CClinicalTrials.gg
Enrolling by invitationNCT07516574Updated Apr 8, 2026

Pre-op Exercise for AIS Surgery

An interventional study of Pre-op Exercise Program in Adolescent Idiopathic Scoliosis (AIS), sponsored by Eric Parent. Enrolling by invitation at 1 site in Canada. Open to participants aged 10 Years to 18 Years. Per ClinicalTrials.gov, last updated 2026-04-08.

Sponsored by Eric Parent · Not applicable, Interventional, and Treatment

From the registry’s dates

  • Registered 4 months after the study started (first participant enrolled Nov 2025, registered Mar 2026).
Phase
Not applicable
Study type
Interventional
Enrollment
40
Allocation
Randomized
Ages
10 Years to 18 Years
Sex
All
01

Study summary

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
02

Conditions studied

  • Adolescent Idiopathic Scoliosis (AIS)

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Keywords

  • Adolescent idiopathic scoliosis
  • AIS
  • scoliosis
  • Schroth
  • flexibility
03

In context

Scoliosis

593 studies on the registry are indexed under Scoliosis; 138 are open to participants now.

This study's planned enrollment of 40 is close to the median of 44 across 344 interventional studies indexed under Scoliosis.

Browse Scoliosis studies →

Lead sponsor

This is the only study on the registry with Eric Parent as lead sponsor.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
10 Years to 18 Years
Sexes eligible
All
Accepts healthy volunteers
No

Inclusion criteria

  • diagnosis of adolescent idiopathic scoliosis
  • aged 10 to 18
  • curve angle >40 degrees
  • waitlisted for posterior spinal fusion surgery at the Stollery Hospital

Exclusion criteria

Exclusion Criteria:

  • previous surgeries
  • current use of scoliosis-specific exercises
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Study design

Phase
Not applicable
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
Single (Outcomes assessor)
Enrollment
40 participants (estimated)

Study arms

  • No intervention
    Standard of Care (Control)

    The Standard of Care (Control) Group is the group that will receive the current standard of care offered in the process of treating AIS with surgery.

  • Experimental
    Pre-op Exercise Intervention

    The Pre-op Exercise Intervention Group will receive the current standard of care offered when treating AIS with surgery, and will also be offered the intervention by the research team that is a pre-op exercise program aimed to increase flexibility of the spine and reduce scoliosis progression.

    Behavioral: Pre-op Exercise Program

Interventions

  • BehavioralPre-op Exercise Program

    The pre-op exercise group will complete a 6-month supervised pre-op exercise program. This program is adapted from the Schroth exercise program we tested for moderate scoliosis, showing good effect on curve angles, muscle endurance, posture, curve severity, and in self-reported pain and QOL scores. This physiotherapy will individualize exercises to specific spinal curvature(s). Exercises will focus on elongating and derotating the spine to improve the flexibility before surgery. The corrective movements required, the targeted curve type, the level of passive support involved, and the dosages recommended, have been published previously. A Schroth curve classification algorithm and algorithms to guide the prescription for the curve type will help standardize treatment. The program begins with 5 supervised visits in the first 2 weeks to help learn the exercises. The following month has supervised visits weekly and then every other week. The aim is to exercise 30mins per day 5x/week.

06

What researchers measure

Primary outcomes

  1. Number of levels fused

    The number of vertebrae levels fused during surgery for AIS. This is an indicator of the amount of flexibility afforded to participants post-op, their risk of adverse wear and tear on unoperated levels, and also can indicate significant cost savings to the hospital and health system.

    Time frame: Indicated during surgical planning, completed during surgery (where it may change from plans)

Secondary outcomes

  1. Italian Spine Youth Quality of Life (ISYQOL) questionnaire

    The Italian Spine Youth Quality of Life questionnaire contains 20 questions with the first 13 answered by all patients with scoliosis and the next 7 answered only by those wearing a brace. The raw sum score of the items is converted to a 0 to 100 quality of life score where 100 indicates the best quality of life.

