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RecruitingNCT03107533Updated Apr 23, 2026

Scoliosis Shared Decision Making

An observational study in Scoliosis, sponsored by Mayo Clinic. Recruiting at 1 site in United States. Open to participants aged 13 Years and older. Per ClinicalTrials.gov, last updated 2026-04-23.

Sponsored by Mayo Clinic · Observational

From the registry’s dates

  • Started Mar 2017; still recruiting 9 years 6 months later.
Study type
Observational
Model
Cohort
Time perspective
Prospective
Enrollment
25
Ages
13 Years and older
Sex
All
01

Study summary

Analysis of video encounters between providers, patients, and families will be used to develop a shared decision making tool for patients deciding between surgery and observation for scoliosis treatment.

Read the detailed description

For patients and parents who are considering scoliosis surgery, a video recording of the encounter will be obtained during their routine clinical visit to discuss surgery/options. This video will then be sent to the shared decision making group at Mayo Clinic, Rochester, Minnesota to run analysis of the data (Shared Decision Making National Resource Center, Knowledge and Evaluation Research Unit, Mayo Clinic). Investigators will follow the patient's electronic medical records for 2 years after their decision of treatment option. No outcome forms will be specifically collected as part of the study, as outcomes forms are currently being collected clinically on all scoliosis patients.

Based off of the initial video recordings, the first visual prototype of the shared decision making tool for scoliosis has been developed. This prototype of the shared decision making tool will be now be used to help test it's efficiency.

02

Conditions studied

  • Scoliosis

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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 25 is below the median of 87 across 232 observational studies indexed under Scoliosis.

Browse Scoliosis studies →

Lead sponsor

Mayo Clinic is the lead sponsor of 3,218 studies on the registry; 670 are open to participants now.

Of its 445 completed or terminated interventional studies of FDA-regulated products, 313 (70%) have results posted.

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

04

Who can participate

Ages eligible
13 Years and older
Sexes eligible
All
Accepts healthy volunteers
No
Sampling method
Non-probability sample

Study population

Children and adults

Inclusion criteria

  • Scoliosis curve >40 degrees, \< 65 degrees
  • Risser score > 2
  • Age > 13 years

Exclusion criteria

Exclusion Criteria:

  • Risser score of 0 or 1
  • Non-ambulatory scoliosis patients
  • Ages 12 year and under
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Study design

Observational model
Cohort
Time perspective
Prospective
Enrollment
25 participants (estimated)
Patient registry
No

Groups and cohorts

  • Video recording of clinical visit

    Investigators will enroll patients from the Department of Orthopedic Surgery for enrollment. The shared decision group will provide staff for data analysis.

    Other: Video recording of clinical visit

Interventions

  • OtherVideo recording of clinical visit

    For patients and parents that are considering scoliosis surgery, a video recording of the encounter will be obtained during their routine clinical visit to discuss surgery/options.

06

What researchers measure

Primary outcomes

  1. Number of patients who understand disease treatment as determined by analysis of video recording

    Video will be recorded then be sent to the shared decision making group at Mayo Clinic, Rochester, Minnesota to run analysis of the data (Shared Decision Making National Resource Center, Knowledge and Evaluation Research Unit, Mayo Clinic).

    Time frame: Baseline

07

Study locations

1 of 1 sites recruiting
  • Mayo Clinic
    Rochester, Minnesota 55905, United States
    • Vickie Treder · Contact · (507) 538-3561
    • Noelle A. Larson, MD · Principal investigator
    Recruiting
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References and documents

Individual participant data

Plan to share: No

09

Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Apr 23, 2026, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
10

Registry details

Key details

Study ID
NCT03107533
Lead sponsor
Mayo Clinic
Responsible party
A. Noelle Larson, MD (Associate Professor of Orthopedics, Mayo Clinic) — Principal investigator
First posted
Apr 11, 2017
Start date
Mar 30, 2017
Primary completion
Mar 2027 (estimated)
Completion
Mar 2027 (estimated)
Last update
Apr 23, 2026

Study contacts

Angela M Severson
Contact
severson.angela2@mayo.edu
(507) 538-3560
Noelle Larson, MD
principal investigator · Mayo Clinic

Oversight

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

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