Actively Recruiting

Age: 18Years +
All Genders
Healthy Volunteers
ID06258161

Functional Reach Test as a Clinical Tool for Assessing Postural Balance Limits Among Adult Spinal Deformity Patients

Led by University of Kansas Medical Center · Updated on 2026-05-06

30

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

Sponsors

U

University of Kansas Medical Center

Lead Sponsor

S

Scoliosis Research Society

Collaborating Sponsor

AI-Summary

What this Trial Is About

Adult spinal deformity (ASD) is a common condition that affects posture and balance, often making daily activities difficult and increasing disability risk. Researchers are studying a new balance assessment called the functional reach test (FRT) to better understand balance limits in ASD patients compared to healthy adults. This study aims to provide spine surgeons with useful data on balance loss risk and guide future research on surgical treatments for ASD. The study involves two groups: adults with ASD undergoing spinal realignment fusion surgery and healthy adults without spine problems as controls. Balance will be assessed using wearable motion sensors and a force plate during normal standing and the functional reach test. The study will track changes before surgery and at 3, 6, 12, and 24 months after surgery to evaluate postural sway and reach distance. Participants will undergo functional balance tests and report pain and disability levels at several time points over two years. Researchers will also assess timed mobility tests to understand overall function. This data will help standardize clinical balance assessments and improve decision-making for ASD care. The total participation time includes preoperative evaluation and multiple follow-up visits up to 24 months post-surgery.

CONDITIONS

Brief Title

Effect of Adult Spinal Deformity Surgery on Functional Reach

Who Can Participate

Age: 18Years +
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults over the age of 18
  • Diagnosed with adult spinal deformity according to the SRS-Schwab Adult Spinal Deformity Classification System
  • Indicated for deformity corrective surgery including multilevel spinal fusion of three or more levels
  • Lowest instrumented level includes S1 or pelvic fixation
  • Able to perform functional activities without the use of any assistance or support devices
  • Adults over the age of 18
  • No current or prior spine pathology or surgery
  • Able to perform the functional activities without the use of any assistance or support devices
Not Eligible

You will not qualify if you...

  • Indicated for spinal fusion due to spinal tumor, trauma, or infection
  • ASD patients who do not plan to be available for all follow-up evaluations at our institution
  • Pregnancy during any time point within the participation duration
  • Any current or prior spine or lower extremity pathology or surgery that impacts the ability to perform functional activities
  • Pregnancy at the time of the evaluation

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surgery and Immediate Post-operative Care

Duration - Up to 1 week or until discharge

Participants diagnosed with adult spinal deformity undergo spinal realignment fusion surgery and receive immediate post-operative care.

1 visit for surgery and immediate hospital stay

Post-operative Follow-up

Duration - 24 months

Participants are assessed over time to monitor functional reach, postural balance, pain levels, disability, and mobility following surgery.

Visits at 3, 6, 12, and 24 months post-surgery

Long-term Monitoring

Duration - 24 months

Asymptomatic adult controls are observed to provide comparison data on functional balance and postural performance without surgical intervention.

Visits at baseline and follow-ups up to 24 months

Trial Site Locations

Total: 1 location

1

University of Kansas Medical Center

Kansas City, Kansas, United States, 66160

Actively Recruiting

Loading map...

Research Team

D

Damon Mar

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

2

Similar Trials

A Comparison Between Palonosetron Versus Granisetron As Post...

Postoperative Nausea and Vomiting

Actively Recruiting

2 locations

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here