    Time frame: Baseline, 3 months, 6 months, and at first routine follow-up post-surgery (6 weeks post-op)

  2. Spinal Appearance Questionnaire (SAQ) v1.1 Appearance score

    The SAQ v1.1 is a questionnaire consisting of 14 items with the first 10 items producing an appearance score reflecting the self-perceived torso appearance. The appearance score ranges from 10 to 50 with low scores indicating better perceived appearance.

    Time frame: Baseline, 3 months, 6 months, and at first routine follow-up post-surgery (6 weeks post-op)

  3. Spinal Appearance Questionnaire (SAQ) v1.1 expectation score

    The SAQ v1.1 is a questionnaire consisting of 14 items with the last 4 items producing an expectation score reflecting the desire to be more even on some asymmetry features. The expectation score ranges from 4 to 20 with low scores indicating less desire to change the appearance.

    Time frame: Baseline, 3 months, 6 months, and at first routine follow-up post-surgery (6 weeks post-op)

  4. Spinal Appearance Questionnaire (SAQ) v1.1 total score

    The SAQ v1.1 is a questionnaire consisting of 14 items producing a score from 14 to 70 with low scores indicating better perceived appearance.

    Time frame: Baseline, 3 months, 6 months, and at first routine follow-up post-surgery (6 weeks post-op)

  5. Pre-operative flexibility measured by 3D Ultrasound Imaging

    The degree (amount) to which the frontal scoliotic curve is reduced during side-bending compared to standing in a radiograph or ultrasound imaging is the curve's flexibility. These will be taken in ultrasound scanning images of participants.

    Time frame: Baseline, 3 months, and 6 months

  6. Other Surgery-related Outcomes

    Other surgical outcomes include: length (duration) of surgery in minutes, length of stay in hospital post-surgery, percentage of curve correction.

    Time frame: During surgery & immediately post-surgery

  7. Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ) Breast

    The TAASQ assesses patient-perceived anterior truncal appearance. This consists of 14 individual questions that fall into a Breast (questions 4 a, b, c; 12; 13; 14) main domain. The TAASQ uses a combination of Likert scales and free text responses. Each multiple-choice question features answer options ranging from 1 to 5, where 5 corresponds to the least amount of concern or asymmetry and 1 corresponds to the most concern. The average score is then calculated for each domain and sub-domain. Higher scores on the TAASQ indicate better quality of life.

    Time frame: Baseline, 3 months, 6 months, and first routine follow-up post-surgery (6 weeks post-op)

  8. Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ) Clothing

    The TAASQ assesses patient-perceived anterior truncal appearance. This consists of 14 individual questions that fall into three main domains including the Clothing (1; 2 a, b, c, d, e; 3; 8 a, b, c; 9) domain. The TAASQ uses a combination of Likert scales and free text responses. Each multiple-choice question features answer options ranging from 1 to 5, where 5 corresponds to the least amount of concern or asymmetry and 1 corresponds to the most concern. The average score is then calculated for each domain and sub-domain. Higher scores on the TAASQ indicate better quality of life.

    Time frame: Baseline, 3 months, 6 months, and first routine follow-up post-surgery (6 weeks post-op)

  9. Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ) Appearance

    The TAASQ assesses patient-perceived anterior truncal appearance. This consists of 14 individual questions that fall into three main domains: including Appearance (5; 6; 7; 10; 11)., Each multiple-choice question features answer options ranging from 1 to 5, where 5 corresponds to the least amount of concern or asymmetry and 1 corresponds to the most concern. The average score is then calculated for each domain and sub-domain. Higher scores on the TAASQ indicate better quality of life.

    Time frame: Baseline, 3 months, 6 months, and first routine follow-up post-surgery (6 weeks post-op)

  10. Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ) Breast Location

    The TAASQ assesses patient-perceived anterior truncal appearance. The Breast domain can be categorized into a Breast location (Q4c, 13) subdomain scored from 1 to 5, where 5 corresponds to the least amount of concern or asymmetry and 1 corresponds to the most concern. The average score is then calculated for each domain and sub-domain. Higher scores on the TAASQ indicate better quality of life.

