Actively Recruiting
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
Eligibility Criteria
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
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
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
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
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
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
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
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