Effect of Adult Spinal Deformity Surgery on Functional Reach

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorUniversity of Kansas Medical Center

About this trial

Adult spinal deformity (ASD) is a common spinal condition that often impacts an individual's ability to stand and maintain an upright posture. Poor balance often limits an individual's ability to perform basic activities of daily life (ADL) and can lead to disability. Current considerations of correcting ASD to improve balance focus on the amount of sway that one exhibits during normal standing. However, current tests do not provide insight into the limits of balance during normal ADL.

The goal of this research is to develop a new balance assessment that includes a functional reach test (FRT) to provide numerical data on the limits of one's ability to maintain balance. The study will include both ASD patients and matched healthy adults and will compare postural sway measures between them. Wearable motion tracking sensors and a force plate will be used to monitor body movement and changes in the center of pressure under foot during normal standing and during a FRT. Data from this study will inform spine surgeons of ASD patient's risk of balance loss in daily life and enable further research on the effects of surgical techniques to restore balance among ASD surgery patients.

Eligibility criteria

Qualifiers

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

Disqualifiers

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

Adults over the age of 18

Trial design

Treatments tested in this trial

  • Spinal Fusion
  • No intervention

Treatment groups

30 Participants
are divided into 2 treatment groups

Sponsors and collaborators

University of Kansas Medical Center

Lead sponsor

Scoliosis Research Society

Collaborator