Validity and Reliability of High-Activity Arthroplasty Score

December 25, 2023 updated by: Emel Taşvuran Horata, Afyonkarahisar Health Sciences University

Turkish Validity and Reliability of High Activity Arthroplasty Score After Total Knee Arthroplasty

Patient-reported Outcome Measures (PROMs) used in total knee arthroplasty focus more on quality of life and pain. For this reason, individuals who can perform activities of daily living normally can get full points. There is a need for PROMs used in the assessment of higher functional skills. This study aimed to translate The High-Activity Arthroplasty Score (HAAS) into Turkish and to conduct a validity and reliability study of the Turkish version.

Study Overview

Status

Recruiting

Conditions

Intervention / Treatment

Detailed Description

Studies show that TKA practice has increased in the young population in recent years. Patient-reported Outcome Measures (PROMs) used in total knee arthroplasty focus more on quality of life and pain. For this reason, individuals who can perform activities of daily living normally can get full points. There is a need for PROMs used in the assessment of higher functional skills. This study aimed to translate The High-Activity Arthroplasty Score into Turkish and to conduct a validity and reliability study of the Turkish version. The adaptation of the questionnaire to Turkish in the study will be made according to the COSMIN and Reliability and Agreement Studies Reporting Guide. The construct validity, concurrent validity, reliability, and floor and ceiling effects of the questionnaire will be evaluated.

Study Type

Observational

Enrollment (Estimated)

70

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Study Locations

  • Turkey
      • Afyonkarahisar, Turkey, 03030
        • Recruiting
        • Emel Taşvuran Horata
        • Contact:
        • Principal Investigator:
          • Emel TAŞVURAN HORATA
        • Sub-Investigator:
          • Fatma EKEN
        • Sub-Investigator:
          • Murat YEŞİL
        • Sub-Investigator:
          • Özal ÖZCAN
      • Afyonkarahisar, Turkey, 03030
        • Recruiting
        • Afyonkarahisar Health Science University
        • Contact:

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 65 years (Adult, Older Adult)

Accepts Healthy Volunteers

No

Sampling Method

Non-Probability Sample

Study Population

Individuals who have undergone primary total knee arthroplasty surgery at least 6 months ago in the Orthopedics and Traumatology Outpatient Clinic will be included. Participants will be contacted via telephone.

Description

Inclusion Criteria:

  • To have undergone primary total knee arthroplasty for osteoarthritis at least 6 months ago,
  • To be between the ages of 18-65.

Exclusion Criteria:

  • Having orthopedic, neurological, cardiovascular, or cognitive problems that may affect physical performance,
  • Presence of previous lower extremity surgery

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
High-Activity Arthroplasty Score (HAAS)
Time Frame: 10 minutes
It consists of 4 sub-dimensions (walking, running, climbing stairs and activity level). 0 (min. score) -18 points (max. score) can be obtained from the survey. Higher score is associated with more functional ability
10 minutes

Collaborators and Investigators

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

Sponsor

Afyonkarahisar Health Sciences University

Investigators

  • Principal Investigator: EMEL TAŞVURAN HORATA, PhD, AFSU

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)

May 1, 2022

Primary Completion (Estimated)

December 1, 2025

Study Completion (Estimated)

December 1, 2025

Study Registration Dates

First Submitted

January 23, 2022

First Submitted That Met QC Criteria

January 23, 2022

First Posted (Actual)

January 27, 2022

Study Record Updates

Last Update Posted (Estimated)

December 27, 2023

Last Update Submitted That Met QC Criteria

December 25, 2023

Last Verified

December 1, 2023

More Information

Terms related to this study

Keywords

Other Study ID Numbers

  • 2022/2

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.

Clinical Trials on Arthroplasty Complications

Clinical Trials on High-Activity Arthroplasty Score (HAAS)

Search Similar Trials

Sponsors and Collaborators

Medical Conditions

Drug Interventions

CROs by country

CROs in Bangladesh

Conditions

Rare Diseases

Drug Interventions

Dietary Supplements

Sponsor/Collaborators

Locations

3
Subscribe