Pre-op Exercise for Scoliosis

Age: < 65
Sex: Any
Trial Phase: Academic
Sponsor: Eric Parent
No Placebo GroupAll trial participants will receive the active study treatment (no placebo)

What You Need to Know Before You Apply

What is the purpose of this trial?

The goal of this clinical trial is to determine if pre-operative scoliosis-specific exercises have a beneficial effect on the health outcomes of surgery for adolescent idiopathic scoliosis. Adolescent idiopathic scoliosis affects adolescents between the age of 10-18.

The main questions this study aims to answer are:

* Can pre-operative exercises help reduce curve progression prior to surgery?

* Can pre-operative exercises help improve the surgery outcomes, such as a lower number of vertebrae needing fusion, increased curve correction, reduced surgery length, and shorter length of stay in the hospital?

* Can a pre-operative exercise intervention result in a reduction of the cost of surgery?

Researchers will compare the current standard of care (the control group) to an intervention group (with pre-op exercises) to see if pre-op exercises have an effect on these outcomes.

Participants will:

* visit the clinic every 3 months to complete ultrasound imaging scans and questionnaires

* if given an exercise intervention, aim to complete it for roughly 30 minutes a day

Are You a Good Fit for This Trial?

Inclusion Criteria

Curve angle >40 degrees
I am on the waitlist for posterior spinal fusion surgery at the Stollery Hospital.
I have been diagnosed with adolescent idiopathic scoliosis.
See 1 more

Exclusion Criteria

Current use of scoliosis-specific exercises
I have had surgery before.

Timeline for a Trial Participant

Screening

Participants are screened for eligibility to participate in the trial

2-4 weeks

Pre-operative Exercise Intervention

Participants in the intervention group perform scoliosis-specific exercises for 30 minutes daily to improve flexibility and reduce curve progression before surgery.

6 months
Clinic visits every 3 months for ultrasound imaging and questionnaires

Surgery

Participants undergo surgery for adolescent idiopathic scoliosis, with outcomes measured such as number of vertebrae fused and surgery duration.

Follow-up

Participants are monitored for safety and effectiveness after surgery, including quality of life assessments and appearance questionnaires.

6 weeks post-op
First routine follow-up post-surgery

What Are the Treatments Tested in This Trial?

Interventions

  • Pre-op Exercise Program

How Is the Trial Designed?

2

Treatment groups

Experimental Treatment

Active Control

Group I: Pre-op Exercise InterventionExperimental Treatment1 Intervention
Group II: Standard of Care (Control)Active Control1 Intervention

Find a Clinic Near You

Who Is Running the Clinical Trial?

Eric Parent

Lead Sponsor

Women and Children's Health Research Institute, Canada

Collaborator

Trials
18
Recruited
24,800+