Translation and Verification of English Lysholm Knee Scoring Scale

July 7, 2021 updated by: Peking University Third Hospital
Through the translation and verification of the Lysholm Knee Score Scale, a Chinese version of the Lysholm Knee Score Scale supported by experimental data was obtained. And on this basis, explore the knee joint score scale that fits the Chinese situation

Study Overview

Status

Completed

Conditions

Intervention / Treatment

Detailed Description

Lysholm Knee Scoring Scale needs to be translated and back translated into Chinese version of Lysholm Knee Scoring Scale. Through data collection and analysis, the reliability, validity and sensitivity of the Chinese version of the Lysholm Knee Score Scale were studied, and on this basis, the advantages and disadvantages of the scale were analyzed, and a new knee score scale was developed based on the domestic situation.

Study Type

Observational

Enrollment (Actual)

92

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

  • China
    • Beijing
      • Beijing, Beijing, China, 100191
        • Peking University Third Hospital

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

18 years to 80 years (Adult, Older Adult)

Accepts Healthy Volunteers

N/A

Genders Eligible for Study

All

Sampling Method

Non-Probability Sample

Study Population

Through the diagnosis of MRI and clinicians, patients who are determined to be ligament rupture, patella dislocation, meniscus injury or total knee replacement surgery before and after surgery, the patient should have the ability to read or communicate with others normally, and the age range is 18-80 years old .

Description

Inclusion Criteria:

  • Patients with ruptured ligaments, dislocation of the patella, meniscus injury or total knee replacement before and after surgery, and have the ability to read or communicate with others normally.

Exclusion Criteria:

  • Patients with other injuries to the joints of the lower limbs, or patients who do not have the ability to read or communicate with others normally.

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

  • Observational Models: Other
  • Time Perspectives: Prospective

Cohorts and Interventions

Group / Cohort
Intervention / Treatment
pre-operation
Within one month before operation of diagnoses with a ligament rupture, patella dislocation, meniscus injury, or total knee replacement surgery
Other: no intervention
no intervention
early after operation
Within three months after operation of ligament rupture, patella dislocation, meniscus injury, or total knee replacement surgery
Other: no intervention
no intervention
lately after operation
within three months to one year after operation of ligament rupture, patella dislocation, meniscus injury, or total knee replacement
Other: no intervention
no intervention
healthy volunteers
Healthy people without abnormalities
Other: no intervention
no intervention

What is the study measuring?

Primary Outcome Measures

Outcome Measure
Measure Description
Time Frame
Chinese version of Lysholm Knee Score Scale
Time Frame: 1 year after operation
Chinese version of Lysholm Knee Score Scale
1 year after operation
IKDC Knee Joint Score Scale
Time Frame: 1 year after operation
IKDC Knee Joint Score Scale
1 year after operation

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

Peking University Third Hospital

Investigators

  • Study Chair: yingfang ao, M.D., Peking University Third Hospital

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)

April 1, 2017

Primary Completion (Actual)

April 11, 2017

Study Completion (Actual)

September 30, 2017

Study Registration Dates

First Submitted

June 28, 2021

First Submitted That Met QC Criteria

July 7, 2021

First Posted (Actual)

July 8, 2021

Study Record Updates

Last Update Posted (Actual)

July 8, 2021

Last Update Submitted That Met QC Criteria

July 7, 2021

Last Verified

July 1, 2021

More Information

Terms related to this study

Other Study ID Numbers

  • M2016001

Plan for Individual participant data (IPD)

Plan to Share Individual Participant Data (IPD)?

Undecided

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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