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Exercise and Body Composition in Juvenile Idiopathic Arthritis (Joint Fitness)

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Johns Hopkins University

Status

Completed

Conditions

Arthritis, Juvenile

Treatments

Other: Dual-Emission X-ray Absorptiometry (DEXA) scan
Other: Ren-Ex Machine
Other: Sub-maximal test
Other: Quality of life questionnaires
Other: Biodex dynamometer

Study type

Interventional

Funder types

Other
NIH

Identifiers

NCT02479373
NA00071505
5R21AR062269-02 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This research is being done to see if resistance exercise (RE) is safe and has a positive effect on children and young adults with juvenile idiopathic arthritis (JIA).

JIA is an inflammatory autoimmune disease that can cause severe impairment and disability. JIA can cause bone loss and decreased muscle strength. The medications used to treat JIA can also have negative effects on growth and development, strength, and ability to function. RE is performing movements in a slow and controlled fashion (i.e., no speeding up or using force in the lifting and lowering of the weight) to lessen force on the joints and tissues. This study will be using Ren-Ex exercise equipment to perform RE.

Currently the American College of Rheumatology recommends exercise for patients with arthritis. This exercise includes range of motion exercise to protect joint mobility as well as low resistance and aerobic exercise (AE) to protect muscle mass, bone health, and fitness. However, a recent study showed no major differences in functionality or quality of life between patients who performed AE and those who did not perform AE. There is a need for more data on the impact of RE on children with JIA. Children and young adults aged 10 to 21 with juvenile idiopathic arthritis may join.

Enrollment

33 patients

Sex

All

Ages

10 to 21 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • American College of Rheumatology criteria for polyarticular JIA
  • Stable medical therapy

Exclusion criteria

  • Non-English speaking
  • Pregnancy
  • Currently breast feeding
  • Cognitive impairment as determined by PI (patient is not responsible for making their own health care decisions)

Trial design

33 participants in 2 patient groups

Resistance Exercise (RE)
Experimental group
Description:
Those assigned to RE will complete baseline and post-testing assessments and participate in 12 weeks of individually-supervised resistance exercise, which will take place in the exercise facility on the Johns Hopkins Bayview Medical Center Campus. Exercises will be performed on Ren-Ex Machines. This equipment is suitable for the proposed study because it provides ultra-low friction movement which creates a personalized resistance profile, which minimizes force on joints and thereby reduces the risk of joint trauma and injury.
Treatment:
Other: Biodex dynamometer
Other: Dual-Emission X-ray Absorptiometry (DEXA) scan
Other: Sub-maximal test
Other: Ren-Ex Machine
Other: Quality of life questionnaires
Control Group (CG)
Other group
Description:
Those assigned to the CG will complete baseline and post-testing assessments and will also be given JIA educational materials, including physical activity and exercise recommendations from the American Academy of Pediatrics (AAP) Council on Sports Medicine and Fitness (COSMF).
Treatment:
Other: Biodex dynamometer
Other: Dual-Emission X-ray Absorptiometry (DEXA) scan
Other: Sub-maximal test
Other: Quality of life questionnaires

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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