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Completed

NCT Number: NCT06226012

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

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

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Key information

Age range

8 year–16 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

Physical Therapy

Kafr ash Shaykh, Kafr Elsheikh, Egypt

About this study

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

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 ).

Treatment and study plan

pulsed magnetic field

Device

Children in this group received pulsed magnetic therapy in addition to traditional exercise program

Low level laser

Device

Children in this group received low level laser therapy in addition to traditional exercise program

Primary outcomes

  1. Swelling

    Time frame: 3 months

    We used Tape Measurement to measure Swelling

  2. Sensation of Pain

    Time frame: 3 months

    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. Range of motion

    Time frame: 3 months

    we used digital geniometer to measure range of motion

Sponsors and collaborators

Lead sponsor

Shrouk Abd Elmohsen Taha Basiony Elnhrawy

Other

Registry information

Important dates

Study start
2023
Primary completion
2023
Study completion
2023
First posted
Jan 26, 2024
Registry last updated
Jan 26, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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