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Quantitative Sensory Testing in Juvenile Idiopathic Arthritis

Quantitative Sensory Testing in Juvenile Idiopathic Arthritis - QST in JIA

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
NL-OMON
Registry ID
NL-OMON40592
Enrollment
44
Registered
2014-01-10
Start date
2014-04-07
Completion date
Unknown
Last updated
2024-04-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Juvenile idiopathic arthritis juvenile rheumatoid arthritis

Interventions

None listed

Sponsors

Academisch Medisch Centrum
Lead Sponsor

Eligibility

Age
2 Years to 17 Years

Inclusion criteria

Inclusion criteria: Healthy controls will be matched to JIA patients based on age and sex. In order to be eligible to participate in this study, a patient must meet all of the following criteria: - From 6 to 17 years of age - Ability to speak Dutch -Be diagnosed with active JIA by their treating physician as defined by the ILAR-classification and patient reported pain rating greater than 10 (on a 0-100mm scale). - The most severe inflammation must be in the knee;Healthy controls must meet all of the following criteria: - From 6 to 17 years of age - Ability to speak Dutch

Exclusion criteria

Exclusion criteria: A potential subject who meets any of the following criteria will be excluded from participation in this study: In the case of patients: - When there is any serious injury to the body regions to be tested - Severe comorbidity including but not limited to cystic fibrosis, cancer, inflammatory bowel disease; history of drug or alcohol abuse; severe psychiatric disorder or dysfunction (e.g., major depression or generalized anxiety disorder) - Inability to understand the instructions;In the case of healthy controls: - When there is any serious injury to the body regions to be tested - Health problems requiring medical treatment, history of drug or alcohol abuse; severe psychiatric disorder or dysfunction (e.g., major depression or generalized anxiety disorder) - Inability to understand the instructions

Design outcomes

Primary

MeasureTime frame
Pain sensitivity levels of the QST battery: Pain thresholds for temperature (hot,cold), pinprick, pressure, temporal summation of pinprick (*wind-up*), and allodynia.

Secondary

MeasureTime frame
Detection sensitivity levels of the QST battery: temperature (warm, cold), mechanical, and vibration.

Countries

Netherlands

Outcome results

None listed

Source: NL-OMON (via WHO ICTRP)