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Recruiting NCT07602595

The BRIDGE Pain Study

Observational Juvenile Idiopathic Arthritis (JIA) Fibromyalgia Lupus Scoliosis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Not applicable- observational study.
Who it may be relevant to
Registry conditions: Juvenile Idiopathic Arthritis (JIA), Fibromyalgia, Lupus, Scoliosis. Basic parameters: 14 years — 26 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Biopsychosocial Risk Influences on the Development and Generation of Early-Onset Chronic Pain

Overview

The purpose of the study is to discover at least two distinct Musculoskeletal pain subtypes. These types are caused by different brain-and-immune system signals that affect how the body feels pain, and they are also shaped by a person's biology, psychology, and social environment. Aim 1. We want to sort adolescents and young adults with long lasting muscle and bone pain into two different groups. To do this, we will look at participants' childhood medical histories, past treatments, when their pain started, the sex they were assigned at birth, what their pain feels like now, tests of how their body senses pain, and immune system markers found in their blood. We think we will find at least two different types of chronic pain groups, plus one group of patients who had a higher risk for pain (because of a rheumatic disease or past surgery) but never developed long term pain. Aim 2. We want to find out if certain patterns of inflammation in the body change how nerve cells react to pain. Aim 3: We want to understand how different biological, psychological, and social factors are connected to the chronic pain groups we identified. We think we will find certain mental, behavioral, and social risks-as well as protective factors-that help explain why some people develop long-lasting pain and others do not. We expect these factors to play different roles in each pain group, including the group that does not develop chronic pain.

Interventions

  • Other Not applicable- observational study
    This is an observational study. No intervention is present.

Primary outcome measures

  • Conditioned Pain Modulation (CPM) Profile (Pressure) [Time frame: Baseline]
  • Conditioned Pain Modulation (CPM) Profile (Heat) [Time frame: Baseline]
  • Temporal Summation (TS) Profile [Time frame: Baseline]

Eligibility criteria

Inclusion criteria

  • Diagnosis of rheumatic/autoimmune disease/pain condition or surgery prior to age 18; Current age 14 to 26 years; Participant (and parent/legal guardian of participants < 18 yo) can read and write in English; At least 1 year from diagnosis of pain or rheumatic disease; For individuals with MSK surgical history, at least 1 year after initial surgical intervention; For individuals with rheumatic disease, their disease must be considered inactive

Exclusion criteria

  • They have active disease, or Other major medical comorbidities have developed after surgery following MSK surgical intervention.

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Observational model
Cohort

Study locations

United States · 1 center
  • Cincinnati Children's Hospital — Cincinnati

Identifiers

NCT: NCT07602595 · BRIDGE Pain · 1UC2AR086503

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