Possibilities and Limitations of a New Method for the Measurement of Spine Dynamics During Gait

NCT ID: NCT01803256

Last Updated: 2016-11-28

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

Get a concise snapshot of the trial, including recruitment status, study phase, enrollment targets, and key timeline milestones.

Recruitment Status

COMPLETED

Total Enrollment

30 participants

Study Classification

OBSERVATIONAL

Study Start Date

2013-04-30

Study Completion Date

2016-01-31

Brief Summary

Review the sponsor-provided synopsis that highlights what the study is about and why it is being conducted.

The full body marker sets that are typically used in opto-electronic 3D gait analyses either disregard the spine entirely or regard it as a rigid structure. Therefore, the purpose of this study is to identify the possibilities and limitations of an enhanced trunk marker set for the measurement of spine dynamics during gait in adolescents with and without structural spine deformities.

It has been hypothesized that the enhance trunk marker set:

1. is a valid method for the measurement of spine deformations in the sagittal, frontal and indirectly transverse planes.
2. is an applicable and reliable method for the measurement of spine dynamics during gait in healthy adolescents and in patients with structural deformities such as seen in scoliosis.
3. is sensitive enough to distinguish the spinal movement pattern during gait measured in scoliosis patients from the one measured in healthy adolescents.

To verify the hypotheses, the following measurements will be carried out:

* Biplanar radiographs (a-p and lateral) with radio-opaque markers in scoliosis patients.
* Instrumented gait analysis with a standard full body marker set and the enhanced trunk marker set in scoliosis patients and healthy controls.

Detailed Description

Dive into the extended narrative that explains the scientific background, objectives, and procedures in greater depth.

Conditions

See the medical conditions and disease areas that this research is targeting or investigating.

Scoliosis

Study Design

Understand how the trial is structured, including allocation methods, masking strategies, primary purpose, and other design elements.

Study Time Perspective

CROSS_SECTIONAL

Study Groups

Review each arm or cohort in the study, along with the interventions and objectives associated with them.

Scoliosis patients:

15 patients with adolescent idiopathic scoliosis.

No interventions assigned to this group

Control subjects:

15 adolescent healthy control subjects

No interventions assigned to this group

Eligibility Criteria

Check the participation requirements, including inclusion and exclusion rules, age limits, and whether healthy volunteers are accepted.

Inclusion Criteria

* Adolescent idiopathic scoliosis
* Able to walk a distance of minimum 50 meters barefoot and without any assistive device

Exclusion Criteria

* Other types of scoliosis (e.g. of neurological origin)
* Previous treatment of scoliosis (conservative or surgery)
* Injuries of the locomotor system which led to persistent deformities

Healthy controls:


* Any pathologies or diseases affecting the locomotor system
* Injuries to the locomotor system which led to persistent deformities
* Obesity (\> 95th BMI-per-age percentile)
* Leg length discrepancy (more than 1% of body height)
Minimum Eligible Age

10 Years

Maximum Eligible Age

18 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

Yes

Sponsors

Meet the organizations funding or collaborating on the study and learn about their roles.

Swiss Federal Institute of Technology

OTHER

Sponsor Role collaborator

Bern University of Applied Sciences

OTHER

Sponsor Role collaborator

University Children's Hospital Basel

OTHER

Sponsor Role lead

Responsible Party

Identify the individual or organization who holds primary responsibility for the study information submitted to regulators.

Prof. Reinald Brunner, MD

Doctor in Charge, Neuro-Orthopedics

Responsibility Role PRINCIPAL_INVESTIGATOR

Principal Investigators

Learn about the lead researchers overseeing the trial and their institutional affiliations.

Reinald Brunner, MD

Role: PRINCIPAL_INVESTIGATOR

University Children's Hospital Basel

Stefan Schmid, PT, PhD

Role: STUDY_CHAIR

Swiss Federal Institute of Technology / Bern University of Applied Sciences

Silvio Lorenzetti, PhD, DSc

Role: STUDY_DIRECTOR

Swiss Federal Institute of Technology

Jacqueline Romkes, PhD

Role: STUDY_DIRECTOR

University Children's Hospital Basel

Carol-Claudius Hasler, MD

Role: STUDY_DIRECTOR

University Children's Hospital Basel

Locations

Explore where the study is taking place and check the recruitment status at each participating site.

University Children's Hospital Basel

Basel, , Switzerland

Site Status

Countries

Review the countries where the study has at least one active or historical site.

Switzerland

References

Explore related publications, articles, or registry entries linked to this study.

Schmid S, Studer D, Hasler CC, Romkes J, Taylor WR, Brunner R, Lorenzetti S. Using Skin Markers for Spinal Curvature Quantification in Main Thoracic Adolescent Idiopathic Scoliosis: An Explorative Radiographic Study. PLoS One. 2015 Aug 13;10(8):e0135689. doi: 10.1371/journal.pone.0135689. eCollection 2015.

Reference Type RESULT
PMID: 26270557 (View on PubMed)

Schmid S, Studer D, Hasler CC, Romkes J, Taylor WR, Lorenzetti S, Brunner R. Quantifying spinal gait kinematics using an enhanced optical motion capture approach in adolescent idiopathic scoliosis. Gait Posture. 2016 Feb;44:231-7. doi: 10.1016/j.gaitpost.2015.12.036. Epub 2015 Dec 29.

Reference Type RESULT
PMID: 27004664 (View on PubMed)

Other Identifiers

Review additional registry numbers or institutional identifiers associated with this trial.

UKBB-Spine-1315-1

Identifier Type: -

Identifier Source: org_study_id