally
Acute complications including pneumonia, urinary tract infection, pressure injury, spasticity, etc.
Time frame: 1 year
Difference in American Spinal Injury Association Impairment Scale grade between baseline and 1 year
Time frame: 1 year
Functional independence
Time frame: 1 year
Severity of spasticity
Time frame: 1 year
International Spinal Cord Injury Pain Basic Data Set
Time frame: 1 year
Physical component of Health-related quality of life
Time frame: 1 year
Mental component of Health-related quality of life
Time frame: 1 year
Difference in motor score from baseline to 1 year
Time frame: 1 year
Difference in sensory scores between baseline and 1 year
Time frame: 1 year
Difference in neurological level of injury between baseline and 1 year
Contact information is provided by the study sponsor or research team.
Andreane Richard-Denis Richard-Denis, MD, MSc
CONTACT
1+514-338-2222
Jean-Marc Mac-Thiong, MD, PhD
CONTACT
1+514-338-2222
Centre Integre Universitaire de Sante et Services Sociaux du Nord de l'ile de Montreal
Other
Acronym: PROMPT-SCI III
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
Published trials that share one or more normalized conditions with this study.
NCT07750808
Brain Diseases, Cardiovascular Diseases
Dhaka, Bangladesh
View Trial DetailsNCT07796035
Central Nervous System Diseases, Communication Barriers
Vancouver, British Columbia, Canada
View Trial DetailsNCT07794072
Ataxia, Basal Ganglia Diseases
Milan, Italy
View Trial DetailsNCT07745712
Acquired Brain Injury (Including Stroke), Brain Damage, Chronic
Girona, Spain
View Trial Details