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Investigation of Catastrophizing of Pain Reported by Parents in JIA Patients

H

Hacettepe University

Status

Enrolling

Conditions

Juvenile Idiopathic Arthritis (JIA)
Childhood Rheumatic Diseases

Treatments

Other: Questionnaire application for JIA cases and their parents

Study type

Observational

Funder types

Other

Identifiers

NCT07185750
SBA 25/530

Details and patient eligibility

About

Juvenile idiopathic arthritis (JIA) is the primary rheumatic disease reported to affect the pediatric population. Research suggests that parents' thoughts and feelings about their child's pain, specifically with JIA diagnosis, may influence treatment compliance. Considering that this situation may also affect children's adherence to treatment, the identification and management of parents' catastrophizing of pain is emphasized as important in improving treatment outcomes. This study aimed to examine the biopsychosocial characteristics of parents of children diagnosed with JIA according to their reported catastrophizing of pain.

Enrollment

50 estimated patients

Sex

All

Ages

7 to 18 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Between 7-18 years of age
  • Diagnosed with JIA
  • Individuals who volunteer to participate in the study will be included.

Exclusion criteria

  • Having advanced heart/lung/liver/kidney disease, neurological disease, or malignancies
  • Having undergone major orthopedic surgery
  • Not volunteering to participate in the study

Trial design

50 participants in 1 patient group

Cases diagnosed with JIA
Description:
JIA patients and their parents who visited the rheumatology outpatient clinic of a university hospital. A questionnaire will be administered to the child cases and their parents.
Treatment:
Other: Questionnaire application for JIA cases and their parents

Trial contacts and locations

1

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Central trial contact

Orkun Tüfekçi, PT, PhD(c)

Data sourced from clinicaltrials.gov

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