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Completed

NCT Number: NCT03892135

Representation and Medication Use in Juvenile Idiopathic Arthritis

According to the International League of Associations for Rheumatology classification, Juvenile Idiopathic Arthritis (JIA) comprises a heterogeneous group of arthritis of unknown cause and with onset before 16 years of age, characterized by joint inflammation lasting for 6 or more weeks. Few studies exist regarding the care experience of children affected by this rheumatic condition. On the other hand, methotrexate and biologics constitute the primary treatment for children with JIA. As with adults undergoing the same treatment, adherence is critical. Difficulties for children to take the drugs have been reported. Notwithstanding, if adherence promotion in pediatric chronic conditions has been the subject of recommendations with regard to care management, the investigators lack information to understand the grounds for adherence specifically in JIA. In order to understand and decipher the parent-child adherence mechanisms and practices, the RUMAJI study will be conducted. Indeed, improving the relational approach between children and their caregivers as well as unrestricted drug adherence involves researching and understanding how appropriation of the disease and treatment could be achieved.

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Key information

Age range

1 year–17 year

Sex eligibility

All sexes

Study type

Observational

Primary location

Uhmontpellier

Montpellier, 34295, France

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • all JIA forms
  • all treatment type (NSAIDs, MTX, bDMARDs)

Exclusion criteria

  • none

Treatment and study plan

Interviews with parents of children with juvenile idiopathic arthritis

Other

Interviews with parents of children with juvenile idiopathic arthritis

Interviews with children with juvenile idiopathic arthritis

Other

Interviews with children with juvenile idiopathic arthritis

Interviews with Physicians

Other

Interviews with Physicians

Primary outcomes

  1. Interview with parents

    Time frame: 1 day

    Interview with parents to learn about role of parents in the management of juvenile idiopathic arthritis in their children

Secondary outcomes

  1. Interview with children

    Time frame: 1 day

    Interview with children to learn about role of children in the management of their juvenile idiopathic arthritis

  2. Interview with physicians

    Time frame: 1 day

    Interview with physicians to learn about role of physicians in the management of juvenile idiopathic arthritis

Sponsors and collaborators

Lead sponsor

University Hospital, Montpellier

Other

Collaborators

  • NORDIC pharma (funding)
  • Research department, unknowns, Strategic & innovation consulting, Paris (anthropologists)

Registry information

Official study title

Representation and Medication Use in Juvenile Idiopathic Arthritis - RUMAJI

Acronym: RUMAJI

Important dates

Study start
2017
Primary completion
2017
Study completion
2017
First posted
Mar 27, 2019
Registry last updated
Apr 29, 2019

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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