    Time frame: Baseline, 3 months, 6 months, and first routine follow-up post-surgery (6 weeks post-op)

  11. Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ) Breast shape

    The TAASQ assesses patient-perceived anterior truncal appearance. The Breast domain can be categorized into a Breast Shape (Q4b, 12) subdomain scored from 1 to 5, where 5 corresponds to the least amount of concern or asymmetry and 1 corresponds to the most concern. The average score is then calculated for each domain and sub-domain. Higher scores on the TAASQ indicate better quality of life.

    Time frame: Baseline, 3 months, 6 months, and first routine follow-up post-surgery (6 weeks post-op)

  12. Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ) Breast size

    The TAASQ assesses patient-perceived anterior truncal appearance. The Breast domain can be categorized into a Breast size (Q4a, 14). subdomain scored from 1 to 5, where 5 corresponds to the least amount of concern or asymmetry and 1 corresponds to the most concern. The average score is then calculated for each domain and sub-domain. Higher scores on the TAASQ indicate better quality of life.

    Time frame: Baseline, 3 months, 6 months, and first routine follow-up post-surgery (6 weeks post-op)

  13. Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ) Clothing General

    The TAASQ assesses patient-perceived anterior truncal appearance. This consists of 14 individual questions that fall into a Clothing-General (Q1, 3, 8a, 9) subdomain. Each multiple-choice question features answer options ranging from 1 to 5, where 5 corresponds to the least amount of concern or asymmetry and 1 corresponds to the most concern. The average score is then calculated for each domain and sub-domain. Higher scores on the TAASQ indicate better quality of life.

    Time frame: Baseline, 3 months, 6 months, and first routine follow-up post-surgery (6 weeks post-op)

  14. Truncal Anterior Asymmetry Scoliosis Questionnaire (TAASQ) Clothing Specific

    The TAASQ assesses patient-perceived anterior truncal appearance. This consists of 14 individual questions that fall into a Clothing-Specific (Q2, 8b, 8c, 8d) subomain. Each multiple-choice question features answer options ranging from 1 to 5, where 5 corresponds to the least amount of concern or asymmetry and 1 corresponds to the most concern. The average score is then calculated for each domain and sub-domain. Higher scores on the TAASQ indicate better quality of life.

    Time frame: Baseline, 3 months, 6 months, and first routine follow-up post-surgery (6 weeks post-op)

07

Study locations

1 site
  • Clinical Science Building, University of Alberta
    Edmonton, Alberta T6G 2R8, Canada
08

References and documents

Publications

  • Calman R, Smithers T, Rowan R. Impact of surgical waiting time on paediatric spinal deformity patients. ANZ J Surg. 2013 Dec;83(12):929-32. doi: 10.1111/ans.12196. Epub 2013 May 8. PubMed 23656433 ↗
  • Fan Y, To MKT, Kuang GM, Lou N, Zhu F, Tao H, Li G, Yeung EHK, Cheung KMC, Cheung JPY. Five days of inpatient scoliosis-specific exercises improve preoperative spinal flexibility and facilitate curve correction of patients with rigid idiopathic scoliosis. Spine Deform. 2025 Jan;13(1):165-175. doi: 10.1007/s43390-024-00965-1. Epub 2024 Sep 26. PubMed 39325330 ↗
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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 8, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT07516574
Lead sponsor
Eric Parent
Collaborators
Women and Children's Health Research Institute, Canada
Responsible party
Eric Parent (Professor, University of Alberta) — Sponsor-investigator
First posted
Apr 8, 2026
Start date
Nov 26, 2025
Primary completion
Dec 2028 (estimated)
Completion
Dec 2028 (estimated)
Last update
Apr 8, 2026

Oversight

Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

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