Crosscultural Adaptation And Validation Of The Italian Version Of The New Knee Society Knee Scoring System

Status

Recruiting

Phases

Unknown

Study type

Observational

Source

ClinicalTrials.gov

Registry ID

NCT06726629

Acronym

KSS-ITALIAN

Enrollment

200

Registered

2024-12-10

Start date

2024-11-01

Completion date

2026-11-30

Last updated

2025-12-26

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Knee Osteoarthritis

Keywords

KSS

Brief summary

The present study aims to be a multicenter prospective analysis aimed at validating the Italian version of the new KSS introduced in 2011 15. To do this it is first necessary to create the translation of the questionnaire. Several steps will be performed to obtain an adequate Italian version of the new KSS: 1. The English version of the KSS will be translated into Italian by 3 bilingual translators 2. The 2 versions will be submitted to the study collaborators (one per centre), the final version (accepted by all the study collaborators) will be translated back into English by 2 bilingual translators (native English) not aware of the initial version. The back translation will then be sent to the original author (Prof. Scott) to ensure that the consistency of the questionnaire has been maintained throughout all processes despite the necessary cultural adaptations. 3. Once the definitive version has been obtained, it will be tested by 300 Italian patients (with an estimated dropout of 20%) suffering from gonarthrosis. The patients will be distributed as follows: approximately 50 patients in each of the 6 centers (total 300). The number of patients was chosen considering approximately 17-18 patients for each of the 17 items, this choice is consistent with previously published studies on translation into other languages

Interventions

OTHERVersion Of The New Knee Society Knee Scoring System

All patients will be subjected to the same clinical and radiographic checks, the data of which will be collected in the different centres

Study design

Observational model

COHORT

Time perspective

PROSPECTIVE

Eligibility

Sex/Gender

ALL

Age

18 Years to 85 Years

Healthy volunteers

Inclusion criteria

* Diagnosis of gonarthrosis and indication for primary TKA surgery * Age between 18 and 85 years * Ability to respond to the proposed questionnaires and provide informed consent * Availability for follow-up for one year after surgery

Exclusion criteria

* Concomitant hip or spinal problems, understood as a cause of patient discomfort even if not yet undergoing medical or rehabilitation therapy * History of ipsilateral or contralateral knee surgery * Congenital knee deformities * Previous septic arthritis * Neuromuscular pathology (e.g. polio) * Simultaneous bilateral prosthesis or within 12 months of both knee, hip and ankle

Design outcomes

Primary

Measure	Time frame	Description
VALIDITY OF THE CONSTRUCT	at baseline (Day 0); post-operative (day 3), at 1 year follow-up	Comparison between the Italian version of the KSS and the tests already validated in Italian .In particular, the Pearson or Spearman coefficient (depending on the sample distribution) will be used to evaluate the correlation.

Countries

Italy

Contacts

Primary Contactgiulio maria marcheggiani muccioli, MD

0516366356

Backup Contacttosca cerasoli, MD

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026