- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT04230733
Pelvis Displacement and Gait Indicators in Patient With Lumbar Disc Herniation
January 13, 2020 updated by: In-Hyuk Ha, KMD, Jaseng Medical Foundation
Correlation Analysis of Pelvis Displacement and Gait Indicators in Patient With Lumbar Disc Herniation : Retrospective Study Using Electronic Medical Record Data
The purpose of this study is to investigate the correlation between pattern of gait and pelvic displacement in patients with lumbar disc herniation.
Study Overview
Status
Completed
Conditions
Detailed Description
Walking is a repetitive movement that moves your body while keeping your posture stable.
The pelvis is located between the hip and lumbar region, where many muscles are attached to regulate the movement of the hip and lumbar spine.
Asymmetrical pelvic alignment affects stability of the lower extremities and trunk, making normal walking difficult.
The purpose of this study is to investigate the pattern of gait according to pelvic displacement in patients with lumbar disc herniation.
Study Type
Observational
Enrollment (Actual)
114
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Locations
-
-
Gangnam-Gu
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Seoul, Gangnam-Gu, Korea, Republic of, 135-896
- Jaseng Hospital of Korean Medicine
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Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
20 years and older (ADULT, OLDER_ADULT)
Accepts Healthy Volunteers
No
Genders Eligible for Study
All
Sampling Method
Non-Probability Sample
Study Population
Patients who are admitted to Jaseng Hospital of Korean Medicine and got gait analysis
Description
Inclusion Criteria:
- Lumbar intervertebral disc herniation as confirmed by a doctor of medicine or a doctor of Korean medicine through an MRI
- Patient who got gait analysis
Exclusion Criteria:
- Patients without MRI and X-ray
- Patient diagnosed with ankle disease
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Correlation between pelvic displacement and gait parameters
Time Frame: A week after data collected
|
<Pelvic displacement>
<Gait parameters> Step, Stance phase, Swing phase, Single support, Double support, Step time, Stride, Cadence, Load response, Pre swing, Gait cycle, Speed, Acceleration, contact phase, foot flat, propulsive, PCI |
A week after data collected
|
Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Numeric Rating Scale
Time Frame: A week after data collected
|
Using NRS-11(0 to 10) which is measured at first visit
|
A week after data collected
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Sponsor
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (ACTUAL)
August 20, 2019
Primary Completion (ACTUAL)
September 30, 2019
Study Completion (ACTUAL)
September 30, 2019
Study Registration Dates
First Submitted
November 13, 2019
First Submitted That Met QC Criteria
January 13, 2020
First Posted (ACTUAL)
January 18, 2020
Study Record Updates
Last Update Posted (ACTUAL)
January 18, 2020
Last Update Submitted That Met QC Criteria
January 13, 2020
Last Verified
November 1, 2019
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- JS-CT-2018-08
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
NO
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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-
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