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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT06197074
Other study ID # 2023/8
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date December 25, 2023
Est. completion date December 25, 2025

Study information

Verified date January 2024
Source Afyonkarahisar Health Sciences University
Contact ERDAL HORATA, PhD
Phone +905056092631
Email erdalhorata@gmail.com
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Studies have reported that individuals with Rheumatoid Arthritis have a smaller muscle cross-sectional area, pennation angle and muscle thickness than healthy controls. Sarcopenia may decrease physical performance and quality of life in individuals with RA. Therefore, morphologic changes in the quadriceps femoris muscle due to sarcopenia may help us to gain insight into physical function and quality of life. This study aims to evaluate the predictive capacity of morphologic characteristics of the quadriceps femoris muscle for disease activity, physical performance, and quality of life in women with Rheumatoid Arthritis.


Description:

Studies have reported that individuals with Rheumatoid Arthritis have a smaller muscle cross-sectional area, pennation angle and muscle thickness than healthy controls. Sarcopenia may decrease physical performance and quality of life in individuals with RA. Therefore, morphologic changes in the quadriceps femoris muscle due to sarcopenia may help us to gain insight into physical function and quality of life. This study aims to evaluate the predictive capacity of morphologic characteristics of the quadriceps femoris muscle for disease activity, physical performance, and quality of life in women with Rheumatoid Arthritis. Within the scope of the study, the morphological characteristics of the quadriceps muscle of the participants will be evaluated by a Physical Medicine and Rehabilitation specialist physician via ultrasound. After appropriate visualization, the image will be captured and saved in JPEG format, and will be exported to the ImageJ program for further analysis and evaluations will be performed by an anatomist. Assessments of quality of life and physical performance will be made by a physiotherapist involved in the study.


Recruitment information / eligibility

Status Recruiting
Enrollment 102
Est. completion date December 25, 2025
Est. primary completion date December 25, 2025
Accepts healthy volunteers No
Gender Female
Age group 18 Years to 60 Years
Eligibility Inclusion Criteria: - 18-60 years old - Female participants with a confirmed diagnosis of RA for at least 3 years according to the 2010 American College of Rheumatology (ACR) criteria - Presence of sarcopenia Exclusion Criteria: - Presence of fractures, burns or lesions in the area to be measured - Presence of any neuromuscular, cardiovascular or metabolic disease, - Individuals with knee endoprosthesis, - Inability to walk

Study Design


Related Conditions & MeSH terms


Intervention

Other:
Ultrasound assessment
The morphological characteristics of the quadriceps muscle of the participants will be assessed using ultrasound.

Locations

Country Name City State
Turkey Afyonkarahisar Health Sciences University Afyonkarahisar

Sponsors (1)

Lead Sponsor Collaborator
Afyonkarahisar Health Sciences University

Country where clinical trial is conducted

Turkey, 

Outcome

Type Measure Description Time frame Safety issue
Primary Vastus lateralis muscle length Vastus Lateralis muscle length will be measured bilaterally by Ultrasound. 10 minutes
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