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NCT06226012 Clinical Trial

Effect of Pulsed Magnetic Field Versus Low Level Laser Therapy on Functional Performance in Children With Juvenile Idiopathic Arthritis

Juvenile Idiopathic Arthritis Clinical Trial

Official title:
Effect of Pulsed Magnetic Field Versus Low Level Laser Therapy on Functional Performance in Children With Juvenile Idiopathic Arthritis

Clinical Trial Details — Status: Completed

Administrative data
NCT number NCT06226012
Other study ID # EG,KFS lab Research 00
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date May 1, 2023
Est. completion date August 1, 2023

Study information
Verified date January 2024
Source Kafrelsheikh University
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

the purpose of this study is to compare between the effect of pulsed magnetic field versus low level laser therapy on functional performance in children with juvenile idiopathic arthritis

Description:

This study directed to investigate effect of pulsed magnetic field versus low level laser therapy on functional performance in children with juvenile idiopathic arthritis children with juvenile idiopathic arthritis suffer from some problems such as pain, swelling and limited motion in knee joints here in this study i used these devices to help in solving these problems pain was measured by visual analogue scale swelling was measured by tape measurement and Range of motion was measured by digital geniometre

Recruitment information / eligibility
Status Completed
Enrollment 40
Est. completion date August 1, 2023
Est. primary completion date August 1, 2023
Accepts healthy volunteers No
Gender All
Age group 8 Years to 16 Years
Eligibility Inclusion Criteria: - 1 Confirmed diagnosis of Juvenile Idiopathic Arthritis (JIA). - 2 Polyarticular onset of JIA with bilateral involvement of the knee joint. - 3 Age between 8 and 16 years - 4 Stable conditions (i.e., receive stable doses of medications in the past three months). - 5 Not participating in a regular exercise program in the past six months. Exclusion Criteria: - 1 Fixed deformities - 2 History of joint surgery - 3 Ankylosing or fractures - 4 Bone destruction ( erosive changes of the knee joints ).

Study Design

Related Conditions & MeSH terms

Intervention

Device:
• pulsed magnetic field
Children in this group received pulsed magnetic therapy in addition to traditional exercise program
• Low level laser
Children in this group received low level laser therapy in addition to traditional exercise program

Locations
Country Name City State
Egypt Physical Therapy Kafr Ash Shaykh Kafr Elsheikh

Sponsors (1)
Lead Sponsor Collaborator
Shrouk Abd Elmohsen Taha Basiony Elnhrawy

Country where clinical trial is conducted

Egypt, 

Outcome
Type Measure Description Time frame Safety issue
Primary Swelling We used Tape Measurement to measure Swelling 3 months
Primary Sensation of Pain we used Visual Analogue Scale (VAS) to measure pain. the scale ranged from 0 to 10. ( 0 means no pain and 10 means maximum pain 3 months
Primary Range of motion we used digital geniometer to measure range of motion 3 months
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