Actively Recruiting

Phase Not Applicable
Age: 18Years - 79Years
All Genders
Healthy Volunteers
NCT04642456

Balance Assessment Scale and Strength Measurement Protocol to Measure Functionality in Adults With Spinal Deformity

Led by Universitaire Ziekenhuizen KU Leuven · Updated on 2026-03-09

30

Participants Needed

1

Research Sites

291 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Develop reliable methods for functional assessment, for trunk strength, of Adult Spinal Deformity (ASD) patients and create a first clinical and normative database 1. Compare functionality of ASD and control subjects 2. Relate functionality of ASD patients to their pathology, in terms of spinal deformity and muscle condition

CONDITIONS

Official Title

Balance Assessment Scale and Strength Measurement Protocol to Measure Functionality in Adults With Spinal Deformity

Who Can Participate

Age: 18Years - 79Years
All Genders
Healthy Volunteers

Eligibility Criteria

Eligible

You may qualify if you...

  • Adults over 18 years old with adult spinal deformity diagnosed on EOS imaging
  • Ability to walk at least 50 meters independently without a walking aid
  • No neurological disease or vestibular lesion affecting balance
  • No current musculoskeletal disorders of the lower limbs affecting movement
  • Adults over 18 years old for control group
  • No current back pain or spinal deformity for control group
  • Ability to walk at least 1000 meters independently without a walking aid for control group
  • No neurological disease or vestibular lesion affecting balance for control group
Not Eligible

You will not qualify if you...

  • Age younger than 18 years or older than 79 years
  • No adult spinal deformity for ASD group
  • Unable to walk at least 50 meters independently for ASD group
  • Missing informed consent
  • Neurological diseases affecting balance other than Parkinson's disease such as stroke or vestibular lesion
  • History of spinal fusion surgery
  • Current severe musculoskeletal disorders affecting movement such as severe hip, knee, or ankle arthrosis or leg length discrepancy greater than 3 cm
  • Back pain or sciatica at time of study for control group
  • Presence of adult spinal deformity causing sagittal misalignment for control group
  • Unable to walk at least 1000 meters independently for control group
  • Neurological diseases affecting balance such as stroke, Parkinson's disease, or vestibular lesions for control group
  • Severe musculoskeletal disorders affecting movement as listed above for control group

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

1
2
3
+1

Trial Site Locations

Total: 1 location

1

UZ Leuven

Leuven, Vlaams-Brabant, Belgium, 3000

Actively Recruiting

Loading map...

Research Team

L

Lieven Moke

CONTACT

A

Anna a Tarasiuk

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

PARALLEL

Primary Purpose

DIAGNOSTIC

Number of Arms

2

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